Literature DB >> 8229026

A randomised clinical trial comparing prednisone and azathioprine in myasthenia gravis. Results of the second interim analysis. Myasthenia Gravis Clinical Study Group.

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Abstract

From January 1983 to October 1990, 41 patients with generalised myasthenia gravis were randomly given either prednisone or azathioprine. The main goal was to record the time to the occurrence of the first episode of deterioration. During a mean follow-up of 30 months, 21 patients showed deterioration, 12 in the prednisone group and nine in the azathioprine group (p = 0.40). No difference was observed between the two groups in muscular score and functional grade, assessed at the end of each treatment year, or in tolerance. Treatment failure occurred in 17 patients, 12 in the prednisone group and five in the azathioprine group (p = 0.02); even after adjustment for imbalances in prognostic features, the failure rate remained 2.8 times higher in the prednisone group than in the azathioprine group (p = 0.5). In the patients in whom treatment failed, symptoms were initially more severe than in the others, but the combination of prednisone and azathioprine resulted in clinical improvement, consisting of remission or only minor deficits in half of the patients after two years of treatment. These findings indicate that azathioprine increases treatment response compared with prednisone, although no difference in the duration of improvement was demonstrated. Nevertheless, it appears that the most severe forms of the disease, often resistant to prednisone or azathioprine alone, could benefit from the combination of both drugs.

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Year:  1993        PMID: 8229026      PMCID: PMC489815          DOI: 10.1136/jnnp.56.11.1157

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  10 in total

1.  Long term treatment of myasthenia gravis with azathioprine.

Authors:  V Fonseca; C W Havard
Journal:  Postgrad Med J       Date:  1990-02       Impact factor: 2.401

2.  Long-term corticosteroid treatment of myasthenia gravis.

Authors:  T R Johns
Journal:  Ann N Y Acad Sci       Date:  1987       Impact factor: 5.691

3.  Planning the size and duration of a clinical trial studying the time to some critical event.

Authors:  S L George; M M Desu
Journal:  J Chronic Dis       Date:  1974-02

4.  Myasthenia gravis: prolonged treatment with steroids.

Authors:  A Sghirlanzoni; D Peluchetti; R Mantegazza; F Fiacchino; F Cornelio
Journal:  Neurology       Date:  1984-02       Impact factor: 9.910

5.  Effect of immunosuppressive drugs (azathioprine).

Authors:  H G Mertens; G Hertel; P Reuther; K Ricker
Journal:  Ann N Y Acad Sci       Date:  1981       Impact factor: 5.691

6.  Long-term corticosteroid treatment of myasthenia gravis: report of 116 patients.

Authors:  R M Pascuzzi; H B Coslett; T R Johns
Journal:  Ann Neurol       Date:  1984-03       Impact factor: 10.422

7.  Evidence for the superiority of immunosuppressive drugs and prednisone over prednisone alone in lupus nephritis. Results of a pooled analysis.

Authors:  D T Felson; J Anderson
Journal:  N Engl J Med       Date:  1984-12-13       Impact factor: 91.245

8.  Controversies about the treatment of myasthenia gravis.

Authors:  L P Rowland
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-07       Impact factor: 10.154

Review 9.  The course of myasthenia gravis and therapies affecting outcome.

Authors:  D Grob; E L Arsura; N G Brunner; T Namba
Journal:  Ann N Y Acad Sci       Date:  1987       Impact factor: 5.691

10.  Azathioprine in the treatment of myasthenia gravis.

Authors:  A S Witte; D R Cornblath; G J Parry; R P Lisak; N J Schatz
Journal:  Ann Neurol       Date:  1984-06       Impact factor: 10.422

  10 in total
  9 in total

Review 1.  Treatment of myasthenia gravis.

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2.  Myasthenia gravis exacerbation after discontinuing mycophenolate: A single-center cohort study.

Authors:  Björn Oskarsson; David M Rocke; Karsten Dengel; David P Richman
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Review 3.  Pharmacotherapy of Generalized Myasthenia Gravis with Special Emphasis on Newer Biologicals.

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4.  Paraneoplastic syndromes of the neuromuscular junction: therapeutic options in myasthenia gravis, lambert-eaton myasthenic syndrome, and neuromyotonia.

Authors:  Agnes van Sonderen; Paul W Wirtz; Jan J G M Verschuuren; Maarten J Titulaer
Journal:  Curr Treat Options Neurol       Date:  2013-04       Impact factor: 3.598

5.  Current and emerging treatments for the management of myasthenia gravis.

Authors:  Sivakumar Sathasivam
Journal:  Ther Clin Risk Manag       Date:  2011-07-22       Impact factor: 2.423

6.  Autoimmune neuromuscular disorders in childhood.

Authors:  Hugh J McMillan; Basil T Darras; Peter B Kang
Journal:  Curr Treat Options Neurol       Date:  2011-12       Impact factor: 3.598

7.  Treatment of myasthenia gravis based on its immunopathogenesis.

Authors:  Jee Young Kim; Kee Duk Park; David P Richman
Journal:  J Clin Neurol       Date:  2011-12-29       Impact factor: 3.077

8.  Immunosuppressive and monoclonal antibody treatment for myasthenia gravis: A network meta-analysis.

Authors:  Liang Wang; Xiao Huan; Jian-Ying Xi; Hui Wu; Lei Zhou; Jia-Hong Lu; Tian-Song Zhang; Chong-Bo Zhao
Journal:  CNS Neurosci Ther       Date:  2019-02-26       Impact factor: 5.243

Review 9.  Current Treatment of Myasthenia Gravis.

Authors:  Mohammed K Alhaidar; Sumayyah Abumurad; Betty Soliven; Kourosh Rezania
Journal:  J Clin Med       Date:  2022-03-14       Impact factor: 4.241

  9 in total

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