Literature DB >> 10426845

A new regimen for heparin use in acute coronary syndromes.

J S Hochman1, A U Wali, D Gavrila, M J Sim, S Malhotra, A M Palazzo, B De La Fuente.   

Abstract

BACKGROUND: Recent trials have demonstrated an association between high activated partial thromboplastin time (aPTT) and bleeding, intracranial hemorrhage, reinfarction, and death in patients with acute coronary syndromes treated with heparin. Of all the factors that affect aPTT in patients treated with heparin, body weight is most strongly correlated.
METHODS: We compared the efficacy of 2 weight-adjusted heparin regimens (groups 2 and 3) and the standard (group 1) non-weight-adjusted 5000-U intravenous bolus/1000 U/hr infusion to achieve an aPTT between 45 and 70 seconds in a nonrandomized prospective cohort of 80 patients admitted with unstable angina and non-ST elevation myocardial infarction.
RESULTS: Patients treated with the lower dose of weight-adjusted heparin (60 U/kg intravenous bolus, maximum of 4000 U; 12 U/kg/hr, maximum 900 U/kg), group 3, were more often within the target range for aPTT at 6 hours (34% vs 5% vs 0%) and required fewer heparin infusion changes (1.0 +/- 1.0 vs 1.9 +/- 1.0 vs 2.0 +/- 0.9) within the first 24 hours compared with the other regimens. Patients in groups 1 and 2 were overwhelmingly above target range at 6 hours (95% and 84%, respectively, compared with 48% in group 3).
CONCLUSIONS: Traditional heparin dosing regimens result in marked initial overanticoagulation in patients with acute coronary syndromes, which may place these patients at higher risk of adverse outcomes. A lower dose weight-adjusted heparin regimen is superior in achieving early aPTTs within the target range and reducing the need for infusion changes over the ensuing 24 hours.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10426845     DOI: 10.1016/s0002-8703(99)70118-3

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  6 in total

1.  Heparin resistance in acute coronary syndromes.

Authors:  Jonathan D Rich; John M Maraganore; Edward Young; Rosa-Maria Lidon; Burt Adelman; Paul Bourdon; Supoat Charenkavanich; Jack Hirsh; Pierre Theroux; Christopher P Cannon
Journal:  J Thromb Thrombolysis       Date:  2007-01-13       Impact factor: 2.300

2.  New treatments in acute ischemic stroke.

Authors:  Michael J Schneck; José Biller
Journal:  Curr Treat Options Neurol       Date:  2005-11       Impact factor: 3.598

Review 3.  The determinants of activated partial thromboplastin time, relation of activated partial thromboplastin time to clinical outcomes, and optimal dosing regimens for heparin treated patients with acute coronary syndromes: a review of GUSTO-IIb.

Authors:  Michael S Lee; Andreas U Wali; Venu Menon; Scott D Berkowitz; Trevor D Thompson; Robert M Califf; Eric J Topol; Christopher B Granger; Judith S Hochman
Journal:  J Thromb Thrombolysis       Date:  2002-10       Impact factor: 2.300

4.  Intravenous heparin dosing strategy in hospitalized patients with atrial dysrhythmias.

Authors:  Robert O Roswell; Brian Greet; Sunny Shah; Samuel Bernard; Alexandra Milin; Iryna Lobach; Yu Guo; Martha J Radford; Jeffrey S Berger
Journal:  J Thromb Thrombolysis       Date:  2016-08       Impact factor: 2.300

5.  Rapid, Label-free Optical Spectroscopy Platform for Diagnosis of Heparin-Induced Thrombocytopenia.

Authors:  Zufang Huang; Soumik Siddhanta; Gang Zheng; Thomas Kickler; Ishan Barman
Journal:  Angew Chem Int Ed Engl       Date:  2020-02-19       Impact factor: 15.336

6.  An automated strategy for bedside aPTT determination and unfractionated heparin infusion adjustment in acute coronary syndromes: insights from PARAGON A.

Authors:  L Kristin Newby; Robert A Harrington; Manjushri V Bhapkar; Frans Van de Werf; Judith S Hochman; Christopher B Granger; R John Simes; Catherine G Davis; Eric J Topol; Robert M Califf; David J Moliterno
Journal:  J Thromb Thrombolysis       Date:  2002-08       Impact factor: 2.300

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.