Suppr超能文献

2015年转诊至拉苏勒·阿克兰医院神经科门诊的重症肌无力患者的人口统计学、临床、实验室及肌电图症状研究。

Study of demographic, clinical, laboratory and electromyographic symptoms in Myasthenia Gravis patients referred to the neurology clinic of Rasoul Akram hospital in 2015.

作者信息

Sadri Y, Haghi-Ashtiani B, Zamani B, Akhundi F H

机构信息

Rasoul Akram Hospital, Iran University of Medical Science, Tehran, Iran.

出版信息

J Med Life. 2015;8(Spec Iss 3):218-221.

Abstract

Myasthenia Gravis is an autoimmune disorder, which is clinically a neuromuscular illness that shows itself as muscular weakness and fatigue. The diagnosis of Myasthenia Gravis depends on clinical evaluation, electrophysiological assessment, and autoantibody detection in serum. Known antibodies could be found in about 90% of the patients, which had a causative relation with disease symptoms. Therefore, the purpose of this paper was a survey on demographic features, clinical, laboratorial, and electromyographic signs of patients with Myasthenia Gravis referred to the neurology clinic of Rasoul Akram hospital. This study was a descriptive cross-sectional one that used an easy sampling method: 54 patients with Myasthenia Gravis who were referred to the neurology clinic of Rasoul Akram were elected in 2015. The patients' information was recorded in the checklists based on the variables and the data were analyzed by using SPSS software version 21. The demographic and the clinical symptoms data of 54 known Myasthenia Gravis patients, whose diagnosis was made according to the clinical symptoms, electrophysiological findings and autoantibody detection, were analyzed in this paper. There were 31 females (57.4%) and 23 males (42.6%) with an average age of 47.3 years. The average age of diagnosis of Myasthenia Gravis in these patients was 42.8 years. Among the patients, 19 (35.2%) had a hospitalization history because of their disease. Due to laboratory findings, 10 patients (18.5%) had Musk antibody, 34 patients (62.9%) had acetylcholine receptor antibodies and 10 patients (18.5%) had none of these two antibodies. Moreover, in electromyographic findings, 38 patients (70.37%) had positive findings and 16 patients (29.6%) had normal findings. Due to the chronic nature of this disease, and its rising trend, educating the people for the early detection of the disease, was necessary as soon as possible so as they would be treated and an acceptable life would be provided for them.

摘要

重症肌无力是一种自身免疫性疾病,临床上是一种神经肌肉疾病,表现为肌肉无力和疲劳。重症肌无力的诊断取决于临床评估、电生理评估以及血清中自身抗体的检测。约90%的患者可检测到已知抗体,这些抗体与疾病症状存在因果关系。因此,本文旨在对转诊至拉苏勒·阿克兰医院神经科门诊的重症肌无力患者的人口统计学特征、临床、实验室及肌电图表现进行调查。本研究为描述性横断面研究,采用简单抽样方法:2015年选取了54例转诊至拉苏勒·阿克兰医院神经科门诊的重症肌无力患者。患者信息根据变量记录在检查表中,并使用SPSS 21版软件进行数据分析。本文分析了54例已知重症肌无力患者的人口统计学和临床症状数据,这些患者的诊断是根据临床症状、电生理检查结果和自身抗体检测做出的。其中女性31例(57.4%),男性23例(42.6%),平均年龄47.3岁。这些患者重症肌无力的平均诊断年龄为42.8岁。患者中,19例(35.2%)因该病有住院史。根据实验室检查结果,10例患者(18.5%)有肌肉特异性酪氨酸激酶抗体,34例患者(62.9%)有乙酰胆碱受体抗体,10例患者(18.5%)这两种抗体均无。此外,在肌电图检查结果中,38例患者(70.37%)检查结果呈阳性,16例患者(29.6%)检查结果正常。由于该病具有慢性性质且呈上升趋势,尽快对民众进行疾病早期检测的教育非常必要,以便他们能够得到治疗并过上可接受的生活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b681/5348943/6d523d6458ad/SIJMedLife-08-03-218-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验