Mabileau Guillaume, Schwarzinger Michael, Flores Juan, Patrat Catherine, Luton Dominique, Epelboin Sylvie, Mandelbrot Laurent, Matheron Sophie, Yazdanpanah Yazdan
Institut National de la Santé et de la Recherche Médicale (INSERM), Infection Antimicrobials Modelling & Evolution (IAME), unity 1137, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Institut National de la Santé et de la Recherche Médicale (INSERM), Infection Antimicrobials Modelling & Evolution (IAME), unity 1137, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Am J Obstet Gynecol. 2015 Sep;213(3):341.e1-12. doi: 10.1016/j.ajog.2015.05.010. Epub 2015 May 13.
We sought to assess the residual risk of HIV transmission, cost, and cost-effectiveness of various strategies that can help fertile HIV-uninfected female/HIV-1-infected male on combination antiretroviral therapy with plasma HIV RNA <50 copies/mL couples to have a child: (1) unprotected sexual intercourse (treatment as prevention); (2) treatment as prevention limited to fertile days (targeting fertile days); (3) treatment as prevention with preexposure prophylaxis (tenofovir/emtricitabine); (4) treatment as prevention and preexposure prophylaxis limited to fertile days; or (5) medically assisted procreation (MAP).
This was a model-based, cost-effectiveness analysis performed from a French societal perspective. Input parameters derived from international literature included: 85% probability of live births in different strategies, 0.0083%/mo HIV transmission risk with unprotected vaginal intercourse, 1% HIV mother-to-child transmission rate, and 4.4% birth defect risk related to combination antiretroviral therapy when the mother is infected at conception. Targeting fertile days and preexposure prophylaxis were estimated to decrease the risk of HIV transmission by 80% and 67%, respectively, and by 93.4% for preexposure prophylaxis limited to fertile days (the relative risk of transmission considering the combination of both strategies assuming to be (1-80%)*(1-67%) = 16.6% in basecase). Tenofovir/emtricitabine monthly cost was set at €540.
The HIV transmission risk was highest with treatment as prevention and lowest for MAP (5.4 and 0.0 HIV-infected women/10,000 pregnancies, respectively). Targeting fertile days was more effective than preexposure prophylaxis (0.9 vs 1.8) and associated with lowest costs. Preexposure prophylaxis limited to fertile days was more effective than targeting fertile days (0.3 vs 0.9) with a cost-effectiveness ratio of €1,130,000/life year saved; MAP cost-effectiveness ratio when compared with preexposure prophylaxis limited to fertile days was €3,600,000/life year saved. Results were robust to multiple sensitivity analyses.
Targeting fertile days is associated with a low risk of HIV transmission in fertile HIV-uninfected female/male with controlled HIV-1 infection couples. The risk is lower with preexposure prophylaxis limited to fertile days, or MAP, but these strategies are associated with unfavorable cost-effectiveness ratios under their current costs.
我们试图评估各种策略在帮助血浆HIV RNA<50拷贝/mL且接受联合抗逆转录病毒治疗的未感染HIV的可育女性/感染HIV-1的男性伴侣生育子女时的HIV传播残余风险、成本及成本效益:(1)无保护性交(治疗即预防);(2)仅在排卵期进行治疗即预防(针对排卵期);(3)采用暴露前预防(替诺福韦/恩曲他滨)进行治疗即预防;(4)仅在排卵期进行治疗即预防和暴露前预防;或(5)医学辅助生殖(MAP)。
这是一项基于模型的成本效益分析,从法国社会视角进行。源自国际文献的输入参数包括:不同策略下活产概率为85%,无保护阴道性交的HIV传播风险为0.0083%/月,HIV母婴传播率为1%,母亲在受孕时感染HIV时与联合抗逆转录病毒治疗相关的出生缺陷风险为4.4%。估计针对排卵期和暴露前预防分别可将HIV传播风险降低80%和67%,仅在排卵期进行暴露前预防可将风险降低93.4%(在基础病例中,考虑两种策略联合时的相对传播风险为(1 - 80%)×(1 - 67%) = 16.6%)。替诺福韦/恩曲他滨的月成本设定为540欧元。
治疗即预防的HIV传播风险最高,MAP最低(分别为每10000次妊娠中有5.4例和0例感染HIV的女性)。针对排卵期比暴露前预防更有效(分别为0.9和1.8),且成本最低。仅在排卵期进行暴露前预防比针对排卵期更有效(分别为0.3和0.9),成本效益比为1130000欧元/生命年;与仅在排卵期进行暴露前预防相比,MAP的成本效益比为3600000欧元/生命年。多项敏感性分析结果稳健。
在HIV-1感染得到控制的未感染HIV的可育女性/男性伴侣中,针对排卵期的HIV传播风险较低。仅在排卵期进行暴露前预防或MAP的风险更低,但在当前成本下,这些策略的成本效益比不佳。