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

被引:29
作者
Nasermoaddeli, Ali
Miura, Katsuyuki [1 ]
Matsumori, Akira
Soyama, Yoshiyuki
Morikawa, Yuko
Kitabatake, Akira
Inaba, Yutaka
Nakagawa, Hideaki
机构
[1] Kanazawa Med Univ, Dept Epidemiol & Publ Hlth, Uchinada, Ishikawa 9200293, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Cardiovasc Med, Kyoto, Japan
[3] Hokkaido Univ, Grad Sch Med, Dept Cardiovasc Med, Sapporo, Hokkaido, Japan
[4] Juntendo Univ, Sch Med, Dept Epidemiol & Environm Hlth, Tokyo 113, Japan
关键词
D O I
10.1136/hrt.2006.095232
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:711 / 715
页数:5
相关论文
共 29 条
[1]   Sex-based comparison of survival in referred patients with hypertrophic cardiomyopathy [J].
Dimitrow, PP ;
Czarnecka, D ;
Kaivecka-Jaszcz, K ;
Dubiel, JS .
AMERICAN JOURNAL OF MEDICINE, 2004, 117 (01) :65-66
[2]   Clinical analysis of hypertrophic cardiomyopathy which evolved into dilated phase during long-term follow-up [J].
Doi, K ;
Toda, G ;
Iliev, II ;
Hayano, M ;
Yano, K .
JAPANESE HEART JOURNAL, 1999, 40 (05) :579-587
[3]   Relation between severity of left-ventricular hypertrophy and prognosis in patients with hypertrophic cardiomyopathy [J].
Elliott, PM ;
Blanes, JRG ;
Mahon, NG ;
Poloniecki, JD ;
McKenna, WJ .
LANCET, 2001, 357 (9254) :420-424
[4]   Long-term outcome in patients with apical hypertrophic cardiomyopathy [J].
Eriksson, MJ ;
Sonnenberg, B ;
Woo, A ;
Rakowski, P ;
Parker, TG ;
Wigle, ED ;
Rakowski, H .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (04) :638-645
[5]   Clinical characteristics of and long-term outcome in Chinese patients with hypertrophic cardiomyopathy [J].
Ho, HH ;
Lee, KLF ;
Lau, CP ;
Tse, HF .
AMERICAN JOURNAL OF MEDICINE, 2004, 116 (01) :19-23
[6]   HYPERTROPHIC CARDIOMYOPATHY [J].
LOUIE, EK ;
EDWARDS, LC .
PROGRESS IN CARDIOVASCULAR DISEASES, 1994, 36 (04) :275-308
[7]   Hypertrophic cardiomyopathy - A systematic review [J].
Maron, BJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (10) :1308-1320
[8]   Clinical course of hypertrophic cardiomyopathy in a regional United States cohort [J].
Maron, BJ ;
Casey, SA ;
Poliac, LC ;
Gohman, TE ;
Almquist, AK ;
Aeppli, DM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (07) :650-655
[9]   Hypertrophic cardiomyopathy: An important global disease [J].
Maron, BJ .
AMERICAN JOURNAL OF MEDICINE, 2004, 116 (01) :63-65
[10]   Clinical course of hypertrophic cardiomyopathy with survival to advanced age [J].
Maron, BJ ;
Casey, SA ;
Hauser, RG ;
Aeppli, DM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 42 (05) :882-888