S1715 Optimal Screening Intervals for Dysplasia in Inflammatory Bowel Disease: Results of a Markov Model

Introduction: Current guidelines recommend frequent colorectal cancer (CRC) screening in patients with inflammatory bowel disease (IBD), but the optimal screening interval remains unclear. We aimed to model dysplasia development in IBD to assess the cost-effectiveness and clinical impact of various CRC screening intervals. Methods: We developed a Markov model in TreeAge Pro 2024 using a base case of a 30-year-old undergoing their first surveillance colonoscopy 8 years after IBD diagnosis. Initial health states of no dysplasia, low grade dysplasia, high grade dysplasia, and CRC were based on recently published prevalence estimates. We compared 3 strategies: (1) a natural history arm with only the initial surveillance colonoscopy, (2) surveillance colonoscopy every 2 years for patients without dysplasia, and (3) an alternative strategy with colonoscopy every 4 years for patients without dysplasia. In all arms, patients could progress to advanced stages of dysplasia or CRC, with follow-up until death or age 100. The model was calibrated to CRC incidence and mortality using DevCan (SEER 2000-2020) and adjusted for IBD using a relative risk from the literature. Deterministic and probabilistic sensitivity analyses included variations in colonoscopy adherence. Results: The cost-effective strategy was continuing with a 4-year surveillance interval for patients without dysplasia. This strategy yielded an incremental cost-effectiveness ratio (ICER) of $6,043 per quality-adjusted life year (QALY), while the 2-year strategy had an ICER of $171,615 per QALY. CRC incidence was slightly higher with the 4-year strategy (4.5% vs 3.8%), with minimal differences in local-stage detection (59% vs 60%) and CRC-related mortality (0.18% vs 0.15%). The 4-year strategy remained cost-effective across sensitivity analyses, with dysplasia detection rates and colonoscopy cost as key drivers. Probabilistic analysis favored the 4-year approach in 70% of simulations. Regarding resource utilization, colonoscopy use per 100 persons screened was 1,283 for the 4-year strategy vs 1,719 for the 2-year strategy, and only 17 in the natural history arm. Conclusion: Our model shows that extending surveillance colonoscopy to every 4 years in IBD patients without dysplasia is the cost-effective strategy. These findings support a more efficient approach to dysplasia surveillance that preserves patient safety while optimizing healthcare resources.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001134320.55807.b6
Primary Topic
Inflammatory Bowel Disease
Type
article
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article

S1715 Optimal Screening Intervals for Dysplasia in Inflammatory Bowel Disease: Results of a Markov Model

The American Journal of Gastroenterology
Inflammatory Bowel Disease
article

S1715 Optimal Screening Intervals for Dysplasia in Inflammatory Bowel Disease: Results of a Markov Model

article en

Abstract

Introduction: Current guidelines recommend frequent colorectal cancer (CRC) screening in patients with inflammatory bowel disease (IBD), but the optimal screening interval remains unclear. We aimed to model dysplasia development in IBD to assess the cost-effectiveness and clinical impact of various CRC screening intervals. Methods: We developed a Markov model in TreeAge Pro 2024 using a base case of a 30-year-old undergoing their first surveillance colonoscopy 8 years after IBD diagnosis. Initial health states of no dysplasia, low grade dysplasia, high grade dysplasia, and CRC were based on recently published prevalence estimates. We compared 3 strategies: (1) a natural history arm with only the initial surveillance colonoscopy, (2) surveillance colonoscopy every 2 years for patients without dysplasia, and (3) an alternative strategy with colonoscopy every 4 years for patients without dysplasia. In all arms, patients could progress to advanced stages of dysplasia or CRC, with follow-up until death or age 100. The model was calibrated to CRC incidence and mortality using DevCan (SEER 2000-2020) and adjusted for IBD using a relative risk from the literature. Deterministic and probabilistic sensitivity analyses included variations in colonoscopy adherence. Results: The cost-effective strategy was continuing with a 4-year surveillance interval for patients without dysplasia. This strategy yielded an incremental cost-effectiveness ratio (ICER) of $6,043 per quality-adjusted life year (QALY), while the 2-year strategy had an ICER of $171,615 per QALY. CRC incidence was slightly higher with the 4-year strategy (4.5% vs 3.8%), with minimal differences in local-stage detection (59% vs 60%) and CRC-related mortality (0.18% vs 0.15%). The 4-year strategy remained cost-effective across sensitivity analyses, with dysplasia detection rates and colonoscopy cost as key drivers. Probabilistic analysis favored the 4-year approach in 70% of simulations. Regarding resource utilization, colonoscopy use per 100 persons screened was 1,283 for the 4-year strategy vs 1,719 for the 2-year strategy, and only 17 in the natural history arm. Conclusion: Our model shows that extending surveillance colonoscopy to every 4 years in IBD patients without dysplasia is the cost-effective strategy. These findings support a more efficient approach to dysplasia surveillance that preserves patient safety while optimizing healthcare resources.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 29%
Inflammatory Bowel Disease
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S1715 Optimal Screening Intervals for Dysplasia in Inflammatory Bowel Disease: Results of a Markov Model · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS