Oral dexamethasone pulse therapy versus daily prednisolone in sub-acute onset myositis, a randomised clinical trial

  • J. van de Vlekkert
  • , J.E. Hoogendijk
  • , R.J. de Haan
  • , A. Algra
  • , I. van der Tweel
  • , W.L. van der Pol
  • , E.V. Uijtendaal
  • , GROUP Dexa Myositis Trial
  • , M. de Visser

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

To determine if high-dose pulsed dexamethasone is more effective and safer than daily high-dose prednisolone in treatment-naive adult patients with inflammatory myopathies (sporadic inclusion body myositis excluded) we performed a multicenter, double-blind randomised controlled clinical trial with 18 months follow-up. Sixty-two patients were randomised into 28-day cycles of oral high-dose dexamethasone or daily high-dose prednisolone. Primary outcome measures included (1) seven point composite score of six clinically relevant outcomes and (2) (time-to) remission and (time-to) relapse. No difference between both treatment groups on the composite score was found. Side-effects occurred significantly less frequently in the dexamethasone group. Median time to relapse was 60 (2.9) weeks in the prednisolone and 44 (4.7) weeks in the dexamethasone group (log-rank test p=0.03). In conclusion, pulsed high-dose oral dexamethasone is not superior to daily prednisolone as first-line treatment of idiopathic inflammatory myopathies, but is a good alternative by causing substantially fewer side-effects.

Original languageEnglish
Pages (from-to)382-389
Number of pages8
JournalNeuromuscular Disorders
Volume20
Issue number6
DOIs
Publication statusPublished - Jun 2010

Keywords

  • Adult
  • Anti-Inflammatory Agents
  • Dexamethasone
  • Double-Blind Method
  • Female
  • Humans
  • Male
  • Middle Aged
  • Myositis
  • Myositis, Inclusion Body
  • Prednisolone
  • Risk Assessment
  • Sample Size
  • Treatment Outcome
  • Comparative Study
  • Journal Article
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

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