TY - JOUR
T1 - Immediate response to prasugrel loading in patients with ST-elevation myocardial infarction
T2 - Predictors and outcome
AU - Koifman, Edward
AU - Beigel, Roy
AU - Herscovici, Romana
AU - Fefer, Paul
AU - Rozenberg, Nurit
AU - Sabbag, Avi
AU - Biton, Yitschak
AU - Segev, Amit
AU - Shechter, Michael
AU - Asher, Elad
AU - Matetzky, Shlomi
N1 - Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/8/1
Y1 - 2016/8/1
N2 - Introduction Information regarding immediate response to novel P2Y12 inhibitors in ST-elevation myocardial infarction (STEMI) is scarce and has been associated with adequate reperfusion. Recent studies have shown that the onset of anti-platelet effects of novel P2Y12 inhibitors in patients with STEMI might be slower and more variable than in stable coronary syndrome. We aimed to assess the predictors and significance of immediate platelet response to prasugrel loading in STEMI. Methods Platelet aggregation (PA) was prospectively evaluated in STEMI patients upon prasugrel loading and at primary percutaneous coronary intervention (PPCI). Early platelet responsiveness was defined as percent reduction of PA from baseline to PPCI, divided by the time lapse from loading to PPCI. High- and low-platelet responsiveness was defined as above and below the median value respectively. Results Fifty consecutive STEMI patients (age 58 ± 8, 90% male) underwent PPCI with a mean door-to-balloon time of 42 ± 15 min. Mean PA upon prasugrel loading and at PPCI was 76 ± 9% and 63 ± 19%, respectively. Older age and prior aspirin use were predictors of low platelet responsiveness to prasugrel [β = (− 0.33), p = 0.02 and β = (− 0.28), p = 0.04, respectively]. Fast compared with slow responders demonstrated more frequent early ST resolution (93% vs. 72%, p = 0.02) and lower peak troponin levels (76 ± 62 μg/L vs. 48 ± 28 μg/L, p = 0.05). Conclusions Immediate platelet responsiveness to prasugrel among STEMI patients is highly variable and inversely associated with older age and prior aspirin use. Fast compared with slow responders have improved reperfusion and infarct size markers.
AB - Introduction Information regarding immediate response to novel P2Y12 inhibitors in ST-elevation myocardial infarction (STEMI) is scarce and has been associated with adequate reperfusion. Recent studies have shown that the onset of anti-platelet effects of novel P2Y12 inhibitors in patients with STEMI might be slower and more variable than in stable coronary syndrome. We aimed to assess the predictors and significance of immediate platelet response to prasugrel loading in STEMI. Methods Platelet aggregation (PA) was prospectively evaluated in STEMI patients upon prasugrel loading and at primary percutaneous coronary intervention (PPCI). Early platelet responsiveness was defined as percent reduction of PA from baseline to PPCI, divided by the time lapse from loading to PPCI. High- and low-platelet responsiveness was defined as above and below the median value respectively. Results Fifty consecutive STEMI patients (age 58 ± 8, 90% male) underwent PPCI with a mean door-to-balloon time of 42 ± 15 min. Mean PA upon prasugrel loading and at PPCI was 76 ± 9% and 63 ± 19%, respectively. Older age and prior aspirin use were predictors of low platelet responsiveness to prasugrel [β = (− 0.33), p = 0.02 and β = (− 0.28), p = 0.04, respectively]. Fast compared with slow responders demonstrated more frequent early ST resolution (93% vs. 72%, p = 0.02) and lower peak troponin levels (76 ± 62 μg/L vs. 48 ± 28 μg/L, p = 0.05). Conclusions Immediate platelet responsiveness to prasugrel among STEMI patients is highly variable and inversely associated with older age and prior aspirin use. Fast compared with slow responders have improved reperfusion and infarct size markers.
KW - Acute platelet aggregation
KW - Myocardial infarction
KW - Prasugrel
UR - http://www.scopus.com/inward/record.url?scp=84977264583&partnerID=8YFLogxK
U2 - 10.1016/j.thromres.2016.05.005
DO - 10.1016/j.thromres.2016.05.005
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 27386796
AN - SCOPUS:84977264583
SN - 0049-3848
VL - 144
SP - 176
EP - 181
JO - Thrombosis Research
JF - Thrombosis Research
ER -