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American College of Critical Care Medicine Clinical Practice Parameters for Hemodynamic Support of Pediatric and Neonatal Septic Shock

Davis, Alan L. MD, MPH, FAAP, FCCM1; Carcillo, Joseph A. MD2; Aneja, Rajesh K. MD2; Deymann, Andreas J. MD3; Lin, John C. MD4; Nguyen, Trung C. MD5; Okhuysen-Cawley, Regina S. MD, FAAP5; Relvas, Monica S. MD, FAAP, MSHA, FCCM6; Rozenfeld, Ranna A. MD, FCCM7; Skippen, Peter W. MD, MBBS, FRCPC8; Stojadinovic, Bonnie J. DNP, CPNP9; Williams, Eric A. MD, MS, MMM10; Yeh, Tim S. MD, MCCM11; Balamuth, Fran MD12; Brierley, Joe MD, MA13; de Caen, Allan R. MD14; Cheifetz, Ira M. MD, FCCM15; Choong, Karen MSc, MB, Bch16; Conway, Edward Jr MD, MS, FCCM17; Cornell, Timothy MD18; Doctor, Allan MD19; Dugas, Marc-Andre MD, MSc20; Feldman, Jonathan D. MD21; Fitzgerald, Julie C. MD, PhD22; Flori, Heidi R. MD23; Fortenberry, James D. MD, MCCM24; Graciano, Ana Lia MD, FAAP, FCCM25; Greenwald, Bruce M. MD, FAAP, FCCM26; Hall, Mark W. MD, FCCM27; Han, Yong Yun MD28; Hernan, Lynn J. MD29; Irazuzta, Jose E. MD, FCCM30; Iselin, Elizabeth MD31; van der Jagt, Elise W. MD, MPH, FAAP, SFHM32; Jeffries, Howard E. MD, MBA33; Kache, Saraswati MD34; Katyal, Chhavi MD35; Kissoon, Niranjan (Tex) MD, MCCM, FCCM36; Kon, Alexander A. MD, FCCM37; Kutko, Martha C. MD, FCCM38; MacLaren, Graeme MD, FCCM39–41; Maul, Timothy PhD42; Mehta, Renuka MD, MBBS, FAAP43; Odetola, Fola MD, MPH44; Parbuoni, Kristine BCPS, PharmD45; Paul, Raina MD46; Peters, Mark J. MD, PhD47; Ranjit, Suchitra MD, FCCM48; Reuter-Rice, Karin E. PhD, CPNP-AC, FCCM49; Schnitzler, Eduardo J. MD50; Scott, Halden F. MD51; Torres, Adalberto Jr MD, MS, FCCM52; Weingarten-Abrams, Jacki MD53; Weiss, Scott L. MD24; Zimmerman, Jerry J. MD, PhD, FCCM54; Zuckerberg, Aaron L. MD55,56

doi: 10.1097/CCM.0000000000002425
Special Article

Objectives: The American College of Critical Care Medicine provided 2002 and 2007 guidelines for hemodynamic support of newborn and pediatric septic shock. Provide the 2014 update of the 2007 American College of Critical Care Medicine “Clinical Guidelines for Hemodynamic Support of Neonates and Children with Septic Shock.”

Design: Society of Critical Care Medicine members were identified from general solicitation at Society of Critical Care Medicine Educational and Scientific Symposia (2006–2014). The PubMed/Medline/Embase literature (2006–14) was searched by the Society of Critical Care Medicine librarian using the keywords: sepsis, septicemia, septic shock, endotoxemia, persistent pulmonary hypertension, nitric oxide, extracorporeal membrane oxygenation, and American College of Critical Care Medicine guidelines in the newborn and pediatric age groups.

Measurements and Main Results: The 2002 and 2007 guidelines were widely disseminated, translated into Spanish and Portuguese, and incorporated into Society of Critical Care Medicine and American Heart Association/Pediatric Advanced Life Support sanctioned recommendations. The review of new literature highlights two tertiary pediatric centers that implemented quality improvement initiatives to improve early septic shock recognition and first-hour compliance to these guidelines. Improved compliance reduced hospital mortality from 4% to 2%. Analysis of Global Sepsis Initiative data in resource rich developed and developing nations further showed improved hospital mortality with compliance to first-hour and stabilization guideline recommendations.

Conclusions: The major new recommendation in the 2014 update is consideration of institution—specific use of 1) a “recognition bundle” containing a trigger tool for rapid identification of patients with septic shock, 2) a “resuscitation and stabilization bundle” to help adherence to best practice principles, and 3) a “performance bundle” to identify and overcome perceived barriers to the pursuit of best practice principles.

1No institution affiliation.

2Department of Critical Care Medicine and Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA.

3Department of Pediatric Critical Care, Riley Hospital for Children, Indiana University, IN.

4Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.

5Department of Pediatrics, Baylor College of Medicine/Texas Children’s Hospital, Houston, TX.

6Pediatric Critical Care Medicine, Covenant Women and Children’s Hospital, Texas Tech University, Lubbock, TX.

7Division of Pediatric Critical Care Medicine, Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL.

8Division of Pediatric Critical Care, University of British Columbia, Vancouver, BC, Canada.

9Division of Pediatric Critical Care Medicine, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI.

10Department of Pediatrics, Baylor College of Medicine, Houston, TX.

11Department of Pediatrics, Saint Barnabas Medical Center, Livingston, NJ.

12Division of Emergency Medicine and Center for Pediatric Clinical Effectiveness, University of Pennsylvania Perelman School of Medicine, Children’s Hospital of Philadelphia, Philadelphia, PA.

13Intensive Care & Bioethics, Great Ormond St Hospital for Sick Children, London, United Kingdom.

14Pediatric Critical Care Medicine, Department of Pediatrics, Stollery Children’s Hospital/University of Alberta, Edmonton, AB, Canada.

15Division of Pediatric Critical Care Medicine, Department of Pediatrics, Duke Children’s, Durham, NC.

16Departments of Pediatrics and Critical Care, Clinical Epidemiology and Biostatistics, McMaster University, Pediatric Intensive Care Unit, McMaster Children’s Hospital, Hamilton, ON, Canada.

17Beth Israel Medical Center, Hartsdale, NY.

18Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI.

19Departments of Pediatrics and Biochemistry, Washington University in Saint Louis School of Medicine, Saint Louis, MO.

20Department of Pediatrics, Centre mère-enfant Soleil du CHU de Québec-Université Laval, Québec City, QC, Canada.

21Department of Inpatient Pediatrics, Kaiser Santa Clara Medical Center, Santa Clara, CA.

22Department of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Children’s Hospital of Philadelphia, Philadelphia, PA.

23Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Mott C.S. Children’s Hospital, Ann Arbor, MI.

24Division of Critical Care, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.

25Department of Pediatrics-Critical Care Medicine, University of Maryland School of Medicine, Baltimore, MD.

26Division of Pediatric Critical Care Medicine, Weill Cornell Medical College, New York, NY.

27Division of Critical Care Medicine, Department of Pediatrics, Nationwide Children’s Hospital, Columbus, OH.

28Department of Critical Care Medicine, Children’s Mercy Hospital, Kansas City, MO.

29Department of Pediatrics, Texas Tech University Health Sciences Center, El Paso, TX.

30Division of Pediatric Critical Care, University of Florida, Jacksonville, FL.

31Bon Secours St. Mary’s Hospital, Glen Allen, VA.

32Division of Pediatric Critical Care, Department of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY.

33Department of Pediatrics, University of Washington School of Medicine, Seattle, WA.

34Division of Critical Care, Department of Pediatrics, Stanford University School of Medicine, Palo Alto, CA.

35Pediatric Critical Care Medicine, The Children’s Hospital at Montefiore, The Pediatric Hospital for Albert Einstein College of Medicine, Bronx, NY.

36Department of Pediatrics, University of British Columbia, UBC & BC Children’s Hospital Professor in Critical Care—Global Child Health, Vancouver, BC, Canada.

37Department of Pediatrics, Naval Medical Center San Diego and University of California San Diego School of Medicine, San Diego, CA.

38Department of Pediatrics and Pediatric Critical Care Medicine, The Valley Hospital, Ridgewood, NJ.

39Cardiothoracic ICU, National University Hospital, Singapore.

40Paediatric ICU, The Royal Children’s Hospital, Melbourne, Australia.

41Department of Paediatrics, University of Melbourne, Melbourne, Australia.

42Children’s Hospital of Pittsburgh, Pittsburgh, PA.

43Department of Pediatrics, Medical College of Georgia at Augusta University, Augusta, GA.

44Division of Critical Care Medicine, Department of Pediatrics, University of Michigan, Ann Arbor, MI.

45Department of Pharmacy Practice, Loma Linda University School of Pharmacy, Loma Linda, CA.

46Division of Emergency Medicine, Ann and Robert Lurie Children’s Hospital of Chicago, Feinberg School of Medicine at Northwestern University, Chicago, IL.

47UCL Great Ormond Street Institute of Child Health and Paediatric Intensive Care Unit, Great Ormond Street Hospital for Children, NHS Trust, London, United Kingdom.

48Pediatric Intensive Care and Emergency Services, Apollo Children’s Hospital, Chennai, India.

49Division of Pediatric Critical Care, Department of Pediatrics, Duke University School of Nursing and School of Medicine, Durham, NC.

50Pediatrics School of Medicine, Austral University, Pcia de Buenos Aires, Argentina.

51Departments of Pediatrics and Emergency Medicine, University of Colorado School of Medicine, Aurora, CO.

52Critical Care and Transport, Nemours Children’s Hospital, Orlando, FL.

53Department of Pediatrics, Critical Care Medicine, Albert Einstein College of Medicine, Bronx, NY.

54Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Washington School of Medicine, Seattle, WA.

55Departments of Pediatrics & Anesthesiology, Sinai Hospital/NAPA, Baltimore, MD.

56Department of Pediatrics, University of Maryland Medical School, Baltimore, MD.

Group leaders and subgroups are identified in Appendix 1.

Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal’s website (

The American College of Critical Care Medicine (ACCM), which honors individuals for their achievements and contributions to multidisciplinary critical care medicine, is the consultative body of the Society of Critical Care Medicine (SCCM) that possesses recognized expertise in the practice of critical care. The College has developed administrative guidelines and clinical practice parameters for the critical care practitioner. New guidelines and practice parameters are continually developed, and current ones are systematically reviewed and revised.

Dr. Davis served as an expert witness regarding a patient who herniated post operatively. Dr. Aneja received funding from UpToDate royalties. Dr. Relvas participates in AAP PrepICU (editorial board member). Dr. Williams participates in American Academy of Pediatrics (guidelines committee work). Dr. Yeh participates in American Academy of Pediatrics (guidelines committee work). Dr. Brierley received funding from Astellas Pharmaceuticals Speakers Bureau (regarding anti-fungals in the ICU). He participates as a member in the American Academy of Pediatrics, Academic Pediatric Association, and Society for Academic Emergency Medicine. Dr. de Caen participates in the Royal College of Physicians and Surgeons of Canada and the American Heart Association. Dr. Cheifetz received funding from Philips (medical advisor) and Ikaria (medical advisor). He participates in various volunteer activities for AARC and ATS, and he has served as an expert witness for testimony for medical malpractice cases. Dr. Choong participates as an Executive Member of the Canadian Critical Care Trials Group, and is an employee of the Hamilton Health Sciences. Dr. Conway participates as Chair of Section on Pediatric CCM for the AAP. He has served as an expert witness for pediatric CCM/ED defense cases. Dr. Cornwell received grant funding from the Coulter Foundation. He participates in the Society of Pediatric Research. Dr. Doctor received funding from consulting for Novartis, Galera Pharmaceuticals, and Terumo BCT. Dr. Fortenberry participates in American Academy of Pediatrics, Extracorporeal Life Support Organization. He served as an expert witness for review of PICU cases and testimony in support of physicians providing PICU care. Dr. Greenwald served as an expert witness for testimony regarding course of illness and risk of mortality. Dr. Hall serves as the Editor for the ATS Online Journal Club. Dr. Irazuzta participates in the National Institutes of Health. Dr. van der Jagt received grant funding from University of Rochester (employee/faculty). She participates in NYS Emergency Medical Services for Children Advisory Committee (Vice-Chair); University of Rochester School of Medicine (faculty); AHA Pediatric Advanced Life Support Advanced Life Support Writing Group (member); IPSO National Expert Advisory Committee (member); FAAP, Sr. Fellow Society of Hospital Medicine; and Fellow College of Pediatricians. Dr. Jeffries participates in AAP, Ped Cardiac Intensive Care Society, and ACC. Dr. Kache participates on the Global health Educators Committee in Association of Pediatric Program Directors, and on the Global Health Education Sub-Comittee in Consortium of Universities for Global Health. Dr. Kon participates as the President-elect for the American Society for Bioethics and Humanities. He disclosed he is a government employee. He has served as an expert witness for peds critical care and bioethics. Dr. MacLaren received funding from UpToDate (royalties). He participates in the Asia-pacific Chapter of ELSO (Chair) and the Pediatric Cardiac Intensive Care Society (Vice President). Dr. Maul received funding from consulting for Mallinkrodt, Thoratec, and Alung. He received grant funding. He participates in ASAIO (editor) and ELSO (committee member). Dr. Odetola participates as a member of the Sub-Board of Critical Care Medicine, American Board of Pediatrics. Dr. Parbuoni participates in the American Society of Health-System Pharmacists and California Society of Health-System Pharmacists. Dr. Reuter-Rice received funding from J & B Learning (textbook royalties). She received grant funding from RWJK. She participates in PNCB-IPN, AAN, and ISONG. Dr. Schnitzler participates in Sociedad Argentina de Terapia Intensiva, Sociedad Argentina de Calidad en Asistencia Sanitaria, and Instituto Técnico de Acreditación de Establecimientos Sanitarios. Dr. Torres received funding from Abbott Point of Care (speaker). He served as an expert witness for the defense paid for his time. Dr. Weiss received funding from honoraria to grand rounds lectures from ThermoFisher Scientific (but content of lecture was solely his own responsibility). He participates in AAP and Shock Society. The remaining authors have disclosed that they do not have any potential conflicts of interest.

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In 1998, the Institute of Medicine called for establishment of best practice guidelines across medicine. In 2002 and 2007, the American College of Critical Care Medicine (ACCM) Clinical Practice Parameters for Hemodynamic Support of Pediatric and Neonatal Shock (1, 2) were published in part to replicate the reported outcomes associated with implementation of “best clinical practices” (mortality rates of 0–5% in previously healthy [3–5] and 10% in chronically ill children with septic shock [5]). Of note, neonatal and pediatric severe sepsis outcomes were already improving prior to 2002 with the advent of neonatal and pediatric intensive care (reduction in mortality from 97% to 9%) (6–9) and were markedly better than in adults (9% compared with 28% mortality) (8). There are two purposes served by this 2014 update of these 2002/2007 Clinical Practice Parameters. First, this 2014 update examines and grades new studies performed to test the utility and efficacy of the 2007 recommendations. Second, this 2014 update examines and grades relevant new treatment and outcome studies to determine to what degree, if any, the 2007 guidelines should be modified.

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Clinical investigators and clinicians affiliated with the Society of Critical Care Medicine (SCCM) who had special interest in hemodynamic support of pediatric patients with sepsis volunteered to be members of the update task force. Subcommittees were formed to review the literature and make recommendations using Grading of Recommendations Assessment, Development and Evaluation methodology. A strong recommendation received the “number” grade 1 and a weak recommendation received the number grade 2. The strength of the literature used to support these number recommendations was given “letter” grades with A equals to multiple randomized controlled trials and at least one meta-analysis, B equals to one randomized controlled trial, C equals to cohort, case control studies, and D equals to expert opinion and case reports. There is common discordance between strength of recommendation and strength of literature providing impetus to study most all recommendations made. The recommendations are largely based on opinion regarding the systematic review by a number of subcommittees, with editorial decision regarding content done initially by group leaders, and ultimately by the chairperson.

The PubMed/Medline/Embase literature (2006–2014) was searched by the SCCM librarian using the keywords: sepsis, septicemia, septic shock, endotoxemia, persistent pulmonary hypertension, nitric oxide, extracorporeal membrane oxygenation (ECMO), and ACCM guidelines in the newborn and pediatric age groups who identified 3,382 potential references. The search was refined by each of the subgroup leaders to identify studies specifically relevant to children and newborns (n = 143; see supplement for CONSORT, Supplemental Digital Content 1, The group members were asked to change the recommendations from 2007 in the new 2014 update only if there was new pediatric evidence since 2007 that warranted such change. The committee members graded all old and new recommendations (see above) because different systems had been used in the prior 2002 or 2007 documents. Due to the diverse, multidisciplinary, international composition of the SCCM membership, and the document’s task force committee members, this update continues to follow the lead of the previous guidelines making recommendations on hemodynamic support medications which may or may not be approved by the U.S. Food and Drug Administration, but which are approved and used in other nations, such as levosimendan, terlipressin, and enoximone.

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Evolution of the 2002, 2007, and 2014 Guidelines

Many studies have tested the observations and recommendations of the 2002 and 2007 guidelines (1, 2). Studies in the resource rich setting, where mechanical ventilators, IV infusion pumps, inotrope medications, and intensive care monitoring are available, have uniformly favored use of the ACCM/Pediatric Advanced Life Support (PALS) guidelines. Han et al (10) showed an association between early use of practice consistent with the 2002 guidelines in the community hospital and improved outcomes in newborns and children (mortality rate 8% vs 38%; number needed to treat = 3.3). Every hour that went by without restoration of normal blood pressure for age and capillary refill less than 3 seconds was associated with a two-fold increase in adjusted mortality odds ratio (10). Ninis et al (11) similarly reported an association between delay in inotrope resuscitation and a 22.6-fold increased adjusted mortality odds ratio in meningococcal septic shock which led to the new guideline recommendation in 2007 that inotropes be started through peripheral infusion in children with fluid-refractory septic shock until central access is attained. Ventura et al (12) tested this 2007 recommendation in a randomized trial and found that use of peripheral adrenaline infusion reduced mortality to 7% compared with 20% with use of peripheral dopamine infusion until central access was attained. de Oliveira et al (13) reported in a randomized trial that use of the 2002 guidelines with continuous central venous oxygen saturation (ScVO2) monitoring and therapy directed to maintenance of ScVO2 greater than 70%, reduced mortality from 39% to 12% (NNT = 3.6) compared with therapy directed only to blood pressure and capillary refill. Sankar et al (14) corroborated this finding in a cohort study in a population of Indian children showing that directing therapy to ScVO2 was associated with improved outcome with a number needed to treat equals to five. In a before and after study, Karapinar et al (15) reported that implementation of the 2002 guidelines in a U.S. tertiary center achieved best practice outcome with a fluid-refractory shock 28-day mortality of 3% and hospital mortality of 6% (3% in previously healthy children; 9% in chronically ill children). This outcome matched the “best practice outcomes” targeted by the 2002 guidelines (3–5). Similar to the experience of St. Mary’s Hospital before 2002 (4), Sophia Children’s Hospital in Rotterdam also reported a reduction in mortality rate from purpura and severe sepsis from 20% to 1% after implementation of 2002 guideline-based therapy in the referral center, transport system, and tertiary care settings (16). Both of these centers also used high flux continuous renal replacement therapy (CRRT) and fresh frozen plasma infusion directed to the goal of normal international normalized ratio (prothrombin time [PT]).

In contrast, the findings have been mixed in the “resource poor setting” where there is not access to mechanical ventilators, IV infusion pumps, inotrope medications, and intensive care monitoring. Wills et al (17) demonstrated near 100% survival when fluid resuscitation was provided to children with dengue shock in the first hour. In contrast, Maitland et al (18) (NEJM, 2011) found fluid boluses were harmful compared with maintenance IV fluid infusion and blood transfusion in severe malaria endemic sub-Saharan Africa. The Maitland study included a large population of children with severe malaria and anemia, and excluded cases with gastroenteritis or hypovolemia, whereas the Wills study only included a population of children with dengue shock, with capillary leak, hemoconcentration, and dehydration with gastroenteritis and hypovolemia. Importantly, neither of these studies formally tested fluid bolus use as recommended in the 2002 and 2007 ACCM guidelines because boluses were given without attention to the presence of rales and hepatomegaly in the patients, and without attention to electrolyte balance, or subsequent fluid removal as needed.

The 2002 and 2007 ACCM guidelines specifically recommend against fluid boluses when rales or hepatomegaly are present, instead recommend inotropic support for these patients (1, 2). The basic tenet of fluid resuscitation proposed in the ACCM guidelines is that “some do” and “some do not” require fluid resuscitation. Hypovolemic shock patients require fluid boluses, whereas euvolemic and hypervolemic patients do not. Severely anemic patients require blood transfusion, severely malnourished children require slow feeding, and patients with congestive heart failure or fluid overload require inotropes and diuretics, not fluid boluses.

There is general consensus among the committee members that these studies indirectly and directly support the utility and efficacy of implementation of the time-sensitive, goal-directed recommendations of the 2002 and 2007 ACCM/PALS guidelines in the “resource rich” setting. In this regard, since 2007 there has been a major effort in the United States to test the first-hour recommendations in pediatric academic centers in the American Academy of Pediatrics collaborative Septic Shock consortium which is dedicated to quality improvement in septic shock recognition and treatment. There have been four studies conducted in tertiary pediatric emergency departments that have examined adherence to ACCM/PALS guidelines for sepsis resuscitation in the first hour (19–22). Together, these studies demonstrated incomplete adherence to recommended goals for administration of IV fluids, antibiotics, and vasoactive agents. Subsequent quality-directed efforts from these studies showed improvement in both process metrics (e.g., decreased time to administration of IV fluids, antibiotics, and peripheral vasoactive agents) (19–22) and outcome metrics, including hospital and PICU length of stay and mortality (20–22). Importantly, all quality improvement studies were predicated on rapid identification of patients with suspected septic shock to trigger rapid clinician evaluation and implementation of appropriate resuscitation efforts. Multiple elements have been incorporated into trigger tools with success by several institutions (23, 24); however, there has been notable variation in the algorithms used at each institution, and none have sufficient evidence to fully endorse as a specific tool. Given the complexity of resource allocation and implementation, it seems reasonable that each institution could locally develop their trigger tool, whereas further studies refine the derivation and validation of an optimally sensitive and specific sepsis trigger tool (24).

From the best practice model standpoint, Paul et al (22) implemented a hospital-wide quality improvement initiative to improve compliance with all five elements of the ACCM/PALS guidelines first-hour recommendations: 1) recognition, 2) establishing IV access, 3) starting IV fluids and resuscitation as needed, 4) administering antibiotics, and 5) starting vasoactive agents if needed. Achievement of 100% compliance required a number of human interaction interventions including use of time clocks set to have time going from 0 to 60 minutes rather than from 60 to 0 minutes that resulted in an increase in number of cases between death occurrences (p < 0.05) with an overall reduction in hospital mortality from 4.0% to 1.7%.

Han et al (25) analyzed the international Global Sepsis Initiative database which included children from resource rich settings in Europe, North America, and South America in order to derive “three-element” bundles associated with improved outcomes. The first-hour/emergency department three-element bundle included 1) reversal of shock defined by normal blood pressure and capillary refill less than 3 seconds, 2) provision of antibiotics, and 3) provision of D10 and sodium containing IV fluid infusion. The stabilization/PICU three-element bundle included 1) reversal of shock defined by maintaining normal mean arterial pressure (MAP)-central venous pressure (CVP) for age and ScVO2 greater than 70%, 2) timely provision of the appropriate sensitive antibiotic and source control, and 3) maintenance of effective tidal volumes between 6 and 8 mL/kg in children mechanically ventilated with acute respiratory distress syndrome (ARDS). Reversal of shock was associated with use of the 2007 ACCM/PALS guidelines in both the resuscitation and stabilization bundles (2).

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Major New Recommendations in the 2014 Update

Due to the success of the 2002 and 2007 guidelines (1, 2), the 2014 update compilation and discussion of the new literature were directed to the question of what changes, if any, should be implemented in the update. The members of the committee were asked whether there are clinical practices which the “best outcome practices” are using in 2014 that are not recommended in the 2002 and 2007 guidelines and should be recommended in the 2014 guidelines? “The changes recommended were few. Most importantly, there was no change in emphasis between the 2002 guidelines and the 2014 update. The continued emphasis is directed to 1) first-hour fluid resuscitation and inotrope therapy directed to goals of threshold heart rates, normal blood pressure, and capillary refill less than or equal to 2 seconds with specific evaluation after each bolus for signs of fluid overload, as well as first-hour antibiotic administration and 2) subsequent ICU hemodynamic support directed to goals of ScVO2 greater than 70% and cardiac index (CI) 3.3–6.0 L/min/m2 with appropriate antibiotic coverage and source control.”

The major new recommendation in the 2014 update is that hemodynamic support of septic shock now be addressed at the institutional level rather than only at the practitioner level with well-planned coordination between the family, community, prehospital, emergency department, hospital, and ICU settings. The new guidelines recommend that each institution implements their own adopted or home-grown bundles that include the following:

1) Recognition bundle containing a trigger tool for rapid identification of patients with suspected septic shock at that institution,

2) Resuscitation and stabilization bundle to drive adherence to consensus best practice at that institution, and

3) Performance bundle to monitor, improve, and sustain adherence to that best practice.

The new 2014 guidelines provide examples of each bundle (Fig. 1) for consideration and review by each hospital’s expert committee.

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Developmental Differences in the Hemodynamic Response to Sepsis in Newborns, Children, and Adults

The predominant cause of mortality in adult septic shock is vasomotor paralysis (26). Adults have myocardial dysfunction manifested as a decreased ejection fraction; however, cardiac output (CO) is usually maintained or increased by two mechanisms: tachycardia and ventricular dilation. Adults who do not develop this adaptive process to maintain CO have a poor prognosis (27, 28). “Pediatric septic shock” is typically associated with severe hypovolemia, and children frequently respond well to aggressive volume resuscitation; however, the hemodynamic response of fluid resuscitated children seems diverse compared with adults. Contrary to the adult experience, low CO, not low systemic vascular resistance (SVR), is associated with mortality in pediatric septic shock (29–40). Attainment of the therapeutic goal of CI 3.3–6.0 L/min/m2 may result in improved survival (30, 38). Also contrary to adults, a reduction in oxygen delivery rather than a defect in oxygen extraction is the major determinant of oxygen consumption (VO2) in children (31). Attainment of the therapeutic goal of VO2 greater than 200 mL/min/m2 may also be associated with improved outcome (30).

It was not until 1998 that investigators reported patient outcome when aggressive volume resuscitation (60 mL/kg fluid in the first hour) and goal-directed therapies (goal = CI, 3.3–6.0 L/min/m2 and normal pulmonary artery occlusion pressure [PAOP]) were applied to children with septic shock (38). Ceneviva et al (38) reported 50 children with fluid-refractory (≥ 60 mL/kg in the first hour), dopamine-resistant shock. The majority (58%) showed a low CO/high SVR state, and 22% had low CO and low vascular resistance. Hemodynamic states frequently progressed and changed over the first 48 hours. Persistent shock occurred in 33% of the patients. There was a significant decrease in cardiac function over time, requiring addition of inotropes and vasodilators. Although decreasing cardiac function accounted for the majority of patients with persistent shock, some showed a complete change from a low output state to a high output/low SVR state (41–44). Inotropes, vasopressors, and vasodilators were directed to maintain normal CI and SVR in the patients. Mortality from fluid-refractory, dopamine-resistant septic shock in this study (18%) was markedly reduced compared with mortality in the 1985 study (58%) (30), in which aggressive fluid resuscitation could not be accomplished in part because intraosseous vascular access was not yet commonly used and attainment of intravascular access in the resuscitation bay was difficult. More recently investigators in the United Kingdom confirmed these observations using Doppler ultrasound to measure CO (39, 40). They found that previously healthy children with community-acquired sepsis often had a low CO with a higher mortality rate, whereas CO was high and mortality rate was low in septic shock related to catheter-associated blood stream infections (39).

“Neonatal septic shock” can be complicated by the physiologic transition from fetal to neonatal circulation. In utero, 85% of fetal circulation bypasses the lungs through the patent ductus arteriosus (PDA) and foramen ovale. This flow pattern is maintained by supra systemic pulmonary vascular resistance in the prenatal period. At birth, inhalation of oxygen triggers a cascade of biochemical events that ultimately result in reduction in pulmonary vascular resistance and artery pressure and transition from fetal to neonatal circulation with blood flow now being directed through the pulmonary circulation. Closure of the PDA and foramen ovale (that can occur much later) complete this transition. Pulmonary vascular resistance and artery pressures can remain elevated and the ductus arteriosus can remain open for the first 6 weeks of life, whereas the foramen ovale may remain probe patent for years. Sepsis-induced acidosis and hypoxia can increase pulmonary vascular resistance and artery pressure and maintain patency of the ductus arteriosus, resulting in persistent pulmonary hypertension of the newborn (PPHN) and persistent fetal circulation. Neonatal septic shock with PPHN is associated with increased right ventricle work. Despite in utero conditioning, the thickened right ventricle may fail in the presence of systemic pulmonary artery pressures. Decompensated right ventricular failure can be clinically manifested by tricuspid regurgitation and hepatomegaly. Newborn animal models of Group B streptococcal and endotoxin shock have also documented reduced CO, and increased pulmonary, mesenteric, and SVR (45–48). Therapies directed at reversal of right ventricle failure, through reduction of pulmonary artery pressures, are commonly needed in neonates with fluid-refractory shock and PPHN.

The hemodynamic response in premature, very low birth weight (VLBW) infants with septic shock (< 32-wk gestation, < 1,000 gm) is least understood. Most hemodynamic information is derived only from echocardiographic evaluation, and there are few septic shock studies in this population. Neonatology investigators often fold septic shock patients into “respiratory distress syndrome” and “shock” studies rather than conduct septic shock studies alone. Hence, the available clinical evidence on the hemodynamic response in premature infants for the most part is in babies with respiratory distress syndrome or shock of undescribed etiology. In the first 24 hours after birth during the “transitional phase,” the neonatal heart must rapidly adjust to a high vascular resistance state compared with the low resistance placenta. CO and blood pressure may decrease when vascular resistance is increased (49). However, the literature indicates that premature infants with shock can respond to volume and inotropic therapies with improvements in stroke volume (SV), contractility, and blood pressure (50–63).

Several other developmental considerations influence shock therapy in the premature infant. Relative initial deficiencies in the thyroid and parathyroid hormone axes have been reported and can result in the need for thyroid hormone and/or calcium replacement (64, 65). Hydrocortisone has been examined in this population as well. Since 2002, randomized controlled trials showed that prophylactic use of hydrocortisone on day 1 of life reduced the proportion of patients with hypotension in this population (66), and a 7-day course of hydrocortisone reduced the need for inotropes in VLBW infants with septic shock (67–69). Immature mechanisms of thermogenesis require attention to external warming. Reduced glycogen stores and muscle mass for gluconeogenesis require attention to maintenance of serum glucose concentration. Standard practices in resuscitation of preterm infants in septic shock employ a more graded approach to volume resuscitation and vasopressor therapy compared with resuscitation of term neonates and children. This more cautious approach is a response to anecdotal reports that preterm infants at risk for intraventricular hemorrhage (< 30-wk gestation) can develop hemorrhage after rapid shifts in blood pressure; however, some now question whether long-term neurologic outcomes are related to periventricular leukomalacia (a result of prolonged under perfusion) more than to intraventricular hemorrhage. Another complicating factor in VLBW infants is the persistence of the PDA. This can occur because immature muscle is less able to constrict. The majority of infants with this condition are treated medically with indomethacin, or in some circumstances with surgical ligation. Rapid administration of fluid may further increase left to right shunting through the ductus with resultant pulmonary edema.

One single-center, randomized control trial reported improved outcome with use of daily 6-hour pentoxyfilline infusions in very premature infants with sepsis (70, 71). This compound is both a vasodilator and an anti-inflammatory agent. A Cochrane analysis agrees that this promising therapy deserves evaluation in the multicenter trial setting (72).

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What Clinical Signs and Hemodynamic Variables Can Be Used to Direct Treatment of Newborn and Pediatric Shock?

Shock can be defined by clinical variables, hemodynamic variables, oxygen utilization variables, and/or cellular variables. However, after review of the literature, the committee continues to choose to define septic shock by clinical, hemodynamic, and oxygen utilization variables only.

Ideally, septic shock should be diagnosed by clinical signs, which include hypothermia or hyperthermia, altered mental status, and peripheral vasodilation (warm shock) or vasoconstriction with capillary refill greater than 2 seconds (cold shock) before hypotension occurs. Threshold heart rates (HRs) associated with increased mortality in critically ill (not necessarily septic) infants are a HR less than 90 or greater than 160 beats/min, and in children are a HR less than 70 or greater than 150 beats/min (73). Emergency department therapies should be directed toward restoring normal mental status, threshold HRs, peripheral perfusion (capillary refill < 3 s), palpable distal pulses, and blood pressure for age (10). Carcillo et al (74) reported that specific hemodynamic abnormalities in the emergency department were associated with progressive increase in mortality (%): eucardia (1%) less than tachycardia/bradycardia (3%) less than hypotension with capillary refill less than 3 seconds (5%) less than normotension with capillary refill longer than 3 seconds (7%) less than hypotension with capillary refill longer than 3 seconds (33%). Reversal of these hemodynamic abnormalities using ACCM/PALS recommended therapy was associated with a 40% reduction in mortality odds ratio regardless of the stage of hemodynamic abnormality at the time of presentation (74).

In both neonates and children, shock should be further evaluated and resuscitation treatment guided by hemodynamic variables including perfusion pressure (MAP – CVP) and CO. Invasive blood pressure monitoring provides more accurate reflection of vasomotor state. Shock has historically been divided into warm and cold based on clinical examination, inferring vasodilation or vasoconstriction based on warm and cold phenotypes, respectively. This categorization has been demonstrated to be fraught with errors. Indeed, as many as 66% of children judged by experienced clinicians to be in “cold shock” were noted to be vasodilated on invasive monitoring (75). Blood flow (Q) varies directly with perfusion pressure (ΔP) and inversely with resistance (R). This is mathematically represented by Q = ΔP/R. For the systemic circulation, this is represented by CO = MAP – CVP/SVR. This relationship is important for organ perfusion. In the kidney, for example, renal blood flow = mean renal arterial pressure (mRAP) – mean renal venous pressure/renal vascular resistance. Some organs (including the kidney and brain) have vasomotor autoregulation, which maintains blood flow in low blood pressure (MAP or RAP) states; however, at some critical point, perfusion pressure is reduced below the ability of the organ to maintain blood flow.

Therefore, the goal of shock treatment is to maintain perfusion pressure above the critical point below which blood flow cannot be effectively maintained in individual organs. Kumar et al (76) demonstrated in children with severe CNS infections and sepsis that therapies targeted to preservation of a minimum cerebral perfusion pressure (CPP) rather than to intracranial pressure (ICP) reduced mortality from 38.2% in the ICP control group to 18.2% in the CPP preservation group. The mean blood pressure in the CPP targeted group was the 90th percentile for age supporting targeting a mean blood pressure greater than 50th percentile for age (76). The kidney receives the second highest blood flow relative to its mass of any organ in the body, and measurement of urine output (with the exception of patients with hyperosmolar states such as hyperglycemia which leads to osmotic diuresis) and creatinine clearance can be used as an indicator of adequate perfusion pressure. Maintenance of MAP with norepinephrine has been shown to improve urine output and creatinine clearance in hyperdynamic sepsis (77, 78). Producing a supranormal MAP above this point is likely not of benefit (78) and may actually decrease CO by increasing afterload above the capacity of the myocardium to compensate.

In addition, reduction in perfusion pressure below the critical point necessary for adequate splanchnic organ perfusion can also occur in disease states with increased intra-abdominal pressure (IAP) such as bowel wall edema, ascites, or abdominal compartment syndrome. If this increased IAP is not compensated for by an increase in MAP, then splanchnic perfusion pressure is decreased. Therapeutic reduction of IAP (measured by intrabladder pressure) using diuretics and/or peritoneal drainage for IAP greater than 12 mm Hg, and surgical decompression for greater than 30 mm Hg, results in restoration of perfusion pressure and has been shown to improve renal function in children with burn shock (79).

Normative blood pressure values in the VLBW newborn have been reassessed. A MAP less than 30 mm Hg is associated with poor neurologic outcome and survival and is considered the absolute minimum tolerable blood pressure in the extremely premature infant (51). Since blood pressure does not necessarily reflect CO, it is recommended that normal CO and/or superior vena cava (SVC) flow, measured by Doppler echocardiography, be a primary goal as well (80–90).

Although perfusion pressure is used as a surrogate marker of adequate flow, the previous equation shows that organ blood flow (Q) correlates directly with perfusion pressure but indirectly with vascular resistance. If the ventricle is healthy, an elevation of SVR results in hypertension with maintenance of CO. Conversely, if ventricular function is reduced, the presence of normal blood pressure with high vascular resistance means that CO is reduced. If the elevation in vascular resistance is marked, the reduction in blood flow results in shock. A CI between 3.3 and 6.0 L/min/m2 is associated with best outcomes in septic shock patients (29, 39, 40) compared to patients without septic shock for whom a CI above 2.0 L/min/m2 is sufficient (91). Attainment of this CO goal is often dependent on attaining threshold HRs. However, if the HR is too high, then there is not enough time to fill the coronary arteries during diastole, and contractility and CO will decrease. Coronary perfusion may be further reduced when an unfavorable transmural coronary artery filling pressure is caused by low diastolic blood pressure (DBP) and/or high end-diastolic ventricular pressure. In this scenario, efforts should be made to improve coronary perfusion pressure and reverse the tachycardia by giving volume if the end-diastolic volume is low, or an inotrope if contractility is low. Because CO = HR × SV, therapies directed to increasing SV will often reflexively reduce HR and improve CO. This will be evident in improvement of the shock index (HR/systolic blood pressure [SBP]) (92), as well as CO. Children have limited HR reserve compared with adults because they are already starting with high basal HRs. For example, if SV is reduced due to endotoxin-induced cardiac dysfunction, an adult can compensate for the fall in SV by increasing HR two-fold from 70 to 140 beats/min, but a baby cannot increase from 140 to 280 beats/min. Although tachycardia is an important method for maintaining CO in infants and children, the younger the patient, the more likely this response will be inadequate and the CO will fall. In this setting, the compensatory response to falling SV and contractility is to vasoconstrict to maintain blood pressure. Increased vascular resistance is clinically identified by absent or weak distal pulses, cool extremities, prolonged capillary refill, and narrow pulse pressure with relatively increased DBP. The effective approach for these children is vasodilator therapy with additional volume loading as vascular capacity is expanded. Vasodilator therapy reduces afterload and increases vascular capacitance. This shifts the venous compliance curve so that more volume can exist in the right and left ventricle at a lower pressure. In this setting, giving volume to restore filling pressure results in a net increase in end-diastolic volume (i.e., preload) and a higher CO at the same or lower filling pressures. Effective use of this approach results in a decreased HR and improved perfusion.

At the other end of the spectrum, a threshold minimum HR is also needed because if the HR is too low, then CO will be too low (CO = HR × SV). This can be attained by using an inotrope that is also a chronotrope. In addition to threshold HRs, attention must also be paid to DBP. If the DBP-CVP is too low, then addition of an inotrope/vasopressor agent such as norepinephrine will be required to improve diastolic coronary blood flow. Conversely, if wall stress is too high due to an increased end-diastolic ventricular pressure secondary to fluid overload, then a diuretic may be required to improve SV by moving leftward on the overfilled Starling function curve. The effectiveness of these maneuvers will similarly be evidenced by improvement in the HR/SBP shock index, CO, and SVR along with improved distal pulses, skin temperature, and capillary refill.

In addition, shock should be treated according to oxygen utilization measures. Measurement of CO and oxygen consumption was proposed as being of benefit in patients with persistent shock because a CI between 3.3 and 6.0 L/min/m2 and oxygen consumption greater than 200 mL/min/m2 is associated with improved survival (29). Low CO is associated with mortality in pediatric septic shock (29–38). In one study, children with fluid-refractory, dopamine-resistant shock were treated with goal-directed therapy (CI, > 3.3 and < 6 L/min/m2) and found to have improved outcomes compared with historical reports (38). Because low CO is associated with increased oxygen extraction (30), ScVO2 saturation can be used as an indirect indicator of whether CO is adequate to meet tissue metabolic demand. If tissue oxygen delivery is adequate, then assuming a normal SaO2 of 100%, mixed venous saturation is greater than 70%. Assuming a hemoglobin concentration of 10 g/dL and 100% arterial oxygen saturation, then a CI greater than 3.3 L/min/m2 with a normal VO2 of 150 mL/min/m2 (oxygen consumption = CI × [arterial oxygen content – venous oxygen content]) results in a mixed venous saturation of greater than 70%: 150 mL/min/m2 = 3.3 L/min/m2 × (1.36 × 10 g/dL + PaO2 × 0.003) × 10 × (1–0.7). Since 2002, de Oliveira et al (13) performed a randomized controlled trial in children with septic shock showing a reduction in mortality from 39% to 12% when directing therapy to the goal of ScVO2 saturation greater than 70% (NNT, 3.6) (93). Sankar et al (14) observed an association with reduced mortality from 54% to 33.3% (NNT, 5) and lower organ dysfunction with a similar ScVO2 saturation goal of greater than 70%. In contrast, supranormal ScVO2 saturations greater than 80–85% that reflect a narrowed arteriovenous difference in oxygen (AVDO2) content may reflect either mitochondrial dysfunction, a high CO state, or overly aggressive resuscitation (94). In this narrow AVDO2 shock state, practitioners should incorporate in their serial patient assessments other markers of adequate tissue oxygen delivery and utilization and organ perfusion such as serum lactate and urine output.

In isolation, any one of the above clinical or hemodynamic parameters may underestimate or overestimate the true severity of illness, leading to either false reassurance and underresuscitation or overresuscitation. Multimodal monitoring refers to the use of multiple variables and their changes over time to better determine the underlying hemodynamic state. Shock index (HR/SBP) (92) and HR variability analysis (95) both leverage the added value of evaluating combinations of variables and their trends over time and have been suggested as being superior to any individual parameter alone for diagnosing septic shock and assessing response to therapy. By combining information from clinical signs, invasive arterial monitoring, and serial bedside echocardiograms, Ranjit et al (75) were able to titrate hemodynamic therapies more precisely and achieve equivalent mortality outcomes to PICUs using more invasive continuous CO monitoring.

Laboratory markers of cardiac function and oxygen delivery:utilization balance include troponin and lactate. Blood troponin concentrations correlate well with poor cardiac function and response to inotropic support in children with septic shock (96–98). Lactate is recommended in adult septic shock laboratory testing bundles for both diagnosis and subsequent monitoring of therapeutic responses. However, most adult literature continues to define shock by hypotension and recommends using lactate concentration to identify shock in normotensive adults. In pediatric studies, initial elevated lactate levels have correlated with increased mortality, and decreasing lactate trends over time seem to correlate with recovery (99–103). However, each of these studies has been limited by small numbers. Lactate elevation for reasons other than cellular hypoxia further clouds the utility of using lactate to either predict outcome or track response to therapy (104). For now, the committee recommends early recognition of pediatric septic shock using clinical examination, not biochemical tests. Nevertheless, given the broad adoption of lactate in the adult guidelines and the suggestive data in small pediatric studies, lactate measurements if high on initial measurement may be useful to judge resolution of shock. Early elevated lactate (from a free flowing sample) may grab a clinician’s attention, when clinical signs are difficult to decipher—it is inexpensive, readily available, and over time performed well as an indicator of shock and its resolution. Because clinical signs of compensated and decompensated shock are always present in children whereas high lactate is commonly not (12, 13), we stress early recognition with clinical signs, not lactate.

In VLBW infants, ultrasound-derived SVC blood flow measurement was reportedly useful in assessing the effectiveness of shock therapies. The SVC flow approximates blood flow from the brain. A value greater than 40 mL/kg/min is associated with improved neurologic outcomes and survival (86–90). ScVO2 saturation can be used in low birth weight infants but may be misleading in the presence of left to right shunting through the PDA.

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Intravascular Access

Vascular access for fluid resuscitation and inotrope/vasopressor infusion is more difficult to attain in newborns and children compared with adults. Portable near-infrared imaging devices may assist with placement of peripheral vascular access (105, 106). To facilitate a rapid approach to vascular access in critically ill infants and children, the American Heart Association and the American Academy of Pediatrics developed Neonatal Resuscitation Program (NRP) and PALS guidelines for emergency establishment of intravascular support (107–110). Essential age-specific differences include use of umbilical artery catheter (UAC) and umbilical venous catheter access in newborns and rapid use of intraosseous access in children (108–114). Ultrasound guidance facilitates placement of central catheters in children but is technologist dependent (113–119).

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Fluid Therapy

Fluid resuscitation trials have been performed since 2002. Several randomized trials showed that when children with mostly stage III (narrow pulse pressure/tachycardia) and some stage IV (hypotension) World Health Organization classification dengue shock received fluid resuscitation in the emergency department, there was near 100% survival regardless of the fluid composition used (3, 17, 120, 121). In a randomized controlled trial, Maitland et al (122) demonstrated a reduction in malaria septic shock mortality from 18% to 4% when albumin was used compared with crystalloid. In contrast, Maitland et al (18) subsequently demonstrated harm in the Fluid Expansion as Supportive Therapy (FEAST) trial when fluid boluses were given rather than IV fluid at a maintenance rate and blood transfusion contradicting this earlier study. The adult Saline versus Albumin Fluid Evaluation (SAFE) trial that compared crystalloid versus albumin fluid resuscitation reported a hypothesis generating trend toward improved outcome (p < 0.1) in septic shock patients who received albumin (123). Preference was given for exclusive use of colloid resuscitation in a clinical practice position article from a group who reported outstanding clinical results in resuscitation of meningococcal septic shock (5% mortality) both using 4% albumin exclusively (20 mL/kg boluses over 5–10 min) and intubating patients who required greater than 40 mL/kg (4). In an Indian trial of fluid resuscitation of pediatric septic shock, there was no difference in outcome with gelatin compared with crystalloid (124). In the initial clinical case series that popularized the use of aggressive volume resuscitation for reversal of pediatric septic shock, a combination of crystalloid and colloid therapies was used (125). Several new investigations examined both the feasibility of the 2002 guideline recommendation of rapid fluid resuscitation and the need for fluid removal in patients with subsequent oliguria following fluid resuscitation. The 2002 guideline recommended rapid 20 mL/kg fluid boluses over 5 minutes followed by assessment for improved perfusion or fluid overload as evidenced by new onset rales, increased work of breathing and hypoxemia from pulmonary edema, hepatomegaly, or a diminishing MAP-CVP. Emergency medicine investigators reported that 20 mL/kg of crystalloid or colloid can be pushed over 5 minutes, or administered via a pressure bag over 5 minutes through a peripheral and/or central IV catheter (126). Ranjit et al (127) reported improved outcome from dengue and bacterial septic shock when they implemented a protocol of aggressive fluid resuscitation followed by fluid removal using diuretics and/or peritoneal dialysis if oliguria ensued. In this regard, Foland et al (128) similarly reported that patients with multiple organ failure who received CRRT when they were less than 10% fluid overloaded had better outcomes than those who were greater than 10% fluid overloaded. Similarly, two best outcome practices reported routine use of CRRT to prevent fluid overload while correcting prolonged INR with plasma infusion in patients with purpura and septic shock (4, 16).

The use of blood as a volume expander was examined in two small pediatric studies, but no recommendations were given by the investigators (129, 130). In the previously mentioned study by de Oliveira et al (13) reporting improved outcome with use of the 2002 ACCM guidelines and continuous ScVO2 saturation monitoring, the treatment group received more blood transfusions directed to improvement of ScVO2 saturation to greater than 70% (40% vs 7%). Although the members of the task force use conservative goals for blood transfusion in stable critical illness (Hgb > 7 g/dL without cardiopulmonary compromise) (131), the observation that patients who have septic shock with a ScVO2 less than 70% and Hgb less than 10 g/dL had better outcomes when transfused to a goal Hgb greater than 10 g/dL supports a higher hemoglobin goal in this population.

Fluid infusion is best initiated with boluses of 20 mL/kg, titrated to assuring an adequate blood pressure and clinical monitors of CO including HR, quality of peripheral pulses, capillary refill, level of consciousness, and urine output. Initial volume resuscitation requirements may be 0 mL/kg if rales or hepatomegaly are present but commonly are 40–60 mL/kg (41, 125, 132–138). Patients who do not respond rapidly to initial fluid boluses, or those with insufficient physiologic reserve, should be considered for invasive hemodynamic monitoring. Monitoring filling pressures can be helpful to optimize preload and thus CO. Observation of little change in the CVP in response to a fluid bolus suggests that the venous capacitance system is not overfilled and that more fluid is indicated. Observation that an increasing CVP is met with reduced MAP-CVP suggests that too much fluid has been given. Large volumes of fluid for acute stabilization in children have not been shown to increase the incidence of the ARDS or cerebral edema (13, 138). Increased fluid requirements may be evident for several days secondary to loss of fluid from the intravascular compartment when there is profound capillary leak (17). Fluid choices include crystalloids (normal saline or lactated Ringers solution) and colloids (dextran, gelatin, or 5% albumin) (139–144). Fresh frozen plasma may be infused to correct abnormal PT and partial thromboplastin time values. Since oxygen delivery depends on hemoglobin concentration, hemoglobin can be maintained at a minimum of 10 g/dL during the initial resuscitation phase with good results (13). Diuretics/peritoneal dialysis/CRRT is indicated for patients who develop signs and symptoms of fluid overload.

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Sedation for Invasive Procedures or Intubation

Supplemental oxygen and optimal airway positioning should be provided at presentation for all patients with shock, consistent with PALS guidelines. Although patients presenting with hypopnea or frank apnea may need immediate intubation, in most instances, there is time for fluid resuscitation, at least 20 mL/kg of either isotonic crystalloid or 5% albumin, and starting a peripheral epinephrine infusion within the first hour of presentation. Children with persistent or worsening shock, as manifested by failure to approximate normal vital signs for age and inadequate perfusion, should be considered to be at high risk for deterioration and should receive ventilatory support. High-flow nasal cannula and other modes of noninvasive respiratory support can be evaluated in selected patients (145). Patients with shock of any etiology are particularly vulnerable to the hemodynamic effects of sedatives and analgesics, emphasizing the importance of prompt appropriate fluid resuscitation and inotrope infusion (peripheral or central) prior to airway instrumentation in spontaneously breathing patients.

Intubation for controlled ventilation plays an important role in the management of neonates and children with septic shock, and timing and should be thoughtfully considered. Sedation, analgesia and positive-pressure ventilation prior to adequate volume resuscitation (146-148), may cause profound drops in preload and precipitate severe hemodynamic instability during intubation. Also, severe diastolic and systolic ventricular dysfunction may predispose the child to pulmonary edema and rapid desaturation during intubation, providing rationale for considering peripheral epinephrine infusion before intubation. Mechanical ventilation can eliminate work of breathing and improve oxygenation and organ perfusion, all of which are typically compromised in the septic child (149–152).

Atropine increases the HR and protects against the deleterious effects of bradycardia, particularly in babies (153). Atropine does not cause cardiac dysrhythmias and is not contraindicated in children exhibiting tachycardia. Ketamine remains an important agent for intubation of pediatric patients with shock (154, 155), given its pharmacologic effects of dissociation while maintaining or augmenting SVR. Side effects may be minimized by administering IV boluses over 30–60 seconds.

The use of ketamine with atropine pretreatment is considered to be the sedative/induction regimen which best promotes cardiovascular integrity (155). The use of etomidate is generally discouraged at this time, given its known effects on adrenal function (156, 157), despite some reports suggesting no direct effect on patient mortality (158–160). Etomidate can be considered in the presence of profound shock if ketamine is unavailable. The role of hydrocortisone supplementation in this setting is unclear. It is possible that etomidate analogs currently in development may have a role in urgent pediatric airway management.

Other options to consider for intubation of neonates and children include the opioids fentanyl and remifentanil (161, 162). These agents should be used instead of morphine, when available, because they have fewer hemodynamic effects. Opioids such as fentanyl should be given in titrated aliquots of 1–2 µg/kg, administered over 60 seconds. Although chest wall rigidity is usually associated with larger doses given as a bolus, this complication and altered hemodynamics can also occur with smaller doses. Benzodiazepines, if used, should be likewise carefully titrated to effect, using small doses.

Pentobarbital and other barbiturates are direct myocardial depressants and decrease SVR, commonly causing hemodynamic instability. These drugs are also devoid of intrinsic analgesic effects, making them unsuitable for tracheal intubation of patients with shock. Inhalational agents are not appropriate for isolated airway instrumentation in shock. Propofol commonly causes hypotension and should be avoided during intubation or sedation in the presence of shock, particularly during transport and before admission to the ICU.

Neuromuscular blocking agents such as rocuronium, or succinylcholine (absent a contraindication), may facilitate intubation by qualified providers. Hypotension may occur even in children who have received appropriate volume resuscitation and pharmacotherapy for intubation. It is advisable, therefore, to have additional isotonic crystalloid and vasoactive infusions available for immediate use during or following the procedure. Additional vascular access should be obtained as soon as practical. Sedation and analgesia may be maintained in ventilated patients requiring transport using agents such as fentanyl and midazolam, supplemented by neuromuscular blockade. Ketamine infusions may be used as well, but there is concern regarding neuroapoptosis following exposure to ketamine in infants (161, 162). Unplanned extubation may occur as the child recovers from shock. The endotracheal tube should be carefully secured once adequate placement is achieved. Appropriately titrated analgesia and sedation are essential for safe transport. Neuromuscular blockade and physical restraints may be appropriate under some circumstances, always in the presence of adequate analgesia and sedation.

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Intravascular Catheters and Noninvasive or Minimally Invasive Monitoring

Minimal invasive monitoring is necessary in children with fluid-responsive shock; however, in children with fluid-refractory shock, physical signs of cold versus warm shock may be unreliable, and central venous access and arterial pressure monitoring is recommended. Intensivists have long used the ultrasound for central venous catheter placement in children, but its role is now expanding to direct resuscitation goals and therapeutic endpoints in shock resuscitation. Echocardiography is considered an appropriate noninvasive tool to rule out the presence of pericardial effusion, evaluate myocardial contractility and intravascular volume. Ranjit et al (75) incorporated the use of echocardiography in their usual practice to categorize the hemodynamics in 48 patients with fluid-refractory septic shock. Based on their findings on the echocardiogram and invasive blood pressure monitoring, fluid and inotrope/vasopressor therapy was changed in almost 88% of the patients (75). Early placement of invasive arterial catheters helped in the identification and subsequent management of a cohort of patients who presented with cold shock but had wide pulse pressure with low diastolic pressure (75). Similarly, Brierly et al (39) categorized the hemodynamic patterns of pediatric septic shock with the use of Doppler ultrasonography and observed that the manifestation of hemodynamics was cause dependent, that is, CVC-associated sepsis presented with high CO and low SVR, whereas community-acquired infections sepsis presented with low CO. A CO greater than 3.3 less than 6.0 L/min/m2 is associated with improved survival and neurologic function. Other noninvasive monitors undergoing evaluation in newborns and children include percutaneous venous oxygen saturation, aortic ultrasound, perfusion index (pulse oximetry), near-infrared spectroscopy, sublingual PCO2, and sublingual microvascular orthogonal polarization spectroscopy scanning. All show promise; however, none has been tested in goal-directed therapy trials (163–166).

Maintenance of perfusion pressure (MAP – CVP), or (MAP – IAP) if the abdomen is tense secondary to bowel edema or ascitic fluid, is considered necessary for organ perfusion (79). Goal-directed therapy to achieve an ScVO2 saturation greater than 70% is associated with improved outcome (13, 14). To gain accurate measures of ScVO2, the tip of the catheter must be at the superior vena cava-right atrium or inferior vena cava-right atrium junction (164). A pulmonary artery catheter (PAC), pulse index contour CO (PiCCO) (165, 166), or femoral artery thermodilution catheter can be used to measure CO in those who remain in shock despite therapies directed to clinical signs of perfusion, MAP-CVP, ScVO2, and echocardiographic analyses (165–172). The PAC measures the PAOP to help identify selective left ventricular dysfunction and can be used to determine the relative contribution of right and left ventricle work. A less invasive PiCCO catheter estimates global end-diastolic volume in the heart (both chambers) and extra vascular lung water and can be used to assess whether preload is adequate. This measure of intravascular volume by global end-diastolic volume has been demonstrated in both children and adults to be more predictive than either CVP or PAOP for changes in CO associated with volume challenge.

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Cardiovascular Drug Therapy

When considering the use of cardiovascular agents in the management of infants and children with septic shock, several important points need to be emphasized. The first is that septic shock represents a dynamic process so that the agents selected and their infusion dose may need to be changed over time based on the need to maintain adequate organ perfusion. It is also important to recognize that the vasoactive agents are characterized by varying effects on SVR and pulmonary vascular resistance (i.e., vasodilators or vasopressors), contractility (i.e., inotropy), HR (chronotropy), and lusotropy (ventricle relaxation). These pharmacologic effects are determined by the pharmacokinetics of the agent and the pharmacodynamics of the patient’s response to the agent. In critically ill septic children, perfusion of the liver and kidney is often altered leading to changes in the pharmacokinetics of these drugs with higher concentrations observed than anticipated. Thus, the infusion doses quoted in many textbooks are approximations of starting rates and should be adjusted based on the patient’s response. “We recommend frequent reevaluation of hemodynamic parameters when a patient requires the use of vasopressors, especially in relation to CO, SVR, and peripheral perfusion so as to choose the appropriate combination with inotropic or vasodilator drugs ± fluids.”

The latter is also determined by the pharmacodynamic response to the agent, which is commonly altered in septic patients. For example, patients with sepsis have a well-recognized reduced response to α-adrenergic agonists that is mediated by excess nitric oxide production and alterations in the α-adrenergic receptor system. Similarly, cardiac β-adrenergic responsiveness may be reduced by the effect of nitric oxide and other inflammatory cytokines.

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Dopamine (5–9 µg/kg/min), dobutamine, or epinephrine (0.05–0.3 µg/kg/min) can be used as first-line inotropic support. Dobutamine may be used when there is a low CO state with adequate or increased SVR (38, 173–201). Dobutamine or mid-dosage dopamine can be used as the first line of inotropic support if supported by clinical and objective data (e.g., assessment of contractility by echocardiogram) when one of the initial goals is to increase cardiac contractility in patients with normal blood pressure. However, children less than 12 months may be less responsive (195).

Dobutamine- or dopamine-refractory low CO shock may be reversed with epinephrine infusion (12, 38, 173, 174, 176). Epinephrine is more commonly used in children than in adults. Some members of the committee recommended use of low-dose epinephrine as a first-line choice for cold hypodynamic shock (12). It is clear that epinephrine has potent inotropic and chronotropic effects, but its effects on peripheral vascular resistance and the endocrine stress response may result in additional problems. At lower infusion doses (≤ 0.3 µg/kg/min), epinephrine has greater β2-adrenergic effects in the peripheral vasculature with little α-adrenergic effect so that SVR falls, particularly in the skeletal musculature and skin. This may redirect blood flow away from the splanchnic circulation even though blood pressure and CO increases. This effect of epinephrine likely explains the observation that epinephrine transiently reduces gastric intramucosal pH in adults and animals with hyperdynamic sepsis (177), but there are no data available to evaluate whether gut injury does or does not occur with epinephrine use in children. Epinephrine stimulates gluconeogenesis and glycogenolysis, and inhibits the action of insulin, leading to increased blood glucose concentrations. In addition, as part of the stimulation of gluconeogenesis, epinephrine increases the shuttle of lactate to liver as a substrate for glucose production (the Cori cycle). Thus, patients on epinephrine infusion have increased plasma lactate concentrations independent of changes in organ perfusion, making this parameter somewhat more difficult to interpret in children with septic shock.

Ideally, epinephrine should be administered by a secure central venous route, but in an emergency, it may be infused through a peripheral IV route or through an intraosseous needle while attaining central access (12). The AHA/PALS guidelines for children recommend the initial use of epinephrine by peripheral IV or intraosseous for CPR or post CPR shock, and by the subcutaneous or intramuscular route for anaphylaxis. Even though a common perception, there are no data clarifying if the peripheral infiltration of epinephrine produces more local damage than observed with dopamine. The severity of local symptoms likely depends on the concentration of the vasoactive drug infusion and the duration of the peripheral infiltration before being discovered. If peripheral infiltration occurs with any catecholamine, its adverse effects may be antagonized by local infiltration with phentolamine, 1–5 mg diluted in 5 mL of normal saline.

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When pediatric patients are normotensive with a low CO and high SVR, initial treatment of fluid-refractory patients consists of the use of an inotropic agent such as epinephrine or dobutamine that tends to lower SVR. In addition, a short-acting vasodilator may be added, such as sodium nitroprusside or nitroglycerin to recruit microcirculation (202–208). Orthogonal polarizing spectroscopy showed that addition of systemic IV nitroglycerin to dopamine/norepinephrine infusion restored tongue microvascular blood flow during adult septic shock (208). Nitrovasodilators can be titrated to the desired effect, but use of nitroprusside is limited if there is reduced renal function secondary to the accumulation of sodium thiocyanate. Use of nitroglycerin may also have limited utility over time through the depletion of tissue thiols that are important for its vasodilating effect. Other vasodilators that have been used in children include prostacyclin, pentoxyfilline, dopexamine, and fenoldapam (209–214).

An alternative approach to improve cardiac contractility and lower SVR is based on the use of type III phosphodiesterase inhibitors (PDEIs) (206, 207, 215, 216). This class of agents, which includes milrinone and inamrinone (formerly amrinone, but the name was changed to avoid confusion with amiodarone), has a synergistic effect with β-adrenergic agonists because the latter agents stimulate intracellular cyclic adenylate mono phosphate (cAMP) production while the PDEIs increase intracellular cAMP by blocking its hydrolysis. Since the PDEIs do not depend on a receptor mechanism, they maintain their action even when the β-adrenergic receptors are down-regulated or have reduced functional responsiveness. The main limitation of these agents is their need for normal renal function (for milrinone clearance) and liver function (for inamrinone clearance). Inamrinone and milrinone are rarely used in adults with septic shock because catecholamine refractory low CO and high vascular resistance are uncommon; however, this hemodynamic state represents a major proportion of children with fluid-refractory, dopamine-resistant shock. Fluid boluses are likely to be required if inamrinone or milrinone is administered with full loading doses. Because milrinone and inamrinone have long half-lifes (1–10 hr depending on organ function), it can take 3–30 hours to reach 90% of steady state. Although recommended in the literature, some individuals in the committee choose not to use boluses of inamrinone or milrinone. This group administers the drugs as a continuous infusion only. Other members divide the bolus into five equal aliquots administering each aliquot over 10 minutes if blood pressure remains within an acceptable range. If blood pressure falls, it is typically because of the desired vasodilation and can be reversed by titrated (e.g., 5 mL/kg) boluses of isotonic crystalloid or colloid. Because of the long elimination half-life, these drugs should be discontinued at the first sign of arrhythmia, or hypotension caused by excessively diminished SVR. Hypotension-related toxicity can also be potentially overcome by beginning norepinephrine. Norepinephrine counteracts the effects of increased cyclic adenosine monophosphate in vascular tissue by stimulating the alpha receptor resulting in vasoconstriction. Norepinephrine has little effect at the vascular β2 receptor.

Rescue from refractory shock has been described in case reports and series using two medications with type III phosphodiesterase activity. Levosimendan is a promising medication that increases Ca++/actin/tropomyosin complex binding sensitivity and also has some type III PDEI and adenosine triphosphate–sensitive K+ channel activity. Because one of the pathogenic mechanisms of endotoxin-induced heart dysfunction is desensitization of Ca++/actin/tropomyosin complex binding, this drug allows treatment at this fundamental level of signal transduction overcoming the loss of contractility that characterizes septic shock (217–222). Enoximone is a type III PDEI with 10 times more β1 cAMP hydrolysis inhibition than β2 cAMP hydrolysis inhibition (223–225). Hence, it can be used to increase cardiac performance with less risk of undesired hypotension.

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Vasopressors may also be beneficial in the treatment of pediatric septic shock when applied according to the guideline algorithm. Vasopressors can be titrated to endpoints of perfusion pressure (MAP-CVP) or SVR that promote optimum urine output and creatinine clearance, but excessive vasoconstriction compromising microcirculatory flow should be avoided. Vasopressor effect can be obtained with different sympathicomimetic drugs. There is no clear evidence that supports the use of one specific vasoactive drug over another (dopamine > 15 µg/kg/min, epinephrine > 0.3 µg/kg/min, or norepinephrine) (77, 179, 226–231). When epinephrine is administrated in doses greater than 0.3 µg/kg/min or dopamine in doses greater than 10 µg/kg/min, there is a vasopressor effect additional to their inotropic action. However, if the patient has ongoing shock and/or shows findings consistent with warm shock (flash capillary refill, warm extremities, low diastolic pressure, and bounding pulses), the additional use of norepinephrine is suggested (231). Some committee members advocate the use of low-dose norepinephrine as a first-line agent for fluid-refractory hypotensive hyperdynamic shock. Based on experimental and clinical data, norepinephrine is recommended as the first-line agent in adults with fluid-refractory shock. If the patient’s clinical state is characterized by low SVR (e.g., wide pulse pressure with DBP that is < half the systolic pressure), norepinephrine is recommended alone. Other experts have recommended combining norepinephrine with dobutamine, recognizing that dobutamine is a potent inotrope that has intrinsic vasodilating action that may be helpful to counteract excessive vasoconstriction from norepinephrine. Higher norepinephrine doses than those usually suggested in the literature have been described to reverse hypotension and hypoperfusion without inducing significant adverse effects (230, 231).

The infusion of norepinephrine is suggested as the initial vasoactive drug in patients with warm shock, vasodilatation, and low SVR. A study using a noninvasive ultrasound CO monitor device to measure serial hemodynamics showed that patients could present with cold or warm shock and that both types evolved in a heterogeneous manner needing frequent revision of cardiovascular support therapy (40). Children with initial warm shock were commenced on norepinephrine. Despite an initial good response, four patients developed low CI and needed epinephrine (40).

When the use of vasopressor drugs is needed, it must be started as soon as possible but within 60 minutes of resuscitation, using intraosseus access, while central venous access is obtained. Lampin et al (230) describe in a retrospective study the use of norepinephrine in 144 children over a 10-year period; it was used as the first-choice drug in 22% of the patients, and in 19% of the cases, it was used either by peripheral or intraosseus route. Paul et al (21, 22) describe delay in the initiation of vasoactive drugs in 65% of the cases and associate this with an increase in length of stay in intensive care.

Vasopressin and terlipressin have been shown to increase MAP, SVR, and urine output in patients with vasodilatory septic shock and hyporesponsiveness to catecholamines (232–258). Vasopressin’s action is independent of catecholamine receptor stimulation, and therefore, its efficacy is not affected by α-adrenergic receptor down-regulation often seen in septic shock. Low-dose infusion of vasopressin should not be used as routine adjunctive therapy but may be considered as rescue therapy in patients with catecholamine and steroid resistant hypotension. The adult Vasopressin and Septic Shock Trial, a randomized, controlled clinical trial that compared low-dose arginine vasopressin with norepinephrine in adults with septic shock, showed no difference between regimens in the 28-day mortality primary endpoint (247). The results of another randomized control trial evaluating the use of low doses of vasopressin as an adjunctive therapy in vasodilated pediatric septic shock also failed to show benefits (248).

Both vasopressin and terlipressin can be considered as rescue therapy in patients in vasodilatory shock who do not respond to high doses of norepinephrine or other sympathicomimetics. Terlipressin, a long acting form of vasopressin, has been reported to reverse vasodilated shock as well. Administered as a continuous infusion or in bolus, it increases blood pressure and urine output in pediatric patients with refractory septic shock. Decreased CO or distal necrosis has been reported as possible adverse events. Yildizdas et al (258) evaluated the effect of continuous infusion of terlipressin in a randomized control trial in pediatric patients with septic shock and high catecholamine requirement. Terlipressin infusion had no effect on mortality.

Angiotensin can also be used to increase blood pressure in patients who are refractory to norepinephrine; however, its clinical role is not as well defined (259). Phenylephrine is another pure vasopressor with no β-adrenergic activity (260). Its clinical role is also limited. Nitric oxide (NO) inhibitors and methylene blue are considered investigational therapies (261–264). Studies have shown an increased mortality with nonselective NO synthase inhibitors suggesting that increasing blood pressure through excessive vasoconstriction can have adverse effects (261).

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Glucose, Calcium, Thyroid, and Hydrocortisone Replacement

Hypoglycemia, hyperglycemia, and glycemic variability have been associated with worse short-term outcomes in critically ill children (265–268). Hypoglycemia must be rapidly diagnosed and promptly treated. Hyperglycemia in nondiabetic children with sepsis has been associated with worse outcomes (266–268). Branco et al (267) reported a greater risk of death with hyperglycemia (≥ 178 mg/dL) in 57 children with septic shock. Day et al (268) reported hyperglycemia (> 180 mg/dL) negatively correlated with ventilator-free days at 30 days in a retrospective review of 97 children with meningococcal sepsis. Hyperglycemia and hypoglycemia during critical illness may simply represent epiphenomena. In contrast, Mesotten et al (269) reported that brief hypoglycemia (≤ 40 mg/dL) caused by tight glycemic control in a pediatric randomized controlled trial was not associated with worse neurocognitive outcome approximately 4 years later.

Randomized controlled trials of tight glycemic control have been conducted primarily in postcardiac surgery children (270–273). Results are conflicting, with one study showing a reduction in PICU length of stay and inflammatory markers (272) and the other three not showing an improvement in mortality or morbidity (270, 271, 273). Hyperglycemia in children with meningococcal sepsis has been partially attributed to the suppression of insulin production by proinflammatory mediators rather than insulin resistance as seen in other critical illnesses (274, 275).

Calcium replacement should be directed to normalize ionized calcium concentration; however, its safety and efficacy have not been established in septic shock. Replacement with thyroid and/or hydrocortisone can also be lifesaving in children with thyroid and/or adrenal insufficiency and catecholamine-resistant shock (64, 276–291). Hypothyroidism is relatively common in children with trisomy 21 and children with CNS pathology, (e.g., pituitary abnormality). Hypothyroidism may manifest clinically after the administration of corticosteroids for adrenal insufficiency and needs to be recognized and treated promptly. Infusion therapy with triiodothyronine may be beneficial in postoperative congenital heart disease patients but has yet to be studied in children with septic shock.

Multiple studies suggest changes in the hypopituitary adrenal axis (292–294), glucocorticoid receptor changes (295), and changes in cortisol metabolism during sepsis (296, 297). Possible rationales for the use of corticosteroids in sepsis are beneficial pharmacologic effect on the cardiovascular system and anti-inflammatory properties (276, 298, 299). A recent prospective study of critically ill children reported a prevalence of relative adrenal insufficiency in critically ill children of 30.2% on the first day of admission and 19.8% on the second day of admission as defined by an increase in cortisol of less than 9 µg/dL after administration of low dose (1 µg) adrenocorticotropic hormone (ACTH) (300). The prevalence of relative adrenal insufficiency reported in other studies is widely variable depending on the diagnostic criteria used and remains somewhat arbitrary. Low or high serum cortisol concentrations have been associated with increased sepsis mortality (301). A cutoff of less than 25 µg/dL in adults with septic shock has been described as useful to predict hemodynamic response to cortisol administration. In children, a serum cortisol concentration of greater than 36 µg/dL and a lack in response to ACTH stimulation may predict a failure to respond to exogenous corticosteroid administration (302). Several factors contribute to the diagnostic controversy. In one study, patients with relative adrenal insufficiency had higher basal cortisol concentrations than those without relative adrenal insufficiency (28.6 vs 16.7 µg/dL; p < 0.001) (302). A study of total and free cortisol concentrations among critically ill children found a high incidence of biochemical adrenal insufficiency using various definitions but no evidence of corresponding clinical adrenal insufficiency (303).

Hypoproteinemia decreases total cortisol concentrations, but free cortisol concentrations have been observed to be high in patients with serum albumin concentrations less than 2.5 mg/dL despite a low total serum cortisol concentration in nearly 40% of adults tested (304). Reduced cortisol metabolism in critically ill adults suggests a 50% decrease in clearance of corticosteroids due to suppression of activity or expression of metabolizing enzymes. Furthermore, the authors observed a dissociation of cortisol concentrations after ACTH stimulation. In patients with elevated serum cortisol concentrations due to reduced clearance, ACTH concentrations were found to be lower suggesting negative feedback on the HPA axis. Mortality is correlated with a higher degree of suppression of corticosteroid metabolism in adults (296). The role of free cortisol in the diagnosis of adrenal insufficiency determination has not been sufficiently elucidated (303, 304). Administration of etomidate (305), megestrol (306), and ketoconazole (307) have been identified as iatrogenic causes of adrenal insufficiency due to their interference with cortisol production.

Nonsurvivors have exceedingly high ACTH/cortisol ratios within the first 8 hours of meningococcal shock (277–279, 290, 292, 308). The lack of increase in serum cortisol concentration (< 9 µg/dL) in patients undergoing an ACTH stimulation test with baseline cortisol concentrations greater than 18 µg/dL was associated with catecholamine refractory shock but not mortality (309, 310). The value of ACTH stimulation test in the diagnosis and treatment of relative adrenal insufficiency and critical illness-related corticosteroid insufficiency in children and adults remains unclear. No gold standard has been established for the diagnosis of adrenal insufficiency in critical illness. Absolute adrenal insufficiency has been defined as a basal serum cortisol concentration of less than 7 µg/dL and peak serum cortisol of less than 18 µg/dL after stimulation. Others suggested a basal serum cortisol of less than 5 or less than 9 µg/dL and use the same peak cutoff after ACTH stimulation of less than 18 µg/dL for the definition of absolute adrenal insufficiency. Relative adrenal insufficiency has been proposed as a basal serum cortisol concentration of less than 20 µg/dL and Δ less than 9 after ACTH stimulation, or a basal total cortisol less than 10, Δ total cortisol less than 9 or free cortisol less than 2.

Patients at risk of inadequate cortisol/aldosterone production due to absolute adrenal insufficiency in the setting of shock include children with purpura fulminans and Waterhouse-Friderichsen syndrome, children who previously received steroid therapies for chronic illness, and children with pituitary or adrenal abnormalities. These patients may benefit from stress doses of hydrocortisone early in the course of their illness, in the presence of sepsis without shock. The need for separate mineralocorticoid replacement during critical illness is unclear. Serum aldosterone concentrations are markedly depressed in meningococcemia (311). The administration of fludrocortisone in addition to hydrocortisone has been suggested in septic shock (312) with the benefit of shortening the duration of norepinephrine administration in the septic subgroup, over hydrocortisone administration alone. The mineralocorticoid activity of hydrocortisone alone, however, may be sufficient and should not exceed 200 mg/d (equivalent to about 100 mg/m2/d) when given to adults (313–316). Hydrocortisone’s mineralocorticoid activity is deemed to be equivalent to 150 µg/m2/d of 9α-fludrocortisone when a total daily dose of 20–50 mg of hydrocortisone is reached.

Treatment with low-dose hydrocortisone for relative adrenal insufficiency has gained interest since the first randomized controlled trial (RCT) in adults with septic shock was published in 2002, proving a mortality benefit (276). A subsequent RCT in adults did not confirm a mortality advantage for the treatment with stress doses of hydrocortisone, leaving us with conflicting results (316). The pediatric literature lacks large RCTs evaluating the benefit of corticosteroids specifically in septic shock and refractory septic shock, and a pediatric meta-analysis evaluating the role of corticosteroids in shock did not demonstrate benefit (302). Trials in premature newborns, and other studies in children and adults have repeatedly shown a positive effect on the cardiovascular system by decreasing the duration and/or amount of catecholamines administered (2, 67, 284, 287, 317, 318).

Very high-dose corticosteroid administration in septic shock has previously been associated with higher infection rates. Several studies published since 2006 point to the possibility of infectious complications as a result of corticosteroid administration in adults and children. Steroid use was linked to disseminated candidiasis in a case report (319); however, infectious complications were not found to be increased by the administration of corticosteroids in children and adults with shock in other studies. Other side effects in patients receiving corticosteroids have been described, including hyperglycemia and bleeding. Concerns regarding the development of myopathy in association with corticosteroid therapy have been raised but not confirmed in either the adult or pediatric population with shock. A rise in sodium during corticosteroid administration was observed in several studies and self-resolves after discontinuation. Pediatric septic shock is associated with suppression of all aspects of adaptive immunity, and steroid use was associated with further depression of peripheral blood mononuclear cell adaptive immunity messenger RNA expression (320, 321).

Analysis of data obtained during the RESOLVE trial did not reveal treatment benefit associated with the administration of corticosteroids, but the concerns for higher mortality associated with corticosteroid administration raised by the analysis of the Pediatric Health Information System database were not corroborated (321). Studies in patients with serious infectious illnesses, that is, meningococcal meningitis, have shown cortisol production rates between 4 and 15 times the normal daily production rate of 5.7–12.5 mg/m2 (277–279, 290, 322–325) of cortisol. Effects on the cardiovascular system in shock have been shown at the lower end of the stress dose range. Administration of stress doses as low as 0.18 mg/kg/hr of hydrocortisone (about 4 mg/kg/d) shorten the time to cessation of vasopressor support (median time 2 vs 7 d in the placebo group) without improving mortality in adults (326). In a single-center study of term neonates, the administration of 45 mg/m2/d of hydrocortisone resulted in similar complication rates compared with historical controls and resulted in a statistically significant increase in blood pressure at 2, 6, 12, and 24 hours after initiation (67). Cortisol levels in adults after IV boluses of 50 mg of hydrocortisone given 6 hourly showed peak plasma cortisol levels over 100 μg/dL, and nadir levels remained elevated at 40–50 μg/dL (326). Among children, only those with fluid-refractory shock were found to have adrenal insufficiency (327).

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Persistent Pulmonary Artery Hypertension (PPHN) of the Newborn Therapy

Inhaled nitric oxide therapy is the treatment of choice for uncomplicated PPHN (328, 329). However, metabolic alkalinization remains an important initial resuscitative strategy during shock because PPHN can reverse when acidosis is corrected (330). For centers with access to inhaled nitric oxide, this is the only selective pulmonary vasodilator reported to be effective in reversal of PPHN (331–336). Milrinone may be added to improve heart function as tolerated (337, 338). Investigations support use of inhaled iloprost (synthetic analog of prostacyclin) or adenosine infusion as modes of therapy for PPHN (339–345). ECMO remains the therapy of choice for patients with refractory PPHN and sepsis (346–349).

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Extracorporeal Therapies

Various extracorporeal therapies such as ECMO, CRRT, and blood purification (hemofiltration, hemoperfusion, and therapeutic plasma exchange [TPE]) have been reported with various successes in the management of pediatric sepsis and septic shock. ECMO is a viable therapy for refractory septic shock in neonates and children (346–359). Neonates have comparably good outcomes (80% + survival) whether the indication for ECMO is refractory respiratory failure or refractory shock from sepsis. Pediatric and adult patients with sepsis have lower survival (historically ≤ 50%) than neonates, but experienced ECMO centers are now reporting survival rates approaching 75% (356–358) for refractory shock and 90% for refractory pneumonia (359). Although ECMO survival is similar in pediatric patients with and without sepsis, thrombotic complications are common in sepsis. Efforts are warranted to reduce ECMO-induced hemolysis because free heme scavenges nitric oxide, adenosine, and a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (a.k.a. von Willebrand factor-cleaving protease) leading to microvascular thrombosis, reversal of portal blood flow, and multiple organ failure (360–364). Severe hemolysis (plasma Hgb > 1 g/L) is associated with longer ECMO runs, more blood product administration, and increased mortality (362). Independent risk factors for hemolysis on ECMO include very negative inlet pressures, higher pump speeds, kinked or narrowed cannulae, and nonpediatric oxygenators (362). The risk of hemolysis can be mitigated by using the proper sized cannulas for age, avoiding excessive pump speeds, and maintaining the negative inlet pressure close to the specified pressure drop given by the manufacturer for the flow rate and never greater than –100 mm Hg (363, 364).

Outcome benefits of CRRT, either alone or in tandem with ECMO, are uncertain in pediatric sepsis. Theoretical benefits of CRRT in sepsis could include prevention or management of fluid overload, management of acute kidney injury, clearance of lactate and organic acids, binding of inflammatory mediators, reversal of coagulopathy, or some combination of these actions (365, 366). Mortality in children receiving CRRT in sepsis ranges from 39% to 59%, likely reflecting severity of illness of patient selection for CRRT use. The best documented association of CRRT and outcome is related to fluid overload. In general, use of CRRT earlier in the course of multiple organ dysfunction syndrome (MODS), including septic patients, has been associated with decreased mortality in children, even when adjusted for severity of illness (128, 367, 368). No specific randomized trials of CRRT use in pediatric sepsis have been performed. In adults, use of higher CRRT flux rates (> 35 mL/kg/hr filtration-dialysis flux), while initially encouraging, has not shown overall mortality benefit in subsequent randomized trials and meta-analysis (369, 370). Investigators in pediatric settings have reported that the use of high flux flow rate CRRT, with concomitant fresh frozen plasma, antithrombotic protein C infusion, or in combination with plasma exchange on ECMO has been associated with reduced inotrope/vasopressor requirements in children with refractory septic shock and purpura (4, 371–376).

Investigators have reported more experiences with blood purification for pediatric sepsis since the last update. In 2010, guided by the evidence-based adult and pediatric literature, the American Society of Apheresis gives a category III recommendation, which is “Optimum role of apheresis therapy is not established. Decision-making should be individualized,” for the use of TPE for sepsis with multiple organ failure (377). Meta-analysis of adult randomized trials reports survival benefit with the use of blood purification for sepsis by hemoperfusion or TPE but not by hemofiltration (378). In this regard, pediatric case series and small trials have reported survival benefits with the use of TPE for sepsis-induced MODS, and in particular, patients with significant coagulopathy (379–387). These studies use TPE as a strategy to reverse MODS and not for shock resuscitation. As for other blood purification techniques for pediatric sepsis, a large RCT testing plasma filtration was stopped due to poor recruitment and showed no benefit of plasmafiltration for severe sepsis (388), and hemoperfusion experience had been very limited (389–391).

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Pediatric Septic Shock

Diagnosis. The inflammatory triad of fever, tachycardia, and vasodilation is common in children with benign infections (Fig. 2). Septic shock is suspected when children with this triad have a change in mental status manifested as irritability, inappropriate crying, drowsiness, confusion, poor interaction with parents, lethargy, or becoming unarousable. The clinical diagnosis of septic shock is made in children who 1) have a suspected infection manifested by hypothermia or hyperthermia and 2) have clinical signs of inadequate tissue perfusion including any of the following: decreased or altered mental status, prolonged capillary refill greater than 2 seconds, diminished pulses, mottled cool extremities, or flash capillary refill, bounding peripheral pulses and wide pulse pressure or decreased urine output less than 1 mL/kg/hr. Hypotension is not necessary for the clinical diagnosis of septic shock; however, its presence in a child with clinical suspicion of infection is confirmatory.

We recommend that each institution develop a recognition bundle (Fig. 1) to optimize identification of patients at risk for septic shock that is based on vital sign abnormalities and high-risk criteria (1C).

The recognition bundle should contain:

1) A trigger tool. Elements that are recommended for use in a trigger tool include vital signs, physical examination, and at-risk populations (an example trigger tool is located in Fig. 3).

2) Rapid clinician assessment within 15 minutes for any patient that is identified by the trigger tool.

3) Activation of a sepsis resuscitation bundle within 15 minutes for patients with suspected septic shock. We recommend that each institution also develop or adopt a first-hour resuscitation and stabilization bundle (Fig. 1) to optimize time to completion of first hour and stabilization tasks when a patient with suspected septic shock is identified (1C).

The resuscitation bundle may contain:

1) Intraosseous or IV access within 5 minutes

2) Appropriate fluid resuscitation initiated within 30 minutes

3) Initiation of broad spectrum antibiotics within 60 minutes

4) Blood culture if it does not delay antibiotic administration

5) Appropriate use of peripheral or central inotrope within 60 minutes

The stabilization bundle may contain:

1) Multimodal monitoring to guide fluid, hormonal, and cardiovascular therapies to attain a normal MAP-CVP for age (55 + 1.5 × age in yr), and ScVO2 greater than 70% and/or CI 3.3–6.0 L/min/m2

2) Administration of appropriate antibiotic therapy and source control. We recommend that each institution develop or adopt a performance bundle (Fig. 1) to identify barriers to attaining the recognition, resuscitation, and stabilization bundle goals (1C).

The performance bundle should contain:

1) Measurement of adherence as well as achievement of goals and individual components.

2) Assessment of barriers as well as unintended consequences such as inappropriate antibiotic duration or fluid overresuscitation.

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ABCs: The First Hour of Resuscitation (Emergency Department Resuscitation)

Goals: (Level 1C)

* Maintain or restore airway, oxygenation, and ventilation

* Maintain or restore circulation, defined as normal perfusion and blood pressure

* Maintain or restore threshold HR.

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Therapeutic Endpoints (Level 1C).

Capillary refill less than or equal to 2 seconds, normal pulses with no differential between the quality of peripheral and central pulses, warm extremities, urine output greater than 1 mL/kg/hr, normal mental status, normal blood pressure for age (only reliable when pulses palpable), normal glucose concentration, normal ionized calcium concentration.

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Monitoring (Level 1C)

* Pulse oximeter

* Continuous electrocardiogram (ECG)

* Blood pressure and pulse pressure

* Temperature

* Urine output

* Glucose, ionized calcium

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Airway and Breathing (Level 1C).

Airway and breathing should be rigorously monitored and maintained. Supplemental oxygen or high-flow nasal cannula oxygen is titrated as initial therapy to avoid hypoxia and hyperoxia (SpO2 100%). Lung compliance and work of breathing may change precipitously. In early sepsis, patients often have a respiratory alkalosis from centrally mediated hyperventilation. As sepsis progresses, patients may have hypoxemia as well as metabolic acidosis and are at high risk to develop respiratory acidosis secondary to a combination of parenchymal lung disease and/or inadequate respiratory effort due to altered mental status. The decision to intubate and ventilate is based on clinical assessment of increased work of breathing, hypoventilation, or impaired mental status. Waiting for confirmatory laboratory tests is discouraged. If possible, volume loading and peripheral or central inotropic/vasoactive drug support is recommended before and during intubation because of relative or absolute hypovolemia, cardiac dysfunction, and the risk of suppressing endogenous stress hormone response with agents that facilitate intubation. Etomidate is not recommended. Ketamine with atropine pretreatment should be considered the induction combination of choice during intubation, to promote cardiovascular integrity during the procedure. A short-acting neuromuscular blocking agent can facilitate intubation if the provider is confident and skilled.

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Circulation (Level 1C).

Vascular access should be rapidly attained. In addition to direct visualization and/or palpation, portable near-infrared imaging devices may assist in peripheral vascular access. Establish intraosseous access if reliable peripheral intravenous line (PIV) access cannot be attained in minutes. Powered intraosseous devices (i.e., intraosseous drill) can facilitate successful intraosseous placement but should be reserved for use in children greater than 3 kg (device not approved below this size). Fluid resuscitation should commence immediately unless hepatomegaly, rales, or a cardiac gallop are present. In the fluid-refractory patient, begin a peripheral inotrope if a second PIV/intraosseous is in place, while establishing a central venous catheter. When administered through a PIV/intraosseous, the inotrope should be infused either as a dilute solution (peripheral epinephrine dilution may be 10 × central) or with a second carrier solution running at a flow rate to assure that it reaches the heart in a timely fashion. Care must be taken to reduce dosage if evidence of peripheral infiltration/ischemia occurs as α-adrenergic receptor mediated effects occur at higher concentrations for epinephrine and dopamine. Central dopamine, epinephrine, or norepinephrine can be administered as a first-line drug as indicated by hemodynamic state when a central line is in place. It is generally appropriate to begin central venous infusion and wait until a pharmacologic effect is observed before stopping the peripheral infusion. Establishing a central venous catheter during the initial resuscitation may be dependent upon the availability of skilled personnel and appropriate equipment and should not delay or compromise ongoing resuscitation efforts. Utilization of bedside vascular imaging modalities such as ultrasound guidance can facilitate successful central venous access for skilled personnel familiar with such technologies. High frequency (7.5–13 MHz) probes should be used for infants and children, with higher frequencies yielding better resolution for the smallest patients (< 15 kg).

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Fluid Resuscitation (Level 1C).

Rapid fluid boluses of 20 mL/kg (isotonic crystalloid or 5% albumin) can be administered by push or rapid infusion device (pressure bag) while observing for signs of fluid overload (i.e., the development of increased work of breathing, rales, cardiac gallop rhythm, or hepatomegaly). In the absence of these clinical findings, children can require 40–60 mL/kg in the first hour. Fluid can be pushed with the goal of attaining normal perfusion and blood pressure. Hypoglycemia and hypocalcemia should be corrected. A 10% dextrose containing isotonic IV solution can be run at maintenance IV fluid rates to provide age appropriate glucose delivery and to prevent hypoglycemia.

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Hemodynamic Support (Level 1C).

Central dopamine can be titrated to a maximum of 10 μg/kg/min through central access; however, epinephrine or norepinephrine is more likely to be beneficial. Central epinephrine can be started for “cold shock” (0.05–0.3 μg/kg/min) or norepinephrine can be titrated for “warm shock” to restore normal perfusion and blood pressure.

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Hydrocortisone Therapy (Level 1C).

If a child is “at risk of absolute adrenal insufficiency or adrenal pituitary axis failure” (e.g., purpura fulminans, congenital adrenal hyperplasia, prior steroid exposure, hypothalamic/pituitary abnormality, intubation with etomidate induction) and remains in shock despite epinephrine or norepinephrine infusion, then hydrocortisone can be administered ideally after attaining a blood sample for subsequent determination of baseline cortisol concentration.

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Stabilization: Beyond the First Hour (PICU Hemodynamic Support)

Goals: (Level 1C)

* Normal perfusion, capillary refill less than or equal to 2 seconds, threshold HRs

* Perfusion pressure (MAP-CVP or MAP-IAP) appropriate for age. ScVO2 greater than 70%

* CI greater than 3.3 and less than 6.0 L/min/m2

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Therapeutic Endpoints: (Level 1C).

Capillary refill less than or equal to 2 seconds, threshold HRs, normal pulses with no differential between the quality of the peripheral and central pulses, warm extremities, urine output greater than 1 mL/kg/hr, normal mental status, CI greater than 3.3 and less than 6.0 L/min/m2 with normal perfusion pressure (MAP-CVP, or MAP-IAP) for age (Table 1), ScVO2 greater than 70%. Maximize preload in order to maximize CI, MAP-CVP. Normal INR, anion gap, and lactate.

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Monitoring (Level 1C)

* Pulse oximetry

* Continuous ECG

* Continuous intra-arterial blood pressure

* Temperature (core) urine output

* CVP/oxygen saturation and/or pulmonary artery pressure/oxygen saturation CO

* Serial limited echocardiogram

* Glucose and calcium


* Lactate, anion gap

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Fluid Resuscitation (Level 1C).

Fluid losses and persistent hypovolemia secondary to diffuse capillary leak can continue for days. Ongoing fluid replacement should be directed at clinical endpoints including perfusion, PAOP/global end-diastolic volume (when available), and CO. Crystalloid is the fluid of choice in patients with Hgb greater than 10 g/dL. RBC transfusion can be given to children with Hgb less than 10 g/dL. FFP is recommended for patients with prolonged INR but as an infusion, not a bolus. Following shock resuscitation, diuretics/peritoneal dialysis/high flux CRRT can be used to remove fluid in patients who are 10% fluid overloaded and unable to maintain fluid balance with native urine output/extra-renal losses.

Elevated lactate concentration and anion gap measurements can be treated by assuring both adequate oxygen delivery and glucose utilization. Adequate oxygen delivery (indicated by a ScVO2 > 70%) can be achieved by attaining Hgb greater than 10 g/dL and CO greater than 3.3 L/min/m2 using adequate volume loading and inotrope/vasodilator support when needed (as described below). Appropriate glucose delivery can be attained by giving a D10% containing isotonic IV solution at fluid maintenance rate. Appropriate glucose uptake can be attained in subsequently hyperglycemic patients by titrating a glucose/insulin infusion to prevent hyperglycemia (keep glucose concentration ≤ 150 mg/dL) and hypoglycemia (keep glucose concentration > 80 mg/dL). The use of lesser glucose infusion rates (e.g., D5% or lower volumes of D10%) will not provide glucose delivery requirements.

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Hemodynamic Support (Level 1C).

Hemodynamic support can be required for days. Children with “catecholamine-resistant shock” can present with low CO/high SVR, high CO/low SVR, or low CO/low SVR shock. Although children with persistent shock commonly have worsening cardiac failure, hemodynamic states may completely change with time. Titration of vasoactive infusion(s) may be guided by clinical examination (blood pressure, HR, and capillary refill/skin perfusion analysis) and laboratory data (arterial blood gas and ScVO2 analysis). For patients with persistent shock (reduced urine output, poor perfusion, metabolic/lactic acidosis, or hypotension), a more accurate assessment of CO may be warranted. Many modalities for CO assessment currently exist and include pulmonary artery, PiCCO, femoral artery or thermodilution catheters, and/or CO estimated by Doppler ultrasound. These additional data may justify further changes in the vasoactive regimen with resolution of shock. Therapies should be directed to maintain mixed venous/ScVO2 greater than 70%, CI greater than 3.3 less than 6.0 L/min/m2, and a normal perfusion pressure for age (MAP-CVP).

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Shock With Low CI, Normal Blood Pressure, and High SVR (Level 1D).

Milrinone is considered by the authors to be the first-line inodilator in patients with epinephrine-resistant shock and normal blood pressure. As noted above, the long elimination half-life of these drugs can lead to slowly reversible toxicities (hypotension, tachyarrhythmias, or both) particularly if abnormal renal or liver function exists. Such toxicities can be reversed in part with norepinephrine infusion. Additional volume loading may be necessary to prevent hypotension when loading doses are used. Nitroprusside or nitroglycerin may be considered as second-line vasodilators. Monitoring is needed to avoid cyanide or isothiocyanate toxicity. Levosimendan and enoximone may have a role in recalcitrant low CO syndrome. Thyroid replacement with triiodothyronine is warranted for thyroid insufficiency, and hydrocortisone replacement can be warranted for adrenal or HPA axis insufficiency.

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Shock With Low CI, Low Blood Pressure, and Low SVR (Level 1D).

Norepinephrine can be added to/or substituted for epinephrine to increase DBP and SVR. Once an adequate blood pressure is achieved, dobutamine, type III PDEIs such as milrinone or enoximone (which is more cardioselective than milrinone) or levosimendan can be added to norepinephrine to improve CI and ScVO2. Thyroid replacement with triiodothyronine is warranted for thyroid insufficiency, and hydrocortisone replacement is warranted for adrenal or HPA axis insufficiency.

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Shock With High CI and Low SVR (Level 1D).

When titration of norepinephrine and fluid does not resolve hypotension, then low-dose vasopressin, angiotensin, or terlipressin can be helpful in restoring blood pressure; however, these potent vasoconstrictors can reduce CO, therefore it is recommended that “these drugs are used with CO/ScVO2 monitoring.” In this situation, additional inotropic therapies will be required such as low-dose epinephrine or dobutamine. Terlipressin is a longer acting drug than angiotensin or vasopressin, so toxicities are more long-acting. As with other forms of severe shock, thyroid hormone or adrenocortical replacement therapy may be added for appropriate indications. We recommend frequent reevaluation of hemodynamic parameters when a patient requires the use of vasopressors, especially in relation to CO, SVR, and peripheral perfusion so as to choose the appropriate combination with inotropic or vasodilator drugs ± fluids.

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Refractory Shock (Level 2C).

Children with refractory shock must be suspected to have unrecognized morbidities (treatment in parenthesis), including inappropriate source control of infection (remove nidus and use antibiotics with the lowest minimum inhibitory concentration possible, preferably < 1, use IV immunoglobulin for toxic shock), pericardial effusion (pericardiocentesis), pneumothorax (thoracentesis), hypoadrenalism (adrenal hormone replacement), hypothyroidism (thyroid hormone replacement), ongoing blood loss (blood replacement/hemostasis), increased IAP (peritoneal catheter or abdominal release), necrotic tissue (nidus removal), excessive immunosuppression (wean immunosuppressants), or immunocompromise (restore immune function; e.g., white cell growth factors/transfusion for neutropenic sepsis). When these potentially reversible causes are addressed, ECMO becomes an important alternative to consider. The expected survival with ECMO for septic shock is no greater than 50% in children, although some centers have recently reported survival rates as high as 75% by using high flow, goal-directed central ECMO where the right atrium and ascending aorta are cannulated directly. This approach mitigates any differential cyanosis and allows the highest possible flow rates, which may facilitate faster resolution of shock. If high flow rates are necessary to resolve shock, it is important to monitor for, and prevent, hemolysis. Maintaining plasma free hemoglobin concentration less than 0.05 g/L by using adequate catheter, circuit, and oxygenator sizes for age. Monitor the inlet pressure as close to the patient as possible (at the connection between the venous cannula and the tubing) and maintain this pressure between zero and the expected pressure drop for the cannula size and the pump flow that is employed. At pressures below these points, there is an increased risk for creating negative pressure in the vessel leading to vessel damage. Thus, the cannula size should be chosen to stay below this limit at the peak expected flow. If these limits are approached, the pump speed should be temporarily reduced while the cause is urgently sought out and corrected. Aside from unnecessarily high circuit flow targets, causes of extremely negative inlet pressures include hypovolemia, inadequate cannula size, partial cannula obstruction or kinking, or high intrathoracic pressure (e.g., cardiac tamponade, excessive positive end-expiratory pressure, pneumothorax, abdominal compartment syndrome). Adequate cannula placement can be confirmed using both chest x-ray and ultrasound guidance. Use of CRRT should be considered for management of potential or actual fluid overload and in patients with purpura. CRRT dosing of 20–25 mL/kg/hr is adequate. High flux CRRT dosing (> 35 mL/kg/hr) can be used, but benefits are theoretical. Consideration should be given to use of CRRT on ECMO primarily for improvement of fluid balance. TPE should not be used during the initial septic shock resuscitation. Once shock resuscitation is addressed, TPE could be considered as a strategy to reverse MODS, especially in patients with significant coagulopathy. Titration of medications will be needed during the procedure to prevent hemodynamic changes because TPE will also remove inotropes, vasopressors, and sedatives. Citrate, a calcium chelator, is used as an anticoagulant for the TPE circuit; therefore, calcium levels will need to be monitored and replenished during the procedure.

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Septic shock should be suspected in any newborn with tachycardia, respiratory distress, poor feeding, poor tone, poor color, tachypnea, diarrhea, or reduced perfusion, particularly in the presence of a maternal history of chorioamnionitis or prolonged rupture of membranes (Fig. 4). It is important to distinguish newborn septic shock from cardiogenic shock caused by closure of the PDA in newborns with ductal-dependent complex congenital heart disease. Any newborn with shock and hepatomegaly, cyanosis, a cardiac murmur, or differential upper and lower extremity blood pressures or pulses should be started on prostaglandin infusion until complex congenital heart disease is ruled out by echocardiographic analysis. Inborn errors of metabolism resulting in hyperammonemia or hypoglycemia may simulate septic shock, and appropriate laboratory tests should be obtained to rule out these conditions. Newborn septic shock is typically accompanied by increased pulmonary vascular resistance and artery pressures. PPHN can cause right ventricle failure with right-to-left shunting at the atrial/ductal levels causing cyanosis.

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ABCs: The First Hour of Resuscitation (Delivery Room Resuscitation)

Goals: (Level 1C)

* Maintain airway, oxygenation, and ventilation

* Restore and maintain circulation, defined as normal perfusion and blood pressure

* Maintain neonatal circulation

* Maintain threshold HRs.

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Therapeutic Endpoints: (Level 1C)

* Capillary refill less than or equal to 2 seconds, normal pulses with no differential in quality between peripheral and central pulses, warm extremities, urine output greater than 1 mL/kg/hr, normal mental status, normal blood pressure for age, normal glucose, and calcium concentrations.

* Difference in preductal and postductal oxygen saturation less than 5%

* 95% SaO2

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Monitoring: (Level 1C)

* Temperature

* Preductal and postductal pulse oximetry

* Intra-arterial (umbilical or peripheral) blood pressure

* Continuous ECG

* Blood pressure

* Arterial pH

* Urine output

* Glucose, ionized calcium concentration

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Airway and Breathing (Level 1D).

Airway patency and adequate oxygenation and ventilation should be rigorously monitored and maintained. Supplemental or high-flow nasal cannula oxygen is the first choice for respiratory support. The decision to intubate and ventilate is based on clinical diagnosis of increased work of breathing or inadequate respiratory effort or marked hypoxemia. Volume loading and inotrope infusion are often necessary prior to intubation and ventilation because analgesia, sedation, and positive-pressure ventilation can reduce preload, precipitating severe hemodynamic instability or arrest. Critically ill neonates may have rapid decline in systolic and diastolic ventricular function, which implies the need for close reassessment as resuscitation progresses. Expertly timed and performed intubation and mechanical ventilation will enhance physiologic performance at all levels by obviating work of breathing and ensuring the best possible oxygenation and perfusion. Pharmacologic management of intubation includes, in addition to adequate fluid resuscitation, the use of atropine to prevent hemodynamically significant bradycardia, and judicious analgesia, which can be accomplished in many cases with small doses of fentanyl, given slowly as 1–2 μg/kg aliquots. The use of NMDA-receptor antagonists such as ketamine is discouraged by many experts, given concerns regarding neurotoxicity despite it being the only hemodynamically stable drug. Etomidate is associated with adrenal suppression and is generally discouraged, although the agent has been used successfully by some experts in this setting with adjunctive hydrocortisone. Morphine, propofol, barbiturates, high-dose benzodiazepines, and dexmedetomidine are likely to cause hemodynamic instability in the septic neonate and should not be used as first-line agents to secure the airway in this setting.

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Circulation (Level 1D).

Vascular access can be rapidly attained according to NRP/PALS guidelines. Placement of an umbilical arterial and venous catheter is preferred. Intraosseous access, particularly in preterm newborns, is not the preferred route of drug administration.

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Fluid Resuscitation (Level 1C).

Fluid boluses of 10 mL/kg can be administered, observing for the development of hepatomegaly and increased work of breathing. Up to 60 mL/kg may be required in the first hour. Fluid should be infused with a goal of attaining normal perfusion and blood pressure. A D10 containing isotonic IV solution run at maintenance rate will provide age appropriate glucose delivery to prevent hypoglycemia.

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Hemodynamic Support (Level 1C).

Patients with severe shock uniformly require cardiovascular support during fluid resuscitation. Although dopamine can be used as the first-line agent, its effect on pulmonary vascular resistance should be considered. A combination of dopamine at low dosage (< 8 μg/kg/min) and dobutamine (up to 10 μg/kg/min) is initially recommended. If the patient does not adequately respond to these interventions, then epinephrine (0.05–0.3 μg/kg/min) can be infused to restore normal blood pressure and perfusion.

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PPHN Therapy (Level 1B).

Hyperoxygenate initially with 100% oxygen and institute metabolic alkalinization (up to pH 7.50) with NaHCO3 or tromethamine unless and until inhaled NO is available. Mild hyperventilation to produce a respiratory alkalosis can also be instituted until 100% oxygen saturation and less than 5% difference in preductal and postductal saturations are obtained. Inhaled nitric oxide should be administered as the first treatment when available. Back-up therapies include milrinone and inhaled iloprost.

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Stabilization: Beyond the First Hour (NICU Hemodynamic Support)

Goals: (Level 1C)

* Restore and maintain threshold HR.

* Maintain normal perfusion and blood pressure.

* Maintain neonatal circulation.

* ScVO2 greater than 70%

* CI greater than 3.3 L/min/m2

* SVC flow greater than 40 mL/kg/min

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Therapeutic Endpoints (Level 1C)

* Capillary refill less than or equal to 2 seconds, normal pulses with no differential between peripheral and central pulses, warm extremities, urine output greater than 1 mL/kg/hr, normal mental status, and normal blood pressure for age

* greater than 95% SaO2

* less than 5% difference in preductal and postductal SaO2

* ScVO2 greater than 70%

* Absence of right-to-left shunting, tricuspid regurgitation, or right ventricular failure on echocardiographic analysis.

* Normal glucose and ionized calcium concentrations

* SVC flow greater than 40 mL/kg/min

* CI greater than 3.3 L/min/m2

* Normal INR

* Normal anion gap, and lactate Fluid overload less than 10%

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Monitoring (Level 1C)

* Pulse oximetry

* Arterial pH Continuous ECG

* Continuous intra-arterial blood pressure

* Temperature

* Glucose and calcium concentration

* Ins and outs, urine output

* CVP/oxygen saturation

* CO

* SVC flow


* Anion gap and lactate

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Fluid Resuscitation (Level 1C).

Fluid losses and persistent hypovolemia secondary to diffuse capillary leak can continue for days. Ongoing fluid replacement should be directed at clinical endpoints, including perfusion and CVP. Crystalloid is the fluid of choice in patients with Hgb greater than 12 g/dL. Packed RBCs can be transfused in newborns with Hgb less than 12 g/dL. Diuretics are recommended in newborns who are 10% fluid overloaded and unable to attain fluid balance with native urine output/extra-renal losses. A D10% containing isotonic IV solution run at maintenance rate can provide age appropriate glucose delivery to prevent hypoglycemia. Insulin infusion can be used to correct hyperglycemia. Diuretics are indicated in hypervolemic patients to prevent fluid overload.

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Hemodynamic Support (Level 1C).

A 5-day, 6 hour/d course of IV pentoxifylline can be used to reverse septic shock in VLBW babies. In term newborns with PPHN, inhaled nitric oxide is often effective. Its greatest effect is usually observed at 20 ppm. In newborns with poor left ventricle function and normal blood pressure, the addition of nitrosovasodilators or type III PDEIs to epinephrine (0.05–0.3 µg/kg/min) can be effective but must be monitored for toxicities. It is important to volume load based on clinical examination and blood pressure changes when using these systemic vasodilators. Triiodothyronine is an effective inotrope in newborns with thyroid insufficiency. Norepinephrine can be effective for refractory hypotension, but ScVO2 should be maintained greater than 70%. An additional inotrope therapy should be added if warranted. Hydrocortisone therapy can be added if the newborn has adrenal insufficiency (defined by a peak cortisol after ACTH < 18 µg/dL, or basal cortisol < 4 mg/dL, or basal cortisol < 18 with the need for inotropic support). An additional inotrope therapy should be added if warranted.

The total duration of umbilical catheterization should not exceed 5 days for an UAC or 14 days for an umbilical vein catheter. Low doses of heparin (0.25–1.0 U/mL) should be added to the fluid infused through UACs. Prophylactic use of heparin for peripherally inserted silastic percutaneous central venous catheters increases the likelihood that they will complete their intended use (complete therapy) and reduces catheter occlusion.

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Refractory Shock (Level 1C).

Newborns with refractory shock must be suspected to have unrecognized morbidities (requiring specific treatment) including cyanotic or obstructive heart disease (responsive to prostaglandin E1), a critically large PDA (PDA closure), inborn errors of metabolism (responsive to glucose and insulin infusion or ammonia scavengers), pericardial effusion (pericardiocentesis), pneumothorax (thoracentesis), ongoing blood loss (blood replacement/hemostasis), hypoadrenalism (hydrocortisone), and/or hypothyroidism (triiodothyronine). When these causes have been excluded, ECMO becomes an important therapy to consider in term newborns. The current ECMO survival rate for newborn sepsis is 80%. Most centers accept refractory shock or a PaO2 less than 40 mm Hg after maximal therapy to be sufficient indication for ECMO support. When on venovenous ECMO, persistent hypotension and/or shock should be treated with inotropic and/or vasopressor therapy, or conversion to venoarterial support. For newborns with refractory shock related to PPHN-induced right ventricular failure, venovenous ECMO can unload the right ventricle, reduce septal bowing, and improve left ventricle output. However, for newborns with primary left ventricle or biventricular failure refractory to inotropic and vasodilator support, venoarterial ECMO is required to reverse shock. Inotrope requirements can diminish when venoarterial ECMO is used but may persist. Calcium concentration should be normalized in the RBC pump prime (usually requires 300 mg CaCl2 per unit of pRBCs). In newborns with inadequate urine output and 10% fluid overload despite diuretics, CRRT is best performed while on the ECMO circuit. No specific recommendations for CRRT can be made in neonatal sepsis. Venous access for CRRT in neonates can be problematic, but in patients on ECMO, CRRT can be provided in tandem. It is a technical challenge to perform TPE in a neonate weighing less than 5 kg. TPE should not be used during the initial septic shock resuscitation. Once the shock resuscitation is addressed, TPE could be considered as a strategy to reverse MODS, especially in patients with significant coagulopathy. Titration of medications and calcium replenishment will be needed during the procedure to prevent hemodynamic changes.

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1. Carcillo JA, Fields AI; American College of Critical Care Medicine Task Force Committee Members: Clinical practice parameters for hemodynamic support of pediatric and neonatal patients in septic shock. Crit Care Med 2002; 30:1365–1378
2. Brierley J, Carcillo JA, Choong K, et al. Clinical practice parameters for hemodynamic support of pediatric and neonatal septic shock: 2007 update from the American College of Critical Care Medicine. Crit Care Med 2009; 37:666–688
3. Nhan NT, Phuong CXT, Kneen R, et al. Acute management of dengue shock syndrome: A randomized double-blind comparison of 4 intravenous fluid regimens in the first hour Clin Infect Dis 2001; 32:204–212
4. Booy R, Habibi P, Nadel S, et al; Meningococcal Research Group: Reduction in case fatality rate from meningococcal disease associated with improved healthcare delivery. Arch Dis Child 2001; 85:386–390
5. Kutko MC, Calarco MP, Flaherty MB, et al. Mortality rates in pediatric septic shock with and without multiple organ system failure. Pediatr Crit Care Med 2003; 4:333–337
6. DuPont HL, Spink WW. Infections due to gram-negative organisms: An analysis of 860 patients with bacteremia at the University of Minnesota Medical Center, 1958-1966. Medicine (Baltimore) 1969; 48:307–332
7. Stoll BJ, Holman RC, Shuchat A. Decline in sepsis-associated neonatal and infant deaths 1974–1994. Pediatrics 1998; 102:E18
8. Angus DC, Linde-Zwirble WT, Lidicker J, et al. Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care. Crit Care Med 2001; 29:1303–1310
9. Watson RS, Carcillo JA, Linde-Zwirble WT, et al. The epidemiology of severe sepsis in children in the United States. Am J Respir Crit Care Med 2003; 167:695–701
10. Han YY, Carcillo JA, Dragotta MA, et al. Early reversal of pediatric-neonatal septic shock by community physicians is associated with improved outcome. Pediatrics 2003; 112:793–799
11. Ninis N, Phillips C, Bailey L, et al. The role of healthcare delivery in the outcome of meningococcal disease in children: Case-control study of fatal and non-fatal cases. BMJ 2005; 330:1475
12. Ventura AM, Shieh HH, Bousso A, et al. Double-blind prospective randomized controlled trial of dopamine versus epinephrine as first-line vasoactive drugs in pediatric septic shock. Crit Care Med 2015; 43:2292–2302
13. de Oliveira CF, de Oliveira DS, Gottschald AF, et al. ACCM/PALS haemodynamic support guidelines for paediatric septic shock: An outcomes comparison with and without monitoring central venous oxygen saturation. Intensive Care Med 2008; 34:1065–1075
14. Sankar J, Sankar MJ, Suresh CP, et al. Early goal-directed therapy in pediatric septic shock: Comparison of outcomes “with” and “without” intermittent superior venacaval oxygen saturation monitoring: A prospective cohort study. Pediatr Crit Care Med 2014; 15:e157–e167
15. Karapinar B, Lin JC, Carcillo JA. ACCM guidelines use, correct antibiotic therapy, and immune suppressant withdrawal are associated with improved survival in pediatric sepsis, severe sepsis, and septic shock. Crit Care Med 2004; 32(12 Suppl 3):A161
16. Maat M, Buysse CM, Emonts M, et al. Improved survival of children with sepsis and purpura: Effects of age, gender, and era. Crit Care 2007; 11:R112
17. Wills BA, Nguyen MD, Ha TL, et al. Comparison of three fluid solutions for resuscitation in dengue shock syndrome. N Engl J Med 2005; 353:877–889
18. Maitland K, Kiguli S, Opoka RO, et al; FEAST Trial Group: Mortality after fluid bolus in African children with severe infection. N Engl J Med 2011; 364:2483–2495
19. Cruz AT, Perry AM, Williams EA, et al. Implementation of goal-directed therapy for children with suspected sepsis in the emergency department. Pediatrics 2011; 127:e758–e766
20. Larsen GY, Mecham N, Greenberg R. An emergency department septic shock protocol and care guideline for children initiated at triage. Pediatrics 2011; 127:e1585–e1592
21. Paul R, Neuman MI, Monuteaux MC, et al. Adherence to PALS Sepsis Guidelines and Hospital Length of Stay. Pediatrics 2012; 130:e273–e280
22. Paul R, Melendez E, Stack A, et al. Improving adherence to PALS septic shock guidelines. Pediatrics 2014; 133:e1358–e1366
23. Cruz AT, Williams EA, Graf JM, et al. Test characteristics of an automated age- and temperature-adjusted tachycardia alert in pediatric septic shock. Pediatr Emerg Care 2012; 28:889–894
24. Sepanski RJ, Godambe SA, Mangum CD, et al. Designing a pediatric severe sepsis screening tool. Front Pediatr 2014; 2:56
25. Han YY, Kissoon N, Carcillo JA, et al. The Global Pediatric Sepsis Initiative. Pediatr Crit Care Med 2014; 15(suppl):15–16
26. Hollenberg SM, Ahrens TS, Annane D, et al. Practice parameters for hemodynamic support of sepsis in adults patients: 2004 update. Crit Care Med 2004; 32:1928–1948
27. Parker MM, Shelhamer JH, Natanson C, et al. Serial cardiovascular variables in survivors and nonsurvivors of human septic shock: Heart rate as an early predictor of prognosis. Crit Care Med 1987; 15:923–929
28. Parker MM, Shelhamer JH, Bacharach SL, et al. Profound but reversible myocardial depression in patients with septic shock. Ann Intern Med 1984; 100:483–490
29. Pollack MM, Fields AI, Ruttimann UE. Sequential cardiopulmonary variables of infants and children in septic shock. Crit Care Med 1984; 12:554–559
30. Pollack MM, Fields AI, Ruttimann UE. Distributions of cardiopulmonary variables in pediatric survivors and nonsurvivors of septic shock. Crit Care Med 1985; 13:454–459
31. Carcillo JA, Pollack MM, Ruttimann UE, et al. Sequential physiologic interactions in pediatric cardiogenic and septic shock. Crit Care Med 1989; 17:12–16
32. Monsalve F, Rucabado L, Salvador A, et al. Myocardial depression in septic shock caused by meningococcal infection. Crit Care Med 1984; 12:1021–1023
33. Mercier JC, Beaufils F, Hartmann JF, et al. Hemodynamic patterns of meningococcal shock in children. Crit Care Med 1988; 16:27–33
34. Simma B, Fritz MG, Trawöger R, et al. Changes in left ventricular function in shocked newborns. Intensive Care Med 1997; 23:982–986
35. Walther FJ, Siassi B, Ramadan NA, et al. Cardiac output in newborn infants with transient myocardial dysfunction. J Pediatr 1985; 107:781–785
36. Ferdman B, Jureidini SB, Gale G, et al. Severe left ventricular dysfunction and arrhythmias as complications of gram-positive sepsis: Rapid recovery in children. Pediatr Cardiol 1998; 19:482–486
37. Feltes TF, Pignatelli R, Kleinert S, et al. Quantitated left ventricular systolic mechanics in children with septic shock utilizing noninvasive wall-stress analysis. Crit Care Med 1994; 22:1647–1658
38. Ceneviva G, Paschall JA, Maffei F, et al. Hemodynamic support in fluid-refractory pediatric septic shock. Pediatrics 1998; 102:e19
39. Brierly J, Thiruchelvan T, Peters MJ. Hemodynamics of early pediatric fluid resistant septic shock using non-invasive cardiac output (USCOM) distinct profiles of CVC infection and community acquired sepsis. Crit Care Med 2006; 33:171-I
40. Deep A, Goonasekera CD, Wang Y, et al. Evolution of haemodynamics and outcome of fluid-refractory septic shock in children. Intensive Care Med 2013; 39:1602–1609
41. Hoban LD, Paschall JA, Eckstein J, et al. Awake porcine model of intraperitoneal sepsis and altered oxygen utilization. Circ Shock 1991; 34:252–262
42. Green EM, Adams HR. New perspectives in circulatory shock: Pathophysiologic mediators of the mammalian response to endotoxemia and sepsis. J Am Vet Med Assoc 1992; 200:1834–1841
43. McDonough KH, Brumfield BA, Lang CH. In vitro myocardial performance after lethal and nonlethal doses of endotoxin. Am J Physiol 1986; 250:H240–H246
44. Natanson C, Fink MP, Ballantyne HK, et al. Gram-negative bacteremia produces both severe systolic and diastolic cardiac dysfunction in a canine model that simulates human septic shock. J Clin Invest 1986; 78:259–270
45. Dobkin ED, Lobe TE, Bhatia J, et al. The study of fecal E. coli peritonitis-induced septic shock in a neonatal pig model. Circ Shock 1985; 16:325–36
46. Peevy KJ, Chartrand SA, Wiseman HJ, et al. Myocardial dysfunction in group B streptococcal shock. Pediatr Res 1985; 19:511–513
47. Meadow WL, Meus PJ. Unsuspected mesenteric hypoperfusion despite apparent hemodynamic recovery in the early phase of septic shock in piglets. Circ Shock 1985; 15:123–129
48. Meadow WL, Meus PJ. Early and late hemodynamic consequences of group B beta streptococcal sepsis in piglets: Effects on systemic, pulmonary, and mesenteric circulations. Circ Shock 1986; 19:347–356
49. Gill AB, Weindling AM. Echocardiographic assessment of cardiac function in shocked very low birthweight infants. Arch Dis Child 1993; 68(1 Spec No):17–21
50. Kluckow M. Low systemic blood flow and pathophysiology of the preterm transitional circulation. Early Hum Dev 2005; 81:429–437
51. Munro MJ, Walker AM, Barfield CP. Hypotensive extremely low birth weight infants have reduced cerebral blood flow. Pediatrics 2004; 114:1591–1596
52. Jayasinghe D, Gill AB, Levene MI. CBF reactivity in hypotensive and normotensive preterm infants. Pediatr Res 2003; 54:848–853
53. Vavilala MS, Lam AM. CBF reactivity to changes in MAP (cerebral autoregulation) or CO2 (CO2 reactivity) is lost in hypotensive, ventilated, preterm infants. Pediatr Res 2004; 55:898
54. Al-Aweel I, Pursley DM, Rubin LP, et al. Variations in prevalence of hypotension, hypertension, and vasopressor use in NICUs. J Perinatol 2001; 21:272–278
55. Martens SE, Rijken M, Stoelhorst GM, et al; Leiden Follow-Up Project on Prematurity, The Netherlands: Is hypotension a major risk factor for neurological morbidity at term age in very preterm infants? Early Hum Dev 2003; 75:79–89
56. Subhedar NV. Treatment of hypotension in newborns. Semin Neonatol 2003; 8:413–423
57. Seri I, Noori S. Diagnosis and treatment of neonatal hypotension outside the transitional period. Early Hum Dev 2005; 81:405–411
58. Noori S, Seri I. Pathophysiology of newborn hypotension outside the transitional period. Early Hum Dev 2005; 81:399–404
59. Evans JR, Lou Short B, Van Meurs K, et al. Cardiovascular support in preterm infants. Clin Ther 2006; 28:1366–1384
60. Evans N. Which inotrope for which baby? Arch Dis Child Fetal Neonatal Ed 2006; 91:F213–220
61. Osborn DA. Diagnosis and treatment of preterm transitional circulatory compromise. Early Hum Dev 2005; 81:413–422
62. Evans N. Management of hypotension and circulatory assessment on NICU. Early Hum Dev 2005; 81:397–398
63. Seri I. Inotrope, lusitrope, and pressor use in neonates. J Perinatol 2005; 25(Suppl 2):S28–S30
64. Schönberger W, Grimm W, Gempp W, et al. Transient hypothyroidism associated with prematurity, sepsis, and respiratory distress. Eur J Pediatr 1979; 132:85–92
65. Roberton NR, Smith MA. Early neonatal hypocalcaemia. Arch Dis Child 1975; 50:604–609
66. Efird MM, Heerens AT, Gordon PV, et al. A randomized-controlled trial of prophylactic hydrocortisone supplementation for the prevention of hypotension in extremely low birth weight infants. J Perinatol 2005; 25:119–124
67. Ng PC, Lee CH, Bnur FL, et al. A double-blind, randomized, controlled study of a “stress dose” of hydrocortisone for rescue treatment of refractory hypotension in preterm infants. Pediatrics 2006; 117:367–375
68. Fernandez E, Schrader R, Watterberg K. Prevalence of low cortisol values in term and near-term infants with vasopressor-resistant hypotension. J Perinatol 2005; 25:114–118
69. Noori S, Siassi B, Durand M, et al. Cardiovascular effects of low-dose dexamethasone in very low birth weight neonates with refractory hypotension. Biol Neonate 2006; 89:82–87
70. Lauterbach R, Pawlik D, Kowalczyk D, et al. Effect of the immunomodulating agent, pentoxifylline, in the treatment of sepsis in prematurely delivered infants: A placebo-controlled, double-blind trial. Crit Care Med 1999; 27:807–814
71. Zimmerman JJ. Appraising the potential of pentoxifylline in septic premies. Crit Care Med 1999; 27:695–697
72. Haque K, Mohan P. Pentoxifylline for neonatal sepsis. Cochrane Database Syst Rev 2003; CD004205
73. Pollack MM, Ruttimann UE, Getson PR. Pediatric risk of mortality (PRISM) score. Crit Care Med 1988; 16:1110–1116
74. Carcillo JA, Kuch BA, Han YY, et al. Mortality and functional morbidity after use of PALS/APLS by community physicians. Pediatrics 2009; 124:500–508
75. Ranjit S, Aram G, Kissoon N, et al. Multimodal monitoring for hemodynamic categorization and management of pediatric septic shock: A pilot observational study. Pediatr Crit Care Med 2014; 15:e17–e26
76. Kumar R, Singhi S, Singhi P, et al. Randomized controlled trial comparing cerebral perfusion pressure-targeted therapy versus intracranial pressure-targeted therapy for raised intracranial pressure due to acute CNS infections in children. Crit Care Med 2014; 42:1775–1787
77. Redl-Wenzl EM, Armbruster C, Edelmann G, et al. The effects of norepinephrine on hemodynamics and renal function in severe septic shock states. Intensive Care Med 1993; 19:151–154
78. LeDoux D, Astiz ME, Carpati CM, et al. Effects of perfusion pressure on tissue perfusion in septic shock. Crit Care Med 2000; 28:2729–2732
79. Greenhalgh DG, Warden GD. The importance of intra-abdominal pressure measurements in burned children. J Trauma 1994; 36:685–690
80. Evans N, Osborn D, Kluckow M. Preterm circulatory support is more complex than just blood pressure. Pediatrics 2005; 115:1114–1115
81. Osborn DA, Evan N, Kluckow M. Clinical detection of low upper body blood flow in very premature infants using blood pressure, capillary refill time, and central – peripheral temperature difference Arch Dis Child Fetal Neonatal Ed 2004; 69:F168–F173
82. Hunt RW, Evans N, Rieger I, et al. Low superior vena cava flow and neurodevelopment at 3 years in very preterm infants. J Pediatr 2004; 145:588–592
83. Evans N, Kluckow M, Simmons M, et al. Which to measure, systemic or organ blood flow? Middle cerebral artery and superior vena cava blood flow in very preterm infants Arch Dis Child Fetal Neonatal Ed 2002; 87:F181–F184
84. Osborn DA, Evans N, Kluckow M. Hemodynamic and antecedent risk factors of early and late periventricular/intraventricular hemorrhage in premature infants. Pediatrics 2003; 112:33–39
85. Osborn DA, Evans N, Kluckow M. Effect of targeted indomethacin on the ductus arteriosus and blood flow to the upper body and brain in the preterm infant. Arch Dis Child Fetal Neonatal Ed 2003; 88:F477–F482
86. Osborn D, Evans N, Kluckow M. Randomized trial of dobutamine versus dopamine in preterm infants with low systemic blood flow. J Pediatr 2002; 140:183–191
87. Evans N, Osborn D, Kluckow M. Mechanism of blood pressure increase induced by dopamine in hypotensive preterm neonates. Arch Dis Child Fetal Neonatal Ed 2000; 83:F75–F76
88. Kluckow M, Evans N. Low systemic blood flow in the preterm infant. Semin Neonatol 2001; 6:75–84
89. Kluckow M, Evans N. Ductal shunting, high pulmonary blood flow, and pulmonary hemorrhage. J Pediatr 2000; 137:68–72
90. Kluckow M, Evans N. Low superior vena cava flow and intraventricular haemorrhage in preterm infants. Arch Dis Child Fetal Neonatal Ed 2000; 82:–
91. Parr GV, Blackstone EH, Kirklin JW. Cardiac performance and mortality early after intracardiac surgery in infants and young children. Circulation 1975; 51:867–874
92. Yasaka Y, Khemani RG, Markovitz BP. Is shock index associated with outcome in children with sepsis/septic shock?. Pediatr Crit Care Med 2013; 14:e372–e379
93. Rivers E, Nguyen B, Havstad S, et al; Early Goal-Directed Therapy Collaborative Group: Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med 2001; 345:1368–1377
94. Textoris J, Fouché L, Wiramus S, et al. High central venous oxygen saturation in the latter stages of septic shock is associated with increased mortality. Crit Care 2011; 15:R176
95. Ahmad S, Tejuja A, Newman KD, et al. Clinical review: A review and analysis of heart rate variability and the diagnosis and prognosis of infection. Crit Care 2009; 13:232
96. Fenton KE, Sable CA, Bell MJ, et al. Increases in serum levels of troponin I are associated with cardiac dysfunction and disease severity in pediatric patients with septic shock. Pediatr Crit Care Med 2004; 5:533–538
97. Briassoulis G, Narlioglou M, Zavras N, et al. Myocardial injury in meningococcus-induced purpura fulminans in children. Intensive Care Med 2001; 27:1073–1082
98. Thiru Y, Pathan N, Bignall S, et al. A myocardial cytotoxic process is involved in the cardiac dysfunction of meningococcal septic shock. Crit Care Med 2000; 28:2979–2983
99. Hatherill M, Waggie Z, Purves L, et al. Mortality and the nature of metabolic acidosis in children with shock. Intensive Care Med 2003; 29:286–291
100. Dugas MA, Proulx F, de Jaeger A, et al. Markers of tissue hypoperfusion in pediatric septic shock. Intensive Care Med 2000; 26:75–83
101. Scott HF, Donoghue AJ, Gaieski DF, et al. The utility of early lactate testing in undifferentiated pediatric systemic inflammatory response syndrome. Acad Emerg Med 2012; 19:1276–1280
102. Kim YA, Ha EJ, Jhang WK, et al. Early blood lactate area as a prognostic marker in pediatric septic shock. Intensive Care Med 2013; 39:1818–1823
103. Jat KR, Jhamb U, Gupta VK. Serum lactate levels as the predictor of outcome in pediatric septic shock. Indian J Crit Care Med 2011; 15:102–107
104. James JH, Luchette FA, McCarter FD, et al. Lactate is an unreliable indicator of tissue hypoxia in injury or sepsis. Lancet 1999; 354:505–508
105. Chapman LL, Sullivan B, Pacheco AL, et al. VeinViewer-assisted intravenous catheter placement in a pediatric emergency department. Acad Emerg Med 2011; 18:966–971
106. Kim MJ, Park JM, Rhee N, et al. Efficacy of VeinViewer in pediatric peripheral intravenous access: A randomized controlled trial. Eur J Pediatr 2012; 171:1121–1125
107. Aria DJ, Vatsky S, Kaye R, et al. Greater saphenous venous access as an alternative in children. Pediatr Radiol 2014; 44:187–192
108. Guilfoyle FJ, Milner R, Kissoon N. Resuscitation interventions in a tertiary level pediatric emergency department: Implications for maintenance of skills. CJEM 2011; 13:90–95
109. Kanter RK, Zimmerman JJ, Strauss RH, et al. Pediatric emergency intravenous access. Evaluation of a protocol. Am J Dis Child 1986; 140:132–134
110. Voigt J, Waltzman M, Lottenberg L. Intraosseous vascular access for in-hospital emergency use: A systematic clinical review of the literature and analysis. Pediatr Emerg Care 2012; 28:185–199
111. American Heart Association/American Academy of Pediatrics Pediatric Resuscitation Subcommittee: Pediatric Advanced Life Support Provider Manual. 2010, Oak Park, IL, AHA/AAP, p 110
112. Fiorito BA, Mirza F, Doran TM, et al. Intraosseous access in the setting of pediatric critical care transport. Pediatr Crit Care Med 2005; 6:50–53
113. National Institute for Clinical Excellence: Guidance on the Use of Ultrasound Locating Devices for Placing Central Venous Catheters. Technology Appraisal Guidance No. 49, 2002
114. Verghese ST, McGill WA, Patel RI, et al. Ultrasound-guided internal jugular venous cannulation in infants: A prospective comparison with the traditional palpation method. Anesthesiology 1999; 91:71–77
115. Rothschild JM. Ultrasound guidance of central vein catheterization. In: Evidence Report/Technology Assessment, No. 43. Making Health Care Safer: A Critical Analysis of Patient Safety Practices. 2001, Rockville, MD, Agency for Healthcare Research and Quality, 245–53Publication No. 01-E058.
116. Di Nardo M, Tomasello C, Pittiruti M, et al. Ultrasound-guided central venous cannulation in infants weighing less than 5 kilograms. J Vasc Access 2011; 12:321–324
117. Hind D, Calvert N, McWilliams R, et al. Ultrasonic locating devices for central venous cannulation: Meta-analysis. BMJ 2003; 327:361
118. Lamperti M, Caldiroli D, Cortellazzi P, et al. Safety and efficacy of ultrasound assistance during internal jugular vein cannulation in neurosurgical infants. Intensive Care Med 2008; 34:2100–2105
119. Sigaut S, Skhiri A, Stany I, et al. Ultrasound guided internal jugular vein access in children and infant: A meta-analysis of published studies. Paediatr Anaesth 2009; 19:1199–1206
120. Ngo NT, Cao XT, Kneen R, et al. Acute management of dengue shock syndrome: A randomized double-blind comparison of 4 intravenous fluid regimens in the first hour. Clin Infect Dis 2001; 32:204–213
121. Dung NM, Day NP, Tam DT, et al. Fluid replacement in dengue shock syndrome: A randomized, double-blind comparison of four intravenous-fluid regimens. Clin Infect Dis 1999; 29:787–794
122. Maitland K, Pamba A, English M, et al. Randomized trial of volume expansion with albumin or saline in children with severe malaria: Preliminary evidence of albumin benefit. Clin Infect Dis 2005; 40:538–545
123. Finfer S, Bellomo R, Boyce N, et al; SAFE Study Investigators: A comparison of albumin and saline for fluid resuscitation in the intensive care unit. N Engl J Med 2004; 350:2247–2256
124. Upadhyay M, Singhi S, Murlidharan J, et al. Randomized evaluation of fluid resuscitation with crystalloid (saline) and colloid (polymer from degraded gelatin in saline) in pediatric septic shock. Indian Pediatr 2005; 42:223–231
125. Carcillo JA, Davis AL, Zaritsky A. Role of early fluid resuscitation in pediatric septic shock. JAMA 1991; 266:1242–1245
126. Stoner MJ, Goodman DG, Cohen DM, et al. Rapid fluid resuscitation in pediatrics; testing the ACCM guidelines Crit Care Med 2005; 33:A68
127. Ranjit S, Kissoon N, Jayakumar I. Aggressive management of dengue shock syndrome may decrease mortality rate: A suggested protocol. Pediatr Crit Care Med 2005; 6:412–419
128. Foland JA, Fortenberry JD, Warshaw BL, et al. Fluid overload before continuous hemofiltration and survival in critically ill children: A retrospective analysis. Crit Care Med 2004; 32:1771–1776
129. Lucking SE, Williams TM, Chaten FC, et al. Dependence of oxygen consumption on oxygen delivery in children with hyperdynamic septic shock and low oxygen extraction. Crit Care Med 1990; 18:1316–1319
130. Mink RB, Pollack MM. Effect of blood transfusion on oxygen consumption in pediatric septic shock. Crit Care Med 1990; 18:1087–1091
131. Karam O, Tucci M, Ducruet T, et al; Canadian Critical Care Trials Group; PALISI Network: Red blood cell transfusion thresholds in pediatric patients with sepsis. Pediatr Crit Care Med 2011; 12:512–518
132. Carroll GC, Snyder JV. Hyperdynamic severe intravascular sepsis depends on fluid administration in cynomolgus monkey. Am J Physiol 1982; 243:R131–R141
133. Lee PK, Deringer JR, Kreiswirth BN, et al. Fluid replacement protection of rabbits challenged subcutaneous with toxic shock syndrome toxins. Infect Immun 1991; 59:879–884
134. Ottoson J, Dawidson I, Brandberg A, et al. Cardiac output and organ blood flow in experimental septic shock: Effect of treatment with antibiotics, corticosteroids, and fluid infusion. Circ Shock 1991; 35:14–24
135. Wilson MA, Chou MC, Spain DA, et al. Fluid resuscitation attenuates early cytokine mRNA expression after peritonitis. J Trauma 1996; 41:622–627
136. Boldt J, Muller M, Heesen M. Influence of different volume therapies and pentoxifylline infusion on circulating adhesion molecules in critically ill patients. Crit Care Med 1998; 24:385–391
137. Zadrobilek E, Hackl W, Sporn P, et al. Effect of large volume replacement with balanced electrolyte solutions on extravascular lung water in surgical patients with sepsis syndrome. Intensive Care Med 1989; 15:505–510
138. Powell KR, Sugarman LI, Eskenazi AE, et al. Normalization of plasma arginine vasopressin concentrations when children with meningitis are given maintenance plus replacement fluid therapy. J Pediatr 1990; 117:515–522
139. Pladys P, Wodey E, Bétrémieux P, et al. Effects of volume expansion on cardiac output in the preterm infant. Acta Paediatr 1997; 86:1241–1245
140. Lambert HJ, Baylis PH, Coulthard MG. Central-peripheral temperature difference, blood pressure, and arginine vasopressin in preterm neonates undergoing volume expansion. Arch Dis Child Fetal Neonatal Ed 1998; 78:F43–F45
141. Bressack MA, Morton NS, Hortop J. Group B streptococcal sepsis in the piglet: Effects of fluid therapy on venous return, organ edema, and organ blood flow. Circ Res 1987; 61:659–669
142. Pollard AJ, Britto J, Nadel S, et al. Emergency management of meningococcal disease. Arch Dis Child 1999; 80:290–296
143. Boldt J, Heesen M, Welters I, et al. Does the type of volume therapy influence endothelial-related coagulation in the critically ill? Br J Anaesth 1995; 75:740–746
144. Oca MJ, Nelson M, Donn SM. Randomized trial of normal saline versus 5% albumin for the treatment of neonatal hypotension. J Perinatol 2003; 23:473–476
145. Cam BV, Tuan DT, Fonsmark L, et al. Randomized comparison of oxygen mask treatment vs nasal continuous positive airway pressure in dengue shock syndrome with acute respiratory failure. J Trop Pediatr 2002; 48:335–339
146. Maitland K, Pamba A, English M, et al. Pre-transfusion management of children with severe malarial anaemia: A randomised controlled trial of intravascular volume expansion. Br J Haematol 2005; 128:393–400
147. Liet JM, Kuster A, Denizot S, et al. Effects of hydroxyethyl starch on cardiac output in hypotensive neonates: A comparison with isotonic saline and 5% albumin. Acta Paediatr 2006; 95:555–560
148. Pamba A, Maitland K. Capillary refill: Prognostic value in Kenyan children. Arch Dis Child 2004; 89:950–955
149. Yamamoto LG. Ludwig S, Fleisher GR. Rapid sequence intubation. In: Textbook of Pediatric Emergency Care. 2000Philadelphia, PA, Lippincott Williams and Wilkins.
150. Jabre P, Avenel A, Combes X, et al. Morbidity related to emergency endotracheal intubation–a substudy of the KETAmine SEDation trial. Resuscitation 2011; 82:517–522
151. Haubner LY, Barry JS, Johnston LC, et al. Neonatal intubation performance: Room for improvement in tertiary neonatal intensive care units. Resuscitation 2013; 84:1359–1364
152. Li S, Rehder K, Giuliano JS, et al. Development of a quality improvement bundle to reduce tracheal intubation-associated events in PICUs. Am J Med Qual 2016; 31:47–55
153. Jones P, Dauger S, Denjoy I, et al. The effect of atropine on rhythm and conduction disturbances during 322 critical care intubations. Pediatr Crit Care Med 2013; 14:e289–e297
154. Jabre P, Combes X, Lapostolle F, et al; KETASED Collaborative Study Group: Etomidate versus ketamine for rapid sequence intubation in acutely ill patients: A multicentre randomised controlled trial. Lancet 2009; 374:293–300
155. Barois J, Tourneux P. Ketamine and atropine decrease pain for preterm newborn tracheal intubation in the delivery room: An observational pilot study. Acta Paediatr 2013; 102:e534–e538
156. Cuthbertson BH, Sprung CL, Annane D, et al. The effects of etomidate on adrenal responsiveness and mortality in patients with septic shock. Intensive Care Med 2009; 35:1868–1876
157. den Brinker M, Hokken-Koelega AC, Hazelzet JA, et al. One single dose of etomidate negatively influences adrenocortical performance for at least 24h in children with meningococcal sepsis. Intensive Care Med 2008; 34:163–168
158. Albert SG, Ariyan S, Rather A. The effect of etomidate on adrenal function in critical illness: A systematic review. Intensive Care Med 2011; 37:901–910
159. Dmello D, Taylor S, O’Brien J, et al. Outcomes of etomidate in severe sepsis and septic shock. Chest 2010; 138:1327–1332
160. McPhee LC, Badawi O, Fraser GL, et al. Single-dose etomidate is not associated with increased mortality in ICU patients with sepsis: Analysis of a large electronic ICU database. Crit Care Med 2013; 41:774–783
161. Nemergut ME, Yaster M, Colby CE. Sedation and analgesia to facilitate mechanical ventilation. Clin Perinatol 2013; 40:539–558
162. Hall RW. Anesthesia and analgesia in the NICU. Clin Perinatol 2012; 39:239–254
163. Sloth E, Pedersen J, Olsen KH, et al. Transoesophageal echocardiographic monitoring during paediatric cardiac surgery: Obtainable information and feasibility in 532 children. Paediatr Anaesth 2001; 11:657–662
164. Fernandez EG, Green TP, Sweeney M. Low inferior vena caval catheters for hemodynamic and pulmonary function monitoring in pediatric critical care patients. Pediatr Crit Care Med 2004; 5:14–18
165. Mahajan A, Shabanie A, Turner J, et al. Pulse contour analysis for cardiac output monitoring in cardiac surgery for congenital heart disease. Anesth Analg 2003; 97:1283–1288
166. Torgay A, Pirat A, Akpek E, et al. Pulse contour cardiac output system use in pediatric orthotopic liver transplantation: Preliminary report of nine patients. Transplant Proc 2005; 37:3168–3170
167. Reynolds EM, Ryan DP, Sheridan RL, et al. Left ventricular failure complicating severe pediatric burn injuries. J Pediatr Surg 1995; 30:264–269
168. Zaritsky A. Curr Concepts Ped Emergency and Crit Care 1998
169. Duke TD, Butt W, South M. Predictors of mortality and multiple organ failure in children with sepsis. Intensive Care Med 1997; 23:684–692
170. Tibby SM, Hatherill M, Marsh MJ, et al. Clinical validation of cardiac output measurements using femoral artery thermodilution with direct Fick in ventilated children and infants. Intensive Care Med 1997; 23:987–991
171. McLuckie A, Murdoch IA, Marsh MJ, et al. A comparison of pulmonary and femoral artery thermodilution cardiac indices in paediatric intensive care patients. Acta Paediatr 1996; 85:336–338
172. Pauli C, Fakler U, Genz T, et al. Cardiac output determination in children: Equivalence of the transpulmonary thermodilution method to the direct Fick principle. Intensive Care Med 2002; 28:947–952
173. Bollaert PE, Bauer P, Audibert G, et al. Effects of epinephrine on hemodynamics and oxygen metabolism in dopamine-resistant septic shock. Chest 1990; 98:949–953
174. Heckmann M, Trotter A, Pohlandt F, et al. Epinephrine treatment of hypotension in very low birthweight infants. Acta Paediatr 2002; 91:566–570
175. Pellicer A, Valverde E, Elorza MD, et al. Cardiovascular support for low birth weight infants and cerebral hemodynamics: A randomized, blinded, clinical trial. Pediatrics 2005; 115:1501–1512
176. Valverde E, Pellicer A, Madero R, et al. Dopamine versus epinephrine for cardiovascular support in low birth weight infants: Analysis of systemic effects and neonatal clinical outcomes. Pediatrics 2006; 117:e1213–e1222
177. Meier-Hellmann A, Reinhart K, Bredle DL, et al. Epinephrine impairs splanchnic perfusion in septic shock. Crit Care Med 1997; 25:399–404
178. Subhedar NV, Shaw NJ. Dopamine versus dobutamine for hypotensive preterm infants. Cochrane Database Syst Rev 2003; CD001242
179. Sakr Y, Reinhart K, Vincent JL, et al. Does dopamine administration in shock influence outcome? Results of the Sepsis Occurrence in Acutely Ill Patients (SOAP) Study. Crit Care Med 2006; 34:589–597
180. Padbury JF, Agata Y, Baylen BG, et al. Pharmacokinetics of dopamine in critically ill newborn infants. J Pediatr 1990; 117:472–476
181. Bhatt-Mehta V, Nahata MC, McClead RE, et al. Dopamine pharmacokinetics in critically ill newborn infants. Eur J Clin Pharmacol 1991; 40:593–597
182. Allen E, Pettigrew A, Frank D, et al. Alterations in dopamine clearance and catechol-O-methyltransferase activity by dopamine infusions in children. Crit Care Med 1997; 25:181–189
183. Outwater KM, Treves ST, Lang P, et al. Renal and hemodynamic effects of dopamine in infants following cardiac surgery. J Clin Anesth 1990; 2:253–257
184. Lobe TE, Paone R, Dent SR, et al. Benefits of high-dose dopamine in experimental neonatal septic shock. J Surg Res 1987; 42:665–674
185. Seri I, Tulassay T, Kiszel J, et al. Cardiovascular response to dopamine in hypotensive preterm neonates with severe hyaline membrane disease. Eur J Pediatr 1984; 142:3–9
186. Padbury JF, Agata Y, Baylen BG, et al. Dopamine pharmacokinetics in critically ill newborn infants. J Pediatr 1987; 110:293–298
187. Hentschel R, Hensel D, Brune T, et al. Impact on blood pressure and intestinal perfusion of dobutamine or dopamine in hypotensive preterm infants. Biol Neonate 1995; 68:318–324
188. Klarr JM, Faix RG, Pryce CJ, et al. Randomized, blind trial of dopamine versus dobutamine for treatment of hypotension in preterm infants with respiratory distress syndrome. J Pediatr 1994; 125:117–122
189. Liet JM, Boscher C, Gras-Leguen C, et al. Dopamine effects on pulmonary artery pressure in hypotensive preterm infants with patent ductus arteriosus. J Pediatr 2002; 140:373–375
190. Kim KK, Frankel LR. The need for inotropic support in a subgroup of infants with severe life-threatening respiratory syncytial viral infection. J Investig Med 1997; 45:469–473
191. Jardin F, Eveleigh MC, Gurdjian F, et al. Venous admixture in human septic shock: Comparative effects of blood volume expansion, dopamine infusion and isoproterenol infusion on mismatching of ventilation and pulmonary blood flow in peritonitis. Circulation 1979; 60:155–159
192. Harada K, Tamura M, Ito T, et al. Effects of low-dose dobutamine on left ventricular diastolic filling in children. Pediatr Cardiol 1996; 17:220–225
193. Stopfkuchen H, Schranz D, Huth R, et al. Effects of dobutamine on left ventricular performance in newborns as determined by systolic time intervals. Eur J Pediatr 1987; 146:135–139
194. Stopfkuchen H, Queisser-Luft A, Vogel K. Cardiovascular responses to dobutamine determined by systolic time intervals in preterm infants. Crit Care Med 1990; 18:722–724
195. Habib DM, Padbury JF, Anas NG, et al. Dobutamine pharmacokinetics and pharmacodynamics in pediatric intensive care patients. Crit Care Med 1992; 20:601–608
196. Berg RA, Donnerstein RL, Padbury JF. Dobutamine infusions in stable, critically ill children: Pharmacokinetics and hemodynamic actions. Crit Care Med 1993; 21:678–686
197. Martinez AM, Padbury JF, Thio S. Dobutamine pharmacokinetics and cardiovascular responses in critically ill neonates. Pediatrics 1992; 89:47–51
198. Perkin RM, Levin DL, Webb R, et al. Dobutamine: A hemodynamic evaluation in children with shock. J Pediatr 1982; 100:977–983
199. Goto M, Griffin A. Adjuvant effects of beta-adrenergic drugs on indomethacin treatment of newborn canine endotoxic shock. J Pediatr Surg 1991; 26:1156–1160
200. Clark SJ, Yoxall CW, Subhedar NV. Right ventricular performance in hypotensive preterm neonates treated with dopamine. Pediatr Cardiol 2002; 23:167–170
201. Lopez SL, Leighton JO, Walther FJ. Supranormal cardiac output in the dopamine- and dobutamine-dependent preterm infant. Pediatr Cardiol 1997; 18:292–296
202. Keeley SR, Bohn DJ. The use of inotropic and afterload-reducing agents in neonates. Clin Perinatol 1988; 15:467–489
203. Butt W, Bohn D, Whyte H. Clinical experience with systemic vasodilator therapy in the newborn infant. Aust Paediatr J 1986; 22:117–120
204. Benitz WE, Rhine WD, Van Meurs KP, et al. Nitrovasodilator therapy for severe respiratory distress syndrome. J Perinatol 1996; 16:443–448
205. Wong AF, McCulloch LM, Sola A. Treatment of peripheral tissue ischemia with topical nitroglycerin ointment in neonates. J Pediatr 1992; 121:980–983
206. Bailey JM, Miller BE, Kanter KR, et al. A comparison of the hemodynamic effects of amrinone and sodium nitroprusside in infants after cardiac surgery. Anesth Analg 1997; 84:294–298
207. Laitinen P, Happonen JM, Sairanen H, et al. Amrinone versus dopamine-nitroglycerin after reconstructive surgery for complete atrioventricular septal defect. J Cardiothorac Vasc Anesth 1997; 11:870–874
208. Spronk PE, Ince C, Gardien MJ, et al. Nitroglycerin in septic shock after intravascular volume resuscitation. Lancet 2002; 360:1395–1396
209. Heyderman RS, Klein NJ, Shennan GI, et al. Deficiency of prostacyclin production in meningococcal shock. Arch Dis Child 1991; 66:1296–1299
210. Lauterbach R, Zembala M. Pentoxifylline reduces plasma tumour necrosis factor-alpha concentration in premature infants with sepsis. Eur J Pediatr 1996; 155:404–409
211. Kawczynski P, Piotrowski A. Circulatory and diuretic effects of dopexamine infusion in low-birth-weight infants with respiratory failure. Intensive Care Med 1996; 22:65–70
212. Habre W, Beghetti M, Roduit C, et al. Haemodynamic and renal effects of dopexamine after cardiac surgery in children. Anaesth Intensive Care 1996; 24:435–439
213. Moffett BS, Orellana R. Use of fenoldopam to increase urine output in a patient with renal insufficiency secondary to septic shock: A case report. Pediatr Crit Care Med 2006; 7:600–602
214. Morelli A, Rocco M, Conti G, et al. Effects of short-term fenoldopam infusion on gastric mucosal blood flow in septic shock. Anesthesiology 2004; 101:576–582
215. Barton P, Garcia J, Kouatli A, et al. Hemodynamic effects of i.v. milrinone lactate in pediatric patients with septic shock. A prospective, double-blinded, randomized, placebo-controlled, interventional study. Chest 1996; 109:1302–1312
216. Chang AC, Atz AM, Wernovsky G, et al. Milrinone: Systemic and pulmonary hemodynamic effects in neonates after cardiac surgery. Crit Care Med 1995; 23:1907–1914
217. Matejovic M, Krouzecky A, Radej J, et al. Successful reversal of resistent hypodynamic septic shock with levosimendan. Acta Anaesthesiol Scand 2005; 49:127–128
218. Noto A, Giacomini M, Palandi A, et al. Levosimendan in septic cardiac failure. Intensive Care Med 2005; 31:164–165
219. Oldner A, Konrad D, Weitzberg E, et al. Effects of levosimendan, a novel inotropic calcium-sensitizing drug, in experimental septic shock. Crit Care Med 2001; 29:2185–2193
220. Morelli A, Teboul JL, Maggiore SM, et al. Effects of levosimendan on right ventricular afterload in patients with acute respiratory distress syndrome: A pilot study. Crit Care Med 2006; 34:2287–2293
221. Müller K, Peters A, Zeus T, et al. [Therapy of acute decompensated heart failure with levosimendan]. Med Klin (Munich) 2006; 101(Suppl 1):119–122
222. Namachivayam P, Crossland DS, Butt WW, et al. Early experience with Levosimendan in children with ventricular dysfunction. Pediatr Crit Care Med 2006; 7:445–448
223. Ringe HI, Varnholt V, Gaedicke G. Cardiac rescue with enoximone in volume and catecholamine refractory septic shock. Pediatr Crit Care Med 2003; 4:471–475
224. Kern H, Schröder T, Kaulfuss M, et al. Enoximone in contrast to dobutamine improves hepatosplanchnic function in fluid-optimized septic shock patients. Crit Care Med 2001; 29:1519–1525
225. Hoang P, Fosse JP, Fournier JL, et al. [Enoximone-noradrenaline combination in septic shock]. Presse Med 1991; 20:1785
226. Meadows D, Edwards JD, Wilkins RG, et al. Reversal of intractable septic shock with norepinephrine therapy. Crit Care Med 1988; 16:663–666
227. Desjars P, Pinaud M, Potel G, et al. A reappraisal of norepinephrine therapy in human septic shock. Crit Care Med 1987; 15:134–137
228. Morimatsu H, Singh K, Uchino S, et al. Early and exclusive use of norepinephrine in septic shock. Resuscitation 2004; 62:249–254
229. Hall LG, Oyen LJ, Taner CB, et al. Fixed-dose vasopressin compared with titrated dopamine and norepinephrine as initial vasopressor therapy for septic shock. Pharmacotherapy 2004; 24:1002–1012
230. Lampin ME, Rousseaux J, Botte A, et al. Noradrenaline use for septic shock in children: Doses, routes of administration and complications. Acta Paediatr 2012; 101:e426–e430
231. Tourneux P, Rakza T, Abazine A, et al. Noradrenaline for management of septic shock refractory to fluid loading and dopamine or dobutamine in full-term newborn infants. Acta Paediatr 2008; 97:177–180
232. Klinzing S, Simon M, Reinhart K, et al. High-dose vasopressin is not superior to norepinephrine in septic shock. Crit Care Med 2003; 31:2646–2650
233. Delmas A, Leone M, Rousseau S, et al. Clinical review: Vasopressin and terlipressin in septic shock patients. Crit Care 2005; 9:212–222
234. Leibovitch L, Efrati O, Vardi A, et al. Intractable hypotension in septic shock: Successful treatment with vasopressin in an infant. Isr Med Assoc J 2003; 5:596–598
235. Matok I, Vard A, Efrati O, et al. Terlipressin as rescue therapy for intractable hypotension due to septic shock in children. Shock 2005; 23:305–310
236. Tsuneyoshi I, Yamada H, Kakihana Y, et al. Hemodynamic and metabolic effects of low-dose vasopressin infusions in vasodilatory septic shock. Crit Care Med 2001; 29:487–493
237. Peters MJ, Booth RA, Petros AJ. Terlipressin bolus induces systemic vasoconstriction in septic shock. Pediatr Crit Care Med 2004; 5:112–115
238. Liedel JL, Meadow W, Nachman J, et al. Use of vasopressin in refractory hypotension in children with vasodilatory shock: Five cases and a review of the literature. Pediatr Crit Care Med 2002; 3:15–18
239. Vasudevan A, Lodha R, Kabra SK. Vasopressin infusion in children with catecholamine-resistant septic shock. Acta Paediatr 2005; 94:380–383
240. Rodríguez-Núñez A, Fernández-Sanmartín M, Martinón-Torres F, et al. Terlipressin for catecholamine-resistant septic shock in children. Intensive Care Med 2004; 30:477–480
241. Matok I, Leibovitch L, Vardi A, et al. Terlipressin as rescue therapy for intractable hypotension during neonatal septic shock. Pediatr Crit Care Med 2004; 5:116–118
242. Rosenzweig EB, Starc TJ, Chen JM, et al. Intravenous arginine-vasopressin in children with vasodilatory shock after cardiac surgery. Circulation 1999; 100(Suppl 19):II182–II186
243. Agrawal A, Singh VK, Varma A, et al. Intravenous arginine vasopressin infusion in refractory vasodilatory shock: A clinical study. Indian J Pediatr 2012; 79:488–493
244. Bidegain M, Greenberg R, Simmons C, et al. Vasopressin for refractory hypotension in extremely low birth weight infants. J Pediatr 2010; 157:502–504
245. Meyer S, Gottschling S, Baghai A, et al. Arginine-vasopressin in catecholamine-refractory septic versus non-septic shock in extremely low birth weight infants with acute renal injury. Crit Care 2006; 10:R71
246. Meyer S, Löffler G, Polcher T, et al. Vasopressin in catecholamine-resistant septic and cardiogenic shock in very-low-birthweight infants. Acta Paediatr 2006; 95:1309–1312
247. Russell JA, Walley KR, Singer J, et al; VASST Investigators: Vasopressin versus norepinephrine infusion in patients with septic shock. N Engl J Med 2008; 358:877–887
248. Choong K, Bohn D, Fraser DD, et al; Canadian Critical Care Trials Group: Vasopressin in pediatric vasodilatory shock: A multicenter randomized controlled trial. Am J Respir Crit Care Med 2009; 180:632–639
249. Zeballos G, López-Herce J, Fernández C, et al. Rescue therapy with terlipressin by continuous infusion in a child with catecholamine-resistant septic shock. Resuscitation 2006; 68:151–153
250. Radicioni M, Troiani S, Camerini PG. Effects of terlipressin on pulmonary artery pressure in a septic cooled infant: An echocardiographic assessment. J Perinatol 2012; 32:893–895
251. Filippi L, Gozzini E, Daniotti M, et al. Rescue treatment with terlipressin in different scenarios of refractory hypotension in newborns and infants. Pediatr Crit Care Med 2011; 12:e237–e241
252. Filippi L, Poggi C, Serafini L, et al. Terlipressin as rescue treatment of refractory shock in a neonate. Acta Paediatr 2008; 97:500–502
253. Leone M, Martin C. Role of terlipressin in the treatment of infants and neonates with catecholamine-resistant septic shock. Best Pract Res Clin Anaesthesiol 2008; 22:323–333
254. Michel F, Thomachot L, David M, et al. Continuous low-dose infusion of terlipressin as a rescue therapy in meningococcal septic shock. Am J Emerg Med 2007; 25:863.e1–863.e2
255. Papoff P, Mancuso M, Barbara CS, et al. The role of terlipressin in pediatric septic shock: A review of the literature and personal experience. Int J Immunopathol Pharmacol 2007; 20:213–221
256. Rodríguez-Núñez A, Oulego-Erroz I, Gil-Antón J, et al; RETSPED-II Working Group of the Spanish Society of Pediatric Intensive Care: Continuous terlipressin infusion as rescue treatment in a case series of children with refractory septic shock. Ann Pharmacother 2010; 44:1545–1553
257. Rodríguez-Núñez A, López-Herce J, Gil-Antón J, et al; RETSPED Working Group of the Spanish Society of Pediatric Intensive Care: Rescue treatment with terlipressin in children with refractory septic shock: A clinical study. Crit Care 2006; 10:R20
258. Yildizdas D, Yapicioglu H, Celik U, et al. Terlipressin as a rescue therapy for catecholamine-resistant septic shock in children. Intensive Care Med 2008; 34:511–517
259. Yunge M, Petros A. Angiotensin for septic shock unresponsive to noradrenaline. Arch Dis Child 2000; 82:388–389
260. Gregory JS, Bonfiglio MF, Dasta JF, et al. Experience with phenylephrine as a component of the pharmacologic support of septic shock. Crit Care Med 1991; 19:1395–1400
261. López A, Lorente JA, Steingrub J, et al. Multiple-center, randomized, placebo-controlled, double-blind study of the nitric oxide synthase inhibitor 546C88: Effect on survival in patients with septic shock. Crit Care Med 2004; 32:21–30
262. Grover R, Lopez A, Lorente J, et al. Multi-center, randomized, double blind, placebo-controlled, double bind study of nitric oxide inhibitor 546C88: Effect on survival in patients with septic shock. Crit Care Med 1999; 27:A33
263. Driscoll W, Thurin S, Carrion V, et al. Effect of methylene blue on refractory neonatal hypotension. J Pediatr 1996; 129:904–908
264. Taylor K, Holtby H. Methylene blue revisited: Management of hypotension in a pediatric patient with bacterial endocarditis. J Thorac Cardiovasc Surg 2005; 130:566
265. Faustino EV, Bogue CW. Relationship between hypoglycemia and mortality in critically ill children. Pediatr Crit Care Med 2010; 11:690–698
266. Wintergerst KA, Buckingham B, Gandrud L, et al. Association of hypoglycemia, hyperglycemia, and glucose variability with morbidity and death in the pediatric intensive care unit. Pediatrics 2006; 118:173–179
267. Branco RG, Garcia PC, Piva JP, et al. Glucose level and risk of mortality in pediatric septic shock. Pediatr Crit Care Med 2005; 6:470–472
268. Day KM, Haub N, Betts H, et al. Hyperglycemia is associated with morbidity in critically ill children with meningococcal sepsis. Pediatr Crit Care Med 2008; 9:636–640
269. Mesotten D, Gielen M, Sterken C, et al. Neurocognitive development of children 4 years after critical illness and treatment with tight glucose control: A randomized controlled trial. JAMA 2012; 308:1641–1650
270. Macrae D, Grieve R, Allen E, et al; CHiP Investigators: A randomized trial of hyperglycemic control in pediatric intensive care. N Engl J Med 2014; 370:107–118
271. Agus MSD, Stiel GM, Wypij D, et al. Tight glycemic control versus standard care after pediatric cardiac surgery. N Engl J Med 2012; 367; 1208–1219
272. Vlasselaers D, Milants I, Desmet L, et al. Intensive insulin therapy for patients in paediatric intensive care: A prospective, randomised controlled study. Lancet 2009; 373:547–556
273. Rigby M, Maher K, Preissig C, et al. The Pedietrol trial: A 2-center trial of glycemic control in pediatric critical illness. Crit Care Med 2013; 41:A993
274. Verhoeven JJ, den Brinker M, Hokken-Koelega AC, et al. Pathophysiological aspects of hyperglycemia in children with meningococcal sepsis and septic shock: A prospective, observational cohort study. Crit Care 2011; 15:R44
275. van Waardenburg DA, Jansen TC, Vos GD, et al. Hyperglycemia in children with meningococcal sepsis and septic shock: The relation between plasma levels of insulin and inflammatory mediators. J Clin Endocrinol Metab 2006; 91:3916–3921
276. Annane D, Sébille V, Charpentier C, et al. Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock. JAMA 2002; 288:862–871
277. Hodes HL. Care of the critically ill child: Endotoxin shock. Pediatrics 1969; 44:248–260
278. Sonnenschein H, Joos HA. Use and dosage of hydrocortisone in endotoxic shock. Pediatrics 1970; 45:720
279. Migeon CJ, Kenny FM, Hung W, et al. Study of adrenal function in children with meningitis. Pediatrics 1967; 40:163–183
280. Soni A, Pepper GM, Wyrwinski PM, et al. Adrenal insufficiency occurring during septic shock: Incidence, outcome, and relationship to peripheral cytokine levels. Am J Med 1995; 98:266–271
281. Riordan FA, Thomson AP, Ratcliffe JM, et al. Admission cortisol and adrenocorticotrophic hormone levels in children with meningococcal disease: Evidence of adrenal insufficiency? Crit Care Med 1999; 27:2257–2261
282. Sumarmo: The role of steroids in dengue shock syndrome. Southeast Asian J Trop Med Public Health 1987; 18:383–389
283. Min M, U T, Aye M, et al. Hydrocortisone in the management of dengue shock syndrome. Southeast Asian J Trop Med Public Health 1975; 6:573–579
284. Hatherill M, Tibby SM, Hilliard T, et al. Adrenal insufficiency in septic shock. Arch Dis Child 1999; 80:51–55
285. Ryan CA, Wenman W, Henningsen C, et al. Fatal childhood pneumococcal Waterhouse-Friderichsen syndrome. Pediatr Infect Dis J 1993; 12:250–251
286. Matot I, Sprung CL. Corticosteroids in septic shock: Resurrection of the last rites? Crit Care Med 1998; 26:627–630
287. Briegel J, Forst H, Kellermann W, et al. Haemodynamic improvement in refractory septic shock with cortisol replacement therapy. Intensive Care Med 1992; 18:318
288. Moran JL, Chapman MJ, O’Fathartaigh MS, et al. Hypocortisolaemia and adrenocortical responsiveness at onset of septic shock. Intensive Care Med 1994; 20:489–495
289. Todd JK, Ressman M, Caston SA, et al. Corticosteroid therapy for patients with toxic shock syndrome. JAMA 1984; 252:3399–3402
290. Sonnenschein H, Joos HA. Hydrocortisone treatment of endotoxin shock. Another paradox in pediatrics. Clin Pediatr (Phila) 1970; 9:251–252
291. Bettendorf M, Schmidt KG, Grulich-Henn J, et al. Tri-iodothyronine treatment in children after cardiac surgery: A double-blind, randomised, placebo-controlled study. Lancet 2000; 356:529–534
292. Joosten KF, de Kleijn ED, Westerterp M, et al. Endocrine and metabolic responses in children with meningoccocal sepsis: Striking differences between survivors and nonsurvivors. J Clin Endocrinol Metab 2000; 85:3746–3753
293. Menon K, Ward RE, Lawson ML, et al; Canadian Critical Care Trials Group: A prospective multicenter study of adrenal function in critically ill children. Am J Respir Crit Care Med 2010; 182:246–251
294. Marquardt DJ, Knatz NL, Wetterau LA, et al. Failure to recover somatotropic axis function is associated with mortality from pediatric sepsis-induced multiple organ dysfunction syndrome. Pediatr Crit Care Med 2010; 11:18–25
295. Indyk JA, Candido-Vitto C, Wolf IM, et al. Reduced glucocorticoid receptor protein expression in children with critical illness. Horm Res Paediatr 2013; 79:169–178
296. Boonen E, Vervenne H, Meersseman P, et al. Reduced cortisol metabolism during critical illness. N Engl J Med 2013; 368:1477–1488
297. Annane D, Bellissant E, Bollaert PE, et al. Corticosteroids in the treatment of severe sepsis and septic shock in adults: A systematic review. JAMA 2009; 301:2362–2375
298. Wheeler DS, Zingarelli B, Wheeler WJ, et al. Novel pharmacologic approaches to the management of sepsis: Targeting the host inflammatory response. Recent Pat Inflamm Allergy Drug Discov 2009; 3:96–112
299. Oppert M, Schindler R, Husung C, et al. Low-dose hydrocortisone improves shock reversal and reduces cytokine levels in early hyperdynamic septic shock. Crit Care Med 2005; 33:2457–2464
300. Sarthi M, Lodha R, Vivekanandhan S, et al. Adrenal status in children with septic shock using low-dose stimulation test. Pediatr Crit Care Med 2007; 8:23–28
301. Sam S, Corbridge TC, Mokhlesi B, et al. Cortisol levels and mortality in severe sepsis. Clin Endocrinol (Oxf) 2004; 60:29–35
302. Menon K, McNally D, Choong K, et al. A systematic review and meta-analysis on the effect of steroids in pediatric shock. Pediatr Crit Care Med 2013; 14:474–480
303. Zimmerman JJ, Donaldson A, Barker RM, et al; Eunice Kennedy Shriver National Institute of Child Health and Human Development Collaborative Pediatric Critical Care Research Network: Real-time free cortisol quantification among critically ill children. Pediatr Crit Care Med 2011; 12:525–531
304. Hamrahian AH, Oseni TS, Arafah BM. Measurements of serum free cortisol in critically ill patients. N Engl J Med 2004; 350:1629–1638
305. Cotton BA, Guillamondegui OD, Fleming SB, et al. Increased risk of adrenal insufficiency following etomidate exposure in critically injured patients. Arch Surg 2008; 143:62–67
306. Li J, Winkler M. Decompensated septic shock in the setting of megace-induced severe adrenal suppression in an otherwise healthy pediatric patient: A case report. Pediatr Emerg Care 2012; 28:802–804
307. Jeschke MG, Williams FN, Finnerty CC, et al. The effect of ketoconazole on post-burn inflammation, hypermetabolism and clinical outcomes. PLoS One 2012; 7:e35465
308. Aneja R, Carcillo JA. What is the rationale for hydrocortisone treatment in children with infection-related adrenal insufficiency and septic shock? Arch Dis Child 2007; 92:165–169
309. Marik PE, Pastores SM, Annane D, et al; American College of Critical Care Medicine: Recommendations for the diagnosis and management of corticosteroid insufficiency in critically ill adult patients: Consensus statements from an international task force by the American College of Critical Care Medicine. Crit Care Med 2008; 36:1937–1949
310. Annane D, Maxime V, Ibrahim F, et al. Diagnosis of adrenal insufficiency in severe sepsis and septic shock. Am J Respir Crit Care Med 2006; 174:1319–1326
311. Lichtarowicz-Krynska EJ, Cole TJ, Camacho-Hubner C, et al. Circulating aldosterone levels are unexpectedly low in children with acute meningococcal disease. J Clin Endocrinol Metab 2004; 89:1410–1414
312. Hebbar KB, Stockwell JA, Fortenberry JD. Clinical effects of adding fludrocortisone to a hydrocortisone-based shock protocol in hypotensive critically ill children. Intensive Care Med 2011; 37:518–524
313. Arafah BM. Hypothalamic pituitary adrenal function during critical illness: Limitations of current assessment methods. J Clin Endocrinol Metab 2006; 91:3725–3745
314. Jung C, Inder WJ. Management of adrenal insufficiency during the stress of medical illness and surgery. Med J Aust 2008; 188:409–413
315. Padidela R, Hindmarsh PC. Mineralocorticoid deficiency and treatment in congenital adrenal hyperplasia. Int J Pediatr Endocrinol 2010; 2010:656925
316. Sprung CL, Annane D, Keh D, et al; CORTICUS Study Group: Hydrocortisone therapy for patients with septic shock. N Engl J Med 2008; 358:111–124
317. Lodygensky GA, Rademaker K, Zimine S, et al. Structural and functional brain development after hydrocortisone treatment for neonatal chronic lung disease. Pediatrics 2005; 116:1–7
318. Baker CF, Barks JD, Engmann C, et al. Hydrocortisone administration for the treatment of refractory hypotension in critically ill newborns. J Perinatol 2008; 28:412–419
319. Burmester M, Pierce C, Petros A. Disseminated candidiasis after steroid treatment for early neonatal hypotension. Arch Dis Child Fetal Neonatal Ed 2001; 85:F226
320. Wong HR, Cvijanovich NZ, Allen GL, et al. Corticosteroids are associated with repression of adaptive immunity gene programs in pediatric septic shock. Am J Respir Crit Care Med 2014; 189:940–946
321. Zimmerman JJ, Williams MD. Adjunctive corticosteroid therapy in pediatric severe sepsis: Observations from the RESOLVE study. Pediatr Crit Care Med 2011; 12:2–8
322. Esteban NV, Loughlin T, Yergey AL, et al. Daily cortisol production rate in man determined by stable isotope dilution/mass spectrometry. J Clin Endocrinol Metab 1991; 72:39–45
323. Kerrigan JR, Veldhuis JD, Leyo SA, et al. Estimation of daily cortisol production and clearance rates in normal pubertal males by deconvolution analysis. J Clin Endocrinol Metab 1993; 76:1505–1510
324. Kenny FM, Preeyasombat C, Migeon CJ. Cortisol production rate. II. Normal infants, children, and adults. Pediatrics 1966; 37:34–42
325. Kenny FM, Malvaux P, Migeon CJ. Cortisol production rate in newborn babies, older infants, and children. Pediatrics 1963; 31:360–373
326. Briegel J, Forst H, Haller M, et al. Stress doses of hydrocortisone reverse hyperdynamic septic shock: A prospective, randomized, double-blind, single-center study. Crit Care Med 1999; 27:723–732
327. Pizarro CF, Troster EJ. Adrenal function in sepsis and septic shock. J Pediatr (Rio J) 2007; 83(5 Suppl):S155–S162
328. Roberts JD Jr, Fineman JR, Morin FC 3rd, et al. Inhaled nitric oxide and persistent pulmonary hypertension of the newborn. The Inhaled Nitric Oxide Study Group. N Engl J Med 1997; 336:605–610
329. Inhaled Nitric Oxide Study Group: Inhaled nitric oxide in full term and nearly full-term infants with hypoxic respiratory failure. N Engl J Med 1997; 336:597–604
330. Wung JT, James LS, Kilchevsky E, et al. Management of infants with severe respiratory failure and persistence of the fetal circulation, without hyperventilation. Pediatrics 1985; 76:488–494
331. Drummond WH, Gregory GA, Heymann MA, et al. The independent effects of hyperventilation, tolazoline, and dopamine on infants with persistent pulmonary hypertension. J Pediatr 1981; 98:603–611
332. Drummond WH. Use of cardiotonic therapy in the management of infants with PPHN. Clin Perinatol 1984; 11:715–728
333. Gouyon JB, Françoise M. Vasodilators in persistent pulmonary hypertension of the newborn: A need for optimal appraisal of efficacy. Dev Pharmacol Ther 1992; 19:62–68
334. Meadow WL, Meus PJ. Hemodynamic consequences of tolazoline in neonatal group B streptococcal bacteremia: An animal model. Pediatr Res 1984; 18:960–965
335. Sandor GG, Macnab AJ, Akesode FA, et al. Clinical and echocardiographic evidence suggesting afterload reduction as a mechanism of action of tolazoline in neonatal hypoxemia. Pediatr Cardiol 1984; 5:93–99
336. Benitz WE, Malachowski N, Cohen RS, et al. Use of sodium nitroprusside in neonates: Efficacy and safety. J Pediatr 1985; 106:102–110
337. McNamara PJ, Laique F, Muang-In S, et al. Milrinone improves oxygenation in neonates with severe persistent pulmonary hypertension of the newborn. J Crit Care 2006; 21:217–222
338. Bassler D, Choong K, McNamara P, et al. Neonatal persistent pulmonary hypertension treated with milrinone: Four case reports. Biol Neonate 2006; 89:1–5
339. Rashid N, Morin FC 3rd, Swartz DD, et al. Effects of prostacyclin and milrinone on pulmonary hemodynamics in newborn lambs with persistent pulmonary hypertension induced by ductal ligation. Pediatr Res 2006; 60:624–629
340. Concheiro Guisán A, Sousa Rouco C, Suárez Traba B, et al. [Inhaled iloprost: A therapeutic alternative for persistent pulmonary hypertension of the newborn]. An Pediatr (Barc) 2005; 63:175–176
341. Ehlen M, Wiebe B. Iloprost in persistent pulmonary hypertension of the newborn. Cardiol Young 2003; 13:361–363
342. Patole S, Lee J, Buettner P, et al. Improved oxygenation following adenosine infusion in persistent pulmonary hypertension of the newborn. Biol Neonate 1998; 74:345–350
343. Konduri GG, Garcia DC, Kazzi NJ, et al. Adenosine infusion improves oxygenation in term infants with respiratory failure. Pediatrics 1996; 97:295–300
344. Motti A, Tissot C, Rimensberger PC, et al. Intravenous adenosine for refractory pulmonary hypertension in a low-weight premature newborn: A potential new drug for rescue therapy. Pediatr Crit Care Med 2006; 7:380–382
345. Ng C, Franklin O, Vaidya M, et al. Adenosine infusion for the management of persistent pulmonary hypertension of the newborn. Pediatr Crit Care Med 2004; 5:10–13
346. Bartlett RH, Roloff DW, Custer JR, et al. Extracorporeal life support: The University of Michigan experience. JAMA 2000; 283:904–908
347. Meyer DM, Jessen ME. Results of extracorporeal membrane oxygenation in neonates with sepsis. The Extracorporeal Life Support Organization experience. J Thorac Cardiovasc Surg 1995; 109:419–425
348. Bernbaum J, Schwartz IP, Gerdes M, et al. Survivors of extracorporeal membrane oxygenation at 1 year of age: The relationship of primary diagnosis with health and neurodevelopmental sequelae. Pediatrics 1995; 96(5 Pt 1):907–913
349. The collaborative UK ECMO (Extracorporeal Membrane Oxygenation) trial: Follow-up to 1 year of age. Pediatrics 1998; 101:E1
350. Meyer DM, Jessen ME. Results of extracorporeal membrane oxygenation in children with sepsis. The Extracorporeal Life Support Organization. Ann Thorac Surg 1997; 63:756–761
351. Goldman AP, Kerr SJ, Butt W, et al. Extracorporeal support for intractable cardiorespiratory failure due to meningococcal disease. Lancet 1997; 349:466–469
352. Beca J, Butt W. Extracorporeal membrane oxygenation for refractory septic shock in children. Pediatrics 1994; 93:726–729
353. Dalton HJ, Siewers RD, Fuhrman BP, et al. Extracorporeal membrane oxygenation for cardiac rescue in children with severe myocardial dysfunction. Crit Care Med 1993; 21:1020–1028
354. Hallin GW, Simpson SQ, Crowell RE, et al. Cardiopulmonary manifestations of hantavirus pulmonary syndrome. Crit Care Med 1996; 24:252–258
355. Crowley MR, Katz RW, Kessler R, et al. Successful treatment of adults with severe Hantavirus pulmonary syndrome with extracorporeal membrane oxygenation. Crit Care Med 1998; 26:409–414
356. MacLaren G, Butt W, Best D, et al. Central extracorporeal membrane oxygenation for refractory pediatric septic shock. Pediatr Crit Care Med 2011; 12:133–136
357. Maclaren G, Butt W, Best D, et al. Extracorporeal membrane oxygenation for refractory septic shock in children: One institution’s experience. Pediatr Crit Care Med 2007; 8:447–451
358. Bréchot N, Luyt CE, Schmidt M, et al. Venoarterial extracorporeal membrane oxygenation support for refractory cardiovascular dysfunction during severe bacterial septic shock. Crit Care Med 2013; 41:1616–1626
359. Smalley N, MacLaren G, Best D, et al. Outcomes in children with refractory pneumonia supported with extracorporeal membrane oxygenation. Intensive Care Med 2012; 38:1001–1007
360. Jeffers A, Gladwin MT, Kim-Shapiro DB. Computation of plasma hemoglobin nitric oxide scavenging in hemolytic anemias. Free Radic Biol Med 2006; 41:1557–1565
361. Jackson EK, Koehler M, Mi Z, et al. Possible role of adenosine deaminase in vaso-occlusive diseases. J Hypertens 1996; 14:19–29
362. Lou S, MacLaren G, Best D, et al. Hemolysis in pediatric patients receiving centrifugal-pump extracorporeal membrane oxygenation: Prevalence, risk factors, and outcomes. Crit Care Med 2014; 42:1213–1220
363. Pfaender M. Hemodynamics in the extracorporeal aortic cannula: Review of factors affecting choice of the appropriate size. J Extracorp Tech 1981; 13:224–232
364. Mulholland JW, Massey W, Shelton JC. Investigation and quantification of the blood trauma caused by the combined dynamic forces experienced during cardiopulmonary bypass. Perfusion 2000; 15:485–494
365. Dellinger RP, Levy MM, Rhodes A, et al. Surviving sepsis campaign: International guidelines for management of severe sepsis and septic shock: 2012. Crit Care Med 2013; 41:580–637
366. Fortenberry JD, Paden ML, Goldstein SL. Acute kidney injury in children: An update on diagnosis and treatment. Pediatr Clin North Am 2013; 60:669–688
367. Sutherland SM, Zappitelli M, Alexander SR, et al. Fluid overload and mortality in children receiving continuous renal replacement therapy: The prospective pediatric continuous renal replacement therapy registry. Am J Kidney Dis 2010; 55:316–325
368. Goldstein SL, Somers MJ, Baum MA, et al. Pediatric patients with multi-organ dysfunction syndrome receiving continuous renal replacement therapy. Kidney Int 2005; 67:653–658
369. Bellomo R, Cass A, Cole L, et al; RENAL Replacement Therapy Study Investigators: Intensity of continuous renal-replacement therapy in critically ill patients. N Engl J Med 2009; 361:1627–1638
370. Van Wert R, Friedrich JO, Scales DC, et al; University of Toronto Acute Kidney Injury Research Group: High-dose renal replacement therapy for acute kidney injury: Systematic review and meta-analysis. Crit Care Med 2010; 38:1360–1369
371. Fortenberry JD, Paden ML. Extracorporeal therapies in the treatment of sepsis: Experience and promise. Semin Pediatr Infect Dis 2006; 17:72–79
372. Smith OP, White B, Vaughan D, et al. Use of protein-C concentrate, heparin, and haemodiafiltration in meningococcus-induced purpura fulminans. Lancet 1997; 350:1590–1593
373. Ratanarat R, Brendolan A, Ricci Z, et al. Pulse high-volume hemofiltration in critically ill patients: A new approach for patients with septic shock. Semin Dial 2006; 19:69–74
374. Piccinni P, Dan M, Barbacini S, et al. Early isovolaemic haemofiltration in oliguric patients with septic shock. Intensive Care Med 2006; 32:80–86
375. Bock KR. Renal replacement therapy in pediatric critical care medicine. Curr Opin Pediatr 2005; 17:368–371
376. Bridges BC, Hardison D, Pietsch J. A case series of the successful use of ECMO, continuous renal replacement therapy, and plasma exchange for thrombocytopenia-associated multiple organ failure. J Pediatr Surg 2013; 48:1114–1117
377. Szczepiorkowski ZM, Winters JL, Bandarenko N, et al; Apheresis Applications Committee of the American Society for Apheresis: Guidelines on the use of therapeutic apheresis in clinical practice–evidence-based approach from the Apheresis Applications Committee of the American Society for Apheresis. J Clin Apher 2010; 25:83–177
378. Zhou F, Peng Z, Murugan R, et al. Blood purification and mortality in sepsis: A meta-analysis of randomized trials. Crit Care Med 2013; 41:2209–2220
379. De Simone N, Racsa L, Bevan S, et al. Therapeutic plasma exchange in the management of sepsis and multiple organ dysfunction syndrome: A report of three cases. J Clin Apher 2014; 29:127–131
380. Demirkol D, Yildizdas D, Bayrakci B, et al; Turkish Secondary HLH/MAS Critical Care Study Group: Hyperferritinemia in the critically ill child with secondary hemophagocytic lymphohistiocytosis/sepsis/multiple organ dysfunction syndrome/macrophage activation syndrome: What is the treatment? Crit Care 2012; 16:R52
381. Qu L, Kiss JE, Dargo G, et al. Outcomes of previously healthy pediatric patients with fulminant sepsis-induced multisystem organ failure receiving therapeutic plasma exchange. J Clin Apher 2011; 26:208–213
382. Sevketoglu E, Yildizdas D, Horoz OO, et al. Use of therapeutic plasma exchange in children with thrombocytopenia-associated multiple organ failure in the Turkish thrombocytopenia-associated multiple organ failure network. Pediatr Crit Care Med 2014; 15:e354–e359
383. Churchwell KB, McManus ML, Kent P, et al. Intensive blood and plasma exchange for treatment of coagulopathy in meningococcemia. J Clin Apher 1995; 10:171–177
384. van Deuren M, Frieling JT, van der Ven-Jongekrijg J, et al. Plasma patterns of tumor necrosis factor-alpha (TNF) and TNF soluble receptors during acute meningococcal infections and the effect of plasma exchange. Clin Infect Dis 1998; 26:918–923
385. van Deuren M, Santman FW, van Dalen R, et al. Plasma and whole blood exchange in meningococcal sepsis. Clin Infect Dis 1992; 15:424–430
386. Yildirim I, Ceyhan M, Bayrakci B, et al. A case report of thrombocytopenia-associated multiple organ failure secondary to Salmonella enterica serotype Typhi infection in a pediatric patient: Successful treatment with plasma exchange. Ther Apher Dial 2010; 14:226–229
387. Nguyen TC, Han YY, Kiss JE, et al. Intensive plasma exchange increases a disintegrin and metalloprotease with thrombospondin motifs-13 activity and reverses organ dysfunction in children with thrombocytopenia-associated multiple organ failure. Crit Care Med 2008; 36:2878–2887
388. Long EJ, Taylor A, Delzoppo, et al. A randomised controlled trial of plasma filtration in severe paediatric sepsis. Crit Care Resusc 2013; 15:198–204
389. Hirabayashi K, Shiohara M, Saito S, et al. Polymyxin-direct hemoperfusion for sepsis-induced multiple organ failure. Pediatr Blood Cancer 2010; 55:202–205
390. Hirakawa E, Ibara S, Tokuhisa T, et al. Septic neonate rescued by polymyxin B hemoperfusion. Pediatr Int 2013; 55:e70–e72
391. Nakamura T, Sato E, Fujiwara N, et al. Polymyxin B-immobilized fiber hemoperfusion in a high school football player with septic shock caused by osteitis pubis. ASAIO J 2011; 57:470–472
392. Haque IU, Zaritsky AL. Analysis of the evidence for the lower limit of systolic and mean arterial pressure in children. Pediatr Crit Care Med 2007; 8:138–144
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Clinical Signs and Hemodynamic Variables to Direct Treatment of Shock/Goals/Therapeutic Endpoints

John C. Lin (subgroup chair)

Alan L Davis

Niranjan Kissoon

Martha C. Kutko

Suchitra Ranjit

Mark Hall,

Allan Doctor

Timothy Cornell

Jacki Weingarten

Intravascular Access

Tim Yeh (subgroup chair) Yong Yun Han

Heidi Flori

Fluid therapy/Fluid Resuscitation

Alan L. Davis (subgroup chair)

Allan Doctor

Suchitra Ranjit

Mark Peters

Airway and Breathing

Bonnie Stojadinovic (subgroup chair)

Mark Hall,

Jacki Weingarten

Ira Cheifetz

Sedation for Invasive Procedures or Intubation

Regina Okhuysen-Cawley (subgroup chair)

Mark Peters

Fola Odetola

Intravascular Catheters and Invasive and Noninvasive Hemodynamic Monitoring

Rajesh K. Aneja (subgroup chair)

Renuka Mehta

Eduardo Schnizler

Howard Jeffries

Lynn Hernan

Aaron Zuckerberg

Suchitra Ranjit

Inotropes/Hemodynamic Support

Monica Relvas (subgroup chair)

Ana Lia Graciano

Saraswati Kache

Jose Irazuzta

Rajesh K. Aneja

Alexander A. Kon

Elizabeth Iselin

Karen Choong

Vasodilators/Hemodynamic Support and PPHN Therapies

Peter Skippen (subgroup chair)

Marc-Andre Dugas

Howard Jeffries

Andreas Deymann

Karin Reuter-Rice

Saraswati Kache

Joe Brierley

Vasopressors/Hemodynamic Support

Ranna Rozenfeld (subgroup chair) Jon Feldman

Allan de Caen

Eduardo Schnitzler

Glucose, Calcium, Thyroid, and Hydrocortisone Replacement

Andreas Deymann (subgroup chair)

Adalberto Torres Jr.

Eric Williams

Kristine Parbuoni

Jerry Zimmerman (editor, not original group member)

Extracorporeal Therapies

Trung Nguyen (subgroup chair) Peter Skippen

Timothy Cornell

Timothy Maul

Graeme Maclaren

James Fortenberry

Bundle Development Taskforce

Eric Williams (subgroup chair)

Scott L. Weiss

Julie C. Fitzgerald

Bruce Greenwald

Monica Relvas

Chhavi Katyal

Edward Conway

Halden Scott

Fran Balamuth

Raina Paul

Elise van der Jagt

hemodynamics; newborn; pediatric; septic shock

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