Vasopressin for cardiac arrest: Meta-analysis of randomized controlled trials
Mentzelopoulus el al. Resuscitation. Published online 25 July 2011
Abstract
Background
Prior meta-analyses-reported results of randomised controlled trials (RCTs) published between 1997 and 2004 failed to show any vasopressin-related benefit in cardiac arrest. Based on new RCT-data and a hypothesis of a potentially increased vasoconstricting efficacy of vasopressin, we sought to determine whether the cumulative, current evidence supports or refutes an overall and/or selective benefit for vasopressin regarding sustained restoration of spontaneous circulation (ROSC), long-term survival, and neurological outcome.
Methods
Two reviewers independently searched PubMed, EMBASE, and Cochrane Database for RCTs assigning adults with cardiac arrest to treatment with a vasopressin-containing regimen (vasopressin-group) vs adrenaline (epinephrine) alone (control-group) and reporting on long-term outcomes. Data from 4,475 patients in 6 high-methodological quality RCTs were analysed. Subgroup analyses were conducted according to initial cardiac rhythm and time from collapse to drug administration (TDRUG) < 20
min.

Results
Vasopressin vs. control did not improve overall rates of sustained ROSC, long-term survival, or favourable neurological outcome. However, in asystole, vasopressin vs. control was associated with higher long-term survival {odds ratio (OR)
=
1.80, 95% confidence interval (CI)
=
1.04-3.12, P
=
0.04}. In asystolic patients of RCTs with average TDRUG < 20
min, vasopressin vs. control increased the rates of sustained ROSC (data available from 2 RCTs; OR
=
1.70, 95% CI
=
1.17-2.47, P
=
0.005) and long-term survival (data available from 3 RCTs; OR
=
2.84, 95% CI
=
1.19-6.79, P
=
0.02).



















Conclusions
Vasopressin use in the resuscitation of cardiac arrest patients is not associated with any overall benefit or harm. However, vasopressin may improve the long-term survival of asystolic patients, especially when average TDRUG is < 20
min.
