Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2025 Oct 1:252:78-87.
doi: 10.1016/j.amjcard.2025.05.037. Epub 2025 Jun 5.

Proton Pump Inhibitor Use, Gastrointestinal Bleeding Reduction, and Long-Term Prognosis After Percutaneous Coronary Intervention

Affiliations
Free article
Multicenter Study

Proton Pump Inhibitor Use, Gastrointestinal Bleeding Reduction, and Long-Term Prognosis After Percutaneous Coronary Intervention

Tatsuya Tokai et al. Am J Cardiol. .
Free article

Abstract

Proton pump inhibitors (PPI) reduce gastrointestinal bleeding (GIB) after percutaneous coronary intervention (PCI), but their impact on mortality and major adverse cardiovascular events (MACE) remains unclear. This study investigated the association between PPI-related GIB reduction and MACE and mortality using a real-world database. We analyzed 6,457 patients undergoing PCI (2013 to 2019), using the Clinical Deep Data Accumulation System including electronic medical records from 7 Japanese hospitals. Patients were grouped by PPI use. The primary outcome was GIB and secondary outcomes were all-cause mortality and MACE. Propensity score matching (PSM), inverse probability of treatment weighting (IPTW), and Cox regression were used to estimate hazard ratios. To estimate causal inference, mediation analysis was conducted to assess the indirect effects of PPI use via GIB reduction. PSM and IPTW analyses revealed a lower GIB incidence in the PPI group (PSM: <0.1%, IPTW: 1.6%) than in the non-PPI group (PSM: 2.3%, IPTW: 2.7%). No significant association was found between PPI use and all-cause death or MACE. However, in patients with acute coronary syndrome (ACS), IPTW analysis indicated that PPI use was associated with lower all-cause death (HR: 0.582, 95% CI: 0.364 to 0.931) and MACE (HR: 0.570, 95% CI: 0.344 to 0.946). Importantly, mediation analysis suggested that GIB reduction partially mediated the association between PPI use and lower mortality. In conclusion, PPI use after PCI was associated with lower GIB risk. In ACS patients, it may be associated with a reduction in all-cause mortality, partially mediated by GIB reduction.

Keywords: acute coronary syndrome; antiplatelet therapy; cardiovascular disease; gastrointestinal bleeding; proton pump inhibitor.

PubMed Disclaimer

Conflict of interest statement

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Tetsuya Matoba reports financial support was provided by the Cross-ministerial Strategic Innovation Promotion Program on Integrated Health Care System. TM received research grants from Amgen and honoraria from Abbott Medical and Bayer. T Kabutoya received scholarship funding from Abbott Medical and the Joint Research Fund of Novartis Pharmaceutical. YI received honoraria from Daiichi Sankyo and Toa Eiyo, Japan. KK received research grants and honoraria from Sanwa Kagaku and Kenkyusho. AK received honoraria from AstraZeneca, Eli Lilly, and Sumitomo Pharma. YN received research grants and consultations from Bayer. KT received remuneration for lectures from Abbott Medical Co., Ltd., Amgen K.K., Bayer Yakuhin, Ltd., Daiichi Sankyo Co., Ltd., Kowa Pharmaceutical Co. Ltd., Nippon Boehringer Ingelheim Co., Ltd., Novartis Pharma K.K., Otsuka Pharmaceutical Co., Ltd., Pfizer Japan Inc., Takeda Pharmaceutical Co., Ltd., and TERUMO Co, Ltd.; trust research/joint research funds from Bayer Yakuhin, Ltd., Bristol-Myers K.K., Daiichi Sankyo Co., Ltd., MOCHIDA PHARMACEUTICAL CO., LTD., EA Pharma Co., Ltd., TAUNS Laboratories, Inc., Novo Nordisk Pharma Ltd., and PRA Health Sciences; received scholarship funds from Abbott Medical Co., Ltd., ITI Co.,Ltd., Boehringer Ingelheim Japan, Otsuka Pharmaceutical Co., Ltd., and Boston Scientific Japan K.K; and was affiliated with endowed departments at Abbott Japan Co., Ltd., Boston Scientific Japan K.K., Fides-one, Inc., GM Medical Co., Ltd., ITI Co., Ltd., Kaneka Medix Co., Ltd., NIPRO CORPORATION, TERUMO Co, Ltd., Philips Japan Ltd., Getinge Group Japan K.K., Orbusneich Medical K. K., Abbott Medical Co., Ltd., BIOTRONIK JAPAN, INC., Boston Scientific Japan K.K., Fukuda Denshi Co., Ltd., Japan Lifeline Co., Ltd., Medtronic Japan Co., Ltd., Nippon Boehringer Ingelheim Co., Ltd., and NIPRO CORPORATION. HS reported stocks and stock options with precision. HF received consulting fees from Mehergen Group Holdings and honoraria from Novartis Pharma and Otsuka Pharmaceutical. RN received research grants from Novartis Pharma K.K. and honoraria from Kowa, Takeda Pharmaceutical, Tanabe-Mitsubishi Pharmaceuticals, and Boehringer Ingelheim. The authors declare no conflict of interest. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Publication types

Substances

LinkOut - more resources