| Literature DB >> 32024944 |
Elizaveta Panchenko1, Ekaterina Kropacheva2, Anatoly Dobrovolsky2, Elena Titaeva2, Oksana Zemlyanskaya2, Dmitry Trofimov3, Irina Galkina3, Galina Lifshits4, Natalya Vereina5, Sergey Sinitsin5, Nadezda Vorobyeva6, Lyudmila Grehova7, Dmitry Zateyshchikov8, Irina Zotova8, Tatyana Vavilova9, Olga Sirotkina9, Alevtina Grontkovskaya10.
Abstract
A total of 263 warfarin naive patients with indications to long-term anticoagulation were included in prospective multicenter study and randomized into Pharmacogenetics and Standard dosing groups. The loading warfarin dose in Pharmacogenetics group was calculated by Gage algorithm and corrected starting on day 5 of treatment according to INR. In Standard dosing group warfarin initial dose was 5 mg and starting on day 3 of treatment it was titrated according to INR. Pharmacogenetics dosing in comparison with prescription of starting dose of 5 mg decreased major bleedings (0 vs. 6, p = 0.031), time to target INR (11 [9-14] vs. 17 [15-24] days, p = 0.046), and frequency of INR fluctuations ≥4.0 (11% vs. 30.9%, p = 0.002). The advantages of the pharmacogenetics dosing were mainly achieved due to the patients with increased warfarin sensitivity.Entities:
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Year: 2020 PMID: 32024944 DOI: 10.1038/s41397-020-0157-2
Source DB: PubMed Journal: Pharmacogenomics J ISSN: 1470-269X Impact factor: 3.550