Pharmacist-led, digitally enabled transitional care after acute myocardial infarction: design and baseline characteristics of the AMI-HOPE nationwide stepped-wedge trial.

IF 4.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
European heart journal. Digital health Pub Date : 2026-06-20 eCollection Date: 2026-07-01 DOI:10.1093/ehjdh/ztag094
Melody Wang, Zhi Zhen Lim, Siew-Pang Chan, Zhen-Long Teo, Sock-Hwee Tan, Vinay Panday, Ho Jien Sze, Yee-May Wong, Grace Chang, Faclin Ng, Imran Syed, Patrick Lim, Zijuan Huang, Ziliang Lim, Valerie Teo, Ian Phoon, Galih Kunarso, Siang-Chew Chai, Kai-Rong Siau, Yew-Seng Kwan, Samuel Ho, Laurane Lim, Marvin Sim, Hui-Rei Yap, Wan-Lin Oh, Hui-Ping Chong, Angela Yeo, Praveen Deorani, Robert Morris, Hee-Hwa Ho, Derek J Hausenloy, Hwee-Lin Wee, Doreen Tan, Mark Y Chan
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引用次数: 0

Abstract

Aims: To describe the design of AMI-HOPE, a pharmacist-led, digitally enabled transitional care intervention for patients after acute myocardial infarction (AMI), and its nationwide stepped-wedge cluster-randomized evaluation across Singapore's public healthcare system.

Methods and results: AMI-HOPE is designed as a pragmatic, open-label trial across three health clusters (7 hospitals, 18 polyclinics) in which hospitals crossed over from standard cardiologist-led care to intervention at 3 month intervals. We utilize the Health Discovery+ (HD+) platform for remote vital signs monitoring, rule-based alerts, pharmacist-led teleconsultations, and automated patient education. Target N = 1512 (1:1 ratio); primary outcome is a hierarchical win ratio composite (CV death, MI, stroke, CV readmissions, low-density lipoprotein cholesterol, systolic blood pressure, HbA1c, patient-reported outcome measures). Secondary outcomes include guideline-directed medical therapy titration/adherence, LVEF, and cost-effectiveness. Enrolment completed in September 2025 (N = 1634 randomized; 810 control, 824 intervention). Baseline characteristics (N = 1492 in follow-up) showed a median age of 59 years, 12% female, 61% Chinese ethnicity. Twelve-month follow-up will complete on 30 September 2026.

Conclusion: AMI-HOPE demonstrates a scalable, digitally enabled model shifting early post-AMI care from specialist-led clinics to pharmacists with remote monitoring. This nationwide trial evaluates its clinical efficacy, implementation, and value at population scale. ClinicalTrials.gov: NCT07443982.

药剂师主导的、数字化的急性心肌梗死后过渡护理:AMI-HOPE全国阶梯形试验的设计和基线特征
目的:描述AMI- hope的设计,这是一种由药剂师主导的、数字化的急性心肌梗死(AMI)后患者过渡护理干预措施,以及其在新加坡公共医疗保健系统中的全国性楔形聚类随机评估。方法和结果:AMI-HOPE被设计为一项实用的、开放标签的试验,涉及三个卫生集群(7家医院,18家综合诊所),其中医院从标准的心脏病专家主导的护理过渡到间隔3个月的干预。我们利用健康发现+ (HD+)平台进行远程生命体征监测、基于规则的警报、药剂师主导的远程会诊和自动化患者教育。目标N = 1512(1:1比例);主要转归是分层赢比复合(心血管死亡、心肌梗死、卒中、心血管再入院、低密度脂蛋白胆固醇、收缩压、HbA1c、患者报告的转归测量)。次要结局包括指南导向的药物治疗滴度/依从性、LVEF和成本效益。入组于2025年9月完成(N = 1634随机,对照组810,干预组824)。基线特征(随访N = 1492)显示中位年龄59岁,12%为女性,61%为华裔。为期12个月的后续行动将于2026年9月30日完成。结论:AMI-HOPE展示了一种可扩展的数字化模式,将ami后早期护理从专科医生主导的诊所转移到远程监控的药剂师。这项全国性的试验评估了其临床疗效、实施情况和在人群规模上的价值。ClinicalTrials.gov: NCT07443982。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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