Watkins David A, Pickersgill Sarah J, Flood David, Gaziano Thomas A, Huffman Mark D, Islam Shofiqul, Joseph Philip, Malekzadeh Reza, Perel Pablo, Piñeiro Daniel J, Pinto Fausto J, Yusuf Salim
Division of General Internal Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA; Department of Global Health, University of Washington, Seattle, Washington, USA.
Independent research consultant, Oakland, California, USA.
J Am Coll Cardiol. 2025 Jul 22;86(3):149-161. doi: 10.1016/j.jacc.2025.04.043.
Uptake of drugs for primary and secondary prevention of cardiovascular disease is low in many countries. Single-pill combination (SPC) therapies consisting of a statin and 1 or more antihypertensive drugs, with or without aspirin, can reduce rates of fatal and nonfatal cardiovascular disease, but their use is currently limited.
The authors modeled the potential impact of widespread adoption of SPC therapies over 2023 to 2050.
We used state-transition and demographic modeling approaches to project ischemic heart disease- and stroke-related deaths and nonfatal events in 182 countries. We modeled the effects of programs to roll out primary and secondary prevention SPCs in 2 scenarios, compared to non-SPC (current) care: 1) targeted strategies to improve adherence and reduce therapeutic inertia among persons already in care; and 2) population-based strategies to provide SPC therapies to most persons at intermediate-to-high risk. We conducted sensitivity analyses around our assumptions on adoption, long-term adherence, and the effect of aspirin.
Over 2023-2050, use of SPC therapies could prevent up to 29 million deaths and 51 million cases in the targeted scenario and up to 72 million deaths and 130 million cases in the population scenario. The greatest share of fatal and nonfatal events prevented would be in South and East Asia and the Pacific because of population size. SPC therapies could reduce all-cause premature mortality by 2.0% (targeted) to 3.2% (population), facilitating achievement of global health targets.
SPC therapies could substantially accelerate progress on cardiovascular disease mortality by increasing use of preventive drugs, especially in settings where uptake is currently low.
在许多国家,用于心血管疾病一级和二级预防的药物使用率较低。由他汀类药物和1种或多种抗高血压药物组成的单片复方制剂(SPC)疗法,无论是否含有阿司匹林,均可降低致命和非致命心血管疾病的发生率,但其目前的使用有限。
作者模拟了2023年至2050年广泛采用SPC疗法的潜在影响。
我们使用状态转换和人口统计学建模方法来预测182个国家与缺血性心脏病和中风相关的死亡及非致命事件。与非SPC(当前)治疗相比,我们在两种情景下模拟了推广一级和二级预防SPC项目的效果:1)有针对性的策略,以提高已接受治疗者的依从性并减少治疗惰性;2)基于人群的策略,为大多数中高风险人群提供SPC疗法。我们围绕采用率、长期依从性和阿司匹林效果的假设进行了敏感性分析。
在2023 - 2050年期间,在有针对性的情景下,使用SPC疗法可预防多达2900万例死亡和5100万例病例;在人群情景下,可预防多达7200万例死亡和1.3亿例病例。由于人口规模,预防的致命和非致命事件的最大份额将出现在南亚、东亚和太平洋地区。SPC疗法可将全因过早死亡率降低2.0%(有针对性的情景)至3.2%(人群情景),有助于实现全球健康目标。
SPC疗法可通过增加预防性药物的使用,大幅加速心血管疾病死亡率方面的进展,尤其是在目前使用率较低的地区。