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Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study

BACKGROUND: Thrombotic events are common in critically ill patients with COVID-19 and have been linked with COVID-19- induced hyperinflammatory state. In addition to anticoagulant effects, heparin and its derivatives have various anti-inflammatory and immunomodulatory properties that may affect pati...

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Autores principales: Al Sulaiman, Khalid, Aljuhani, Ohoud, Korayem, Ghazwa B., Hafiz, Awatif, Alalawi, Mai, Badreldin, Hisham A., Altebainawi, Ali F., Vishwakarma, Ramesh, Alissa, Abdulrahman, Alghamdi, Albandari, Alenazi, Abeer A., Al Enazi, Huda, Alanazi, Shahad, Alhammad, Abdullah, Alghamdi, Jahad, AlFaifi, Mashael, Al Sehli, Faisal A., Aldossari, Maram A., Alhubaishi, Alaa A., Al-Ali, Anfal Y., Al-Dorzi, Hasan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733230/
https://www.ncbi.nlm.nih.gov/pubmed/36482388
http://dx.doi.org/10.1186/s12959-022-00432-9
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author Al Sulaiman, Khalid
Aljuhani, Ohoud
Korayem, Ghazwa B.
Hafiz, Awatif
Alalawi, Mai
Badreldin, Hisham A.
Altebainawi, Ali F.
Vishwakarma, Ramesh
Alissa, Abdulrahman
Alghamdi, Albandari
Alenazi, Abeer A.
Al Enazi, Huda
Alanazi, Shahad
Alhammad, Abdullah
Alghamdi, Jahad
AlFaifi, Mashael
Al Sehli, Faisal A.
Aldossari, Maram A.
Alhubaishi, Alaa A.
Al-Ali, Anfal Y.
Al-Dorzi, Hasan M.
author_facet Al Sulaiman, Khalid
Aljuhani, Ohoud
Korayem, Ghazwa B.
Hafiz, Awatif
Alalawi, Mai
Badreldin, Hisham A.
Altebainawi, Ali F.
Vishwakarma, Ramesh
Alissa, Abdulrahman
Alghamdi, Albandari
Alenazi, Abeer A.
Al Enazi, Huda
Alanazi, Shahad
Alhammad, Abdullah
Alghamdi, Jahad
AlFaifi, Mashael
Al Sehli, Faisal A.
Aldossari, Maram A.
Alhubaishi, Alaa A.
Al-Ali, Anfal Y.
Al-Dorzi, Hasan M.
author_sort Al Sulaiman, Khalid
collection PubMed
description BACKGROUND: Thrombotic events are common in critically ill patients with COVID-19 and have been linked with COVID-19- induced hyperinflammatory state. In addition to anticoagulant effects, heparin and its derivatives have various anti-inflammatory and immunomodulatory properties that may affect patient outcomes. This study compared the effectiveness and safety of prophylactic standard-doses of enoxaparin and unfractionated heparin (UFH) in critically ill patients with COVID-19.  METHODS: A multicenter, retrospective cohort study included critically ill adult patients with COVID-19 admitted to the ICU between March 2020 and July 2021. Patients were categorized into two groups based on the type of pharmacological VTE thromboprophylaxis given in fixed doses (Enoxaparin 40 mg SQ every 24 hours versus UFH 5000 Units SQ every 8 hours) throughout their ICU stay. The primary endpoint was all cases of thrombosis. Other endpoints were considered secondary. Propensity score (PS) matching was used to match patients (1:1 ratio) between the two groups based on the predefined criteria. Multivariable logistic, Cox proportional hazards, and negative binomial regression analysis were used as appropriate.  RESULTS: A total of 306 patients were eligible based on the eligibility criteria; 130 patients were included after PS matching (1:1 ratio). Patients who received UFH compared to enoxaparin had higher all thrombosis events at crude analysis (18.3% vs. 4.6%; p-value = 0.02 as well in logistic regression analysis (OR: 4.10 (1.05, 15.93); p-value = 0.04). Although there were no significant differences in all bleeding cases and major bleeding between the two groups (OR: 0.40 (0.07, 2.29); p-value = 0.31 and OR: 1.10 (0.14, 8.56); p-value = 0.93, respectively); however, blood transfusion requirement was higher in the UFH group but did not reach statistical significance (OR: 2.98 (0.85, 10.39); p-value = 0.09). The 30-day and in-hospital mortality were similar between the two groups at Cox hazards regression analysis. In contrast, hospital LOS was longer in the UFH group; however, it did not reach the statistically significant difference (beta coefficient: 0.22; 95% CI: -0.03, 0.48; p-value = 0.09). CONCLUSION: Prophylactic enoxaparin use in critically ill patients with COVID-19 may significantly reduce all thrombosis cases with similar bleeding risk compared to UFH.
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spelling pubmed-97332302022-12-10 Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study Al Sulaiman, Khalid Aljuhani, Ohoud Korayem, Ghazwa B. Hafiz, Awatif Alalawi, Mai Badreldin, Hisham A. Altebainawi, Ali F. Vishwakarma, Ramesh Alissa, Abdulrahman Alghamdi, Albandari Alenazi, Abeer A. Al Enazi, Huda Alanazi, Shahad Alhammad, Abdullah Alghamdi, Jahad AlFaifi, Mashael Al Sehli, Faisal A. Aldossari, Maram A. Alhubaishi, Alaa A. Al-Ali, Anfal Y. Al-Dorzi, Hasan M. Thromb J Research BACKGROUND: Thrombotic events are common in critically ill patients with COVID-19 and have been linked with COVID-19- induced hyperinflammatory state. In addition to anticoagulant effects, heparin and its derivatives have various anti-inflammatory and immunomodulatory properties that may affect patient outcomes. This study compared the effectiveness and safety of prophylactic standard-doses of enoxaparin and unfractionated heparin (UFH) in critically ill patients with COVID-19.  METHODS: A multicenter, retrospective cohort study included critically ill adult patients with COVID-19 admitted to the ICU between March 2020 and July 2021. Patients were categorized into two groups based on the type of pharmacological VTE thromboprophylaxis given in fixed doses (Enoxaparin 40 mg SQ every 24 hours versus UFH 5000 Units SQ every 8 hours) throughout their ICU stay. The primary endpoint was all cases of thrombosis. Other endpoints were considered secondary. Propensity score (PS) matching was used to match patients (1:1 ratio) between the two groups based on the predefined criteria. Multivariable logistic, Cox proportional hazards, and negative binomial regression analysis were used as appropriate.  RESULTS: A total of 306 patients were eligible based on the eligibility criteria; 130 patients were included after PS matching (1:1 ratio). Patients who received UFH compared to enoxaparin had higher all thrombosis events at crude analysis (18.3% vs. 4.6%; p-value = 0.02 as well in logistic regression analysis (OR: 4.10 (1.05, 15.93); p-value = 0.04). Although there were no significant differences in all bleeding cases and major bleeding between the two groups (OR: 0.40 (0.07, 2.29); p-value = 0.31 and OR: 1.10 (0.14, 8.56); p-value = 0.93, respectively); however, blood transfusion requirement was higher in the UFH group but did not reach statistical significance (OR: 2.98 (0.85, 10.39); p-value = 0.09). The 30-day and in-hospital mortality were similar between the two groups at Cox hazards regression analysis. In contrast, hospital LOS was longer in the UFH group; however, it did not reach the statistically significant difference (beta coefficient: 0.22; 95% CI: -0.03, 0.48; p-value = 0.09). CONCLUSION: Prophylactic enoxaparin use in critically ill patients with COVID-19 may significantly reduce all thrombosis cases with similar bleeding risk compared to UFH. BioMed Central 2022-12-08 /pmc/articles/PMC9733230/ /pubmed/36482388 http://dx.doi.org/10.1186/s12959-022-00432-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Al Sulaiman, Khalid
Aljuhani, Ohoud
Korayem, Ghazwa B.
Hafiz, Awatif
Alalawi, Mai
Badreldin, Hisham A.
Altebainawi, Ali F.
Vishwakarma, Ramesh
Alissa, Abdulrahman
Alghamdi, Albandari
Alenazi, Abeer A.
Al Enazi, Huda
Alanazi, Shahad
Alhammad, Abdullah
Alghamdi, Jahad
AlFaifi, Mashael
Al Sehli, Faisal A.
Aldossari, Maram A.
Alhubaishi, Alaa A.
Al-Ali, Anfal Y.
Al-Dorzi, Hasan M.
Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study
title Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study
title_full Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study
title_fullStr Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study
title_full_unstemmed Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study
title_short Standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with COVID-19: a multicenter propensity-score matched study
title_sort standard dosing of enoxaparin versus unfractionated heparin in critically ill patient with covid-19: a multicenter propensity-score matched study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733230/
https://www.ncbi.nlm.nih.gov/pubmed/36482388
http://dx.doi.org/10.1186/s12959-022-00432-9
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