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Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial)
OBJECTIVE: To assess the cost-effectiveness of elective induction of labour (IOL) at 41 weeks and expectant management (EM) until 42 weeks. DESIGN: Cost-effectiveness analysis from a healthcare perspective alongside a randomised controlled trial (INDEX). SETTING: 123 primary care midwifery practices...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900343/ https://www.ncbi.nlm.nih.gov/pubmed/36755905 http://dx.doi.org/10.1016/j.eurox.2023.100178 |
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author | Bruinsma, Aafke Keulen, Judit KJ van Eekelen, Rik van Wely, Madelon Kortekaas, Joep C van Dillen, Jeroen van de Post, Joris AM Mol, Ben W de Miranda, Esteriek |
author_facet | Bruinsma, Aafke Keulen, Judit KJ van Eekelen, Rik van Wely, Madelon Kortekaas, Joep C van Dillen, Jeroen van de Post, Joris AM Mol, Ben W de Miranda, Esteriek |
author_sort | Bruinsma, Aafke |
collection | PubMed |
description | OBJECTIVE: To assess the cost-effectiveness of elective induction of labour (IOL) at 41 weeks and expectant management (EM) until 42 weeks. DESIGN: Cost-effectiveness analysis from a healthcare perspective alongside a randomised controlled trial (INDEX). SETTING: 123 primary care midwifery practices and 45 obstetric departments of hospitals in the Netherlands. POPULATION: We studied 1801 low-risk women with late-term pregnancy, randomised to IOL at 41 weeks (N = 900) or EM until 42 weeks (N = 901). METHODS: The incremental cost-effectiveness ratio (ICER) was expressed as the ratio of the difference in costs and the difference in main perinatal outcomes. A Cost-Effectiveness Acceptability Curve (CEAC) was constructed to assess whether induction is cost-effective for a range of monetary values as thresholds. We performed subgroup analysis for parity. MAIN OUTCOME MEASURES: Direct medical costs, composite adverse perinatal outcome (CAPO) (perinatal mortality, NICU admission, Apgar 5 min < 7, plexus brachialis injury and/or meconium aspiration syndrome) and composite severe adverse perinatal outcome (SAPO) (including Apgar 5 min < 4 instead of < 7). RESULTS: The average costs were €3858 in the induction group and €3723 in the expectant group (mean difference €135; 95 % CI −235 to 493). The ICERs of IOL compared to EM to prevent one additional CAPO and SAPO was €9436 and €14,994, respectively. The CEAC showed a 80 % chance of IOL being cost-effective with a willingness-to-pay of €22,000 for prevention of one CAPO and €50,000 for one SAPO. Subgroup analysis showed a willingness-to-pay to prevent one CAPO for nulliparous of €47,000 and for multiparous €190,000. To prevent one SAPO the willingness-to-pay is €62,000 for nulliparous and €970,000 for multiparous women. CONCLUSIONS: Induction at 41 weeks has an 80 % chance of being cost-effective at a willingness-to-pay of €22,000 for prevention of one CAPO and €50,000 for prevention of one SAPO. Subgroup analysis suggests that induction could be cost-effective for nulliparous women while it is unlikely cost-effective for multiparous women. Cost-effectiveness in other settings will depend on baseline characteristics of the population and health system organisation and funding. |
format | Online Article Text |
id | pubmed-9900343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99003432023-02-07 Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial) Bruinsma, Aafke Keulen, Judit KJ van Eekelen, Rik van Wely, Madelon Kortekaas, Joep C van Dillen, Jeroen van de Post, Joris AM Mol, Ben W de Miranda, Esteriek Eur J Obstet Gynecol Reprod Biol X Obstetrics and Maternal Fetal Medicine OBJECTIVE: To assess the cost-effectiveness of elective induction of labour (IOL) at 41 weeks and expectant management (EM) until 42 weeks. DESIGN: Cost-effectiveness analysis from a healthcare perspective alongside a randomised controlled trial (INDEX). SETTING: 123 primary care midwifery practices and 45 obstetric departments of hospitals in the Netherlands. POPULATION: We studied 1801 low-risk women with late-term pregnancy, randomised to IOL at 41 weeks (N = 900) or EM until 42 weeks (N = 901). METHODS: The incremental cost-effectiveness ratio (ICER) was expressed as the ratio of the difference in costs and the difference in main perinatal outcomes. A Cost-Effectiveness Acceptability Curve (CEAC) was constructed to assess whether induction is cost-effective for a range of monetary values as thresholds. We performed subgroup analysis for parity. MAIN OUTCOME MEASURES: Direct medical costs, composite adverse perinatal outcome (CAPO) (perinatal mortality, NICU admission, Apgar 5 min < 7, plexus brachialis injury and/or meconium aspiration syndrome) and composite severe adverse perinatal outcome (SAPO) (including Apgar 5 min < 4 instead of < 7). RESULTS: The average costs were €3858 in the induction group and €3723 in the expectant group (mean difference €135; 95 % CI −235 to 493). The ICERs of IOL compared to EM to prevent one additional CAPO and SAPO was €9436 and €14,994, respectively. The CEAC showed a 80 % chance of IOL being cost-effective with a willingness-to-pay of €22,000 for prevention of one CAPO and €50,000 for one SAPO. Subgroup analysis showed a willingness-to-pay to prevent one CAPO for nulliparous of €47,000 and for multiparous €190,000. To prevent one SAPO the willingness-to-pay is €62,000 for nulliparous and €970,000 for multiparous women. CONCLUSIONS: Induction at 41 weeks has an 80 % chance of being cost-effective at a willingness-to-pay of €22,000 for prevention of one CAPO and €50,000 for prevention of one SAPO. Subgroup analysis suggests that induction could be cost-effective for nulliparous women while it is unlikely cost-effective for multiparous women. Cost-effectiveness in other settings will depend on baseline characteristics of the population and health system organisation and funding. Elsevier 2023-01-17 /pmc/articles/PMC9900343/ /pubmed/36755905 http://dx.doi.org/10.1016/j.eurox.2023.100178 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Obstetrics and Maternal Fetal Medicine Bruinsma, Aafke Keulen, Judit KJ van Eekelen, Rik van Wely, Madelon Kortekaas, Joep C van Dillen, Jeroen van de Post, Joris AM Mol, Ben W de Miranda, Esteriek Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial) |
title | Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial) |
title_full | Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial) |
title_fullStr | Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial) |
title_full_unstemmed | Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial) |
title_short | Cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (INDEX trial) |
title_sort | cost-effectiveness analysis of induction of labour at 41 weeks and expectant management until 42 weeks in low risk women (index trial) |
topic | Obstetrics and Maternal Fetal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900343/ https://www.ncbi.nlm.nih.gov/pubmed/36755905 http://dx.doi.org/10.1016/j.eurox.2023.100178 |
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