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首页> 外文期刊>Clinical neurology and neurosurgery >Efficacy and safety of tacrolimus in Osserman grade III and Osserman grade IV Myasthenia Gravis
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Efficacy and safety of tacrolimus in Osserman grade III and Osserman grade IV Myasthenia Gravis

机译:奥塞尔曼队III级和奥塞尔曼级IV Myasthenia Gravis的疗效和安全性

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ObjectiveA retrospective observational cohort study was conducted to evaluate the efficacy and safety of tacrolimus in Osserman grade III and Osserman grade IV myasthenia gravis (MG) patients. Patients and methodsMG patients admitted to the First Affiliated Hospital of Guangzhou University of Chinese Medicine between June 2011 and January 2017 with grade III and grade IV according to the modified Osserman scale were recruited and received a telephone follow-up in September 2017. Patients treated with tacrolimus plus prednisone were compared with those treated without tacrolimus. The efficacy of tacrolimus was assessed using MG-activities of daily living (MG-ADL) score, Osserman classification, Myasthenia Gravis Foundation of America (MGFA) post intervention status (PIS), the number of hospitalizations, the number of myasthenic crises and deaths. The adverse drug effects of tacrolimus were monitored. ResultsA total of 124 patients were included. The tacrolimus group had a significantly lower MG-ADL score than the control group at follow-up (1.90?±?2.27vs2.97?±?2.78,p= 0.029). The difference of MG-ADL score between baseline and after follow-up was significantly greater in the tacrolimus group than the control group (-7.20?±?2.95vs-5.52?±?2.91,p?=? 0.003). Fewer patients were hospitalized in the tacrolimus group (p?=? 0.011). The Osserman classification, MGFA PIS, the number of myasthenic crises and deaths did not differ significantly between the two groups. Nineteen patients in the tacrolimus group had adverse drug reactions, but no severe adverse effects appeared. ConclusionOur study suggested that tacrolimus could be an effective and safe treatment for Osserman grade III and Osserman grade IV MG patients.
机译:进行了对象的回顾性观察队列研究,以评估奥塞尔曼级和奥塞尔曼级肌无力肌肌肌肌肌肌肌瘤(MG)患者的疗效和安全性。 2011年6月和2017年1月在2011年和2017年1月期间录取了广州中医大学第一个附属医院的患者,并根据修改后的OSSERMAN规模招募并收到了2017年9月的电话随访。治疗患者将Tacrolimus Plus泼尼松与没有凝尾母羊毛司处理的人进行比较。使用Mg-Activity(Mg-Adl)评分,osserman分类,美国肌无力术(MGFA)哨所职位(PIS),住院人数,医院危机和死亡人数的疗效评估疗效。监测Tacrolimus的不良药物作用。结果包括124名患者。 Tacrolimus组的Mg-AdL得分明显低于对照组(1.90?±2.27Vs2.97?±2.78,P = 0.029)。基线之间的Mg-ADL评分与后续后续比对照组的差异显着大于对照组(-7.20?±2.95VS-5.52?±2.91,P?= 0.003)。在Tacrolimus群体中住院较少的患者(p?= 0.011)。奥塞尔曼分类,MgFA PI,两组之间的岩石危机和死亡人数没有显着差异。躯干组中的十九名患者具有不良药物反应,但没有严重的不良反应出现。结论科学研究表明,他克莫司可能是对奥塞尔曼三世和奥塞尔曼级千兆米蛋白患者的有效和安全的待遇。

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