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比较四种不同粪便免疫化学检测系统报告的疑似结直肠癌和严重肠道疾病患者的粪便血红蛋白浓度和诊断准确性。

A comparison of the faecal haemoglobin concentrations and diagnostic accuracy in patients suspected with colorectal cancer and serious bowel disease as reported on four different faecal immunochemical test systems.

机构信息

Clinical Biochemistry, Royal Surrey County Hospital, Berkshire and Surrey Pathology Services, Guildford, Surrey, UK.

NHS Bowel Cancer Screening South of England Hub, Berkshire and Surrey Pathology Services, Guildford, Surrey, UK.

出版信息

Clin Chem Lab Med. 2022 Jun 1;60(8):1278-1286. doi: 10.1515/cclm-2021-1248. Print 2022 Jul 26.

DOI:10.1515/cclm-2021-1248
PMID:35637625
Abstract

OBJECTIVES

Faecal immunochemical tests for haemoglobin (FIT) are used in colorectal cancer (CRC) screening programmes and to triage patients presenting with symptoms suggestive of CRC for further bowel investigations. There are a number of quantitative FIT analytical systems available. Currently, there is no harmonisation or standardisation of FIT methods. The aim of the study was to assess the comparability of numerical faecal haemoglobin concentrations (f-Hb) obtained with four quantitative FIT systems and the diagnostic accuracy at different f-Hb thresholds.

METHODS

A subgroup of the National Institute for Health and Care Excellence (NICE) FIT study, a multicentre, prospective diagnostic accuracy study were sent four FIT specimen collection devices from four different FIT systems or two FIT devices for one FIT system. Faecal samples were examined and analysis of results carried out to assess difference between methods at thresholds of limit of detection (LoD), 10 µg haemoglobin/g faeces (µg/g) and 100 μg/g.

RESULTS

233 patients returned specimen collection devices for examination on four different systems; 189 patients returned two FIT kits for one system. At a threshold of 100 μg/g the sensitivity is the same for all methods. At lower thresholds of LoD and 10 μg/g differences were observed between systems in terms of patients who would be referred and diagnostic accuracies.

CONCLUSIONS

The lack of standardisation or harmonisation of FIT means that differences are observed in f-Hb generated on different systems. Further work is required to understand the clinical impact of these differences and to minimise them.

摘要

目的

粪便血红蛋白免疫化学检测(FIT)用于结直肠癌(CRC)筛查计划,并对有 CRC 症状提示的患者进行分诊,以进一步进行肠道检查。目前有许多定量 FIT 分析系统。目前,FIT 方法没有标准化或统一。本研究旨在评估四种定量 FIT 系统获得的数值粪便血红蛋白浓度(f-Hb)的可比性,以及不同 f-Hb 阈值下的诊断准确性。

方法

英国国家卫生与保健优化研究所(NICE)FIT 研究的一个亚组,是一项多中心、前瞻性诊断准确性研究,将来自四个不同 FIT 系统的四个 FIT 标本采集装置或一个 FIT 系统的两个 FIT 装置发送给四个不同的 FIT 系统。检查粪便样本并进行结果分析,以评估在检测限(LoD)、10μg 血红蛋白/g 粪便(μg/g)和 100μg/g 阈值下方法之间的差异。

结果

233 名患者返回了四个不同系统的标本采集装置进行检查;189 名患者返回了一个系统的两个 FIT 试剂盒。在 100μg/g 的阈值下,所有方法的灵敏度相同。在较低的 LoD 和 10μg/g 阈值下,系统之间在需要转诊的患者和诊断准确性方面存在差异。

结论

FIT 缺乏标准化或统一,导致在不同系统上生成的 f-Hb 存在差异。需要进一步研究以了解这些差异的临床影响,并尽量减少这些差异。

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