Bleeding Risk Following Percutaneous Coronary Intervention in Patients with Diabetes Prescribed Dual Anti-platelet Therapy

Background Patients with diabetes (DM) experience higher rates of in-stent restenosis and greater benefit from DES implant at the time of PCI, necessitating prolonged dual anti-platelet therapy (DAPT). While DAPT reduces risk of ischemic events post-PCI, it also increases risk of bleeding. Whether b...

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Published inThe American heart journal Vol. 182; pp. 111 - 118
Main Authors Grodzinsky, Anna, MD, Arnold, Suzanne V., MD, MHA, Wang, Tracy Y., MD, MSc, Sharma, Praneet, MD, Gosch, Kensey, M.S, Jones, Philip G., M.S, Bhatt, Deepak L., MD, MPH, Steg, Philippe Gabriel, MD, McGuire, Darren K., MD, MHSc, Cohen, David J., MD, MSc, Spertus, John A., MD, MPH, Chhatriwalla, Adnan K., MD, Lind, Marcus, MD, Ph.D, Graham, Garth, MD, MPH, Kosiborod, Mikhail, MD
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.12.2016
Elsevier Limited
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Summary:Background Patients with diabetes (DM) experience higher rates of in-stent restenosis and greater benefit from DES implant at the time of PCI, necessitating prolonged dual anti-platelet therapy (DAPT). While DAPT reduces risk of ischemic events post-PCI, it also increases risk of bleeding. Whether bleeding rates differ among patients with and without DM receiving long-term DAPT is unknown. Methods Among patients who underwent PCI and were maintained on DAPT for 1 year in a multicenter US registry, we assessed patient-reported bleeding over one year following PCI in patients with and without DM. Multivariable, hierarchical Poisson regression was used to evaluate the association of DM with bleeding during follow-up. Results Among 2334 PCI patients from 10 US hospitals (mean age 64, 54% ACS), 32.6% had DM. In unadjusted analyses, patients with DM had fewer bleeding events over the year following PCI (DM vs no DM: BARC =1: 78.0% vs 87.7%, P < .001; BARC ≥2: 4.3% vs 5.3%, P = .33). Following adjustment, patients with (vs. without DM) had a lower risk of BARC ≥1 bleeding during follow-up (relative risk [RR] 0.89, 95% CI 0.83–0.96). This decreased bleeding risk persisted after removing bruising from the endpoint definition. Conclusions In a real-world PCI registry, patients with DM experienced lower risk of bleeding risk on DAPT. As patients with DM also derive greater ischemic benefit from DES, which requires prolonged DAPT, our findings suggest that the balance between benefit and risk of this therapeutic approach may be even more favorable in patients with DM than previously considered.
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ISSN:0002-8703
1097-6744
DOI:10.1016/j.ahj.2016.09.010