Key result
Tegoprazan shows similar GI and MACE outcomes compared to PPIs after PCI.
Why the study?
The comparative clinical outcomes of tegoprazan versus proton pump inhibitors in patients receiving antiplatelet therapy after PCI were not established.
Does tegoprazan reduce upper gastrointestinal and cardiovascular complications compared to proton pump inhibitors in patients receiving antiplatelet therapy after percutaneous coronary intervention?
Observational (n=604)
No
Does tegoprazan reduce upper gastrointestinal and cardiovascular complications compared to proton pump inhibitors in patients receiving antiplatelet therapy after percutaneous coronary intervention?
In patients receiving antiplatelet therapy after percutaneous coronary intervention, tegoprazan demonstrated comparable gastrointestinal and cardiovascular safety profiles to proton pump inhibitors.
Tegoprazan may serve as PPI alternative post-PCI on antiplatelets; leaves open randomized confirmation of cardiovascular safety.
Objectives: Tegoprazan is an alternative to proton pump inhibitors (PPIs). This study evaluated the occurrence of upper gastrointestinal (GI) and cardiovascular (CV) complications in patients with ischemic heart disease undergoing antiplatelet therapy after percutaneous coronary intervention (PCI) who were treated with tegoprazan or PPIs. Methods: Data from 604 patients who received antiplatelet therapy with tegoprazan or PPIs for >6 months after PCI between March 2019 and November 2023 were retrospectively analyzed. The primary GI endpoints were symptomatic gastroduodenal ulcers and upper GI bleeding, while the primary CV endpoints comprised major adverse cardiac events (MACEs), nonfatal myocardial infarction (MI), target vessel revascularization, and death from CV-related causes. Results: Among the 604 patients, 265 received tegoprazan and 339 received PPIs. During a mean follow-up of 17 months, seven patients experienced a GI event (0.4% with tegoprazan vs. 1.8% with PPIs; p=0.112) and 12 experienced MACEs (1.1% with tegoprazan vs. 2.7% with PPIs; p=0.183). Subgroup analysis indicated that target vessel revascularization occurred in six patients, with event rates of 0.8% (n=2) for tegoprazan and 1.2% (n=4) for PPIs (p=0.598). Tegoprazan was associated with similar rates of nonfatal MI (0.8% vs. 2.4%; p=0.125) and death from CV-related causes (0.4% vs. 0%; p=0.258) as PPIs. Conclusions: There were no significant differences in GI- or CV-related complications between patients treated with tegoprazan and those treated with PPIs.
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Lee et al. (2026) conducted an observational in Ischemic heart disease undergoing antiplatelet therapy after percutaneous coronary intervention (n=604). Tegoprazan vs. Proton pump inhibitors was evaluated on Gastrointestinal events (symptomatic gastroduodenal ulcers and upper GI bleeding) (HR 0.34, 95% CI 0.04-2.97, p=0.33). Tegoprazan was associated with similar rates of gastrointestinal events (HR 0.34) and major adverse cardiac events (HR 0.57) compared to proton pump inhibitors in patients receiving antiplatelet therapy after percutaneous coronary intervention.
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