Aims: Acenocoumarol, a vitamin K antagonist anticoagulant, is used in the management of common thromboembolic conditions, such as atrial fibrillation and venous thrombosis. Although it remains a standard treatment in Algeria, its clinical use is hampered by significant interindividual variability in therapeutic response, influenced by several genetic and non-genetic factors. the objective of this work was to evaluate the quality of anticoagulation with acenocoumarol at the University and Hospital Establishment of Oran, Algeria. Methodology: A prospective descriptive cross-sectional study was conducted on patients treated with acenocoumarol. Therapeutic monitoring was performed using the International Normalized Ratio (INR) and the Time in Therapeutic Range (TTR). Results and Discussion: A total of 51 patients were followed. The results showed a female predominance, with a mean age of 55 ± 2.33 years. The mean daily dose of acenocoumarol administered was 2.52 ± 0.7 mg/ day, and the steady-state dose was 2.72 ± 0.89 mg/day; the mean time to steady state was 2.72 ± 0.89 days. Only 41.18% of patients achieved their INR target at the end of the study. The majority of patients (82.35%) had a TTR below 50%, indicating poor control of anticoagulation with acenocoumarol. Conclusion: This study has demonstrated that acenocoumarol dosage optimization by INR is insufficient, and has highlighted the importance of implementing other dosage personalization approaches such as pharmacogenetics.
Oral anticoagulationtherapeutic monitoringtime in therapeutic range ratioTTR
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