Goutallier Charlotte S, Carrandi Alayna, Brennecke Shaun P, Callander Emily J
Pregnancy Research Centre, Royal Women's Hospital, Parkville, Victoria, Australia (Goutallier, Brennecke and Callander).
School of Public Health and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, Victoria, Australia (Carrandi).
AJOG Glob Rep. 2025 Apr 25;5(2):100498. doi: 10.1016/j.xagr.2025.100498. eCollection 2025 May.
Pre-eclampsia (PE) affects approximately 2%-4% of pregnancies. Diagnosis involves repeated assessment of pregnant patients with risk factors. The sFlt-1/PlGF ratio test is shown to have clinical utility in ruling in and out PE among at-risk patients. By excluding the probability of PE, the addition of the sFlt-1/PlGF ratio test to antenatal care may prevent unnecessary hospital admissions, intensive management, and premature delivery, thus reducing costs. The objective of this systematic review is to determine the cost-effectiveness of the sFlt-1/PlGF ratio test globally for pregnant patients at-risk of developing PE.
PubMed, Medline (OVID), National Health Service Economic Evaluation Database, Web of Science, Econlit, and Cost Effectiveness Analysis Registry was systematically searched between 2013-April 2023.
Empirical studies quantifying costs of the sFlt-1/PlGF ratio test compared to other diagnostic options for pregnant patients with suspected PE.
Eleven studies were included in the systematic review; all were cost analyses and modelled economic evaluations, and most used a health system perspective. Cost data were extracted into tables and indexed to 2022 United States Dollars (USD). An assessment of risk of bias for each study was performed using the Drummond critical appraisal checklist.
All studies reported "cost-savings" of the test in antenatal care. Studies varied with costs and assumptions included, therefore a large range of incremental cost savings per patient was reported ($15-$1,881, 2022USD). No Incremental Cost-Effectiveness Ratios or health outcomes including Quality Adjusted Life Years were reported.
The included studies demonstrated "cost-savings" of the sFlt-1/PlGF ratio test in antenatal care for at-risk pregnant patients. However, this does not account for health outcome differences and long-term health care utilisation and expenditure.
子痫前期(PE)影响约2%-4%的妊娠。诊断需要对有风险因素的孕妇进行反复评估。可溶性Fms样酪氨酸激酶1(sFlt-1)/胎盘生长因子(PlGF)比值检测在高危患者中诊断和排除PE方面具有临床应用价值。通过排除PE的可能性,将sFlt-1/PlGF比值检测纳入产前护理可避免不必要的住院、强化管理和早产,从而降低成本。本系统评价的目的是确定全球范围内sFlt-1/PlGF比值检测对有发生PE风险的孕妇的成本效益。
2013年至2023年4月期间对PubMed、Medline(OVID)、国家卫生服务经济评估数据库、科学网、Econlit和成本效益分析注册库进行了系统检索。
量化sFlt-1/PlGF比值检测与疑似PE的孕妇其他诊断方法相比成本的实证研究。
系统评价纳入了11项研究;均为成本分析和建模经济评估,且大多数采用卫生系统视角。成本数据被提取到表格中并换算为2022年美元(USD)。使用德拉蒙德批判性评价清单对每项研究的偏倚风险进行评估。
所有研究均报告该检测在产前护理中“节省成本”。研究在成本和所包含的假设方面存在差异,因此报告的每位患者节省的增量成本范围很大(15-1881美元,2022年USD)。未报告增量成本效益比或包括质量调整生命年在内的健康结果。
纳入的研究表明,sFlt-1/PlGF比值检测在高危孕妇的产前护理中“节省成本”。然而,这并未考虑健康结果差异以及长期医疗保健利用和支出情况。