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Cost effectiveness of treatments for inflammatory bowel disease
1Department of Gastroenterology, University of Liverpool, Liverpool, UK. kbodger@liverpool.ac.uk
Insights
The cost-effectiveness of biological therapies for inflammatory bowel diseases (IBD) remains complex. While these treatments offer benefits, their high cost necessitates careful economic evaluation for long-term affordability.
Area of Science:
- Gastroenterology
- Health Economics
- Pharmacoeconomics
Background:
- Chronic inflammatory bowel diseases (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), incur significant direct costs, historically dominated by inpatient treatments for severe cases.
- The introduction of expensive biological agents has shifted the cost burden towards pharmacotherapy, increasing interest in the cost-effectiveness of IBD treatments.
- Evaluating the affordability of long-term biological therapy is crucial for managing IBD patient care.
Purpose of the Study:
- To review the existing literature on the cost-effectiveness and affordability of IBD therapies.
- To identify research gaps and challenges in current cost-effectiveness modeling for IBD treatments.
Main Methods:
- Literature review of studies assessing the cost-effectiveness of IBD therapies.
- Analysis of cost-utility models for different treatment strategies in UC and CD.
- Examination of head-to-head trials and clinical trial data related to cost-effectiveness.
Main Results:
- Head-to-head trials comparing treatment options are infrequent, and cost-effectiveness is seldom a primary endpoint in clinical trials.
- Cost-utility models for ulcerative colitis (UC) have explored dosing strategies for 5-aminosalicylic acid (5-ASA) and the impact of adherence.
- Cost-utility models for Crohn's disease (CD) indicate that anti-tumour necrosis factor (TNF) drugs provide incremental benefits at a higher overall cost, with wide variations in incremental cost-effectiveness ratios.
Conclusions:
- Existing cost-effectiveness data for IBD therapies, particularly biological agents, are limited and show considerable variability.
- Challenges and limitations exist in current modeling techniques for assessing the economic value of IBD treatments.
- Further research is needed to refine cost-effectiveness analyses and inform decisions regarding the long-term affordability of biological therapies for IBD.
Abstract:
Traditionally, half of the direct costs associated with chronic inflammatory bowel diseases (IBD) [Crohn's disease (CD) and ulcerative colitis (UC)] have related to hospital inpatient treatment for a sub-group of more severely affected, often therapy-resistant individuals. The advent of effective but relatively expensive biological agents has increased the contribution of drugs to overall medical care costs. This has focussed interest on the relative cost effectiveness of rival therapies for IBD and, in particular, on the affordability of long-term biological therapy. The purpose of this article is to review the available literature on this topic and to identify areas for future research. Head-to-head trials of competing treatment options are uncommon and clinical trials have seldom addressed cost effectiveness. In UC, models have explored the cost utility of 'high-' versus 'standard-' dose 5-aminosalicylic acid (5-ASA) therapy and the theoretical impact of improved adherence with once-daily formulations. In CD, cost-utility models for anti-tumour necrosis factor (TNF) drugs versus standard care have suggested consistently that incremental benefits are achieved at increased overall cost. However, studies of varying design have produced a wide spectrum of incremental cost-effectiveness ratio estimates, which highlights the challenges and limitations of existing modelling techniques.
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