PMID- 23306859 OWN - NLM STAT- MEDLINE DCOM- 20130918 LR - 20181202 IS - 2567-689X (Electronic) IS - 0340-6245 (Linking) VI - 109 IP - 3 DP - 2013 Mar TI - Hirudin anticoagulation allows more rapid determination of P2Y(1)(2) inhibition by the VerifyNow P2Y12 assay. PG - 550-5 LID - 10.1160/TH12-10-0718 [doi] AB - VerifyNow (VN) P2Y12 is a point-of-care assay used to assess response to P2Y12 inhibitors. Sodium citrate (citrate) is the standard anticoagulant used for this assay but requires a pre-incubation period. Hirudin is an alternative anticoagulant for platelet function studies that maintains physiological divalent cation levels. We investigated whether hirudin anticoagulation might allow more rapid testing of P2Y(1)(2) inhibition at the time of percutaneous coronary intervention (PCI). Blood was collected from the arterial sheath of aspirin-treated patients undergoing elective, urgent or emergency coronary angiography+/-PCI and aliquots were anticoagulated with either citrate or hirudin. For each anticoagulant, VN P2Y12 was performed both immediately and after 20 minutes. A total of 98 patients were included in this study following pre-treatment with clopidogrel (n=88), prasugrel (n=6) or no P2Y(1)(2) inhibitor (n=4). PRU with hirudin immediately (PRU_H_Imm) and PRU with citrate 20 minutes post sampling (PRU_C_20) were very strongly correlated (R=0.95) though PRU_H_Imm tended to be lower than PRU_C_20 so that optimal correlation was estimated by the equation PRU_H_Imm=0.95xPRU_C_20 (p<0.001). Bland-Altman plots showed good agreement between PRU_H_Imm and (0.95xPRU_C_20). Platelet reactivity was more stable over the studied time course with hirudin as compared to citrate. We therefore conclude that VN P2Y12 with hirudin anticoagulation can be performed more rapidly and results are strongly correlated with delayed citrate measurements. Further studies are warranted to assess the utility of this method for improving clinical outcomes in patients undergoing PCI. FAU - Sumaya, Wael AU - Sumaya W AD - Department of Cardiovascular Science, University of Sheffield, Centre for Biomedical Research, Northern General Hospital, Herries Road, Sheffield, S5 7AU, UK. w.sumaya@sheffield.ac.uk FAU - Daly, Rebecca L AU - Daly RL FAU - Mehra, Sonal AU - Mehra S FAU - Dhutia, Amrita J AU - Dhutia AJ FAU - Howgego, Kate E AU - Howgego KE FAU - Ecob, Rosemary AU - Ecob R FAU - Judge, Heather M AU - Judge HM FAU - Morton, Allison C AU - Morton AC FAU - Storey, Robert F AU - Storey RF LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130110 PL - Germany TA - Thromb Haemost JT - Thrombosis and haemostasis JID - 7608063 RN - 0 (Anticoagulants) RN - 0 (Antithrombins) RN - 0 (Cations) RN - 0 (Citrates) RN - 0 (Hirudins) RN - 0 (P2RY12 protein, human) RN - 0 (Piperazines) RN - 0 (Receptors, Purinergic P2Y12) RN - 0 (Thiophenes) RN - 1Q73Q2JULR (Sodium Citrate) RN - A74586SNO7 (Clopidogrel) RN - G89JQ59I13 (Prasugrel Hydrochloride) RN - OM90ZUW7M1 (Ticlopidine) SB - IM MH - Acute Coronary Syndrome/blood MH - Aged MH - Anticoagulants/*pharmacology MH - Antithrombins/pharmacology MH - Area Under Curve MH - Cations MH - Citrates/*pharmacology MH - Clopidogrel MH - Coronary Angiography/methods MH - Female MH - Hematologic Tests/*methods MH - Hirudins/*pharmacology MH - Humans MH - Male MH - Middle Aged MH - Myocardial Infarction/blood MH - Piperazines/pharmacology MH - Platelet Function Tests/methods MH - Prasugrel Hydrochloride MH - Receptors, Purinergic P2Y12/analysis/*metabolism MH - Sodium Citrate MH - Thiophenes/pharmacology MH - Ticlopidine/analogs & derivatives/pharmacology MH - Treatment Outcome EDAT- 2013/01/12 06:00 MHDA- 2013/09/21 06:00 CRDT- 2013/01/12 06:00 PHST- 2012/10/02 00:00 [received] PHST- 2012/12/07 00:00 [accepted] PHST- 2013/01/12 06:00 [entrez] PHST- 2013/01/12 06:00 [pubmed] PHST- 2013/09/21 06:00 [medline] AID - 12-10-0718 [pii] AID - 10.1160/TH12-10-0718 [doi] PST - ppublish SO - Thromb Haemost. 2013 Mar;109(3):550-5. doi: 10.1160/TH12-10-0718. Epub 2013 Jan 10.