Outcomes Associated with Time in Therapeutic Range for Patients Receiving Intravenous Unfractionated Heparin

Time in therapeutic range (TTR) with intravenous unfractionated heparin (UFH) and its association with outcomes is poorly explored. UFH can be monitored with anti-Xa or aPTT, however, evidence indicates anti-Xa monitoring of UFH improves time to therapeutic anticoagulation. The objective of this stu...

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Published inClinical and applied thrombosis/hemostasis Vol. 31; p. 10760296251371003
Main Authors Mahmud, Mujtaba, Klimatcheva, Maia, Tsang, Angela, La, Andrew, Miklus, Victoria, Becker, Jack, Herrmann, Benjamin, Cremeans, Amanda, Benedict, Neal J, Iasella, Carlo J, Smith, Roy E, Coons, James C
Format Journal Article
LanguageEnglish
Published United States SAGE Publications 01.01.2025
SAGE Publishing
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ISSN1076-0296
1938-2723
1938-2723
DOI10.1177/10760296251371003

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Abstract Time in therapeutic range (TTR) with intravenous unfractionated heparin (UFH) and its association with outcomes is poorly explored. UFH can be monitored with anti-Xa or aPTT, however, evidence indicates anti-Xa monitoring of UFH improves time to therapeutic anticoagulation. The objective of this study was to determine if TTR correlates with thrombotic and safety outcomes for patients receiving UFH, and if differences exist between these methods of monitoring. This retrospective, single center, cohort study stratified patient admissions based on the laboratory monitoring technique used (aPTT vs anti-Xa). The primary outcome was the presence of a new thrombotic event (TE) during the index visit. The secondary outcome was major bleeding during the index visit. Clinical outcomes were each assessed for their association with TTR. TTR was defined as the percentage of time in therapeutic range for each patient, as determined via the linear interpolation method. Of 4773 patient admissions (aPTT, n = 2,939, anti-Xa, n = 1834), TE occurred in 6.5% and 4.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .006). Bleeding events occurred in 33.3% and 31.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .204). TTR was 41.6% [IQR 23.3-57.7%] in the aPTT cohort compared to 56.1% [IQR 33.5-75.2%] in the anti-Xa cohort (p < .001). The monitoring of IV UFH with anti-Xa was associated with significantly fewer TEs and greater overall TTR when compared to those monitored with aPTT.
AbstractList Time in therapeutic range (TTR) with intravenous unfractionated heparin (UFH) and its association with outcomes is poorly explored. UFH can be monitored with anti-Xa or aPTT, however, evidence indicates anti-Xa monitoring of UFH improves time to therapeutic anticoagulation. The objective of this study was to determine if TTR correlates with thrombotic and safety outcomes for patients receiving UFH, and if differences exist between these methods of monitoring. This retrospective, single center, cohort study stratified patient admissions based on the laboratory monitoring technique used (aPTT vs anti-Xa). The primary outcome was the presence of a new thrombotic event (TE) during the index visit. The secondary outcome was major bleeding during the index visit. Clinical outcomes were each assessed for their association with TTR. TTR was defined as the percentage of time in therapeutic range for each patient, as determined via the linear interpolation method. Of 4773 patient admissions (aPTT, n = 2,939, anti-Xa, n = 1834), TE occurred in 6.5% and 4.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .006). Bleeding events occurred in 33.3% and 31.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .204). TTR was 41.6% [IQR 23.3-57.7%] in the aPTT cohort compared to 56.1% [IQR 33.5-75.2%] in the anti-Xa cohort (p < .001). The monitoring of IV UFH with anti-Xa was associated with significantly fewer TEs and greater overall TTR when compared to those monitored with aPTT.Time in therapeutic range (TTR) with intravenous unfractionated heparin (UFH) and its association with outcomes is poorly explored. UFH can be monitored with anti-Xa or aPTT, however, evidence indicates anti-Xa monitoring of UFH improves time to therapeutic anticoagulation. The objective of this study was to determine if TTR correlates with thrombotic and safety outcomes for patients receiving UFH, and if differences exist between these methods of monitoring. This retrospective, single center, cohort study stratified patient admissions based on the laboratory monitoring technique used (aPTT vs anti-Xa). The primary outcome was the presence of a new thrombotic event (TE) during the index visit. The secondary outcome was major bleeding during the index visit. Clinical outcomes were each assessed for their association with TTR. TTR was defined as the percentage of time in therapeutic range for each patient, as determined via the linear interpolation method. Of 4773 patient admissions (aPTT, n = 2,939, anti-Xa, n = 1834), TE occurred in 6.5% and 4.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .006). Bleeding events occurred in 33.3% and 31.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .204). TTR was 41.6% [IQR 23.3-57.7%] in the aPTT cohort compared to 56.1% [IQR 33.5-75.2%] in the anti-Xa cohort (p < .001). The monitoring of IV UFH with anti-Xa was associated with significantly fewer TEs and greater overall TTR when compared to those monitored with aPTT.
Time in therapeutic range (TTR) with intravenous unfractionated heparin (UFH) and its association with outcomes is poorly explored. UFH can be monitored with anti-Xa or aPTT, however, evidence indicates anti-Xa monitoring of UFH improves time to therapeutic anticoagulation. The objective of this study was to determine if TTR correlates with thrombotic and safety outcomes for patients receiving UFH, and if differences exist between these methods of monitoring. This retrospective, single center, cohort study stratified patient admissions based on the laboratory monitoring technique used (aPTT vs anti-Xa). The primary outcome was the presence of a new thrombotic event (TE) during the index visit. The secondary outcome was major bleeding during the index visit. Clinical outcomes were each assessed for their association with TTR. TTR was defined as the percentage of time in therapeutic range for each patient, as determined via the linear interpolation method. Of 4773 patient admissions (aPTT, n = 2,939, anti-Xa, n = 1834), TE occurred in 6.5% and 4.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .006). Bleeding events occurred in 33.3% and 31.6% of visits in the aPTT and the anti-Xa cohort, respectively (p = .204). TTR was 41.6% [IQR 23.3-57.7%] in the aPTT cohort compared to 56.1% [IQR 33.5-75.2%] in the anti-Xa cohort (p < .001). The monitoring of IV UFH with anti-Xa was associated with significantly fewer TEs and greater overall TTR when compared to those monitored with aPTT.
Author Tsang, Angela
Miklus, Victoria
Smith, Roy E
Mahmud, Mujtaba
Benedict, Neal J
Herrmann, Benjamin
Klimatcheva, Maia
La, Andrew
Cremeans, Amanda
Becker, Jack
Coons, James C
Iasella, Carlo J
AuthorAffiliation 3 Department of Pharmacy, 43159 University Health , San Antonio, TX, USA
6 Division of Classical Hematology, 25817 UPMC Presbyterian -Shadyside Hospital, Pittsburgh, PA, USA
2 Lipscomb University, College of Pharmacy, Nashville, TN, USA
4 15523 University of Pittsburgh School of Pharmacy , Pittsburgh, PA, USA
5 Department of Pharmacy, 25817 UPMC Presbyterian -Shadyside Hospital, Pittsburgh, PA, USA
1 Critical Illness, 12328 Brain Dysfunction, and Survivorship (CIBS) Center , Nashville, TN, USA
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Keywords heparin
bleeding
thrombosis
time in therapeutic range
Language English
License This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
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Snippet Time in therapeutic range (TTR) with intravenous unfractionated heparin (UFH) and its association with outcomes is poorly explored. UFH can be monitored with...
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Title Outcomes Associated with Time in Therapeutic Range for Patients Receiving Intravenous Unfractionated Heparin
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