Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.

BACKGROUND: An intravenous rather than oral course of methylprednisolone is often prescribed for treating acute relapses in multiple sclerosis (MS) despite the lack of evidence to support this route of administration. Our double-blind placebo-controlled randomised trial was designed to compare the e...

Mô tả đầy đủ

Chi tiết về thư mục
Những tác giả chính: Barnes, D, Hughes, R, Morris, R, Wade-Jones, O, Brown, P, Britton, T, Francis, D, Perkin, G, Rudge, P, Swash, M, Katifi, H, Farmer, S, Frankel, J
Định dạng: Journal article
Ngôn ngữ:English
Được phát hành: 1997
_version_ 1826272685302218752
author Barnes, D
Hughes, R
Morris, R
Wade-Jones, O
Brown, P
Britton, T
Francis, D
Perkin, G
Rudge, P
Swash, M
Katifi, H
Farmer, S
Frankel, J
author_facet Barnes, D
Hughes, R
Morris, R
Wade-Jones, O
Brown, P
Britton, T
Francis, D
Perkin, G
Rudge, P
Swash, M
Katifi, H
Farmer, S
Frankel, J
author_sort Barnes, D
collection OXFORD
description BACKGROUND: An intravenous rather than oral course of methylprednisolone is often prescribed for treating acute relapses in multiple sclerosis (MS) despite the lack of evidence to support this route of administration. Our double-blind placebo-controlled randomised trial was designed to compare the efficacy of commonly used intravenous and oral steroid regimens in promoting recovery from acute relapses in MS. METHODS: 42 patients with clinically definite relapse in MS received oral, and 38 intravenous, methylprednisolone. Clinical measurements at entry and at 1 week, 4 weeks, 12 weeks, and 24 weeks included Kurtzke's expanded disability status scale (EDSS), Hauser's Ambulatory Index, and an arm-function index. The primary outcome criterion was a difference between the two treatment groups of one or more EDSS grades at 4 weeks. FINDINGS: There were no significant differences between the two groups at any stage of the study in any measurement taken: the mean difference in EDSS at 4 weeks (adjusted for baseline level) was 0.07 grades more in those taking oral steroids (95% CI -0.46 to 0.60). The most optimistic outcome for intravenous therapy is an average benefit of less than half a grade improvement on EDSS over oral treatment. INTERPRETATION: Since our study did not show any clear advantage of the intravenous regime we conclude that it is preferable to prescribe oral rather than intravenous steroids for acute relapses in MS for reasons of patient convenience, safety, and cost.
first_indexed 2024-03-06T22:16:29Z
format Journal article
id oxford-uuid:538b7b72-0ba8-46cf-ac4c-bbe0b36abcb2
institution University of Oxford
language English
last_indexed 2024-03-06T22:16:29Z
publishDate 1997
record_format dspace
spelling oxford-uuid:538b7b72-0ba8-46cf-ac4c-bbe0b36abcb22022-03-26T16:32:27ZRandomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:538b7b72-0ba8-46cf-ac4c-bbe0b36abcb2EnglishSymplectic Elements at Oxford1997Barnes, DHughes, RMorris, RWade-Jones, OBrown, PBritton, TFrancis, DPerkin, GRudge, PSwash, MKatifi, HFarmer, SFrankel, JBACKGROUND: An intravenous rather than oral course of methylprednisolone is often prescribed for treating acute relapses in multiple sclerosis (MS) despite the lack of evidence to support this route of administration. Our double-blind placebo-controlled randomised trial was designed to compare the efficacy of commonly used intravenous and oral steroid regimens in promoting recovery from acute relapses in MS. METHODS: 42 patients with clinically definite relapse in MS received oral, and 38 intravenous, methylprednisolone. Clinical measurements at entry and at 1 week, 4 weeks, 12 weeks, and 24 weeks included Kurtzke's expanded disability status scale (EDSS), Hauser's Ambulatory Index, and an arm-function index. The primary outcome criterion was a difference between the two treatment groups of one or more EDSS grades at 4 weeks. FINDINGS: There were no significant differences between the two groups at any stage of the study in any measurement taken: the mean difference in EDSS at 4 weeks (adjusted for baseline level) was 0.07 grades more in those taking oral steroids (95% CI -0.46 to 0.60). The most optimistic outcome for intravenous therapy is an average benefit of less than half a grade improvement on EDSS over oral treatment. INTERPRETATION: Since our study did not show any clear advantage of the intravenous regime we conclude that it is preferable to prescribe oral rather than intravenous steroids for acute relapses in MS for reasons of patient convenience, safety, and cost.
spellingShingle Barnes, D
Hughes, R
Morris, R
Wade-Jones, O
Brown, P
Britton, T
Francis, D
Perkin, G
Rudge, P
Swash, M
Katifi, H
Farmer, S
Frankel, J
Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.
title Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.
title_full Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.
title_fullStr Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.
title_full_unstemmed Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.
title_short Randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis.
title_sort randomised trial of oral and intravenous methylprednisolone in acute relapses of multiple sclerosis
work_keys_str_mv AT barnesd randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT hughesr randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT morrisr randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT wadejoneso randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT brownp randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT brittont randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT francisd randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT perking randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT rudgep randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT swashm randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT katifih randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT farmers randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis
AT frankelj randomisedtrialoforalandintravenousmethylprednisoloneinacuterelapsesofmultiplesclerosis