Service de Dermatologie, AP-HP, Hôpital Henri Mondor, Créteil, France.
Service de Dermatologie et Allergologie, AP-HP, Hôpital Tenon, Paris, France.
J Eur Acad Dermatol Venereol. 2019 May;33(5):842-849. doi: 10.1111/jdv.15447. Epub 2019 Feb 28.
Treatment of erythema multiforme (EM) is not codified. We performed a systematic review of the effect of any topical or systemic treatment on time to healing and frequency of episodes with acute and chronic forms of EM in adults. Four databases (MEDLINE, CENTRAL, EMBASE and LILACS) and other sources were searched for articles published up to 20 March 2018. Randomized control trials (RCTs), observational studies and case series (n ≥ 10) were considered. From 1558 references, we included one RCT and six case series. The RCT (n = 20) showed a significant difference in complete remission of EM with continuous acyclovir vs. placebo over 6 months. One case series found a mean reduction in flare duration with thalidomide for recurrent EM (5.1 vs. 16.2 days; n = 20). Adverse events were poorly or not reported in included studies. Quality of life was never assessed. One limitation of our study is that we excluded the cases of isolated mucosal EM in order to prevent inclusion of Stevens-Johnson syndrome cases. In conclusion, there is low-level evidence for continuous acyclovir treatment for recurrent EM (one RCT). Evidence for other treatments is only based on retrospective case series. Results for thalidomide, in particular, encourage further research. Data concerning safety are insufficient. PROSPERO registration no. CRD42016053175.
多形性红斑(EM)的治疗方法尚未确定。我们对任何局部或全身治疗在成人急性和慢性 EM 形式的愈合时间和发作频率方面的影响进行了系统评价。我们在 4 个数据库(MEDLINE、CENTRAL、EMBASE 和 LILACS)和其他来源中搜索了截至 2018 年 3 月 20 日发表的文章。我们考虑了随机对照试验(RCT)、观察性研究和病例系列(n≥10)。从 1558 篇参考文献中,我们纳入了 1 项 RCT 和 6 项病例系列研究。该 RCT(n=20)显示,在 6 个月的时间内,连续使用阿昔洛韦与安慰剂相比,EM 完全缓解的差异有统计学意义。一项病例系列研究发现,对于复发性 EM,沙利度胺可使皮疹发作持续时间的平均值缩短(5.1 天 vs. 16.2 天;n=20)。纳入研究中不良事件报告情况较差或未报告。从未评估过生活质量。我们研究的一个局限性是,为了防止包括史蒂文斯-约翰逊综合征病例,我们排除了孤立性黏膜 EM 的病例。总之,有低水平证据表明连续使用阿昔洛韦治疗复发性 EM(1 项 RCT)。其他治疗方法的证据仅基于回顾性病例系列研究。沙利度胺的结果,特别是,鼓励进一步的研究。关于安全性的数据不足。PROSPERO 注册号 CRD42016053175。