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Evaluating the cost-effectiveness of artificial intelligence in Barrett's surveillance
Jin Lin Tan1,2, Jeremy Wei Quan Chan3, Mohamed Asif Chinnaratha1,2
1Lyell McEwin Hospital, SA Health, Department of Gastroenterology and Hepatology, Australia, Elizabeth Vale.
Background:
Artificial intelligence (AI) has emerged as a promising tool to detect early dysplasia in Barrett's esophagus (BE). However, the cost-effectiveness of AI-assisted BE surveillance has not been evaluated.
Methods:
A Markov model simulated 1000 Australian individuals with nondysplastic Barrett's esophagus (NDBE) undergoing surveillance from age 50 to 80 years, with follow-up until age 100. We compared AI-assisted surveillance with targeted biopsies against standard endoscopy with four-quadrant biopsies under 3-yearly and 5-yearly surveillance. The primary outcome was the incremental cost-effectiveness ratio (ICER). Secondary outcomes included cumulative incidence of high grade dysplasia (HGD)/T1 lesions and advanced esophageal adenocarcinoma (EAC), as well as their relative differences. A health care system perspective was employed, with costs and utilities discounted at an annual rate of 3%.
Results:
AI-assisted surveillance was cost effective across both intervals, with ICERs of AUD 14 039/quality-adjusted life year (QALY) (3-yearly) and 3609/QALY (5-yearly). Compared with standard surveillance, AI reduced the cumulative incidence of advanced EAC by 5 and 3 cases per 1000 people (relative reductions of 3.5% and 1.6%) for 3- and 5-yearly surveillance, respectively. Conversely, AI increased HGD/T1 detection by 27 and 38 cases per 1000 people (relative increases of 21.8% and 27.7%) for 3- and 5-yearly surveillance, respectively. Additionally, AI reduced missed HGD/T1 incidence by 37 and 45 cases per 1000 people (relative reductions of 72.9% and 72.2%) for 3- and 5-yearly surveillance, respectively.
Conclusion:
AI-assisted endoscopic surveillance in BE was a cost-effective strategy in the Australian health care setting, reducing the cumulative incidence of advanced EAC and missed HGD/T1 lesions.
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