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比较不同批次的活化部分凝血活酶时间试剂:两种方法的分析

Comparing different lots of activated partial thromboplastin time reagent: analysis of two methods.

作者信息

Rosborough T K

机构信息

Department of Medical Education, Abbott Northwestern Hospital, Minneapolis, Minnesota 55407, USA.

出版信息

Am J Clin Pathol. 1998 Aug;110(2):173-7. doi: 10.1093/ajcp/110.2.173.

Abstract

This study was conducted to compare the performance of 2 different lots of activated partial thromboplastin time (APTT) reagent from the same manufacturer. Two hundred plasma samples were analyzed for APTT on the same instrument using 2 separate APTT reagent lots. Results were compared with those obtained from duplicate APTT determinations with 1 reagent lot on an additional 267 plasma samples. Regression analysis of paired APTT data was suboptimal because the disagreement of the results increased as the APTT values became higher. A better approach was the use of the Bland and Altman assessment of agreement method on logarithmically transformed data, which showed that the new reagent lot produced values that were 88.9% of the values produced by the old lot. This importantly reduced the APTT therapeutic range for unfractionated heparin (UH). In comparison, duplicate APTT values were 97.6% of a first APTT value. However, 95% limits of agreement for duplicate APTT determinations were +/-10% over the range of values considered therapeutic for UH. The variability of APTT results within and between reagent lots is one reason that APTT may not be optimum for monitoring UH therapy.

摘要

本研究旨在比较同一制造商生产的两批不同活化部分凝血活酶时间(APTT)试剂的性能。使用两批不同的APTT试剂,在同一仪器上对200份血浆样本进行APTT分析。将结果与另外267份血浆样本使用一批试剂进行重复APTT测定所得结果进行比较。对配对的APTT数据进行回归分析并不理想,因为随着APTT值升高,结果的差异增大。更好的方法是对对数转换后的数据使用Bland和Altman一致性评估方法,结果显示新试剂批次产生的值是旧批次产生值的88.9%。这显著降低了普通肝素(UH)的APTT治疗范围。相比之下,重复APTT值是首次APTT值的97.6%。然而,在UH治疗的有效范围内,重复APTT测定的95%一致性界限为±10%。APTT结果在试剂批次内和批次间的变异性是APTT可能不适用于监测UH治疗的一个原因。

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