首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Clinical predictors of steroid-induced exacerbation in myasthenia gravis.
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Clinical predictors of steroid-induced exacerbation in myasthenia gravis.

机译:重症肌无力的类固醇诱导加重的临床预测指标。

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Although oral corticosteroids are effective for the treatment of myasthenia gravis (MG), the possibility of steroid-induced exacerbation of symptoms, especially during the initial course of steroid therapy, has limited their use patients with severe MG. However, the factors influencing or predicting in exacerbation are not well understood. The purpose of this study was to identify the clinical factors that predict the initial paradoxical exacerbation of MG in response to steroid therapy. Fifty-five consecutive patients who were administered for the first time high doses of prednisone (40-80 mg) in a tertiary medical centre in Seoul, were included. Prednisone-induced exacerbation was defined as a significant reduction in a patient's Myasthenia Gravis Severity Scale (MSS) score within 4 weeks of prednisone administration. We divided the patients into two groups on the basis of whether or not they experienced prednisone-induced exacerbation, and investigated the differences between the two groups with respect to clinical, laboratory and electrophysiological features. Twenty-three patients (42%) experienced definite exacerbation after prednisone therapy. Older age, predominantly severe bulbar symptoms, and low MSS score were found to be significant clinical predictors of exacerbation by multivariate logistic regression analysis. A high daily dosage of prednisone relative to body weight was found to be neither a predictor of exacerbation nor a predictor of early improvement in bivariate correlation analysis. Steroid-induced exacerbation in MG is a frequently encountered and challenging problem. Clinicians should be aware of the possibility of exacerbation of MG when prescribing prednisone, especially when treating elderly, bulbar dominant, or severely myasthenic patients.
机译:尽管口服皮质类固醇激素可有效治疗重症肌无力(MG),但类固醇激素引起的症状加重的可能性,尤其是在类固醇激素治疗的最初阶段,限制了其对重症MG患者的使用。但是,影响或预测加重的因素尚不十分清楚。这项研究的目的是确定可预测类固醇疗法对MG初始矛盾加重的临床因素。包括在首尔一家三级医疗中心首次接受高剂量泼尼松(40-80毫克)的连续连续患者55名。泼尼松引起的急性发作定义为泼尼松给药后4周内患者的重症肌无力严重程度评分(MSS)评分显着降低。我们根据患者是否接受泼尼松引起的病情加重将其分为两组,并研究两组在临床,实验室和电生理特征方面的差异。泼尼松治疗后有23例患者(42%)病情加重。通过多因素logistic回归分析,发现年龄较大,主要是严重的延髓症状和MSS评分低是加重的重要临床指标。相对于体重,高剂量的泼尼松每日剂量既不能预测病情恶化,也不能预测双变量相关分析的早期改善。 MG中类固醇诱导的恶化是一个经常遇到且具有挑战性的问题。临床医生应在开泼尼松处方时意识到MG加重的可能性,尤其是在治疗老年,延髓为主或重症肌无力患者时。

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