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用皮质类固醇治疗慢性心肌炎。

Treatment of chronic myocarditis with corticosteroids.

作者信息

Kühl U, Schultheiss H P

机构信息

Department of Cardiology, Benjamin Franklin Hospital, University of Berlin, Germany.

出版信息

Eur Heart J. 1995 Dec;16 Suppl O:168-72. doi: 10.1093/eurheartj/16.suppl_o.168.

DOI:10.1093/eurheartj/16.suppl_o.168
PMID:8682089
Abstract

Dilated cardiomyopathy (DCM) continues to be an aetiologically unknown heart muscle disease. Recent clinical and experimental data have suggested a temporal relationship with viral myocarditis. The clinical diagnosis of a chronic myocarditis is unspecific. The evaluation of endomyocardial biopsies by light microscopy and their histological classification according to the Dallas criteria is limited by the difficulty in differentiating and quantifying infiltrating lymphocytes from non-inflammatory interstitial cells. Using immunohistological methods that allow better identification and quantification of infiltrating lymphocytes and which provide further evidence for an activated immunological process within the myocardium, myocarditis was diagnosed on endomyocardial biopsy in 48 of 130 patients (37%). According to both haemodynamic and immunohistological findings, 31 of these patients were allocated for immunosuppressive treatment. After a 6 month treatment period with 6-methylprednisolone, 23 patients reported an improvement according to the NYHA classification. Lymphocytic infiltrations were abolished by corticoid treatment in 24 patients. Left ventricular systolic function was improved in 20 patients (64%) as indicated by an increased ejection fraction and stroke volume with a concomitant decrease of left ventricular end diastolic pressure. Our study suggests that immunosuppressive treatment in a subgroup of patients with dilated cardiomyopathy who have a continuing active immunohistologically proven inflammatory process results in a clinical, haemodynamic and immunohistological improvement in 60-70% of patients.

摘要

扩张型心肌病(DCM)仍然是一种病因不明的心肌疾病。最近的临床和实验数据表明它与病毒性心肌炎存在时间上的关联。慢性心肌炎的临床诊断缺乏特异性。通过光学显微镜对心内膜活检组织进行评估,并根据达拉斯标准进行组织学分类,存在局限性,因为难以区分浸润淋巴细胞与非炎性间质细胞并对其进行定量。使用免疫组织学方法可以更好地识别和定量浸润淋巴细胞,并为心肌内激活的免疫过程提供进一步证据,在130例患者中的48例(37%)的心内膜活检中诊断出心肌炎。根据血流动力学和免疫组织学结果,其中31例患者被分配接受免疫抑制治疗。在用6-甲基泼尼松龙治疗6个月后,23例患者根据纽约心脏协会(NYHA)分级报告病情有所改善。皮质类固醇治疗使24例患者的淋巴细胞浸润消失。20例患者(64%)的左心室收缩功能得到改善,表现为射血分数和每搏输出量增加,同时左心室舒张末期压力降低。我们的研究表明,在一组经免疫组织学证实存在持续活动性炎症过程的扩张型心肌病患者中,免疫抑制治疗可使60 - 70%的患者在临床、血流动力学和免疫组织学方面得到改善。

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Eur Heart J. 1995 Dec;16 Suppl O:168-72. doi: 10.1093/eurheartj/16.suppl_o.168.
2
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