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Published Online First: 3 November 2006. doi:10.1136/hrt.2006.095232
Heart 2007;93:711-715
Copyright © 2007 BMJ Publishing Group Ltd & British Cardiovascular Society

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HEART FAILURE AND CARDIOMYOPATHY

Prognosis and prognostic factors in patients with hypertrophic cardiomyopathy in Japan: results from a nationwide study

Ali Nasermoaddeli1, Katsuyuki Miura1, Akira Matsumori2, Yoshiyuki Soyama1, Yuko Morikawa1, Akira Kitabatake3, Yutaka Inaba4, Hideaki Nakagawa1

1 Department of Epidemiology and Public Health, Kanazawa Medical University, Ishikawa, Japan
2 Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan
3 Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine, Sapporo, Japan
4 Department of Epidemiology and Environmental Health, Juntendo University School of Medicine, Tokyo, Japan

Correspondence to:
Correspondence to:
Dr K Miura
Department of Epidemiology and Public Health, Kanazawa Medical University, 1–1 Daigaku, Uchinada, Ishikawa 920–0293, Japan; miura{at}kanazawa-med.ac.jp


ABSTRACT
Objective: To investigate prognosis and prognostic factors in patients with hypertrophic cardiomyopathy (HCM) in Japan.

Design: A nationwide epidemiological study.

Setting: Hospitals selected randomly from among all hospitals in Japan.

Patients: Clinical and epidemiological information for 2155 patients with HCM were collected in 1999.

Main outcome measures: Patients were classified on the basis of baseline prognostic factors. Survival rates up to 5 years were calculated by Cox’s proportional hazard model for 1605 patients.

Results: During the follow-up period, 241 deaths were recorded. The crude 5-year survival rate for the entire cohort was 86% (95% CI 84 to 88), and annual mortality ranged from 2.2% to 3.0%. A higher cardiothoracic ratio on chest x ray (HR 1.61; 95% CI 1.26 to 2.05, with 1 SD (6.2%) increase), a lower left ventricular ejection fraction (HR 1.42; 95% CI 1.20 to 1.69, with 1 SD (13%) decrease) and the presence of left bundle branch block (HR 3.14; 95% CI 1.28 to 7.71) were independently associated with a poorer prognosis, whereas the presence of apical hypertrophy at baseline (HR 0.58; 95%CI 0.36 to 0.92) predicted a better chance of survival.

Conclusions: The nationwide survey of patients with hypertrophic cardiomyopathy yielded important information on its prognosis and prognostic factors. These observations afford, for the first time, a measure of risk stratification in patients with HCM in Japan.


Abbreviations: AF, atrial fibrillation; BMI, body mass index; HCM, hypertrophic cardiomyopathy; IVS, interventricular septum; LBBB, left bundle branch block; LVEF, left ventricular ejection fraction; LV, left ventricular; NYHA, New York Heart Association







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