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During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
Tegoprazan, a potassium-competitive acid blocker (P-CAB), has been widely prescribed in South Korea since 2018. Despite its increasing use, data on the long-term renal safety of tegoprazan, especially in patients with chronic kidney disease (CKD), remains limited. This study aimed to assess the long-term effect of tegoprazan on progression to end-stage kidney disease (ESKD) among CKD stage 3–4 patients.
We conducted a nationwide, retrospective cohort study using the Korean Health Insurance Review and Assessment (HIRA) database from 2013 to 2022. Patients with CKD stages 3–4 who were newly prescribed tegoprazan were matched 1:1 by propensity score with those receiving histamine-2 receptor antagonists (H2RAs) or proton pump inhibitors (PPIs). The composite outcome was all-cause mortality or ESKD. Hazard ratios (HRs) were estimated using Cox proportional hazards models, and a network meta-analysis was performed to integrate pairwise comparisons.
After matching, 674, 902, and 4,583 pairs were included in the tegoprazan–H2RA, tegoprazan–PPI, and PPI–H2RA comparisons, respectively. The mean age exceeded 75 years, and comorbidities were frequent (hypertension 85%, diabetes 45%, ischemic heart disease 28%).
Long-term tegoprazan use was not associated with increased risk of death or ESKD compared with H2RAs (HR 0.91, 95% CI 0.66–1.26, p=0.565) or PPIs (HR 0.87, 95% CI 0.66–1.15, p=0.321). The network meta-analysis confirmed consistent findings across treatment groups.
Among patients with CKD stages 3–4, long-term tegoprazan use did not significantly increase the risk of death or ESKD progression compared with H2RAs or PPIs. These findings suggest no apparent renal toxicity signal associated with tegoprazan use. Further prospective studies are warranted to confirm its long-term renal safety.