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Long‐term corticosteriod treatment of myasthenia gravis: Report of 116 Patients
Author(s) -
Pascuzzi Robert M.,
Coslett H. Branch,
Johns T. R.
Publication year - 1984
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.410150316
Subject(s) - myasthenia gravis , medicine , prednisone , thymoma , weakness , surgery , pediatrics
One hundred sixteen patients, aged 8 to 82 years, with myasthenia gravis were treated with prednisone, 6o to 80 mg daily, until the onset of improvement, followed by lower‐dose alternate‐day therapy of several years' duration. Of all patients, 80.2%achived wither remission(27.6%) or marked improvement (52.6%). Moderate improvement occurred in 14.7%, and 5.2% showed no improvement. Increasing age correlated with a favorable outcome, but sex, duration of illness prior to treatment, severity and distribution of weaskness at the time of onset of treatment, and presence of thymoma were not factors in the response to therapy.

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