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首页> 外文期刊>Journal of neurology >Rituximab as induction therapy in refractory myasthenia gravis: 18month follow-up study
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Rituximab as induction therapy in refractory myasthenia gravis: 18month follow-up study

机译:Rituximab作为难治性Myasthenia的诱导疗法,Remis:18个月后续研究

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BackgroundMyasthenia gravis is an immune-mediated disorder characterized by easy fatigability and diurnal variation in skeletal muscle weakness. Aim of therapy is to prevent crisis and maintain remission. However, despite standard therapy, some remain refractory to treatment.Aims and objectivesTo look for efficacy of rituximab in treating refractory myasthenia gravis (MG) in the form of MGFA-PIS score, number of crisis, and dose reduction in immunotherapies.Material and methodsA retrospective study was performed in patients with myasthenia gravis (MG) referred to the All India Institute of Medical Sciences (AIIMS) from January 2012 to December 2017 with follow-up of at least 6 months.ResultsEight refractory MG patients (six AchR positive and two Musk-positive) were identified on oral corticosteroids and azathioprine. After four cycles of rituximab, all patients showed a dose reduction of whom seven were completely tapered off prednisone and there was a 53.8% dose reduction in azathioprine. All patients were continued on AZA after RTX infusion unless contraindicated. Seven achieved minimal manifestation (MM)2 status as per the MGFA-PIS scale. None of the patients had infusion associated reactions or cytopenia post-RTX infusion.ConclusionIn this small retrospective study, we used RTX as induction therapy and results suggest that repeated RTX infusions may not be necessary as it adds to cost of therapy, especially in LMIC like India.
机译:BackgroundMyasthenia Gravis是一种免疫介导的疾病,其特征在于骨骼肌弱点的易脂肪性和昼夜变化。治疗的目的是防止危机并保持缓解。然而,尽管标准治疗,但有些仍然是治疗令人难以难以理解的。事宜和Objectivesto寻找毒素肢体以MgFA-PIS评分,危机数量和剂量减少的形式治疗难治性Myasthenia Gravis(Mg)的疗效。材料和方法从2012年1月到2017年12月,肌球血症(MG)患者对肌颌骨(MG)的患者进行了回顾性研究,其中包括至少6个月的后续行动。令人难以置力的MG患者(六ACHR阳性和两个在口腔皮质类固醇和AzathioLine上鉴定了麝香阳性。经过四个rituximab循环后,所有患者均显示出七种血小酮完全逐渐变细的剂量减少,并且在氮嘌呤中减少了53.8%。除非禁忌,否则所有患者均继续静止AZA。根据MGFA-PIS量表,七项实现了最小的表现(mm)2状态。没有一个患者患有输液相关的反应或细胞缺陷后rtx infusion.clusurusivein,我们使用RTX作为感应治疗,结果表明反复的RTX输注可能不是必要的,因为它增加了治疗成本,特别是在LMIC中可能不需要印度。

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