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Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018
Myeloproliferative neoplasms (MPNs) are a leading cause of splanchnic vein thrombosis (SVT). SVT is observed in all MPNs and frequently affects young patients. Therapy should be addressed to three main goals: preventing thrombosis recurrence, managing the underlying MPN, and supporting liver dysfunc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018786/ https://www.ncbi.nlm.nih.gov/pubmed/29946154 http://dx.doi.org/10.1038/s41408-018-0100-9 |
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author | Finazzi, Guido De Stefano, Valerio Barbui, Tiziano |
author_facet | Finazzi, Guido De Stefano, Valerio Barbui, Tiziano |
author_sort | Finazzi, Guido |
collection | PubMed |
description | Myeloproliferative neoplasms (MPNs) are a leading cause of splanchnic vein thrombosis (SVT). SVT is observed in all MPNs and frequently affects young patients. Therapy should be addressed to three main goals: preventing thrombosis recurrence, managing the underlying MPN, and supporting liver dysfunction. Life-long oral anticoagulation with vitamin K antagonists is the cornerstone of the antithrombotic treatment. However, recurrences of SVT or other thrombosis may occur in 15–20% of patients. Direct oral anticoagulants can represent an alternative and preliminary data encourage comparative studies. Survival of patients with SVT in MPN is primarily influenced by the natural history of the underlying neoplasms, rather than the SVT event. An aggressive management is recommended and a treatment algorithm based on the different MPN subtypes is proposed. Hydroxyurea is the cytoreductive drug of choice in polycythemia vera and essential thrombocythemia, whereas ruxolitinib is indicated in intermediate and high-risk patients with myelofibrosis and in PV patients resistant or intolerant to hydroxyurea. The management of SVT in MPNs requires a multidisciplinary approach that may include a hematologist, a gastroenterologist, an interventional radiologist, and a surgeon. In the case of clinical deterioration despite pharmacological therapy, patients with SVT should be considered for invasive procedures or liver transplantation. |
format | Online Article Text |
id | pubmed-6018786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60187862018-06-27 Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 Finazzi, Guido De Stefano, Valerio Barbui, Tiziano Blood Cancer J Current Treatment Algorithm Myeloproliferative neoplasms (MPNs) are a leading cause of splanchnic vein thrombosis (SVT). SVT is observed in all MPNs and frequently affects young patients. Therapy should be addressed to three main goals: preventing thrombosis recurrence, managing the underlying MPN, and supporting liver dysfunction. Life-long oral anticoagulation with vitamin K antagonists is the cornerstone of the antithrombotic treatment. However, recurrences of SVT or other thrombosis may occur in 15–20% of patients. Direct oral anticoagulants can represent an alternative and preliminary data encourage comparative studies. Survival of patients with SVT in MPN is primarily influenced by the natural history of the underlying neoplasms, rather than the SVT event. An aggressive management is recommended and a treatment algorithm based on the different MPN subtypes is proposed. Hydroxyurea is the cytoreductive drug of choice in polycythemia vera and essential thrombocythemia, whereas ruxolitinib is indicated in intermediate and high-risk patients with myelofibrosis and in PV patients resistant or intolerant to hydroxyurea. The management of SVT in MPNs requires a multidisciplinary approach that may include a hematologist, a gastroenterologist, an interventional radiologist, and a surgeon. In the case of clinical deterioration despite pharmacological therapy, patients with SVT should be considered for invasive procedures or liver transplantation. Nature Publishing Group UK 2018-06-26 /pmc/articles/PMC6018786/ /pubmed/29946154 http://dx.doi.org/10.1038/s41408-018-0100-9 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Current Treatment Algorithm Finazzi, Guido De Stefano, Valerio Barbui, Tiziano Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 |
title | Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 |
title_full | Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 |
title_fullStr | Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 |
title_full_unstemmed | Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 |
title_short | Splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 |
title_sort | splanchnic vein thrombosis in myeloproliferative neoplasms: treatment algorithm 2018 |
topic | Current Treatment Algorithm |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018786/ https://www.ncbi.nlm.nih.gov/pubmed/29946154 http://dx.doi.org/10.1038/s41408-018-0100-9 |
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