Uses of polypills for cardiovascular disease and evidence to date

被引:86
作者
Huffman, Mark D. [1 ]
Xavier, Denis [2 ,3 ,4 ]
Perel, Pablo [5 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL 60611 USA
[2] St Johns Natl Acad Hlth Sci, Dept Pharmacol, Bangalore, Karnataka, India
[3] St Johns Natl Acad Hlth Sci, Div Clin Res, St Johns Med Coll, Bangalore, Karnataka, India
[4] St Johns Natl Acad Hlth Sci, Res Inst, Bangalore, Karnataka, India
[5] London Sch Hyg & Trop Med, Ctr Global Noncommunicable Dis Epidemiol, London, England
基金
加拿大健康研究院;
关键词
DOSE COMBINATION THERAPY; HIGH-RISK; PRIMARY PREVENTION; DOUBLE-BLIND; RANDOMIZED-TRIAL; NATIONAL-HEALTH; BLOOD-PRESSURE; STRATEGY; ADHERENCE; HYPERTENSION;
D O I
10.1016/S0140-6736(17)30553-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Polypills have been approved in more than 30 countries, but worldwide experience with and availability of polypills remain limited, unlike fixed-dose combinations in other diseases such as HIV, tuberculosis, and malaria. In this Series review, we aim to propose a guide for the use of polypills in future research and clinical activities and to synthesise contemporary evidence supporting the use of polypills for prevention of atherosclerosis. Polypill uses can be categorised by population and indication, both of which influence the balance between benefits and risks. Populations include secondary prevention, high-risk primary prevention based on formal risk assessment, and primary prevention based on single risk factor measurement, such as age, also known as mass treatment. For each population, potential indications are initiation, step-up of current drug therapy, and straight substitution of individual drug components. We summarise efficacy and safety results from 13 polypill trials (9059 participants) done in 32 countries. Polypills improve adherence, are generally well tolerated, and reduce risk factor levels, although heterogeneity limits the certainty of the effect on risk factors. Trials published to date have not been designed to detect differences in clinical outcomes, and thus no significant differences between polypill and comparator groups have been reported. Polypill therapy could be one of the most scalable strategies to reduce the risk of premature mortality from atherosclerosis by 25% by 2025 by improving medication adherence and access, but further trial data and clinical experience will be useful to determine how polypills can best be implemented to achieve this goal.
引用
收藏
页码:1055 / 1065
页数:11
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