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Elecsys 2010的分析性能——一项多中心评估

Analytical performance of Elecsys 2010--a multicentre evaluation.

作者信息

Stockmann W, Bablok W, Luppa P

机构信息

Boehringer Mannheim GmbH, Mannheim, Germany.

出版信息

Wien Klin Wochenschr. 1998;110 Suppl 3:10-21.

PMID:9677668
Abstract

The analytical performance of Elecsys 2010 has been assessed in a multicentre evaluation, which involved twelve laboratories from eight countries worldwide. Eleven alanytes (TSH, T4, FT4, T3, FT3, T-up, TNT, CK-MB, HCG, CEA and PSA) were tested using a protocol related to the ECCLS guidelines and the Standard Operating Procedures of the manufacturer. The evaluation was supported by a "Computer Aided Evaluation" (CAEv) program system and telecommunications. Within-run and between-day imprecision for the various analytes with 3% CV and 3 to 8% CV, resp. was comparable to homogeneous immunoassays e.g. for specific proteins on clinical chemistry analysers. The functional sensitivity for TSH, TNT and PSA was met by low concentrations: < 0.02 microIU/ml TSH, < 0.05 ng/ml TNT and < 0.07 ng/ml PSA. TSH is an assay of the third generation according to the recommendation of Spencer. The measured lower detection limit was less or equal to the manufacturer's specifications with the exception of the PSA assay. Drift effects (over eight hours) and signal carry-over effects were not observed. A high-dose hook effect became relevant for concentrations higher than 430,000 IU/HCG--an assay with a dynamic range of 10,000 IU/I. The Elecsys assays showed a high dynamic range and rarely necessary predilutions could be performed by the Elecsys instrument using the Elecsys multidiluent. Endogenous interferences were not observed. Calibration stability was confirmed for one week and data indicated that it could be extended at least for three weeks. The quality assurance experiment showed a good transferability of the results between the participating laboratories. The assigned values of two interlaboratory survey materials were found for most of the analytes within a deviation of +/- 10%. Higher deviations could be explained by differences in standardization and methods. The Elecsys 2010 system offers a high analytical sensitivity in combination with relatively low sample volumes and short measuring times (< or = 18 minutes); a high dynamic measuring range reduces the number of reruns and makes the work-flow more convenient. The electrochemiluninescence technology of Elecsys 2010 shows advantages in system performance without having any drawbacks compared to existing technologies.

摘要

Elecsys 2010的分析性能已在一项多中心评估中得到评估,该评估涉及来自全球八个国家的12个实验室。使用与ECCLS指南及制造商标准操作规程相关的方案,对11种分析物(促甲状腺激素、总甲状腺素、游离甲状腺素、三碘甲状腺原氨酸、游离三碘甲状腺原氨酸、甲状腺素结合球蛋白、肌钙蛋白T、肌酸激酶同工酶、人绒毛膜促性腺激素、癌胚抗原和前列腺特异性抗原)进行了检测。该评估得到了一个“计算机辅助评估”(CAEv)程序系统和电信技术的支持。各种分析物的批内不精密度和批间不精密度分别为3%CV和3%至8%CV,与同类免疫分析方法相当,例如临床化学分析仪上特定蛋白质的检测。促甲状腺激素、肌钙蛋白T和前列腺特异性抗原在低浓度时达到功能灵敏度:促甲状腺激素<0.02微国际单位/毫升,肌钙蛋白T<0.05纳克/毫升,前列腺特异性抗原<0.07纳克/毫升。根据斯宾塞的建议,促甲状腺激素检测为第三代检测方法。除前列腺特异性抗原检测外,实测最低检测限小于或等于制造商规定值。未观察到漂移效应(超过8小时)和信号残留效应。对于浓度高于430,000国际单位/人绒毛膜促性腺激素(动态范围为10,000国际单位/升的一种检测方法),高剂量钩状效应较为明显。Elecsys检测方法显示出高动态范围,Elecsys仪器使用Elecsys多稀释剂很少需要进行预稀释。未观察到内源性干扰。校准稳定性已确认一周,数据表明其至少可延长至三周。质量保证实验表明,参与实验室之间结果的可转移性良好。对于大多数分析物,两种实验室间调查材料的指定值在±10%的偏差范围内。偏差较大可由标准化和方法的差异来解释。Elecsys 2010系统结合相对较少的样本量和较短的测量时间(≤18分钟)提供了高分析灵敏度;高动态测量范围减少了复测次数,使工作流程更便捷。Elecsys 2010的电化学发光技术在系统性能方面显示出优势,与现有技术相比没有任何缺点。

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