Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan.
Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan
BMJ Open. 2020 Oct 15;10(10):e038294. doi: 10.1136/bmjopen-2020-038294.
Neither the pathophysiology nor an effective treatment for heart failure with preserved ejection fraction (HFpEF) has been elucidated to date. The purpose of this ongoing study is to elucidate the pathophysiology and prognostic factors for patients with HFpEF admitted to participating institutes. We also aim to obtain insights into the development of new diagnostic and treatment methods by analysing patient background factors, clinical data and follow-up information.
This study is a prospective, multicentre, observational study of patients aged ≥20 years admitted due to acute decompensated heart failure with preserved left ventricular ejection fraction (≥50%) and elevated N-terminal-pro brain natriuretic peptide (NT-proBNP) (≥400 pg/mL). The study began in June 2016, with the participation of Osaka University Hospital and 31 affiliated facilities. We will collect data on history in detail, accompanying diseases, quality of life, frailty score, medication history, and laboratory and echocardiographic data. We will follow-up each patient for 5 years, and collect outcome data on mortality, cause of death, and the number and cause of hospitalisation. The target number of registered cases is 1500 cases in 5 years.
The protocol was approved by the Institutional Review Board (IRB) of Osaka University Hospital on 24 February 2016 (ID: 15471), and by the IRBs of the all participating facilities. The findings will be disseminated through peer-reviewed publications and conference presentations.
目前尚未阐明射血分数保留的心力衰竭(HFpEF)的病理生理学和有效治疗方法。本研究旨在阐明入住参与研究所的 HFpEF 患者的病理生理学和预后因素。我们还旨在通过分析患者的背景因素、临床数据和随访信息,深入了解新的诊断和治疗方法的发展。
这是一项针对年龄≥20 岁的患者的前瞻性、多中心、观察性研究,这些患者因急性失代偿性射血分数保留的心力衰竭(≥50%)和升高的 N 末端前脑利钠肽(NT-proBNP)(≥400pg/ml)而入院。该研究于 2016 年 6 月开始,由大阪大学医院和 31 个附属机构参与。我们将详细收集病史、伴随疾病、生活质量、虚弱评分、用药史以及实验室和超声心动图数据。我们将对每位患者进行为期 5 年的随访,并收集死亡率、死因以及住院次数和原因等结果数据。预计在 5 年内登记的病例数为 1500 例。
该方案于 2016 年 2 月 24 日获得大阪大学医院机构审查委员会(IRB)的批准(ID:15471),并获得所有参与机构的 IRB 批准。研究结果将通过同行评审的出版物和会议报告进行传播。