无声的负担:识别和管理视神经脊髓炎的不可见症状。

IF 8.7 1区 医学 Q1 CLINICAL NEUROLOGY
Lorena Lorefice, Antonio Carotenuto, Giuseppe Fenu
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引用次数: 0

摘要

水通道蛋白-4阳性视神经脊髓炎谱系障碍(AQP4+NMOSD)是一种自身免疫性星形细胞病,主要表现为视觉、运动和感觉症状,取决于病变部位。然而,患者经常会出现看不见的症状,如疲劳、疼痛、神经精神症状和膀胱/肠功能障碍,尽管这些症状对生活质量有重大影响,但往往被忽视。使用PubMed进行系统文献综述,关键词为AQP4+NMOSD的疲劳、疼痛、膀胱/肠功能障碍和神经精神症状。这篇综述探讨了这些经常被忽视的症状的流行、评估和管理。急需改进AQP4+NMOSD中不可见症状的检测和监测。加强评估不仅对于开发靶向治疗,而且对于确定这些症状是否反映潜在的疾病活动,最终导致优化的治疗策略至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Silent burden: recognising and managing invisible symptoms in neuromyelitis optica.

Aquaporin-4-positive neuromyelitis optica spectrum disorder (AQP4+NMOSD) is an autoimmune astrocytopathy primarily characterised by visual, motor, and sensory symptoms, depending on lesion location. However, patients frequently experience invisible symptoms such as fatigue, pain, neuropsychiatric symptoms, and bladder/bowel dysfunction, which are often overlooked despite their substantial impact on quality of life. A systematic literature review was conducted using PubMed, with keywords related to fatigue, pain, bladder/bowel dysfunction, and neuropsychiatric symptoms in the context of AQP4+NMOSD. The review explores the prevalence, assessment, and management of these frequently neglected symptoms. There is a critical need for improved detection and monitoring of invisible symptoms in AQP4+NMOSD. Enhanced assessment is crucial not only for developing targeted therapies but also for determining whether these symptoms reflect underlying disease activity, ultimately leading to optimised treatment strategies.

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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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