Why the study?
Does discontinuing phenprocoumon 5 days preoperatively achieve a safe preoperative INR (<1.8) in patients undergoing elective surgery?
Does discontinuing phenprocoumon 5 days preoperatively achieve a safe preoperative INR (<1.8) in patients undergoing elective surgery?
Discontinuing phenprocoumon 5 days before elective surgery is insufficient to reach a safe INR (<1.8) in over one-third of patients, suggesting a need for individualized or extended discontinuation periods.
Stopping phenprocoumon 5 days preoperatively left >1/3 with INR ≥1.8; leaves open need for individualized timing or prospective validation before practice change.
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.
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Knol et al. (2018) studied this question.
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