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Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients

Heparin-induced thrombocytopenia (HIT) is a disorder originating from exposure to heparin and has a spectrum of presentation ranging from asymptomatic positive antibodies to thrombotic complications. When symptomatic, it is associated with morbidity and mortality. The incidence of HIT in the ESRD po...

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Autores principales: Hamadi, Rachelle, Sakr, Fouad, Aridi, Hussam, Alameddine, Zakaria, Dimachkie, Reem, Assaad, Marc, Asmar, Samer, ElSayegh, Suzanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233607/
https://www.ncbi.nlm.nih.gov/pubmed/37253454
http://dx.doi.org/10.1177/10760296231177993
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author Hamadi, Rachelle
Sakr, Fouad
Aridi, Hussam
Alameddine, Zakaria
Dimachkie, Reem
Assaad, Marc
Asmar, Samer
ElSayegh, Suzanne
author_facet Hamadi, Rachelle
Sakr, Fouad
Aridi, Hussam
Alameddine, Zakaria
Dimachkie, Reem
Assaad, Marc
Asmar, Samer
ElSayegh, Suzanne
author_sort Hamadi, Rachelle
collection PubMed
description Heparin-induced thrombocytopenia (HIT) is a disorder originating from exposure to heparin and has a spectrum of presentation ranging from asymptomatic positive antibodies to thrombotic complications. When symptomatic, it is associated with morbidity and mortality. The incidence of HIT in the ESRD population is yet to be defined. End-stage renal disease (ESRD) patients are at particular risk due to constant exposure to heparin. The main treatment of HIT is to avoid heparin and pursue alternative anticoagulants. Since 1 of the main advantages of heparin in ESRD patients is the ease of its use due to non-renal clearance, the use of alternative anticoagulants poses yet another challenge for this population due to cost, availability, and adverse effects on ESRD patients. Argatroban seems like the best alternative to heparin in hemodialysis (HD) patients due to its liver clearance. Despite having limited studies in HIT, direct oral anticoagulants (DOACs) were added as a potential treatment for HIT, with apixaban favored in kidney dysfunction as it is the least dependent on kidney clearance. Other treatment modalities exist but are still being studied in ESRD patients. The presence of HIT antibodies is not always associated with clinical syndrome, and some studies suggested that heparin antibodies are transient, and the reintroduction of heparin is still being evaluated as a treatment option. Hence, HIT is a challenging diagnosis in ESRD patients, a population that has frequent exposure to anticoagulants, and a risk/benefit ratio should be weighed between the risk of progression to symptomatic HIT and the benefit of switching to a non-heparin anticoagulant bearing in mind the difficulties associated with the latter.
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spelling pubmed-102336072023-06-02 Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients Hamadi, Rachelle Sakr, Fouad Aridi, Hussam Alameddine, Zakaria Dimachkie, Reem Assaad, Marc Asmar, Samer ElSayegh, Suzanne Clin Appl Thromb Hemost Review Heparin-induced thrombocytopenia (HIT) is a disorder originating from exposure to heparin and has a spectrum of presentation ranging from asymptomatic positive antibodies to thrombotic complications. When symptomatic, it is associated with morbidity and mortality. The incidence of HIT in the ESRD population is yet to be defined. End-stage renal disease (ESRD) patients are at particular risk due to constant exposure to heparin. The main treatment of HIT is to avoid heparin and pursue alternative anticoagulants. Since 1 of the main advantages of heparin in ESRD patients is the ease of its use due to non-renal clearance, the use of alternative anticoagulants poses yet another challenge for this population due to cost, availability, and adverse effects on ESRD patients. Argatroban seems like the best alternative to heparin in hemodialysis (HD) patients due to its liver clearance. Despite having limited studies in HIT, direct oral anticoagulants (DOACs) were added as a potential treatment for HIT, with apixaban favored in kidney dysfunction as it is the least dependent on kidney clearance. Other treatment modalities exist but are still being studied in ESRD patients. The presence of HIT antibodies is not always associated with clinical syndrome, and some studies suggested that heparin antibodies are transient, and the reintroduction of heparin is still being evaluated as a treatment option. Hence, HIT is a challenging diagnosis in ESRD patients, a population that has frequent exposure to anticoagulants, and a risk/benefit ratio should be weighed between the risk of progression to symptomatic HIT and the benefit of switching to a non-heparin anticoagulant bearing in mind the difficulties associated with the latter. SAGE Publications 2023-05-30 /pmc/articles/PMC10233607/ /pubmed/37253454 http://dx.doi.org/10.1177/10760296231177993 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/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).
spellingShingle Review
Hamadi, Rachelle
Sakr, Fouad
Aridi, Hussam
Alameddine, Zakaria
Dimachkie, Reem
Assaad, Marc
Asmar, Samer
ElSayegh, Suzanne
Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients
title Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients
title_full Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients
title_fullStr Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients
title_full_unstemmed Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients
title_short Heparin-Induced Thrombocytopenia in Chronic Hemodialysis Patients
title_sort heparin-induced thrombocytopenia in chronic hemodialysis patients
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233607/
https://www.ncbi.nlm.nih.gov/pubmed/37253454
http://dx.doi.org/10.1177/10760296231177993
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