IF 0.9 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiology in the Young Pub Date : 2025-02-27 DOI:10.1017/S1047951125000587
Paul Esteso, Scott R Auerbach, Neha Bansal, Rachel Harris, Jonathan H Soslow, Brian F Birnbaum, Jennifer Conway, Linda H Cripe, Deipanjan Nandi, Emily Hayes, Katheryn E Gambetta, E Kevin Hall, Daphne T Hsu, Beth D Kaufman, David Rosenthal, Sonya Kirmani, Michelle S Ploutz, Ashwin K Lal, David M Peng, Chet R Villa, Svetlana Shugh, Carol A Wittlieb-Weber, Renata Shih
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引用次数: 0

摘要

简介杜兴氏肌营养不良症是一种破坏性神经肌肉疾病,其特征是肌营养不良蛋白的缺失,不可避免地会导致心肌病。尽管有关预防和治疗心肌病药物以缓解心肌病进展的文章已发表,但在药物的启动和优化的具体细节方面仍存在差距:本文件是一份专家意见陈述,旨在解决杜兴氏肌肉萎缩症心脏治疗方面的一个关键缺口。它根据疾病的进展和患者的反应,为心脏药物的启动和滴定提供了详尽的建议。这些建议来源于 "先进心脏治疗改善结果网络 "的专业知识,并参考了美国心脏协会、美国心脏病学会和杜氏肌肉萎缩症护理考虑因素的既定指南。这些源自专家的建议旨在帮助人们了解杜兴氏肌肉萎缩症相关心脏护理的复杂性:结果:针对杜氏肌营养不良症相关心肌病,提供了启动、滴定和优化关键心脏药物的综合建议:讨论:杜氏肌营养不良症的治疗需要采用多学科方法。然而,参与杜氏肌营养不良症治疗的医疗服务提供者的多样性可能导致心脏护理的差异,使治疗标准化和患者预后复杂化。本报告旨在为管理杜氏肌营养不良症相关心肌病提供一个路线图,阐明最佳疗效的关键时机和剂量的细微差别,最终改善心脏预后,提高杜氏肌营养不良症患者的生活质量:本文件旨在为杜氏肌营养不良症患者的心脏护理建立一个标准化框架,以改善心脏预后。
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Cardiac treatment for Duchenne muscular dystrophy: consensus recommendations from the ACTION muscular dystrophy committee.

Introduction: Duchenne muscular dystrophy is a devastating neuromuscular disorder characterized by the loss of dystrophin, inevitably leading to cardiomyopathy. Despite publications on prophylaxis and treatment with cardiac medications to mitigate cardiomyopathy progression, gaps remain in the specifics of medication initiation and optimization.

Method: This document is an expert opinion statement, addressing a critical gap in cardiac care for Duchenne muscular dystrophy. It provides thorough recommendations for the initiation and titration of cardiac medications based on disease progression and patient response. Recommendations are derived from the expertise of the Advance Cardiac Therapies Improving Outcomes Network and are informed by established guidelines from the American Heart Association, American College of Cardiology, and Duchenne Muscular Dystrophy Care Considerations. These expert-derived recommendations aim to navigate the complexities of Duchenne muscular dystrophy-related cardiac care.

Results: Comprehensive recommendations for initiation, titration, and optimization of critical cardiac medications are provided to address Duchenne muscular dystrophy-associated cardiomyopathy.

Discussion: The management of Duchenne muscular dystrophy requires a multidisciplinary approach. However, the diversity of healthcare providers involved in Duchenne muscular dystrophy can result in variations in cardiac care, complicating treatment standardization and patient outcomes. The aim of this report is to provide a roadmap for managing Duchenne muscular dystrophy-associated cardiomyopathy, by elucidating timing and dosage nuances crucial for optimal therapeutic efficacy, ultimately improving cardiac outcomes, and improving the quality of life for individuals with Duchenne muscular dystrophy.

Conclusion: This document seeks to establish a standardized framework for cardiac care in Duchenne muscular dystrophy, aiming to improve cardiac prognosis.

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来源期刊
Cardiology in the Young
Cardiology in the Young 医学-小儿科
CiteScore
1.70
自引率
10.00%
发文量
715
审稿时长
4-8 weeks
期刊介绍: Cardiology in the Young is devoted to cardiovascular issues affecting the young, and the older patient suffering the sequels of congenital heart disease, or other cardiac diseases acquired in childhood. The journal serves the interests of all professionals concerned with these topics. By design, the journal is international and multidisciplinary in its approach, and members of the editorial board take an active role in the its mission, helping to make it the essential journal in paediatric cardiology. All aspects of paediatric cardiology are covered within the journal. The content includes original articles, brief reports, editorials, reviews, and papers devoted to continuing professional development.
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