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Guidelines for evaluation of new fever in critically ill adult patients: 2008 update from the American College of Critical Care Medicine and the Infectious Diseases Society of America

O’Grady, Naomi P. MD; Barie, Philip S. MD, MBA, FCCM; Bartlett, John G. MD; Bleck, Thomas MD, FCCM; Carroll, Karen RN; Kalil, Andre C. MD; Linden, Peter MD; Maki, Dennis G. MD; Nierman, David MD, FCCM; Pasculle, William MD; Masur, Henry MD, FCCM

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doi: 10.1097/CCM.0b013e318169eda9
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Abstract

In some intensive care units (ICUs), the measurement of a newly elevated temperature triggers an automatic order set that includes many tests that are time consuming, costly, and disruptive to the patient and staff. Moreover, the patient may experience discomfort, be exposed to unneeded radiation, require transport outside the controlled environment of the ICU, or experience considerable blood loss due to this testing, which is often repeated several times within 24 hrs and daily thereafter. In an era when utilization of hospital and patient resources is under intensive scrutiny, it is appropriate to assess how such fevers should be evaluated in a prudent and cost-effective manner.

The American College of Critical Care Medicine of the Society of Critical Care Medicine and the Infectious Diseases Society of America reconvened a Task Force to update practice parameters for the evaluation of a new fever in adult patients (i.e., ≥18 yrs of age) in an ICU (1). The goal of this update is to continue to promote the rational consumption of resources and an efficient evaluation. This guideline presumes that any unexplained temperature elevation merits a clinical assessment by a healthcare professional that includes a review of the patient’s history and a focused physical examination before any laboratory tests or imaging procedures are ordered.

This update specifically addresses how to evaluate a new fever in an adult patient already in the ICU who has previously been afebrile and in whom the source of fever is not initially obvious. This update will assist intensivists and consultants as a starting point for developing an effective and cost-conscious approach appropriate for their patient populations. The specific recommendations are rated by the strength of evidence, using the published criteria of the Society of Critical Care Medicine (Table 1).

Table 1
Table 1:
Society of Critical Care Medicine’s rating system for references and recommendations

Initiating a Fever Evaluation: Measuring Body Temperature and Defining Fever as Thresholds for Diagnostic Effort

Definition of Fever.

The definition of fever is arbitrary and depends on the purpose for which it is defined. Some literature defines fever as a core temperature of >38.0°C (100.4°F) (2–4), whereas other sources define fever as two consecutive elevations of >38.3°C (101.0°F). In patients who are neutropenic, fever has been defined as a single oral temperature of >38.3°C (101.0°F) in the absence of an obvious environmental cause, or a temperature elevation of >38.0°C (100.4°F) for >1 hr (4). A variety of definitions of fever are acceptable, depending on how sensitive an indicator of thermal abnormality an ICU practitioner wants to utilize. Normal body temperature is generally considered to be 37.0°C (98.6°F) (4, 5). In healthy individuals, this temperature varies by 0.5 to 1.0°C, according to circadian rhythm and menstrual cycle (6). With heavy exercise, temperature can rise by 2 to 3°C (7). Whereas many biological processes can alter body temperature, a variety of environmental forces in an ICU can also alter temperature, such as specialized mattresses, hot lights, air conditioning, cardiopulmonary bypass, peritoneal lavage, dialysis, and continuous hemofiltration (8–10). Thermoregulatory mechanisms can also be disrupted by drugs or by damage to the central or the autonomic nervous systems. Thus, it is often difficult to determine whether an abnormal temperature is a reflection of a physiologic process, a drug, or an environmental influence.

A substantial proportion of infected patients are not febrile: such patients may be euthermic or hypothermic. These patients include the elderly, patients with open abdominal wounds, patients with large burns, patients receiving extracorporeal membrane oxygenation or continuous renal replacement therapy (11), patients with congestive heart failure, end-stage liver disease, or chronic renal failure, and patients taking anti-inflammatory or antipyretic drugs. A patient who is hypothermic or euthermic may have a life-threatening infection. Other symptoms and signs in the absence of fever, such as otherwise unexplained hypotension, tachycardia, tachypnea, confusion, rigors, skin lesions, respiratory manifestations, oliguria, lactic acidosis, leukocytosis, leukopenia, immature neutrophils (i.e., bands) of >10%, or thrombocytopenia, might appropriately mandate a comprehensive search for infection and aggressive, immediate empirical therapy.

As a broad generalization, it is reasonable in many ICUs to consider everyone with a temperature of ≥38.3°C (≥101°F) to be febrile and to warrant special attention to determine whether infection is present. However, a lower threshold may be used for immunocompromised patients because they are not able to manifest a similar fever response as the one seen in immunocompetent patients. Effective management of patients in an ICU mandates that infection be considered in patients regardless of temperature but that laboratory tests to search for infection should be initiated in febrile patients only after a clinical assessment indicates a reasonable possibility that infection might be present.

Site and Technology of Temperature Measurement.

The ideal system for measuring temperature should provide reliable, reproducible values safely and conveniently. Any device must be calibrated properly and checked periodically according to the manufacturer’s specifications.

Most authorities consider the thermistor of a pulmonary artery catheter to be the standard for measuring core temperature against which other devices must be compared (6, 12–16). Not all patients have such a thermistor in place. Even when available, these thermistors are not all equal in technical performance. Thermistors in indwelling bladder catheters provide essentially identical readings to thermistors in intravascular sites, are less invasive, provide continuous readings, and provide stable measurements, regardless of urine flow rate (12, 13, 16–18). However, bladder thermistor catheters are costly and require a monitor. Esophageal probes placed in the distal third of the esophagus provide readings comparable with thermistors in intravascular sites and with bladder catheters (19). However, confirming accurate placement is difficult because they are not radiopaque. In addition, they are uncomfortable in alert or spontaneously breathing patients. The theoretical risk of an esophageal probe eroding or perforating the esophagus when left in place for extended periods of time makes this probe impractical for use in the critically ill patient.

Rectal temperatures obtained with a mercury thermometer or an electronic probe (intermittent or continuous) are traditional measurement devices. Readings from the rectum are often a few tenths of a degree higher than core temperature (12, 14, 20, 21). The patient often perceives rectal temperature measurement as unpleasant and intrusive. Access to the rectum may be limited by patient position. Moreover, there is a small risk of trauma or perforation to the rectum, which is a particular problem in patients who are neutropenic, coagulopathic, or who have had recent rectal surgery. Rectal temperature measurements have also been implicated in spreading enteric pathogens such as Clostridium difficile or vancomycin-resistant enterococci via the device or the operator (22–24).

Oral temperature measurement is safe, convenient, and familiar for alert and cooperative patients. Mouth breathing, heated gases, and hot or cold fluids can distort the reading (13, 25). Oral probes can damage oral mucosa, especially in patients with abnormal mucosa due to trauma, thermal injury, infection, surgery, cancer, or cytotoxic drugs. In critically ill patients, oral temperatures are often not practical due to intubation or inability of the patient to cooperate.

Tympanic membrane temperature is believed to reflect the temperature of the hypothalamus and, thus, the core body temperature. Direct measurement of the tympanic membrane temperature requires an electronic probe, is painful in awake patients, and risks trauma to the tympanic membrane. Infrared ear thermometry is also available to detect radiant energy from the tympanic membrane and ear canal through an otoscopic probe. These devices are not accurate if inflammation of the auditory canal or tympanic membrane is present or if there is obstruction of the external canal. Tympanic membrane and infrared devices do not always agree with other measurement devices. Multiple studies have shown consistently poor agreement between measurements made by infrared ear devices and those made by pulmonary artery catheters (12–16, 18, 26).

Infrared thermometry measurement technology used in tympanic membrane thermometers has been adapted to a noninvasive temporal artery thermometer (27). Because the temporal artery has a high arterial perfusion rate that remains unchanged under most conditions, measurement of temperature via skin areas perfused by the temporal artery provide an easy, noninvasive estimate of the core temperature (28). Environmental temperature and sweating have been associated with unreliable temperature measurements compared with rectal and esophageal temperature (29), and the temporal artery thermometer provides similar accuracy to axillary measurements that are not recommended (27).

The chemical dot thermometer is a single-use, flexible polystyrene plastic strip with 50 heat-sensitive dots (temperature sensors) applied to the forehead; each dot represents a temperature increment of 0.1°C over a range of 35.5–40.4°C; the last dot to turn blue constitutes the body temperature (30). Lack of agreement between measurements made using this device and pulmonary artery catheters limits their usefulness in critically ill patients (26).

Recommendations for Measuring Temperature

  1. Choose the most accurate and reliable method to measure temperature based on the clinical circumstances of the patient. Temperature is most accurately measured by an intravascular, esophageal, or bladder thermistor, followed by rectal, oral, and tympanic membrane measurements, in that order (Table 2). Axillary measurements, temporal artery estimates, and chemical dot thermometers should not be used in the ICU (level 2). Rectal thermometers should be avoided in neutropenic patients (level 2).
  2. Table 2
    Table 2:
    Accuracy of methods used for measuring temperature (6, 12–16)
  3. Any device used to measure temperature must be maintained and calibrated appropriately, using the manufacturer’s guidelines as a reference (level 2).
  4. Any device used to measure temperature must be used in a manner that does not facilitate spread of pathogens by the instrument or the operator (level 2).
  5. The site of temperature measurement should be recorded with the temperature in the chart (level 1).
  6. A new onset of temperature of ≥38.3°C is a reasonable trigger for a clinical assessment but not necessarily a laboratory or radiologic evaluation for infection (level 3).
  7. A new onset of temperature of <36.0°C in the absence of a known cause of hypothermia (e.g., hypothyroidism, cooling blanket, etc.) is a reasonable trigger for a clinical assessment but not necessarily a laboratory or radiologic evaluation for infection (level 3).
  8. Critical care units could reduce the cost of fever evaluations by eliminating automatic laboratory and radiologic tests for patients with new temperature elevation (level 2). Instead, these tests should be ordered based on clinical assessment. A clinical and laboratory evaluation for infection, conversely, may be appropriate in euthermic or hypothermic patients, depending on clinical presentation.

Blood Cultures

Because the information provided by a positive blood culture can have such important prognostic and therapeutic implications, blood cultures should be obtained in patients with a new fever when clinical evaluation does not strongly suggest a noninfectious cause.

Skin Preparation.

The site of venipuncture should be cleaned with either 2% chlorhexidine gluconate in 70% isopropyl alcohol (2% alcoholic chlorhexidine), or 1–2% tincture of iodine (iodine in alcohol). Povidone iodine (10%), although acceptable, is a less efficient agent. The access to an intravascular device and to the stopper on all blood culture bottles should be cleaned with 70–90% alcohol (31, 32). Most blood culture bottles should not be swabbed with iodine-containing antiseptics because these solutions may degrade the stoppers. Chlorhexidine and tincture of iodine are equally effective for cleaning the site of venipuncture and more effective than aqueous povidone iodine in reducing the rate of blood culture contamination (33–36). Iodophors (aqueous iodine solutions) must be allowed to dry 1.5–2 mins to provide maximal antiseptic activity and thus to minimize the risk of contamination (37). Both alcoholic chlorhexidine and tincture of iodine have an alcohol base, so they dry more rapidly (∼30 secs) than iodophors. This reduces the time required for phlebotomy.

When blood is to be inoculated into a culture or transport tube, the needle used for venipuncture should not be replaced by a sterile needle. The risk of a needle stick injury during the switch in needles is currently thought to outweigh the risk of contamination (37, 38).

Blood Volume and Collection System.

One blood culture is defined as a sample of 20–30 mL of blood drawn at a single time from a single site, regardless of how many bottles or tubes the laboratory may use to process the specimen. The sensitivity of blood cultures for detection of true bacteremia or fungemia is related to many factors, the most important being obtaining the cultures before the initiation of anti-infective therapy and the volume of blood drawn (32, 39–44). The full amount of blood recommended for each bottle should be drawn (37). The volumes required for blood cultures are typically determined by laboratories based on the various media used and on recommendations of the manufacturer of the blood culture instrument employed (37). A variety of commercial blood culture systems can provide excellent results (Table 3). Laboratories need to make their own decisions about the best system, considering their budget, their manpower, and the patient population they serve. Special media or blood culture systems can be added in designated circumstances. The utility of antibiotic removal devices in blood culture systems is controversial, although some laboratories still use them routinely. Some studies have shown that, when compared with conventional culture systems, these devices can enhance the recovery of staphylococci and yeasts, regardless of whether the patient is receiving antibiotics (37, 45, 46); they do not seem to enhance the recovery of Gram-negative bacilli. Considering varying experiences related to benefit, and the substantial additive costs and increased number of contaminants (37, 47), their use is considered optional.

Table 3
Table 3:
Blood culture systems

In general, commercial pediatric collection systems should not be used for adults: the smaller volume of blood sampled will diminish the yield of pathogens for adults (42). If it is not possible to secure the recommended volume of blood required for the adult collection system and <5 mL of blood is obtained, it is acceptable to inject the entire amount into the aerobic blood culture bottle.

Cultures of Blood for Unusual Pathogens.

In special patient populations or in special geographic areas, it may be appropriate in the evaluation of fever to include special media or special blood culture systems for organisms other than common aerobic and anaerobic bacteria. For example, cultures containing resins or lytic agents may be helpful in isolating yeast, and lysis-centrifugation may be useful for isolating Bartonella species, dimorphic fungi, Mycobacterium avium, and Mycobacterium tuberculosis. Most often, these pathogens are sought in patients with specific underlying diseases (solid organ transplant and stem cell transplant recipients or patients with prolonged granulocytopenia), or they are sought because of epidemiologic circumstances (Francisella, Bartonella, or Histoplasma). In such situations, communication with the microbiology laboratory is essential to determine whether special culture systems, in addition to routine blood cultures, are needed or if incubating the routine culture for a longer period of time would be useful.

Number of Cultures and Sites.

Recent data suggest that the cumulative yield of pathogens is optimized when three to four blood cultures with adequate volume (20–30 mL each) are drawn within the first 24 hrs of suspected bacteremia or fungemia (39, 48). Each culture should be drawn by separate venipuncture or through a separate intravascular device but not through multiple ports of the same intravascular catheter (49, 50). Ideally, blood cultures should not be drawn through nonintact or infected skin (e.g., burns). There is no evidence that the yield of cultures drawn from an artery is different from the yield of cultures drawn from a vein. If the patient has limited access for venipuncture, it is acceptable to draw blood cultures from separate intravascular devices. However, this may increase the number of contaminated blood cultures.

In most cases of true bacteremia/fungemia, when organisms are detected, all specimens, whether drawn through a catheter or through a venipuncture, will yield positive results (51). In the majority of cases of discordant results, the culture drawn through the device will be positive and the culture drawn by venipuncture will be negative; in such instances, the positive culture may represent a contaminant or a catheter-related infection, but clinical judgment rather than any rigid criteria is needed to interpret the significance of discordant results (50, 52, 53).

Drawing three to four blood cultures with appropriate volume from separate sites of access within the first 24 hrs of the onset of fever is the most effective way to discern whether an organism found in blood culture represents a true pathogen (multiple cultures are often positive), a contaminant (only one of multiple blood cultures is positive for an organism commonly found on skin and clinical correlation does not support infection), or a bacteremia/fungemia from an infected catheter (one culture from the source catheter is positive, often with a positive catheter tip, and other cultures are not) (32, 37, 54). Clinical judgment must determine which catheter(s) and which lumen(s) are used for drawing the culture(s). Clinical data that might determine drawing blood cultures from certain catheters include catheter dwell time (carefully inserted catheters that have been in place for <3 days are less likely to be infected than longer-dwelling catheters), conditions of insertion (emergency vs. routine), and local signs of inflammation. Many experts would use the distal port of a catheter to obtain blood cultures. If all blood cultures are obtained from catheters, the blood culture replacing the venipuncture should be obtained from the most recently inserted catheter. Blood cultures should not be obtained via a peripherally inserted venous catheter at the time of insertion as this leads to an unacceptably high rate of contamination (55). Finally, separating blood cultures by defined, spaced intervals (such as every 10 mins) has not been shown to enhance microbial recovery, is not practical, and may lead to a delay in therapy in critically ill patients (56).

Labeling.

Blood cultures should be clearly labeled with the exact time, date, and anatomic site or catheter lumen from which blood is drawn and also include other information (concomitant antimicrobial therapy) that may be appropriate. This labeling is extremely useful for interpreting the significance of the result (see section on catheter-related infections below).

Recommendations for Obtaining Blood Cultures

  1. Obtain three to four blood cultures within the first 24 hrs of the onset of fever. Every effort must be made to draw the first cultures before the initiation of antimicrobial therapy. They can be drawn consecutively or simultaneously, unless there is suspicion of an endovascular infection, in which case separate venipunctures by timed intervals can be drawn to demonstrate continuous bacteremia (level 2).
  2. Additional blood cultures should be drawn thereafter only when there is clinical suspicion of continuing or recurrent bacteremia or fungemia or for test of cure, 48–96 hrs after initiation of appropriate therapy for bacteremia/fungemia. Additional cultures should not be drawn as a single specimen but should always be paired (level 2).
  3. For patients without an indwelling vascular catheter, obtain at least two blood cultures using strict aseptic technique from peripheral sites by separate venipunctures after appropriate disinfection of the skin (level 2).
  4. For cutaneous disinfection, 2% chlorhexidine gluconate in 70% isopropyl alcohol is the preferred skin antiseptic, but tincture of iodine is equally effective. Both require ≥30 secs of drying time before proceeding with the culture procedure. Povidone iodine is an acceptable alternative, but it must be allowed to dry for >2 mins (level 1).
  5. The injection port of the blood culture bottles should be wiped with 70–90% alcohol before injecting the blood sample into the bottle to reduce the risk of introduced contamination (level 3).
  6. If the patient has an intravascular catheter, one blood culture should be drawn by venipuncture and at least one culture should be drawn through an intravascular catheter. Obtaining blood cultures exclusively through intravascular catheters yields slightly less precise information than information obtained when at least one culture is drawn by venipuncture (level 2).
  7. Label the blood culture with the exact time, date, and anatomic site from which it was taken (level 2).
  8. Draw 20–30 mL of blood per culture (level 2).
  9. Paired blood cultures provide more useful information than single blood cultures. Single blood cultures are not recommended, except in neonates (level 2).
  10. Once blood cultures have been obtained after the onset of new fever, additional blood cultures should be ordered based on clinical suspicion of continuous or recurrent bacteremia or fungemia (level 2).

Intravascular Devices and Fever

Stable vascular access is essential to the management of the critically ill patient. Most patients will have at least one central venous catheter, and many may have an arterial catheter as well. An increasing number of patients will have some type of tunneled, cuffed central venous catheter or some type of subcutaneous central venous port.

The relative risk of bloodstream infection caused by various intravascular devices ranges widely, depending on the length of the device, the type of device, the patient population, the techniques used in insertion, the frequency of manipulation, and the time they have been in place (57, 58). The highest risk is with short-term, noncuffed central venous catheters, in the range of 2–5 per 1,000 catheter days, and is especially high with noncuffed temporary hemodialysis catheters. Arterial catheters used for hemodynamic monitoring and peripherally inserted central venous catheters used in hospitalized patients seem to have a risk of catheter-related bloodstream infection (2–3 per 1,000 catheter days) similar to conventional subclavian, internal jugular, or femoral short-term, noncuffed central venous catheters. In contrast, the risk of bloodstream infection with small, peripheral intravenous catheters is <0.1 cases per 1,000 catheter days. With good care, surgically implanted ports are associated with a much lower risk of bacteremia/fungemia than temporary percutaneous catheters, approximating 0.2–1 per 1,000 catheter days (57).

Location of Infection.

All intravascular devices need to be assessed daily, to determine whether they are still needed and whether there are signs of local infection at the site of insertion (manifested by inflammation or purulence at the exit site or along the tunnel), or systemically (manifested by positive blood cultures or thrombosis).

It is important to recognize that contaminated hubs are common portals of entry for organisms colonizing the endoluminal surface of the catheter (59, 60). In addition, infusate (parenteral fluid, blood products, or intravenous medications) administered through an intravascular device can become contaminated and produce device-related bacteremia or fungemia, which is more likely to culminate in septic shock than are other catheter-related infections.

Diagnosis.

Patients with abrupt onset of signs and symptoms of sepsis without risk factors for nosocomial infection (e.g., young, immunocompetent), especially without any local site of infection, should prompt suspicion of infection of an intravascular device. Difficulty drawing or infusing through the catheter may point to the catheter as a source of infection. The presence of inflammation, with or without purulence, at the insertion site, though absent in most cases (61), when combined with signs and symptoms of sepsis, has been shown to be predictive of device-related bacteremia. Finally, recovery of certain microorganisms in multiple blood cultures, such as staphylococci, Corynebacterium jeikeium, Bacillus species, atypical mycobacteria, Candida, or Malassezia species, strongly suggest infection of an intravascular device.

Evaluation.

As part of the comprehensive physical examination, the access site should be examined at least daily, and any expressible purulence or exudate should be Gram stained and cultured. A minimum of two peripheral blood cultures, or one culture drawn percutaneously and one drawn through the catheter, should be obtained. Standard blood cultures drawn through intravascular devices provide excellent sensitivity for diagnosis of bloodstream infection (62, 63).

Removal and culture of the catheter has historically been the gold standard for the diagnosis of catheter-related bloodstream infection, particularly with short-term catheters. Studies have demonstrated the reliability of semiquantitative or quantitative catheter tip culture methods for the diagnosis of catheter-related bacteremia (64, 65) (Table 4). The diagnosis of catheter-related bloodstream infection is completed when a colonized catheter is associated with concomitant bloodstream infection with the identical organism, with no other plausible source. Gram-negative stain (66) or acridine orange stain (67) of intravascular segments of removed catheters also correlates with semiquantitative or quantitative cultures but are technically challenging, time consuming, and expensive to perform and thus are offered by few hospitals.

Table 4
Table 4:
Common pathogens and diagnostic tests available

Some ICU clinicians routinely culture central venous catheters on removal, regardless of whether there is fever or any other reason to suspect catheter sepsis. Because up to 20% of removed central venous catheters are colonized at removal, most unassociated with local infection or bacteremia/fungemia, this practice adds to microbiology laboratory expense and can lead to unnecessary therapies if interpreted inappropriately. The predictive value of a positive catheter culture is very low when there is a low pretest probability of catheter sepsis (65), and catheters removed from ICU patients should only be cultured if there is strong clinical suspicion of catheter sepsis (68).

Cultures of catheters obviously require their removal, which presents a disadvantage in patients with long-term central venous devices. Prospective studies have shown that only 25–45% of episodes of sepsis in patients with long-term devices represent true device-related bloodstream infection (69). Thus, it would seem that development of methods for detecting device-related bloodstream infection that do not require removal of the device would be of great value. Although exit site swabs are not sensitive for detecting catheter-related infection, a negative catheter exit site swab culture has a high negative predictive value and may reduce the proportion of unnecessary catheter withdrawals (70, 71).

Blood cultures drawn through the catheter in combination with blood cultures drawn percutaneously may be especially useful for detecting catheter-related bloodstream infection. Microbial growth can be quantitated using a quantitative blood culture system, or by using the differential time to positivity for peripheral vs. catheter blood cultures drawn simultaneously. If both sets of cultures are positive for the same organism and the set drawn through the catheter becomes positive ≥120 mins earlier than the culture drawn peripherally, this is highly suggestive of catheter-related bloodstream infection. This method is less sensitive but as specific as quantitative culture.

A quantitative blood culture drawn through an infected catheter characteristically shows a marked step-up in concentration of organisms, usually ten-fold or greater, as compared with a quantitative blood culture drawn concomitantly from a peripheral vein. Due to the additional expense and expertise necessary for processing, quantitative cultures of catheter-drawn blood are not routinely performed as part of the usual evaluation of fever. They can, however, provide useful information, especially for surgically implanted catheters that cannot easily be removed.

For patients with fever alone who are not septic (i.e., temperature of >38°C or <36°C, white blood cell count of >12,000 cells/mm3 or <4,000 cells/mm3, heart rate of >90 beats/min, respiratory rate of >20 breaths/min, or Paco2 of <32 [3]), there is usually no need to remove or change all indwelling catheters immediately, although such an approach would be the most cautious management strategy and might be desirable in a patient with a prosthetic heart valve or a fresh arterial graft (68). If patients have sepsis or septic shock refractory to vasopressors, peripheral embolization, disseminated intravascular coagulation, or acute respiratory distress syndrome, removal of all intravascular catheters and reinsertion at new sites is indicated, even if the catheters are cuffed or tunneled devices (72). If there is clinical evidence of vascular compromise (i.e., signs of occlusive venous thrombosis or arterial insufficiency), the catheter should be removed. If a radiographic study is performed and there is evidence of thrombosis, clinical judgment is needed to determine whether anticoagulation, thrombolysis, or surgical interventions are necessary.

Septic phlebitis of a central vein due to a centrally placed catheter is unusual (73, 74). With suppurative phlebitis, bloodstream infection characteristically persists after the catheter has been removed, producing a clinical picture of overwhelming sepsis with high-grade bacteremia or fungemia or with septic embolization. This syndrome is most often encountered in burn patients or other ICU patients who develop catheter-related infection that goes unrecognized, permitting microorganisms to proliferate to high levels within an intravascular thrombus (73–75). In patients with persistent bacteremia with Staphylococcus aureus or persistent fungemia, echocardiography is appropriate to assess for endocarditis and guide further therapy (68).

Recommendations for Management of Intravascular Catheters

  1. Examine the patient at least daily for inflammation or purulence at the exit site or along the tunnel, and assess the patient for signs of venous thrombosis or evidence of embolic phenomena (level 2).
  2. Any expressed purulence from the insertion site should be Gram stained and cultured (level 2).
  3. If there is evidence of a tunnel infection, embolic phenomenon, vascular compromise, or septic shock, the catheter should be removed and cultured and a new catheter inserted at a different site (level 2).
  4. With short-term temporary catheters—peripheral venous catheters, noncuffed central venous catheters, or arterial catheters—if catheter-related sepsis (i.e., source of the infection is a colonized catheter) is considered likely, the suspect catheter or catheters should be removed and a catheter segment cultured. Blood cultures should be obtained as well. With all short-term catheters, a 5- to 7-cm intracutaneous segment should be cultured to document the source of bacteremia; with short peripheral venous or arterial catheters, the tip should be cultured; with longer central venous catheters, the intracutaneous segment and tip should be cultured; and with pulmonary artery catheters, the introducer and the pulmonary artery catheter should be cultured (level 1).
  5. At least two blood cultures should be obtained. At least one blood culture should be obtained peripherally by venipuncture. One specimen should be obtained from the suspected catheter (level 1). If a quantitative culture system is available, it should be used to diagnose the catheter as the source of bacteremia/fungemia. Alternatively, differential time to positivity can be used if both blood cultures are positive for the same organism. The distal port is the logical port from which to draw cultures. When short-term, uncuffed central venous catheters are suspected of infection, it is usually more efficient to remove the existing catheter and replace it than to draw quantitative cultures (level 2).
  6. Do not routinely culture all catheters removed from ICU patients. Culture only those catheters suspected of being the source of infection (level 2).
  7. It is not necessary to routinely culture infusate specimens as part of the evaluation for catheter-related infections, unless there is clinical suspicion for infected infusate or blood products (level 2).

Pulmonary Infections and ICU-Acquired Pneumonia

Pneumonia is the second most common cause of infection acquired in the ICU and a ubiquitous cause of fever, with the majority of cases occurring in mechanically ventilated patients (76, 77). In an ICU, it can be difficult to determine whether fever is due to pneumonia when patients commonly have other noninfectious processes producing abnormal chest radiographs and gas exchange (i.e., congestive heart failure, atelectasis, acute respiratory distress syndrome). Many patients in an ICU are intubated and sedated, cannot cough, and have other reasons for abnormal secretions. In addition, immunocompromised patients, such as solid organ transplant recipients, may have severe pneumonia without fever, cough, sputum production, or leukocytosis (78, 79).

Diagnostic Evaluation.

Physical examination, chest radiograph, and examination of pulmonary secretions comprise the initial evaluation. For initial fever evaluations, portable chest radiographs are generally adequate. All radiographs should be performed in an erect sitting position, during deep inspiration if possible. Among all radiographic signs in ICU patients, unilateral air bronchograms have been shown to have the best predictive value for pneumonia; however, no single radiographic finding is highly predictive (80–82). The absence of infiltrates, masses, or effusions does not exclude pneumonia, abscess, or empyema as a cause of fever. Clinical judgment is needed to determine whether the suspicion of infection is high enough to warrant transporting the patient to the radiology suite for a higher resolution study such as computerized tomographic (CT) imaging. Such studies are particularly sensitive for demonstrating parenchymal or pleural disease in the posterior-inferior lung bases (83, 84), although there is only a fair correlation with a diagnosis of pneumonia in complex patients (85). CT imaging is also valuable in immunocompromised patients, in whom small nodular or cavitary lesions are more prevalent and difficult to detect by standard chest radiographs (86, 87). Respiratory secretions can be obtained for examination by a variety of techniques. Expectoration, nasopharyngeal washing, saline induction, deep tracheal suctioning, bronchoscopic protected specimen brush samples or aspiration, or bronchoscopic or nonbronchoscopic (mini-BAL) bronchoalveolar lavage are the principle diagnostic options. Each of these techniques has advantages and disadvantages (77, 88). For initial evaluation of fever in the nonintubated patient, before it is apparent whether pneumonia is present, evaluation of an expectorated sputum, nasotracheal or endotracheal aspirate, as opposed to a more invasively obtained specimen, is usually sufficient. In the intubated patient, saline should be instilled in the endotracheal tube only if an adequate specimen cannot be obtained by deep suctioning in the absence of saline. There is concern that saline dilutes the specimen and could introduce pathogens present in the tube biofilm or upper airway into the lower airway.

The utility of fiberoptic bronchoscopy is variable and depends on the patient populations, causative organism, and current and previous use of antibiotics. Aspirates from the inner channel of the bronchoscope are characteristically contaminated by upper respiratory flora (89, 90). If bronchoscopic sampling is not immediately available, nonbronchoscopic sampling (mini-BAL) can reliably obtain lower respiratory secretions for microscopic evaluation (88, 91). Bronchoscopy, however, may be especially useful for the detection of selected pathogens such as Pneumocystis jiroveci, Aspergillus and other filamentous fungi, Nocardia, Legionella, cytomegalovirus (CMV), and Mycobacterium species (92, 93).

When pulmonary secretions are acquired for analysis, the specimen should be transported to the laboratory and processed within 2 hrs so that fastidious organisms such as Streptococcus pneumoniae remain viable (94). For any expectorated specimen, it is important for the laboratory to perform direct microscopy on the specimen to determine whether it represents saliva (i.e., if the predominant cells are squamous epithelial) or lower respiratory secretions (i.e., if the predominant cells are leukocytes, assuming the patient is nonneutropenic).

If the specimen is of lower respiratory origin, in most situations, a Gram-negative stain should be performed, and the specimen should be cultured for routine aerobic bacterial pathogens. In appropriate circumstances, principally defined by the host category, rapidity of clinical presentation, and radiographic features, it may be desirable to perform other direct tests, such as a potassium hydroxide with calcofluor stain for fungus, an enzyme-immunoassay, or direct fluorescent antibody tests for respiratory viruses and P. jiroveci, and an acid-fast stain for mycobacteria. It may also be desirable to culture the specimen for fungi, mycobacteria, Legionella, and respiratory viruses. Urinary antigen tests are currently available for Legionella pneumophila type 1 and S. pneumoniae. Some laboratories have developed and verified nucleic acid amplification tests for some of these pathogens. However, there are currently no assays approved by the Food and Drug Administration, except those available for M. tuberculosis. The use of such assays must be driven by institution-specific expertise and in consultation with clinicians. Because local and referral center testing methods may vary across different centers, the most common laboratory technique options for each pathogen are summarized in Table 4.

Clinicians need to be aware of the organisms that are virtually always pathogens when recovered from respiratory secretions. Although not all-inclusive, these organisms might include Legionella, Chlamydia, M. tuberculosis, Rhodococcus equi, influenza virus, respiratory syncytial virus, parainfluenza virus, Strongyloides, Toxoplasma gondii, P. jiroveci, Histoplasma capsulatum, Coccidioides immitis, Blastomyces dermatitidis, and Cryptococcus neoformans. Conversely, isolation of enterococci, viridans streptococci, coagulase-negative staphylococci, and Candida species (93, 95, 96) should rarely if ever be considered the cause of respiratory dysfunction. Potential bacterial pathogens such as Pseudomonas aeruginosa, Enterobacteriaceae, S. pneumoniae, S. aureus, and Haemophilus influenzae are frequently encountered in respiratory specimens and may represent contaminants that colonize the upper airways, or they may be true pathogens of pneumonia. The distinction between pathogen and colonizer is facilitated by detection of pathogenic organisms as the dominant flora on direct Gram-negative stain or their recovery in respiratory secretions in moderate or heavy growth. Quantitative cultures of bronchoscopic or other specimens from lower airways may also facilitate the distinction between colonizing bacteria and pathogens. The use of these quantitative techniques has been shown to increase the specificity of the diagnosis of healthcare-associated pneumonia in some studies but requires bronchoscopic expertise, considerable labor by the microbiology department, and well-standardized methodology (88).

Clinical interpretation of quantitative cultures is likely to be hampered by previous antibiotic administration, which may lower the observed quantitative inoculum after 24 hrs of ongoing antibiotic therapy and up to 72 hrs after cessation of antibiotics (97, 98). The utility of quantitative cultures to identify the causative pathogen has been reviewed elsewhere (99–101).

It is appropriate to draw blood cultures to attempt to identify the cause of pneumonia. Blood tests other than cultures may also yield the etiology of pneumonia, especially in immunocompromised patients: a) antigenemia for CMV in non–human immunodeficiency virus-infected patients, histoplasmosis, and cryptococcosis; b) polymerase chain reaction for CMV, varicella-zoster virus, human herpes virus-6, and adenovirus; and c) galactomannan and beta-d-glucan for aspergillosis and Candida may be useful as supportive evidence of infections but may be most useful to exclude invasive fungal infection, given their high negative predictive value.

Many febrile patients in an ICU have small amounts of pleural fluid due to congestive heart failure, hypoalbuminemia, or postoperative processes. It is not necessary to obtain a sample of such fluid for culture in every febrile patient. Thoracentesis to obtain fluid for stain, culture, and cytology (and for measurement of pH, protein, glucose, and lactate dehydrogenase) would be especially appropriate if there is enough fluid to aspirate safely using ultrasound guidance and if there is either an adjacent pulmonary infiltrate, suspicion of tuberculosis, or possible contamination of the pleural space by surgery, trauma, or a fistula (102, 103). The fluid should be cultured for aerobic and anaerobic bacteria. Cultures for fungi and mycobacteria should be performed as epidemiologically appropriate.

Once cultures are obtained and the laboratory grows pathogens, antimicrobial susceptibility tests should be performed on isolates of aerobic and facultative bacteria, including S. pneumoniae. Susceptibility tests should be performed and interpreted using the most recent criteria published by the Clinical and Laboratory Standards Institute. Susceptibility tests for anaerobic bacteria, fungi, or viruses are not routinely indicated.

Recommendations for Evaluation of Pulmonary Infections.

If a febrile patient is suspected of having a lower respiratory tract infection by clinical or radiographic assessment:

  1. A chest imaging study should be obtained. In most cases, an upright portable anteroposterior chest radiograph is the most feasible study to obtain. Posterior-anterior chest radiographs with lateral view or CT scan offer more information and should be obtained when clinically indicated, especially to rule out opportunistic infections in immunocompromised patients (level 1).
  2. Obtain one sample of lower respiratory tract secretions for direct examination and culture before initiation of or change in antibiotics. Expectorated sputum, induced sputum, tracheal secretions, or bronchoscopic or nonbron-choscopic alveolar lavage material can be used effectively. If pneumonia is documented by physical examination and radiographic evaluation, a decision to employ bronchoscopy or other invasive diagnostic approaches should be considered based on an individual basis and the availability of local expertise (level 2).
  3. Respiratory secretions obtained for microbiological evaluation should be transported to the laboratory and processed in <2 hrs (level 2).
  4. Respiratory secretions that are judged to be appropriate samples by the laboratory should be evaluated by Gram-negative stain and cultured for routine aerobic and facultative bacteria. Additional stains, rapid tests, cultures, and other tests should be performed as epidemiologically appropriate (level 2).
  5. Quantitative cultures can provide useful information in certain patient populations when assessed in experienced laboratories; however, quantitative cultures have not yet been sufficiently standardized nor have they been shown to alter outcome for this technique to be considered part of routine evaluation (level 2).
  6. Pleural fluid should be obtained with ultrasound guidance for Gram-negative stain and routine culture (with other studies as clinically indicated) if there is an adjacent infiltrate or another reason to suspect infection and the fluid can be safely aspirated (level 2).

Stool Evaluation in the Febrile Patient in the ICU

Many patients in the ICU have diarrhea, which is often caused by enteral feedings or drugs. By far the most common enteric cause of fever in the ICU is Clostridium difficile, which should be suspected in any patient with fever or leukocytosis and diarrhea who received an antibacterial agent or chemotherapy within 60 days before the onset of the diarrhea (104, 105). C. difficile accounts for 10–25% of all cases of antibiotic-associated diarrhea and virtually all of the cases of antibiotic-associated pseudomembranous colitis (106). Other organisms that can cause fever and diarrhea include Salmonella, Shigella, Campylobacter jejuni, Aeromonas, Yersinia, Escherichia coli, Entamoeba histolytica, and multiple viruses that are not usually identified by standard techniques. In general, these are community-acquired diseases and only rarely cause infectious diarrhea acquired after a patient has been admitted to the ICU. If the patient was not initially admitted to the hospital with diarrhea and is not infected with HIV, it is unlikely that these organisms would produce diarrhea and fever in the ICU. Thus, sending stools for bacterial cultures or ova and parasite examination should generally be avoided as part of a fever evaluation unless the patient was admitted to the hospital with diarrhea, is infected with HIV, or is a part of an outbreak evaluation.

Presentation.

Most patients with C. difficile as the cause for their fever present with diarrhea. (Diarrhea is defined in this document as more than two stools per day that conform to the container in which they are placed.) However, some patients, especially those who are postoperative, may present with ileus or toxic megacolon or leukocytosis without diarrhea as the manifestation of C. difficile disease. In these patients, the diagnosis of C. difficile disease may be difficult to establish because stool specimens are not accessible (107). C. difficile–associated diarrhea may occur with any antibacterial agent, but the most common causes are clindamycin, cephalosporins, and fluoroquinolones (108). Other clinical clues are fever, toxic megacolon, leukocytosis (especially with a leukemoid reaction), and hypoalbuminemia (109).

Evaluation for C. difficile.

Testing algorithms differ markedly among institutions. The most sensitive and specific test most laboratories can perform to establish this diagnosis is the tissue culture assay (110, 111). Disadvantages with this test are the 24- to 48-hr delay in results, lack of experience with tissue culture techniques in many laboratories, and cost. As a result, most laboratories now use enzyme immunoassay (EIA) tests, which are commercially available, provide results within minutes to hours, and are technically easy to perform. They are less sensitive than the tissue culture assay and consequently may require two to three repeat tests to document disease (112). The EIA for toxin A is available, but 2–3% of stains produce only toxin B, so the EIA for toxin A and B is preferred (113). Once toxin is demonstrated, there is no utility in follow-up assays to demonstrate cure, as patients may shed toxin long after they are clinically cured. A two-step algorithm that screens samples for glutamate dehydrogenase, the C. difficile common antigen, followed by testing only positives for toxin has been demonstrated to have high negative predictive value (114, 115).

Cultures for C. difficile are technically demanding, require 2 to 3 days for growth, and are not specific in distinguishing toxin-positive strains, toxin-negative strains, and asymptomatic carriage (112, 116). Cultures may be useful in the setting of nosocomial outbreaks when isolates are needed for strain typing for epidemiologic purposes (105). The NAP1 strain has been epidemic in many hospitals in the United States, Canada, and Europe; it is associated with serious complications (toxic megacolon, leukemoid reactions, sepsis, and death) and is often refractory to standard therapy (108, 117, 118). There are strain differences in virulence, which may be important to recognize for epidemiologic purposes (119). However, the methods to identify specific strains are not generally available, and strain identification does not alter management of individual patients.

Direct visualization of pseudomembranes is nearly diagnostic for C. difficile colitis (120). Most diagnoses by visualization come from proctoscopic evaluation rather than more extensive lower gastrointestinal evaluation. In terms of sensitivity, in patients with severe disease, only 71% of patients had pseudomembranes documented by direct visualization, whereas pseudomembranes were present in only 23% of patients with mild disease (121). Concerns about cost, risk of perforation during the examination, and the relative ease of cytotoxin assays have removed flexible sigmoidoscopy and colonoscopy from routine use for diagnosis. However, a role for direct visualization may exist in cases requiring rapid diagnosis if laboratory results will be delayed or if false-negative C. difficile toxin assays are suspected (105). Many clinicians would treat such patients empirically rather than perform sigmoidoscopy or colonoscopy.

Evaluation for Other Enteric Pathogens.

Infection with Klebsiella oxytoca should be considered in patients with antibiotic-associated colitis who are negative for C. difficile (122). Patients who have a recent and significant travel history to developing countries, patients with HIV disease, and patients with unusual domestic exposures may require a more extensive evaluation. Patients with a recent travel history should have their evaluation directed by the most likely pathogens that occur in their area of travel, although the most common cause of travelers’ diarrhea, enterotoxigenic E. coli, is not detected with the usual laboratory tests. Patients who have traveled to areas where parasitic disease is common should have their stool evaluated by stool ova and parasite examination for other organisms such as Cyclospora, E. histolytica, and Strongyloides. Norovirus should be considered in the setting of employee illness, patients with a travel history, or when multiple patients on a particular hospital unit are having fever, vomiting, and diarrhea.

Patients with HIV disease and CD4 <100/μL often have chronic diarrhea caused by Salmonella, Microsporidium, CMV, or M. avium complex. Microsporidium detection requires special stains of the stool or small bowel biopsy. The diagnosis of CMV should be made endoscopically by means of a biopsy. CMV colitis should be highly suspected in the solid organ transplant recipient with fever and diarrhea, particularly in the recipient who received an allograft from a donor with positive CMV serology. Acute neutropenic enterocolitis or typhlitis caused by enteric Gram-negative bacilli (i.e., Pseudomonas species) or anaerobes (i.e., Clostridium septicum) should be sought in cancer or stem cell transplant recipients by imaging studies or endoscopy.

Recommendations for Evaluation of the Gastrointestinal Tract.

If more than two stools per day conform to the container in which they are placed in a patient at risk for C. difficile and if clinical evaluation indicates that a laboratory evaluation is necessary:

  1. Send one stool sample for C. difficile common antigen, EIA for toxin A and B, or tissue culture assay (level 2).
  2. If the first specimen for C. difficile is negative and testing is performed by an EIA method, send an additional sample for C. difficile EIA evaluation. A second specimen is not necessary if the common antigen test was negative (level 2).
  3. If severe illness is present and rapid tests for C. difficile are negative or unavailable, consider flexible sigmoidoscopy (level 3).
  4. If severe illness is present, consider empirical therapy with vancomycin while awaiting diagnostic studies. Empirical therapy is not generally recommended if two stool evaluations are negative using a reliable assay. Although it may be more cost-effective than making the diagnosis, the empirical use of antibiotics, especially vancomycin, is discouraged because of the risk of producing resistant pathogens (level 2).
  5. Stool cultures for other enteric pathogens are rarely indicated in a patient who did not present to the hospital with diarrhea or in patients who are not HIV infected. Send stool cultures for other enteric pathogens and examine for ova and parasites only if epidemiologically appropriate or evaluating an immunocompromised host (level 2).
  6. Test stool for norovirus if the clinical and epidemiologic setting is appropriate. Testing for norovirus is usually only available in state laboratories and is usually performed in outbreak settings. Obtain consultation with infection control and public health authorities (level 3).

Urinary Tract Infection

Catheter-associated bacteriuria or candiduria usually represents colonization, is rarely symptomatic, and is rarely the cause of fever or secondary bloodstream infection (123), even in immunocompromised patients (124), unless there is urinary tract obstruction, the patient has had recent urologic manipulation or surgery, or is granulocytopenic (125, 126). The traditional clinical signs and symptoms (dysuria, urgency, pelvic or flank pain, fever or chills), that correlate well with significant bacteriuria in noncatheterized patients are rarely reported in ICU patients with documented catheter-associated bacteriuria or candiduria of >105 colony-forming units (cfu)/mL (123, 124).

Etiology.

In the ICU, the majority of urinary tract infections are related to urinary catheters and are caused by multiresistant nosocomial Gram-negative bacilli other than E. coli, Enterococcus species, and yeasts (123, 127, 128).

Diagnosis.

When clinical evaluation indicates the urinary tract is a source of fever, a specimen of urine should be obtained and evaluated by direct microscopy, Gram-negative stain, and quantitative culture.

The specimen should not be collected from the drainage bag because multiplication of bacteria to high levels can occur while the urine is in the bag (129). Rather, a specimen of urine should be aspirated from the catheter sampling port. Healthcare personnel should wear clean gloves whenever manipulating a urinary device and should scrupulously clean the port with 70–90% alcohol before collecting the specimen. For patients without a catheter in place, a conventional midstream clean-catch urine specimen should be obtained. Urine collected for culture should be transported to the laboratory and processed promptly to prevent the multiplication of insignificant numbers of microorganisms to high levels within the receptacle, which might lead to the misdiagnosis of infection. If the transport of urine will be delayed longer than approximately 1 hr, the specimen should be refrigerated. For transport to a remote laboratory site, the use of a urine preservative device containing boric acid is recommended (130).

In contrast to community-acquired urinary tract infections, where pyuria is highly predictive of significant bacteriuria, pyuria may be absent in patients with catheter-associated urinary tract infection and, even if present, is not reliably predictive of infection or associated with symptoms referable to the urinary tract (123).

The concentration of urinary bacteria or yeast needed to cause symptomatic urinary tract infection or fever is unclear. Whereas it is clear that counts of >103 cfu/mL represent true bacteriuria or candiduria in catheterized patients (131), there are no data to show that higher counts are more likely to represent symptomatic infection than lower ones. Gram-negative stain of a centrifuged urinary specimen, however, will show microorganisms most of the time if infection is present (132) and can provide valuable information to the clinician selecting empirical antimicrobial therapy for suspected urosepsis.

Although it is appropriate to collect urinary specimens in the investigation of fever, routine monitoring or “surveillance” cultures of urine contribute little to patient management (133). The rapid dipstick tests, which detect leukocyte esterase and nitrite, are unreliable tests in the setting of catheter-related urinary tract infection. The leukocyte esterase test correlates with significant pyuria, which may or may not be present in a catheter-related urinary tract infection. The nitrite test corresponds to Enterobacteriaceae, which convert nitrate to nitrite. In the setting of active bacteriuria caused by Enterococcus species, Candida species, and coagulase-positive Staphylococcus species, it is not reliable and is not recommended for use in patients with urinary catheters in place (134, 135).

Recommendations for Evaluation of the Urinary Tract

  1. For patients at high risk for urinary tract infection (kidney transplant patients, granulocytopenic patients, or patients with recent urologic surgery or obstruction), if clinical evaluation suggests a patient may have symptomatic urinary tract infection, a laboratory evaluation is necessary. Obtain urine for microscopic exam, Gram-negative stain, and culture (level 2).
  2. Patients who have urinary catheters in place should have urine collected from the sampling port of the catheter and not from the drainage bag (level 2).
  3. Urine should be transported to the laboratory and processed within 1 hr to avoid bacterial multiplication. If transport to the laboratory will be delayed for >1 hr, the specimen should be refrigerated. Alternatively, a preservative could be used but is less preferable to refrigeration (level 2).
  4. Cultures from catheterized patients showing >103 cfu/mL represent true bacteriuria or candiduria, but neither higher counts nor the presence of pyuria alone are of much value in determining if the catheter-associated bacteriuria or candiduria is the cause of a patient’s fever; in most cases, it is not the cause of fever (level 1).
  5. Gram stains of centrifuged urine will reliably show the infecting organisms and can aid in the selection of anti-infective therapy if catheter-associated urosepsis is suspected (level 1).
  6. Rapid dipstick tests are not recommended for patients with urinary catheters in the analysis of possible catheter-associated infection (level 1).

Sinusitis

In the ICU setting, nosocomial sinusitis is a closed-space infection that is infrequent and may be clinically occult but, when it occurs, can have serious consequences (136). Whereas sinusitis is often part of the differential diagnosis of fever, the prevalence is low in comparison with other nosocomial infections in the ICU, and the diagnosis can be difficult to document convincingly.

Etiology.

The most common risk factor for sinusitis is anatomic obstruction of the ostia draining the facial sinuses, especially the maxillary sinuses. Transnasal intubations of the stomach and especially of the trachea are the leading risk factors, with transnasal intubation of the airway carrying a prevalence of sinusitis estimated to be 33% after 7 days of intubation. Maxillofacial trauma, with obstruction of drainage by retained blood clots, is another clear risk factor. The paranasal sinuses are normally sterile, but bacterial overgrowth occurs when drainage is impeded. The etiological agents responsible for most cases of nosocomial sinusitis are those that colonize the naso-oropharynx (137–139), which occur at high frequency among hospitalized patients, and especially among critically ill patients. Gram-negative bacilli (particularly P. aeruginosa) constitute 60% of bacteria isolated from nosocomial sinusitis, whereas Gram-positive cocci (typically S. aureus and coagulase-negative staphylococci) comprise one third of isolates and fungi the remaining 5–10% (138–141). Infections are often polymicrobial.

Diagnosis of Sinusitis.

Either two major criteria (cough, purulent nasal discharge) or one major and two minor criteria (headache or earache, facial or tooth pain, fever, malodorous breath, sore throat, wheezing) suggest acute bacterial sinusitis in outpatients when these manifestations have been present for ≥7 days (142). A diagnostic challenge even among outpatients, the diagnosis of sinusitis in critically ill, intubated patients is even more difficult. Complaints of facial pain or headache may be impossible to elicit, and purulent nasal discharge is present in only 25% of proved cases of sinusitis (139).

Acute sinusitis can be suggested by plain radiographs, ultrasound, CT, or magnetic resonance imaging (143). Sinus opacification by plain radiography is sensitive but nonspecific for the diagnosis (139, 141, 144, 145). A combination of nasal endoscopy and plain radiography can increase accuracy but depends on the skill of the endoscopist (146). However, obtaining good-quality plain sinus radiographs is a practical impossibility using portable equipment in the ICU. CT scanning provides better sensitivity than plain radiography alone (147, 148).

Microbial analysis of fluid obtained by minimally invasive sinus puncture and aspiration under antiseptic conditions is definitive for the diagnosis of infectious sinusitis. In addition, tissue biopsy may need to be performed to rule out invasive fungal sinusitis in the immunocompromised patient. Although less well studied, endoscopically guided middle meatal tissue culture has been shown to be a safe alternative for septic patients who are not candidates for antral puncture, such as patients with coagulopathies (149). Sampling is mandatory because of the discordant accuracy between radiographic and microbiological testing, whereas pathogen identification and susceptibility testing permit focused, narrow-spectrum antimicrobial therapy. However, specimen collection is susceptible to contamination by bacteria colonizing the overlying mucosa if rigorous antisepsis is not practiced when obtaining the specimen.

Recommendations for Evaluation of the Sinuses

  1. If clinical evaluation suggests that sinusitis may be a cause of fever, a CT scan of the facial sinuses should be obtained (level 2).
  2. If the patient has not responded to empirical therapy, puncture and aspiration of the involved sinuses under antiseptic conditions should be performed (level 2).
  3. Aspirated fluid should be sent for Gram-negative stain and culture for aerobic and anaerobic bacteria and fungi to determine the causative pathogen and its antimicrobial susceptibility (level 1).

Postoperative Fever

Fever is a common phenomenon during the initial 48 hrs after surgery. It can be useful to remember that fever in this early postoperative period is usually noninfectious in origin (150), presuming that unusual breaks in sterile technique or pulmonary aspiration did not occur. Considerable money can be wasted in overzealous evaluation of early postoperative fever. However, once a patient is >96 hrs postoperative, fever is likely to represent infection.

A chest radiograph is not mandatory for evaluation of postoperative fever unless respiratory rate, auscultation, abnormal blood gas, or pulmonary secretions suggest a high probability of utility. Atelectasis is often considered to be a cause of postoperative fever, although this should be a diagnosis of exclusion. The clinician must be alert to the possibility that the patient could have aspirated during the perioperative period or that the patient was incubating a community-acquired process, for instance, influenza A or Legionella pneumonia, before the operation.

Urinary tract infection is common postoperatively because of the use of urinary drainage catheters (151). The duration of catheterization is the most important risk factor for the development of nosocomial cystitis or pyelonephritis. A urinalysis or culture is not mandatory to evaluate fever during the initial 2 to 3 days postoperatively unless there is reason by history or examination to suspect an infection at this site.

Fever can be related to hematoma or infection of the surgical field. Wound infection is rare in the first few days after operation, except for group A streptococcal infections and clostridial infections, which can develop 1–3 days after surgery. These causes should be suspected on the basis of inspection of the wound.

Many emergency abdominal operations are performed for control of an infection (e.g., peritonitis due to perforated diverticulitis). Even under optimal circumstances (definitive surgical source control and timely administration of appropriate broad-spectrum antibiotics), it may take ≥72 hrs for such patients to defervesce. New or persistent fever >4 days after surgery should raise a strong suspicion of persistent pathology or a new complication. Thus, it is mandatory to remove the surgical dressing to inspect the wound. Swabbing the wound for culture is rarely helpful if clinical assessment reveals no symptoms or signs suggesting infection (152). When erysipelas or myonecrosis is present, the diagnosis is often suspected by inspection alone, and such patients are usually “toxic” appearing. Muscle compression injury (either direct trauma or as a result of compartment syndrome) and tetanus are two other rare complications of traumatic wounds that may cause fever. Toxic shock may accompany infection with group A β-hemolytic streptococci or S. aureus.

Other potentially serious causes of postoperative fever include deep venous thrombosis, suppurative phlebitis, pulmonary embolism (153–156), drug-induced fever, anesthesia-induced malignant hyperthermia, acute allograft rejection, and catheter-related infection.

Recommendations for Evaluation of Fever Within 72 Hours of Surgery

  1. A chest radiograph is not mandatory during the initial 72 hrs postoperatively if fever is the only indication (level 3).
  2. A urinalysis and culture are not mandatory during the initial 72 hrs postoperatively if fever is the only indication. Urinalysis and culture should be performed for those febrile patients having indwelling bladder catheters for >72 hrs (level 3).
  3. Surgical wounds should be examined daily for infection. They should not be cultured if there is no symptom or sign suggesting infection (see below) (level 2).
  4. A high level of suspicion should be maintained for deep venous thrombosis, superficial thrombophlebitis, and pulmonary embolism, especially in patients who are sedentary, have lower limb immobility, have a malignant neoplasm, or are taking an oral contraceptive (level 2).

Surgical Site Infections

Surgical site infections alone account for approximately 25% of overall costs related to treatment of nosocomial infections. The rate of surgical site infection is approximately 3%, based on infections and operative case loads sampled from many hospitals (157, 158). This varies based on the degree of contamination of the incision, the medical comorbidity of the patient (e.g., diabetes mellitus and obesity increase the risk), whether surgery is prolonged or an emergency, and whether antimicrobial prophylaxis is administered correctly (e.g., appropriate narrow spectrum of activity, administration just before incision, and discontinuation within 24 hrs [48 hrs for cardiac surgery]), if indicated (152).

Microbiology.

In clean surgical procedures, S. aureus from the patient’s skin flora or the exogenous environment is the most common cause of surgical site infection (159, 160). However, Gram-negative bacilli may be causative for surgical site infections of clean infra-inguinal operations. For all other categories of procedures, the indigenous polymicrobial aerobic-anaerobic flora of the organ or tissue being operated on are the most common pathogens of surgical site infection. Infections of contaminated operations of perioral, perirectal, and vulvovaginal tissues yield bacteria that are similar to the normal microbial flora of the adjacent mucous membrane. Infections of areas remote from those sites are caused primarily by indigenous skin microflora, especially if no body cavity has been entered. Rarely, necrotizing incisional surgical site infection (superficial or deep) may be caused by group A Streptococcus or Clostridium species, which, if identified or suspected, carries the same diagnostic and therapeutic urgency as other manifestations of necrotizing soft-tissue infection.

Although patients commonly receive antibiotics when surgical site infection is first diagnosed, there is little or no evidence supporting this practice. Studies of subcutaneous abscesses found no benefit for antibiotic therapy when combined with drainage (161, 162). A trial of antibiotic administration for surgical site infections found no clinical benefit associated with this treatment (163). A common practice endorsed by most experts is to open all infected wounds (152).

Recommendations for Evaluation of Surgical Site Infection

  1. Examine the surgical incision at least once daily for erythema, purulence, or tenderness as part of the fever evaluation (level 2).
  2. If there is suspicion of infection, the incision should be opened and cultured (level 2).
  3. Gram-negative stain and cultures should be obtained from any expressed purulence obtained from levels within the incision consistent with a deep incisional or organ/space surgical site infection. Tissue biopsies or aspirates are preferable to swabs (level 3).
  4. Drainage from superficial surgical site infections may not require Gram-negative stain and culture because incision, drainage, and local care may be sufficient treatment and antibiotic therapy may not be required. Superficial swab cultures are likely to be contaminated with commensal skin flora and are not recommended (level 2).
  5. Standard guidelines should be used to define burn wound infection (level 3).

Central Nervous System Infection

A prospective study of fever in neurocritical care patients indicates that although fever occurs in about 25% of such patients, almost half are noninfectious in etiology (164). Hence, the intensivist needs to maintain a high index of suspicion for central nervous system infection.

Diagnostic Evaluation.

Central nervous system infection rarely causes encephalopathy without focal abnormalities on neurologic examination. However, in any febrile ICU patient, even without focal findings, infection must be considered because of the inherent limitations of the neurologic examination in critically ill patients. However, the yield of lumbar puncture in patients without immune compromise or central nervous system instrumentation who develop mental status changes in the ICU may be low (165).

Imaging studies and culture of the cerebrospinal fluid are the cardinal features of a diagnostic evaluation. Patients with focal neurologic findings suggesting disease above the foramen magnum will generally require an imaging study before a lumbar puncture. A noncontrast CT scan is adequate to exclude mass lesions or obstructive hydrocephalus, which might contraindicate a lumbar puncture. If bacterial meningitis is suspected and the lumbar puncture is delayed for any reason, including an imaging study, then appropriate empirical antibiotic therapy for meningitis due to rapidly fatal etiologies (such as S. pneumoniae) should be started after blood cultures are obtained. The usual contraindications to lumbar puncture detected by CT scanning include lateral shift of midline structures, loss of the suprachiasmatic and basilar cisterns, obliteration of the fourth ventricle, or obliteration of the superior cerebellar and quadrigeminal plate cisterns with sparing of the ambient cisterns (166). If the physical examination suggests involvement of the spinal cord, consultation with a neurologist or neurosurgeon should be obtained because of the potential for spinal cord herniation with an intra-axial mass. Whether to postpone a lumbar puncture for an imaging study in a patient who is unresponsive without focal findings is a clinical decision.

Patients with suspected brain abscesses should not undergo a lumbar puncture until the degree of cerebral edema and intracranial hypertension are determined (167). Aspiration of the suspected abscess is the diagnostic procedure of choice. The optimal timing of aspiration is currently debated; if it is delayed, empirical antibiotic therapy should be considered.

Patients with Intracranial Devices.

When a patient with an intracranial device, such as a ventriculostomy catheter or a ventriculoperitoneal shunt, becomes febrile, cerebrospinal fluid (CSF) should almost always be obtained for analysis. The site of CSF access in the patient with a ventriculostomy is straightforward. The patient with a shunt system that includes a CSF reservoir should have the reservoir aspirated; this is also the case for patients with Ommaya reservoirs. Patients in whom CSF flow to the lumbar subarachnoid space is obstructed may also need a lumbar puncture because one space may be infected while the other is sterile. In patients with ventriculostomies who develop stupor or signs of meningitis, the catheter should be removed and the tip cultured.

Tests to Be Performed on CSF.

Basic tests to be performed on CSF from patients with suspected central nervous system infection include cell counts and differential, glucose and protein concentrations, Gram-negative stain, and bacterial cultures. Whether to perform cryptococcal antigen testing, fungal staining and cultures, acid-fast bacillus smears and cultures, cytologic examination for neoplasia, polymerase chain reaction tests, or a serologic test for syphilis depends on the clinical situation. The immunocompromised patient may require additional tests such as polymerase chain reaction for herpes simplex virus, CMV, Epstein-Barr virus, human herpes virus-6, JC virus, West Nile virus, adenovirus, and enterovirus. The precise combination of tests with the greatest likelihood of detecting bacterial infection depends on the patient population. The normal protein content of CSF varies with the site from which it was withdrawn; ventricular fluid usually has an upper protein content limit of 15 mg/dL, cisternal fluid of 20 mg/dL, and lumbar fluid of 45 mg/dL.

Patients with bacterial meningitis typically have a CSF glucose of <35 mg/dL, a CSF-blood glucose ratio of <0.23, a CSF protein level concentration of >220 mg/dL, >2,000 total white blood cells/μL, or >1,180 neutrophils/μL (168). Conversely, in immunologically normal hosts, the presence of a normal opening pressure, <5 white blood cells/μL, and a normal CSF protein concentration essentially exclude meningitis (169). The applicability of these findings to the critically ill immunocompromised patient is uncertain, and a high index of suspicion for infection should be maintained, regardless of cell count and glucose concentration, until cultures are final. CSF lactate measurements may be useful in neurosurgical patients to distinguish infection from postoperative aseptic meningitis (170, 171).

Recommendations for Evaluation of Central Nervous System Infections

  1. If altered consciousness or focal neurologic signs are unexplained, lumbar puncture should be considered in any patient with a new fever, unless there is a contraindication to lumbar puncture (level 3).
  2. For a patient with a new fever and new focal neurologic findings suggesting disease above the foramen magnum, an imaging study is usually required before lumbar puncture. If a mass is present, neurology/neurosurgery consultation is required to determine the optimal diagnostic approach (level 2).
  3. In febrile patients with an intracranial device, CSF should be obtained for analysis from the CSF reservoir. If CSF flow to the subarachnoid space is obstructed, it may be prudent to also obtain CSF from the lumbar space (level 3).
  4. In patients with ventriculostomies who develop stupor or signs of meningitis, the catheter should be removed and the tip cultured (level 3).
  5. CSF should be evaluated by Gram-negative stain and culture, glucose, protein, and cell count with differential. Additional tests for tuberculosis, viral and fungal disease, neoplasia, etc., should be performed as dictated by the clinical situation (level 2).

Other Considerations

Mononucleosis syndrome after blood transfusion has been broadly recognized as a cause of hectic fever in postsurgical patients for more than four decades. Infection may be caused by transmission of CMV by way of transfused white blood cells in the blood product or from reactivation of CMV by transfusion-induced antigenic stimulation (172). The spectrum of disease related to posttransfusion CMV ranges from asymptomatic conversion to a self-limited mononucleosis syndrome. In symptomatic patients, symptoms usually begin 1 month after transfusion. The classic features of mononucleosis are usually absent. Rather, patients develop high fever, which often leads to empirical antimicrobial therapy for sepsis. This syndrome should be suspected when patients with spiking fevers do not respond to antimicrobial therapy or when cultures for bacterial pathogens are negative. Immunocompetent patients with this syndrome lack clinical toxicity, despite daily fever as high as 40°C. The presence of pancytopenia with atypical lymphocytosis and mild elevations of liver function tests may also be clues to this entity (173, 174). In contrast, immunocompromised patients can develop serious consequences, including fatal disseminated disease or diffuse interstitial pneumonia, especially in the setting of primary infection (seronegative patient transfused with seropositive blood). In general, transplant services attempt to administer screened, filtered, or leukocyte-reduced blood components to this group of seriously ill patients to prevent CMV disease. This has substantially reduced but not completely eliminated the risk of this infection. Diagnosis can be made by using quantitative molecular nucleic acid amplification tests to measure serum viral load.

Silent sources of infection, including but not limited to otitis media, decubitus ulcers at the sacrum or the back or the head, perineal or perianal abscesses, and undetected retained tampons need to be carefully ruled out. The recognition and identification of these other less common infectious causes of fever require a careful history and physical examination, including the examination of all devices, drains, and hardware on a daily basis.

Use of Adjunctive Markers for the Evaluation of Fever.

Several biomarkers have been investigated for their utility in rapidly discriminating true infection from other inflammatory processes causing fever. Several generations of serum procalcitonin assays with variable cutoff points have been examined (175–180). A more sensitive serum procalcitonin assay is now approved for the early detection of bacterial infections and sepsis in patients during the first day of ICU admission. Procalcitonin level elevations of >0.5 ng/mL occur within 2–3 hrs of onset, with higher levels observed along the continuum from systemic inflammatory response syndrome (0.6–2.0 ng/mL), severe sepsis (2–10 ng/mL), and septic shock (>10 ng/mL). Most importantly, viral infections, recent surgery, and chronic inflammatory states are not associated with an increment in procalcitonin levels.

Traditional endotoxin detection systems, such as the chromogenic limulus lysate assay, have been hampered by contamination concerns, cumbersome techniques, and variable sensitivity, with inconsistent correlation to the presence of true Gram-negative infection (181, 182). However, kinetic luminometric anti-assay (endotoxin activity assay) uses an antibody to the conserved lipid A component of endotoxin to form an antibody-antigen complex capable of stimulating a detectable host neutrophil respiratory burst in an ex vivo assay (183). In a multicenter ICU study, the endotoxin activity assay demonstrated a high negative predictive value (98.6%) for Gram-negative infection (184).

Tumor necrosis factor-α, interleukin-6, C-reactive protein, and triggering receptor expressed on myeloid cells-1 (TREM-1) have been tested as methods to discriminate true infection from other inflammatory states but have not yet been validated.

Recommendation for Using Biomarkers to Determine the Cause of Fever

  1. Serum procalcitonin levels and endotoxin activity assay can be employed as an adjunctive diagnostic tool for discriminating infection as the cause for fever or sepsis presentations (level 2).

Noninfectious Causes of Fever in the ICU

Drug-Related Fever.

Any drug can cause fever due to hypersensitivity (185–187). Hypersensitivity reactions may manifest as fever alone to life-threatening hypersensitivity, such as those that have been associated with abacavir and nevirapine. In addition, some drugs cause fever by producing local inflammation at the site of administration (phlebitis, sterile abscesses, or soft-tissue reaction): amphotericin B, erythromycin, potassium chloride, sulfonamides, and cytotoxic chemotherapies are prime examples. Drugs or their delivery systems (diluent, intravenous fluid, or intravascular delivery devices) may also contain pyrogens or, rarely, microbial contaminants (188). Some drugs may also stimulate heat production (e.g., thyroxine), limit heat dissipation (e.g., atropine or epinephrine), or alter thermoregulation (e.g., butyrophenone tranquilizers, phenothiazines, antihistamines, or antiparkinson drugs).

Among drug categories, fever is most often attributed to antimicrobials (especially β-lactam drugs), anti-epileptic drugs (especially phenytoin), antiarrhythmics (especially quinidine and procainamide), and antihypertensives (methyldopa). There is nothing characteristic about the fevers induced by these drugs (186). Fevers do not invariably occur immediately after drug administration: it may be days after administration that fever occurs and many more days before the fever abates. In one series, the lag time between initiating a drug and fever was a mean of 21 days (median, 8). Fever often took 1 to 3 days to return to normal but can take >7 days to return to normal after removing the offending agent (189). Rash occurs in a small fraction of cases. Eosinophilia is also uncommon.

The diagnosis of drug-induced fever is usually established by temporal relationship of the fever to starting and stopping the drug. Patients can be rechallenged with the drug to confirm the diagnosis, but this is rarely done unless the drug in question is essential and alternatives are not available. Patients who had anaphylaxis or toxic epidermal necrolysis as a result of drug exposure should not be rechallenged.

Two important syndromes, malignant hyperthermia and neuroleptic malignant syndrome, deserve consideration when fever is especially high because the results can be devastating if left untreated (190, 191). Malignant hyperthermia is more often identified in the operating room than in the ICU, but onset can be delayed for as long as 24 hrs, especially if the patient is on steroids. It can be caused by succinylcholine and the inhalation anesthetics, of which halothane is the most frequently identified. This hyperthermic syndrome is believed to be a genetically determined response mediated by a dysregulation of cytoplasmic calcium control in skeletal muscle. The result of this calcium dysregulation is intense muscle contraction, generating fever and increasing creatinine phosphokinase concentrations.

The neuroleptic malignant syndrome is rare but more often identified in the ICU than malignant hyperthermia. It has been strongly associated with antipsychotic neuroleptic medications—phenothiazines, thioxanthenes, and butyrophenones (190, 192). In the ICU, haloperidol is perhaps the most frequently reported drug. It manifests as muscle rigidity, generating fever and increasing creatinine phosphokinase concentrations. However, unlike malignant hyperthermia, the initiator of muscle contraction is central.

The serotonin syndrome may be confused with neuroleptic malignant syndrome, but it is a distinct entity (193). The mechanism is related to excessive stimulation of the 5-HT1A–receptor and is increasingly seen with the popularity of serotonin reuptake inhibitors in the treatment of various psychiatric disorders. The serotonin syndrome may be exacerbated with concomitant use of linezolid (194).

Importantly, withdrawal of certain drugs may be associated with fever, often with associated tachycardia, diaphoresis, and hyperreflexia. Alcohol, opiates (including methadone), barbiturates, and benzodiazepines have all been associated with this febrile syndrome. It is important to recognize that a history of use of these drugs may not be available when the patient is admitted to the ICU. Withdrawal and related fever may therefore occur several hours or days after admission. Fever related to other therapies and inflammatory states are listed in Table 5.

Table 5
Table 5:
Fever related to other therapies and noninfectious inflammatory states

Recommendations for Recognizing Noninfectious Causes of Fever

  1. Consider all new medications and blood products the patient has received. Ideally, if the suspected drug can be stopped, do so. If the drug cannot be stopped, consider a comparable substitute (level 2).
  2. Fever induced by drugs may take several days to resolve. Establishing a temporal relationship between fever and the offending agent may be helpful in establishing the diagnosis (level 3).

Considerations for Empiric Therapy During Diagnostics

Initiation of therapy may be necessary for unstable or high-risk patients while the diagnostic evaluation is ongoing, and certainly before the results of cultures are available. Usually, this entails antimicrobial therapy, but treatment may also have to be considered for noninfectious causes of fever as well.

If an infectious cause of fever is suspected, empirical antimicrobial therapy may be urgent. Delay of effective antimicrobial therapy has been associated with increased mortality from infection and sepsis (195–201). Antibiotic therapy should begin within 1 hr after the diagnosis of sepsis is considered (202). The choice of regimen depends on the suspected infectious etiology, whether the infection is community-, healthcare-, or hospital-onset, and whether the patient is immunocompromised. If drug-resistant pathogens are suspected, initial broad-spectrum empirical antimicrobial therapy directed against both resistant Gram-positive cocci (including methicillin-resistant S. aureus) and Gram-negative bacilli is indicated. This may require several agents to ensure that resistant pathogens are covered. In addition, empirical antifungal coverage may be appropriate in selected patients.

Recommendations for Empiric Therapy of Fever

  1. When clinical evaluation suggests that infection is the cause of fever, consideration should be given to administering empirical antimicrobial therapy as soon as possible after cultures are obtained, especially if the patient is seriously ill or deteriorating (level 1).
  2. Initial empirical antibiotic therapy should be directed against likely pathogens, as suggested by the suspected source of infection, the patient risk for infection by multidrug-resistant pathogens, and local knowledge of antimicrobial susceptibility patterns (level 1).

REFERENCES

Letters after the reference numbers indicate Society of Critical Care Medicine’s rating system (see Table 1).

1c. O’Grady NP, Barie PS, Bartlett JG, et al: Practice guidelines for evaluating new fever in critically ill adult patients: Task Force of the Society of Critical Care Medicine and the Infectious Diseases Society of America. Clin Infect Dis 1998; 26:1042–1059
2b. Arbo MJ, Fine MJ, Hanusa BH, et al: Fever of nosocomial origin: Etiology, risk factors, and outcomes. Am J Med 1993; 95:505–512
3d. Bone RC, Balk RA, Cerra FB, et al: Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis: The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine. Chest 1992; 101:1644–1655
4c. Hughes WT, Armstrong D, Bodey GP, et al: 2002 guidelines for the use of antimicrobial agents in neutropenic patients with cancer. Clin Infect Dis 2002; 34:730–751
5c. Mackowiak PA, Wasserman SS, Levine MM: A critical appraisal of 98.6 degrees F, the upper limit of the normal body temperature, and other legacies of Carl Reinhold August Wunderlich. JAMA 1992; 268:1578–1580
6c. Dinarello CA, Cannon JG, Wolff SM: New concepts on the pathogenesis of fever. Rev Infect Dis 1988; 10:168–189
7b. Waterhouse J, Edwards B, Bedford P, et al: Thermoregulation during mild exercise at different circadian times. Chronobiol Int 2004; 21:253–275
8c. Insler SR, Sessler DI: Perioperative thermoregulation and temperature monitoring. Anesthesiol Clin 2006; 24:823–837
9d. van der Sande FM, Kooman JP, Leunissen KM: Haemodialysis and thermoregulation. Nephrol Dial Transplant 2006; 21:1450–1451
10b. van der Sande FM, Rosales LM, Brener Z, et al: Effect of ultrafiltration on thermal variables, skin temperature, skin blood flow, and energy expenditure during ultrapure hemodialysis. J Am Soc Nephrol 2005; 16:1824–1831
11c. Le Blanc L, Lesur O, Valiquette L, et al: Role of routine blood cultures in detecting unapparent infections during continuous renal replacement therapy. Intensive Care Med 2006; 32:1802–1807
12b. Erickson RS, Kirklin SK: Comparison of ear-based, bladder, oral, and axillary methods for core temperature measurement. Crit Care Med 1993; 21:1528–1534
13b. Erickson RS, Meyer LT: Accuracy of infrared ear thermometry and other temperature methods in adults. Am J Crit Care 1994; 3:40–54
14b. Schmitz T, Bair N, Falk M, et al: A comparison of five methods of temperature measurement in febrile intensive care patients. Am J Crit Care 1995; 4:286–292
15b. Milewski A, Ferguson KL, Terndrup TE: Comparison of pulmonary artery, rectal, and tympanic membrane temperatures in adult intensive care unit patients. Clin Pediatr (Phila) 1991; 30(4 Suppl):13–16
16b. Nierman DM: Core temperature measurement in the intensive care unit. Crit Care Med 1991; 19:818–823
17b. Fallis WM: The effect of urine flow rate on urinary bladder temperature in critically ill adults. Heart Lung 2005; 34:209–216
18b. Moran JL, Peter JV, Solomon PJ, et al: Tympanic temperature measurements: Are they reliable in the critically ill? A clinical study of measures of agreement. Crit Care Med 2007; 35:155–164
19b. Lefrant JY, Muller L, de La Coussaye JE, et al: Temperature measurement in intensive care patients: Comparison of urinary bladder, oesophageal, rectal, axillary, and inguinal methods versus pulmonary artery core method. Intensive Care Med 2003; 29:414–418
20b. Eichna LW, Berger AR, Rader B, et al: Comparison of intracardiac and intravascular temperatures with rectal temperatures in man. J Clin Invest 1951; 30:353–359
21b. Ilsley AH, Rutten AJ, Runciman WB: An evaluation of body temperature measurement. Anaesth Intensive Care 1983; 11:31–39
22b. Brooks S, Khan A, Stoica D, et al: Reduction in vancomycin-resistant Enterococcus and Clostridium difficile infections following change to tympanic thermometers. Infect Control Hosp Epidemiol 1998; 19:333–336
23b. Livornese LL Jr, Dias S, Samel C, et al: Hospital-acquired infection with vancomycin-resistant Enterococcus faecium transmitted by electronic thermometers. Ann Intern Med 1992; 117:112–116
24d. Gerding DN, Johnson S, Peterson LR, et al: Clostridium difficile–associated diarrhea and colitis. Infect Control Hosp Epidemiol 1995; 16:459–477
25b. Cranston WI, Gerbrandy J, Snell ES: Oral, rectal and oesophageal temperatures and some factors affecting them in man. J Physiol 1954; 126:347–358
26b. Farnell S, Maxwell L, Tan S, et al: Temperature measurement: Comparison of non-invasive methods used in adult critical care. J Clin Nurs 2005; 14:632–639
27b. Hebbar K, Fortenberry JD, Rogers K, et al: Comparison of temporal artery thermometer to standard temperature measurements in pediatric intensive care unit patients. Pediatr Crit Care Med 2005; 6:557–561
28b. Harioka T, Matsukawa T, Ozaki M, et al: “Deep-forehead” temperature correlates well with blood temperature. Can J Anaesth 2000; 47:980–983
29b. Kistemaker JA, Den Hartog EA, Daanen HA: Reliability of an infrared forehead skin thermometer for core temperature measurements. J Med Eng Technol 2006; 30:252–261
30b. Potter P, Schallom M, Davis S, et al: Evaluation of chemical dot thermometers for measuring body temperature of orally intubated patients. Am J Crit Care 2003; 12:403–407
31a. Strand CL, Wajsbort RR, Sturmann K: Effect of iodophor vs iodine tincture skin preparation on blood culture contamination rate. JAMA 1993; 269:1004–1006
32b. Weinstein MP, Reller LB, Murphy JR, et al: The clinical significance of positive blood cultures: A comprehensive analysis of 500 episodes of bacteremia and fungemia in adults. I. Laboratory and epidemiologic observations. Rev Infect Dis 1983; 5:35–53
33b. Trautner BW, Clarridge JE, Darouiche RO: Skin antisepsis kits containing alcohol and chlorhexidine gluconate or tincture of iodine are associated with low rates of blood culture contamination. Infect Control Hosp Epidemiol 2002; 23:397–401
34b. Barenfanger J, Drake C, Lawhorn J, et al: Comparison of chlorhexidine and tincture of iodine for skin antisepsis in preparation for blood sample collection. J Clin Microbiol 2004; 42:2216–2217
35a. Little JR, Murray PR, Traynor PS, et al: A randomized trial of povidone-iodine compared with iodine tincture for venipuncture site disinfection: Effects on rates of blood culture contamination. Am J Med 1999; 107:119–125
36a. Mimoz O, Karim A, Mercat A, et al: Chlorhexidine compared with povidone-iodine as skin preparation before blood culture: A randomized, controlled trial. Ann Intern Med 1999; 131:834–837
37d. Clinical and Laboratory Standards Institute: Principles and procedures for blood cultures: Proposed Guideline. Wayne, PA, Clinical and Laboratory Standards Institute, CLSI Document M47-P 2006
38b. Leisure MK, Moore DM, Schwartzman JD, et al: Changing the needle when inoculating blood cultures: A no-benefit and high-risk procedure. JAMA 1990; 264:2111–2112
39b. Cockerill FR III, Wilson JW, Vetter EA, et al: Optimal testing parameters for blood cultures. Clin Infect Dis 2004; 38:1724–1730
40b. Tenney JH, Reller LB, Mirrett S, et al: Controlled evaluation of the volume of blood cultured in detection of bacteremia and fungemia. J Clin Microbiol 1982; 15:558–561
41b. Salventi JF, Davies TA, Randall EL, et al: Effect of blood dilution on recovery of organisms from clinical blood cultures in medium containing sodium polyanethol sulfonate. J Clin Microbiol 1979; 9:248–252
42b. Mermel LA, Maki DG: Detection of bacteremia in adults: Consequences of culturing an inadequate volume of blood. Ann Intern Med 1993; 119:270–272
43b. Ilstrup DM, Washington JA Jr: The importance of volume of blood cultured in the detection of bacteremia and fungemia. Diagn Microbiol Infect Dis 1983; 1:107–110
44b. Hall MM, Ilstrup DM, Washington JA Jr. Effect of volume of blood cultured on detection of bacteremia. J Clin Microbiol 1976; 3:643–645
45b. Mirrett S, Everts RJ, Reller LB: Controlled comparison of original vented aerobic fan medium with new nonvented BacT/ALERT FA medium for culturing blood. J Clin Microbiol 2001; 39:2098–2101
46b. Jorgensen JH, Mirrett S, McDonald LC, et al: Controlled clinical laboratory comparison of BACTEC plus aerobic/F resin medium with BacT/Alert aerobic FAN medium for detection of bacteremia and fungemia. J Clin Microbiol 1997; 35:53–58
47b. Weinstein MP, Mirrett S, Reimer LG, et al: Controlled evaluation of BacT/Alert standard aerobic and FAN aerobic blood culture bottles for detection of bacteremia and fungemia. J Clin Microbiol 1995; 33:978–981
48b. Lee A, Mirrett S, Reller LB, et al: Detection of bloodstream infections in adults: How many blood cultures are needed? J Clin Microbiol 2007; 45:3546–3548
49b. Hudson-Civetta JA, Civetta JM, Martinez OV, et al: Risk and detection of pulmonary artery catheter-related infection in septic surgical patients. Crit Care Med 1987; 15:29–34
50b. Bates DW, Goldman L, Lee TH: Contaminant blood cultures and resource utilization: The true consequences of false-positive results. JAMA 1991; 265:365–369
51b. Wormser GP, Onorato IM, Preminger TJ, et al: Sensitivity and specificity of blood cultures obtained through intravascular catheters. Crit Care Med 1990; 18:152–156
52b. Tokars JI: Predictive value of blood cultures positive for coagulase-negative staphylococci: Implications for patient care and health care quality assurance. Clin Infect Dis 2004; 39:333–341
53b. Bryant JK, Strand CL: Reliability of blood cultures collected from intravascular catheter versus venipuncture. Am J Clin Pathol 1987; 88:113–116
54c. Washington JA Jr, Ilstrup DM: Blood cultures: Issues and controversies. Rev Infect Dis 1986; 8:792–802
55c. Weinstein MP: Current blood culture methods and systems: Clinical concepts, technology, and interpretation of results. Clin Infect Dis 1996; 23:40–46
56b. Li J, Plorde JJ, Carlson LG: Effects of volume and periodicity on blood cultures. J Clin Microbiol 1994; 32:2829–2831
57c. Maki DG, Kluger DM, Crnich CJ: The risk of bloodstream infection in adults with different intravascular devices: A systematic review of 200 published prospective studies. Mayo Clin Proc 2006; 81:1159–1171
58d. Crnich CJ: Infections caused by intravascular devices: Epidemiology, pathogenesis, diagnosis, prevention, and treatment. In: APIC Text of Infection Control and Epidemiology. Second Edition. Carrico R (Ed). Washington, DC, Association for Professionals in Infection Control and Epidemiology, 2005, pp 24.1–24.6
59a. Leon C, Alvarez-Lerma F, Ruiz-Santana S, et al: Antiseptic chamber-containing hub reduces central venous catheter-related infection: A prospective, randomized study. Crit Care Med 2003; 31:1318–1324
60b. Mermel LA, McCormick RD, Springman SR, et al: The pathogenesis and epidemiology of catheter-related infection with pulmonary artery Swan-Ganz catheters: A prospective study utilizing molecular subtyping. Am J Med 1991; 91(3B):197S–205S
61b. Safdar N, Maki DG: Inflammation at the insertion site is not predictive of catheter-related bloodstream infection with short-term, noncuffed central venous catheters. Crit Care Med 2002; 30:2632–2635
62b. Blot F, Nitenberg G, Chachaty E, et al: Diagnosis of catheter-related bacteraemia: A prospective comparison of the time to positivity of hub-blood versus peripheral-blood cultures. Lancet 1999; 354:1071–1077
63b. DesJardin JA, Falagas ME, Ruthazer R, et al: Clinical utility of blood cultures drawn from indwelling central venous catheters in hospitalized patients with cancer. Ann Intern Med 1999; 131:641–647
64b. Maki DG, Weise CE, Sarafin HW: A semiquantitative culture method for identifying intravenous-catheter-related infection. N Engl J Med 1977; 296:1305–1309
65b. Safdar N, Fine JP, Maki DG: Meta-analysis: Methods for diagnosing intravascular device-related bloodstream infection. Ann Intern Med 2005; 142:451–466
66b. Cooper GL, Hopkins CC: Rapid diagnosis of intravascular catheter-associated infection by direct Gram staining of catheter segments. N Engl J Med 1985; 312:1142–1147
67b. Zufferey J, Rime B, Francioli P, et al: Simple method for rapid diagnosis of catheter-associated infection by direct acridine orange staining of catheter tips. J Clin Microbiol 1988; 26:175–177
68c. Mermel LA, Farr BM, Sherertz RJ, et al: Guidelines for the management of intravascular catheter-related infections. Clin Infect Dis 2001; 32:1249–1272
69c. Tacconelli E, Tumbarello M, Pittiruti M, et al: Central venous catheter-related sepsis in a cohort of 366 hospitalised patients. Eur J Clin Microbiol Infect Dis 1997; 16:203–209
70c. Raad II, Baba M, Bodey GP: Diagnosis of catheter-related infections: The role of surveillance and targeted quantitative skin cultures. Clin Infect Dis 1995; 20:593–597
71b. Catton JA, Dobbins BM, Kite P, et al: In situ diagnosis of intravascular catheter-related bloodstream infection: A comparison of quantitative culture, differential time to positivity, and endoluminal brushing. Crit Care Med 2005; 33:787–791
72c. Mayhall CG: Diagnosis and management of infections of implantable devices used for prolonged venous access. Curr Clin Top Infect Dis 1992; 12:83–110
73c. Kaufman J, Demas C, Stark K, et al: Catheter-related septic central venous thrombosis: Current therapeutic options. West J Med 1986; 145:200–203
74c. Strinden WD, Helgerson RB, Maki DG: Candida septic thrombosis of the great central veins associated with central catheters: Clinical features and management. Ann Surg 1985; 202:653–658
75c. Verghese A, Widrich WC, Arbeit RD: Central venous septic thrombophlebitis: The role of medical therapy. Medicine (Baltimore) 1985; 64:394–400
76b. Rello J, Ollendorf DA, Oster G, et al: Epidemiology and outcomes of ventilator-associated pneumonia in a large US database. Chest 2002; 122:2115–2121
77c. Chastre J, Fagon JY: Ventilator-associated pneumonia. Am J Respir Crit Care Med 2002; 165:867–903
78b. Sawyer RG, Crabtree TD, Gleason TG, et al: Impact of solid organ transplantation and immunosuppression on fever, leukocytosis, and physiologic response during bacterial and fungal infections. Clin Transplant 1999; 13:260–265
79b. Pelletier SJ, Crabtree TD, Gleason TG, et al: Characteristics of infectious complications associated with mortality after solid organ transplantation. Clin Transplant 2000; 14(4 Pt 2):401–408
80b. Combes A, Figliolini C, Trouillet JL, et al: Factors predicting ventilator-associated pneumonia recurrence. Crit Care Med 2003; 31:1102–1107
81c. Winer-Muram HT, Rubin SA, Ellis JV, et al: Pneumonia and ARDS in patients receiving mechanical ventilation: Diagnostic accuracy of chest radiography. Radiology 1993; 188:479–485
82c. Wunderink RG, Woldenberg LS, Zeiss J, et al: The radiologic diagnosis of autopsy-proven ventilator-associated pneumonia. Chest 1992; 101:458–463
83c. Barkhausen J, Stoblen F, Dominguez-Fernandez E, et al: Impact of CT in patients with sepsis of unknown origin. Acta Radiol 1999; 40:552–555
84c. Miller WT Jr, Tino G, Friedburg JS: Thoracic CT in the intensive care unit: Assessment of clinical usefulness. Radiology 1998; 209:491–498
85c. Winer-Muram HT, Steiner RM, Gurney JW, et al: Ventilator-associated pneumonia in patients with adult respiratory distress syndrome: CT evaluation. Radiology 1998; 208:193–199
86c. Franquet T: High-resolution computed tomography (HRCT) of lung infections in non-AIDS immunocompromised patients. Eur Radiol 2006; 16:707–718
87c. Hiorns MP, Screaton NJ, Muller NL: Acute lung disease in the immunocompromised host. Radiol Clin North Am 2001; 39:1137–1151
88c. Guidelines for the management of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia. Am J Respir Crit Care Med 2005; 171:388–416
89c. Bartlett JG, Alexander J, Mayhew J, et al: Should fiberoptic bronchoscopy aspirates be cultured? Am Rev Respir Dis 1976; 114:73–78
90c. Jain P, Sandur S, Meli Y, et al: Role of flexible bronchoscopy in immunocompromised patients with lung infiltrates. Chest 2004; 125:712–722
91c. Campbell GD Jr: Blinded invasive diagnostic procedures in ventilator-associated pneumonia. Chest 2000; 117(4 Suppl 2):207S–211S
92c. Peikert T, Rana S, Edell ES: Safety, diagnostic yield, and therapeutic implications of flexible bronchoscopy in patients with febrile neutropenia and pulmonary infiltrates. Mayo Clin Proc 2005; 80:1414–1420
93c. Rello J, Esandi ME, Diaz E, et al: The role of Candida sp isolated from bronchoscopic samples in nonneutropenic patients. Chest 1998; 114:146–149
94b. Rishmawi N, Ghneim R, Kattan R, et al: Survival of fastidious and nonfastidious aerobic bacteria in three bacterial transport swab systems. J Clin Microbiol 2007; 45:1278–1283
95b. el-Ebiary M, Torres A, Fabregas N, et al: Significance of the isolation of Candida species from respiratory samples in critically ill, non-neutropenic patients: An immediate postmortem histologic study. Am J Respir Crit Care Med 1997; 156(2 Pt 1):583–590
96b. Barenfanger J, Arakere P, Cruz RD, et al: Improved outcomes associated with limiting identification of Candida spp. in respiratory secretions. J Clin Microbiol 2003; 41:5645–5649
97a. Heyland D, Dodek P, Muscedere J, et al: A randomized trial of diagnostic techniques for ventilator-associated pneumonia. N Engl J Med 2006; 355:2619–2630
98b. Souweine B, Veber B, Bedos JP, et al: Diagnostic accuracy of protected specimen brush and bronchoalveolar lavage in nosocomial pneumonia: Impact of previous antimicrobial treatments. Crit Care Med 1998; 26:236–244
99b. Fagon JY, Chastre J, Hance AJ, et al: Detection of nosocomial lung infection in ventilated patients: Use of a protected specimen brush and quantitative culture techniques in 147 patients. Am Rev Respir Dis 1988; 138:110–116
100c. Niederman MS, Torres A, Summer W: Invasive diagnostic testing is not needed routinely to manage suspected ventilator-associated pneumonia. Am J Respir Crit Care Med 1994; 150:565–569
101b. Pugin J, Auckenthaler R, Mili N, et al: Diagnosis of ventilator-associated pneumonia by bacteriologic analysis of bronchoscopic and nonbronchoscopic “blind” bronchoalveolar lavage fluid. Am Rev Respir Dis 1991; 143(5 Pt 1):1121–1129
102b. Lipscomb DJ, Flower CD, Hadfield JW: Ultrasound of the pleura: An assessment of its clinical value. Clin Radiol 1981; 32:289–290
103a. Grogan DR, Irwin RS, Channick R, et al: Complications associated with thoracentesis: A prospective, randomized study comparing three different methods. Arch Intern Med 1990; 150:873–877
104c. Fekety R: Guidelines for the diagnosis and management of Clostridium difficile– associated diarrhea and colitis: American College of Gastroenterology, Practice Parameters Committee. Am J Gastroenterol 1997; 92:739–750
105d. DeMaio J, Bartlett JG: Update on diagnosis of Clostridium difficile–associated diarrhea. Curr Clin Top Infect Dis 1995; 15:97–114
106c. Bartlett JG: Clostridium difficile: History of its role as an enteric pathogen and the current state of knowledge about the organism. Clin Infect Dis 1994; 18(Suppl 4):S265–S272
107c. Fekety R, Shah AB: Diagnosis and treatment of Clostridium difficile colitis. JAMA 1993; 269:71–75
108b. Pepin J, Saheb N, Coulombe MA, et al: Emergence of fluoroquinolones as the predominant risk factor for Clostridium difficile–associated diarrhea: A cohort study during an epidemic in Quebec. Clin Infect Dis 2005; 41:1254–1260
109b. Pepin J, Valiquette L, Alary ME, et al: Clostridium difficile–associated diarrhea in a region of Quebec from 1991 to 2003: A changing pattern of disease severity. CMAJ 2004; 171:466–472
110c. Bartlett JG: Narrative review: The new epidemic of Clostridium difficile–associated enteric disease. Ann Intern Med 2006; 145:758–764
111c. Borek AP, Aird DZ, Carroll KC: Frequency of sample submission for optimal utilization of the cell culture cytotoxicity assay for detection of Clostridium difficile toxin. J Clin Microbiol 2005; 43:2994–2995
112b. Manabe YC, Vinetz JM, Moore RD, et al: Clostridium difficile colitis: An efficient clinical approach to diagnosis. Ann Intern Med 1995; 123:835–840
113c. Johnson S, Kent SA, O’Leary KJ, et al: Fatal pseudomembranous colitis associated with a variant Clostridium difficile strain not detected by toxin A immunoassay. Ann Intern Med 2001; 135:434–438
114b. Zheng L, Keller SF, Lyerly DM, et al: Multicenter evaluation of a new screening test that detects Clostridium difficile in fecal specimens. J Clin Microbiol 2004; 42:3837–3840
115c. Ticehurst JR, Aird DZ, Dam LM, et al: Effective detection of toxigenic Clostridium difficile by a two-step algorithm including tests for antigen and cytotoxin. J Clin Microbiol 2006; 44:1145–1149
116b. Walker RC, Ruane PJ, Rosenblatt JE, et al: Comparison of culture, cytotoxicity assays, and enzyme-linked immunosorbent assay for toxin A and toxin B in the diagnosis of Clostridium difficile–related enteric disease. Diagn Microbiol Infect Dis 1986; 5:61–69
117c. Loo VG, Poirier L, Miller MA, et al: A predominantly clonal multi-institutional outbreak of Clostridium difficile–associated diarrhea with high morbidity and mortality. N Engl J Med 2005; 353:2442–2449
118c. McDonald LC, Killgore GE, Thompson A, et al: An epidemic, toxin gene-variant strain of Clostridium difficile. N Engl J Med 2005; 353:2433–2441
119c. Warny M, Pepin J, Fang A, et al: Toxin production by an emerging strain of Clostridium difficile associated with outbreaks of severe disease in North America and Europe. Lancet 2005; 366:1079–1084
120b. Tedesco FJ, Corless JK, Brownstein RE: Rectal sparing in antibiotic-associated pseudomembranous colitis: A prospective study. Gastroenterology 1982; 83:1259–1260
121b. Talbot RW, Walker RC, Beart RW Jr: Changing epidemiology, diagnosis, and treatment of Clostridium difficile toxin–associated colitis. Br J Surg 1986; 73:457–460
122c. Hogenauer C, Langner C, Beubler E, et al: Klebsiella oxytoca as a causative organism of antibiotic-associated hemorrhagic colitis. N Engl J Med 2006; 355:2418–2426
123c. Tambyah PA, Maki DG: Catheter-associated urinary tract infection is rarely symptomatic: A prospective study of 1,497 catheterized patients. Arch Intern Med 2000; 160:678–682
124b. Safdar N, Slattery WR, Knasinski V, et al: Predictors and outcomes of candiduria in renal transplant recipients. Clin Infect Dis 2005; 40:1413–1421
125c. Bryan CS, Reynolds KL: Hospital-acquired bacteremic urinary tract infection: Epidemiology and outcome. J Urol 1984; 132:494–498
126c. Quintiliani R, Klimek J, Cunha BA, et al: Bacteraemia after manipulation of the urinary tract: The importance of pre-existing urinary tract disease and compromised host defences. Postgrad Med J 1978; 54:668–671
127b. Laupland KB, Zygun DA, Davies HD, et al: Incidence and risk factors for acquiring nosocomial urinary tract infection in the critically ill. J Crit Care 2002; 17:50–57
128b. Laupland KB, Bagshaw SM, Gregson DB, et al: Intensive care unit-acquired urinary tract infections in a regional critical care system. Crit Care 2005; 9:R60–R65
129b. Shah PS, Cannon JP, Sullivan CL, et al: Controlling antimicrobial use and decreasing microbiological laboratory tests for urinary tract infections in spinal-cord-injury patients with chronic indwelling catheters. Am J Health Syst Pharm 2005; 62:74–77
130d. Thongboonkerd V, Saetun P: Bacterial overgrowth affects urinary proteome analysis: Recommendation for centrifugation, temperature, duration, and the use of preservatives during sample collection. J Proteome Res 2007; 6:4173–4181
131c. Stark RP, Maki DG: Bacteriuria in the catheterized patient: What quantitative level of bacteriuria is relevant? N Engl J Med 1984; 311:560–564
132c. Cornia PB, Takahashi TA, Lipsky BA: The microbiology of bacteriuria in men: A 5-year study at a Veterans’ Affairs hospital. Diagn Microbiol Infect Dis 2006; 56:25–30
133c. Warren JW, Muncie HL Jr, Bergquist EJ, et al: Sequelae and management of urinary infection in the patient requiring chronic catheterization. J Urol 1981; 125:1–8
134b. Schwartz DS, Barone JE: Correlation of urinalysis and dipstick results with catheter-associated urinary tract infections in surgical ICU patients. Intensive Care Med 2006; 32:1797–1801
135b. Schiotz HA: The value of leucocyte stix results in predicting bacteriuria and urinary tract infection after gynaecological surgery. J Obstet Gynaecol 1999; 19:396–398
136c. Stein M, Caplan ES: Nosocomial sinusitis: A unique subset of sinusitis. Curr Opin Infect Dis 2005; 18:147–150
137c. Westergren V, Forsum U, Lundgren J: Possible errors in diagnosis of bacterial sinusitis in tracheal intubated patients. Acta Anaesthesiol Scand 1994; 38:699–703
138b. Rouby JJ, Laurent P, Gosnach M, et al: Risk factors and clinical relevance of nosocomial maxillary sinusitis in the critically ill. Am J Respir Crit Care Med 1994; 150:776–783
139b. Caplan ES, Hoyt NJ: Nosocomial sinusitis. JAMA 1982; 247:639–641
140b. Grindlinger GA, Niehoff J, Hughes SL, et al: Acute paranasal sinusitis related to nasotracheal intubation of head-injured patients. Crit Care Med 1987; 15:214–217
141c. Aebert H, Hunefeld G, Regel G: Paranasal sinusitis and sepsis in ICU patients with nasotracheal intubation. Intensive Care Med 1988; 15:27–30
142c. Shapiro GG, Rachelefsky GS: Introduction and definition of sinusitis. J Allergy Clin Immunol 1992; 90(3 Pt 2):417–418
143c. Vargas F, Bui HN, Boyer A, et al: Transnasal puncture based on echographic sinusitis evidence in mechanically ventilated patients with suspicion of nosocomial maxillary sinusitis. Intensive Care Med 2006; 32:858–866
144c. Chidekel N, Jensen C, Axelsson A, et al: Diagnosis of fluid in the maxillary sinus. Acta Radiol Diagn (Stockh) 1970; 10:433–440
145b. Hamory BH, Sande MA, Sydnor A Jr, et al: Etiology and antimicrobial therapy of acute maxillary sinusitis. J Infect Dis 1979; 139:197–202
146b. Roberts DN, Hampal S, East CA, et al: The diagnosis of inflammatory sinonasal disease. J Laryngol Otol 1995; 109:27–30
147c. Osguthorpe JD, Hadley JA: Rhinosinusitis: Current concepts in evaluation and management. Med Clin North Am 1999; 83:27–41
148c. Zinreich SJ: Rhinosinusitis: Radiologic diagnosis. Otolaryngol Head Neck Surg 1997; 117(3 Pt 2):S27–S34
149b. Kountakis SE, Skoulas IG: Middle meatal vs antral lavage cultures in intensive care unit patients. Otolaryngol Head Neck Surg 2002; 126:377–381
150b. Garibaldi RA, Brodine S, Matsumiya S, et al: Evidence for the non-infectious etiology of early postoperative fever. Infect Control 1985; 6:273–277
151c. Cheadle WG: Current perspectives on antibiotic use in the treatment of surgical infections. Am J Surg 1992; 164(4A Suppl):44S–47S
152c. Stevens DL, Bisno AL, Chambers HF, et al: Practice guidelines for the diagnosis and management of skin and soft-tissue infections. Clin Infect Dis 2005; 41:1373–1406
153b. Agnelli G, Bolis G, Capussotti L, et al: A clinical outcome-based prospective study on venous thromboembolism after cancer surgery: The @RISTOS project. Ann Surg 2006; 243:89–95
154b. Jaffer AK, Barsoum WK, Krebs V, et al: Duration of anesthesia and venous thromboembolism after hip and knee arthroplasty. Mayo Clin Proc 2005; 80:732–738
155b. White RH, Gettner S, Newman JM, et al: Predictors of rehospitalization for symptomatic venous thromboembolism after total hip arthroplasty. N Engl J Med 2000; 343:1758–1764
156b. White RH, Zhou H, Romano PS: Incidence of symptomatic venous thromboembolism after different elective or urgent surgical procedures. Thromb Haemost 2003; 90:446–455
157b. Haley RW, Culver DH, White JW, et al: The efficacy of infection surveillance and control programs in preventing nosocomial infections in US hospitals. Am J Epidemiol 1985; 121:182–205
158b. Haley RW: Measuring the costs of nosocomial infections: Methods for estimating economic burden on the hospital. Am J Med 1991; 91(3B):32S–38S
159c. Brook I, Frazier EH: Aerobic and anaerobic bacteriology of wounds and cutaneous abscesses. Arch Surg 1990; 125:1445–1451
160c. File TM Jr, Tan JS: Treatment of skin and soft-tissue infections. Am J Surg 1995; 169(5A Suppl):27S–33S
161c. Meislin HW, Lerner SA, Graves MH, et al: Cutaneous abscesses: Anaerobic and aerobic bacteriology and outpatient management. Ann Intern Med 1977; 87:145–149
162b. Macfie J, Harvey J: The treatment of acute superficial abscesses: A prospective clinical trial. Br J Surg 1977; 64:264–266
163b. Huizinga WK, Kritzinger NA, Bhamjee A: The value of adjuvant systemic antibiotic therapy in localised wound infections among hospital patients: A comparative study. J Infect 1986; 13:11–16
164b. Commichau C, Scarmeas N, Mayer SA: Risk factors for fever in the neurologic intensive care unit. Neurology 2003; 60:837–841
165c. Jackson WL Jr, Shorr AF: The yield of lumbar puncture to exclude nosocomial meningitis as aetiology for mental status changes in the medical intensive care unit. Anaesth Intensive Care 2006; 34:21–24
166c. Gower DJ, Baker AL, Bell WO, et al: Contraindications to lumbar puncture as defined by computed cranial tomography. J Neurol Neurosurg Psychiatry 1987; 50:1071–1074
167c. Schliamser SE, Backman K, Norrby SR: Intracranial abscesses in adults: an analysis of 54 consecutive cases. Scand J Infect Dis 1988; 20:1–9
168b. Spanos A, Harrell FE Jr, Durack DT: Differential diagnosis of acute meningitis: An analysis of the predictive value of initial observations. JAMA 1989; 262:2700–2707
169b. Hayward RA, Shapiro MF, Oye RK: Laboratory testing on cerebrospinal fluid: A reappraisal. Lancet 1987; 1:1–4
170b. Leib SL, Boscacci R, Gratzl O, et al: Predictive value of cerebrospinal fluid (CSF) lactate level versus CSF/blood glucose ratio for the diagnosis of bacterial meningitis following neurosurgery. Clin Infect Dis 1999; 29:69–74
171c. Tunkel AR, Hartman BJ, Kaplan SL, et al: Practice guidelines for the management of bacterial meningitis. Clin Infect Dis 2004; 39:1267–1284
172c. Adler SP: Transfusion-associated cytomegalovirus infections. Rev Infect Dis 1983; 5:977–993
173c. Drew WL, Miner RC: Transfusion-related cytomegalovirus infection following noncardiac surgery. JAMA 1982; 247:2389–2391
174c. Lerner PI, Sampliner JE: Transfusion-associated cytomegalovirus mononucleosis. Ann Surg 1977; 185:406–410
175b. Ugarte H, Silva E, Mercan D, et al: Procalcitonin used as a marker of infection in the intensive care unit. Crit Care Med 1999; 27:498–504
176b. Suprin E, Camus C, Gacouin A, et al: Procalcitonin: A valuable indicator of infection in a medical ICU? Intensive Care Med 2000; 26:1232–1238
177b. Selberg O, Hecker H, Martin M, et al: Discrimination of sepsis and systemic inflammatory response syndrome by determination of circulating plasma concentrations of procalcitonin, protein complement 3a, and interleukin-6. Crit Care Med 2000; 28:2793–2798
178b. Rothenburger M, Markewitz A, Lenz T, et al: Detection of acute phase response and infection: The role of procalcitonin and C-reactive protein. Clin Chem Lab Med 1999; 37:275–279
179b. Muller B, Becker KL, Schachinger H, et al: Calcitonin precursors are reliable markers of sepsis in a medical intensive care unit. Crit Care Med 2000; 28:977–983
180b. Aouifi A, Piriou V, Bastien O, et al: Usefulness of procalcitonin for diagnosis of infection in cardiac surgical patients. Crit Care Med 2000; 28:3171–3176
181c. Cohen J: The detection and interpretation of endotoxaemia. Intensive Care Med 2000; 26(Suppl 1):S51–6
182c. Cohen J, McConnell JS: Observations on the measurement and evaluation of endotoxemia by a quantitative limulus lysate microassay. J Infect Dis 1984; 150:916–924
183b. Marshall JC, Walker PM, Foster DM, et al: Measurement of endotoxin activity in critically ill patients using whole blood neutrophil dependent chemiluminescence. Crit Care 2002; 6:342–348
184b. Marshall JC, Foster D, Vincent JL, et al: Diagnostic and prognostic implications of endotoxemia in critical illness: Results of the MEDIC study. J Infect Dis 2004; 190:527–534
185c. Lipsky BA, Hirschmann JV: Drug fever. JAMA 1981; 245:851–854
186d. Mackowiak PA: Drug fever: Mechanisms, maxims and misconceptions. Am J Med Sci 1987; 294:275–286
187c. Mackowiak PA, LeMaistre CF: Drug fever: A critical appraisal of conventional concepts. An analysis of 51 episodes in two Dallas hospitals and 97 episodes reported in the English literature. Ann Intern Med 1987; 106:728–733
188c. Mermel LA: Bacteriology, safety and prevention of infection associated with continuous intravenous infusions. Blood Coagul Fibrinolysis 1996; 7(Suppl 1):S45–S51
189c. Cunha BA: Drug fever: The importance of recognition. Postgrad Med 1986; 80:123–129
190c. Heiman-Patterson TD: Neuroleptic malignant syndrome and malignant hyperthermia: Important issues for the medical consultant. Med Clin North Am 1993; 77:477–492
191c. Nimmo SM, Kennedy BW, Tullett WM, et al: Drug-induced hyperthermia. Anaesthesia 1993; 48:892–895
192c. Caroff SN, Mann SC: Neuroleptic malignant syndrome and malignant hyperthermia. Anaesth Intensive Care 1993; 21:477–478
193c. Mason PJ, Morris VA, Balcezak TJ: Serotonin syndrome: Presentation of 2 cases and review of the literature. Medicine (Baltimore) 2000; 79:201–209
194c. Lawrence KR, Adra M, Gillman PK: Serotonin toxicity associated with the use of linezolid: A review of postmarketing data. Clin Infect Dis 2006; 42:1578–1583
195b. Garnacho-Montero J, Garcia-Garmendia JL, Barrero-Almodovar A, et al: Impact of adequate empirical antibiotic therapy on the outcome of patients admitted to the intensive care unit with sepsis. Crit Care Med 2003; 31:2742–2751
196b. Garnacho-Montero J, Aldabo-Pallas T, Garnacho-Montero C, et al: Timing of adequate antibiotic therapy is a greater determinant of outcome than are TNF and IL-10 polymorphisms in patients with sepsis. Crit Care 2006; 10:R111
197b. Ibrahim EH, Sherman G, Ward S, et al: The influence of inadequate antimicrobial treatment of bloodstream infections on patient outcomes in the ICU setting. Chest 2000; 118:146–155
198b. Harbarth S, Garbino J, Pugin J, et al: Inappropriate initial antimicrobial therapy and its effect on survival in a clinical trial of immunomodulating therapy for severe sepsis. Am J Med 2003; 115:529–535
199b. Kollef MH, Sherman G, Ward S, et al: Inadequate antimicrobial treatment of infections: A risk factor for hospital mortality among critically ill patients. Chest 1999; 115:462–474
200b. Micek ST, Lloyd AE, Ritchie DJ, et al: Pseudomonas aeruginosa bloodstream infection: Importance of appropriate initial antimicrobial treatment. Antimicrob Agents Chemother 2005; 49:1306–1311
201b. Kumar A, Roberts D, Wood KE, et al: Duration of hypotension before initiation of effective antimicrobial therapy is the critical determinant of survival in human septic shock. Crit Care Med 2006; 34:1589–1596
202b. Ibrahim EH, Ward S, Sherman G, et al: Experience with a clinical guideline for the treatment of ventilator-associated pneumonia. Crit Care Med 2001; 29:1109–1115

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Keywords:

fever; intensive care unit; critical illness; blood cultures; catheter infection; pneumonia; colitis; sinusitis; surgical site infection; nosocomial infection; temperature measurement; urinary tract infection

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