Efficacy and safety of more potent antiplatelet therapy with vorapaxar in patients with impaired renal function

J Thromb Thrombolysis. 2019 Apr;47(3):353-360. doi: 10.1007/s11239-018-1779-y.

Abstract

Patients with renal disease are often undertreated with antiplatelet therapy due to concerns about bleeding. Vorapaxar blocks platelet activation via the PAR-1 receptor and reduces cardiovascular events in patients with stable atherosclerosis, but with increased bleeding. We examined the efficacy and safety of vorapaxar in patients with impaired renal function. TRA2°P-TIMI 50 randomized patients with stable atherosclerosis to vorapaxar or. We analyzed patients with eGFR assessed who qualified with a history of MI or PAD (without stroke or TIA) (n = 19,932). Cox models assessed the risk of CV events and bleeding by quartile of baseline eGFR in the placebo arm and then by randomized assignment. Net clinical outcome (NCO) was predefined as CV death, MI, stroke, or GUSTO severe bleeding. Patients with lower eGFR tended to be older, female, have hypertension, hyperlipidemia or prior PAD. In the placebo arm, baseline eGFR in the lowest quartile was associated with a 26% higher risk of CV death, MI or stroke (Q1:Q4 HRadj 1.26, 1.03-1.55) and 73% higher risk of GUSTO moderate or severe bleeding (HRadj 1.73, 1.12-2.65). Vorapaxar reduced the risk of MACE to a similar extent (14-26%) across quartiles of baseline eGFR (P interaction = 0.70) and increased the relative risk of GUSTO moderate or severe bleeding (P interaction = 0.54). NCO was similar across quartiles of eGFR (P interaction = 0.65). Intensification of antiplatelet therapy with vorapaxar offers comparable net clinical benefit regardless of baseline renal function. These data support the use of more potent antiplatelet regimens in patients with renal dysfunction.

Keywords: Antiplatelet agents; PAR-1 receptor; Renal dysfunction; Secondary prevention; Vorapaxar.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Atherosclerosis / drug therapy
  • Cardiovascular Diseases / drug therapy
  • Female
  • Glomerular Filtration Rate*
  • Hemorrhage / chemically induced
  • Humans
  • Kidney Diseases / drug therapy*
  • Lactones / adverse effects
  • Lactones / therapeutic use*
  • Male
  • Middle Aged
  • Platelet Aggregation Inhibitors / therapeutic use
  • Pyridines / adverse effects
  • Pyridines / therapeutic use*
  • Receptor, PAR-1 / metabolism
  • Risk
  • Secondary Prevention
  • Treatment Outcome

Substances

  • Lactones
  • Platelet Aggregation Inhibitors
  • Pyridines
  • Receptor, PAR-1
  • vorapaxar