A meta-analysis of methylprednisolone in recovery from multiple sclerosis exacerbations

被引:47
作者
Miller, DM
Weinstock-Guttman, B
Béthoux, F
Lee, JC
Beck, G
Block, V
Durelli, L
LaMantia, L
Barnes, D
Sellebjerg, F
Rudick, RA
机构
[1] Cleveland Clin Fdn, IH Page Ctr Hlth Outcomes Res, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Biostat & Epidemiol, Cleveland, OH 44195 USA
[3] Cleveland Clin Fdn, Dept Neurol, Cleveland, OH 44195 USA
[4] SUNY Buffalo, Buffalo Gen Hosp, Dept Neurol, Buffalo, NY 14260 USA
[5] Univ Turin, Dipartimento Neurosci, Turin, Italy
[6] Inst Nazl Neurol C Besta, Milan, Italy
[7] Atkinson Morleys Hosp, Dept Neurol, London, England
[8] Univ Copenhagen, Glostrup Hosp, Dept Neurol, DK-1168 Copenhagen, Denmark
来源
MULTIPLE SCLEROSIS | 2000年 / 6卷 / 04期
关键词
multiple sclerosis; methylprednisolone; meta-analysis;
D O I
10.1191/135245800678827770
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Despite recent advances in multiple sclerosis treatment, patients experience relapses for which standard treatment remains glucocorticosteroids (GCS). However, there is limited information comparing doses or routes of administration for different GCS types or the benefit of GCS compared to natural recovery. Currently, high dose (HD) methylprednisolone (MP) is the preferred therapy We conducted meta-analyses of published studies assessing MP at different doses and in comparison to other steroid products or no treatment Relevant studies were identified through predetermined processes and five articles met the inclusion criteria. Three studies compared HD MP to placebo; two studies compared the effect of HD MP and low dose (LD) MP; only one accepted report compared HD MP to another GCS. This report could not be included in a meta-analysis. The meta-analysis of HD MP vs placebo studies indicated a mean treatment difference of 0.76 in Expanded Disability Status Score (EDSS) changes from baseline. The meta-analysis of HD and LD MP demonstrated no difference in EDSS change. Despite these rather obvious findings, these meta-analyses have been valuable in identifying further research questions. We recommend studies to determine optimum benefit related to dosage, timing for starting therapy and the most appropriate GCS type. Given the advances in MS therapeutics these studies will have to include patients on additional disease modifying therapy.
引用
收藏
页码:267 / 273
页数:7
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