Clinical Impact of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy Results From Kochi RYOMA Study

Toru Kubo(Kochi Medical School Hospital), Hiroaki Kitaoka(Kochi Medical School Hospital), Makoto Okawa(Kochi Medical School Hospital), Takayoshi Hirota(Kochi Medical School Hospital), Kayo Hayato(Kochi Medical School Hospital), Naohito Yamasaki(Kochi Medical School Hospital), Yoshihisa Matsumura(Kochi Medical School Hospital), Toshikazu Yabe(Kochi Medical School Hospital), Jun Takata(Kochi Medical School Hospital), Yoshinori Doi(Kochi Medical School Hospital)
Circulation Journal
January 1, 2009
Cited by 100Open Access
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Abstract

BACKGROUND: There have been few studies of the clinical features of hypertrophic cardiomyopathy (HCM) in a community-based patient cohort in Japan. METHODS AND RESULTS: Cardiomyopathy registration was established in Kochi Prefecture and named the Kochi RYOMA (registry of myocardial diseases) study, consisting of 9 hospitals that registered 261 patients with a diagnosis of HCM. At registration, 74 patients (28%) had documented paroxysmal or chronic atrial fibrillation (AF). Although most patients (93%) were in New York Heart Association (NYHA) class I or II, 17 of the 18 patients in NYHA III had AF; 37 of the 74 patients with AF suffered from morbid events (embolism and/or heart failure (HF) admission), and 15 of 19 patients with embolic events had AF prior to or at the time of embolism. Of the 29 patients who had a history of HF admission, 8 had left ventricular systolic dysfunction, and the other 21 patients were hospitalized because of diastolic HF. AF occurred prior to HF in 20 of those 21 patients. Furthermore, 19 of those 20 patients with AF and diastolic HF were hospitalized within 1 year after detection of AF. CONCLUSIONS: In an unselected regional registry, AF was the major determinant of clinical deteriorations in patients with HCM.


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