Omar K Siddiqi1, Kyle J Smoot2, Alyssa B Dufour3, Kelly Cho4, Melissa Young2, David R Gagnon5, Samantha Ly6, Sara Temiyasathit6, David P Faxon7, J Michael Gaziano8, Scott Kinlay7. 1. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA Cardiovascular Division, Boston Medical Center, Boston, Massachusetts, USA. 2. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA MAVERIC, Veterans Affairs Boston Healthcare System, Boston, Massachusetts, USA. 3. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA MAVERIC, Veterans Affairs Boston Healthcare System, Boston, Massachusetts, USA Harvard Medical School, Boston, Massachusetts, USA Institute for Aging Research, Hebrew SeniorLife, Boston, Massachusetts, USA. 4. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA MAVERIC, Veterans Affairs Boston Healthcare System, Boston, Massachusetts, USA Harvard Medical School, Boston, Massachusetts, USA. 5. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA MAVERIC, Veterans Affairs Boston Healthcare System, Boston, Massachusetts, USA Boston University School of Public Health, Boston, Massachusetts, USA. 6. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA. 7. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA Harvard Medical School, Boston, Massachusetts, USA Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts, USA. 8. Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury, Massachusetts, USA MAVERIC, Veterans Affairs Boston Healthcare System, Boston, Massachusetts, USA Harvard Medical School, Boston, Massachusetts, USA Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Abstract
OBJECTIVES: Patients with chronic kidney disease (CKD) are at high risk of death or myocardial infarction (MI) after percutaneous coronary interventions (PCI). We assessed whether prolonged dual antiplatelet therapy beyond the recommended 12 months may prevent adverse outcomes in patients with CKD receiving drug-eluting stents (DES) or bare-metal stents (BMS). METHODS: We studied all Veterans receiving PCI with BMS or first-generation DES in the Veterans Affairs (VA) Healthcare System between 2002 and 2006, classified by CKD (estimated glomerular filtration rate <60 mL/min) or normal renal function. We used landmark analyses from 12 months after PCI with Cox proportional hazards multivariable and propensity-adjusted models to assess the effect of prolonged clopidogrel (more than 12 months) versus 12 months or less after PCI on clinical outcomes from 1 year to 4 years after PCI. RESULTS: Of 23 042 eligible subjects receiving PCI, 4880 (21%) had CKD. Compared with normal renal function, patients with CKD had higher risks of death or MI 1-4 years after DES (21% vs 12%, HR=1.75; 95% CI 1.51 to 2.04) or BMS (28% vs 15%, HR=2.10; 95% CI 1.90 to 2.32). In patients with CKD receiving DES, clopidogrel use of more than 12 months after PCI was associated with lower risks of death or MI (18% vs 24%, HR=0.74; 95% CI 0.58 to 0.95), and death (15% vs 23%, HR=0.61; 95% CI 0.47 to 0.80), but had no effect on repeat revascularisation 1-4 years after PCI. CONCLUSIONS: In patients with CKD, prolonging clopidogrel beyond 12 months after PCI may decrease the risk of death or MI only in patients receiving first-generation DES. These results support a patient-tailored approach to prolonging clopidogrel after PCI. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
OBJECTIVES:Patients with chronic kidney disease (CKD) are at high risk of death or myocardial infarction (MI) after percutaneous coronary interventions (PCI). We assessed whether prolonged dual antiplatelet therapy beyond the recommended 12 months may prevent adverse outcomes in patients with CKD receiving drug-eluting stents (DES) or bare-metal stents (BMS). METHODS: We studied all Veterans receiving PCI with BMS or first-generation DES in the Veterans Affairs (VA) Healthcare System between 2002 and 2006, classified by CKD (estimated glomerular filtration rate <60 mL/min) or normal renal function. We used landmark analyses from 12 months after PCI with Cox proportional hazards multivariable and propensity-adjusted models to assess the effect of prolonged clopidogrel (more than 12 months) versus 12 months or less after PCI on clinical outcomes from 1 year to 4 years after PCI. RESULTS: Of 23 042 eligible subjects receiving PCI, 4880 (21%) had CKD. Compared with normal renal function, patients with CKD had higher risks of death or MI 1-4 years after DES (21% vs 12%, HR=1.75; 95% CI 1.51 to 2.04) or BMS (28% vs 15%, HR=2.10; 95% CI 1.90 to 2.32). In patients with CKD receiving DES, clopidogrel use of more than 12 months after PCI was associated with lower risks of death or MI (18% vs 24%, HR=0.74; 95% CI 0.58 to 0.95), and death (15% vs 23%, HR=0.61; 95% CI 0.47 to 0.80), but had no effect on repeat revascularisation 1-4 years after PCI. CONCLUSIONS: In patients with CKD, prolongingclopidogrel beyond 12 months after PCI may decrease the risk of death or MI only in patients receiving first-generation DES. These results support a patient-tailored approach to prolongingclopidogrel after PCI. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
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