首页|期刊导航|中国合理用药探索|重症肌无力多病共存患者高风险药物识别与靶向治疗进展

重症肌无力多病共存患者高风险药物识别与靶向治疗进展OA

High-Risk Drug Identification and Targeted Therapy Progress in Patients with Myasthenia Gravis Complicated with Multiple Diseases

中文摘要英文摘要

重症肌无力(MG)是一种由自身抗体介导、累及神经肌肉接头(NMJ)传递的自身免疫性疾病.由于中老年 MG 患者常处于多病共存状态,多重用药的临床管理面临严峻挑战.本文以1例高龄 MG 多病共存患者的多药联用风险为切入点,系统梳理了MG多病共存患者高风险药物识别、相关机制及用药建议;剖析了胆碱酯酶抑制剂、糖皮质激素、免疫抑制剂等传统 MG 治疗药物的联用风险.针对 MG 传统治疗方案特异性不足且联合用药风险较高的临床困境,进一步阐述了艾加莫德、依库珠单抗和泰它西普 3 种用于 MG 治疗的靶向生物制剂的作用机制、适用人群、给药方式、安全性特征及药物相互作用信息,以期实现疾病平稳控制与用药安全的双重目标,改善患者的长期生活质量.

Myasthenia gravis(MG)is an autoimmune disease mediated by autoantibodies and involved in neuromuscular junction(NMJ)transmission.Elderly MG patients are often complicated with multiple diseases,bringing severe challenges to clinical polypharmacy management.Starting with the medication risks of one elderly MG patient with multimorbidity,this article systematically summarizes the identification of high-risk drugs and related medication suggestions for MG patients with multiple diseases,and analyzes the combined medication risks of traditional MG drugs such as cholinesterase inhibitors,glucocorticoids and immunosuppressants.In view of the clinical dilemma of insufficient specificity and high combined medication risk of traditional MG regimens,this paper further expounds the mechanism of action,applicable population,administration route,safety characteristics and drug interaction of three targeted biological agents including efgartigimod,eculizumab and telitacicept,so as to achieve the dual goals of stable disease control and medication safety,and improve the long-term quality of life of patients.

杨玉娇;张涵煦;陈丽婷;易湛苗

北京大学第三医院药学部,北京 100191||山东第一医科大学第一附属医院(山东省千佛山医院)药学部,济南 250014北京大学第三医院药学部,北京 100191||天津医科大学总医院药剂科,天津 300052北京大学第三医院药学部,北京 100191||广西医科大学第一附属医院药学部,南宁 530021北京大学第三医院药学部,北京 100191||北京大学医学部药物评价中心,北京 100191

医药卫生

重症肌无力多病共存多重用药用药风险靶向生物制剂

myasthenia gravismultiple diseasespolypharmacymedication risktargeted biological agents

《中国合理用药探索》 2026 (5)

19-23,5

北京慢性病防治与健康教育研究会、中关村人才协会医工领域"未来人才"培养计划(MBRC0012025062)

10.3969/j.issn.2096-3327.2026.05.002

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