A-104 宫颈结节细针穿刺中甲状腺球蛋白和降钙素的基质效应研究

IF 7.1 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
D Canali, G Zampieri, C Bonato, G Francisco, C Sabino, V Oliveira, A Lopes
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Such parameters involved doping, which corresponds to the introduction of a calibrator with a known and traceable value into a pool of puncture material that is known to be negative, in order to analyze the behavior of the results obtained, paying attention to the deviations that may eventually occur due to the interference of the characteristics of the puncture material. puncture. After doping the material, dilutions were performed up to the sensitivity limit of the test, also analyzing the functional sensitivity, where ten replicates of the material were dosed, thus obtaining CV%, mean and Standard Deviation values. The same process was carried out and evaluated using the serum material. During the entire process, the materials received and analyzed were centrifuged and always kept in a refrigerated environment. 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引用次数: 0

摘要

背景 在 ACCESS 设备上使用贝克曼库尔特试剂分析宫颈甲状腺球蛋白结节的细针穿刺材料,在 Immulite 设备上使用西门子试剂分析降钙素。分析了基质效应、线性度和分析灵敏度极限。本研究旨在分析供应商包装说明书中描述的血清/血浆检测结果与穿刺基质检测结果之间的相关性。方法 根据 ANVISA RDC 166/2017 的建议,按照实验室操作程序对性能特征进行测试。这些参数涉及掺杂,即在已知为阴性的穿刺材料池中引入已知且可溯源的校准物,以分析所获结果的行为,同时注意由于穿刺材料特性的干扰而最终可能出现的偏差。掺入材料后,稀释至测试的灵敏度极限,同时分析功能灵敏度,在此过程中掺入 10 次材料,从而获得 CV%、平均值和标准偏差值。对血清材料也进行了同样的处理和评估。在整个过程中,接收和分析的材料都经过离心,并始终保存在冷藏环境中。结果 宫颈吸液穿刺基质效应研究的回收率在预期范围内,从 80% 到 120% 不等,与供应商包装说明书中提到的血清/血浆相比也是如此。甲状腺球蛋白的功能灵敏度研究显示,CV% 为 1.77%,低于包装说明书中的建议值(2.2%);降钙素分析物的功能灵敏度研究显示,CV% 为 8.49%,低于包装说明书中的建议值(15.7%),此外,CV 值还低于 ANVISA 建议的 20%。血清基质效应研究的结果也显示出 80% 到 120% 之间的数值,两者一致。结论 结果表明,细针抽吸法测得的降钙素和甲状腺球蛋白性能优异,与供应商包装说明书中描述的血清数据一致,因此该试剂可用于宫颈穿刺基质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A-104 Study of the matrix effect for thyroglobulin and calcitonin in fine-needle aspiration of cervical nodules
Background Analysis of material from fine needle aspiration of cervical thyroglobulin nodules with Beckman Coulter reagents on the ACCESS equipment and Calcitonin using the Siemens reagent on the Immulite equipment. The matrix effect, linearity and the limit of analytical sensitivity were analyzed. This study aims to analyze the correlation between the serum/plasma results described in the suppliers' package inserts with the results obtained with the puncture matrix. Methods The performance characteristics were tested according to the laboratory's operating procedures, based on the recommendations of ANVISA RDC 166/2017. Such parameters involved doping, which corresponds to the introduction of a calibrator with a known and traceable value into a pool of puncture material that is known to be negative, in order to analyze the behavior of the results obtained, paying attention to the deviations that may eventually occur due to the interference of the characteristics of the puncture material. puncture. After doping the material, dilutions were performed up to the sensitivity limit of the test, also analyzing the functional sensitivity, where ten replicates of the material were dosed, thus obtaining CV%, mean and Standard Deviation values. The same process was carried out and evaluated using the serum material. During the entire process, the materials received and analyzed were centrifuged and always kept in a refrigerated environment. Results The recovery% of the matrix effect study for cervical aspirate puncture showed results within the expected range, ranging from 80% to 120%, as well as the results compared with serum/plasma referenced in the supplier's package insert. The functional sensitivity study for Thyroglobulin showed a CV% of 1.77%, being lower than that recommended by the package insert (2.2%) and for the Calcitonin analyte, the functional sensitivity study showed a CV% of 8.49%, being lower than recommended by the package leaflet (15.7%), in addition to having CV's lower than the 20% recommended by ANVISA. The results obtained with the matrix effect study for serum also showed values between 80% and 120%, both of which agreed. Conclusions The results showed excellent performance for material from fine needle aspiration for both Calcitonin and Thyroglobulin, being consistent with the serum data described by the suppliers' package inserts, thus making the reagent usable for the cervical aspirate puncture matrix.
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来源期刊
Clinical chemistry
Clinical chemistry 医学-医学实验技术
CiteScore
11.30
自引率
4.30%
发文量
212
审稿时长
1.7 months
期刊介绍: Clinical Chemistry is a peer-reviewed scientific journal that is the premier publication for the science and practice of clinical laboratory medicine. It was established in 1955 and is associated with the Association for Diagnostics & Laboratory Medicine (ADLM). The journal focuses on laboratory diagnosis and management of patients, and has expanded to include other clinical laboratory disciplines such as genomics, hematology, microbiology, and toxicology. It also publishes articles relevant to clinical specialties including cardiology, endocrinology, gastroenterology, genetics, immunology, infectious diseases, maternal-fetal medicine, neurology, nutrition, oncology, and pediatrics. In addition to original research, editorials, and reviews, Clinical Chemistry features recurring sections such as clinical case studies, perspectives, podcasts, and Q&A articles. It has the highest impact factor among journals of clinical chemistry, laboratory medicine, pathology, analytical chemistry, transfusion medicine, and clinical microbiology. The journal is indexed in databases such as MEDLINE and Web of Science.
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