Treatment of Myasthenic Crisis in Late Life
- 1 October 1985
- journal article
- research article
- Published by Southern Medical Association in Southern Medical Journal
- Vol. 78 (10) , 1208-1210
- https://doi.org/10.1097/00007611-198510000-00017
Abstract
In 32 patients with the onset of myasthenia gravis after age 50, myasthenic crisis occurred in 53% and persisted for a mean of 33 days (range six to 84 days). Three of the patients has a second crisis. Precipitating factors were found in 60% of the episodes. Treatment of 20 episodes of crisis resulted in excellent recovery. No patient died in crisis. All regained enough function to return home. Those patients (50%) who had no medical complications recovered most rapidly. The most common medical complications were aspiration and bacterial pneumonia, cardiac arrhythmias, and congestive heart failure. Large doses of prednisone in combination with serial plasma exchanges was the most effective therapy. This group of patients had the fewest medical complications (29%) and the fastest recovery.This publication has 2 references indexed in Scilit:
- Functional Activities of Autoantibodies to Acetylcholine Receptors and the Clinical Severity of Myasthenia GravisNew England Journal of Medicine, 1982
- CRITICAL REAPPRAISAL OF THE USE OF EDROPHONIUM (TENSILON) CHLORIDE TESTS IN MYASTHENIA GRAVIS AND SIGNIFICANCE OF CLINICAL CLASSIFICATION*†Annals of the New York Academy of Sciences, 1966