Department of Obstetrics and Gynecology, Centre Hospitalier Universitaire de Liège, CHR Citadelle, Liège, Belgium.
Department of Obstetrics and Gynaecology, University Hospitals, KULeuven, Leuven, Belgium.
Pregnancy Hypertens. 2021 Dec;26:31-37. doi: 10.1016/j.preghy.2021.08.113. Epub 2021 Aug 18.
To evaluate the economic impact of introducing the soluble fms-like tyrosine kinase (sFlt-1) to placental growth factor (PlGF) ratio test into clinical practice in Belgium for the prediction of preeclampsia (PE).
We developed a one-year time-horizon decision tree model to evaluate the short-term costs associated with the introduction of the sFlt-1/PlGF test for guiding the management of women with suspected PE from the Belgian public healthcare payers' perspective. The model estimated the costs associated with the diagnosis and management of PE in pregnant women managed in either a test scenario, in which the sFlt-1/PlGF test is used in addition to current clinical practice, or a no test scenario, in which clinical decisions are based on current practice alone. Test characteristics were derived from PROGNOSIS, a non-interventional study in women presenting with clinical suspicion of PE. Unit costs were obtained from Belgian-specific sources. The main model outcome was the total cost per patient.
Introduction of the sFlt-1/PlGF ratio test is expected to result in a cost saving of €712 per patient compared with the no test scenario. These savings are generated mainly due to a reduction in unnecessary hospitalizations.
The sFlt-1/PlGF test is projected to result in substantial cost savings for the Belgian public healthcare payers through reduction of unnecessary hospitalization of women with clinical suspicion of PE that ultimately do not develop the condition. The test also has the potential to ensure that women at high risk of developing PE are identified and appropriately managed.
评估在比利时将可溶性 fms 样酪氨酸激酶(sFlt-1)与胎盘生长因子(PlGF)比值检测引入临床实践,用于预测先兆子痫(PE)的经济影响。
我们开发了一个为期一年的时间框架决策树模型,从比利时公共医疗保健支付者的角度评估引入 sFlt-1/PlGF 检测以指导疑似 PE 孕妇管理的短期成本。该模型估计了在测试情景中(sFlt-1/PlGF 检测与当前临床实践一起使用)或非测试情景中(临床决策仅基于当前实践)管理的孕妇的 PE 诊断和管理相关成本。测试特征来自 PROGNOSIS,这是一项针对有临床疑似 PE 表现的女性的非干预性研究。单位成本来自比利时特定来源。主要模型结果是每位患者的总成本。
与非测试情景相比,引入 sFlt-1/PlGF 比值检测预计将使每位患者的成本节省 712 欧元。这些节省主要是由于减少了不必要的住院治疗。
sFlt-1/PlGF 检测有望通过减少最终未发生该疾病的具有临床疑似 PE 的女性不必要的住院治疗,为比利时公共医疗保健支付者节省大量成本。该检测还有可能确保识别出患有 PE 高风险的女性并进行适当的管理。