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Polypharmacy and Bleeding Outcomes After Percutaneous Coronary Intervention
Ko Yamamoto1, Takeshi Morimoto2, Masahiro Natsuaki3
1Department of Cardiology, Kokura Memorial Hospital.
Insights
Polypharmacy, or using multiple medications, increases major bleeding risk in patients after percutaneous coronary intervention (PCI). This study found higher bleeding rates with more medications, but no increase in ischemic events.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Polypharmacy is linked to major bleeding in general populations.
- Data on polypharmacy and bleeding risk in percutaneous coronary intervention (PCI) patients were lacking.
Purpose of the Study:
- To investigate the association between the number of medications and major bleeding risk in patients undergoing PCI.
- To assess the impact of polypharmacy on both bleeding and ischemic events post-PCI.
Main Methods:
- Analysis of 12,291 patients from the CREDO-Kyoto PCI Registry Cohort-3.
- Medication counts at discharge were categorized into tertiles.
- Major bleeding (Bleeding Academic Research Consortium Type 3 or 5) incidence was compared across medication tertiles over 5 years.
Main Results:
- Approximately 90% of PCI patients used five or more medications.
- A significant, incremental increase in 5-year major bleeding risk was observed with higher medication counts.
- Adjusted analyses confirmed increased major bleeding risk for patients on 6-7 (HR 1.21) and ≥8 (HR 1.27) medications compared to ≤5.
- No significant association was found between medication count and the risk of myocardial infarction or ischemic stroke.
Conclusions:
- In real-world PCI patients, polypharmacy is common and associated with a significantly higher adjusted risk of major bleeding.
- The number of medications did not correlate with an increased risk of ischemic events like myocardial infarction or stroke.
Background:
Polypharmacy was reported to be associated with major bleeding in various populations. However, there are no data on polypharmacy and its association with bleeding in patients undergoing percutaneous coronary intervention (PCI).
Methods And Results:
Among 12,291 patients in the CREDO-Kyoto PCI Registry Cohort-3, we evaluated the number of medications at discharge and compared major bleeding, defined as Bleeding Academic Research Consortium Type 3 or 5 bleeding, across tertiles (T1-3) of the number of medications. The median number of medications was 6, and 88.0% of patients were on ≥5 medications. The cumulative 5-year incidence of major bleeding increased incrementally with increasing number of medications (T1 [≤5 medications] 12.5%, T2 [6-7] 16.5%, and T3 [≥8] 20.4%; log-rank P<0.001). After adjusting for confounders, the risks for major bleeding of T2 (hazard ratio [HR] 1.21; 95% confidence interval [CI] 1.08-1.36; P=0.001) and T3 (HR 1.27; 95% CI 1.12-1.45; P<0.001) relative to T1 remained significant. The adjusted risks of T2 and T3 relative to T1 were not significant for a composite of myocardial infarction or ischemic stroke (HR 0.95 [95% CI 0.83-1.09; P=0.47] and HR 1.06 [95% CI 0.91-1.23; P=0.48], respectively).
Conclusions:
In a real-world population of patients undergoing PCI, approximately 90% were on ≥5 medications. Increasing number of medications was associated with a higher adjusted risk for major bleeding, but not ischemic events.
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