Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Department of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Clin Infect Dis. 2021 Aug 2;73(3):e672-e679. doi: 10.1093/cid/ciaa1903.
We aimed to determine if treatment of male sexual partners of women with recurrent bacterial vaginosis (BV) with oral metronidazole 2×/day for 7 days (ie, multidose metronidazole) significantly decreased BV recurrence rates in the female.
This was a multicenter, 2-arm, double-blind, placebo-controlled study. Women with recurrent BV and current diagnosis of BV by Amsel and Nugent were enrolled. Multidose metronidazole for 7 days was dispensed to women. Male partners were randomized to placebo versus multidose metronidazole for 7 days and asked to refrain from unprotected sex for 14 days. Female follow-up visits were conducted at day 21 and 8 and 16 weeks. Male follow-up visits occurred at days 14-21. BV cure was defined as 0-2 Amsel criteria and Nugent score 0-6 in the female partner with the primary endpoint at 16 weeks.
214 couples were enrolled. In the intent-to-treat population, there was no significant difference between treatment arms for the primary outcome. BV treatment failure occurred in 81% and 80% of women in the metronidazole and placebo arms through the third follow-up visit, respectively (P > .999). However, women whose male partners adhered to study medication were less likely to fail treatment (adjusted relative risk, .85; 95% CI, .73-.99; P = .035). This finding persisted in post hoc comparisons in the metronidazole arm.
Overall, this study did not find that male partner treatment with multidose metronidazole significantly reduces BV recurrence in female partners, although women whose partners adhered to multidose metronidazole were less likely to fail treatment.
(NCT02209519).
我们旨在确定女性复发性细菌性阴道病(BV)患者的男性性伴侣接受每日 2 次、每次 2 片的口服甲硝唑(即多剂量甲硝唑)治疗 7 天,是否能显著降低女性的 BV 复发率。
这是一项多中心、2 臂、双盲、安慰剂对照研究。招募了复发性 BV 且当前符合 Amsel 和 Nugent 诊断标准的 BV 女性患者。给予女性患者 7 天的多剂量甲硝唑。男性伴侣被随机分配至安慰剂组或多剂量甲硝唑组(7 天),并被要求在 14 天内避免无保护性行为。女性的随访在第 21 天和第 8、16 周进行。男性的随访在第 14-21 天进行。主要终点是 16 周时,女性伴侣的 Amsel 标准评分为 0-2 分且 Nugent 评分 0-6 分定义为 BV 治愈。
共纳入 214 对夫妇。在意向性治疗人群中,治疗组之间在主要结局上没有显著差异。在第三次随访时,甲硝唑组和安慰剂组中分别有 81%和 80%的女性治疗失败(P>.999)。然而,男性伴侣遵守研究药物治疗的女性更不太可能治疗失败(调整后的相对风险,0.85;95%CI,0.73-0.99;P=0.035)。这一发现在后序贯比较甲硝唑组中仍然存在。
总的来说,这项研究没有发现男性伴侣接受多剂量甲硝唑治疗会显著降低女性伴侣的 BV 复发率,尽管女性伴侣的男性伴侣遵守多剂量甲硝唑治疗方案的女性不太可能治疗失败。
(NCT02209519)。