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Vasopressin, Epinephrine, and Corticosteroids for In-Hospital Cardiac Arrest
Spyros D. Mentzelopoulos, MD, PhD;
Spyros G. Zakynthinos, MD, PhD;
Maria Tzoufi, MD, PhD;
Nikos Katsios, MD;
Androula Papastylianou, MD;
Sotiria Gkisioti, MD;
Anastasios Stathopoulos, MD;
Androniki Kollintza, PhD;
Elissavet Stamataki, MD, PhD;
Charis Roussos, MD, PhD
Arch Intern Med. 2009;169(1):15-24.
Background Animal data on cardiac arrest showed improved long-term survival with combined vasopressin-epinephrine. In cardiac arrest, cortisol levels are relatively low during and after cardiopulmonary resuscitation. We hypothesized that combined vasopressin-epinephrine and corticosteroid supplementation during and after resuscitation may improve survival in refractory in-hospital cardiac arrest.
Methods We conducted a single-center, prospective, randomized, double-blind, placebo-controlled, parallel-group trial. We enrolled 100 consecutive patients with cardiac arrest requiring epinephrine according to current resuscitation guidelines. Patients received either vasopressin (20 IU per cardiopulmonary resuscitation cycle) plus epinephrine (1 mg per resuscitation cycle) (study group; n = 48) or isotonic sodium chloride solution placebo plus epinephrine (1 mg per resuscitation cycle) (control group; n = 52) for the first 5 resuscitation cycles after randomization, followed by additional epinephrine if needed. On the first resuscitation cycle, study group patients received methylprednisolone sodium succinate (40 mg) and controls received saline placebo. Postresuscitation shock was treated with stress-dose hydrocortisone sodium succinate (300 mg daily for 7 days maximum, with gradual taper) (27 patients in the study group) or saline placebo (15 patients in the control group). Primary end points were return of spontaneous circulation for 15 minutes or longer and survival to hospital discharge.
Results Study group patients vs controls had more frequent return of spontaneous circulation (39 of 48 patients [81%] vs 27 of 52 [52%]; P = .003) and improved survival to hospital discharge (9 [19%] vs 2 [4%]; P = .02). Study group patients with postresuscitation shock vs corresponding controls had improved survival to hospital discharge (8 of 27 patients [30%] vs 0 of 15 [0%]; P = .02), improved hemodynamics and central venous oxygen saturation, and more organ failure–free days. Adverse events were similar in the 2 groups.
Conclusion In this single-center trial, combined vasopressin-epinephrine and methylprednisolone during resuscitation and stress-dose hydrocortisone in postresuscitation shock improved survival in refractory in-hospital cardiac arrest.
Trial Registration clinicaltrials.gov Identifier: NCT00411879
Author Affiliations: First Department of Intensive Care Medicine, University of Athens Medical School (Drs Mentzelopoulos, Zakynthinos, Tzoufi, Kollintza, and Roussos); and Department of Anesthesiology, Evaggelismos General Hospital (Drs Katsios, Papastylianou, Gkisioti, Stathopoulos, and Stamataki), Athens, Greece.
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