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口服阿昔洛韦抑制单纯疱疹病毒生殖器感染复发的双盲研究。

A double-blind study of oral acyclovir for suppression of recurrences of genital herpes simplex virus infection.

作者信息

Douglas J M, Critchlow C, Benedetti J, Mertz G J, Connor J D, Hintz M A, Fahnlander A, Remington M, Winter C, Corey L

出版信息

N Engl J Med. 1984 Jun 14;310(24):1551-6. doi: 10.1056/NEJM198406143102402.

Abstract

Patients with frequently recurring genital herpes were enrolled in a double-blind placebo-controlled trial comparing 200-mg acyclovir capsules, given five or two times daily, with placebo. Of 47 placebo recipients, 44 (94 per cent) had recurrences during the 120-day treatment period, compared with 13 (29 per cent) of 45 patients treated with acyclovir five times daily and 18 of 51 (35 per cent) treated with acyclovir twice daily (P less than 0.001 for each regimen compared with placebo). The median time to the first clinical recurrence was 18 days in placebo recipients, compared with over 120 days in both acyclovir-treated groups (P less than 0.001 for both groups compared with placebo). The mean monthly recurrence rate during the medication period was 0.86 in placebo recipients, compared with 0.13 in patients treated with acyclovir five times daily and 0.14 in patients treated with acyclovir twice daily (P less than 0.001 for both groups compared with placebo). While receiving therapy, 86 of 96 acyclovir-treated patients had over a 50 per cent reduction in their pretreatment recurrence rate. Breakthrough recurrences in acyclovir recipients were of shorter duration and associated with a lower frequency of viral shedding than recurrences in placebo recipients. After medication was discontinued, the subsequent recurrence rate returned to pretreatment frequencies. Daily oral acyclovir was well tolerated. We conclude that oral acyclovir given for four months markedly reduces but does not completely prevent recurrences of genital herpes and does not influence the long-term natural history of the disease.

摘要

复发性生殖器疱疹患者被纳入一项双盲安慰剂对照试验,该试验比较了每天服用5次或2次的200毫克阿昔洛韦胶囊与安慰剂的效果。47名接受安慰剂治疗的患者中,有44名(94%)在120天的治疗期内复发,而每天服用5次阿昔洛韦的45名患者中有13名(29%)复发,每天服用2次阿昔洛韦的51名患者中有18名(35%)复发(与安慰剂相比,每种治疗方案的P值均小于0.001)。安慰剂组患者首次临床复发的中位时间为18天,而两个阿昔洛韦治疗组均超过120天(与安慰剂相比,两组的P值均小于0.001)。服药期间安慰剂组患者的平均每月复发率为0.86,每天服用5次阿昔洛韦的患者为0.13,每天服用2次阿昔洛韦的患者为0.14(与安慰剂相比,两组的P值均小于0.001)。在接受治疗期间,96名接受阿昔洛韦治疗的患者中有86名的治疗前复发率降低了50%以上。与安慰剂组患者的复发相比,阿昔洛韦组患者的突破性复发持续时间更短,病毒排出频率更低。停药后,随后的复发率恢复到治疗前的频率。口服阿昔洛韦的耐受性良好。我们得出结论,口服阿昔洛韦四个月可显著减少但不能完全预防生殖器疱疹的复发,且不影响该疾病的长期自然病程。

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