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• W1630391490 startingPage "e0129305" @default.
• W1630391490 abstract "International guidelines recommend dopamine or norepinephrine as first-line vasopressor agents in septic shock. Phenylephrine, epinephrine, vasopressin and terlipressin are considered second-line agents. Our objective was to assess the evidence for the efficiency and safety of all vasopressors in septic shock.Systematic review and meta-analysis. We searched electronic database of MEDLINE, CENTRAL, LILACS and conference proceedings up to June 2014. We included randomized controlled trials comparing different vasopressors for the treatment of adult patients with septic shock. Primary outcome was all-cause mortality. Other clinical and hemodynamic measurements were extracted as secondary outcomes. Risk ratios (RR) and mean differences with 95% confidence intervals (CI) were pooled.Thirty-two trials (3,544 patients) were included. Compared to dopamine (866 patients, 450 events), norepinephrine (832 patients, 376 events) was associated with decreased all-cause mortality, RR 0.89 (95% CI 0.81-0.98), corresponding to an absolute risk reduction of 11% and number needed to treat of 9. Norepinephrine was associated with lower risk for major adverse events and cardiac arrhythmias compared to dopamine. No other mortality benefit was demonstrated for the comparisons of norepinephrine to epinephrine, phenylephrine and vasopressin / terlipressin. Hemodynamic data were similar between the different vasopressors, with some advantage for norepinephrine in central venous pressure, urinary output and blood lactate levels.Evidence suggests a survival benefit, better hemodynamic profile and reduced adverse events rate for norepinephrine over dopamine. Norepinephrine should be regarded as the first line vasopressor in the treatment of septic shock." @default.
• W1630391490 created "2016-06-24" @default.
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• W1630391490 date "2015-08-03" @default.
• W1630391490 modified "2023-10-12" @default.
• W1630391490 title "Vasopressors for the Treatment of Septic Shock: Systematic Review and Meta-Analysis" @default.
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• W1630391490 doi "https://doi.org/10.1371/journal.pone.0129305" @default.
• W1630391490 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4523170" @default.
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• W1630391490 hasPublicationYear "2015" @default.
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