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Cardiac Rehabilitation for Patients With Stable Ischemic Heart Disease Without Revascularization ― Rationale and Design of a Single-Arm Pilot Study ―

Background: Clinical practice guidelines strongly recommend optimal medical therapy (OMT), including lifestyle modification, pharmacotherapy, and exercise-based cardiac rehabilitation (CR), in patients with stable ischemic heart disease (SIHD). However, the efficacy and safety of CR in patients with...

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Detalles Bibliográficos
Autores principales: Seki, Tomotsugu, Murata, Makoto, Takabayashi, Kensuke, Yanagisawa, Takashi, Ogihara, Masayuki, Kurimoto, Ritsuko, Kida, Keisuke, Tamita, Koichi, Song, Xiaoyang, Ozasa, Neiko, Taniguchi, Ryoji, Nishitani-Yokoyama, Miho, Koba, Shinji, Murai, Ryosuke, Furukawa, Yutaka, Hamasaki, Maki, Kondo, Hirokazu, Hayashi, Hironori, Ootakara-Katsume, Asako, Tateishi, Kento, Matoba, Satoaki, Adachi, Hitoshi, Shiraishi, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Circulation Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992498/
https://www.ncbi.nlm.nih.gov/pubmed/36909138
http://dx.doi.org/10.1253/circrep.CR-22-0131
Descripción
Sumario:Background: Clinical practice guidelines strongly recommend optimal medical therapy (OMT), including lifestyle modification, pharmacotherapy, and exercise-based cardiac rehabilitation (CR), in patients with stable ischemic heart disease (SIHD). However, the efficacy and safety of CR in patients with SIHD without revascularization remain unclear. Methods and Results: The Prospective Registry of STable Angina RehabiliTation (Pre-START) study is a multicenter, prospective, single-arm, open-label pilot study to evaluate the efficacy and safety of CR on health-related quality of life (HRQL), exercise capacity, and clinical outcomes in Japanese patients with SIHD without revascularization. In this study, all patients will undergo guideline-based OMT and are encouraged to have 36 outpatient CR sessions within 5 months after enrollment. The primary endpoint is the change in the Seattle Angina Questionnaire-7 summary score between baseline and the 6-month visit; an improvement of ≥5 points will be defined as a clinically important change. Secondary endpoints include changes in other HRQL scores and exercise capacity between baseline and the 6-month visit, as well as clinical outcomes between enrollment and the 6-month visit. Conclusions: The Pre-START study will provide valuable evidence to elucidate the efficacy and safety of CR in patients with SIHD and indispensable information for a subsequent randomized controlled trial. The study was registered with the University Hospital Medical Information Network (UMIN) Clinical Trials Registry (ID: UMIN000045415) on April 1, 2022.