Rishniw Mark, Pion Paul D
Veterinary Information Network, Davis, CA, USA.
Vet Clin Pathol. 2016 Dec;45(4):604-614. doi: 10.1111/vcp.12398. Epub 2016 Oct 7.
A previous study provided information regarding the quality of in-clinic veterinary biochemistry testing. However, no similar studies for in-clinic veterinary hematology testing have been conducted.
The objective of this study was to assess the quality of hematology testing in veterinary in-clinic laboratories using results obtained from testing 3 levels of canine EDTA blood samples.
Clinicians prepared blood samples to achieve measurand concentrations within, below, and above their RIs and evaluated the samples in triplicate using their in-clinic analyzers. Quality was assessed by comparison of calculated total error with quality requirements, determination of sigma metrics, use of a quality goal index, and agreement between in-clinic and reference laboratory instruments. Suitability for statistical quality control was determined using adaptations from the computerized program, EZRules3.
Evaluation of 10 veterinary in-clinic hematology analyzers showed that these instruments often fail to meet quality requirements. At least 60% of analyzers reasonably determined RBC, WBC, HCT, and HGB, when assessed by most quality goal criteria; platelets were less reliably measured, with 80% deemed suitable for low platelet counts, but only 30% for high platelet counts, and automated differential leukocyte counts were generally considered unsuitable for clinical use with fewer than 40% of analyzers meeting the least stringent quality goal requirements. Fewer than 50% of analyzers were able to meet requirements for statistical quality control for any measurand.
These findings reflect the current status of in-clinic hematology analyzer performance and provide a basis for future evaluations of the quality of veterinary laboratory testing.
先前的一项研究提供了有关临床兽医生物化学检测质量的信息。然而,尚未开展类似的临床兽医血液学检测研究。
本研究的目的是利用检测3个水平犬EDTA血样的结果,评估兽医临床实验室血液学检测的质量。
临床医生制备血样,使其测量值浓度处于参考区间内、低于参考区间和高于参考区间,并使用其临床分析仪对样本进行一式三份评估。通过将计算出的总误差与质量要求进行比较、确定西格玛指标、使用质量目标指数以及临床分析仪与参考实验室仪器之间的一致性来评估质量。使用计算机程序EZRules3的改编版本来确定统计质量控制的适用性。
对10台兽医临床血液学分析仪的评估表明,这些仪器常常无法满足质量要求。根据大多数质量目标标准评估时,至少60%的分析仪能够合理测定红细胞、白细胞、血细胞比容和血红蛋白;血小板测量的可靠性较低,80%的分析仪被认为适用于低血小板计数,但只有30%适用于高血小板计数,自动白细胞分类计数通常被认为不适合临床使用,只有不到40%的分析仪符合最宽松的质量目标要求。对于任何测量值,能够满足统计质量控制要求的分析仪不到50%。
这些发现反映了临床血液学分析仪性能的现状,并为未来评估兽医实验室检测质量提供了依据。