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Costs and Use of Health Care in Patients With Celiac Disease: A Population-Based Longitudinal Study
Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg, Sweden; Department of Pediatric Gastroenterology, Queen Silvia Children's Hospital, Gothenburg, Sweden.
Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.ORCID-id: 0000-0003-2862-8855
Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
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2020 (Engelska)Ingår i: American Journal of Gastroenterology, ISSN 0002-9270, E-ISSN 1572-0241, Vol. 115, nr 8, s. 1253-1263Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

INTRODUCTION: Celiac disease (CD) affects 1% of the population. Its effect on healthcare cost, however, is barely understood. We estimated healthcare use and cost in CD, including their temporal relationship to diagnosis.

METHODS: Through biopsy reports from Sweden's 28 pathology departments, we identified 40,951 prevalent patients with CD (villous atrophy) as of January 1, 2015, and 15,086 incident patients with CD diagnosed in 2008-2015, including 2,663 who underwent a follow-up biopsy to document mucosal healing. Each patient was compared with age- and sex-matched general population comparators (n = 187,542). Using nationwide health registers, we retrieved data on all inpatient and nonprimary outpatient care, prescribed diets, and drugs.

RESULTS: Compared with comparators, healthcare costs in 2015 were, on average, $1,075 (95% confidence interval, $864-1,278) higher in prevalent patients with CD aged <18 years, $715 ($632-803) in ages 18-64 years, and $1,010 ($799-1,230) in ages ≥65 years. Half of all costs were attributed to 5% of the prevalent patients. Annual healthcare costs were $391 higher 5 years before diagnosis and increased until 1 year after diagnosis; costs then declined but remained 75% higher than those of comparators 5 years postdiagnosis (annual difference = $1,044). Although hospitalizations, nonprimary outpatient visits, and medication use were all more common with CD, excess costs were largely unrelated to the prescription of gluten-free staples and follow-up visits for CD. Mucosal healing in CD did not reduce the healthcare costs.

DISCUSSION: The use and costs of health care are increased in CD, not only before, but for years after diagnosis. Mucosal healing does not seem to lower the healthcare costs.

Ort, förlag, år, upplaga, sidor
Blackwell Publishing, 2020. Vol. 115, nr 8, s. 1253-1263
Nationell ämneskategori
Klinisk medicin Gastroenterologi och hepatologi
Identifikatorer
URN: urn:nbn:se:oru:diva-88842DOI: 10.14309/ajg.0000000000000652ISI: 000619500100022PubMedID: 32349030Scopus ID: 2-s2.0-850891705022-s2.0-85089170502OAI: oai:DiVA.org:oru-88842DiVA, id: diva2:1521478
Anmärkning

Funding Agencies:

Swedish government  

Swedish county councils, the A.L.F. agreement  

Bengt Ihre Research Foundation  

Bengt Ihre Research Fellowship  

The Louis and Gloria Flanzer Philanthropic Trust  

Tillgänglig från: 2021-01-22 Skapad: 2021-01-22 Senast uppdaterad: 2025-02-11Bibliografiskt granskad

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Bozorg, Soran R.Ludvigsson, Jonas F.

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American Journal of Gastroenterology
Klinisk medicinGastroenterologi och hepatologi

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