Suppr超能文献

日本心肌病研究

Research on cardiomyopathy in Japan.

作者信息

Toshima H

出版信息

Heart Vessels Suppl. 1985;1:14-7. doi: 10.1007/BF02072352.

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%).

摘要

自1974年日本厚生省赞助的特发性心肌病研究委员会成立以来,日本进行了许多实验和临床研究。心肌炎作为扩张型心肌病可能的发病机制备受关注,人们进行了大量的实验研究,并在尸检或活检时进行了组织病理学评估。在临床领域,疑似心肌炎的病例并不少见,但除急性期外,大多数患者很难确定病因病毒。因此,日本13家以上的机构最近引入了心内膜活检,以努力获得更准确的诊断。1983年,特发性心肌病研究委员会对1255例心肌病患者(786例肥厚型和469例扩张型)的预后进行了研究。扩张型心肌病的预后较差,5年生存率仅为54.3%。这一数字与肥厚型心肌病患者较好的预后(92%)形成了对比。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验