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Systematic review of the healthcare cost of bronchopulmonary dysplasia

OBJECTIVES: To determine the costs directly or indirectly related to bronchopulmonary dysplasia (BPD) in preterm infants. The secondary objective was to stratify the costs based on gestational age and/or birth weight. DESIGN: Systematic literature review. SETTING: PubMed and Scopus were searched on...

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Autores principales: Humayun, Jhangir, Löfqvist, Chatarina, Ley, David, Hellström, Ann, Gyllensten, Hanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356184/
https://www.ncbi.nlm.nih.gov/pubmed/34376441
http://dx.doi.org/10.1136/bmjopen-2020-045729
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author Humayun, Jhangir
Löfqvist, Chatarina
Ley, David
Hellström, Ann
Gyllensten, Hanna
author_facet Humayun, Jhangir
Löfqvist, Chatarina
Ley, David
Hellström, Ann
Gyllensten, Hanna
author_sort Humayun, Jhangir
collection PubMed
description OBJECTIVES: To determine the costs directly or indirectly related to bronchopulmonary dysplasia (BPD) in preterm infants. The secondary objective was to stratify the costs based on gestational age and/or birth weight. DESIGN: Systematic literature review. SETTING: PubMed and Scopus were searched on 3 February 2020. Studies were selected based on eligibility criteria by two independent reviewers. Included studies were further searched to identify eligible references and citations. Two independent reviewers extracted data with a prespecified data extraction sheet, including items from a published checklist for quality assessment. The costs in the included studies are reported descriptively. PRIMARY OUTCOME MEASURE: Costs of BPD. RESULTS: The 13 included studies reported the total costs or marginal costs of BPD. Most studies reported costs during birth hospitalisation (cost range: Int$21 392–Int$1 094 509 per child, equivalent to €19 103–€977 397, in 2019) and/or during the first year of life. One study reported costs during the first 2 years; two other studies reported costs later, during the preschool period and one study included a long-term follow-up. The highest mean costs were associated with infants born at extremely low gestational ages. The quality assessment indicated a low risk of bias in the reported findings of included studies. CONCLUSIONS: This study was the first systematic review of costs associated with BPD. We confirmed previous reports of high costs and described the long-term follow-up necessary for preterm infants with BPD, particularly infants of very low gestational age. Moreover, we identified a need for studies that estimate costs outside hospitals and after the first year of life. PROSPERO REGISTRATION NUMBER: CRD42020173234.
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spelling pubmed-83561842021-08-24 Systematic review of the healthcare cost of bronchopulmonary dysplasia Humayun, Jhangir Löfqvist, Chatarina Ley, David Hellström, Ann Gyllensten, Hanna BMJ Open Health Economics OBJECTIVES: To determine the costs directly or indirectly related to bronchopulmonary dysplasia (BPD) in preterm infants. The secondary objective was to stratify the costs based on gestational age and/or birth weight. DESIGN: Systematic literature review. SETTING: PubMed and Scopus were searched on 3 February 2020. Studies were selected based on eligibility criteria by two independent reviewers. Included studies were further searched to identify eligible references and citations. Two independent reviewers extracted data with a prespecified data extraction sheet, including items from a published checklist for quality assessment. The costs in the included studies are reported descriptively. PRIMARY OUTCOME MEASURE: Costs of BPD. RESULTS: The 13 included studies reported the total costs or marginal costs of BPD. Most studies reported costs during birth hospitalisation (cost range: Int$21 392–Int$1 094 509 per child, equivalent to €19 103–€977 397, in 2019) and/or during the first year of life. One study reported costs during the first 2 years; two other studies reported costs later, during the preschool period and one study included a long-term follow-up. The highest mean costs were associated with infants born at extremely low gestational ages. The quality assessment indicated a low risk of bias in the reported findings of included studies. CONCLUSIONS: This study was the first systematic review of costs associated with BPD. We confirmed previous reports of high costs and described the long-term follow-up necessary for preterm infants with BPD, particularly infants of very low gestational age. Moreover, we identified a need for studies that estimate costs outside hospitals and after the first year of life. PROSPERO REGISTRATION NUMBER: CRD42020173234. BMJ Publishing Group 2021-08-10 /pmc/articles/PMC8356184/ /pubmed/34376441 http://dx.doi.org/10.1136/bmjopen-2020-045729 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Health Economics
Humayun, Jhangir
Löfqvist, Chatarina
Ley, David
Hellström, Ann
Gyllensten, Hanna
Systematic review of the healthcare cost of bronchopulmonary dysplasia
title Systematic review of the healthcare cost of bronchopulmonary dysplasia
title_full Systematic review of the healthcare cost of bronchopulmonary dysplasia
title_fullStr Systematic review of the healthcare cost of bronchopulmonary dysplasia
title_full_unstemmed Systematic review of the healthcare cost of bronchopulmonary dysplasia
title_short Systematic review of the healthcare cost of bronchopulmonary dysplasia
title_sort systematic review of the healthcare cost of bronchopulmonary dysplasia
topic Health Economics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356184/
https://www.ncbi.nlm.nih.gov/pubmed/34376441
http://dx.doi.org/10.1136/bmjopen-2020-045729
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