4.6 Article

Procalcitonin increase in early identification of critically ill patients at high risk of mortality

Journal

CRITICAL CARE MEDICINE
Volume 34, Issue 10, Pages 2596-2602

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01.CCM.0000239116.01855.61

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Objective. To investigate day-by-day changes in procalcitonin and maximum obtained levels as predictors of mortality in critically ill patients. Design: Prospective observational cohort study. Setting. Multidisciplinary intensive care unit at Rigshospitalet, Copenhagen University Hospital, a tertiary reference hospital in Denmark. Patients: Four hundred seventy-two patients with diverse comorbidity and age admitted to this intensive care unit. Interventions. Equal in all patient groups: antimicrobial treatment adjusted according to the procalcitonin level. Measurements and Main Results., Daily procalcitonin measurements were carried out during the study period as well as measurements of white blood cell count and C-reactive protein and registration of comorbidity. The primary end point was all-cause mortality in a 90-day follow-up period. Secondary end points were mortality during the stay in the intensive care unit and in a 30-day follow-up period. A total of 3,642 procalcitonin measurements were evaluated in 472 critically ill patients. We found that a high maximum procalcitonin level and a procalcitonin increase for 1 day were independent predictors of 90-day all-cause mortality in the multivariate Cox regression analysis model. C-reactive protein and leukocyte increases did not show these qualities. The adjusted hazard ratio for procalcitonin increase for 1 day was 1.8 (95% confidence interval 1.3-2.7). The relative risk for mortality in the intensive care unit for patients with an increasing procalcitonin was as follows: after 1 day increase, 1.8 (95% confidence interval 1.4-2.4); after 2 days increase, 2.2 (95% confidence interval 1.6-3.0); and after 3 days increase: 2.8 (95% confidence interval 2.0-3.8). Conclusions. A high maximum procalcitonin level and a procalcitonin increase for 1 day are early independent predictors of all-cause mortality in a 90-day follow-up period after intensive care unit admission. Mortality risk increases for every day that procalcitonin increases. Levels or increases of C-reactive protein and white blood cell count do not seem to predict mortality.

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