Department of Neurology, Mayo Clinic College of Medicine and Science, Phoenix, AZ.
Neurologist. 2023 Mar 1;28(2):129-134. doi: 10.1097/NRL.0000000000000479.
The clinical benefit of intravenous immunoglobulin (IVIG) in adult individuals with neuroinvasive West Nile virus (niWNV) infection is not well substantiated. We sought to critically assess current evidence regarding the efficacy of IVIG in treating patients with niWNV.
The objective was addressed through the development of a critically appraised topic that included a clinical scenario, structured question, literature search strategy, critical appraisal, assessment of results, evidence summary, commentary, and bottom-line conclusions. Participants included consultant and resident neurologists, a medical librarian, clinical epidemiologists, and a content expert in the field of neuro-infectious diseases.
The appraised study enrolled 62 participants with suspected niWNV, randomized into 3 different arms [37 participants in the Omr-IgG-am group, 12 in the Polygam group, and 13 in the normal saline (NS) group]. Omr-IgG-am and Polygam are different formulations of IVIG. IVIG safety, measured as rates of serious adverse events, was the primary study outcome while IVIG efficacy, measured as rates of unfavorable outcomes, was a secondary endpoint. The estimated rates of SAE were statistically similar in all groups (51.4% Omr-IgG-am, 58.3% Polygam, and 23.1% NS groups). Unfavorable outcomes also occurred at a similar rate between all the groups (51.5% Omr-IgG-am, 54.5% Polygam, and 27.3% NS).
The appraised trial showed that Omr-IgG-am and Polygam are as safe as NS. Data on efficacy from this trial were limited by a small sample size. Phase III clinical trials on IVIG efficacy in NiWNV infection are needed.
静脉注射免疫球蛋白(IVIG)在成人神经侵袭性西尼罗河病毒(niWNV)感染中的临床获益尚未得到充分证实。我们旨在批判性评估 IVIG 治疗 niWNV 患者的疗效的现有证据。
通过制定一个批判性评价主题来实现目标,该主题包括临床情况、结构化问题、文献搜索策略、批判性评价、结果评估、证据总结、评论和底线结论。参与者包括顾问和住院医师神经科医生、医学图书馆员、临床流行病学家以及神经感染性疾病领域的内容专家。
评价研究纳入了 62 名疑似患有 niWNV 的患者,随机分为 3 个不同的治疗组[37 名患者接受 Omr-IgG-am 治疗,12 名患者接受 Polygam 治疗,13 名患者接受生理盐水(NS)治疗]。Omr-IgG-am 和 Polygam 是两种不同的 IVIG 制剂。IVIG 的安全性,以严重不良事件(SAE)发生率来衡量,是主要的研究结局,而 IVIG 的疗效,以不良结局发生率来衡量,则是次要终点。所有组的 SAE 发生率均具有统计学相似(51.4% Omr-IgG-am 组、58.3% Polygam 组和 23.1% NS 组)。所有组的不良结局发生率也相似(51.5% Omr-IgG-am 组、54.5% Polygam 组和 27.3% NS 组)。
评价试验表明,Omr-IgG-am 和 Polygam 与 NS 一样安全。本试验关于疗效的数据受到样本量小的限制。需要进行 III 期临床试验以评估 IVIG 在 NiWNV 感染中的疗效。