TY - JOUR
T1 - Comparative cost-effectiveness analysis of quinidine, procainamide and mexiletine
AU - Podrid, Philip J.
AU - Kowey, Peter R.
AU - Frishman, William H.
AU - Goldberg Arnold, Renée J.
AU - Kaniecki, Diana J.
AU - Beck, J. Robert
AU - Beshansky, Joni R.
N1 - Funding Information:
From the Cardiac Arrhythmia Service, University Hospital, Boston, Massachusetts; Lankenau Hospital, and Jefferson Medical School, Philadelphia, Pennsylvania; the Departments of Medicine and Epidemiology, Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, New York; Pharmacon International, Inc., New York, New York, and the Arnold and Marie Schwartz College of Pharmacy and Health Scienceso f Long Island University, Brooklyn, New York; the Biomedical Information Communication Center and the Department of Pathology, Oregon Health SciencesU niversity, Portland, Ore gon; and the Division of Clinical Decision Making, Department of Medicine, New England Medical Center and Tufts University School of Medicine, Boston, MassachusettsT. his study was supported in part by a grant from Boehringer Ingelheim Pharmaceuticals,I nc., Danbury, Connecticut, and by ResearchC areer Development Award LMO0086 from the National Library of Medicine, Bethesda, Maryland. Manuscript received April 22,199l; revised manuscript receivedA ugust 14, 1991,a nd acceptedA ugust 18.
PY - 1991/12/15
Y1 - 1991/12/15
N2 - Quinidine and procainamide have the potential for major organ toxicity, whereas mexiletine has been reported to have little risk of organ toxicity, serious proarrhythmia or congestive heart failure, but a relatively high incidence of nuisance side effects. In light of the potential adverse effects of all antiarrhythmic agents as highlighted by the Cardiac Arrhythmia Suppression Trial, the relative cost-effectiveness of these 3 agents was assessed. Based on a review of >1,000 published reports, studies included in the analysis examined ≥1 of these agents in adults, with adequate efficacy or safety data, or both. The majority of studies assessed patients with symptomatic or malignant arrhythmias, or both. Data were analyzed using a decision analysis/cost-effectiveness model. Probabilities were averaged using techniques of meta-analysis. Costs were obtained from a university medical center costaccounting system and from expected follow-up visits to university clinics. Thirty-seven separate side effects were included in the analysis. In terms of overall cost, 12 months of mexiletine would engender $875, quinidine $1,239 and procainamide $1,911 of expenses. Mexiletine dominates the older agents in terms of cost per successful drug response, a result that holds over a wide range of efficacy and safety data. Analyses demonstrated no increase in all-cause mortality for quinidine and mexiletine over placebo, but a trend toward higher mortality with procainamide. The results suggest that mexiletine is a cost-saving alternative therapy for ventricular arrhythmias when adverse reactions are considered in addition to pharmaceutical costs and treatment efficacy.
AB - Quinidine and procainamide have the potential for major organ toxicity, whereas mexiletine has been reported to have little risk of organ toxicity, serious proarrhythmia or congestive heart failure, but a relatively high incidence of nuisance side effects. In light of the potential adverse effects of all antiarrhythmic agents as highlighted by the Cardiac Arrhythmia Suppression Trial, the relative cost-effectiveness of these 3 agents was assessed. Based on a review of >1,000 published reports, studies included in the analysis examined ≥1 of these agents in adults, with adequate efficacy or safety data, or both. The majority of studies assessed patients with symptomatic or malignant arrhythmias, or both. Data were analyzed using a decision analysis/cost-effectiveness model. Probabilities were averaged using techniques of meta-analysis. Costs were obtained from a university medical center costaccounting system and from expected follow-up visits to university clinics. Thirty-seven separate side effects were included in the analysis. In terms of overall cost, 12 months of mexiletine would engender $875, quinidine $1,239 and procainamide $1,911 of expenses. Mexiletine dominates the older agents in terms of cost per successful drug response, a result that holds over a wide range of efficacy and safety data. Analyses demonstrated no increase in all-cause mortality for quinidine and mexiletine over placebo, but a trend toward higher mortality with procainamide. The results suggest that mexiletine is a cost-saving alternative therapy for ventricular arrhythmias when adverse reactions are considered in addition to pharmaceutical costs and treatment efficacy.
UR - http://www.scopus.com/inward/record.url?scp=0026321759&partnerID=8YFLogxK
U2 - 10.1016/0002-9149(91)90326-G
DO - 10.1016/0002-9149(91)90326-G
M3 - Article
C2 - 1836102
AN - SCOPUS:0026321759
SN - 0002-9149
VL - 68
SP - 1662
EP - 1667
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 17
ER -