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Published ahead of print on November 5, 2004, doi:10.1164/rccm.200403-324OC
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American Journal of Respiratory and Critical Care Medicine Vol 171. pp. 461-468, (2005)
© 2005 American Thoracic Society
doi: 10.1164/rccm.200403-324OC


Original Article

Systemic Inflammatory Response and Progression to Severe Sepsis in Critically Ill Infected Patients

Corinne Alberti, Christian Brun-Buisson, Sylvie Chevret, Massimo Antonelli, Sergey V. Goodman, Claudio Martin, Rui Moreno, Ana R. Ochagavia, Mark Palazzo, Karl Werdan and Jean Roger Le Gall for the European Sepsis Study Group

Clinical Epidemiology Unit, Hôpital Robert Debré; Department of Medical Biostatistics, Hôpital Saint-Louis; and Medical Intensive Care Unit, Hôpital Saint-Louis, Assistance Publique—Hôpitaux de Paris, Université Paris VII, Paris; and Medical Intensive Care Unit, Hôpital Henri-Mondor, Assistance Publique-Hôpitaux de Paris, Université Paris XII, Créteil, France; Istituto di Anestesiologia e Rianimazione, Universita Cattolica del Sacro Cuore, Policlinico A. Gemelli, Rome, Italy; General Intensive Care Unit, Department of Anesthesiology and Critical Care Medicine, Hadassah Hebrew University Medical Center, Jerusalem, Israël; Critical Care-Trauma Centre, London Health Sciences Centre, London, Ontario, Canada; Intensive Care Unit, Santo Antonio dos Capuchos Hospital, Lisboa, Portugal; Intensive Care Unit, Parc Tauli Hospital, Red Gina, Spain; Intensive Care Unit, Charing Cross Hospital, London, United Kingdom; and Universitatsklinik und Poliklinik fur Innere Medizin III, Klinikum Krollwitz der Martin-Luther-Universitat Halle-Wittenberg, Halle, Germany

Correspondence and requests for reprints should be addressed to Dr Christian Brun-Buisson, Service de Réanimation Médicale, Hôpital Henri Mondor, 94000 Créteil, France. Email: christian.brun-buisson{at}hmn.ap-hop-paris.fr

Rationale: The systemic inflammatory response syndrome has low specificity to identify infected patients at risk of worsening to severe sepsis or shock. Objective: To examine the incidence of and risk factors for worsening sepsis in infected patients. Methods: A 1-year inception cohort study in 28 intensive care units of patients (n = 1,531) having a first episode of infection on admission or during the stay. Measurements and main results: The cumulative incidence of progression to severe sepsis or shock was 20% and 24% at Days 10 and 30, respectively. Variables independently associated (hazard ratio [HR]) with worsening sepsis included: temperature higher than 38.2°C (1.6), heart rate greater than 120/minute (1.3), systolic blood pressure higher than 110 mm Hg (1.5), platelets higher than 150 x 109/L (1.5), serum sodium higher than 145 mmol/L (1.5), bilirubin higher than 30 µmol/L (1.3), mechanical ventilation (1.5), and five variables characterizing infection (pneumonia [HR 1.5], peritonitis [1.5], primary bacteremia [1.8], and infection with gram-positive cocci [1.3] or aerobic gram-negative bacilli [1.4]). The 12 weighted variables were included in a score (Risk of Infection to Severe Sepsis and Shock Score, range 0–49), summarized in four classes of "low" (score 0–8) and "moderate" (8.5–16) risk (9% and 17% probability of worsening, respectively), and of "high" (16.5–24) and "very high" (score > 24) risk (31% and 55% probability, respectively). Conclusions: One of four patients presenting with infection/sepsis worsen to severe sepsis or shock. A score estimating this risk, using objectively defined criteria for systemic inflammatory response syndrome, could be used by physicians to stratify patients for clinical management and to test new interventions.

Key Words: infection, intensive care units, multivariable models, risk prediction, sepsis, septic shock




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