van Doorn Iris N, Eftimov Filip, Wieske Luuk, van Schaik Ivo N, Verhamme Camiel
Department of Neurology and Clinical Neurophysiology, Amsterdam Neuroscience and University of Amsterdam, Amsterdam UMC, location AMC, the Netherlands.
Department of Clinical Neurophysiology, Sint Antonius Hospital, Nieuwegein, the Netherlands.
Ther Clin Risk Manag. 2024 Feb 14;20:111-126. doi: 10.2147/TCRM.S360249. eCollection 2024.
Diagnosing Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) poses numerous challenges. The heterogeneous presentations of CIDP variants, its mimics, and the complexity of interpreting electrodiagnostic criteria are just a few of the many reasons for misdiagnoses. Early recognition and treatment are important to reduce the risk of irreversible axonal damage, which may lead to permanent disability. The diagnosis of CIDP is based on a combination of clinical symptoms, nerve conduction study findings that indicate demyelination, and other supportive criteria. In 2021, the European Academy of Neurology (EAN) and the Peripheral Nerve Society (PNS) published a revision on the most widely adopted guideline on the diagnosis and treatment of CIDP. This updated guideline now includes clinical and electrodiagnostic criteria for CIDP variants (previously termed atypical CIDP), updated supportive criteria, and sensory criteria as an integral part of the electrodiagnostic criteria. Due to its many rules and exceptions, this guideline is complex and misinterpretation of nerve conduction study findings remain common. CIDP is treatable with intravenous immunoglobulins, corticosteroids, and plasma exchange. The choice of therapy should be tailored to the individual patient's situation, taking into account the severity of symptoms, potential side effects, patient autonomy, and past treatments. Treatment responses should be evaluated as objectively as possible using disability and impairment scales. Applying these outcome measures consistently in clinical practice aids in recognizing the effectiveness (or lack thereof) of a treatment and facilitates timely consideration of alternative diagnoses or treatments. This review provides an overview of the current perspectives on the diagnostic process and first-line treatments for managing the disease.
诊断慢性炎症性脱髓鞘性多发性神经病(CIDP)面临诸多挑战。CIDP 变体的异质性表现、其模仿病症以及解读电诊断标准的复杂性,只是误诊的众多原因中的一部分。早期识别和治疗对于降低不可逆轴索损伤的风险很重要,这种损伤可能导致永久性残疾。CIDP 的诊断基于临床症状、表明脱髓鞘的神经传导研究结果以及其他支持性标准的综合判断。2021 年,欧洲神经病学学会(EAN)和周围神经学会(PNS)发布了对 CIDP 诊断和治疗最广泛采用指南的修订版。这份更新后的指南现在包括 CIDP 变体(以前称为非典型 CIDP)的临床和电诊断标准、更新后的支持性标准以及作为电诊断标准组成部分的感觉标准。由于其有许多规则和例外情况,该指南很复杂,对神经传导研究结果的误解仍然很常见。CIDP 可用静脉注射免疫球蛋白、皮质类固醇和血浆置换进行治疗。治疗方案的选择应根据个体患者的情况进行调整,要考虑症状的严重程度、潜在副作用、患者自主性和既往治疗情况。应使用残疾和损伤量表尽可能客观地评估治疗反应。在临床实践中持续应用这些结果指标有助于认识治疗的有效性(或缺乏有效性),并便于及时考虑替代诊断或治疗方法。本综述概述了目前关于该疾病诊断过程和一线治疗的观点。