Circulation Journal
Online ISSN : 1347-4820
Print ISSN : 1346-9843
ISSN-L : 1346-9843

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Prognostic Impact of Echocardiographic Diastolic Dysfunction on Outcomes in Patients With Heart Failure With Preserved Ejection Fraction ― Insights From the PURSUIT-HFpEF Registry ―
Bolrathanak OeunShungo HikosoDaisaku NakataniHiroya MizunoShinichiro SunaTetsuhisa KitamuraKatsuki OkadaTomoharu DohiYohei SotomiTakayuki KojimaHirota KidaAkihiro SunagaTaiki SatoYasuharu TakedaHiroyuki KurakamiTomomi YamadaShunsuke TamakiHaruhiko AbeYusuke NakagawaYoshiharu HiguchiHisakazu FujiToshiaki ManoMasaaki UematsuYoshio YasumuraTakahisa YamadaYasushi Sakataon behalf of the OCVC-Heart Failure Investigators
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論文ID: CJ-21-0300

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Background:Although diastolic dysfunction is important pathophysiology in heart failure with preserved ejection fraction (HFpEF), its prognostic impact in HFpEF patients, including those with atrial fibrillation (AF), remains to be elucidated.

Methods and Results:We included the data for 863 patients (321 patients with AF) registered in a prospective multicenter observational study of patients with HFpEF. Patients were divided into 3 groups according to the 2016 ASE/EACVI recommendations. The primary endpoint was a composite of all-cause death or HF rehospitalization. Median age was 83 years, and 55.5% were female. 196 (22.7%) were classified with normal diastolic function (ND), 253 (29.3%) with indeterminate (ID) and 414 (48.0%) with diastolic dysfunction (DD). The primary endpoint occurred more frequently in patients with DD than in those with ND or ID (log-rank P<0.001 for DD vs. ND, and log-rank P=0.007 for DD vs. ID, respectively). Taking ND as the reference, multivariable Cox regression analysis revealed that DD (hazard ratio (HR): 1.57, 95% confidence interval (CI):1.06–2.32, P=0.024) was independently associated with the composite endpoint, whereas ID (HR: 1.28, 95% CI: 0.84–1.95, P=0.255) was not. DD was associated with the composite endpoint in both patients with and without AF.

Conclusions:HFpEF patients classified with DD using the 2016 ASE/EACVI recommendations had worse clinical outcomes than those with ND or ID. DD may be considered a prognostic marker in patients with HFpEF regardless of AF.

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© 2021, THE JAPANESE CIRCULATION SOCIETY

This article is licensed under a Creative Commons [Attribution-NonCommercial-NoDerivatives 4.0 International] license.
https://creativecommons.org/licenses/by-nc-nd/4.0/
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