Kroon S, Petersen C S, Andersen L P, Rasmussen J R, Vestergaard B F
Department of Dermato-Venereology, Bispebjerg Hospital, University of Copenhagen, Denmark.
Genitourin Med. 1990 Apr;66(2):101-4. doi: 10.1136/sti.66.2.101.
Twenty immunocompetent patients, four females and 16 males, with severe recurrent genital herpes (median number of recurrences the previous year 16, range (8-24] entered an open continuous long-term suppressive treatment with oral acyclovir (ACV) for 12 months. The study included a dose-titration schedule: (ACV, 200 mg x 4/1-3 months, ACV, 400 mg x 2/4-6 months, ACV, 200 mg x 2/7-9 months, and ACV, 400 mg x 1/10-12 months). Patients with recurrences on steps two and three received an alternative dose of ACV, 200 mg x 3. Otherwise patients entered the previous dose-step. Five (20%) of patients were completely free of symptoms (recurrences and abortive lesions) during the four dose-reduction periods. A further nine patients (50%) could be dose-reduced to 200 mg x 3 without symptoms. Isolates from three patients showed a decrease in virus sensitivity after ceasing treatment. In conclusion, 14/20 of treated patients could be dose reduced to 200 mg x 2-3 without selection of HSV strains showing clinically important decreases in sensitivity towards ACV.
20名免疫功能正常的患者(4名女性和16名男性)患有严重复发性生殖器疱疹(前一年复发次数中位数为16次,范围在8 - 24次),接受了为期12个月的口服阿昔洛韦(ACV)开放连续性长期抑制治疗。该研究包括一个剂量滴定方案:(阿昔洛韦,200毫克×4次/第1 - 3个月,阿昔洛韦,400毫克×2次/第4 - 6个月,阿昔洛韦,200毫克×2次/第7 - 9个月,以及阿昔洛韦,400毫克×1次/第10 - 12个月)。在第二和第三步出现复发的患者接受替代剂量的阿昔洛韦,200毫克×3次。否则患者进入上一个剂量步骤。5名(20%)患者在四个剂量减少期内完全没有症状(复发和顿挫性损害)。另外9名患者(50%)可以将剂量减少到200毫克×3次且无症状。三名患者的分离株在停止治疗后显示病毒敏感性降低。总之,20名接受治疗的患者中有14名可以将剂量减少到200毫克×2 - 3次,而不会选择对阿昔洛韦敏感性出现临床显著降低的单纯疱疹病毒株。