Pneumothorax in the Intensive Care Unit: Incidence, Risk Factors, and Outcome
de Lassence, Arnaud M.D.*; Timsit, Jean-François M.D., Ph.D.†; Tafflet, Muriel M.Sc.‡; Azoulay, Élie M.D., Ph.D.§; Jamali, Samir M.D.∥; Vincent, François M.D.#; Cohen, Yves M.D.**; Garrouste-Orgeas, Maïté M.D.††; Alberti, Corinne M.D., Ph.D.‡‡; Dreyfuss, Didier M.D.§§; on behalf of the OUTCOMEREA Study Group
Background: The risk factors and outcomes of critically ill patients with iatrogenic pneumothorax (IP) have not been studied in a large unselected intensive care unit (ICU) population.
Methods: The authors studied a prospective cohort of adults admitted for more than 24 h. Data were collected at ICU admission and daily by senior physicians until ICU discharge. Risk factors for IP were identified in the entire cohort. A matched nested case–control study was used to evaluate the excess risk of IP in decedents.
Results: Of the 3,499 patients, 69 with pneumothorax before ICU admission were excluded. Of the remaining 3,430 patients, 94 experienced IP within 30 days (42 due to barotrauma and 52 due to invasive procedures). The cumulative incidence of IP was 1.4% (95% confidence interval [CI], 1.0–1.8) on day 5 and 3.0% (95% CI, 2.4–3.6) on day 30. Risk factors for IP (hazard ratio [95% CI]) were body weight less than 80 kg (2.4 [1.3–4.2]), history of adult immunodeficiency syndrome (2.8 [1.2–6.4]), diagnosis of acute respiratory distress syndrome (5.3 [2.6–11]) or cardiogenic pulmonary edema at admission (2.0 [1.1–3.6]), central vein or pulmonary artery catheter insertion (1.7 [1.0–2.7]), and use of inotropic agents during the first 24 h (2.1 [1.3–3.4]). Excess risk of IP in decedents was 2.6 (95% CI, 1.3–4.9; P = 0.004).
Conclusion: Iatrogenic pneumothorax is a life-threatening complication seen in 3% of ICU patients. Incorporating risk factors for IP into preventive strategies should reduce the occurrence of IP.
IATROGENIC pneumothorax (IP) is one of the main iatrogenic complications in intensive care unit (ICU) patients.1
The incidence of IP in the ICU was greater than 20% in the 1990s2–8
and has since decreased to 3%.9,10
IP in the ICU occurs chiefly as a complication of barotrauma related to mechanical ventilation (IP-MV) or as a postprocedural event (e.g.
, after central venous catheter insertion, thoracentesis, or surgery). Most studies of the prognosis and outcome of IP were retrospective and focused on a single category of IP.9,11–17
The development of lung-protective strategies for ventilation and of new material, techniques, and recommendations for inserting central vein catheters makes IP largely preventable in routine practice.18
Nevertheless, the occurrence of IP is closely related to the underlying disease, such as adult respiratory distress syndrome (ARDS) for IP-MV. Identifying patients with risk factors in order to take specific preventive steps may be beneficial.
The aim of this study was to investigate the incidence, risk factors, morbidity, and mortality of IP in the large OUTCOMEREA® database.
Materials and Methods
We conducted a prospective observational study in a multicenter database (OUTCOMEREA®) from January 1997 to June 2003. The database, fed by 11 French medical or surgical ICUs, is specifically designed to record daily disease severity and occurrence of iatrogenic events and nosocomial infections. A random sample of patients older than 16 yr and having ICU stays longer than 24 h was entered into the database each year. Briefly, the center could choose among two methods for random sampling: (1) consecutive admissions in n ICU beds or (2) consecutive admissions in a given month. Beds (or month) were allocated to the database once a year by the database steering committee. We studied all patients in the OUTCOMEREA® database except those admitted to the ICU for pneumothorax (n = 69).
Method of Data Collection.
Data were collected daily by senior physicians in each participating unit. For each patient, the investigator entered the data into a computer case-report form using the data capture software VIGIREA® (OUTCOMEREA; Rosny sous bois, France) and imported all records to the OUTCOMEREA® database. All codes and definitions were established before study initiation.
All study ICUs followed the same rules for mechanical ventilation and catheter insertion. In mechanically ventilated patients, tidal volume was set to maintain a plateau pressure below 30 cm H2
O in most cases and no greater than 35 cm H2
O in all patients.19
Central venous access was chosen according to a previously suggested algorithm.20
Briefly, to avoid catheter-related infection, subclavian access was preferred except in patients with severe hemostasis disorders or arterial oxygen tension (Pao2
)/fraction of inspired oxygen (Fio2
) less than 150, in whom the choice between the femoral and internal jugular routes was at the discretion of the attending physician. Written protocols were shared among the participating ICUs, but practices were not audited.
The following data were recorded: patient characteristics at admission (age, sex, origin, and body weight), admission diagnosis (pneumonia, cardiogenic pulmonary edema, acute exacerbation of chronic obstructive pulmonary disease, or ARDS21
), admission category, main symptom, diabetes, acquired immunodeficiency syndrome (AIDS),22
main clinical features and laboratory findings, treatment modalities (most notably mechanical ventilation [yes/no] and endotracheal mechanical ventilation [yes/no], inotropic agents, and antimicrobials), and catheters. The following scores were computed at admission and daily thereafter: Simplified Acute Physiologic Score (SAPS II),25
Logistic Organ Dysfunction (LOD),26
Sequential Organ Failure Assessment,27
and Glasgow Coma Scale score. Last, duration of invasive ventilation, duration of ICU and hospital stays, and outcomes at ICU and hospital discharges were recorded.
Quality of the Database.
Data were collected daily on computers by ICU physicians closely involved in establishing the database. The software immediately conducts an automatic check of most of the variables entered by the investigator. Multiple automatic checking of internal consistency generated queries that were sent to the ICUs before the new data were incorporated into the database. At each study ICU, the quality control procedure involved having a senior ICU physician from another study ICU check a 2% random sample of study data. Interrater correlation coefficients ranged from 0.67 to 1 for clinical variables, severity scores, and organ dysfunction scores, and κ coefficients for qualitative variables ranged from 0.5 to 0.9. Missing values occurred only for age and weight (less than 1% of the cohort), which were replaced by median sex-specific values.
Chest radiographs were obtained at least once a day during the first month in all ventilated patients, routinely after thoracentesis or central venous catheter insertion, and when clinically indicated. Computed tomography was performed when the chest radiograph did not confirm a clinically suspected diagnosis. IP was also diagnosed when drainage of a tension pneumothorax was required before chest radiography.
All patients were screened daily for IP throughout the ICU stay. Four categories of IP were distinguished: IP secondary to barotrauma caused by invasive mechanical ventilation (IP-MV), IP after central venous catheter insertion (IP-CVC), IP after thoracentesis, and IP related to other causes.
Quantitative and qualitative variables are reported as medians [interquartile range (IQR)] and n (%), respectively. We studied the incidence of first IP (within the first 30 days), taking “discharge from the ICU alive without experiencing IP” as a competing risk. We used the cumulative incidence instead of Kaplan-Meier plots.28
The first episode of IP within the first 30 days in the ICU was considered. A proportional hazard model was used to compute the time to IP and to investigate risk factors for IP. We used the Fine and Gray extension of the Cox model to take competing risks into account.29
Variables significantly associated with IP at a 0.05 level of risk were selected using a bivariate Cox model. Multivariate analysis was performed with stepwise forward selection. Because we anticipated colinearity between severity and organ dysfunction scores, these were introduced successively at the first step of the multivariate analysis.
The proportional risk and log-linearity hypotheses were checked for all models. For continuous variables, when log linearity was not confirmed, we cut variables on the break points of the spline curves. A pooled two-way interaction test was used to unmask significant interactions between variables in the final model. Results are reported as hazard ratios and 95% confidence intervals (CIs).
A pneumothorax risk score was developed from the regression coefficients associated with each variable. Internal validation of the pneumothorax risk score was performed by bootstrapping, which involves analyzing a large number (400 independent replicates) of subsamples with replacement from the full sample. Bootstrapping provides nearly unbiased estimates of β coefficients of the final regression. External validation was also performed using an external data set of patients included in the database between June 2003 and November 2004 (n = 1,798).
Hospital mortality rate in patients with IP, invasive ventilation on the day of IP occurrence, duration of stay before and after IP, mortality after IP, and changes in daily LOD before and after IP were studied consecutively.
We investigated whether the risk of IP was increased in decedents, taking into account confounding factors such as severity and duration of ICU stay. To this end, we designed a nested case–control study comparing patients who died in the hospital and patients who were discharged alive from the hospital. At least 631 cases and controls were needed to detect an increase in the odds ratio (OR) for IP of 2 assuming a 3% IP prevalence in survivors (with α 0.05 and β 0.20). The case–control (1:1) matching criteria were probability of hospital death (SAPS II) ± 5%, duration of ICU stay ± 20%, invasive ventilation at admission, and transfer from a ward.##
We used conditional logistic regression with and without adjustment on matching criteria, risk factors for death, and risk factors for IP. Clinically relevant two-way interactions were selected in the final model and tested.
Sensitivity analyses of the IP risk were performed in patients ventilated for at least 24 h, in those with intermediary SAPS II values (27–48 points, i.e., from the 25th to the 75th percentiles), and in those without decisions to forego life-sustaining treatments (withdrawal or withholding decisions taken by consensus among ICU staff members and communicated to intensivists on duty or written in the patient’s medical record).
All statistical tests were two tailed, and P values less than 0.05 were considered significant. All statistical analyses were performed using the SAS 8.02 software package (SAS Inc., Cary, NC) and S-plus 2000 (MathSoft Inc., Seattle, WA).
Of the 10,339 patients admitted to all OUTCOMEREA® ICUs during the study period, 3,430 (29%) were enrolled in the 11 participating ICUs (40,472 ICU days). Among these, 94 (2.7%; 95% CI, 2.2–3.2%) experienced at least one episode of IP within the first 30 days (fig. 1
); 7 patients had two episodes (including 1 episode on day 31).
Among the 3,430 study patients, 2,299 (67%) received invasive mechanical ventilation for at least 24 h and 1,949 (57%) for at least 48 h. IP was associated with longer durations of the ICU stay (7 [IQR, 4–13] vs. 17.5 [IQR, 9–32] days; P < 0.001) and hospital stay (18 [IQR, 10–33] vs. 31 [IQR, 14–46] days; P < 0.001). Mortality rates in the ICU (22 vs. 45%; P < 0.001) and hospital (28 vs. 51%; P < 0.001) were also higher in patients with IP.
Incidence and Epidemiology of IP
The first episode of IP was secondary to barotrauma during invasive ventilation (IP-MV) in 42 patients, with a median time from admission to IP of 5 days [IQR, 3–10 days] and from mechanical ventilation initiation to IP of 4 days [IQR, 2–8 days]. IP followed central venous catheter insertion (IP-CVC) in 28 patients, with a median time from admission to IP of 3.5 days [IQR, 2.5–9 days]. IP occurred after thoracentesis in 21 patients, with a median time from admission to IP of 7 days [IQR, 3–12 days]. IP was due to other causes in 3 patients, with a median time from admission to IP of 20 days [IQR, 10–26 days]. Overall, the median time from admission to the first episode of IP was 5.5 days [IQR, 3–11 days].
The cumulative incidence of IP was 1.4% (95% CI, 1.0–1.8) on day 5, 2.1% (95% CI, 1.6–2.6) on day 10, and 3.0% (95% CI, 2.4–3.6) on day 30 (fig. 2
). On day 30, cumulative incidences were as follows: IP-MV, 1.3% (95% CI, 0.9–1.7); IP-CVC, 0.9% (95% CI, 0.5–1.2); and IP after thoracocentesis, 0.7% (95% CI, 0.4–1.0).
Disease severity according to SAPS II, LOD, and Sequential Organ Failure Assessment values was greater in the patients with IP (table 1
). A larger proportion of patients with than without IP had AIDS, pneumonia at admission, pulmonary edema, or ARDS. Patients with IP were more likely to receive invasive ventilation and to require insertion of arterial, central, and pulmonary artery catheters.
Of the 94 patients with IP, 10 died on the same day of or the day after the event. Tension IP caused cardiac arrest in 10 patients (10.6%).
Chest tube drainage was required in 87 patients (93%), for a median duration of 6 days [3–10 days]. The medical records of the remaining 7 patients were reviewed retrospectively by the attending physicians. Two of these patients had severe hemostasis disorders and experienced localized IP after being weaned off mechanical ventilation. In the other 5 patients, localized IP occurred during spontaneous breathing, after thoracentesis (n = 2), central vein catheter insertion (n = 2), or transbronchial biopsy (n = 1) and resolved with oxygen therapy.
Severity according to LOD values increased significantly between the day before and the day after IP. The mean LOD score increase was +0.59 [+0.13 to +1.05], P = 0.004, on the day of IP and +1.38 [+0.57 to +1.86], P < 0.001, on the day after IP.
Risk Factors for IP
The univariate and multivariate analyses of risk factors for IP are reported in tables 1 and 2
. At the last step of the multivariate analysis, six factors were independently associated with IP: history of AIDS, diagnosis of cardiogenic pulmonary edema at admission, diagnosis of ARDS at admission, insertion during the first 24 h of a central vein catheter or pulmonary artery catheter, and use of vasoactive agents during the first 24 h (table 2
). Bootstrap analysis did not influence the type or significance of the independent risk factors (table 2
The risk factors for IP showed little change when the analysis was rerun on mechanically ventilated patients only or on patients with at least one central venous catheter or with a pulmonary artery catheter. AIDS was a risk factor for IP-MV but not for IP-CVC.
Based on the adjusted hazards ratios of variables included in the final model, an IP risk score was built (table 3
). This score could range from 0 to 6. Two points were assigned to ARDS at admission, and one point was assigned to each of the other risk factors. The cumulative incidence of IP according to the risk score is shown in figure 3
. The cumulative risk on day 30 ranged from 0.9% (95% CI, 0–1.9%) with a score of zero to 34% (95% CI, 9.5–59%) with a score of 5 or greater (fig. 3A
). The model was tested on an external data set based on a more recent population entered in the database (n = 1,798 patients). Thirty-two IPs occurred (1.9%). As shown in figure 3B
, the risk of IP within the first 30 days in this external population was 0% when the IP risk score was 0, 9.1% when the risk score was 4, and 15.1% when the risk score was 5 or 6.
Increased Risk of IP in Decedents: Case–Control Study
Among the 982 decedents, 745 were successfully matched with a survivor. The adequacy of matching was 100% for the probability of hospital death according to SAPS II at admission and ICU duration of stay, 87% for invasive ventilation, and 83% for transfer from ward. In the 745 matched pairs (1,490 patients), 39 IPs (5.2%) occurred in decedents, and 17 (2.2%) occurred in survivors (P
= 0.003). The population enrolled in the nested case–control study is shown in table 4
Multivariate Analysis: Conditional Logistic Regression
In the multivariate analysis, we took into account all variables used for matching and several additional variables expected to affect outcome, such as LOD, chronic diseases, admission category, and age, as well as risk factors for IP such as an admission diagnosis of pneumonia, pulmonary edema, or ARDS; body weight; pulmonary artery or central catheter insertion; and AIDS. Clinically relevant two-way interactions were also tested (LOD with age, chronic disease, body weight < 80 kg, unscheduled surgery, and invasive ventilation; diagnosis of pneumonia with unscheduled surgery; and chronic disease with unscheduled surgery, hospital death probability, and body weight).
Iatrogenic pneumothorax was more common in decedents: The unadjusted OR was 2.37 (95% CI, 1.32–4.26; P = 0.0028), and the OR adjusted on the above-listed variables was 2.56 (95% CI, 1.34–4.89; P = 0.0043).
Finally, the excess risk of death associated with IP-MV (OR, 2.44; 95% CI, 0.96–6.24) was not different from that associated with IP-CVC (OR, 2.67; 95% CI, 1.1–6.45).
The estimated excess risk of death was unchanged in separate analyses of ventilated patients (530 pairs; OR, 2.68; 95% CI, 1.32–5.45; P = 0.0065), patients with intermediate severity (SAPS II between 27 and 48; 254 pairs; OR, 3.19; 95% CI, 0.98–10.4; P = 0.055), and patients without decisions to forego life-sustaining treatment (450 pairs; OR, 2.72; 95% CI, 1.08–7.22; P = 0.032).
The results from this large multicenter study show that IP is a life-threatening complication associated with a more than twofold increase in the risk of death. The 30-day incidence of IP was 3% in the overall population. The occurrence of IP was heavily dependent on risk factors that can be easily collected at ICU admission.
The overall incidence of IP secondary to mechanical ventilation in ICUs is not well known because most of the published studies investigated barotrauma related to mechanical ventilation without distinguishing clearly among pneumothorax, pneumomediastinum, pneumoperitoneum, and subcutaneous emphysema.1,5,9,11,17,21,30
Furthermore, postprocedural IP was either not taken into account or lumped together with other mechanical procedure–related events such as hemorrhage, faulty catheter position, or failure of a central venous catheter.11,17
The overall rate of IP in ICU patients was 8% in the 1980s2
and subsequently decreased to 3–4%.1,10
Even in recent series, however, the incidence rate of pneumothorax was as high as 7–14% in patients receiving mechanical ventilation5,9,16
and was highest in patients with acute lung injury and ARDS.12,15,30–33
Mechanical ventilation was the most common cause of IP in our series, in keeping with previous reports9,15
However, invasive procedures remained a major cause of IP,10
most notably central vein catheter insertion,11,20
and bronchoscopy with transbronchial biopsy.10
Cumulative incidence curves showed a 3% risk of IP after 30 days. The risk was highest during the first 5 ICU days and decreased slightly thereafter. The occurrence of IP increased the duration of ICU and hospital stays. Moreover, using a case–control nested study with careful adjustment on severity at admission and duration of risk exposure, we demonstrated that IP was associated with a greater than twofold increase in the risk of death. In contrast to Chen et al.
we observed that the increased risk of death was similar for IP-MV and for postprocedural IP. This result is in accordance with evaluations of mechanically ventilated patients,9
patients with acute lung injury,15
and patients with AIDS.35
In one study involving a specific group of ARDS patients, IP-MV was not associated with an increased risk of death.30
However, even in this study, mortality in patients with no air leak (39%) was not significantly lower than that in patients with IP-MV (46%). We also found a significant LOD score increase after IP. Moreover, IP was associated with cardiac arrest in 10 patients and occurred immediately before death in 10 other patients, supporting a major risk of death related to IP.
In our study, AIDS, body weight less than 80 kg, admission diagnosis of cardiogenic pulmonary edema or ARDS, insertion of a pulmonary artery or central venous catheter, and inotropic support on the first ICU day were independent risk factors for IP in ICU patients. Our findings are consistent with previous studies for ARDS9,16
and lower body weight.17,30
AIDS patients are often admitted for interstitial lung diseases or Pneumocystis carinii
which have been associated with a high risk of IP. Finally superior vena cava catheter insertion has been associated with a 0.5–3% risk of IP.20
Several limitations of our study should be discussed. First, symptomatic barotrauma without IPs was not recorded. This may have impacted the β estimates of the covariates and decreased the power of the study. In addition, because computed tomography was not performed routinely, the incidence of IP may have been underestimated. Also, because chest radiographs were not obtained routinely after death, cases of IP secondary to cardiac pumping during unsuccessful cardiac resuscitation procedures may have been missed. Second, the absence of plateau pressure and tidal volume in the database may have influenced the results of the risk factor evaluation and the IP risk score. However, plateau pressure was carefully maintained below 30 cm H2
O in all of the study ICUs. In this situation, plateau was not a risk factor for IP in two recent studies9,30
Third, the relatively low number of IPs may have limited the power of the study for identifying risk factors. Finally, cardiogenic pulmonary edema was diagnosed by the investigators based on physical findings, echocardiography results, and the course. Pulmonary capillary pressure was not measured routinely. Therefore, the reproducibility of this variable is open to question.
We used our results to build an IP risk score that can be evaluated at ICU admission. The risk of experiencing IP within the first 30 days was less than 1% when the score was 0 and 15% when the score was 4. This risk score needs further external validation on another database. However, results obtained with a more recent data set of the OUTCOMEREA® database support the reliability of the IP risk score.
Iatrogenic pneumothorax should be a good quality indicator because it is clearly associated with ICU mortality. Requisites for valid comparisons of outcomes among ICUs include an accurate and comprehensive outcome measure, a sufficient sample size with unbiased sampling, and appropriate risk adjustment via
application of a valid model to reliably collected data.37
The IP risk score could be useful for comparing the IP rate across ICUs according to a specific level of risk. It could also be used to identify patients at high risk of IP, who would probably benefit from specific procedures for central venous catheter placement such as a careful risk–benefit estimation of central vein or pulmonary artery catheter insertion,8
use of an insertion site that does not carry a risk of IP (femoral vessels), Doppler ultrasound guidance if subclavian or internal jugular vein insertion is required,38
placement by an experienced physician,11,17,20,39
and discontinuation of the procedure if the first two venipuncture attempts fail.11
Pneumothorax is one of the main iatrogenic events observed in ICU patients1
and is relatively easy to diagnose. Our study confirms that IP is associated with subsequent increases in ICU stay duration, resource use, and mortality. Interventions such as new ventilatory strategies for patients with ARDS,9,40
improved experience of physicians with catheter insertion,20
and use of ultrasound-located devices for central vein cannulation38
reduce the rate of barotrauma. We suggest that the rate of IP could serve as an outcome measure in the ICU. Use of the IP risk score could allow reliable comparisons across groups, centers, or years.
1. Giraud T, Dhainaut JF, Vaxelaire JF, Joseph T, Journois D, Bleichner G, Sollet JP, Chevret S, Monsallier JF: Iatrogenic complications in adult intensive care units: A prospective two-center study. Crit Care Med 1993; 21:40–51
2. Petersen GW, Baier H: Incidence of pulmonary barotrauma in a medical ICU. Crit Care Med 1983; 11:67–9
3. Wasserberger J, Ordog GJ, Turner AF, Eskridge J, Bryon G, Eubanks DH, Wali V: Iatrogenic pulmonary overpressure accident. Ann Emerg Med 1986; 15:947–51
4. Ovenfors CO: Iatrogenic trauma to the thorax. J Thorac Imaging 1987; 2:18–31
5. Gammon RB, Shin MS, Buchalter SE: Pulmonary barotrauma in mechanical ventilation: Patterns and risk factors. Chest 1992; 102:568–72
6. Sassoon CS, Light RW, O’Hara VS, Moritz TE: Iatrogenic pneumothorax: Etiology and morbidity. Results of a Department of Veterans Affairs Cooperative Study. Respiration 1992; 59:215–20
7. Williams TJ, Tuxen DV, Scheinkestel CD, Czarny D, Bowes G: Risk factors for morbidity in mechanically ventilated patients with acute severe asthma. Am Rev Respir Dis 1992; 146:607–15
8. Rouby JJ, Lherm T, Martin de Lassale E, Poete P, Bodin L, Finet JF, Callard P, Viars P: Histologic aspects of pulmonary barotrauma in critically ill patients with acute respiratory failure. Intensive Care Med 1993; 19:383–9
9. Anzueto A, Frutos-Vivar F, Esteban A, Alia I, Brochard L, Stewart T, Benito S, Tobin MJ, Elizalde J, Palizas F, David CM, Pimentel J, Gonzalez M, Soto L, D’Empaire G, Pelosi P: Incidence, risk factors and outcome of barotrauma in mechanically ventilated patients. Intensive Care Med 2004; 30:612–9
10. Chen KY, Jerng JS, Liao WY, Ding LW, Kuo LC, Wang JY, Yang PC: Pneumothorax in the ICU: Patient outcomes and prognostic factors. Chest 2002; 122:678–83
11. Lefrant JY, Muller L, De La Coussaye JE, Prudhomme M, Ripart J, Gouzes C, Peray P, Saissi G, Eledjam JJ: Risk factors of failure and immediate complication of subclavian vein catheterization in critically ill patients. Intensive Care Med 2002; 28:1036–41
12. Boussarsar M, Thierry G, Jaber S, Roudot-Thoraval F, Lemaire F, Brochard L: Relationship between ventilatory settings and barotrauma in the acute respiratory distress syndrome. Intensive Care Med 2002; 28:406–13
13. Afessa B, Morales I, Cury JD: Clinical course and outcome of patients admitted to an ICU for status asthmaticus. Chest 2001; 120:1616–21
14. Amato MB, Barbas CS, Medeiros DM, Magaldi RB, Schettino GP, Lorenzi-Filho G, Kairalla RA, Deheinzelin D, Munoz C, Oliveira R, Takagaki TY, Carvalho CR: Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome. N Engl J Med 1998; 338:347–54
15. Schnapp LM, Chin DP, Szaflarski N, Matthay MA: Frequency and importance of barotrauma in 100 patients with acute lung injury. Crit Care Med 1995; 23:272–8
16. Gammon RB, Shin MS, Groves Jr, RH Hardin JM, Hsu C, Buchalter SE: Clinical risk factors for pulmonary barotrauma: A multivariate analysis. Am J Respir Crit Care Med 1995; 152:1235–40
17. Mansfield PF, Hohn DC, Fornage BD, Gregurich MA, Ota DM: Complications and failures of subclavian-vein catheterization. N Engl J Med 1994; 331:1735–8
18. Domino KB, Bowdle TA, Posner KL, Spitellie PH, Lee LA, Cheney FW: Injuries and liability related to central vascular catheters: A closed claims analysis. Anesthesiology 2004; 100:1411–8
19. Slutsky AS: Consensus conference on mechanical ventilation—January 28-30, 1993 at Northbrook, Illinois, USA: II. Intensive Care Med 1994; 20:150–62
20. Timsit JF: Central venous access in intensive care unit patients: Is the subclavian vein the royal route? Intensive Care Med 2002; 28:1006–8
21. Esteban A, Anzueto A, Frutos F, Alia I, Brochard L, Stewart TE, Benito S, Epstein SK, Apezteguia C, Nightingale P, Arroliga AC, Tobin MJ: Characteristics and outcomes in adult patients receiving mechanical ventilation: A 28-day international study. JAMA 2002; 287:345–55
22. Centers for Disease Control and Prevention: Guidelines for national human immunodeficiency virus case surveillance, including monitoring for human immunodeficiency virus infection and acquired immunodeficiency syndrome. MMWR Recomm Rep 1999; 48:1–27, 29–31
23. Knaus WA, Draper EA, Wagner DP, Zimmerman JE: APACHE II: A severity of disease classification system. Crit Care Med 1985; 13:818–29
24. McCabe WR, Jackson GG: Gram-negative bacteremia: I. Etiology and ecology. Arch Intern Med 1962; 110:847–53
25. Le Gall JR, Lemeshow S, Saulnier F: A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. JAMA 1993; 270:2957–63
26. Le Gall JR, Klar J, Lemeshow S, Saulnier F, Alberti C, Artigas A, Teres D: The Logistic Organ Dysfunction system: A new way to assess organ dysfunction in the intensive care unit. ICU Scoring Group. JAMA 1996; 276:802–10
27. Vincent JL, Moreno R, Takala J, Willatts S, De Mendonca A, Bruining H, Reinhart CK, Suter PM, Thijs LG: The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med 1996; 22:707–10
28. Alberti C, Metivier F, Landais P, Thervet E, Legendre C, Chevret S: Improving estimates of event incidence over time in populations exposed to other events: Application to three large databases. J Clin Epidemiol 2003; 56:536–45
29. Fine JP, Gray RJ: A proportional hazards model for the model for the subdistribution of a competing risk. JASA 1999; 94:496–509
30. Weg JG, Anzueto A, Balk RA, Wiedemann HP, Pattishall EN, Schork MA, Wagner LA: The relation of pneumothorax and other air leaks to mortality in the acute respiratory distress syndrome. N Engl J Med 1998; 338:341–6
31. Eisner MD, Thompson BT, Schoenfeld D, Anzueto A, Matthay MA: Airway pressures and early barotrauma in patients with acute lung injury and acute respiratory distress syndrome. Am J Respir Crit Care Med 2002; 165:978–82
32. Brochard L, Roudot-Thoraval F, Roupie E, Delclaux C, Chastre J, Fernandez-Mondejar E, Clementi E, Mancebo J, Factor P, Matamis D, Ranieri M, Blanch L, Rodi G, Mentec H, Dreyfuss D, Ferrer M, Brun-Buisson C, Tobin M, Lemaire F: Tidal volume reduction for prevention of ventilator-induced lung injury in acute respiratory distress syndrome. The Multicenter Trail Group on Tidal Volume Reduction in ARDS. Am J Respir Crit Care Med 1998; 158:1831–8
33. Acute Respiratory Distress Syndrome Network: Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med 2000; 342:1301–8
34. Despars JA, Sassoon CS, Light RW: Significance of iatrogenic pneumothoraces. Chest 1994; 105:1147–50
35. Bedos JP, Dumoulin JL, Gachot B, Veber B, Wolff M, Regnier B, Chevret S: Pneumocystis carinii pneumonia requiring intensive care management: Survival and prognostic study in 110 patients with human immunodeficiency virus. Crit Care Med 1999; 27:1109–15
36. Afessa B: Pleural effusion and pneumothorax in hospitalized patients with HIV infection: The Pulmonary Complications, ICU support, and Prognostic Factors of Hospitalized Patients with HIV (PIP) Study. Chest 2000; 117:1031–7
37. Randolph AG, Guyatt GH, Carlet J: Understanding articles comparing outcomes among intensive care units to rate quality of care. Evidence Based Medicine in Critical Care Group. Crit Care Med 1998; 26:773–81
38. Hind D, Calvert N, McWilliams R, Davidson A, Paisley S, Beverley C, Thomas S: Ultrasonic locating devices for central venous cannulation: Meta-analysis. BMJ 2003; 327:361
39. Sznajder JI, Zveibil FR, Bitterman H, Weiner P, Bursztein S: Central vein catheterization: Failure and complication rates by three percutaneous approaches. Arch Intern Med 1986; 146:259–61
40. Ricard JD: Barotrauma during mechanical ventilation: Why aren’t we seeing any more? Intensive Care Med 2004; 30:533–5
Appendix: List of Members of the OUTCOMEREA® Study Group
Jean-François Timsit, M.D., Ph.D., Staff Physician, ICU, Centre Hospitalier Universitaire Grenoble, France; Gilles Troché, M.D., Staff Physician, Hôpital A. Béclère, Clamart France; Pierre Moine, M.D., Ph.D., Staff Physician, Département d’Anesthesie-Réanimation, Hôpital Lariboisière, Paris, France; Arnaud de Lassence, M.D., Staff Physician, ICU, Hôpital Louis Mourier, Colombes, France; Élie Azoulay, M.D., Ph.D., Staff Physician, ICU, Hôpital Saint Louis, Paris, France; Yves Cohen, M.D., Professor, ICU, Hôpital Avicenne, Bobigny, France; Maïté Garrouste-Orgeas, M.D., Staff Physician, ICU, Hôpital Saint Joseph, Paris, France; Jean-Philippe Fosse, M.D., Staff Physician, ICU, Hôpital Avicenne, Bobigny, France; Lilia Soufir, M.D., Staff Physician, ICU, Hôpital Saint Joseph, Paris, France; Jean-Ralph Zahar, M.D., Attending Physician, Microbiology Department, Hôpital Necker, Paris, France; Christophe Adrie, M.D., Staff Physician, ICU, Hôpital de la Fontaine, Saint Denis, France; Jean Carlet, M.D., Staff Physician, ICU, Hôpital Saint Joseph, Paris, France; and François L’Hériteau, M.D., Attending Physician, ICU, Hôpital Bichat, Paris, France.
Biostatistical and Informatics Expertise
Sylvie Chevret, M.D. Ph.D., Professor, Medical Computer Sciences and Biostatistics Department, Hôpital Saint Louis, Paris, France; CorinneAlberti, M.D., Staff Physician, Medical Computer Sciences and Biostatistics Department, Hôpital Saint Louis, Paris, France; Frederik Lecorre, Informatician, Supelec, Gif sur Yvette, France; Didier Nakache, Informatic Engineer, Conservatoire National des Arts et Métiers, Paris, France; and Muriel Tafflet, Biostatistical Engineer, Outcomerea Organization, Rosny sous bois, France.
Investigators of the OUTCOMEREA® Database
Caroline Bornstain, M.D., Staff Physician, ICU, Hôpital Européen Georges Pompidou, Paris, France; Marie Thuong, M.D., Staff Physician, ICU, Hôpital de la Fontaine, Saint Denis, France; Marie-Alliette Costa de Beauregard, M.D., Staff Physician, Nephrology, Hôpital Tenon, Paris, France; Jean-Pierre Colin, M.D., Staff Physician, ICU, Hôpital de Dourdan, Dourdan, France; Eric Le Miere, M.D., Attending Physician, ICU, Hôpital Louis Mourier, Colombes, France; Antoine Caubel, M.D., Attending Physician, ICU, Hôpital Saint Joseph, Paris, France; William Marie, M.D., Attending Physician, ICU, Hôpital Saint Joseph, Paris, France; Christine Cheval, M.D., Staff Physician, SICU, Hôpital Saint Joseph, Paris, France; Eric Vantalon, M.D., Staff Physician, SICU, Hôpital Saint Joseph, Paris, France; Christophe Clec’h, M.D., Staff Physician, ICU, Hôpital Avicenne, Bobigny, France; François Vincent, M.D., Staff Physician, Nephrology, Hôpital Tenon, Paris, France; Amar Salah, M.D., Staff Physician, ICU, Hôpital Louis Mourier, Colombes, France; Laurent Montesino, M.D., Attending Physician, ICU, Hôpital Bichat, Paris, France; Etienne Pigné, M.D., Staff Physician, ICU, Hôpital Louis Mourier, Colombes, France; Alexandre Boyer, M.D., Staff Physician, ICU, Hôpital Pellegrin, Bordeaux, France; Olivier Tuil, M.D., Staff Physician, ICU, Hôpital Avicenne, Bobigny, France; Bruno Mourvillier, M.D., Staff Physician, ICU, Hôpital d’Aulnay sous bois, France; Samir Jamali, M.D., Staff Physician, ICU, Hôpital de Dourdan, Dourdan, France; Delphine Moreau, M.D., Staff Physician, ICU, Hôpital Saint Louis, Paris, France; Guillaume Thiery, M.D., Staff Physician, ICU, Hôpital Saint Louis, Paris, France; Alexandre Duguet, M.D., Attending Physician, Hôpital Pitié-Salpétriere, Paris, France; Christian Laplace, M.D., Attending Physician, ICU, Hôpital Kremlin-Bicêtre, Bicêtre, France; and Thierry Lazard, M.D., Staff Physician, ICU, Hôpital de la Croix St Simon, Paris, France. Cited Here...
## SAS macro procedure. Available at: http://www.outcomerea.org/ehtm/matchmacro.pdf
. Accessed September 30, 2005. Cited Here...
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