Registry for Evaluating Healthy Life Expectancy and Long-Term Outcomes after Catheter Ablation of Atrial Fibrillation in the Very Elderly (REHEALTH AF) study: rationale and design of a prospective, multicentre, observational, comparative study
Author:
Okumura YasuoORCID, Nagashima Koichi, Watanabe Ryuta, Yokoyama Katsuaki, Kato Takeshi, Fukaya Hidehira, Hayashi Hidemori, Nakahara Shiro, Shimizu Wataru, Iwasaki Yu-ki, Fujimoto Yuhi, Mukai Yasushi, Ejima Koichiro, Otsuka Takayuki, Suzuki Shinya, Murakami Masato, Kimura Masaomi, Harada Masahide, Koyama Junjiroh, Okamatsu Hideharu, Yamane Teiichi, Yamashita Seigo, Tokuda MichifumiORCID, Narui Ryohsuke, Takami Mitsuru, Shoda Morio, Harada Tomoo, Nakajima Ikutaro, Fujiu Katsuhito, Hiroshima Kenichi, Tanimoto Kojiro, Fujino Tadashi, Nakamura Keijiro, Kumagai Koji, Okada Ayako, Kobayashi Hideki, Hayashi Tatsuya, Watari Yuji, Hatsuno Mina, Tachibana Eizo, Iso Kazuki, Sonoda Kazumasa, Aizawa Yoshiyasu, Chikata Akio, Sakagami Satoru, Inoue Masaru, Minamiguchi Hitoshi, Makino Nobuhiko, Satomi Kazuhiro, Yazaki Yoshinao, Aoyagi Hideshi, Ichikawa Makoto, Haruta Hironori, Hiro Takafumi, Okubo Kimie, Arima Ken, Tojo Taiki, Kihara Hajime, Miyanaga Satoru, Fukuda Yoshiaki, Oiwa Koji, Fujiishi Tamami, Akabane Masashi, Ishikawa Norikazu, Kusano Kengo, Miyamoto Koji, Tabuchi Haruna, Shiozawa Tomoyuki, Miyamoto Kenjiro, Mase Hiroshi, Murotani KentaORCID
Abstract
IntroductionData are lacking on the extent to which patients with non-valvular atrial fibrillation (AF) who are aged ≥80 years benefit from ablation treatment. The question pertains especially to patients’ postablation quality of life (QoL) and long-term clinical outcomes.Methods and analysisWe are initiating a prospective, registry-based, multicentre observational study that will include patients aged ≥80 years with non-valvular AF who choose to undergo treatment by catheter ablation and, for comparison, such patients who do not choose to undergo ablation (either according to their physician’s advice or their own preference). Study subjects are to be enrolled from 52 participant hospitals and three clinics located throughout Japan from 1 June 2022 to 31 December 2023, and each will be followed up for 1 year. The planned sample size is 660, comprising 220 ablation group patients and 440 non-ablation group patients. The primary endpoint will be the composite incidence of stroke/transient ischaemic attack (TIA) or systemic embolism (SE), another cardiovascular event, major bleeding and/or death from any cause. Other clinical events such as postablation AF recurrence, a fall or bone fracture will be recorded. We will collect standard clinical background information plus each patient’s Clinical Frailty Scale score, AF-related symptoms, QoL (Five-Level Version of EQ-5D) scores, Mini-Mental State Examination (optional) score and laboratory test results, including measures of nutritional status, on entry into the study and 1 year later, and serial changes in symptoms and QoL will also be secondary endpoints. Propensity score matching will be performed to account for covariates that could affect study results.Ethics and disseminationThe study conforms to the Declaration of Helsinki and the Ethical Guidelines for Clinical Studies issued by the Ministry of Health, Labour and Welfare, Japan. Results of the study will be published in one or more peer-reviewed journals.Trial registration numberUMIN000047023.
Funder
Johnson&Johnson Medical Research Grant
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