Mitchell C D, Bean B, Gentry S R, Groth K E, Boen J R, Balfour H H
Lancet. 1981 Jun 27;1(8235):1389-92. doi: 10.1016/s0140-6736(81)92569-1.
11 of 24 immunocompromised patients with mucocutaneous herpes simplex virus (HSV) infections were given intravenous acyclovir in a randomised double-blind placebo-controlled study. Patients receiving acyclovir experienced no major adverse effects. The median times to cessation of new lesion formation, lesion crusting, lesion healing, cessation of pain, and termination of viral shedding were shorter in the acyclovir-treated group than in the placebo group. The time-to-event probability curves for the acyclovir and placebo groups were significantly different for cessation of pain (p=0.032) and termination of viral shedding (p=0.004). The median times to termination of viral shedding were also statistically different (p=0.045). Acyclovir seems to be a non-toxic and effective treatment for mucocutaneous HSV infections in immunocompromised patients.
在一项随机双盲安慰剂对照研究中,24名患有皮肤黏膜单纯疱疹病毒(HSV)感染的免疫功能低下患者中有11名接受了静脉注射阿昔洛韦治疗。接受阿昔洛韦治疗的患者未出现重大不良反应。与安慰剂组相比,阿昔洛韦治疗组中停止形成新病灶、病灶结痂、病灶愈合、疼痛停止以及病毒脱落终止的中位时间更短。阿昔洛韦组和安慰剂组在疼痛停止(p = 0.032)和病毒脱落终止(p = 0.004)方面的事件发生时间概率曲线存在显著差异。病毒脱落终止的中位时间在统计学上也存在差异(p = 0.045)。阿昔洛韦似乎是免疫功能低下患者皮肤黏膜HSV感染的一种无毒且有效的治疗方法。