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宾夕法尼亚医药健康心脏研究的设计与原理:一项针对动脉粥样硬化性心血管疾病高危患者血压和胆固醇改善的中心组织方法有效性的随机试验。

Design and rationale of penn medicine healthy heart, a randomized trial of effectiveness of a centrally organized approach to blood pressure and cholesterol improvement among patients at elevated risk of atherosclerotic cardiovascular disease.

机构信息

Penn Center for Health Incentives and Behavioral Economics, University of Pennsylvania, Philadelphia, PA; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Wharton School, University of Pennsylvania, Philadelphia PA; Leonard Davis Institute of Health Economics, University of Pennsylvania, Philadelphia, PA.

Penn Center for Health Incentives and Behavioral Economics, University of Pennsylvania, Philadelphia, PA; Penn Medicine Center for Health Care Transformation and Innovation, Philadelphia, PA.

出版信息

Am Heart J. 2024 Dec;278:208-222. doi: 10.1016/j.ahj.2024.09.029. Epub 2024 Sep 27.

Abstract

RATIONALES

Atherosclerotic Cardiovascular Disease (ASCVD) is the leading cause of morbidity and mortality in the United States. Suboptimal control of hypertension and hyperlipidemia are common factors contributing to ASCVD risk. The Penn Medicine Healthy Heart (PMHH) Study is a randomized clinical trial testing the effectiveness of a system designed to offload work from primary care clinicians and improve patient follow-through with risk reduction strategies by using a centralized team of nonclinical navigators and advanced practice providers, remote monitoring, and bi-directional text messaging, augmented by behavioral science engagement strategies. The intervention builds on prior nonrandomized evaluations of these design elements that demonstrated significant improvement in patients' systolic blood pressure and LDL Cholesterol (LDL-C).

PRIMARY HYPOTHESIS

Penn Medicine Healthy Heart will significantly improve systolic blood pressure and LDL-C compared to usual care over the 6 months of this intervention.

DESIGN

Randomized clinical trial of Penn Medicine Healthy Heart in patients aged 35-80 years at elevated risk of ASCVD whose systolic blood pressure and LDL-C are not well controlled. The intervention consists of 4 modules that address blood pressure management, lipid management, nutrition, and smoking cessation, offered in a phased approach to give the participant time to learn about each topic, adopt any recommendations, and build a relationship with the care team.

SITES

University of Pennsylvania Health System at primary care practices located in inner-city urban and rural/semi-rural areas.

PRIMARY OUTCOMES

Improvement in systolic blood pressure and LDL-C.

SECONDARY OUTCOMES

Cost-effectiveness analyses are planned to evaluate the health care costs and health outcomes of the intervention approach. An implementation evaluation is planned to understand factors influencing success of the intervention.

ESTIMATED ENROLLMENT

2,420 active patients of Penn Medicine primary care practices who have clinical ASCVD, or who are at elevated risk for ASCVD, and who are (a) not on statins or have LDL-C >100 despite being on statins and (b) had systolic blood pressure >140 at 2 recent ambulatory visits.

ENROLLMENT DATES

March 2024-March 2025. The intervention will last 6 months with a 12-month follow-up to determine whether its effects persist.

CURRENT STATUS

Enrolling (1,240 enrolled as of August 15, 2024) CLINICAL TRIAL REGISTRATION: NCT06062394.

摘要

理由

动脉粥样硬化性心血管疾病(ASCVD)是美国发病率和死亡率的主要原因。高血压和血脂异常控制不佳是导致 ASCVD 风险的常见因素。宾夕法尼亚大学医学中心健康心脏(PMHH)研究是一项随机临床试验,旨在测试一种系统的有效性,该系统旨在通过使用非临床导航员和高级实践提供者的集中团队、远程监测和双向短信、以及行为科学参与策略来减轻初级保健临床医生的工作负担,并提高患者对降低风险策略的后续跟进,从而改善 ASCVD 风险。该干预措施基于对这些设计元素的先前非随机评估,这些评估显示患者的收缩压和 LDL 胆固醇(LDL-C)显著改善。

主要假设

与常规护理相比,宾夕法尼亚大学医学中心健康心脏在 6 个月的干预期间将显著改善收缩压和 LDL-C。

设计

对患有 ASCVD 高危、收缩压和 LDL-C 控制不佳的 35-80 岁患者进行宾夕法尼亚大学医学中心健康心脏的随机临床试验。该干预措施由 4 个模块组成,用于管理血压、血脂、营养和戒烟,采用分阶段方法提供,以便参与者有时间了解每个主题,采用任何建议,并与护理团队建立关系。

地点

宾夕法尼亚大学健康系统在位于城市内城区和农村/半农村地区的初级保健诊所。

主要结局

收缩压和 LDL-C 的改善。

次要结局

计划进行成本效益分析,以评估干预措施的医疗保健成本和健康结果。计划进行实施评估,以了解影响干预成功的因素。

估计入组人数

宾夕法尼亚大学医学中心初级保健诊所的 2420 名活跃患者,这些患者患有临床 ASCVD,或 ASCVD 风险升高,且(a)未服用他汀类药物,或(b)在最近 2 次门诊就诊时收缩压>140,即使正在服用他汀类药物且 LDL-C>100。

入组日期

2024 年 3 月-2025 年 3 月。干预将持续 6 个月,随访 12 个月,以确定其效果是否持续。

当前状态

正在入组(截至 2024 年 8 月 15 日,已入组 1240 人)临床试验注册:NCT06062394。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c71e/11560706/6813d8371983/nihms-2025987-f0001.jpg

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