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15 July 1993 | Volume 119 Issue 2 | Pages 104-109
Objective: To compare two methods of determining a therapeutic range of activated partial thromboplastin time (aPT) results.
Design: Cohort studies.
Setting: Referral teaching hospital.
Patients: Inpatients who received unfractionated heparin intravenously for venous thromboembolic disease.
Measurements: A therapeutic range determined by aPT ratios of 1.5 to 2.5 times the control value as compared with a therapeutic range determined by protamine titration heparin levels of 0.2 to 0.4 U/mL.
Results: For all aPT reagents studied, a ratio of 1.5 times the control value is much less than a minimum protamine titration heparin level of 0.2 U/mL. Various manufacturers' aPT reagents and reagent lots from the same manufacturer show considerable variation in response to heparin and therefore have different therapeutic ranges.
Conclusions: A different dose of heparin would be required to produce an aPT ratio of 1.5 times the control value, depending on the reagent used. Establishing a therapeutic range for aPT results using protamine titration heparin levels of 0.2 to 0.4 U/mL as a reference standard is practical and compensates for the variable response of aPT reagents to heparin.
Author and Article Information
From McMaster University Medical Center and Hamilton Civic Hospitals Research Centre, Hamilton, Ontario, Canada.
ARTICLE
Establishing a Therapeutic Range for Heparin Therapy
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Requests for Reprints: Dr. P. Brill-Edwards, MD, McMaster University Medical Center, 1200 Main Street West, HSC-3W12, Hamilton, Ontario L8N 3Z5, Canada.
Acknowledgments: The authors thank Dianne Donovan, RN, Robin Roberts, PhD, and David Sackett, MD, for their contributions to and support of this study.
Grant Support: Dr. Ginsberg is the recipient of a Research Scholarship of the Heart and Stroke Foundation of Canada. Dr. Hirsh is a Distinguished Research Professor of the Heart and Stroke Foundation of Canada and a Trillium Award Recipient of the Ministry of Health.
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