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了解视神经脊髓炎谱系障碍的治疗决策:一项结合患者访谈的全球临床记录回顾

Understanding Treatment Decisions in Neuromyelitis Optica Spectrum Disorder: A Global Clinical Record Review with Patient Interviews.

作者信息

Min Ju-Hong, Capobianco Marco, Welsh Carly, Lobo Patricia, deFiebre Gabrielle, Lana-Peixoto Marco, Wingerchuk Dean M, Wang Jiawei, Ringelstein Marius

机构信息

Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Neurology Department, "S. Croce E Carle" Hospital, Cuneo, Italy.

出版信息

Neurol Ther. 2023 Apr;12(2):619-633. doi: 10.1007/s40120-022-00431-y. Epub 2023 Feb 24.

Abstract

INTRODUCTION

We sought insights into neuromyelitis optica spectrum disorder (NMOSD) treatment practices worldwide.

METHODS

Neurologists from the USA, Germany, Italy, Brazil, South Korea, and China completed an online survey, contributing clinical records for aquaporin-4 (AQP4) immunoglobulin G (IgG)-seropositive adults with NMOSD, which included patient demographics, diagnosis, maintenance treatment history, relapse occurrence, and severity. Interviewed patients receiving NMOSD maintenance therapy provided information about their diagnosis, treatment, perceptions about relapse severity or disease stability, and treatment switches.

RESULTS

A total of 389 neurologists submitted clinical records for 1185 patients with AQP4-IgG-seropositive NMOSD; 33 patients with NMOSD were interviewed. Approximately 25% (228/910) of patients from the clinical record review (CRR) were initially misdiagnosed; 24% (8/33) of patients interviewed reported formal misdiagnosis. Misdiagnosis was associated with treatment delay and more relapses compared with correct diagnosis (mean 3.3 vs 2.8). Maintenance therapy was not initiated within 2 months for 47% (221/472) of patients from the CRR and 24% (8/33) of interviewed patients. Oral corticosteroids/immunosuppressive therapies were typically the first maintenance treatment initiated, except for the USA, where monoclonal antibodies were equally likely to be prescribed. Relapse severity influenced the decision to initiate/change therapy and use monoclonal antibodies. Of interviewed patients, 76% (25/33) did not recall having a choice of treatment and many did not know the rationale for treatment choice.

CONCLUSION

Misdiagnosis of NMOSD appears to be common and is associated with a delay in initiation of maintenance therapy, with decisions influenced by relapse severity. Further real-world studies assessing relapse severity in treatment initiation/switch are required to revise NMOSD treatment recommendations.

摘要

引言

我们旨在深入了解全球范围内视神经脊髓炎谱系障碍(NMOSD)的治疗实践。

方法

来自美国、德国、意大利、巴西、韩国和中国的神经科医生完成了一项在线调查,提供了水通道蛋白4(AQP4)免疫球蛋白G(IgG)血清阳性的NMOSD成年患者的临床记录,其中包括患者人口统计学信息、诊断、维持治疗史、复发情况及严重程度。接受NMOSD维持治疗的受访患者提供了有关其诊断、治疗、对复发严重程度或疾病稳定性的看法以及治疗转换的信息。

结果

共有389名神经科医生提交了1185例AQP4-IgG血清阳性NMOSD患者的临床记录;对33例NMOSD患者进行了访谈。临床记录回顾(CRR)中的患者约25%(228/910)最初被误诊;受访患者中有24%(8/33)报告曾被正式误诊。与正确诊断相比,误诊与治疗延迟和更多复发相关(平均3.3次 vs 2.8次)。CRR中的患者47%(221/472)以及受访患者24%(8/33)在2个月内未开始维持治疗。除美国外,口服糖皮质激素/免疫抑制疗法通常是最初开始的维持治疗,在美国,单克隆抗体的处方可能性相同。复发严重程度影响了开始/改变治疗以及使用单克隆抗体的决定。在受访患者中,有76%(25/33)不记得有治疗选择,许多人也不知道治疗选择的依据。

结论

NMOSD的误诊似乎很常见,并且与维持治疗开始延迟有关,决策受复发严重程度影响。需要进一步的真实世界研究来评估治疗开始/转换时的复发严重程度,以修订NMOSD的治疗建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70d9/10043119/bd5a97ae77de/40120_2022_431_Fig1_HTML.jpg

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