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The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study
BACKGROUND: Clinicians lack substantiated guidance on when vitamin K antagonist (VKA) treatment should be interrupted preoperatively, especially with regard to phenprocoumon, with its long half‐life of 5.5 days. OBJECTIVE: To evaluate the efficacy of discontinuing phenprocoumon 5 days preoperatively...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332713/ https://www.ncbi.nlm.nih.gov/pubmed/30656280 http://dx.doi.org/10.1002/rth2.12159 |
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author | Knol, Silke Mallo, Mascha Tromp Meesters, Reinier Westerink, Jan van de Ree, Marcel |
author_facet | Knol, Silke Mallo, Mascha Tromp Meesters, Reinier Westerink, Jan van de Ree, Marcel |
author_sort | Knol, Silke |
collection | PubMed |
description | BACKGROUND: Clinicians lack substantiated guidance on when vitamin K antagonist (VKA) treatment should be interrupted preoperatively, especially with regard to phenprocoumon, with its long half‐life of 5.5 days. OBJECTIVE: To evaluate the efficacy of discontinuing phenprocoumon 5 days preoperatively and determine whether a safe international normalized ratio (INR) was reached. METHODS: This was a retrospective review of 118 patients using phenprocoumon prior to elective surgery. Preoperative INRs and factors that could potentially influence these values were identified and described. A safe preoperative INR was defined as <1.8. RESULTS: Of the 118 included patients, 42 patients (35.6%) had an off‐target INR. The male sex was significantly and independently associated with an off‐target INR (odds ratio [OR] 2.4, 95% confidence interval [CI] 1.022‐5.445). A high American Society of Anesthesiologists (ASA) classification was also significantly and independently associated with an off‐target INR (OR 2.3, 95% CI: 1.029‐5.173). CONCLUSION: Discontinuation of phenprocoumon 5 days preoperatively resulted in an INR < 1.8 in more than one‐third of patients. Individualizing or extending the period of phenprocoumon discontinuation may be a necessary treatment option. |
format | Online Article Text |
id | pubmed-6332713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63327132019-01-17 The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study Knol, Silke Mallo, Mascha Tromp Meesters, Reinier Westerink, Jan van de Ree, Marcel Res Pract Thromb Haemost Original Articles: Thrombosis BACKGROUND: Clinicians lack substantiated guidance on when vitamin K antagonist (VKA) treatment should be interrupted preoperatively, especially with regard to phenprocoumon, with its long half‐life of 5.5 days. OBJECTIVE: To evaluate the efficacy of discontinuing phenprocoumon 5 days preoperatively and determine whether a safe international normalized ratio (INR) was reached. METHODS: This was a retrospective review of 118 patients using phenprocoumon prior to elective surgery. Preoperative INRs and factors that could potentially influence these values were identified and described. A safe preoperative INR was defined as <1.8. RESULTS: Of the 118 included patients, 42 patients (35.6%) had an off‐target INR. The male sex was significantly and independently associated with an off‐target INR (odds ratio [OR] 2.4, 95% confidence interval [CI] 1.022‐5.445). A high American Society of Anesthesiologists (ASA) classification was also significantly and independently associated with an off‐target INR (OR 2.3, 95% CI: 1.029‐5.173). CONCLUSION: Discontinuation of phenprocoumon 5 days preoperatively resulted in an INR < 1.8 in more than one‐third of patients. Individualizing or extending the period of phenprocoumon discontinuation may be a necessary treatment option. John Wiley and Sons Inc. 2018-11-09 /pmc/articles/PMC6332713/ /pubmed/30656280 http://dx.doi.org/10.1002/rth2.12159 Text en © 2018 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles: Thrombosis Knol, Silke Mallo, Mascha Tromp Meesters, Reinier Westerink, Jan van de Ree, Marcel The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study |
title | The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study |
title_full | The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study |
title_fullStr | The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study |
title_full_unstemmed | The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study |
title_short | The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study |
title_sort | effect of stopping phenprocoumon 5 days preoperatively: a retrospective study |
topic | Original Articles: Thrombosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332713/ https://www.ncbi.nlm.nih.gov/pubmed/30656280 http://dx.doi.org/10.1002/rth2.12159 |
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