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Costs and Use of Health Care in Patients With Celiac Disease: A Population-Based Longitudinal Study
Karl Mårild1,2, Jonas Söderling3, Soran R Bozorg4
1Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg, Sweden.
Insights
Celiac disease (CD) significantly increases healthcare costs before and for years after diagnosis. Even with mucosal healing, these elevated costs persist, impacting patient care and resource allocation.
Area of Science:
- Gastroenterology
- Health Economics
- Public Health
Background:
- Celiac disease (CD) affects 1% of the population, but its economic burden remains poorly understood.
- Estimating healthcare utilization and costs associated with CD is crucial for resource planning.
Purpose of the Study:
- To estimate healthcare use and costs in celiac disease patients.
- To analyze the temporal relationship between CD diagnosis and healthcare expenditures.
Main Methods:
- Identified 40,951 prevalent and 15,086 incident CD cases from Swedish biopsy reports (2008-2015).
- Compared CD patients with 187,542 age- and sex-matched general population controls.
- Utilized nationwide registers for inpatient, outpatient, diet, and medication data.
Main Results:
- Healthcare costs were higher in CD patients across all age groups ($715-$1,075 more annually in 2015).
- Costs increased pre-diagnosis, peaked post-diagnosis, and remained elevated for at least 5 years.
- Mucosal healing did not significantly reduce healthcare costs in CD patients.
Conclusions:
- Celiac disease leads to sustained increases in healthcare utilization and costs.
- Healthcare costs associated with CD extend long after diagnosis, irrespective of mucosal healing status.
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.
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