Evidence map›Paper›PMID 35418441›Full record

ArticleBMJ open2022

A cohort study of duplicate faecal immunochemical testing in patients at risk of colorectal cancer from North-West England.

Natalie Hunt, Christopher Rao, Robert Logan, Vishnu Chandrabalan, Jane Oakey, Claire Ainsworth, Neil Smith, Saswata Banerjee, Martin Myers

Abstract read
In one paragraph

Article in BMJ open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Observational
  3. Article
  4. Article
  5. Observational
  6. Review
  7. Faecal haemoglobin concentration and colorectal cancer site, stage and grade in a symptomatic cohort.Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland · 2024
    Article
  8. Review
  9. FIT for the future.Frontline gastroenterology · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Natalie HuntDepartment of Clinical Biochemistry, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK Natalie.Hunt@lthtr.nhs.uk.ORCID 0000-0003-3121-0740
Christopher RaoDepartment of Surgery and Cancer, Imperial College London, London, UK.
Robert LoganDepartment of Gastroenterology, King's College London, London, UK.
Vishnu ChandrabalanDepartment of Colorectal Surgery, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK.
Jane OakeyClinical Biochemistry, East Lancashire Hospitals NHS Trust, Blackburn, UK.
Claire AinsworthLancashire and South Cumbria Cancer Alliance, Preston, UK.
Neil SmithNHS Blackburn with Darwen CCG, Blackburn, UK.
Saswata BanerjeeBarking Havering and Redbridge Hospitals NHS Trust, Romford, UK.
Martin MyersDepartment of Clinical Biochemistry, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe sought to investigate if duplicate faecal immunochemical testing (FIT) sampling improves the negative and positive predictive value of patients thought to be at risk of colorectal cancer (CRC). Specifically, we aimed to investigate whether the proportion of FIT-negative CRC missed by a single FIT test in symptomatic patients could be reduced by duplicate FIT testing.

designA retrospective service evaluation cohort study of the diagnostic accuracy of duplicate FIT testing.

settingPatients referred from primary care with suspected CRC to four secondary care trusts in North-West England.

participants28 622 patients over 18-years-old with lower gastrointestinal symptoms suggestive of CRC who completed two FIT samples. PRIMARY AND SECONDARY OUTCOME MEASURES: The performance of duplicate FIT for detecting CRC at a threshold of 10 µgHb/g.

resultsThe sensitivity if either test was >10 µgHb/g was 0.978 (0.955-0.989), specificity was 0.662 (0.657-0.668), positive predictive value 0.031 (0.028-0.035) and negative predictive value 1.00 (0.999-1.00). Despite two-thirds of patients (18952) being negative following two tests, at this threshold only seven CRC were missed over a 26-month period. All seven patients had other high-risk features which should have prompted investigation.

conclusionsThis study suggests that in routine NHS practice, a duplicate FIT sample strategy together with clinical evaluation for evidence of anaemia and weight loss is superior to a single FIT sample alone and would allow symptomatic patients to be managed in primary care without the need for urgent referral to secondary care for urgent colonic imaging.

Indexed as

Colorectal NeoplasmsEarly Detection of CancerAdolescentCohort StudiesColonoscopyEnglandFecesHemoglobinsHumansOccult BloodRetrospective StudiesSensitivity and SpecificityHemoglobinsbiochemistryendoscopygastroenterologypathologyprimary care

Identifiers

PMID35418441
PMCPMC9014104

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.