TY - JOUR
T1 - Therapeutic monitoring of unfractionated heparin - trials and tribulations
AU - Baluwala, Israfil
AU - Favaloro, Emmanuel J
AU - Pasalic, Leonardo
N1 - Includes bibliographical references
PY - 2017/7
Y1 - 2017/7
N2 - INTRODUCTION: Heparin is one of the oldest biological medicines with an established role in prevention and treatment of arterial and venous thromboembolism. Published therapeutic ranges for unfractionated heparin (UFH) mostly precede the large increase in the number of activated partial thromboplastin time (APTT) reagent/instrument combinations that now show wide variability. Areas covered: This paper explores the use of UFH, the development of heparin therapeutic ranges (HTRs), and the strengths and limitations of the methods used to monitor heparin's anticoagulant effect. Expert commentary: Despite longstanding use of UFH for management of thromboembolic conditions, the optimal test for monitoring UFH remains undetermined. Although used extensively for monitoring UFH, routine APTT-derived HTRs are based on limited science that may have little relevance to current laboratory practice. Anti-FXa levels may provide better and more reliable HTRs; however, even these levels show considerable inter-laboratory variation, and there are insufficient clinical studies proving improved clinical efficacy. Alternative tests for monitoring UFH reported over time have not been proven effective nor feasible, secondary to technical or cost issues, or lack of general adoption. Thus, despite limited evidence of clinical utility, an uncomfortable marriage of convenience represented by heparin laboratory monitoring is unlikely to be terminated in the immediate future.
AB - INTRODUCTION: Heparin is one of the oldest biological medicines with an established role in prevention and treatment of arterial and venous thromboembolism. Published therapeutic ranges for unfractionated heparin (UFH) mostly precede the large increase in the number of activated partial thromboplastin time (APTT) reagent/instrument combinations that now show wide variability. Areas covered: This paper explores the use of UFH, the development of heparin therapeutic ranges (HTRs), and the strengths and limitations of the methods used to monitor heparin's anticoagulant effect. Expert commentary: Despite longstanding use of UFH for management of thromboembolic conditions, the optimal test for monitoring UFH remains undetermined. Although used extensively for monitoring UFH, routine APTT-derived HTRs are based on limited science that may have little relevance to current laboratory practice. Anti-FXa levels may provide better and more reliable HTRs; however, even these levels show considerable inter-laboratory variation, and there are insufficient clinical studies proving improved clinical efficacy. Alternative tests for monitoring UFH reported over time have not been proven effective nor feasible, secondary to technical or cost issues, or lack of general adoption. Thus, despite limited evidence of clinical utility, an uncomfortable marriage of convenience represented by heparin laboratory monitoring is unlikely to be terminated in the immediate future.
KW - Anticoagulants/chemistry
KW - Clinical Trials as Topic
KW - Drug Monitoring
KW - Factor Xa Inhibitors/therapeutic use
KW - Heparin/chemistry
KW - Heparin, Low-Molecular-Weight/chemistry
KW - Humans
KW - Partial Thromboplastin Time
KW - Thromboembolism/blood
KW - Treatment Outcome
KW - Venous Thromboembolism/blood
KW - Unfractionated heparin
KW - low molecular weight heparin
KW - therapeutic range
KW - APTT
KW - anti-FXa assay
U2 - 10.1080/17474086.2017.1345306
DO - 10.1080/17474086.2017.1345306
M3 - Review article
C2 - 28632418
SN - 1747-4094
VL - 10
SP - 595
EP - 605
JO - Expert Review of Hematology
JF - Expert Review of Hematology
IS - 7
ER -