4.6 Article

Effect of Chronic Kidney Disease in Women Undergoing Percutaneous Coronary Intervention With Drug-Eluting Stents A Patient-Level Pooled Analysis of Randomized Controlled Trials

Journal

JACC-CARDIOVASCULAR INTERVENTIONS
Volume 9, Issue 1, Pages 28-38

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcin.2015.09.023

Keywords

chronic kidney disease; drug-eluting stents; outcomes; women

Funding

  1. Women in Innovation Initiative of the Society of Cardiovascular Angiography and Interventions
  2. Abbott Vascular
  3. AstraZeneca
  4. Biosensors
  5. Biotronik
  6. Medicines Company
  7. Sanofi
  8. Servier
  9. Amarin
  10. Bayer
  11. Boehringer Ingelheim
  12. Bristol-Myers Squibb
  13. Daiichi-Sankyo-Lilly
  14. GlaxoSmithKline
  15. Medtronic
  16. Merck
  17. Novartis
  18. Pfizer
  19. Regeneron
  20. Abbott
  21. Boston Scientific
  22. Cordis
  23. St. Jude
  24. Boston
  25. Terumo
  26. Iroko
  27. Eli Lilly
  28. Merck Sharp and Dohme
  29. Lilly
  30. Daiichi Sankyo
  31. CSL Behring
  32. Covidien
  33. Janssen Pharmaceuticals
  34. Maya Medical
  35. Osprey Medical Inc.
  36. Regado Biosciences
  37. Watermark Research Partners

Ask authors/readers for more resources

OBJECTIVES This study sought to evaluate: 1) the effect of impaired renal function on long-term clinical outcomes in women undergoing percutaneous coronary intervention (PCI) with drug-eluting stent (DES); and 2) the safety and efficacy of new-generation compared with early-generation DES in women with chronic kidney disease (CKD). BACKGROUND The prevalence and effect of CKD in women undergoing PCI with DES is unclear. METHODS We pooled patient-level data for women enrolled in 26 randomized trials. The study population was categorized by creatinine clearance (CrCl) <45 ml/min, 45 to 59 ml/min, and >= 60 ml/min. The primary endpoint was the 3-year rate of major adverse cardiovascular events (MACE). Participants for whom baseline creatinine was missing were excluded from the analysis. RESULTS Of 4,217 women included in the pooled cohort treated with DES and for whom serum creatinine was available, 603 (14%) had a CrCl <45 ml/min, 811 (19%) had a CrCl 45 to 59 ml/min, and 2,803 (66%) had a CrCl >= 60 ml/min. A significant stepwise gradient in risk for MACE was observed with worsening renal function (26.6% vs. 15.8% vs. 12.9%; p < 0.01). Following multivariable adjustment, CrCl <45 ml/min was independently associated with a higher risk of MACE (adjusted hazard ratio: 1.56; 95% confidence interval: 1.23 to 1.98) and all-cause mortality (adjusted hazard ratio: 2.67; 95% confidence interval: 1.85 to 3.85). Compared with older-generation DES, the use of newer-generation DES was associated with a reduction in the risk of cardiac death, myocardial infarction, or stent thrombosis in women with CKD. The effect of new-generation DES on outcomes was uniform, between women with or without CKD, without evidence of interaction. CONCLUSIONS Among women undergoing PCI with DES, CKD is a common comorbidity associated with a strong and independent risk for MACE that is durable over 3 years. The benefits of newer-generation DES are uniform in women with or without CKD. (J Am Coll Cardiol Intv 2016;9:28-38) (C) 2016 by the American College of Cardiology Foundation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available