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Volume 37, Issue 1, Pages 67-71 (January 2008)


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The impact of carvedilol on the defibrillation threshold

Brian F. McBride, PharmDa, C. Michael White, PharmD, FCCP, FCPbc, James S. Kalus, PharmD, BCPSbc, Danette C. Guertin, MSN, APRNd, Christopher A. Clyne, MDd, William L. Baker, PharmD, BCPSe, Jeffery Kluger, MD, FACCdfCorresponding Author Informationemail address

Background

Defibrillation threshold (DFT) is the minimum energy required to successfully terminate ventricular fibrillation. Epinephrine has been shown to increase the DFT in the beta-blocker naïve, but using cardioselective beta-blockers leads to a reduction in the DFT on infusion of epinephrine and norepinephrine. We sought to determine the impact of carvedilol therapy on the DFT after infusion of epinephrine and norepinephrine.

Methods

DFT was determined in patients receiving carvedilol by the step-down method (baseline DFT), and then patients (n = 27, 67.3 years, 70.0% were male, average left ventricular ejection fraction = 19%) were randomized to a 7-minute infusion of norepinephrine, epinephrine, or placebo in a double-blind manner. After the study drug infusion, DFT testing was repeated (experimental DFT) and results were compared between groups.

Results

No differences in intragroup DFTs were observed among carvedilol-treated patients receiving norepinephrine (9.4 ± 4.6 J vs 11.1 ± 7.8 J; P = .589), epinephrine (10.6 ± 5.3 J vs 9.8 ± 6.3 J; P = .779), or placebo (11.1 ± 7.0 vs 8.5 ± 4.2; P = .349).

Conclusions

Carvedilol prevents alterations in DFT produced by stress levels of catecholamines.

a Division of Clinical Pharmacology and John A. Oates Institute for Experimental Therapeutics, Vanderbilt University School of Medicine, Nashville, Tennessee

b University of Connecticut School of Pharmacy, Storrs, Connecticut

c Hartford Hospital Division of Cardiology and Drug Information, Hartford, Connecticut

d Hartford Hospital Division of Cardiology, Hartford, Connecticut

e Hartford Hospital/University of Connecticut, Hartford, Connecticut

f University of Connecticut School of Medicine; Farmington, Connecticut.

Corresponding Author InformationReprint requests: Jeffrey Kluger, MD, FACC, Hartford Hospital, 80 Seymour Street Suite 1001 Hartford, CT 06102-5037.

 This study was funded by a Hartford Hospital Research Grant.

PII: S0147-9563(07)00090-8

doi:10.1016/j.hrtlng.2007.04.005


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