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Original Research: CRITICAL CARE |

Severe Sepsis in Community-Acquired Pneumonia*: When Does It Happen, and Do Systemic Inflammatory Response Syndrome Criteria Help Predict Course?

Tony Dremsizov, MBA; Gilles Clermont, MD, CM, FCCP; John A. Kellum, MD, FCCP; Kenneth G. Kalassian, MD, FCCP; Michael J. Fine, MD; Derek C. Angus, MD, MPH, FCCP
Author and Funding Information

*From the CRISMA Laboratory, Department of Critical Care Medicine (Mr. Dremsizov, and Drs. Clermont, Kellum, and Angus), and Division of General Internal Medicine, Department of Medicine (Dr. Fine), University of Pittsburgh School of Medicine, Pittsburgh, PA; and Surgical Intensive Care (Dr. Kalassian), Emory University Hospital, Atlanta, GA.

Correspondence to: Gilles Clermont, MD, CM, 606 Scaife Hall, the CRISMA Laboratory, Critical Care Medicine, University of Pittsburgh, 3550 Terrace St, Pittsburgh, PA 15261; e-mail: clermontg@ccm.upmc.edu



Chest. 2006;129(4):968-978. doi:10.1378/chest.129.4.968
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Study objectives: Most natural history studies of severe sepsis are limited to ICU populations. We describe the onset and timing of severe sepsis during the hospital course for patients hospitalized with community-acquired pneumonia (CAP). We also determine the ability of the systemic inflammatory response syndrome (SIRS) and other proposed risk stratification scores measured at emergency department (ED) presentation to predict progression to severe sepsis, septic shock, or death.

Design: Retrospective analysis of a prospective observational outcome study from the Pneumonia Patient Outcomes Research Team (PORT).

Setting: Four academic medical centers in the United States and Canada between October 1991 and March 1994.

Participants: The 1,339 patients hospitalized for CAP in the PORT study cohort, and a random subset of 686 patients for whom we had information for SIRS criteria.

Interventions: None.

Measurements and results: All subjects had infection (CAP). Severe sepsis was defined as new-onset acute organ dysfunction in this cohort, using consensus criteria. Severe sepsis developed in one half of the patients (n = 639, 48%), nonpulmonary organ dysfunction developed in 520 patients (39%), and septic shock developed in 61 subjects (4.5%). Severe sepsis and septic shock were present at ED presentation in 457 patients (71% of severe sepsis cases) and 27 patients (44% of septic shock cases), respectively. While SIRS was common at presentation (82% of the subset of 686 had two SIRS criteria), it was not associated with increased odds for progression to severe sepsis (odds ratios [ORs], 0.65 and 0.89 for two or more SIRS criteria and three or more SIRS criteria, respectively), septic shock (ORs, 0.80 and 0.55), or death (ORs, 0.65 and 0.39), with poor discrimination (all receiver operating characteristic [ROC] areas under the curve < 0.5). The pneumonia severity index was associated with severe sepsis (p < 0.001) with moderate discrimination (ROC, 0.63).

Conclusions: Severe sepsis is common in hospitalized CAP patients, occurring early in the hospital course. SIRS criteria do not appear to be useful predictors for progression to severe sepsis in CAP.

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