• Surgical infections · Apr 2007

    Clinical Trial

    Addition of vasopressin to norepinephrine as independent predictor of mortality in patients with refractory septic shock: an observational study.

    • Scott T Micek, Poorvi Shah, James M Hollands, Rina A Shah, William D Shannon, and Marin H Kollef.
    • Department of Pharmacy, Barnes-Jewish Hospital, St Louis, MO, USA.
    • Surg Infect (Larchmt). 2007 Apr 1;8(2):189-200.

    ObjectiveTo identify predictors of 28-day mortality among patients with refractory septic shock treated with norepinephrine with or without vasopressin.DesignProspective observational cohort study.SettingA 1,200-bed academic medical center.PatientsOne hundred thirty-seven patients with septic shock treated with norepinephrine with or without vasopressin.InterventionsNone.Measurements And Main ResultsThe 28-day mortality rate was 37.2% (n = 51). By multivariate analysis, significant predictors of death were norepinephrine plus vasopressin administration (adjusted odds ratio [AOR], 13.96; 95% confidence interval [CI] 6.47, 30.08; p = 0.001), lack of goal-directed fluid administration during initial resuscitation (AOR 15.82; 95% CI 6.16, 40.61; p = 0.003), inappropriate initial antimicrobial therapy (AOR 8.95; 95% CI 2.93, 27.33; p = 0.05), and higher Acute Physiology and Chronic Health Evaluation (APACHE) II score (AOR 1.14; 95% CI 1.07, 1.21; p = 0.033). Patients who received norepinephrine plus vasopressin (n = 68) had a significantly higher mortality rate than patients managed with norepinephrine alone (n = 69) 28 days after the initiation of vasopressors (54.4% vs. 20.3%; p < 0.001). This finding was confirmed in patients matched optimally across treatment groups.ConclusionsOur study found an association between the use of norepinephrine plus vasopressin and 28-day mortality in refractory septic shock. In view of its known mechanism of action, vasopressin contributed to this excess mortality. Further recommendations regarding the use of vasopressin await the results of large randomized trials evaluating its efficacy and safety for septic shock.

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