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Upper gastrointestinal bleeding in patients receiving dual antiplatelet therapy after coronary stenting
Hiroshi Yasuda1, Masaya Yamada, Susumu Sawada
1Division of Gastroenterology, Showa University Fujigaoka Hospital. hyasuda@marianna-u.ac.jp
Insights
Anti-secretory drugs reduce upper gastrointestinal bleeding risk in patients on dual antiplatelet therapy after drug-eluting stent implantation. However, proton pump inhibitors may reduce antiplatelet therapy effectiveness.
Area of Science:
- Cardiology
- Gastroenterology
- Pharmacology
Background:
- Dual antiplatelet therapy (DAPT) is crucial after drug-eluting stent (DES) implantation for coronary heart disease.
- Upper gastrointestinal (UGI) bleeding is a significant risk associated with DAPT.
- Proton pump inhibitors (PPIs) are commonly used to prevent UGI bleeding but may interact with antiplatelet agents.
Purpose of the Study:
- To evaluate the risk of UGI bleeding in patients undergoing DES implantation and receiving DAPT.
- To assess the protective effect of anti-secretory drugs, including PPIs and H2 receptor antagonists (H2RAs), against UGI bleeding.
- To investigate the impact of anti-secretory drugs on cardiovascular outcomes in patients on DAPT.
Main Methods:
- Retrospective analysis of 243 patients who received DES implantation and DAPT.
- Assessment of UGI bleeding events as the primary outcome.
- Coronary angiography (CAG) findings used to evaluate cardiovascular outcomes.
- Data collected from medical records.
Main Results:
- No UGI bleeding occurred in patients taking anti-secretory drugs.
- The 1- and 2-year cumulative incidences of UGI bleeding were 4.5% and 9.2% in patients not taking anti-secretory drugs.
- Significantly more coronary artery stenotic lesions were observed in patients taking PPIs compared to those not taking anti-secretory drugs or taking H2RAs.
Conclusions:
- Concomitant use of anti-secretory agents significantly reduces the risk of UGI bleeding in patients on DAPT post-DES.
- Proton pump inhibitor use may attenuate the effectiveness of DAPT, potentially impacting cardiovascular outcomes.
Objective:
We investigated the risk of upper gastrointestinal (UGI) bleeding and the protective effect of concomitant anti-secretory drugs during dual antiplatelet therapy administered following implantation of drug-eluting stents (DES) for coronary heart disease. Because proton pump inhibitors (PPIs) are reported to decrease the platelet inhibitory effects of clopidogrel, we also assessed cardiovascular outcomes in patients taking thienopyridine derivatives with or without anti-secretory drug.
Methods:
We retrospectively analyzed 243 patients, who underwent DES implantation between January 2006 and December 2007 and were receiving dual anti-platelet therapy post-surgery. The main outcome measurement was the presence of UGI bleeding. Cardiovascular outcomes were assessed by follow-up coronary angiography (CAG) findings. Data were collected from medical records.
Results:
Eight cases of UGI bleeding were observed during the follow-up period, none of whom were taking anti-secretory drugs. Among the 243 cases, 108 cases were taking anti-secretory drugs: a PPI (67 cases), and an H2 receptor antagonist (41 cases). No UGI bleeding was observed among patients who were taking concomitant anti-secretory drugs. The 1- and 2-year cumulative incidences of UGI bleeding among patients who were not taking anti-secretory drugs were 4.5% and 9.2%, respectively. When CAG findings were compared between patients not taking any anti-secretory drug, taking PPI, or taking H2RA, significantly more stenotic lesions of the coronary artery were observed in the PPI-treatment group.
Conclusion:
Concomitant use of an anti-secretory agent was associated with a reduced risk of UGI bleeding. Use of PPI may be associated with an attenuation of the effect of dual antiplatelet therapy.
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