Algahtani Hussein, Shirah Bader, Alshehri Ali, Al Hassani Abdulaziz N, Binseddeq Hosam H, Mukhtar Rayan M, Saleh Bashar, Taj Jamal A
Department of Medicine, Neurology Section, King Abdulaziz Medical City, Jeddah, SAU.
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, SAU.
Cureus. 2021 Dec 27;13(12):e20765. doi: 10.7759/cureus.20765. eCollection 2021 Dec.
A limited number of research studies were published to delineate the clinical pattern of myasthenia gravis in Saudi Arabia. This paper is an attempt to describe some of the clinical aspects related to this disease in two large centers from two main cities in Saudi Arabia.
A retrospective multi-center observational study of patients diagnosed with myasthenia gravis was conducted. The study setting was King Abdulaziz Medical City in Jeddah and Riyadh, Saudi Arabia. The study period was 12 years, starting from January 2007 to May 2019.
A total of 144 patients were included in this study (60 males and 84 females). The most common symptoms at diagnosis were ocular symptoms in 118 patients (81.9%), diplopia in 84 patients (58.3%), and/or blurred vision in 30 patients (20.8%). The majority had positive anti-acetylcholine receptor antibodies (72.2%). Pyridostigmine was the most prescribed medication for 136 patients (94.4%). Immunosuppressive medications were prescribed for 114 patients (79.2%). Around 40% of patients had exacerbations, and approximately 20% were admitted to the ICU. Thymectomy was performed for 97 patients (67.4%).
The present study indicates that the clinical presentation and management of myasthenia gravis remained the same in the last few years despite the introduction of new modalities of diagnosis such as the anti-muscle-specific kinase (anti-MuSK) and other autoantibodies tests. Furthermore, we observed that the number of exacerbations and ICU admission were high, which may indicate inadequate therapy. We are stressing the need for establishing specialized neuromuscular clinics with neurologists trained in neurophysiology to improve the diagnostic accuracy and outcomes for patients with myasthenia gravis.
在沙特阿拉伯,仅有少数研究发表以描述重症肌无力的临床模式。本文旨在描述沙特阿拉伯两个主要城市的两个大型中心中与该疾病相关的一些临床方面。
对诊断为重症肌无力的患者进行回顾性多中心观察性研究。研究地点为沙特阿拉伯吉达和利雅得的阿卜杜勒阿齐兹国王医疗城。研究期为12年,从2007年1月至2019年5月。
本研究共纳入144例患者(60例男性和84例女性)。诊断时最常见的症状为118例患者(81.9%)出现眼部症状,84例患者(58.3%)出现复视,和/或30例患者(20.8%)出现视力模糊。大多数患者抗乙酰胆碱受体抗体呈阳性(72.2%)。136例患者(94.4%)最常使用的药物是溴吡斯的明。114例患者(79.2%)使用了免疫抑制药物。约40%的患者病情加重,约20%的患者入住重症监护病房。97例患者(67.4%)接受了胸腺切除术。
本研究表明,尽管引入了新的诊断方法,如抗肌肉特异性激酶(抗MuSK)和其他自身抗体检测,但重症肌无力的临床表现和治疗在过去几年中保持不变。此外,我们观察到病情加重和入住重症监护病房的人数较多,这可能表明治疗不足。我们强调需要建立专门的神经肌肉诊所,配备接受过神经生理学培训的神经科医生,以提高重症肌无力患者的诊断准确性和治疗效果。