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临床及 CN-SFEMG 评估新斯的明试验在重症肌无力中的应用。

Clinical and CN-SFEMG evaluation of neostigmine test in myasthenia gravis.

机构信息

Department "G. F. Ingrassia", Section of Neurosciences, University of Catania, Via Santa Sofia 78, 95123, Catania, Italy.

Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, University of Catania, Catania, Italy.

出版信息

Neurol Sci. 2018 Feb;39(2):341-345. doi: 10.1007/s10072-017-3194-0. Epub 2018 Jan 12.

Abstract

Neostigmine test (NT) is a pharmacological test, demonstrating a clinical improvement in patients affected by myasthenia gravis (MG). We aim to compare clinical evaluation and neurophysiological recordings by concentric-needle single-fiber electromyography (CN-SFEMG) in response to acute administration of neostigmine in ocular and generalized MG patients. Twenty-three MG patients (10 with ocular MG and 13 with generalized MG) were evaluated before and after 90 min neostigmine 0.5-mg administration. Clinical responsiveness was assessed by MG composite (MGC) scale. Neurophysiological evaluation by CN-SFEMG considered analysis of mean value of consecutive differences (MCD), single-pair jitter, and blocks. MGC scores significantly improved after NT in generalized MG patients (MGC 11.1 ± 7.6 vs 9.1 ± 6.7, p = 0.02), whereas the improvement was not significant in the ocular group. CN-SFEMG recordings significantly improved after NT in generalized MG patients (MCD 58.9 ± 18.8 vs 45.9 ± 23.2 μs, p = 0.003; single-pair jitter 49.8 ± 26.9 vs 24.1 ± 26.7%, p = 0.0001; blocks 6.2 ± 9.5 vs 2.6 ± 7.4%, p = 0.03) as well as in ocular MG patients (MCD 50.8 ± 22.7 vs 40.1 ± 22.9 μs, p = 0.01; single-pair jitter 35.9 ± 23.7 vs 20.0 ± 25.1%, p = 0.001). CN-SFEMG is a reliable tool to evaluate responsiveness to acute administration of neostigmine in MG. Moreover, neurophysiological modifications to NT could show subclinical improvement in ocular MG better than that of the clinical scale.

摘要

新斯的明试验(NT)是一种药理学试验,可证明患有重症肌无力(MG)的患者的临床改善。我们旨在比较急性新斯的明给药后眼肌型和全身型 MG 患者的临床评估和神经生理学记录,使用同心针单纤维肌电图(CN-SFEMG)进行。23 例 MG 患者(10 例眼肌型 MG 和 13 例全身型 MG)在新斯的明 0.5mg 给药前和给药后 90 分钟进行评估。临床反应性通过 MG 综合评分(MGC)量表评估。CN-SFEMG 的神经生理学评估包括连续差值平均值(MCD)、单对肌颤搐和阻滞分析。新斯的明试验后,全身型 MG 患者的 MGC 评分显著改善(MGC 11.1±7.6 对 9.1±6.7,p=0.02),而眼肌型 MG 组的改善不显著。新斯的明试验后,全身型 MG 患者的 CN-SFEMG 记录显著改善(MCD 58.9±18.8 对 45.9±23.2μs,p=0.003;单对肌颤搐 49.8±26.9 对 24.1±26.7%,p=0.0001;阻滞 6.2±9.5 对 2.6±7.4%,p=0.03),眼肌型 MG 患者也如此(MCD 50.8±22.7 对 40.1±22.9μs,p=0.01;单对肌颤搐 35.9±23.7 对 20.0±25.1%,p=0.001)。CN-SFEMG 是评估 MG 患者对急性新斯的明给药反应的可靠工具。此外,新斯的明试验的神经生理学改变可能比临床量表更能显示眼肌型 MG 的亚临床改善。

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