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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...

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Detalles Bibliográficos
Autores principales: Knol, Silke, Mallo, Mascha, Tromp Meesters, Reinier, Westerink, Jan, van de Ree, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
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
Descripción
Sumario: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.