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Effects of Obesity on Warfarin Reversal With Vitamin K

机译:肥胖对维生素K逆转华法林的影响

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摘要

Phytonadione (vitamin K1, VK) is fat soluble and may be sequestered by adipose tissue, thus potentially altering drug distribution in obese patients requiring warfarin reversal. This single-center retrospective cohort study aimed to determine the effects of obesity (defined as body mass index [BMI] ≥ 30 kg/m2) on warfarin reversal following administration of VK in adult patients. The primary outcome was complete or partial warfarin reversal (defined as an international normalized ratio [INR] ≤ 2.0) within 72 hours post-VK administration. Of 688 identified patients, 215 were included in primary INR analysis. Mean BMIs for obese (n = 84) and nonobese (n = 131) patients were 37.3 and 24.3 kg/m2 (P < .001), and mean baseline INRs were 4.73 and 4.42 (P = .534), respectively. Within 72 hours post-VK administration, 70% and 69% of the obese and nonobese groups, respectively, achieved complete or partial warfarin reversal (P = .904). Multiple logistic regression determined baseline INR and concomitant fresh frozen plasma administration to be factors influencing warfarin reversal. These findings do not suggest obesity is significantly associated with a decreased likelihood of warfarin reversal within 72 hours post-VK administration.
机译:苯乙二酮(维生素K1,VK)是脂溶性的,可能被脂肪组织隔离,因此有可能改变需要华法林逆转的肥胖患者的药物分布。这项单中心回顾性队列研究旨在确定成人患者接受VK后肥胖对华法林逆转的影响(定义为体重指数[BMI]≥30 kg / m 2 )。 VK给药后72小时内,主要结果为完全或部分华法林逆转(定义为国际标准化比率[INR]≤2.0)。在确定的688位患者中,有215位被纳入了主要INR分析。肥胖(n = 84)和非肥胖(n = 131)患者的平均BMI为37.3和24.3 kg / m 2 (P <.001),平均基线INR为4.73和4.42(P = .534)。服用VK后72小时内,肥胖和非肥胖组分别有70%和69%的华法林完全或部分逆转(P = .904)。多元logistic回归确定基线INR和伴随的新鲜冷冻血浆给药是影响华法林逆转的因素。这些发现并不表明肥胖与服用VK后72小时内华法林逆转的可能性降低显着相关。

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