PMID- 22323092 OWN - NLM STAT- MEDLINE DCOM- 20121031 LR - 20211021 IS - 1573-742X (Electronic) IS - 0929-5305 (Linking) VI - 34 IP - 1 DP - 2012 Jul TI - Activated partial thromboplastin time measurement is not associated with clinical outcomes in patients with high-risk non-ST-segment elevation acute coronary syndromes treated with unfractionated heparin. PG - 114-9 LID - 10.1007/s11239-012-0693-y [doi] AB - Our objective was to determine the association of activated partial thromboplastin time (aPTT) with recurrent ischemic events and non-coronary artery bypass surgery-related thrombolysis in myocardial infarction major bleeding. We studied 4,985 patients with high-risk non-ST-segment elevation acute coronary syndromes (NSTE ACS) participating in SYNERGY, a prospective, randomized, international trial designed to emulate contemporary practice wherein unfractionated heparin (UFH) is given intravenously and titrated according to a weight-adjusted dosing nomogram to a target aPTT of 1.5-2 times the upper limit of normal (approximately 50-70 s). Aspirin was administered to 95% of patients, clopidogrel to 63%, and glycoprotein IIb/IIIa receptor inhibitors to 58%. More than 90% of patients underwent early coronary angiography, and 69% were revascularized. Used as a time-dependent covariate, aPTT was evaluated as a predictor of time to ischemic or major hemorrhagic events in proportional hazards regression models. Using discrete variable analysis, aPTT was categorized as persistently below a lower threshold of anticoagulation (<50 vs. >/=50 s) for recurrent ischemic events and above an upper threshold (>70 vs. 6-12 (n = 3,021), >12-24 (n = 3,406), and >24-48 (n = 2,497) h, 34, 41, and 46% of patients achieved the target aPTT range, respectively. Both before and after adjusting for baseline predictors of anticoagulant response and risk score (age, hypertension, diabetes, smoking, ST depression, and renal function), no significant relationship between aPTT values and recurrent ischemic events or major bleeding was found. No relationship was observed between clinical outcomes and aPTT values persistently above or below the designated thresholds. Measurements of aPTT were not associated with clinical outcomes among patients with NSTE ACS treated with UFH. The required intensity of anticoagulation for benefit may be relatively modest when UFH is administered concomitantly with dual or triple platelet-directed therapy, particularly in patients undergoing early coronary revascularization. FAU - Thomas, Michael P AU - Thomas MP AD - Duke Clinical Research Institute, 2400 Pratt Street, Durham, NC 27705, USA. michptho@med.umich.edu FAU - Mahaffey, Kenneth W AU - Mahaffey KW FAU - Chiswell, Karen AU - Chiswell K FAU - Cohen, Marc AU - Cohen M FAU - Kontos, Michael C AU - Kontos MC FAU - Antman, Elliott M AU - Antman EM FAU - Ferguson, James J AU - Ferguson JJ FAU - Califf, Robert M AU - Califf RM FAU - Goodman, Shaun G AU - Goodman SG FAU - Becker, Richard C AU - Becker RC LA - eng PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - Netherlands TA - J Thromb Thrombolysis JT - Journal of thrombosis and thrombolysis JID - 9502018 RN - 0 (Fibrinolytic Agents) RN - 0 (Platelet Aggregation Inhibitors) RN - 9005-49-6 (Heparin) SB - IM MH - Acute Coronary Syndrome/*blood/complications/therapy MH - Aged MH - Aged, 80 and over MH - Angioplasty, Balloon, Coronary MH - Female MH - Fibrinolytic Agents/administration & dosage MH - Hemorrhage/blood/drug therapy/etiology MH - Heparin/administration & dosage MH - Humans MH - Male MH - Middle Aged MH - *Partial Thromboplastin Time MH - Platelet Aggregation Inhibitors/administration & dosage MH - Predictive Value of Tests MH - Proportional Hazards Models MH - Prospective Studies MH - Risk Factors EDAT- 2012/02/11 06:00 MHDA- 2012/11/01 06:00 CRDT- 2012/02/11 06:00 PHST- 2012/02/11 06:00 [entrez] PHST- 2012/02/11 06:00 [pubmed] PHST- 2012/11/01 06:00 [medline] AID - 10.1007/s11239-012-0693-y [doi] PST - ppublish SO - J Thromb Thrombolysis. 2012 Jul;34(1):114-9. doi: 10.1007/s11239-012-0693-y.