眼阻
医学
免疫疗法
重症肌无力
强的松
外科
胃肠病学
内科学
免疫学
免疫系统
上睑下垂
作者
Tarin A. Europa,Melissa Nel,Jeannine M. Heckmann
摘要
ABSTRACT Introduction : Although immunotherapies such as prednisone are effective in treating myasthenic muscle weakness, their effect on resolution of myasthenic‐induced persistent ophthalmoparesis is unknown. Methods : We observed patients with myasthenia gravis during their first year of immunotherapy, documenting ophthalmoplegia scores and drug doses. Results : Seventy‐six of 87 cases had persistent ophthalmoparesis. With immunotherapy, the median time to resolution of ophthalmoparesis was 7 months, and 37% of cases resolved within 3 months. Patients starting therapy within 12 months of symptom onset were twice as likely to have resolution in the first year ( P = 0.028). Resolution of ophthalmoparesis within 3 months, compared with later resolution, was associated with higher initial prednisone doses (mean 0.5 vs. 0.3 mg/kg/day; P = 0.014). However, 25% of the higher dose group also received intravenous immunoglobulin/plasma exchange; after their exclusion, the finding was not significant. Discussion : One‐third of cases with myasthenic ophthalmoparesis resolved within 3 months of immunotherapy, particularly in response to more aggressive immunotherapy. Muscle Nerve 58 : 542–549, 2018
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