Department of Experimental and Clinical Medicine, Neurological Clinic, Marche Polytechnic University, Via Conca 71, 60020, Ancona, Italy.
J Neurol. 2017 Aug;264(8):1697-1704. doi: 10.1007/s00415-017-8505-0. Epub 2017 May 10.
Glucocorticoids are the standard of care for multiple sclerosis (MS) relapses, but the most desirable route of administration is still matter of debate. The aim of the study was to compare the efficacy and safety of oral versus intravenous steroids for treatment of acute relapses in patients with MS. Randomized or quasi-randomized, parallel group trials with direct comparison between oral and intravenous steroid treatment in MS patients with acute relapse were identified through a systematic literature search. Six trials were included involving 419 participants, 210 for oral, and 209 for intravenous groups, respectively. The weighted mean differences (WMDs) in the Kurtzke's Expanded Disability Status Scale (EDSS) score reduction between the oral and intravenous groups were 0.32 [(-0.09 to 0.73); p = 0.129] and 0.11 [(-0.12 to 0.33); p = 0.355] at 1 and 4 weeks after treatment, respectively. The risk ratios (RRs) for improvement by at least one EDSS point were 0.79 [(0.37-1.68); p = 0.539] at week 1 and 0.92 (0.76-1.12); p = 0.400] at week 4. There were no differences in the relapse rate and relapse freedom at 6 months between groups. The WMDs in the mean percentage reduction of Gadolinium-enhancing lesions between oral and intravenous arms were 0.14 (-0.02, 0.29); p = 0.083] and 0.04 (-0.19, 0.28); p = 0.705] at 1 and 4 weeks from treatment. Among the adverse events, insomnia was significantly associated with the oral route of steroid administration [RR 1.25 (1.07-1.46); p = 0.005]. In adult patients with acute MS relapse, there were no clear-cut differences in the efficacy and overall tolerability between oral and intravenous steroids.
糖皮质激素是多发性硬化症(MS)复发的标准治疗方法,但最理想的给药途径仍存在争议。本研究旨在比较口服和静脉注射类固醇治疗 MS 急性发作的疗效和安全性。通过系统文献检索,确定了随机或半随机、平行组试验,比较了 MS 急性发作患者的口服和静脉类固醇治疗。共纳入 6 项试验,涉及 419 名参与者,其中 210 名接受口服治疗,209 名接受静脉治疗。治疗后 1 周和 4 周时,口服组和静脉组 Kurtzke 扩展残疾状况量表(EDSS)评分降低的加权均数差值(WMD)分别为 0.32 [(-0.09 至 0.73);p=0.129]和 0.11 [(-0.12 至 0.33);p=0.355]。治疗后 1 周和 4 周时,EDSS 评分至少改善 1 分的风险比(RR)分别为 0.79 [(0.37 至 1.68);p=0.539]和 0.92 [(0.76 至 1.12);p=0.400]。两组 6 个月时的复发率和复发缓解率无差异。口服组和静脉组的钆增强病变平均百分比减少的 WMD 分别为 0.14 [(-0.02 至 0.29);p=0.083]和 0.04 [(-0.19 至 0.28);p=0.705]。治疗后 1 周和 4 周时。在不良反应中,失眠与口服类固醇给药明显相关[RR 1.25(1.07-1.46);p=0.005]。在急性 MS 复发的成年患者中,口服和静脉类固醇治疗的疗效和总体耐受性没有明显差异。