Rombouts E K, Rosendaal F R, Van Der Meer F J M
Department of Thrombosis and Haemostasis, Leiden University Medical Center, Leiden.
J Thromb Haemost. 2007 Oct;5(10):2043-8. doi: 10.1111/j.1538-7836.2007.02715.x. Epub 2007 Jul 31.
One of the causes of unstable anticoagulant control in patients using vitamin K antagonists is a fluctuating intake of vitamin K. Research suggests that patients with a low dietary intake of vitamin K have a less stable anticoagulant control than patients with a higher intake.
To study whether supplementation with a low daily dose of vitamin K improves anticoagulant control.
We performed a double-blind, randomized, placebo-controlled trial. 200 patients of the Leiden anticoagulation clinic, who used the vitamin K antagonist phenprocoumon, were randomized to receive either adjusted-dose phenprocoumon and 100 mug vitamin K once daily or adjusted-dose phenprocoumon and a placebo. Treatment duration was 24 weeks. The primary outcome was the percentage of time the International Normalized Ratio was within the therapeutic range.
The time in the therapeutic range was 85.5% in the placebo group and 89.5% in the vitamin K group (adjusted difference 3.6%; 95% CI -0.8% to 8.0%). The time below the therapeutic range was 3.1% in the placebo group and 2.1% in the vitamin K group (adjusted difference -0.7%; 95% CI -2.5% to 1.1%) and the time above the therapeutic range was 11.4% in the placebo group and 8.5% in the vitamin K group (adjusted difference -2.9%; 95% CI -6.9% to 1.1%). The relative risk (RR) of a maximal stability in the vitamin K group compared to the placebo group was 1.8 (95%, CI 1.1-2.7).
Supplementation of vitamin K antagonists with 100 mug vitamin K improves stability of anticoagulant therapy. Because the risk of side effects is inversely related to anticoagulant stability, such an improvement is likely to reduce the number of bleeding and thrombotic events.
使用维生素K拮抗剂的患者抗凝控制不稳定的原因之一是维生素K摄入量波动。研究表明,维生素K膳食摄入量低的患者比摄入量高的患者抗凝控制更不稳定。
研究每日补充低剂量维生素K是否能改善抗凝控制。
我们进行了一项双盲、随机、安慰剂对照试验。莱顿抗凝门诊的200名使用维生素K拮抗剂苯丙香豆素的患者被随机分为两组,一组接受调整剂量的苯丙香豆素和每日一次100微克维生素K,另一组接受调整剂量的苯丙香豆素和安慰剂。治疗持续时间为24周。主要结局是国际标准化比值处于治疗范围内的时间百分比。
安慰剂组处于治疗范围内的时间为85.5%,维生素K组为89.5%(校正差异3.6%;95%CI -0.8%至8.0%)。安慰剂组低于治疗范围的时间为3.1%,维生素K组为2.1%(校正差异-0.7%;95%CI -2.5%至1.1%),高于治疗范围的时间在安慰剂组为11.4%,维生素K组为8.5%(校正差异-2.9%;95%CI -6.9%至1.1%)。与安慰剂组相比,维生素K组最大稳定性的相对风险(RR)为1.8(95%,CI 1.1 - 2.7)。
维生素K拮抗剂补充100微克维生素K可提高抗凝治疗的稳定性。由于副作用风险与抗凝稳定性呈负相关,这种改善可能会减少出血和血栓形成事件的数量。