Predicting new-onset heart failure hospitalization of patients with atrial fibrillation: development and external validations of a risk score

Author:

Ishii Kai1,Matsue Yuya1ORCID,Miyauchi Katsumi1,Miyazaki Sakiko1,Hayashi Hidemori1,Nishizaki Yuji123,Nojiri Shuko2,Saito Yuki4,Nagashima Koichi4,Okumura Yasuo4ORCID,Daida Hiroyuki15,Minamino Tohru16

Affiliation:

1. Department of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine , 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421 , Japan

2. Medical Technology Innovation Center, Juntendo University , 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421 , Japan

3. Division of Medical Education, Juntendo University School of Medicine , 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421 , Japan

4. Division of Cardiology, Department of Medicine, Nihon University School of Medicine , 30-1 Oyaguchi Kami-cho, Itabashi-ku, Tokyo, 173-8610 , Japan

5. Faculty of Health Science, Juntendo University , 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421 , Japan

6. Japan Agency for Medical Research and Development-Core Research for Evolutionary Medical Science and Technology (AMED-CREST), Japan Agency for Medical Research and Development , 1-7-1 Otemachi, Chiyoda-ku, Tokyo, 100-0004 , Japan

Abstract

Abstract Aim Atrial fibrillation (AF) is a well-known risk factor for heart failure (HF). We sought to develop and externally validate a risk model for new-onset HF admission in patients with AF and those without a history of HF. Methods and results Using two multicentre, prospective, observational AF registries, RAFFINE (2857 patients, derivation cohort) and SAKURA (2516 patients without a history of HF, validation cohort), we developed a risk model by selecting variables with regularized regression and weighing coefficients by Cox regression with the derivation cohort. External validity testing was used for the validation cohort. Overall, 148 (5.2%) and 104 (4.1%) patients in the derivation and validation cohorts, respectively, developed HF during median follow-ups of 1396 (interquartile range [IQR]: 1078–1820) and 1168 (IQR: 844–1309) days, respectively. In the derivation cohort, age, haemoglobin, serum creatinine, and log-transformed brain natriuretic peptide were identified as potential risk factors for HF development. The risk model showed good discrimination and calibration in both derivations (area under the curve [AUC]: 0.80 [95% confidence interval (CI) 0.76–0.84]; Hosmer–Lemeshow, P = 0.257) and validation cohorts (AUC: 0.78 [95%CI 0.74–0.83]; Hosmer–Lemeshow, P = 0.475). Conclusion The novel risk model with four readily available clinical characteristics and biomarkers performed well in predicting new-onset HF admission in patients with AF.

Funder

Abbott Japan

Astellas Pharma

AstraZeneca

Bayer HealthCare

Boehringer Ingelheim

Boston Scientific

Bristol-Myers Squibb

Crosswill Medical

Daiichi-Sankyo

Eisai

Fukuda Denshi

FUJIFILM RI Pharma

Japan Lifeline

Kowa Pharmaceutical Europe

Kyowa Hakko Kirin

Mitsubishi Tanabe Pharma

Medical Hearts

Medtronic Japan

Mochida Pharmaceutical Company

MSD

Nippon Shinyaku

Otsuka Pharmaceutical

Pfizer

Philips Respironics

Roshe Diagnostics

Sanwa Kagaku Kenkyusho

Sanofi

Shionogi

Sumitomo Dainippon Pharma

Takeda Pharmaceuticals U.S.A.

Nihon Medi-Physics

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Health Policy

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