Suppr超能文献

全自动降钙素原化学发光免疫分析方法的评估

Evaluation of a fully automated procalcitonin chemiluminescence immunoassay.

作者信息

Hubl Walter, Krassler Jens, Zingler Christiana, Pertschy Annette, Hentschel Jörg, Gerhards-Reich Christina, Mack Michael, Demant Thomas

机构信息

Institut für Klinische Chemie und Laboratoriumsmedizin, Krankenhaus Dresden-Friedrichstadt, Dresden, Germany.

出版信息

Clin Lab. 2003;49(7-8):319-27.

Abstract

We evaluated a new fully automated microparticle immunoassay for procalcitonin (LIAISON BRAHMS PCT) in comparison with a previously established manual chemiluminescence assay from the same manufacturer (LUMItest PCT, BRAHMS AG). Procalcitonin (PCT) is an early and rather specific marker of systemic bacterial infection. In addition, the efficacy of antibiotic therapy can be monitored by sequential analysis of PCT values. This is why rapid and accurate determinations of PCT are urgently required by intensive care units. The aim of this study was to evaluate in a clinical set-up a new fully automated rapid PCT test. Analytical results are compared with results obtained by a previously introduced quantitative manual test. Intra-assay coefficients of variation (CV) were found in the range of 0.94 to 7.1% at concentrations between 0.46 and 97.2 microg/l. Over a time period of 27 days the inter-assay CV was found below 4.0% at concentrations of 1.93 and 14.29 microg/l and 9.9% at 0.40 microg/l. The functional sensitivity at a CV level of 20% was determined as 0.2 microg/l. Linearity could be demonstrated in a concentration range from 0 to 445 microg/l. When serum and plasma with EDTA, citrate or heparin anti-coagulation were analyzed in parallel, no systematic bias was found. A method comparison by regression analysis showed PCT values determined by both tests in very good agreement (r = 0.99). PCT concentrations in apparently healthy subjects (n =101) were below 0.58 microg/l in line with previously published results. Patients with sepsis (n = 43) or with infectious adult respiratory distress syndrome (ARDS) (n = 28) showed median values of 22.2 and 18.9 microg/l, respectively. In a clinical set-up the LIAISON Brahms PCT assay provided rapid and accurate PCT results supporting the early detection of severe sepsis, the differentiation between systemic bacterial infection and other inflammatory diseases, and the monitoring of antibiotic therapy in septic patients. The results of the new LIAISON BRAHMS PCT assay show an excellent concordance with the LUMItest PCT. The clinical information derived from the measurements is well comparable to the results obtained with the LUMItest PCT, too.

摘要

我们评估了一种新的降钙素原全自动微粒免疫分析方法(LIAISON BRAHMS PCT),并与同一制造商先前建立的手动化学发光分析方法(LUMItest PCT,BRAHMS AG)进行了比较。降钙素原(PCT)是全身性细菌感染的一种早期且相当特异的标志物。此外,通过连续分析PCT值可监测抗生素治疗的效果。这就是重症监护病房迫切需要快速、准确测定PCT的原因。本研究的目的是在临床环境中评估一种新的全自动快速PCT检测方法。将分析结果与先前引入的定量手动检测方法所获得的结果进行比较。在浓度为0.46至97.2微克/升之间时,批内变异系数(CV)在0.94%至7.1%范围内。在27天的时间段内,浓度为1.93和14.29微克/升时批间CV低于4.0%,在0.40微克/升时为9.9%。在CV水平为20%时的功能灵敏度确定为0.2微克/升。在0至445微克/升的浓度范围内可证明线性关系。当对含有EDTA、柠檬酸盐或肝素抗凝剂的血清和血浆进行平行分析时,未发现系统偏差。通过回归分析进行的方法比较显示,两种检测方法测定的PCT值非常一致(r = 0.99)。明显健康受试者(n = 101)的PCT浓度低于0.58微克/升,与先前发表的结果一致。脓毒症患者(n = 43)或感染性成人呼吸窘迫综合征(ARDS)患者(n = 28)的中位数分别为22.2和18.9微克/升。在临床环境中,LIAISON Brahms PCT检测方法提供了快速、准确的PCT结果,有助于早期检测严重脓毒症、区分全身性细菌感染和其他炎症性疾病以及监测脓毒症患者的抗生素治疗。新的LIAISON BRAHMS PCT检测方法的结果与LUMItest PCT显示出极好的一致性。从测量中获得的临床信息与LUMItest PCT所获得的结果也具有很好的可比性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验