Literature DB >> 3843577

Research on cardiomyopathy in Japan.

H Toshima.   

Abstract

Many experimental and clinical studies have been performed in Japan, since the Idiopathic Cardiomyopathy Research Committee sponsored by the Ministry of Health and Welfare of Japan was organized in 1974. Much interest has been focused on myocarditis as a possible pathogenesis of dilated cardiomyopathy and extensive experimental studies have been performed as well as histopathologic assessment at autopsy or biopsy. In the clinical field, suspected cases of myocarditis are not uncommon, but determination of etiological viruses is quite difficult in most patients except at the acute stage. Therefore, endomyocardial biopsy has been recently introduced in more than 13 institutes in Japan in an effort to obtain more accurate diagnosis. In 1983, the Idiopathic Cardiomyopathy Research Committee performed a study on the prognosis of cardiomyopathy in 1255 patients (786 hypertrophic and 469 dilated). The prognosis of dilated cardiomyopathy was poor, with a 5-year survival rate of only 54.3%. This figure contrasted with the better prognosis in those with hypertrophic cardiomyopathy (92%).

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Year:  1985        PMID: 3843577     DOI: 10.1007/bf02072352

Source DB:  PubMed          Journal:  Heart Vessels Suppl        ISSN: 0935-736X


  5 in total

1.  Clinical features of idiopathic hypertrophic cardiomyopathy.

Authors:  H Toshima; T Fukami
Journal:  Jpn Circ J       Date:  1971-07

2.  Hypertrophic nonobstructive cardiomyopathy with giant negative T waves (apical hypertrophy): ventriculographic and echocardiographic features in 30 patients.

Authors:  H Yamaguchi; T Ishimura; S Nishiyama; F Nagasaki; S Nakanishi; F Takatsu; T Nishijo; T Umeda; K Machii
Journal:  Am J Cardiol       Date:  1979-09       Impact factor: 2.778

3.  Symposium on idiopathic myocardial fibrosis and allied diseases. 2. Intracardiac heart biopsy.

Authors:  S Konno; S Sakakibara
Journal:  Jpn Circ J       Date:  1966-12

4.  Hypertrophic cardiomyopathy with ventricular septal hypertrophy localized to the apical region of the left ventricle (apical hypertrophic cardiomyopathy).

Authors:  B J Maron; R O Bonow; T N Seshagiri; W C Roberts; S E Epstein
Journal:  Am J Cardiol       Date:  1982-06       Impact factor: 2.778

5.  Giant T wave inversion as a manifestation of asymmetrical apical hypertrophy (AAH) of the left ventricle. Echocardiographic and ultrasono-cardiotomographic study.

Authors:  T Sakamoto; C Tei; M Murayama; H Ichiyasu; Y Hada
Journal:  Jpn Heart J       Date:  1976-09
  5 in total
  2 in total

1.  Resolution of acromegalic cardiomyopathy in mild acromegalic physical abnormality after short-term octreotide therapy.

Authors:  Myung-Woo Hwang; Akira Shimatsu; Yoshio Sasaki; Hiroyuki Ayukawa; Katsura Inenaga; Rei Takeoka; Tomoyuki Iwase; Chuichi Kawai
Journal:  Heart Vessels       Date:  2007-05-21       Impact factor: 2.037

2.  What explains black-white differences in survival in idiopathic dilated cardiomyopathy? The Washington, DC, Dilated Cardiomyopathy Study.

Authors:  S S Coughlin; L Myers; R K Michaels
Journal:  J Natl Med Assoc       Date:  1997-04       Impact factor: 1.798

  2 in total

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