Whitley R, Barton N, Collins E, Whelchel J, Diethelm A G
Am J Med. 1982 Jul 20;73(1A):236-40. doi: 10.1016/0002-9343(82)90098-5.
Forty-three immunocompromised patients with progressive cutaneous herpes simplex virus infections were studied in a double-blind, placebo-controlled evaluation of topically applied acyclovir. Patients were randomized and 22 received acyclovir and 21 placebo; medications were applied four times daily for 10 days. Both study populations were balanced for all demographic characteristics. Acyclovir therapy resulted in no median differences in time to total healing compared with placebo responses, p = 0.13. However, those patients who received the acyclovir ceased shedding virus more rapidly, p less than 0.001, and lost pain more readily, p = 0.04, than placebo counterparts. Neither group experienced adverse effects. Because of the protracted nature of mucocutaneous herpes simplex infections in these patients, the immunocompromised host provides a good model for evaluation of topical antiviral therapy.
对43例患有进行性皮肤单纯疱疹病毒感染的免疫功能低下患者进行了一项双盲、安慰剂对照的局部应用阿昔洛韦评估研究。患者被随机分组,22例接受阿昔洛韦治疗,21例接受安慰剂治疗;药物每天应用4次,持续10天。两个研究人群在所有人口统计学特征方面均保持平衡。与安慰剂组相比,阿昔洛韦治疗在总愈合时间上无中位数差异,p = 0.13。然而,接受阿昔洛韦治疗的患者病毒脱落停止得更快,p < 0.001,且比接受安慰剂的患者更容易减轻疼痛,p = 0.04。两组均未出现不良反应。由于这些患者黏膜皮肤单纯疱疹感染病程迁延,免疫功能低下宿主为评估局部抗病毒治疗提供了一个良好模型。