伊拉克患者重症肌无力加重的相关因素

Ahmed Abdalrazak Al Dulaimy, SarmadA. Al-Mashtah, M. Ahmed
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引用次数: 0

摘要

背景:重症肌无力是一种神经肌肉接头的自身免疫性疾病,可导致波动性肌无力和严重疲劳。疾病恶化是一种危急情况,需要确定其诱发因素,以改进预防措施。目的:我们的研究旨在确定一组伊拉克患者重症肌无力恶化的易感因素。受试者和方法:共有30名重症肌无力患者在入院前一个月内症状恶化,确定为功能残疾、吞咽困难或呼吸衰竭。通过病史采集、临床检查和调查对每位患者进行评估,以确定可能的加重因素。结果:感染者占56.7%。(26.7%)的患者不遵守治疗,(16.7%)的患者出现药物引起的病情恶化。结论:感染是疾病恶化的最常见诱因,并与不良结局有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors associated with Exacerbation of Myasthenia Gravis in a Group of Iraqi Patients
Background: Myasthenia gravis is an autoimmune disease of the neuromuscular junction that results in fluctuating muscle weakness as well as significant fatigue. Disease exacerbation is a critical condition, and the predisposing factors for it need to be identified to improve preventive measures. Objectives:  Our study aims to determine the predisposing factors for myasthenia gravis exacerbations in a group of Iraqi patients. Subjects and Methods: A total number of 30 myasthenia gravis patients were admitted to the hospital with an exacerbation of their symptoms, determined as the development of functional disability, dysphagia, or respiratory failure within one month prior to admission. Each patient was assessed by history taking, clinical examination, and investigations to determine the possible exacerbating factor. Results: There were (56.7%) of patients with infection. Non-compliance to treatment was found in (26.7%) of patients, and medication induced exacerbation was found in (16.7%) of the patients. Conclusion: Infection is the most common predisposing factor for disease exacerbation and is associated with an unfavorable outcome.
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来源期刊
CiteScore
0.10
自引率
0.00%
发文量
34
审稿时长
12 weeks
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