Document Detail


Effect of amiodarone and sotalol on ventricular defibrillation threshold: the optimal pharmacological therapy in cardioverter defibrillator patients (OPTIC) trial.
MedLine Citation:
PMID:  16818810     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Many patients with implanted cardioverter defibrillators (ICDs) receive adjunctive antiarrhythmic drug therapy, most commonly amiodarone or sotalol. The effects of these drugs on defibrillation energy requirements have not been previously assessed in a randomized controlled trial.
METHODS AND RESULTS: The Optimal Pharmacological Therapy in Cardioverter Defibrillator Patients (OPTIC) trial was a randomized clinical trial evaluating the efficacy of amiodarone plus beta-blocker and sotalol versus beta-blocker alone for reduction of ICD shocks. Within OPTIC, a prospectively designed substudy evaluated the effects of the 3 treatment arms on defibrillation energy requirements. Defibrillation thresholds (DFTs) were measured (binary step-down protocol) at baseline and again after 8 to 12 weeks of therapy in 94 patients, of whom 29 were randomized to receive beta-blocker therapy (control group), 35 to amiodarone plus beta-blocker, and 30 to sotalol. In the control group, the mean DFT decreased from 8.77+/-5.15 J at baseline to 7.13+/-3.43 J (P=0.027); in the amiodarone group, DFT increased from 8.53+/-4.29 to 9.82+/-5.84 J (P=0.091). In the sotalol group, DFT decreased from 8.09+/-4.81 to 7.20+/-5.30 J (P=0.21). DFT changes in the beta-blocker and the amiodarone group were significantly different (P=0.006). In all patients, adequate safety margins for defibrillation were maintained. No clinical variable predicted baseline DFT or changes in DFT on therapy.
CONCLUSIONS: Although amiodarone increased DFT, the effect size with modern ICD systems is very small. Therefore, DFT reassessment after the institution of antiarrhythmic drug therapy with amiodarone or sotalol is not routinely required.
Authors:
Stefan H Hohnloser; Paul Dorian; Robin Roberts; Michael Gent; Carsten W Israel; Eric Fain; Jean Champagne; Stuart J Connolly
Publication Detail:
Type:  Comparative Study; Journal Article; Randomized Controlled Trial     Date:  2006-07-03
Journal Detail:
Title:  Circulation     Volume:  114     ISSN:  1524-4539     ISO Abbreviation:  Circulation     Publication Date:  2006 Jul 
Date Detail:
Created Date:  2006-07-11     Completed Date:  2006-08-14     Revised Date:  2013-05-28    
Medline Journal Info:
Nlm Unique ID:  0147763     Medline TA:  Circulation     Country:  United States    
Other Details:
Languages:  eng     Pagination:  104-9     Citation Subset:  AIM; IM    
Affiliation:
Department of Medicine, Division of Cardiology, J.W. Goethe University, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany. Hohnloser@em.uni-frankfurt.de
Data Bank Information
Bank Name/Acc. No.:
ClinicalTrials.gov/NCT00257959
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MeSH Terms
Descriptor/Qualifier:
Adrenergic beta-Antagonists / therapeutic use
Aged
Amiodarone / therapeutic use*
Anti-Arrhythmia Agents / therapeutic use*
Atrial Fibrillation / physiopathology
Bisoprolol / therapeutic use
Carbazoles / therapeutic use
Combined Modality Therapy
Defibrillators, Implantable*
Female
Heart Arrest
Humans
Male
Metoprolol / therapeutic use
Middle Aged
Myocardial Infarction / physiopathology
Propanolamines / therapeutic use
Sotalol / therapeutic use*
Ventricular Fibrillation / drug therapy*,  surgery*
Ventricular Function, Left
Chemical
Reg. No./Substance:
0/Adrenergic beta-Antagonists; 0/Anti-Arrhythmia Agents; 0/Carbazoles; 0/Propanolamines; 0K47UL67F2/carvedilol; 1951-25-3/Amiodarone; 37350-58-6/Metoprolol; 3930-20-9/Sotalol; 66722-44-9/Bisoprolol
Comments/Corrections
Comment In:
Circulation. 2006 Jul 11;114(2):98-100   [PMID:  16831995 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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