Guideline-Directed Medical Therapy Use in the STRONG-HF Trial.

IF 8.4 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Xiang Zhang, Beth Davison, Marianna Adamo, Mattia Arrigo, Jan Biegus, Ovidiu Chioncel, Alain Cohen-Solal, Gad Cotter, Christopher Edwards, Antoine Kimmoun, Carolyn S P Lam, Alexandre Mebazaa, Marco Metra, Maria Novosadova, Peter S Pang, Karen Sliwa, Koji Takagi, Adriaan A Voors, Justin A Ezekowitz
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引用次数: 0

Abstract

Background: Assessment of medication changes in heart failure trials and registries is complex and may not capture the entirety of care. A comprehensive and standardized method is needed. We used different methods to assess the use of guideline-directed medical therapies (GDMT) and verified the association between GDMT intensity score with the STRONG-HF trial (Safety, Tolerability and Efficacy of Rapid Optimization, Helped by NT-proBNP Testing of Heart Failure Therapies) clinical outcomes.

Methods: We used data from the STRONG-HF trial to examine the baseline GDMT use for all randomized patients by applying the GDMT intensity score and evaluated its change over time. We also examined their basic adherence, indication-corrected adherence, and dose-corrected adherence, and the association with clinical outcomes up to 180 days.

Results: At 90 days, triple therapy indication-corrected use increased from 4.5% to 36% in the usual care group, and from 5.2% to 93.5% in the high-intensity care group (P<0.001 between the 2 groups). Triple therapy dose-corrected use increased from 4.5% to 20.5% in the usual care group, and from 3.3% to 77.4% in the high-intensity care group (P<0.001). The GDMT intensity score at baseline was <6 in 358 (33%) patients, 6 to 7 in 329 (31%) patients, and >7 in 386 (36%) patients. At 90 days, 88.4% of patients in the high-intensity arm achieved a score >7 versus 14.3% in the usual care arm (P<0.0001). The GDMT intensity score was correlated with clinical outcomes at 180 days.

Conclusions: The GDMT intensity score provides a comprehensive description of medication use by means of standardized measurements and is linked to clinical outcomes. Future studies should consider utilizing this as a trial end point.

Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03412201.

指南指导药物治疗在STRONG-HF试验中的应用。
背景:心力衰竭试验和登记中药物变化的评估是复杂的,可能无法捕捉到整个治疗过程。需要一种全面和标准化的方法。我们使用不同的方法来评估指南导向药物治疗(GDMT)的使用,并验证GDMT强度评分与STRONG-HF试验(快速优化的安全性、耐受性和有效性,帮助NT-proBNP测试心力衰竭治疗)临床结果之间的关联。方法:我们使用STRONG-HF试验的数据,通过应用GDMT强度评分来检查所有随机患者的基线GDMT使用情况,并评估其随时间的变化。我们还检查了他们的基本依从性、适应症纠正依从性和剂量纠正依从性,以及与180天临床结果的关系。结果:在90天,常规护理组的三联疗法适应症纠正使用率从4.5%增加到36%,高强度护理组从5.2%增加到93.5%(386例(36%)患者的PP7)。在90天,高强度组中88.4%的患者达到了bb70分,而常规护理组中为14.3%(结论:GDMT强度评分通过标准化测量提供了对药物使用的全面描述,并与临床结果相关。未来的研究应考虑将其作为试验终点。注册:网址:https://www.clinicaltrials.gov;唯一标识符:NCT03412201。
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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来源期刊
Circulation: Heart Failure
Circulation: Heart Failure 医学-心血管系统
CiteScore
12.90
自引率
3.10%
发文量
271
审稿时长
6-12 weeks
期刊介绍: Circulation: Heart Failure focuses on content related to heart failure, mechanical circulatory support, and heart transplant science and medicine. It considers studies conducted in humans or analyses of human data, as well as preclinical studies with direct clinical correlation or relevance. While primarily a clinical journal, it may publish novel basic and preclinical studies that significantly advance the field of heart failure.
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