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接受阿哌沙班或利伐沙班治疗的患者的抗Xa活性比较。

Comparison of Anti-Xa Activity in Patients Receiving Apixaban or Rivaroxaban.

作者信息

Bookstaver David A, Sparks Kimberly, Pybus Brandon S, Davis Dustin K, Marcsisin Sean R, Sousa Jason C

机构信息

1 Eisenhower Army Medical Center, Fort Gordon, GA, USA.

2 Walter Reed Army Institute of Research, Silver Spring, MD, USA.

出版信息

Ann Pharmacother. 2018 Mar;52(3):251-256. doi: 10.1177/1060028017738262. Epub 2017 Oct 19.

Abstract

BACKGROUND

There is no established method for monitoring the anticoagulant effects of apixaban and rivaroxaban. Linear correlation between serum levels and anti-Xa activity has been shown, with r ranging from 0.88 to 0.99. However, there are minimal data in patients receiving apixaban 5 mg twice daily or rivaroxaban 20 mg once daily.

OBJECTIVE

To evaluate the anti-Xa activity and serum levels at those doses and compare the trough anti-Xa activity.

METHODS

This was a single-center prospective study,approved by the institutional review board. Patients on an inappropriate dose or receiving an interacting drug were excluded. Blood samples were drawn 0.5 to 3 hours before a dose for both agents, 2 to 3 hours after an apixaban dose, and 12 to 16 hours after a rivaroxaban dose. Anti-Xa activity and serum levels were determined, and correlation was done via regression analysis. Trough anti-Xa activity was compared using a t-test.

RESULTS

The study enrolled 88 patients receiving each drug. The r values were 0.79 and 0.87 for apixaban and rivaroxaban, respectively. The mean trough anti-Xa activity was 1.79 ± 0.96 IU/mL for apixaban and 1.25 ± 0.88 IU for rivaroxaban ( P < 0.01). The trough sample was drawn a mean of 1.3 and 1.8 hours prior to the next dose for apixaban and rivaroxaban, respectively ( P < 0.01).

CONCLUSIONS

Good correlation was shown between anti-Xa activity and serum levels. The clinical utility of monitoring anti-Xa activity and the significance of the difference in trough anti-Xa activity for these agents remains to be established.

摘要

背景

目前尚无监测阿哌沙班和利伐沙班抗凝效果的确立方法。已显示血清水平与抗Xa活性之间存在线性相关性,r值范围为0.88至0.99。然而,关于每日两次服用5mg阿哌沙班或每日一次服用20mg利伐沙班的患者的数据极少。

目的

评估这些剂量下的抗Xa活性和血清水平,并比较谷值抗Xa活性。

方法

这是一项经机构审查委员会批准的单中心前瞻性研究。排除服用剂量不当或正在接受相互作用药物治疗的患者。在服用两种药物前0.5至3小时、阿哌沙班服药后2至3小时以及利伐沙班服药后12至16小时采集血样。测定抗Xa活性和血清水平,并通过回归分析进行相关性分析。使用t检验比较谷值抗Xa活性。

结果

该研究纳入了88名服用每种药物的患者。阿哌沙班和利伐沙班的r值分别为0.79和0.87。阿哌沙班的平均谷值抗Xa活性为1.79±0.96IU/mL,利伐沙班为1.25±0.88IU(P<0.01)。阿哌沙班和利伐沙班的谷值样本分别在下一次服药前平均1.3小时和1.8小时采集(P<0.01)。

结论

抗Xa活性与血清水平之间显示出良好的相关性。监测抗Xa活性的临床实用性以及这些药物谷值抗Xa活性差异的意义仍有待确定。

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