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Drotrecogin alfa (activated) for severe sepsis: Could we consider a shorter treatment period in patients with a favorable course? Journal of critical care [J Crit Care] Journal article

 
TitleDrotrecogin alfa (activated) for severe sepsis: Could we consider a shorter treatment period in patients with a favorable course?
Author(s)Ahishakiye D, Lorent S, De Backer D, Gottignies P, Vincent JL 
InstitutionDepartment of Intensive Care, Erasme Hospital, Université Libre de Bruxelles, 1070 Brussels, Belgium.
SourceJ Crit Care 2009 Jul 2.
AbstractPURPOSE: The objective of this study was to develop a model to identify patients in whom drotrecogin alfa (activated) (DAA) might be administered for periods shorter than the recommended 96 hours.
METHODS: We did a retrospective chart review of all 124 patients treated with a standard 96-hour infusion of DAA in a 31-bed department of intensive care. Using a stepwise approach, we identified and combined parameters that could help predict outcomes to achieve the best sensitivity associated with 100% specificity.
RESULTS: Twenty-one (17%) of the 124 patients had a favorable outcome (left the intensive care unit within 5 days of DAA initiation); of these, 11 had an increase in arterial pH in the first 24 hours of treatment compared with 22 (21%) of the 103 patients with intermediate (intensive care unit stay >5 days after DAA initiation) or unfavorable (died within 5 days of DAA initiation) outcomes (P = not significant). Eight (72.7%) of these 11 patients and no other patient showed a decrease in sequential organ failure assessment score of at least 50% during the first 24 hours (P < .001). By combining these 2 variables, we could identify, with 100% specificity, 8 of the patients with a favorable outcome (38%) who made a prompt recovery.
CONCLUSIONS: A simple model based on sequential organ failure assessment score and arterial pH can help identify patients with a rapid favorable course in whom a shorter duration of DAA treatment may be justified.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19577419
  
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