在华法林治疗中使用个性化决策支持算法:一项随机对照试验

Peter Brønnum Nielsen , Søren Lundbye-Christensen , Meriam van der Male , Torben Bjerregaard Larsen
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引用次数: 6

摘要

背景:维生素k拮抗剂如华法林治疗仍然是预防各种情况下血栓栓塞事件的主要药物。治疗质量随时间反映在治疗(INR)范围(TTR)中,阈值≥70%表示“良好质量”;实现这种品质并非易事。我们进行了一项随机对照试验,以评估决策辅助模型对高质量维生素k拮抗剂治疗环境中治疗质量的影响。方法:我们调查了在涉及自我管理华法林患者的高质量环境中,算法建议的华法林剂量是否优于标准剂量。患者最初被分配到算法建议的华法林剂量或标准护理治疗,并在三个月后交叉。试验期共6个月,主要终点为TTR;我们还研究了对数变换INR变异性的次要终点。结果191例患者参与主分析,平均随访140天;75%为男性,平均年龄为65岁。干预组的TTR为81.6,而安慰剂组的TTR为80.9(差异[干预组与安慰剂组]:0.67(95%可信区间为- 2.93至4.27)。INR变异性的差异为0.30(0.14至0.47),就较低的对数转换变异性而言,安慰剂组更有利。结论:我们发现两个试验组在高质量华法林治疗设置上没有差异。然而,总的来说,该模型的表现与常规患者自我管理护理相似。(ClinicalTrials.gov号码:NCT02705976)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using a personalized decision support algorithm for dosing in warfarin treatment: A randomised controlled trial

Background

Vitamin K-antagonists such as warfarin treatment remain the mainstay to prevent thromboembolic events in various conditions. The quality of the treatment is reflected through time in therapeutic (INR) range (TTR) with a threshold at ≥ 70% indicating ‘good quality’; achieving this quality is not trivial. We conducted a randomised controlled trial to assess the impact of decision aiding model on treatment quality in a high quality vitamin K-antagonist treatment setting.

Methods

We investigated if algorithm-suggested warfarin dosing was superior to standard dosing in a high-quality setting involving self-managing warfarin patients. Patients were initially allocated to either algorithm-suggested warfarin dosing or to standard care treatment, and were crossed over after three months. The trial period was a total of six months, and the primary endpoint was TTR; we also investigated a secondary endpoint of log-transformed INR variability.

Results

A total of 191 patients contributed to the main analysis with a mean follow-up time of 140 days; 75% were males and the mean age was 65 years old. The intervention arm achieved a TTR of 81.6, while the placebo arm attained a TTR of 80.9 (difference [intervention arm minus placebo arm]: 0.67 (95% confidence interval − 2.93 to 4.27). The difference in INR variability was 0.30 (0.14 to 0.47), favouring the placebo arm in terms of lower log transformed variability.

Conclusions

We found no difference between the two trial-arms in a high-quality warfarin treatment setup. However in general, the model performed similarly as to routine patient self-management care. (ClinicalTrials.gov number: NCT02705976)

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