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Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases
BACKGROUND: Nephrotic syndrome (NS) is associated with increased risk of thromboembolic events (TE) adding to the morbidity and mortality. International guidelines recommend prophylactic anticoagulation in patients with NS and high risk of TE, but no studies have identified the optimal type of antic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446569/ https://www.ncbi.nlm.nih.gov/pubmed/36064370 http://dx.doi.org/10.1186/s12882-022-02929-x |
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author | Kelddal, Sarah Hvas, Anne-Mette Grove, Erik Lerkevang Birn, Henrik |
author_facet | Kelddal, Sarah Hvas, Anne-Mette Grove, Erik Lerkevang Birn, Henrik |
author_sort | Kelddal, Sarah |
collection | PubMed |
description | BACKGROUND: Nephrotic syndrome (NS) is associated with increased risk of thromboembolic events (TE) adding to the morbidity and mortality. International guidelines recommend prophylactic anticoagulation in patients with NS and high risk of TE, but no studies have identified the optimal type of anticoagulation in NS. We aimed to assess the effectiveness and safety of direct oral anticoagulant (DOAC) by analyzing the thromboembolic and bleeding events in NS patients prescribed DOAC as primary prophylaxis to prevent TE or as treatment for TE occurring in relation to NS. METHODS: We performed a single-center, retrospective study including patients with NS, a plasma albumin less than 25 g/L and prophylactic anticoagulation treatment with DOAC at the Department of Renal Medicine at Aarhus University Hospital, Denmark from July 2016 to June 2021. Patients treated with DOAC as thromboprophylaxis for other indications than NS were excluded. Baseline characteristics and outcomes, including TE, bleeding and other adverse effects associated with DOAC were obtained from medical records. RESULTS: We identified 268 patients treated with DOAC of which 21 patients with NS were included in the study. Nineteen patients were prescribed DOAC as thromboprophylaxis and two patients received DOAC due to previous TE, which was considered associated with the NS. The type of DOAC prescribed was apixaban (n = 10) and rivaroxaban (n = 11). No patients experienced TE during DOAC treatment, while five patients had a minor bleeding episode. Patients who experienced bleeding episodes were older (median 62 vs 51 years), more often female (80%) and had been on DOAC for a longer period (204 days vs 47 days). Neither the HAS-BLED score nor GN-risk-score predicted the risk of minor bleedings in this population. CONCLUSIONS: In this case series, no new TE and only minor bleeding complications were observed among adult NS patients treated with DOAC. |
format | Online Article Text |
id | pubmed-9446569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94465692022-09-07 Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases Kelddal, Sarah Hvas, Anne-Mette Grove, Erik Lerkevang Birn, Henrik BMC Nephrol Research BACKGROUND: Nephrotic syndrome (NS) is associated with increased risk of thromboembolic events (TE) adding to the morbidity and mortality. International guidelines recommend prophylactic anticoagulation in patients with NS and high risk of TE, but no studies have identified the optimal type of anticoagulation in NS. We aimed to assess the effectiveness and safety of direct oral anticoagulant (DOAC) by analyzing the thromboembolic and bleeding events in NS patients prescribed DOAC as primary prophylaxis to prevent TE or as treatment for TE occurring in relation to NS. METHODS: We performed a single-center, retrospective study including patients with NS, a plasma albumin less than 25 g/L and prophylactic anticoagulation treatment with DOAC at the Department of Renal Medicine at Aarhus University Hospital, Denmark from July 2016 to June 2021. Patients treated with DOAC as thromboprophylaxis for other indications than NS were excluded. Baseline characteristics and outcomes, including TE, bleeding and other adverse effects associated with DOAC were obtained from medical records. RESULTS: We identified 268 patients treated with DOAC of which 21 patients with NS were included in the study. Nineteen patients were prescribed DOAC as thromboprophylaxis and two patients received DOAC due to previous TE, which was considered associated with the NS. The type of DOAC prescribed was apixaban (n = 10) and rivaroxaban (n = 11). No patients experienced TE during DOAC treatment, while five patients had a minor bleeding episode. Patients who experienced bleeding episodes were older (median 62 vs 51 years), more often female (80%) and had been on DOAC for a longer period (204 days vs 47 days). Neither the HAS-BLED score nor GN-risk-score predicted the risk of minor bleedings in this population. CONCLUSIONS: In this case series, no new TE and only minor bleeding complications were observed among adult NS patients treated with DOAC. BioMed Central 2022-09-05 /pmc/articles/PMC9446569/ /pubmed/36064370 http://dx.doi.org/10.1186/s12882-022-02929-x 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 Kelddal, Sarah Hvas, Anne-Mette Grove, Erik Lerkevang Birn, Henrik Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases |
title | Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases |
title_full | Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases |
title_fullStr | Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases |
title_full_unstemmed | Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases |
title_short | Safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases |
title_sort | safety and effectiveness of direct oral anticoagulants in patients with nephrotic syndrome: a report of 21 cases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446569/ https://www.ncbi.nlm.nih.gov/pubmed/36064370 http://dx.doi.org/10.1186/s12882-022-02929-x |
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