Key result
Intralesional GPIs increase odds of TIMI 3 flow ~138% vs intracoronary delivery during ACS PCI.
Why the study?
Limited data exist comparing intracoronary versus intralesional glycoprotein IIb/IIIa inhibitor delivery during PCI for acute coronary syndromes.
Does intralesional administration of glycoprotein IIb/IIIa inhibitors improve postprocedural angiographic outcomes compared to intracoronary administration in patients with acute coronary syndromes undergoing PCI?
Meta-Analysis (n=995)
Does intralesional administration of glycoprotein IIb/IIIa inhibitors improve postprocedural angiographic outcomes compared to intracoronary administration in patients with acute coronary syndromes undergoing PCI?
Effect estimate: OR 2.38 (95% CI 1.52-3.72)
p-value: p=0.0001
Intralesional administration of glycoprotein IIb/IIIa inhibitors during PCI for ACS improves postprocedural TIMI grade 3 flow compared to intracoronary administration, but does not significantly improve hard clinical outcomes.
Intralesional GPI shows no advantage over intracoronary in ACS PCI; leaves open the preferred local delivery method.
BACKGROUND: Intracoronary glycoprotein IIb/IIIa inhibitors (GPIs) after percutaneous coronary intervention (PCI) have shown better outcomes than intravenous administration. However, limited data exist comparing intracoronary versus intralesional GPI delivery during PCI for acute coronary syndromes (ACS). METHODS: PubMed, Embase, and the Cochrane Library were searched for randomized controlled trials comparing intralesional and intracoronary GPI administration in ACS patients undergoing PCI. Odds ratios (ORs) and mean differences were used to combine dichotomous and continuous outcomes, respectively, using a random-effects model. Analyses were conducted in RevMan 5.4 and CRAN-R. RESULTS: Nine randomized controlled trials comparing the intralesional (n = 509) with intracoronary route (n = 486) were included. In the primary analysis, the intralesional route demonstrated significantly better postprocedural thrombolysis in myocardial infarction (TIMI) grade 3 flow [OR = 2.38, 95% confidence interval (CI) = 1.52-3.72, P = 0.0001], corrected TIMI frame count (mean difference = -4.63, 95% CI = -8.83 to -0.43, P = 0.03), myocardial blush grade 3 (OR = 2.60, 95% CI = 1.51-4.49, P = 0.0006), and complete ST-segment resolution (OR = 1.64, 95% CI = 1.16-2.33, P = 0.005). After Hartung-Knapp restricted maximum likelihood adjustment, only TIMI grade 3 flow remained significant (OR = 2.38, 95% CI = 1.36-4.15, P = 0.009). No significant differences were observed in major adverse cardiovascular events, bleeding, or thrombocytopenia (P > 0.05). CONCLUSION: During PCI for ACS, intralesional GPI administration improves postprocedural TIMI grade 3 flow, with no significant differences in corrected TIMI frame count, complete ST-segment resolution, or hard clinical outcomes.
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Basit et al. (2026) conducted a meta-analysis in Acute coronary syndromes (n=995). Intralesional glycoprotein IIb/IIIa inhibitors vs. Intracoronary glycoprotein IIb/IIIa inhibitors was evaluated on Postprocedural thrombolysis in myocardial infarction (TIMI) grade 3 flow (OR 2.38, 95% CI 1.52-3.72, p=0.0001). Intralesional glycoprotein IIb/IIIa inhibitors during PCI for ACS improved postprocedural TIMI grade 3 flow compared to intracoronary delivery (OR 2.38; 95% CI 1.36-4.15; P=0.009).
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