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糖化血红蛋白:101个实验室在一项外部质量保证计划中,对12种分析方法应用于冻干溶血产物的比较。

Glycohaemoglobin: comparison of 12 analytical methods, applied to lyophilized haemolysates by 101 laboratories in an external quality assurance programme.

作者信息

Weykamp C W, Penders T J, Muskiet F A, van der Slik W

机构信息

Department of Clinical Chemistry, Queen Beatrix Hospital, Winterswijk, The Netherlands.

出版信息

Ann Clin Biochem. 1993 Mar;30 ( Pt 2):169-74. doi: 10.1177/000456329303000210.

Abstract

Stable lyophilized ethylenediaminetetra-acetic acid (EDTA)-blood haemolysates were applied in an external quality assurance programme (SKZL, The Netherlands) for glycohaemoglobin assays in 101 laboratories using 12 methods. The mean intralaboratory day-to-day coefficient of variation (CV), calculated from the assay of 12 unidentified pairs over a period of 1 year, was 5.2% (range: 0.2-28.7). Forty-seven per cent of laboratories did not meet the criterion of CV < 5%, whereas 68% did not meet the clinically more desirable 3.3-3.6%. Linearity, as derived from the analysis of five combinations of two haemolysates with low and high glycohaemoglobin percentages over 6 months, was excellent (mean correlation coefficient 0.9953; range: 0.9188-0.9999). Analysis of two samples with high and low glycohaemoglobin percentages gave mean interlaboratory coefficients of variation of 10% for one method performed by several laboratories and 22% for all methods performed by all laboratories. It is concluded that the majority of laboratories do not meet the clinically desirable intralaboratory precision and that an unacceptably high interlaboratory precision exists.

摘要

稳定的冻干乙二胺四乙酸(EDTA)-血溶血产物被应用于荷兰SKZL的一项外部质量保证计划中,该计划涉及101个实验室使用12种方法进行糖化血红蛋白检测。通过对12对未识别样本在1年时间内的检测计算得出,实验室内部日常变异系数(CV)的平均值为5.2%(范围:0.2 - 28.7)。47%的实验室未达到CV < 5%的标准,而68%的实验室未达到临床上更理想的3.3 - 3.6%。通过对两种糖化血红蛋白百分比高低不同的溶血产物的五种组合进行6个月的分析得出,线性关系极佳(平均相关系数0.9953;范围:0.9188 - 0.9999)。对两种糖化血红蛋白百分比高低不同的样本进行分析,对于多个实验室采用的一种方法,实验室间变异系数平均值为10%,对于所有实验室采用的所有方法,变异系数平均值为22%。得出的结论是,大多数实验室未达到临床上理想的实验室内部精密度,且存在高得不可接受的实验室间精密度。

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