Objective Patients undergoing percutaneous coronary intervention require dual antiplatelet therapy. Proton-pump inhibitor (PPI) therapy is recommended for the prevention of upper GI complications. No study has determined the rate and type of GI bleeding events in such patients in routine clinical practice.
Design Observational study with a prospective follow-up to confirm medication use and occurrence of events, which were validated.
Patients and setting We have followed up a cohort of 1219 consecutive patients admitted for percutaneous coronary intervention in Zaragoza (Spain).
Main outcome measures Major GI bleeding and cardiovascular events.
Results At discharge, 96.7% of patients were on dual antiplatelet therapy and 76.6% on PPI therapy, which increased up to 87.9% during follow-up of 2107.6 patient (pt) s-years (1.72±1.07 years/patient). There were eight patients who developed GI bleeding during hospitalisation and 27 patients during follow-up, (1.52 bleeds per 100 pt-years). Most GI bleeding events (81.4%) occurred during the first year (mean time to bleeding event: 7.03±7.65 months) and 84.6% of patients were on long-term PPI at the time of the bleed. Lower GI bleeding occurred more frequently than upper GI bleeding (74% lower vs 26% upper). Peptic ulcer history and concomitant warfarin therapy were the only risk factors identified for upper or lower GI bleeding respectively.
Conclusions Among patients on dual antiplatelet therapy and PPI co-therapy, gastrointestinal bleeding episodes are more frequent in the lower GI tract. This changing pattern of bleeding may reflect the success of gastroprotection and focuses attention on research to address lower GI bleeding in this population.
- Antiplatelet treatment
- interventional cardiology
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Funding This study was funded by a grant for international research post-residency, Spanish Society of Cardiology (RC); B01 from the Regional Aragone's Government in Spain (AL).
Competing interests ICMJE conflicts of interest form for each author of this manuscript. Angel Lanas has served as consultant to AstraZeneca, Pfizer, and Bayer, and has received research funding from AstraZeneca and Pfizer for investigator-initiated research. James Scheiman has served as consultant to AstraZeneca as well as and Pozen, and Novartis Inc. Ruben Casado-Arroyo, Mónica Polo-Tomas and Maria P Roncales report no conflict of interest.
Patient consent The ethics committee of our hospital approved the study, and all the patients gave oral informed consent before the telephone interview.
Ethics approval The ethics committee of Hospital Clínico Universitario Lozano Blesa approved the study.
Provenance and peer review Not commissioned; internally peer reviewed.
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