Morosetti M, Meloni C, Iani C, Caramia M, Galderisi C, Palombo G, Gallucci M T, Bernardi G, Casciani C U
Clinica Chirurgica, Università Tor Vergata, Rome, Italy.
Artif Organs. 1998 Feb;22(2):129-34. doi: 10.1046/j.1525-1594.1998.05061.x.
In this study we introduce a new combination treatment of plasma exchange (PE) and high daily doses of prednisone for severe forms of myasthenia gravis (MG). The clinical efficacy of the combined therapy has been tested in 18 patients suffering from severe forms of MG. The protocol included 5 sessions of PE, performed in a range of 15 days, 1 session every 3 days, with concurrent administration of oral prednisone (1 mg/kg of body weight), starting at the first session of PE and given daily for at least 3 months. At the end of the entire cycle of PE, almost complete recovery (more than 90% of the initial clinical score) was obtained in 8 of 18 patients while an improvement between 60 and 90% of the initial score was achieved in 9 of 18 patients. An early improvement was noted 24 h after the beginning of plasmapheresis in 11 of 18 patients. No recurrence of symptoms was reported after 36 months of follow-up for 17 patients. The administration of steroid therapy was never followed by an early exacerbation of myasthenic symptoms as reported when it is administered in the absence of concomitant PE. According to our results, we can conclude that high doses of oral prednisone therapy in simultaneous association with PE lead to successful control of severe forms of MG, significantly superior to the therapeutic strategies until now adopted and reported in literature.
在本研究中,我们引入了一种针对重症肌无力(MG)严重形式的血浆置换(PE)和高剂量每日泼尼松联合治疗方法。该联合疗法的临床疗效已在18例重症MG患者中进行了测试。方案包括在15天内进行5次PE,每3天进行1次,同时口服泼尼松(1mg/kg体重),从PE的第一次治疗开始,每日服用至少3个月。在整个PE周期结束时,18例患者中有8例几乎完全恢复(超过初始临床评分的90%),18例患者中有9例改善程度在初始评分的60%至90%之间。18例患者中有11例在血浆置换开始后24小时出现早期改善。17例患者随访36个月后未报告症状复发。与在未同时进行PE时使用类固醇疗法时所报告的情况不同,该疗法从未导致肌无力症状早期加重。根据我们的结果,我们可以得出结论,高剂量口服泼尼松疗法与PE同时联合使用可成功控制重症MG,明显优于目前文献中报道的治疗策略。