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Abstract 11149: Pretreatment With P2Y12 Inhibitors in ST-Elevation Myocardial Infarction & Systematic Review and Meta-Analysis
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Background:
the practice of pretreatment with oral P
2
Y
12
inhibitors in ST-Elevation Myocardial Infarction (STEMI) remains common; however, its association with improved cardiovascular outcomes is unclear, since no large RCT has addressed this issue.
Hypothesis:
We aimed to evaluate the association of oral P2Y12 inhibitor pretreatment in STEMI patients with cardiovascular and bleeding outcomes.
Methods:
PubMed, MEDLINE, Embase, Cochrane, Scopus, Web of Science were systematically searched for studies that compared pretreatment with P
2
Y
12
versus no pretreatment in STEMI, and reported efficacy and safety outcomes. A meta-analysis using a fixed and random effects model was used to calculated outcomes of interest. Heterogeneity was assessed with I
2
statistics.
Results:
A total of 3 RCTs and 14 observational studies assigning 91,771 patients to either pretreatment (65,598 patients) or no pretreatment (26,171 patients) were included. Follow-up ranged from 7 days to 19 months. The P
2
Y
12
inhibitors included clopidogrel, prasugrel and ticagrelor. At 30 days, P
2
Y
12
pretreatment was associate with lower 30-day mortality (risk ratio [RR], 0.71; 95% CI, 0.56-0.91; p=0.006; I
2
=75%), stent thrombosis (RR, 0.33; 95% CI, 0.12-0.95; p=0.04; I
2
=83%), and major bleeding (RR, 0.81; 95% CI, 0.74-0.90; p<0.0001; I
2
=0%). No difference in the incidence of 30-day myocardial infarction (MI), target vessel revascularization (TVR), MACE (death/MI/TVR), stroke, pre-PCI TIMI 0 flow, and post-PCI TIMI 0-2 flow was observed. Subgroup analysis including only randomized studies indicated no difference in all-cause mortality between groups (RR, 1.49; 95% CI, 0.89-2.52; p=0.13; I
2
=38%).
Conclusion:
In this study, pretreatment with oral P2Y12 inhibitors among patients with STEMI before cath lab, compared with treatment once coronary anatomy is known, was associated with decreased all-cause mortality and bleeding risk.
Ovid Technologies (Wolters Kluwer Health)
Title: Abstract 11149: Pretreatment With P2Y12 Inhibitors in ST-Elevation Myocardial Infarction & Systematic Review and Meta-Analysis
Description:
Background:
the practice of pretreatment with oral P
2
Y
12
inhibitors in ST-Elevation Myocardial Infarction (STEMI) remains common; however, its association with improved cardiovascular outcomes is unclear, since no large RCT has addressed this issue.
Hypothesis:
We aimed to evaluate the association of oral P2Y12 inhibitor pretreatment in STEMI patients with cardiovascular and bleeding outcomes.
Methods:
PubMed, MEDLINE, Embase, Cochrane, Scopus, Web of Science were systematically searched for studies that compared pretreatment with P
2
Y
12
versus no pretreatment in STEMI, and reported efficacy and safety outcomes.
A meta-analysis using a fixed and random effects model was used to calculated outcomes of interest.
Heterogeneity was assessed with I
2
statistics.
Results:
A total of 3 RCTs and 14 observational studies assigning 91,771 patients to either pretreatment (65,598 patients) or no pretreatment (26,171 patients) were included.
Follow-up ranged from 7 days to 19 months.
The P
2
Y
12
inhibitors included clopidogrel, prasugrel and ticagrelor.
At 30 days, P
2
Y
12
pretreatment was associate with lower 30-day mortality (risk ratio [RR], 0.
71; 95% CI, 0.
56-0.
91; p=0.
006; I
2
=75%), stent thrombosis (RR, 0.
33; 95% CI, 0.
12-0.
95; p=0.
04; I
2
=83%), and major bleeding (RR, 0.
81; 95% CI, 0.
74-0.
90; p<0.
0001; I
2
=0%).
No difference in the incidence of 30-day myocardial infarction (MI), target vessel revascularization (TVR), MACE (death/MI/TVR), stroke, pre-PCI TIMI 0 flow, and post-PCI TIMI 0-2 flow was observed.
Subgroup analysis including only randomized studies indicated no difference in all-cause mortality between groups (RR, 1.
49; 95% CI, 0.
89-2.
52; p=0.
13; I
2
=38%).
Conclusion:
In this study, pretreatment with oral P2Y12 inhibitors among patients with STEMI before cath lab, compared with treatment once coronary anatomy is known, was associated with decreased all-cause mortality and bleeding risk.
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