2022年日本重症肌无力和Lambert–Eaton肌无力综合征临床指南

Q4 Immunology and Microbiology
Hiroyuki Murai, Kimiaki Utsugisawa, Masakatsu Motomura, Tomihiro Imai, Akiyuki Uzawa, Shigeaki Suzuki
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引用次数: 6

摘要

修订后的日本重症肌无力(MG)和Lambert-Eaton肌无力综合征(LEMS)临床指南于2022年出版。这些指南(GLs)中值得注意的要点如下:(i)这是第一个包含LEMS描述的日本GLs;(ii)修改MG的诊断标准,以减少假阴性患者的发生率;(iii) MG临床分为6个亚型;(iv) GLs不推荐高剂量口服类固醇治疗方案的升级和降级计划;(v) gl促进了之前gl中最初提出的早期快速治疗策略;(vi)定义难熔MG;(七)包括分子靶向药物的使用;(viii)提出LEMS的诊断标准;(ix)给出了MG和LEMS的处理算法。这些新的GLs有望改善患者的生活质量,并将为当前时代和分子靶向治疗时代架起一座桥梁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Japanese clinical guidelines 2022 for myasthenia gravis and Lambert–Eaton myasthenic syndrome

The Japanese clinical guidelines 2022 for myasthenia gravis and Lambert–Eaton myasthenic syndrome

The revised Japanese clinical guidelines for myasthenia gravis (MG) and Lambert–Eaton myasthenic syndrome (LEMS) were published in 2022. The notable points in these guidelines (GLs) are as follows: (i) these are the first Japanese GLs to include a description of LEMS; (ii) diagnostic criteria of MG are revised to lessen the incidence of false negative patients; (iii) MG is divided into six clinical subtypes; (iv) a high-dose oral steroid regimen with escalation and de-escalation schedule is not recommended by the GLs; (v) the GLs promote the early fast-acting treatment strategy initially proposed in the previous GLs; (vi) refractory MG is defined; (vii) the use of molecular targeted drugs is included; (viii) diagnostic criteria of LEMS are proposed; and (ix) treatment algorithms for both MG and LEMS are presented. These new GLs are expected to improve the patients' quality of life and will serve to bridge the present era with the molecular targeted treatment eras.

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来源期刊
Clinical and Experimental Neuroimmunology
Clinical and Experimental Neuroimmunology Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
52
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