An activated clotting time >196 seconds at 2 hours after PCI predicted access-site bleeding or hematoma (AUC 0.72; 95% CI 0.56-0.85; P=0.008) in patients with chronic coronary syndromes.
Observational (n=40)
Do platelet reactivity and activated clotting time predict hemorrhagic site complications in patients with chronic coronary syndromes undergoing percutaneous coronary interventions?
Point-of-care testing of ACT and platelet reactivity after PCI can help identify patients at higher risk of access-site bleeding.
Effect estimate: AUC 0.72 (95% CI 0.56-0.85)
p-value: p=0.008
BACKGROUND: Radial access is preferred in patients with chronic coronary syndromes (CCSs) treated with ad hoc percutaneous coronary intervention (PCI). Antithrombotic and antiplatelet treatment before PCI may affect outcomes at vascular access sites. QuikClot Radial is a kaolin-based band that may shorten hemostasis time. Using point-of-care testing, we investigated the effect of antithrombotic and antiplatelet treatment on access-site complications. METHODS: This prospective observational study included consecutive patients with CCS on chronic aspirin therapy referred for ad hoc PCI. The activated clotting time (ACT), global thrombosis test and VerifyNow P2Y 12 test were done sequentially after unfractionated heparin (UFH) and clopidogrel administration. Patients were monitored for radial artery patency, bleeding and local hematoma until discharge. RESULTS: We enrolled 40 patients mean age, 68.8 ± 8.8 years; men, 30 (75%) who received UFH (median dose, 8000 IU; interquartile range, 7000-9000 IU) and clopidogrel (600 mg). All radial arteries remained patent during follow-up. Local bleeding and hematomas were noted in 11 patients (27.5%) each. Patients with bleeding had lower mean platelet activity at 2 h 122.5 ± 51 platelet reactivity units (PRU) vs. 158.7 ± 43 PRU, P = 0.04 and higher ACT (216.9 ± 40 s vs. 184.6 ± 28 s, P = 0.006) than patients without bleeding. An ACT >196 s at 2 h predicted bleeding or hematoma (AUC, 0.72; 95% CI, 0.56-0.85, P = 0.008). CONCLUSION: Lower platelet activity and higher ACT after PCI were associated with higher bleeding risk at a vascular access site. Point-of-care testing of ACT after the procedure may help identify patients with CCS undergoing PCI who are at higher risk of access-site bleeding.
Ramotowski et al. (Fri,) conducted a observational in chronic coronary syndromes (n=40). Activated clotting time and platelet reactivity vs. Lower activated clotting time and higher platelet reactivity was evaluated on Bleeding or hematoma (AUC 0.72, 95% CI 0.56-0.85, p=0.008). An activated clotting time >196 seconds at 2 hours after PCI predicted access-site bleeding or hematoma (AUC 0.72; 95% CI 0.56-0.85; P=0.008) in patients with chronic coronary syndromes.