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基层医疗中疱疹后神经痛管理的循证指南。

Evidence-based guidance for the management of postherpetic neuralgia in primary care.

机构信息

Director, Center for Pain Studies, Rehabilitation Institute of Chicago, IL, USA.

出版信息

Postgrad Med. 2013 Jul;125(4):191-202. doi: 10.3810/pgm.2013.07.2690.

DOI:10.3810/pgm.2013.07.2690
PMID:23933906
Abstract

This article aims to help primary care physicians negotiate gaps in current guidelines for postherpetic neuralgia (PHN). The objectives of this article are to: 1) briefly review the available guidelines and identify their strengths and weaknesses; 2) review the gaps in the guidelines; 3) review new data that were not included in the most recent guidelines; 4) provide expert opinion on how the new data and current guidelines can be used to make treatment decisions; and 5) review several important dimensions of care (eg, tolerability, dosing) and provide guidance. In general, all guidelines recognize the α2δ ligands, tricyclic antidepressants (TCAs), opioids, and tramadol as efficacious systemic options, with topical lidocaine serving as an efficacious nonsystemic approach for localized PHN treatment. The first-line treatment options typically recommended in the guidelines are α2δ ligands and TCAs, while opioids and tramadol are often recommended as second- or third-line options. Since the latest guidelines were published, newer agents (eg, topical capsaicin [8%] patch and gastroretentive gabapentin) have met the standard as first-line therapy with the publication of ≥ 1 randomized controlled trial. However, gabapentin enacarbil has not met this standard due to a lack of a published randomized controlled trial in PHN.

摘要

这篇文章旨在帮助初级保健医生解决带状疱疹后神经痛(PHN)现行指南中的差距问题。本文的目的是:1)简要回顾现有的指南,并确定其优缺点;2)审查指南中的差距;3)审查未包含在最新指南中的新数据;4)就如何使用新数据和当前指南做出治疗决策提供专家意见;5)审查护理的几个重要方面(例如,耐受性,剂量)并提供指导。一般来说,所有指南都承认 α2δ 配体、三环类抗抑郁药(TCAs)、阿片类药物和曲马多是有效的全身性选择,局部 PHN 治疗的局部利多卡因是有效的非系统性方法。指南中通常推荐的一线治疗选择是 α2δ 配体和 TCAs,而阿片类药物和曲马多通常被推荐为二线或三线选择。自最新指南发布以来,由于 PHN 缺乏发表的随机对照试验,新型药物(例如,局部辣椒素[8%]贴剂和胃滞留型加巴喷丁)已符合一线治疗标准。然而,加巴喷丁恩卡他比因缺乏发表的 PHN 随机对照试验而未达到这一标准。

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