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首页> 外文期刊>Current pharmaceutical design >Multi-constituent cardiovascular pills (MCCP)--challenges and promises of population-based prophylactic drug therapy for prevention of heart attack.
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Multi-constituent cardiovascular pills (MCCP)--challenges and promises of population-based prophylactic drug therapy for prevention of heart attack.

机译:多成分心血管药(MCCP)-预防心脏病发作的人群预防药物治疗的挑战和希望。

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摘要

Risk factors for atherosclerotic cardiovascular disease (CVD) are highly co-prevalent but poorly identified and treated. The Screening for Heart Attack Prevention and Education (SHAPE) Task Force from the Association for Eradication of Heart Attack (AEHA) has recently proposed a new strategy that recommends screening for subclinical atherosclerosis and implementing aggressive treatment of "vulnerable patients". The Task Force has also envisioned future developments that may shift mass screening strategies to mass prophylactic therapy. The "Polypill" concept, introduced by Wald and Law suggests a combination of statin, low-dose antihypertensives, aspirin and folic acid, in a single pill, taken prophylactically by high risk population can cut CVD event rates by as much as 80%. In this communication, we review the challenges and promises of such a strategy. "Polypill" is but one of an astronomical number of possible multiconstituent pills (MCCP). Attractive as the MCCP concept is, it lacks evidence from randomized controlled trials, and begs numerous questions about the credibility of the concept, the design and synthesis of such complex pills, pharmacokinetics, pharmacodynamics, bioequivalence, "class" vs. unique properties, interactions, evidence of clinical efficacy and safety, regulatory approval, post-marketing surveillance, prescription vs. over-the-counter use, responsibility for initiating and monitoring therapy, patient education, counterfeiting and importation, reimbursement, advertisement, patent protection, commercial viability, etc. If these issues are favorably addressed, MCCP stand to dramatically change the manner in which CVD is prevented particularly in developing societies. Notwithstanding, assuming low commercial interests, realizing the promises of MCCP will demand serious attention from national public health policymakers. The clinical and regulatory implications of population-based secondary prevention (which rely on a different evidence base, and in which entirely different risk-benefit and cost-effectiveness considerations apply) remain issues for active debate.
机译:动脉粥样硬化性心血管疾病(CVD)的风险因素普遍存在,但识别和治疗不力。根除心脏病发作协会(AEHA)进行的心脏病预防和教育筛查(SHAPE)工作组最近提出了一项新策略,建议筛查亚临床动脉粥样硬化并积极治疗“弱势患者”。该工作组还预见了未来的发展,可能会将大规模筛查策略转向大规模预防性治疗。 Wald and Law提出的“ Polypill”概念表明,由高风险人群预防性服用的他汀类药物,他汀类药物,低剂量降压药,阿司匹林和叶酸的组合可将CVD发生率降低多达80%。在本交流中,我们回顾了这种策略的挑战和希望。 “多药”只是可能的多成分药(MCCP)的天文数字之一。由于MCCP概念很吸引人,它缺乏来自随机对照试验的证据,并且就该概念的可信度,此类复杂药丸的设计和合成,药代动力学,药效学,生物等效性,“类别”与独特特性,相互作用的关系提出了许多问题。 ,临床疗效和安全性证明,监管批准,上市后监督,处方与非处方药的使用,治疗的发起和监控责任,患者教育,假冒和进口,费用报销,广告,专利保护,商业可行性,如果能够很好地解决这些问题,MCCP将会极大地改变预防CVD的方式,特别是在发展中社会中。尽管如此,假设商业利益低,实现MCCP的承诺将需要国家公共卫生政策制定者的认真关注。基于人群的二级预防的临床和法规含义(依赖不同的证据基础,并且在其中应用了完全不同的风险效益和成本效益考量)仍然是积极辩论的问题。

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