Cost-utility of a first-trimester screening strategy versus the standard of care for nulliparous women to prevent pre-term pre-eclampsia in Belgium.


Journal

Pregnancy hypertension
ISSN: 2210-7797
Titre abrégé: Pregnancy Hypertens
Pays: Netherlands
ID NLM: 101552483

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 23 02 2021
revised: 09 06 2021
accepted: 28 06 2021
pubmed: 17 7 2021
medline: 15 12 2021
entrez: 16 7 2021
Statut: ppublish

Résumé

To assess the cost-effectiveness of the Fetal Medicine Foundation (FMF) combined first-trimester pre-eclampsia (PE) screening algorithm, coupled with low-dose aspirin treatment in high-risk patients, compared to the standard of care (SOC; screening based on maternal risk factors) for nulliparous pregnancies in Belgium. A decision analytic model was used to estimate the costs and outcomes for patients screened using the SOC and for those using the FMF screening algorithm, from the Belgian payers' perspective. Where possible, the probabilities and associated costs at each decision point were calculated based on published literature and public databases. Cost-effectiveness was assessed using an incremental cost-effectiveness ratio. One-way sensitivity analyses were performed to assess the impact of independent variations in each model parameter. A probabilistic sensitivity analysis was used to estimate the impact of the overall uncertainty of the model on the estimated cost-effectiveness. Considering an estimated 51,309 pregnancies in nulliparous women in Belgium per year, the FMF screening algorithm resulted in fewer cases of pre-term PE compared with the SOC (479 versus 816 cases) and a cost saving of €28.67 per patient. The outcome in quality-adjusted life-years was similar for both screening approaches (FMF screening algorithm 1.8521 versus SOC 1.8518). The FMF screening algorithm was cost-saving and more effective in 99.4% of simulations. The FMF screening algorithm coupled with early intervention using low-dose aspirin has the potential to prevent an additional 337 cases of pre-term PE per year compared with the current SOC in this population, along with a cost saving.

Identifiants

pubmed: 34271426
pii: S2210-7789(21)00073-8
doi: 10.1016/j.preghy.2021.06.012
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

219-224

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Ana Dubon Garcia (A)

Roche Diagnostics Belgium NV/SA, Berkenlaan 8, 1831 Diegem, Belgium. Electronic address: ana.dubon_garcia@roche.com.

Roland Devlieger (R)

Department of Obstetrics and Gynaecology, University Hospitals Leuven, Herestraat 49, 3000 Leuven, Belgium. Electronic address: roland.devlieger@uzleuven.be.

Ken Redekop (K)

Erasmus School of Health Policy and Management, Erasmus University Rotterdam, Burgemeester Oudlaan 50, 3062 PA Rotterdam, The Netherlands. Electronic address: redekop@eshpm.eur.nl.

Katleen Vandeweyer (K)

Roche Diagnostics Belgium NV/SA, Berkenlaan 8, 1831 Diegem, Belgium. Electronic address: katleen.vandeweyer1@gmail.com.

Stefan Verlohren (S)

Department of Obstetrics (S.V.), Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Charitéplatz 1, Berlin 10117, Germany. Electronic address: stefan.verlohren@charite.de.

Liona C Poon (LC)

Department of Obstetrics and Gynaecology, Chinese University of Hong Kong, Sha Tin, Hong Kong. Electronic address: liona.poon@cuhk.edu.hk.

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