Mortality and Morbidity During and After the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial

被引:47
作者
Cushman, William C. [2 ]
Davis, Barry R.
Pressel, Sara L. [1 ]
Cutler, Jeffrey A. [3 ]
Einhorn, Paula T. [3 ]
Ford, Charles E.
Oparil, Suzanne [4 ]
Probstfield, Jeffrey L. [5 ]
Whelton, Paul K. [6 ]
Wright, Jackson T., Jr. [7 ]
Alderman, Michael H. [8 ]
Basile, Jan N. [9 ]
Black, Henry R. [10 ]
Grimm, Richard H., Jr. [11 ]
Hamilton, Bruce P. [12 ]
Haywood, L. Julian [13 ]
Ong, Stephen T. [14 ]
Piller, Linda B.
Simpson, Lara M.
Stanford, Carol [15 ]
Weiss, Robert J. [16 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Univ Texas Houston, ALLHAT Clin Trials Ctr, Sch Publ Hlth, Houston, TX 77030 USA
[2] Memphis Vet Affairs Med Ctr, Memphis, TN USA
[3] Natl Heart Lung & Blood Inst, Bethesda, MD USA
[4] Univ Alabama Birmingham, Sch Med, Birmingham, AL USA
[5] Univ Washington, Med Ctr, Seattle, WA 98195 USA
[6] Loyola Univ, Med Ctr, Maywood, IL 60153 USA
[7] Case Western Reserve Univ, Med Ctr, Cleveland, OH 44106 USA
[8] Albert Einstein Coll Med, Bronx, NY 10467 USA
[9] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC USA
[10] NYU, Langone Med Ctr, New York, NY USA
[11] Berman Ctr Outcomes & Clin Res, Minneapolis, MN USA
[12] Baltimore Vet Adm, Med Ctr, Baltimore, MD USA
[13] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[14] Healthcare Greater Washington, Oxon Hill, MD USA
[15] Univ Missouri, Kansas City Sch Med, Kansas City, MO 64110 USA
[16] Androscoggin Cardiol Associates, Auburn, AL USA
关键词
CONVERTING-ENZYME-INHIBITOR; CARDIOVASCULAR EVENTS; BLOOD-PRESSURE; FOLLOW-UP; RAMIPRIL; OUTCOMES; THERAPY; RISK; PARTICIPANTS; HYPERTENSION;
D O I
10.1111/j.1751-7176.2011.00568.x
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
A randomized, double-blind, active-controlled, multicenter trial assigned 32,804 participants aged 55 years and older with hypertension and =1 other coronary heart disease risk factors to receive chlorthalidone (n=15,002), amlodipine (n=8898), or lisinopril (n=8904) for 4 to 8 years, when double-blinded therapy was discontinued. Passive surveillance continued for a total follow-up of 8 to 13 years using national administrative databases to ascertain deaths and hospitalizations. During the post-trial period, fatal outcomes and nonfatal outcomes were available for 98% and 65% of participants, respectively, due to lack of access to administrative databases for the remainder. This paper assesses whether mortality and morbidity differences persisted or new differences developed during the extended follow-up. Primary outcome was cardiovascular mortality and secondary outcomes were mortality, stroke, coronary heart disease, heart failure, cardiovascular disease, and end-stage renal disease. For the post-trial period, data are not available on medications or blood pressure levels. No significant differences (P<.05) appeared in cardiovascular mortality for amlodipine (hazard ratio [HR], 1.00; 95% confidence interval [CI], 0.931.06) or lisinopril (HR, 0.97; CI, 0.901.03), each compared with chlorthalidone. The only significant differences in secondary outcomes were for heart failure, which was higher with amlodipine (HR, 1.12; CI, 1.021.22), and stroke mortality, which was higher with lisinopril (HR, 1.20; CI, 1.011.41), each compared with chlorthalidone. Similar to the previously reported in-trial result, there was a significant treatment-by-race interaction for cardiovascular disease for lisinopril vs chlorthalidone. Black participants had higher risk than non-black participants taking lisinopril compared with chlorthalidone. After accounting for multiple comparisons, none of these results were significant. These findings suggest that neither calcium channel blockers nor angiotensin-converting enzyme inhibitors are superior to diuretics for the long-term prevention of major cardiovascular complications of hypertension. J Clin Hypertens (Greenwich). 2012; 14: 20-31. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:20 / 31
页数:12
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