Evaluation of point-of-care activated partial thromboplastin time testing by comparison to laboratory-based assay for control of intravenous heparin.
INTRODUCTION: Patients on intravenous heparin require regular activated partial thromboplastin time monitoring. Laboratory-based activated partial thromboplastin time assays necessitate a delay between blood sampling and dose adjustment. Point-of-care testing could permit immediate dose adjustments...
Principais autores: | Douglas, A, Jefferis, J, Sharma, R, Parker, R, Handa, A, Chantler, J |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado em: |
2009
|
Registros relacionados
-
Evaluation of Antifactor-Xa Heparin Assay and Activated Partial Thromboplastin Time Values in Patients on Therapeutic Continuous Infusion Unfractionated Heparin Therapy
por: Kevin McLaughlin PharmD, BCPS, et al.
Publicado em: (2019-09-01) -
The use of activated partial thromboplastin time versus antifactor Xa assay in monitoring continuous unfractionated heparin infusion therapy in obstetric intensive care unit
por: Hany V. Zaki, et al.
Publicado em: (2019-02-01) -
PARTIAL THROMBOPLASTIN TIME CHANGES IN ASTHMA
por: A MIRALAEI, et al.
Publicado em: (2003-03-01) -
A Recurrent Neural Network Model for Predicting Activated Partial Thromboplastin Time After Treatment With Heparin: Retrospective Study
por: Sebastian Daniel Boie, et al.
Publicado em: (2022-10-01) -
An Agreement Study Between Point-of-Care and Laboratory Activated Partial Thromboplastin Time for Anticoagulation Monitoring During Extracorporeal Membrane Oxygenation
por: Yuan Teng, et al.
Publicado em: (2022-06-01)