0
ARTICLE |

Incidence, Risk Factors, and Outcome of Severe Sepsis and Septic Shock in Adults: Title and subTitle BreakA Multicenter Prospective Study in Intensive Care Units FREE

Christian Brun-Buisson, MD; Françoise Doyon, MSc; Jean Carlet, MD; Pierre Dellamonica, MD; François Gouin, MD; Agnès Lepoutre, MD; Jean-Christophe Mercier, MD; Georges Offenstadt, MD; Bernard Régnier, MD
[+] Author Affiliations

A complete list of the participants in the French ICU Group for Severe Sepsis appears at the end of this article.

Reprint requests to Service de Réanimation Médicale, Hôpital Henri Mondor, 94010, Créteil, France (Dr Brun-Buisson).

Concepts in Emergency and Critical Care section editor: Roger C. Bone, MD, Consulting Editor, JAMA.

Advisory Panel: Bart Chernow, MD, Baltimore, Md; David Dantzker, MD, New Hyde Park, NY; Jerrold Leiken, MD, Chicago, Ill; Joseph E. Parrillo, MD, Chicago, Ill; William J. Sibbald, MD, London, Ontario; and Jean-Louis Vincent, MD, PhD, Brussels, Belgium.


JAMA. 1995;274(12):968-974. doi:10.1001/jama.1995.03530120060042
Text Size: A A A
Published online

Objective.  —To examine the incidence, risk factors, and outcome of severe sepsis in intensive care unit (ICU) patients.

Design and Setting.  —Inception cohort study from a 2-month prospective survey of 11 828 consecutive admissions to 170 adult ICUs of public hospitals in France.

Patients.  —Patients meeting clinical criteria for severe sepsis were included and classified as having documented infection (ie, documented severe sepsis, n=742), or a clinical diagnosis of infection without microbiological documentation (ie, culture-negative severe sepsis, n=310).

Main Outcome Measures.  —Hospital and 28-day mortality after severe sepsis.

Results.  —Clinically suspected sepsis and confirmed severe sepsis occurred in 9.0 (95% confidence interval [CI], 8.5 to 9.5) and 6.3 (95% CI, 5.8 to 6.7) of 100 ICU admissions, respectively. The 28-day mortality was 56% (95% CI, 52% to 60%) in patients with severe sepsis, and 60% (95% CI, 55% to 66%) in those with culture-negative severe sepsis. Major determinants of both early (<3 days) and secondary deaths in the whole cohort were the Simplified Acute Physiology Score (SAPS) II and the number of acute organ system failures. Other risk factors for early death included a low arterial blood pH (<7.33) (P<.001) and shock (P=.03), whereas secondary deaths were associated with the admission category (P<.001), a rapidly or ultimately fatal underlying disease (P<.001), a preexisting liver (P=.01) or cardiovascular (P=.002) insufficiency, hypothermia (P=.02), thrombocytopenia (P=.01), and multiple sources of infection (P=.02). In patients with documented sepsis, bacteremia was associated with early mortality (P=.03).

Conclusions.  —Only three of four patients presenting with clinically suspected severe sepsis have documented infection. However, patients with clinically suspected sepsis but without microbiological documentation and patients with documented infection share common risk factors and are at similarly high risk of death. In addition to the severity of illness score, acute organ failures and the characteristics of underlying diseases should be accounted for in stratification of patients and outcome analyses.(JAMA. 1995;274:968-974)

REFERENCES

American College of Chest Physicians/Society of Critical Care Medicine Consensus Committee.  Definitions for sepsis and organ failures and guidelines for the use of innovative therapies in sepsis. Chest . 1992;;101:1658-1662.
Bone RC.  Sepsis, the sepsis syndrome, multiorgan failure: a plea for comparable definitions. Ann Intern Med . 1991;;114:332-334.
Bone RC.  A critical evaluation of new agents for the treatment of sepsis. JAMA . 1991;;266:1686-1691.
Natanson C, Hoffman WD, Suffredini AF, Eichacker PQ, Danner RL.  Selected treatment strategies for septic shock based on proposed mechanisms of pathogenesis. Ann Intern Med . 1994;;120:771-783.
Wenzel RP.  Anti-endotoxin monoclonal antidodies: a second look. N Engl J Med . 1992;;326:1151-1152.
Warren HS, Danner RL, Munford RS.  Anti-endotoxin monoclonal antibodies. N Engl J Med . 1992;; 326:1153-1156.
Ziegler EJ, Fischer CJ, Sprung CL, et al.  Treatment of gram-negative bacteremia and septic shock with HA-IA human monoclonal antibody against endotoxin. N Engl J Med . 1991;;324:429-436.
Greenman RL, Schein RMH, Martin MA, et al.  A controlled clinical trial of E5 murine monoclonal IgM antibody to endotoxin in the treatment of gram-negative sepsis. JAMA . 1991;;266:1097-1102.
Knaus WA, Wagner DP, Draper EA, et al.  The APACHE III prognostic system: risk prediction of hospital mortality for critically ill hospitalized adults. Chest . 1991;;100:1619-1636.
Le Gall J-R, Lemeshow S, Saulnier F.  A new simplified acute physiology score based on a European-North American multicenter study. JAMA . 1993;;270:2957-2963.
Knaus WA, Draper EA, Wagner DP, Zimmerman JE.  APACHE II, a severity of disease classification system. Crit Care Med . 1985;;13:818-829.
McCabe WA, Jackson GG.  Gram-negative bacteremia, I: etiology and ecology. Arch Intern Med . 1962;;110:847-855.
Knaus WA, Draper EA, Wagner DP, Zimmerman JE.  Prognosis in acute organ system failure. Ann Surg . 1985;;202:685-693.
Dean AD, Dean JA, Burton JH, Dicker RC. Epi Info, Version 5.1: A Word Processing, Database, and Statistics Program for Epidemiology . Atlanta, Ga: Centers for Disease Control and Prevention; 1993;.
Epidemiological Graphic Estimation and Testing Package: Version 26.6 , 4th ed. Seattle, Wash: Statistics and Epidemiology Research Corp; 1993;.
SAS/STAT User's Guide: Version 6 , 4th ed. Cary, NC: SAS Institute Inc; 1990;.
Breslow NE, Day NE.  The analysis of case-control studies.  In: Statistical Methods in Cancer Research . Lyon, France: International Agency for Research on Cancer; 1980;.
Kaplan EL, Meier P.  Nonparametric estimation from incomplete information. J Am Stat Assoc . 1958;;53:457-481.
Cox DR.  Regression models and life-tables (with discussion). J R Stat Soc . 1972;;34( (B) ):248-275.
The Intravenous Immunoglobulin Collaborative Study Group.  Prophylactic intravenous administration of standard immune globulin as compared with core-lipopolysaccharide immune globulin in patients at high risk of postsurgical infection. N Engl J Med . 1992;;327:234-240.
The National Committee for the Evaluation of Centoxin.  The French national registry of HA-1A in septic shock: a cohort study of 600 patients. Arch Intern Med . 1994;;154:2484-2491.
Fisher CJ, Dhainaut JF, Opal SM, et al.  Recombinant human interleukin-1 receptor antagonist in the treatment of patients with the sepsis syndrome: results from a randomized, double-blind, placebo-controlled trial. JAMA . 1994;;271:1836-1843.
Peduzzi P, Shatney C, Sheagren J, Sprung C.  Predictors of bacteremia and gram-negative bacteremia in patients with sepsis. Arch Intern Med . 1992;;152:529-535.
Bone RC, Fisher CJ, Clemmer TP, et al.  Sepsis syndrome: a valid clinical entity. Crit Care Med . 1989;;17:389-393.
Rangel-Frausto MS, Pittet D, Costignan M, Hwang T, Davis CS, Wenzel RP.  The natural history of the systemic inflammatory response syndrome (SIRS): a prospective study. JAMA . 1995;; 273:117-123.
Weinstein MP, Reller LB, Murphy JR, Lichtenstein KA.  The clinical significance of positive blood cultures: a comprehensive analysis of 500 episodes of bacteremia and fungemia in adults, II: clinical observations with special reference to factors influencing prognosis. Rev Infect Dis . 1983;;5: 54-70.
Roberts FJ, Geere IW, Coldman A.  A threeyear study of positive blood cultures, with emphasis on prognosis. Rev Infect Dis . 1991;;13:34-46.
Knaus WA, Sun X, Nystrom PO, Wagner DP.  Evaluation of definitions for sepsis. Chest . 1992;; 101:1656-1662.
Knaus WA, Harrel FE, Fisher CJ, et al.  The clinical evaluation of new drugs for sepsis: a prospective study design based on survival analysis. JAMA . 1993;;270:1233-1241.
Lemeshow S, Le Gall J-R.  Modeling the severity of illness of ICU patients. JAMA . 1994;;272: 1049-1055.
Le Gall J-R, Lemeshow S, Leleu G, et al.  Customized probability models for early severe sepsis in adult intensive care patients. JAMA . 1995;;273: 644-650.

Figures

Tables

Interactive Graphics

Video

Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal

American College of Chest Physicians/Society of Critical Care Medicine Consensus Committee.  Definitions for sepsis and organ failures and guidelines for the use of innovative therapies in sepsis. Chest . 1992;;101:1658-1662.
Bone RC.  Sepsis, the sepsis syndrome, multiorgan failure: a plea for comparable definitions. Ann Intern Med . 1991;;114:332-334.
Bone RC.  A critical evaluation of new agents for the treatment of sepsis. JAMA . 1991;;266:1686-1691.
Natanson C, Hoffman WD, Suffredini AF, Eichacker PQ, Danner RL.  Selected treatment strategies for septic shock based on proposed mechanisms of pathogenesis. Ann Intern Med . 1994;;120:771-783.
Wenzel RP.  Anti-endotoxin monoclonal antidodies: a second look. N Engl J Med . 1992;;326:1151-1152.
Warren HS, Danner RL, Munford RS.  Anti-endotoxin monoclonal antibodies. N Engl J Med . 1992;; 326:1153-1156.
Ziegler EJ, Fischer CJ, Sprung CL, et al.  Treatment of gram-negative bacteremia and septic shock with HA-IA human monoclonal antibody against endotoxin. N Engl J Med . 1991;;324:429-436.
Greenman RL, Schein RMH, Martin MA, et al.  A controlled clinical trial of E5 murine monoclonal IgM antibody to endotoxin in the treatment of gram-negative sepsis. JAMA . 1991;;266:1097-1102.
Knaus WA, Wagner DP, Draper EA, et al.  The APACHE III prognostic system: risk prediction of hospital mortality for critically ill hospitalized adults. Chest . 1991;;100:1619-1636.
Le Gall J-R, Lemeshow S, Saulnier F.  A new simplified acute physiology score based on a European-North American multicenter study. JAMA . 1993;;270:2957-2963.
Knaus WA, Draper EA, Wagner DP, Zimmerman JE.  APACHE II, a severity of disease classification system. Crit Care Med . 1985;;13:818-829.
McCabe WA, Jackson GG.  Gram-negative bacteremia, I: etiology and ecology. Arch Intern Med . 1962;;110:847-855.
Knaus WA, Draper EA, Wagner DP, Zimmerman JE.  Prognosis in acute organ system failure. Ann Surg . 1985;;202:685-693.
Dean AD, Dean JA, Burton JH, Dicker RC. Epi Info, Version 5.1: A Word Processing, Database, and Statistics Program for Epidemiology . Atlanta, Ga: Centers for Disease Control and Prevention; 1993;.
Epidemiological Graphic Estimation and Testing Package: Version 26.6 , 4th ed. Seattle, Wash: Statistics and Epidemiology Research Corp; 1993;.
SAS/STAT User's Guide: Version 6 , 4th ed. Cary, NC: SAS Institute Inc; 1990;.
Breslow NE, Day NE.  The analysis of case-control studies.  In: Statistical Methods in Cancer Research . Lyon, France: International Agency for Research on Cancer; 1980;.
Kaplan EL, Meier P.  Nonparametric estimation from incomplete information. J Am Stat Assoc . 1958;;53:457-481.
Cox DR.  Regression models and life-tables (with discussion). J R Stat Soc . 1972;;34( (B) ):248-275.
The Intravenous Immunoglobulin Collaborative Study Group.  Prophylactic intravenous administration of standard immune globulin as compared with core-lipopolysaccharide immune globulin in patients at high risk of postsurgical infection. N Engl J Med . 1992;;327:234-240.
The National Committee for the Evaluation of Centoxin.  The French national registry of HA-1A in septic shock: a cohort study of 600 patients. Arch Intern Med . 1994;;154:2484-2491.
Fisher CJ, Dhainaut JF, Opal SM, et al.  Recombinant human interleukin-1 receptor antagonist in the treatment of patients with the sepsis syndrome: results from a randomized, double-blind, placebo-controlled trial. JAMA . 1994;;271:1836-1843.
Peduzzi P, Shatney C, Sheagren J, Sprung C.  Predictors of bacteremia and gram-negative bacteremia in patients with sepsis. Arch Intern Med . 1992;;152:529-535.
Bone RC, Fisher CJ, Clemmer TP, et al.  Sepsis syndrome: a valid clinical entity. Crit Care Med . 1989;;17:389-393.
Rangel-Frausto MS, Pittet D, Costignan M, Hwang T, Davis CS, Wenzel RP.  The natural history of the systemic inflammatory response syndrome (SIRS): a prospective study. JAMA . 1995;; 273:117-123.
Weinstein MP, Reller LB, Murphy JR, Lichtenstein KA.  The clinical significance of positive blood cultures: a comprehensive analysis of 500 episodes of bacteremia and fungemia in adults, II: clinical observations with special reference to factors influencing prognosis. Rev Infect Dis . 1983;;5: 54-70.
Roberts FJ, Geere IW, Coldman A.  A threeyear study of positive blood cultures, with emphasis on prognosis. Rev Infect Dis . 1991;;13:34-46.
Knaus WA, Sun X, Nystrom PO, Wagner DP.  Evaluation of definitions for sepsis. Chest . 1992;; 101:1656-1662.
Knaus WA, Harrel FE, Fisher CJ, et al.  The clinical evaluation of new drugs for sepsis: a prospective study design based on survival analysis. JAMA . 1993;;270:1233-1241.
Lemeshow S, Le Gall J-R.  Modeling the severity of illness of ICU patients. JAMA . 1994;;272: 1049-1055.
Le Gall J-R, Lemeshow S, Leleu G, et al.  Customized probability models for early severe sepsis in adult intensive care patients. JAMA . 1995;;273: 644-650.
CME Course for:


You need to register in order to view this quiz.


To understand the clinical management of acute heart failure syndromes.
Accreditation Information The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
Note: You must get at least of the answers correct to pass this quiz.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
To view and print your certificate and access a summary of your CME courses go to My CME.
NOTE:
Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s “Cited By” API will populate this tab (http://www.crossref.org/citedby.html).
Submit a Response

Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging & repositioning the boxes below.