Li Qifu, Chen Ning, Yang Jie, Zhou Muke, Zhou Dong, Zhang Quanwei, He Li
Department of Neurology, West China Hospital, Sichuan University, Guoxuexiang No.37, Chengdu, China, 610041.
Cochrane Database Syst Rev. 2009 Apr 15(2):CD006866. doi: 10.1002/14651858.CD006866.pub2.
Postherpetic neuralgia (PHN) is a painful and refractory complication of herpes zoster. Treatments are either partially or totally ineffective for many people with PHN. Antiviral agents, used at the time of the rash, are one of the best-established approaches that may prevent the development of PHN.
To investigate the effectiveness of antiviral agents in preventing PHN.
We searched the Cochrane Neuromuscular Disease Group Trials Register (January 13 2009), the Cochrane Central Register of Controlled Trials (The Cochrane Library 2008, Issue 4), MEDLINE (January 1966 to November Week 3 2008), EMBASE (January 1980 to Week 02 2009), LILACS (January 1982 to 13 January 2009), and the Chinese Biomedical Retrieval System (January 1978 to 13 January 2009). We checked the references of published studies to identify additional trials.
All randomised and quasi-randomised controlled trials for antiviral treatment given within 72 hours after the onset of herpes zoster for preventing PHN irrespective of any language restrictions.
Two authors independently selected trials and evaluated the methodological quality, then extracted and analysed data from the included trials.
Twenty trials were identified. Twelve trials were excluded and two trials are awaiting classification. Six randomised controlled trials, with a total of 1211 participants were eligible; five trials evaluated oral acyclovir, and one trial with 419 participants evaluated oral famciclovir. There was no significant difference between the oral acyclovir and control groups on the incidence of PHN four months (risk ratio (RR), 0.75; 95% CI 0.51 to 1.11; P = 0.15) or six months (RR 1.05, 95% CI 0.87 to 1.27; P = 0.62) after the onset of the acute herpetic rash. There was some evidence for a reduction in the incidence of pain four weeks after the onset of rash. In the trial of famciclovir versus placebo, neither 500 mg and 750 mg doses of famciclovir reduced the incidence of herpetic neuralgia significantly.
AUTHORS' CONCLUSIONS: Oral acyclovir did not reduce the incidence of PHN significantly. There is insufficient evidence from randomised controlled trials to determine whether other antiviral treatments prevent PHN. Additional well-designed, randomised controlled trials of famciclovir or other new antiviral agents, with a greater number of participants are needed. Future trials should pay more attention to the severity of pain and quality of life of participants, and should be conducted among different subgroups of people, such as people who are immunocompromised.
带状疱疹后神经痛(PHN)是带状疱疹的一种疼痛且难治的并发症。对于许多PHN患者,治疗要么部分无效,要么完全无效。在出疹时使用的抗病毒药物是可能预防PHN发生的最成熟方法之一。
研究抗病毒药物预防PHN的有效性。
我们检索了Cochrane神经肌肉疾病组试验注册库(2009年1月13日)、Cochrane对照试验中央注册库(《Cochrane图书馆》2008年第4期)、MEDLINE(1966年1月至2008年11月第3周)、EMBASE(1980年1月至2009年第2周)、LILACS(1982年1月至2009年1月13日)以及中国生物医学文献数据库(1978年1月至2009年1月13日)。我们检查了已发表研究的参考文献以识别其他试验。
所有在带状疱疹发作后72小时内给予抗病毒治疗以预防PHN的随机和半随机对照试验,不受任何语言限制。
两位作者独立选择试验并评估方法学质量,然后从纳入试验中提取和分析数据。
共识别出20项试验。12项试验被排除,2项试验等待分类。6项随机对照试验符合条件,共1211名参与者;5项试验评估口服阿昔洛韦,1项有419名参与者的试验评估口服泛昔洛韦。在急性疱疹性皮疹发作后四个月(风险比(RR),0.75;95%可信区间0.51至1.11;P = 0.15)或六个月(RR 1.05,95%可信区间0.87至1.27;P = 0.62)时,口服阿昔洛韦组与对照组在PHN发生率上无显著差异。有一些证据表明皮疹发作后四周疼痛发生率有所降低。在泛昔洛韦与安慰剂的试验中,500毫克和750毫克剂量的泛昔洛韦均未显著降低疱疹后神经痛的发生率。
口服阿昔洛韦未显著降低PHN的发生率。随机对照试验中没有足够证据确定其他抗病毒治疗是否能预防PHN。需要更多设计良好、参与者数量更多的泛昔洛韦或其他新型抗病毒药物的随机对照试验。未来的试验应更多关注参与者的疼痛严重程度和生活质量,并且应在不同亚组人群中进行,如免疫功能低下者。