Evaluation of Antifactor-Xa Heparin Assay and Activated Partial Thromboplastin Time Values in Patients on Therapeutic Continuous Infusion Unfractionated Heparin Therapy

Author:

McLaughlin Kevin1ORCID,Rimsans Jessica1,Sylvester Katelyn W.1,Fanikos John1,Dorfman David M.2,Senna Patricia3,Connors Jean M.4,Goldhaber Samuel Z.5

Affiliation:

1. Department of Pharmacy, Brigham and Women’s Hospital, Boston, MA, USA

2. Department of Pathology, Brigham and Women’s Hospital, Boston, MA, USA

3. Department of Clinical Laboratories, Brigham and Women’s Hospital, Boston, MA, USA

4. Hematology Division, Brigham and Women’s Hospital, Boston, MA, USA

5. Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

Abstract

Clinical uncertainty exists regarding which assay should be designated as the standard monitoring coagulation test for intravenous unfractionated heparin (UFH). Several studies have compared the use of activated partial thromboplastin time (aPTT) and antifactor-Xa (anti-Xa) and have come out with varying results. The correlation between these 2 tests varied, markedly from strong to weak. Some have demonstrated that monitoring with anti-Xa heparin assay leads to fewer dose adjustments, resulting in fewer laboratory tests, while others have not. In the current study, we evaluated the correlation between aPTT and anti-Xa values to guide clinical management of UFH, with the intention to develop a new correlation nomogram.

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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