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用于预测华法林反应的贝叶斯回归程序的评估。

Evaluation of a Bayesian regression program for predicting warfarin response.

作者信息

Boyle D A, Ludden T M, Carter B L, Becker A J, Taylor J W

机构信息

Division of Drug Metabolism, Smith-Kline and French Laboratories, King of Prussia, Pennsylvania.

出版信息

Ther Drug Monit. 1989;11(3):276-84. doi: 10.1097/00007691-198905000-00010.

Abstract

The ability of a Bayesian regression program (Warfcalc) to predict warfarin response was evaluated retrospectively in 48 inpatients and prospectively in 10 inpatients. The prothrombin ratio (PR) on the last day of inpatient therapy was predicted using zero (naive) to five sequential, daily PR feedbacks. Bias and precision were measured using mean error (ME) and mean absolute error (MAE), respectively. Root mean squared error (RMSE) was used as a combined measure of bias and precision. In the retrospective group, the use of five PR feedbacks yielded the lowest ME, MAE, and RMSE (0.22, 0.30, and 0.45, respectively). The use of two and three daily PR feedbacks resulted in larger prediction errors compared with the use of naive parameters. Further evaluation of the retrospective patient data indicated that deletion of PR feedbacks associated with an activated partial thromboplastin time greater than 100 s and exclusion of metabolic inhibitors in the estimation of warfarin clearance resulted in more reliable predictions (ME = 0.07, MAE = 0.20, RMSE = 0.28). Similarly, deletion of such PR feedbacks and metabolic inhibitors from the prospective data and use of PRs for the first 5 days of therapy yielded ME, MAE, and RMSE values of 0.07, 0.21, and 0.27, respectively. The variance for prothrombin complex activity (PCA) as a function of the variance in the prothrombin time (PT) was investigated using Monte Carlo simulation assuming four different random error models for the PT measurements. These error models yielded functions that exhibit a maximum coefficient of variation at PCA values of 40-70%.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对一个贝叶斯回归程序(Warfcalc)预测华法林反应的能力进行了回顾性评估,涉及48名住院患者,并前瞻性评估了10名住院患者。使用零(朴素)到五个连续的每日凝血酶原比值(PR)反馈来预测住院治疗最后一天的凝血酶原比值。分别使用平均误差(ME)和平均绝对误差(MAE)来衡量偏差和精度。均方根误差(RMSE)用作偏差和精度的综合度量。在回顾性组中,使用五个PR反馈产生了最低的ME、MAE和RMSE(分别为0.22、0.30和0.45)。与使用朴素参数相比,使用两个和三个每日PR反馈导致更大的预测误差。对回顾性患者数据的进一步评估表明,删除与活化部分凝血活酶时间大于100秒相关的PR反馈,并在估计华法林清除率时排除代谢抑制剂,可得到更可靠的预测(ME = 0.07,MAE = 0.20,RMSE = 0.28)。同样,从前瞻性数据中删除此类PR反馈和代谢抑制剂,并使用治疗前5天的PR,得到的ME、MAE和RMSE值分别为0.07、0.21和0.27。使用蒙特卡罗模拟研究了凝血酶原复合物活性(PCA)的方差作为凝血酶原时间(PT)方差的函数,假设PT测量有四种不同的随机误差模型。这些误差模型产生的函数在PCA值为40 - 70%时表现出最大变异系数。(摘要截断于250字)

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