Comparative performance of two methods that assess the quality of international normalized ratio measures

被引:1
|
作者
Shermock, Kenneth M. [1 ]
Tandon, Sangeeta [2 ]
Sorgen, Patrick J. [3 ]
Lavallee, Danielle C. [4 ]
Clarke, William [5 ]
Streiff, Michael B. [6 ]
机构
[1] Johns Hopkins Med Inst, Ctr Pharmaceut Outcomes, Baltimore, MD 21205 USA
[2] Univ Iowa, Coll Pharm, Iowa City, IA 52242 USA
[3] Purdue Univ, Coll Pharm, W Lafayette, IN 47907 USA
[4] Ctr Med Technol Policy, Baltimore, MD USA
[5] Johns Hopkins Sch Med, Dept Pathol, Div Clin Chem, Baltimore, MD USA
[6] Johns Hopkins Sch Med, Div Hematol, Dept Med, Baltimore, MD USA
关键词
Coagulation monitoring; Point-of-care testing; POCT; PT INR; Healthcare quality assurance; AGREEMENT;
D O I
10.1016/j.clinbiochem.2012.01.032
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Two methods, Petersen's error grid analysis and Shermock's method to detect clinically important differences, were recently developed to advance the assessment of analytic performance of point-of-care INR devices. Both methods predict when alternate INR measures lead to different clinical decisions. Our goal was to compare their performance characteristics. Design and methods: Performance characteristics were assessed by comparing the models' predictions to clinical decisions that were directly measured in a previous experiment. Results: Shermock's method (82% of predictions correct) demonstrated superior predictive performance compared with the error grid analysis (75% of predictions correct, p = 0.008). Shermock's method was particularly superior at identifying the clinical decisions that actually disagreed (79% for Shermock's method vs. 47% for error grid). Consequently, Shermock's method was superior at identifying a POC device with poor performance (79% accuracy vs. 70%, p = 0.006). Conclusion: Shermock's method had superior performance characteristics and should be integrated into analytic strategies to assess POC INR devices. (C) 2012 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:530 / 534
页数:5
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