PMID- 10510988 OWN - NLM STAT- MEDLINE DCOM- 19991019 LR - 20190812 IS - 0003-9926 (Print) IS - 0003-9926 (Linking) VI - 159 IP - 17 DP - 1999 Sep 27 TI - Recurrent venous thrombosis and heparin therapy: an evaluation of the importance of early activated partial thromboplastin times. PG - 2029-32 AB - BACKGROUND: The presence of an association between early subtherapeutic activated partial thromboplastin times (aPTTs) and recurrent venous thromboembolism (VTE) remains controversial. OBJECTIVE: To determine the relation between early subtherapeutic aPTTs and recurrent VTE in patients who were treated with intravenous (i.v.) unfractionated heparin (UFH). PATIENTS AND METHODS: We studied 961 patients with acute VTE who received i.v. UFH in 3 randomized trials that compared the use of i.v. UFH (loading dose: 5000 U i.v.; initial infusion, 1250-1280 U/h) with that of subcutaneous low-molecular-weight heparin. According to aPTT criteria, patients were classified as being in a subtherapeutic or a therapeutic state during the first 24 and 48 hours of treatment. All episodes of possible recurrent VTE were adjudicated by an independent committee that was unaware of the aPTTs. RESULTS: At 24 hours, in 886 patients who were eligible for the analysis, the rate of recurrent VTE in the subtherapeutic group was 6.7% (11/163) compared with 5.3% (38/723) in the therapeutic group. The odds ratio for recurrence in patients in the subtherapeutic vs the therapeutic group at 24 hours was 1.30 (95% confidence interval: 0.64-2.63; P = .46). At 48 hours, in 917 patients who were eligible for the analysis, the rate of recurrent VTE in the subtherapeutic group was 7.8% (5/64) compared with 5.7% (49/853) in the therapeutic group. The odds ratio for recurrence in patients in the subtherapeutic vs the therapeutic group at 48 hours was 1.32 (95% confidence interval: 0.51-3.44; P = .56). CONCLUSION: In patients with acute VTE who receive an i.v. bolus of 5000 U, followed by a starting dose of at least 1250 U/h of UFH, a subtherapeutic aPTT response during the first 48 hours of treatment is not associated with a large increase in the risk of recurrent VTE. FAU - Anand, S S AU - Anand SS AD - Department of Medicine, McMaster University, Hamilton, Ontario, Canada. anands@fhs.mcmaster.ca FAU - Bates, S AU - Bates S FAU - Ginsberg, J S AU - Ginsberg JS FAU - Levine, M AU - Levine M FAU - Buller, H AU - Buller H FAU - Prins, M AU - Prins M FAU - Haley, S AU - Haley S FAU - Kearon, C AU - Kearon C FAU - Hirsh, J AU - Hirsh J FAU - Gent, M AU - Gent M LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Arch Intern Med JT - Archives of internal medicine JID - 0372440 RN - 0 (Anticoagulants) RN - 9005-49-6 (Heparin) SB - IM MH - Aged MH - Anticoagulants/administration & dosage/*therapeutic use MH - Drug Administration Schedule MH - Female MH - Heparin/administration & dosage/*therapeutic use MH - Humans MH - Infusions, Intravenous MH - Injections, Intravenous MH - Male MH - Middle Aged MH - Odds Ratio MH - *Partial Thromboplastin Time MH - Randomized Controlled Trials as Topic MH - Recurrence MH - Time Factors MH - Treatment Outcome MH - Venous Thrombosis/blood/*drug therapy/*prevention & control EDAT- 1999/10/08 00:00 MHDA- 1999/10/08 00:01 CRDT- 1999/10/08 00:00 PHST- 1999/10/08 00:00 [pubmed] PHST- 1999/10/08 00:01 [medline] PHST- 1999/10/08 00:00 [entrez] AID - 10.1001/archinte.159.17.2029 [doi] PST - ppublish SO - Arch Intern Med. 1999 Sep 27;159(17):2029-32. doi: 10.1001/archinte.159.17.2029.