Pharmacodynamic Profile and Prevalence of Bleeding Episode in East Asian Patients with Acute Coronary Syndromes Treated with Prasugrel Standard-Dose versus De-escalation Strategy: A Randomized A-MATCH Trial
- Author(s)
- Young-Hoon Jeong; Ju-Hyeon Oh; Hyuck-Jun Yoon; Yongwhi Park; Jon Suh; Se-Whan Lee; Kyounghoon Lee; Jeong-Su Kim; Woo-Jung Chun; Yong-Hwan Park; Chang-Wook Nam; June-Hong Kim; Jong-Hwa Ahn; Seok-Jae Hwang; Jin-Yong Hwang; Udaya S. Tantry; Paul A. Gurbel; Eun-Seok Shin
- Keimyung Author(s)
- Yoon, Hyuck Jun; Nam, Chang Wook
- Department
- Dept. of Internal Medicine (내과학)
- Journal Title
- Thromb Haemost
- Issued Date
- 2021
- Volume
- 121
- Issue
- 10
- Keyword
- acute coronary syndrome; prasugrel; East Asians; de-escalation strategy; platelet function test
- Abstract
- Compared with Caucasian patients, East Asian patients have the unique risk–benefit trade-off and different responsiveness to antithrombotic regimens. The aim of this study was to compare pharmacodynamic profile in East Asian patients with acute coronary syndromes (ACSs) treated with prasugrel standard-dose versus a de-escalation strategy. Before discharge, ACS patients with age <75 years or weight ≥60 kg (n = 255) were randomly assigned to the standard-dose (10-mg group) or de-escalation strategy (5-mg group or platelet function test [PFT]-guided group). After 1 month, VerifyNow P2Y12 assay-based platelet reactivity (P2Y12 reaction unit [PRU]) and bleeding episodes were evaluated. Primary endpoint was the percentage of patients with the therapeutic window (85 ≤ PRU ≤ 208). The 250 patients completed 1-month treatment. The percentage of patients within the therapeutic window was significantly lower in the 10-mg group (n = 85) compared with the 5-mg (n = 83) and PFT-guided groups (n = 82) (35.3 vs. 67.5 vs. 65.9%) (odds ratio [OR]: 3.80 and 3.54; 95% confidence interval [CI]: 2.01–7.21 and 1.87–6.69, respectively). Compared with the 10-mg group, the bleeding rate was tended to be lower with de-escalation strategies (35.3 vs. 24.1% vs. 23.2%) (hazard ratio [HR]: 0.58 and 0.55; 95% CI: 0.30–1.14 and 0.28–1.09, respectively). "PRU < 127" was the optimal cut-off for predicting 1-month bleeding events (area under the curve: 0.616; 95% CI: 0.543–0.689; p = 0.005), which criteria was significantly associated with early discontinuation of prasugrel treatment (HR: 2.00; 95% CI: 1.28–3.03; p = 0.001). In conclusion, compared with the standard-dose prasugrel, the prasugrel de-escalation strategy in East Asian patients presented with ACS showed a higher chance within the therapeutic window and a lower tendency toward bleeding episodes.
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