Division of Neurology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Division of Neurology, Department of Medicine, The Ellen and Prosserman Centre for Neuromuscular Diseases, University Health Network, Toronto, Ontario, Canada.
Eur J Neurol. 2021 Apr;28(4):1375-1384. doi: 10.1111/ene.14675. Epub 2020 Dec 31.
Defining refractory myasthenia gravis is important, as this can drive clinical decision making, for example, by escalating treatments in refractory individuals. There are several definitions of refractory myasthenia, and their performances have not been compared. Having valid and reliable criteria can help select patients in whom more aggressive treatments may be needed.
We applied five different refractory myasthenia criteria (Drachman, Mantegazza, Suh, the International Consensus Guideline (ICG), and the randomised controlled trial of eculizumab in refractory, anti-acetylcholine receptor positive, generalised myasthenia gravis (REGAIN), to a cohort of 237 patients. We compared the proportion of refractory patients among different criteria and their scores on disease severity, fatigue, and quality-of-life (QoL) scales. We also assessed the agreement for each criterion between two trained assessors.
The Drachman, Mantegazza, and Suh criteria resulted in high proportions of refractory individuals (40.1%, 39.2%, and 38.8%, respectively), compared with the ICG and REGAIN criteria (9.7% and 3.0%, respectively). Refractory patients by the ICG and REGAIN criteria had worse disease severity, QoL, and fatigue scores, compared with patients classified as refractory by other criteria. All criteria had high agreement between raters (between 70% and 100%).
There is high variability in the proportion of refractory myasthenia gravis patients depending on the criteria used, with ICG and REGAIN criteria capturing patients with worse disease severity. This reflects conceptual differences as to what refractory means. Further multicenter studies are needed to determine appropriate criteria for refractory myasthenia gravis.
定义难治性重症肌无力很重要,因为这可以指导临床决策,例如在难治性患者中升级治疗。有几种难治性重症肌无力的定义,但其性能尚未进行比较。拥有有效的和可靠的标准可以帮助选择可能需要更积极治疗的患者。
我们将五种不同的难治性重症肌无力标准(Drachman、Mantegazza、Suh、国际共识指南(ICG)和难治性、抗乙酰胆碱受体阳性、全身性重症肌无力(REGAIN)的依库珠单抗随机对照试验)应用于 237 例患者。我们比较了不同标准下难治性患者的比例及其疾病严重程度、疲劳和生活质量(QoL)评分。我们还评估了两位训练有素的评估员对每个标准的一致性。
与 ICG 和 REGAIN 标准(分别为 9.7%和 3.0%)相比,Drachman、Mantegazza 和 Suh 标准导致的难治性个体比例较高(分别为 40.1%、39.2%和 38.8%)。与其他标准分类为难治性的患者相比,根据 ICG 和 REGAIN 标准分类为难治性的患者疾病严重程度、QoL 和疲劳评分更差。所有标准的评估者之间的一致性都很高(70%-100%)。
根据使用的标准,难治性重症肌无力患者的比例存在很大差异,ICG 和 REGAIN 标准可捕获疾病严重程度更差的患者。这反映了对难治性意味着什么的概念差异。需要进一步的多中心研究来确定难治性重症肌无力的适当标准。