The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study
- PMID: 30656280
- PMCID: PMC6332713
- DOI: 10.1002/rth2.12159
The effect of stopping phenprocoumon 5 days preoperatively: A retrospective study
Abstract
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.
Keywords: anticoagulant; international normalized ratio; phenprocoumon; preoperative care; vitamin k antagonists.
Comment in
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The effect of oral vitamin K on the pre-operative reversal of vitamin K antagonists in elective noncardiac surgery.Eur J Anaesthesiol. 2023 Jan 1;40(1):54-74. doi: 10.1097/EJA.0000000000001777. Eur J Anaesthesiol. 2023. PMID: 36409167 No abstract available.
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