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Critical Care Medicine:
February 2009 - Volume 37 - Issue 2 - pp 410-416
doi: 10.1097/CCM.0b013e3181958b1c
Feature Articles

Influence of vasopressor agent in septic shock mortality. Results from the Portuguese Community-Acquired Sepsis Study (SACiUCI study) *

Póvoa, Pedro R. MD, PhD; Carneiro, António H. MD; Ribeiro, Orquídea S. BSc; Pereira, Altamiro C. MD, PhD; on behalf of the Portuguese Community-Acquired Sepsis Study Group

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Abstract

Objective: Guidelines for the adrenergic support of septic shock are controversial. In patients with community-acquired septic shock, we assessed the impact of the choice of vasopressor support on mortality.

Design: Cohort, multiple center, observational study.

Setting: Seventeen Portuguese intensive care units (ICUs).

Patients: All adult patients admitted to a participating ICU between December 2004 and November 2005.

Interventions: None.

Measurements and Main Results: Patients were followed up during the first five ICU days, the day of discharge or death, and hospital outcome. Eight hundred ninety-seven consecutive patients with community-acquired sepsis (median age, 63 years; 577 men; and hospital mortality, 38%) were studied. Of the 458 patients with septic shock, 73% received norepinephrine and 50.5% dopamine. The norepinephrine group had a higher hospital mortality (52% vs. 38.5%, p = 0.002). A Kaplan-Meier survival curve showed diminished 28-day survival in the norepinephrine group (log-rank = 22.6, p < 0.001). A Cox proportional hazard analysis revealed that the administration of norepinephrine was associated with an increased risk of death (adjusted hazard ratio, 2.501; 95% confidence interval, 1.413-4.425; p = 0.002). In a multivariate analysis with ICU mortality as the dependent factor, Simplified Acute Physiology Score II and norepinephrine administration were independent risk factors for ICU mortality in patients with septic shock.

Conclusions: In patients with community-acquired septic shock, our data suggest that norepinephrine administration could be associated with worse outcome.

© 2009 Lippincott Williams & Wilkins, Inc.

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