Faecal immunochemical test (FIT) based prioritisation of new patient symptomatic cases referred for colorectal investigation.

IF 1.2 Q2 MEDICINE, GENERAL & INTERNAL NEW ZEALAND MEDICAL JOURNAL Pub Date : 2024-09-06 DOI:10.26635/6965.6582
James Falvey, Catherine M Stedman, Joel Dunn, Chris Sies, Susan Levin
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Abstract

Aim: Quantitative faecal haemoglobin (fHb) measurement by faecal immunochemical test (FIT) is a powerful biomarker for colorectal cancer (CRC) and is incorporated in referral, prioritisation and triage protocols for symptomatic cases in other countries. We report our use of FIT to prioritise new patient symptomatic cases referred for colorectal investigation.

Method: Cases referred for investigation of new colorectal symptoms who were aged ≥50 years (≥40 years Māori/Pacific peoples), who would otherwise be triaged to non-urgent colonoscopy, were asked to provide a stool sample for FIT. Following FIT testing, cases were re-triaged to either urgent colonoscopy, non-urgent colonoscopy or computed tomography colonography (CTC) depending on fHb concentration (measured in micrograms haemoglobin per gram of stool [mcg/g]) and incorporating clinical judgement. At pathway initiation, cases already waiting for colonoscopy on the non-urgent new patient waiting list were approached first, and then new patient (NP) referrals for colonoscopy could be triaged to the pathway at the discretion of the triaging consultant.

Results: Out of 739 cases, 715 (97%) returned FIT samples, and 691 cases completed colorectal investigations. Overall FIT positivity ≥10mcg/g was 17.1%. Fifteen colorectal cancers (CRC) were detected (2.2%). The sensitivity and specificity of FIT ≥10mcg/g for CRC were 80.0% (54.0-93.7%) and 84.3 (81.4-86.9%) respectively. A total of 432 cases (62.5%) completed the pathway without recourse to colonoscopy, and the median time to CRC diagnosis for NP from referral was 25 days.

Conclusion: FIT based prioritisation of cases referred with symptoms concerning for CRC is feasible and reduces time to CRC diagnosis.

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根据粪便免疫化学检验 (FIT) 确定转诊接受结直肠检查的无症状新病例的优先次序。
目的:通过粪便免疫化学试验(FIT)进行粪便血红蛋白(fHb)定量测定是结直肠癌(CRC)的有力生物标志物,其他国家已将其纳入无症状病例的转诊、优先排序和分流方案中。我们报告了使用 FIT 对转诊进行结直肠癌检查的新发无症状病例进行优先排序的情况:方法:要求年龄≥50 岁(毛利人/太平洋岛屿族裔≥40 岁)的新结直肠症状转诊病例提供粪便样本进行 FIT 检测,否则这些病例将被分流至非急诊结肠镜检查。FIT 检测后,根据 fHb 浓度(以每克粪便微克血红蛋白 [mcg/g] 为单位)并结合临床判断,病例被重新分流至急诊结肠镜检查、非急诊结肠镜检查或计算机断层扫描结肠成像 (CTC)。在路径启动时,首先接触非急诊新病人候诊名单上已在等待结肠镜检查的病例,然后由分诊顾问酌情将结肠镜检查的新病人(NP)转诊至路径:在 739 例病例中,715 例(97%)交回了 FIT 样本,691 例完成了结直肠检查。FIT阳性率≥10mcg/g的总体比例为17.1%。检测出 15 例结直肠癌 (CRC)(2.2%)。FIT ≥10mcg/g 对 CRC 的敏感性和特异性分别为 80.0% (54.0-93.7%) 和 84.3 (81.4-86.9%)。共有 432 个病例(62.5%)在未进行结肠镜检查的情况下完成了检查,NP 从转诊到确诊为 CRC 的中位时间为 25 天:结论:对有 CRC 相关症状的转诊病例进行基于 FIT 的优先排序是可行的,并能缩短 CRC 诊断时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
NEW ZEALAND MEDICAL JOURNAL
NEW ZEALAND MEDICAL JOURNAL MEDICINE, GENERAL & INTERNAL-
CiteScore
2.30
自引率
23.50%
发文量
229
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