Abstract
Background: In contrast to the vast majority of pharmaceuticals on the market, antiplatelet agents are widely prescribed in a uniform, 'one size fits all' manner, without conventional dose adjustments. However, strong evidence yielded from clinical trials repeatedly suggests that patients with a low body weight (LBW), the elderly and those with renal or hepatic impairment may benefit from reduced doses, while younger, heavier patients, males and diabetics may benefit from a dose escalation. Vorapaxar, a thrombin protease-activated receptor-1 inhibitor, has been tested in the TRA2P and TRACER clinical trials, but its efficacy and safety in patients with a LBW is unclear. Objective: To determine the impact of LBW on primary end point rates (PER) and bleeding risk after vorapaxar, as yielded from the TRA2P and TRACER secondary FDA review. Results: The LBW (
Original language | English (US) |
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Pages (from-to) | 69-72 |
Number of pages | 4 |
Journal | Cardiology |
Volume | 133 |
Issue number | 2 |
DOIs | |
State | Published - Jan 1 2016 |
Keywords
- Bleeding
- Body weight
- Dose adjustment
- Vorapaxar
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
- Pharmacology (medical)