PMID- 12575965 OWN - NLM STAT- MEDLINE DCOM- 20030225 LR - 20191210 IS - 0735-1097 (Print) IS - 0735-1097 (Linking) VI - 41 IP - 3 DP - 2003 Feb 5 TI - The activated clotting time can be used to monitor the low molecular weight heparin dalteparin after intravenous administration. PG - 394-402 AB - OBJECTIVES: This study was designed to compare the dose response of dalteparin versus unfractionated heparin (UFH) on the activated clotting time (ACT), and to determine whether the ACT can be used to monitor intravenous (IV) dalteparin during percutaneous coronary intervention (PCI). BACKGROUND: The use of low molecular weight heparin (LMWH) during PCI has been limited by the presumed inability to monitor its anticoagulant effect using bedside assays. METHODS: This study was performed in three phases. In vitro, ACTs were measured on volunteer (n = 10) blood samples spiked with increasing concentrations of dalteparin or UFH. To extend these observations in vivo, ACTs were then measured in patients (n = 15) who were sequentially treated with IV dalteparin and then UFH. Finally, a larger monitoring study was undertaken involving patients (n = 110) who received dalteparin 60 or 80 international U (IU)/kg alone or followed by abciximab. We measured ACT (Hemochron), activated partial thromboplastin time (aPTT), plasma anti-Xa and anti-IIa levels, tissue factor pathway inhibitor (TFPI) concentration, and plasma dalteparin concentration. RESULTS: Dalteparin induced a significant rise in the ACT with a smaller degree of variance as compared to UFH. Five min after administration of IV dalteparin 80 IU/kg the ACT increased from 125 s (122 s, 129 s) to 184 s (176 s, 191 s) (p < 0.001). The aPTT, anti-Xa and anti-IIa activities, and TFPI concentration also demonstrated significant increases following IV dalteparin. CONCLUSIONS: The ACT and aPTT are sensitive to IV dalteparin at clinically relevant doses. These data suggest that the ACT may be useful in monitoring the anticoagulant effect of intravenously administered dalteparin during PCI. FAU - Marmur, Jonathan D AU - Marmur JD AD - Department of Medicine, Division of Cardiology, SUNY Health Science Center at Brooklyn, 450 Clarkson Avenue, Box 1257, Brooklyn, NY 11203, USA. jonathan@marmur.com FAU - Anand, Sunil X AU - Anand SX FAU - Bagga, Ramanjit S AU - Bagga RS FAU - Fareed, Jawed AU - Fareed J FAU - Pan, Chi-Miau AU - Pan CM FAU - Sharma, Samin K AU - Sharma SK FAU - Richard, Merwin F AU - Richard MF LA - eng PT - Comparative Study PT - Evaluation Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Am Coll Cardiol JT - Journal of the American College of Cardiology JID - 8301365 RN - 0 (Anticoagulants) RN - 9005-49-6 (Heparin) RN - S79O08V79F (Dalteparin) SB - IM MH - Aged MH - *Angioplasty, Balloon, Coronary MH - Anticoagulants/*administration & dosage/*therapeutic use MH - Coronary Disease/*therapy MH - Dalteparin/*administration & dosage/*therapeutic use MH - Dose-Response Relationship, Drug MH - Female MH - Heparin/*administration & dosage/*therapeutic use MH - Humans MH - Infusions, Intravenous MH - Male MH - Middle Aged MH - Monitoring, Intraoperative/*methods MH - Partial Thromboplastin Time MH - *Whole Blood Coagulation Time EDAT- 2003/02/11 04:00 MHDA- 2003/02/26 04:00 CRDT- 2003/02/11 04:00 PHST- 2003/02/11 04:00 [pubmed] PHST- 2003/02/26 04:00 [medline] PHST- 2003/02/11 04:00 [entrez] AID - S0735109702027626 [pii] AID - 10.1016/s0735-1097(02)02762-6 [doi] PST - ppublish SO - J Am Coll Cardiol. 2003 Feb 5;41(3):394-402. doi: 10.1016/s0735-1097(02)02762-6.