Evidence map›Paper›PMID 38252165›Full record

ArticlePediatric surgery international2024

Hirschsprung disease: a cost analysis study of the direct, indirect costs and financial coping strategies for the surgical management in Western Uganda.

Ahmed Hamad Binde, Felix Oyania, Sarah Ullrich, Martin Situma, Meera Kotagal, Edgar Mugema Mulogo

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Article in Pediatric surgery international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ahmed Hamad BindeMbarara University of Science and Technology, Mbarara, Uganda. ahmedbinde@gmail.com.
Felix OyaniaMbarara University of Science and Technology, Mbarara, Uganda.
Sarah UllrichYale University, New Haven, USA.
Martin SitumaMbarara University of Science and Technology, Mbarara, Uganda.
Meera KotagalCincinnati Children's Hospital Medical Center, Cincinnati, USA.
Edgar Mugema MulogoMbarara University of Science and Technology, Mbarara, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSurgical management of Hirschsprung disease (HD) in low- and middle-income countries is typically a staged procedure, necessitating multiple hospitalizations and clinic visits increasing family financial burden. Currently, there is limited information on the costs borne by caretakers of children with Hirschsprung disease seeking surgical intervention. This study seeks to measure the costs and economic burden of surgical treatment for Hirschsprung disease in western Uganda.

methodsA cross-sectional study using cost analysis was conducted among caretakers of patients who completed surgical treatment of HD between January 2017 and December 2021 at two hospitals in western Uganda. The average direct and indirect costs incurred by caretakers presenting at a public and private hospital were computed.

resultsA total of 69 patients (M: F = 7:1) were enrolled in the study. The median age at diagnosis was 60.5 (IQR 3-151.25) days for children and two-staged pull-through procedure was the common surgery performed. The mean overall cost for treatment was US $960 (SD = $720), with the majority of costs coming from direct medical costs. Nearly half (48%) of participants resorted to distress financing to finance their child's surgical care. The overwhelming majority of patients (n = 64, 93%) incurred catastrophic expenditure from the total costs of surgery for HD, and 97% of participants fell below the international poverty line at the time treatment was completed.

conclusionDespite the availability of 'free care' from government hospital and non-profit services, this study found that surgical management of Hirschsprung disease imposed substantial cost burden on families with Hirschsprung disease patients.

Indexed as

Coping SkillsHirschsprung DiseaseChildCosts and Cost AnalysisCross-Sectional StudiesHumansUgandaCatastrophic health expenditureDirect costFinancial coping strategiesHirschsprung diseaseIndirect cost

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.