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机械循环支持联合免疫抑制治疗巨细胞性心肌炎 - 日本单中心经验。

Mechanical Circulatory Support Combined With Immunosuppression for the Treatment of Giant Cell Myocarditis - A Single-Center Experience in Japan.

机构信息

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Department of Adult Cardiac Surgery, National Cerebral and Cardiovascular Center.

出版信息

Circ J. 2020 Apr 24;84(5):815-819. doi: 10.1253/circj.CJ-19-0847. Epub 2020 Mar 14.

DOI:10.1253/circj.CJ-19-0847
PMID:32173690
Abstract

BACKGROUND

The therapeutic strategy for giant cell myocarditis (GCM) remains controversial, so we reviewed the clinical status of Japanese patients with GCM.

METHODS AND RESULTS

We retrospectively reviewed 6 consecutive patients with GCM requiring percutaneous mechanical circulatory support (p-MCS), with 3 further requiring ventricular assist devices. One patient died during p-MCS. Cardiac function improved in the other 5 with immunosuppressive therapy, but only 3 patients treated with dual immunosuppressants, including cyclosporine (CyA), achieved >1-year survival.

CONCLUSIONS

The prognosis of patients with fulminant GCM is poor, but a treatment that combines MCS and early administration of CyA-based immunosuppressants will be useful.

摘要

背景

巨细胞心肌炎(GCM)的治疗策略仍存在争议,因此我们回顾了日本 GCM 患者的临床状况。

方法和结果

我们回顾性分析了 6 例连续接受经皮机械循环支持(p-MCS)的 GCM 患者,其中 3 例进一步需要心室辅助装置。1 例患者在 p-MCS 期间死亡。另外 5 例患者经免疫抑制治疗后心功能改善,但仅 3 例接受包括环孢素(CyA)在内的双免疫抑制剂治疗的患者存活时间超过 1 年。

结论

暴发性 GCM 患者的预后较差,但联合 MCS 和早期使用 CyA 为基础的免疫抑制剂治疗将是有用的。

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Successful bridge to recovery in a patient with fulminant giant cell myocarditis that developed from multiple autoimmune disorders including myasthenia gravis: a case report.一名患有包括重症肌无力在内的多种自身免疫性疾病并发暴发性巨细胞心肌炎的患者成功康复:病例报告。
Eur Heart J Case Rep. 2022 Feb 3;6(2):ytac046. doi: 10.1093/ehjcr/ytac046. eCollection 2022 Feb.
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Clinical Identification and Characteristic Analysis of Giant Cell Myocarditis in 12 Cases.
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