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Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series
BACKGROUND: Low-molecular-weight heparins (LMWHs) are frequently used to treat arterial and venous thrombo-embolic events. LMWHs accumulate with renal failure, but only limited clinical data regarding appropriate dosage adjustments are available. Nevertheless, LMWHs are routinely used in these patie...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438398/ https://www.ncbi.nlm.nih.gov/pubmed/26064511 http://dx.doi.org/10.1093/ckj/sft083 |
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author | Russcher, Marije Josephus Jitta, Nienke Kraaijenhagen, Rob J. Fijnheer, Rob Pasker-de Jong, Pieternel C. M. Gaillard, Carlo A. J. M. |
author_facet | Russcher, Marije Josephus Jitta, Nienke Kraaijenhagen, Rob J. Fijnheer, Rob Pasker-de Jong, Pieternel C. M. Gaillard, Carlo A. J. M. |
author_sort | Russcher, Marije |
collection | PubMed |
description | BACKGROUND: Low-molecular-weight heparins (LMWHs) are frequently used to treat arterial and venous thrombo-embolic events. LMWHs accumulate with renal failure, but only limited clinical data regarding appropriate dosage adjustments are available. Nevertheless, LMWHs are routinely used in these patients worldwide. Although many clinics apply renal function-based dosage reductions, anti-factor Xa (anti-Xa) activity is not measured routinely. METHODS: We determined anti-Xa activity in 51 patients with MDRD-eGFR <60 mL/min/1.73 m(2), treated with therapeutic doses of nadroparin according to a standard, renal function-based guideline. RESULTS: An a priori dosage reduction resulted in anti-Xa activity within, below and above the reference range in 51, 30 and 19% of the measurements, respectively. Treatment resulted in different anti-Xa activities compared with dosages that were not given according to official advice (P < 0.001). Anti-Xa values increased with longer treatment duration (P = 0.038). CONCLUSIONS: A preemptive fixed reduction (25%) of the nadroparin dosage in all patients with renal failure seems appropriate. However, because target anti-Xa activities were reached in only half of the patients, we submit that the use of nadroparin, dosage reduction and monitoring of anti-Xa activity in combination with clinical outcome monitoring in this patient population urgently needs further investigation. |
format | Online Article Text |
id | pubmed-4438398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44383982015-06-10 Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series Russcher, Marije Josephus Jitta, Nienke Kraaijenhagen, Rob J. Fijnheer, Rob Pasker-de Jong, Pieternel C. M. Gaillard, Carlo A. J. M. Clin Kidney J Original Contributions BACKGROUND: Low-molecular-weight heparins (LMWHs) are frequently used to treat arterial and venous thrombo-embolic events. LMWHs accumulate with renal failure, but only limited clinical data regarding appropriate dosage adjustments are available. Nevertheless, LMWHs are routinely used in these patients worldwide. Although many clinics apply renal function-based dosage reductions, anti-factor Xa (anti-Xa) activity is not measured routinely. METHODS: We determined anti-Xa activity in 51 patients with MDRD-eGFR <60 mL/min/1.73 m(2), treated with therapeutic doses of nadroparin according to a standard, renal function-based guideline. RESULTS: An a priori dosage reduction resulted in anti-Xa activity within, below and above the reference range in 51, 30 and 19% of the measurements, respectively. Treatment resulted in different anti-Xa activities compared with dosages that were not given according to official advice (P < 0.001). Anti-Xa values increased with longer treatment duration (P = 0.038). CONCLUSIONS: A preemptive fixed reduction (25%) of the nadroparin dosage in all patients with renal failure seems appropriate. However, because target anti-Xa activities were reached in only half of the patients, we submit that the use of nadroparin, dosage reduction and monitoring of anti-Xa activity in combination with clinical outcome monitoring in this patient population urgently needs further investigation. Oxford University Press 2013-10 2013-09-05 /pmc/articles/PMC4438398/ /pubmed/26064511 http://dx.doi.org/10.1093/ckj/sft083 Text en © The Author 2013. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For permissions, please email: journals.permissions@oup.com. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Contributions Russcher, Marije Josephus Jitta, Nienke Kraaijenhagen, Rob J. Fijnheer, Rob Pasker-de Jong, Pieternel C. M. Gaillard, Carlo A. J. M. Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series |
title | Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series |
title_full | Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series |
title_fullStr | Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series |
title_full_unstemmed | Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series |
title_short | Preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series |
title_sort | preemptive dosage reduction of nadroparin in patients with renal failure: a retrospective case series |
topic | Original Contributions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438398/ https://www.ncbi.nlm.nih.gov/pubmed/26064511 http://dx.doi.org/10.1093/ckj/sft083 |
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