通过床旁检测平台 IchromaTM II 对样本类型和储存条件对肿瘤标志物测量的分析前影响进行性能评估和特征描述。

IF 3.2 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinica Chimica Acta Pub Date : 2024-08-05 DOI:10.1016/j.cca.2024.119902
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引用次数: 0

摘要

为有效预防、诊断和监测癌症,应定期准确测量肿瘤标志物。我们旨在分析影响床旁检测(POCT)平台 IchromaTM II(韩国江原道 Boditech Med 公司)甲胎蛋白(AFP)、癌胚抗原(CEA)和前列腺特异性抗原(PSA)分析性能的分析前因素,并评估其在临床实践中的影响。根据 CLSI 指南对 IchromaTM II 的分析性能(包括精密度、线性和方法比较)进行了全面评估,并对样品类型和条件的分析前因素进行了广泛分析。共使用了来自 40 名患者的 5 种样本类型(血清、血浆(PL)和 EDTA 管全血(WB)、肝素钠管全血和 WB),以比较样本类型之间的差异。此外,还评估了室温下 21 小时、冷藏 8 天和冷冻 16 周的稳定性。所有三种肿瘤标记物的精确度、线性度以及与中心实验室分析仪的相关性都在可接受的标准范围内。然而,根据样本类型和储存条件的不同,观察到的百分比偏差程度也不同。只有 EDTA PL 样品在室温或冷藏条件下储存时,三种肿瘤标记物的百分比偏差都在临床可接受的范围内。在冷冻保存条件下,CEA 和 PSA 在 16 周前的保存时间内都出现了正偏差。虽然 IchromaTM II 作为一种操作程序简单的 POCT 平台,在肿瘤标志物的测量方面显示出了足够的分析性能,但临床实验室在实际使用不同类型的血液标本时应注意稳定性问题。
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Performance evaluation and characterization of pre-analytical effects by sample types and storage conditions on tumor marker measurement by the point-of-care test platform IchromaTM II

Tumor markers should be measured regularly and accurately to prevent, diagnose, and monitor cancers efficiently. We aimed to characterize the pre-analytical factors effecting on the analytical performance of point-of-care test (POCT) platform IchromaTM II (Boditech Med Inc., Gangwon-do, Korea) for alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), and prostate specific antigen (PSA) and evaluate their consequences in clinical practice. Based on comprehensive evaluation for the analytical performance of IchromaTM II including precision, linearity, and method comparison performed according to CLSI guidelines, pre-analytical factors of sample types and conditions were extensively analyzed. A total of five sample types [serum, plasma (PL) and whole blood (WB) from EDTA tube, PL and WB from sodium heparin tube] from 40 patients were used for comparing among specimen types. Additionally, stability was assessed up to 21 h at room temperature, refrigerated for 8 days, and frozen for 16 weeks by using 4 levels of pooled patient samples which were measured in triplicate. Precision, linearity and correlation with central laboratory analyzers observed in all three tumor markers were within acceptable criteria. However, variable degrees of percent deviations were observed according to sample type and storage conditions. Only EDTA PL samples presented clinically acceptable percentage biases for all three tumor markers when stored at room temperature or refrigerated condition. Positive bias of CEA and PSA in storage duration until 16 weeks were observed when stored in frozen condition. While IchromaTM II showed an adequate analytical performance as a POCT platform with simple operating procedures for the measurement of tumor markers, clinical laboratories should be aware of stability issues when different types of blood specimens are practically utilized.

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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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