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Comparative Effectiveness and Safety of Oral P2Y12 Inhibitors in Patients on Chronic Dialysis.
Jain, Nishank; Phadnis, Milind A; Hunt, Suzanne L; Dai, Junqiang; Shireman, Theresa I; Davis, Clayton L; Mehta, Jawahar L; Rasu, Rafia S; Hedayati, S Susan.
  • Jain N; Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Phadnis MA; Medicine Service, Central Arkansas Veterans Affairs Medical Center, Little Rock, Arkansas, USA.
  • Hunt SL; Department of Biostatistics and Data Science, University of Kansas School of Medicine, Kansas City, Kansas, USA.
  • Dai J; Department of Biostatistics and Data Science, University of Kansas School of Medicine, Kansas City, Kansas, USA.
  • Shireman TI; Department of Biostatistics and Data Science, University of Kansas School of Medicine, Kansas City, Kansas, USA.
  • Davis CL; Department of Health Services, Policy and Practice, School of Public Health, Brown University, Providence, Rhode Island, USA.
  • Mehta JL; Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Rasu RS; Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Hedayati SS; Medicine Service, Central Arkansas Veterans Affairs Medical Center, Little Rock, Arkansas, USA.
Kidney Int Rep ; 6(9): 2381-2391, 2021 Sep.
Article en En | MEDLINE | ID: mdl-34514199
INTRODUCTION: Although oral P2Y12 inhibitors (P2Y12-Is) are one of the most commonly prescribed medication classes in patients with end stage kidney disease on dialysis (ESKD), scarce data exist regarding their benefits and risks. METHODS: We compared effectiveness and safety of clopidogrel, prasugrel, and ticagrelor in a longitudinal study using the United States Renal Data System registry of Medicare beneficiaries with ESKD. Individuals who filled new P2Y12-I prescriptions between 2011 and 2015 were included and followed until death or censoring. The primary exposure variable was P2Y12-I assignment. The primary outcome variable was death. Secondary outcomes included cardiovascular (CV) death, coronary revascularization, and gastrointestinal (GI) hemorrhage. Survival analyses were performed after propensity matching. RESULTS: Of 44,619 patients with ESKD who received P2Y12-Is, 95% received clopidogrel (n = 42,523), 3% prasugrel (n = 1205), and 2% ticagrelor (n = 891). To balance baseline differences, propensity-matching was performed: 1:6 for prasugrel (n = 1189) versus clopidogrel (n = 7134); 1:4 for ticagrelor (n = 880) versus clopidogrel (n = 3520); and 1:1 for ticagrelor versus prasugrel (n = 880). Prasugrel was associated with a reduced risk for death versus clopidogrel and ticagrelor (adjusted hazard ratio [HR] = 0.82; 95% CI: 0.73-0.93 and 0.78; 95% CI: 0.64-0.95). Compared with clopidogrel, prasugrel reduced risk for coronary revascularization (HR = 0.91; 95% CI: 0.86-0.96). There were no differences in GI hemorrhage between P2Y12-Is. CONCLUSION: In patients with ESKD, prasugrel compared with others reduced risk of death possibly by reducing risk for coronary revascularizations and without worsening gastrointestinal hemorrhage. Future trials are imperative to compare efficacy and safety of P2Y12-Is in patients with ESKD.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Año: 2021 Tipo del documento: Article