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首页> 外文期刊>Muscle and Nerve >Low‐dose rituximab every 6?months for the treatment of acetylcholine receptor–positive refractory generalized myasthenia gravis
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Low‐dose rituximab every 6?months for the treatment of acetylcholine receptor–positive refractory generalized myasthenia gravis

机译:每6个月乙酰胆碱受体阳性耐火炎肌肌炎肌炎的低剂量蓖麻油肢体

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摘要

Abstract Introduction In this prospective, open‐label study we explore the effectiveness of low‐dose rituximab every 6?months in treating refractory generalized myasthenia gravis (GMG). Methods Twelve patients with acetylcholine receptor (AChR)‐positive refractory GMG were enrolled for the study. The primary endpoint was the change in quantitative myasthenia gravis (QMG) score from baseline to the study end. Secondary endpoints included changes in manual muscle testing (MMT), MG‐Related Activities of Daily Living (MG‐ADL), and 15‐item Quality‐of‐Life (MGQOL‐15) scores, as well as prednisolone reduction. Results MG decreased from 18.25?±?4.03 to 8.42?±?3.99 ( P = .0001), MMT from 27.50?±?17.78 to 4.58?±?4.34 ( P = .0001), ADL from 8.50?±?2.84 to 1.17?±?1.27 ( P ??.0001), MGQOL‐15 from 37.25?±?13.78 to 17.50?±?9.73 ( P = .0015), and prednisolone dose from 29.38?±?11.92?mg/day to 8.86?±?1.88?mg/day ( P ?≤?.01). Discussion Low‐dose rituximab every 6?months is effective in treating refractory GMG patients.
机译:摘要在这项前瞻性的介绍中,开放标签研究我们探讨了每6个月治疗难治性广义肌肌肌肌肌(GMG)的每6个月每6个月的有效性。方法乙酰胆碱受体(ACHR) - 阳性难催化Gmg的12例进行了研究。主要终点是从基线到研究结束的定量myasthenia的重量(qmg)的变化。辅助端点包括手动肌肉测试(MMT)的变化,日常生活(MG-ADL)的MG相关活动,以及15项寿命质量(MGQOL-15)分数,以及泼尼松还原。结果Mg从18.25°(±4.03到8.42)下降到8.42?±3.99(p = .0001),mmt从27.50?±17.78至4.58?±4.34(p = .0001),ADL从8.50?±2.84到1.17?±±1.27(p?0001),mgqol-15,从37.25Δ±13.78至17.50?±9.73(p = .0015),和泼尼松酮剂量从29.38?±11.92?mg /天至8.86?±1.88?mg /天(p?≤≤01)。讨论低剂量rituximab每6?个月是有效治疗难敏的GMG患者。

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