Why the study?
Does co-prescription of a proton pump inhibitor or H2-receptor antagonist reduce the occurrence of upper gastrointestinal bleeding in patients on aspirin and clopidogrel co-therapy?
Does co-prescription of a proton pump inhibitor or H2-receptor antagonist reduce the occurrence of upper gastrointestinal bleeding in patients on aspirin and clopidogrel co-therapy?
In patients receiving dual antiplatelet therapy with aspirin and clopidogrel, co-prescription of a proton pump inhibitor significantly reduces the risk of upper gastrointestinal bleeding.
May support PPI gastroprotection in DAPT; leaves open causal confirmation by RCTs.
INTRODUCTION: The major complication of aspirin and clopidogrel (A+C) co-therapy is upper gastrointestinal bleeding (UGIB). However, data are unavailable for real-life situations. Furthermore, the treatment effect of antisecretory agents is unknown. AIM: This cohort study aimed to determine the occurrence of UGIB. The treatment effect of H2-receptor antagonist (H2RA) and proton pump inhibitor (PPI) was also analyzed. METHOD: The records of 987 consecutive patients on A+C co-therapy between January 2001 and September 2006 were analyzed. The follow-up ended on the dates of a first occurrence of UGIB, stopping A+C co-therapy, a change in the antisecretory class, death, or March 2007. RESULTS: After a follow-up of 5.8 +/- 6.5 months, UGIB occurred in 39 (4.0%) patients. PPI, H2RA and control were prescribed in 213, 287 and 487 patients respectively. After adjustment for age, dose of aspirin, previous UGIB and duration of treatment, the risk was marginally reduced by H2RA (OR = 0.43, 95% CI 0.18-0.91, p = 0.04) and significantly reduced by PPI (OR = 0.04, 95% CI 0.002-0.21, p = 0.002), as compared to control. CONCLUSION: The occurrence of UGIB associated with A+C co-therapy for a median of 5.8 months was 4.0%. Co-prescription with PPI was associated with a lower risk.
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Ng et al. (2008) studied this question.
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