London School of Hygiene & Tropical Medicine, Keppel Street, London, UK.
ISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.
Lancet Glob Health. 2015 Mar;3(3):e143-53. doi: 10.1016/S2214-109X(14)70385-7.
In 2012, WHO changed its recommendation for intermittent preventive treatment of malaria during pregnancy (IPTp) from two doses to monthly doses of sulfadoxine-pyrimethamine during the second and third trimesters, but noted the importance of a cost-effectiveness analysis to lend support to the decision of policy makers. We therefore estimated the incremental cost-effectiveness of IPTp with three or more (IPTp-SP3+) versus two doses of sulfadoxine-pyrimethamine (IPTp-SP2).
For this analysis, we used data from a 2013 meta-analysis of seven studies in sub-Saharan Africa. We developed a decision tree model with a lifetime horizon. We analysed the base case from a societal perspective. We did deterministic and probabilistic sensitivity analyses with appropriate parameter ranges and distributions for settings with low, moderate, and high background risk of low birthweight, and did a separate analysis for HIV-negative women. Parameters in the model were obtained for all countries included in the original meta-analysis. We did simulations in hypothetical cohorts of 1000 pregnant women receiving either IPTp-SP3+ or IPTp-SP2. We calculated disability-adjusted life-years (DALYs) for low birthweight, severe to moderate anaemia, and clinical malaria. We calculated cost estimates from data obtained in observational studies, exit surveys, and from public procurement databases. We give financial and economic costs in constant 2012 US$. The main outcome measure was the incremental cost per DALY averted.
The delivery of IPTp-SP3+ to 1000 pregnant women averted 113·4 DALYs at an incremental cost of $825·67 producing an incremental cost-effectiveness ratio (ICER) of $7·28 per DALY averted. The results remained robust in the deterministic sensitivity analysis. In the probabilistic sensitivity analyses, the ICER was $7·7 per DALY averted for moderate risk of low birthweight, $19·4 per DALY averted for low risk, and $4·0 per DALY averted for high risk. The ICER for HIV-negative women was $6·2 per DALY averted.
Our findings lend strong support to the WHO guidelines that recommend a monthly dose of IPTp-SP from the second trimester onwards.
Malaria in Pregnancy Consortium and the Bill & Melinda Gates Foundation.
2012 年,世界卫生组织(WHO)将孕妇间歇性预防治疗疟疾(IPTp)的推荐剂量从两剂改为妊娠第二和第三孕期每月一剂磺胺多辛-乙胺嘧啶,但指出需要进行成本效益分析来支持决策者的决策。因此,我们估计了三剂或更多剂量的 IPTp(IPTp-SP3+)与两剂磺胺多辛-乙胺嘧啶(IPTp-SP2)相比的增量成本效益。
我们使用了来自撒哈拉以南非洲的七项研究的 2013 年荟萃分析的数据。我们开发了一个具有终生时间范围的决策树模型。我们从社会角度分析了基础案例。我们对低、中、高出生体重低风险背景下的设定进行了确定性和概率敏感性分析,并为 HIV 阴性妇女进行了单独分析。模型中的参数是从原始荟萃分析中包含的所有国家获得的。我们在接受 IPTp-SP3+或 IPTp-SP2 的 1000 名孕妇的假设队列中进行了模拟。我们计算了低出生体重、严重至中度贫血和临床疟疾的残疾调整生命年(DALY)。我们从观察性研究、退出调查和公共采购数据库中获得成本估算。我们以 2012 年不变的美元表示财务和经济成本。主要结果指标是每避免一个 DALY 的增量成本。
为 1000 名孕妇提供 IPTp-SP3+可避免 113.4 个 DALY,增量成本为 825.67 美元,增量成本效益比(ICER)为每避免一个 DALY 7.28 美元。在确定性敏感性分析中,结果仍然稳健。在概率敏感性分析中,对于中等出生体重低风险,ICER 为每避免一个 DALY 7.7 美元,对于低风险,ICER 为每避免一个 DALY 19.4 美元,对于高风险,ICER 为每避免一个 DALY 4.0 美元。对于 HIV 阴性妇女,ICER 为每避免一个 DALY 6.2 美元。
我们的研究结果为 WHO 建议从妊娠中期开始每月给予 IPTp-SP 的指南提供了有力支持。
妊娠疟疾联盟和比尔及梅琳达·盖茨基金会。