Adherence and arrhythmic mortality in the Cardiac Arrhythmia Suppression Trial (CAST)

被引:17
作者
ObiasManno, D
Friedmann, E
Brooks, MM
Thomas, SA
Haakenson, C
Morris, M
Wimbush, F
Somelofski, C
Goldner, F
机构
[1] WASHINGTON HOSP CTR, WASHINGTON, DC 20010 USA
[2] CUNY BROOKLYN COLL, BROOKLYN, NY 11210 USA
[3] LIFE CARE HLTH FDN, ELLICOTT CITY, MD USA
[4] CLIN RES PHARM CTR, COOPERAT STUDIES PROGRAM, ALBUQUERQUE, NM USA
[5] MED COLL OHIO, TOLEDO, OH 43699 USA
[6] SAN FRANCISCO GEN HOSP, SAN FRANCISCO, CA 94110 USA
[7] VANDERBILT UNIV, NASHVILLE, TN USA
[8] CAST COORDINATING CTR, TOLEDO, OH USA
基金
美国国家卫生研究院;
关键词
coronary heart disease; myocardial infarction; survival; treatment efficacy; medication compliance; clinical trials; drug adherence;
D O I
10.1016/1047-2797(95)00134-4
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Patient adherence to therapy is essential to assess treatment efficacy, particularly in clinical trials. Active treatment usually is expected to benefit patients. The healthy adherer effect, the association or greater adherence to all health-promoting behaviors, including medication and overall concern for health, explains the improved survival of more adherent patients in both active and placebo medication groups of several clinical trials. The Cardiac Arrhythmia Suppression Trial (CAST), a placebo-controlled double-blind clinical trial of post-myocardial infarction (MI) patients with asymptomatic ventricular arrhythmias, in which active medication (encainide or flecainide) led to increased mortality, provided an opportunity to examine the relationship of adherence to survival from a different perspective. We consider whether adherence to active treatment was related to arrhythmic mortality and whether a healthy adherer effect might counteract the effect of treatment on mortality among patients taking active medication. Adherence (average pill count) at the first follow-up visit did not differ in the active treatment (92.2%, standard deviation (SD) = 11.97, n = 574) and placebo (90.8%, SD = 13.66, n = 579) groups. In a Cox proportional hazard regression model, medication adherence Predicted arrhythmic mortality among the active (P < 0.0062) but not the placebo medication group. The effect of adherence on arrhythmic mortality was significant beyond the effects of ejection fraction, race, spouse, smoking status, diuretic medication, and history of MI. A 10% increase in adherence led to more than a threefold increase of risk of arrhythmic death. The design of the CAST, which included a titration phase, may have tended to select relatively adherent patients since only those whose arrhythmias were suppressed with active medication were randomized into the trial. The data do not support a strong healthy adherer effect in the CAST. There was no evidence in this study that a healthy adherer effect counterbalanced the effect of the active medication.
引用
收藏
页码:93 / 101
页数:9
相关论文
共 18 条
[1]  
[Anonymous], 1989, NEW ENGL J MED, V321, P406
[2]  
[Anonymous], 1979, Compliance in Health Care
[3]   COMPLIANCE TO TREATMENT FOR HYPERTENSION IN ELDERLY PATIENTS - THE SHEP PILOT-STUDY [J].
BLACK, DM ;
BRAND, RJ ;
GREENLICK, M ;
HUGHES, G ;
SMITH, J .
JOURNALS OF GERONTOLOGY, 1987, 42 (05) :552-557
[4]   THE RUN-IN PERIOD IN CLINICAL-TRIALS - THE EFFECT OF MISCLASSIFICATION ON EFFICIENCY [J].
BRITTAIN, E ;
WITTES, J .
CONTROLLED CLINICAL TRIALS, 1990, 11 (05) :327-338
[5]  
CANNER PL, 1980, NEW ENGL J MED, V303, P1038
[6]   MORTALITY AND MORBIDITY IN PATIENTS RECEIVING ENCAINIDE, FLECAINIDE, OR PLACEBO - THE CARDIAC-ARRHYTHMIA SUPPRESSION TRIAL [J].
ECHT, DS ;
LIEBSON, PR ;
MITCHELL, LB ;
PETERS, RW ;
OBIASMANNO, D ;
BARKER, AH ;
ARENSBERG, D ;
BAKER, A ;
FRIEDMAN, L ;
GREENE, HL ;
HUTHER, ML ;
RICHARDSON, DW .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (12) :781-788
[7]  
FEINSTEIN AR, 1979, COMPLIANCE HLTH CARE, P309
[8]   CAN DROPOUT AND OTHER NON-COMPLIANCE BE MINIMIZED IN A CLINICAL-TRIAL - REPORT FROM THE VETERANS-ADMINISTRATIVE-NATIONAL-HEART-LUNG-AND-BLOOD-INSTITUTE COOPERATIVE STUDY ON ANTIHYPERTENSIVE THERAPY - MILD HYPERTENSION [J].
GOLDMAN, AI ;
HOLCOMB, R ;
PERRY, HM ;
SCHNAPER, HW ;
FITZ, AE ;
FROHLICH, ED .
CONTROLLED CLINICAL TRIALS, 1982, 3 (02) :75-89
[9]  
GOLDSMITH CH, 1979, COMPLIANCE HLTH CARE, P297
[10]  
GRIFFITH S, 1990, BRIT J GEN PRACT, V40, P114