Impact of introducing a faecal immunochemical test (FIT) for haemoglobin into primary care on the outcome of patients with new bowel symptoms: a prospective cohort study.

bowel disease colorectal cancer colorectal disease faecal biomarkers faecal haemoglobin faecal immunochemical test primary care

Journal

BMJ open gastroenterology
ISSN: 2054-4774
Titre abrégé: BMJ Open Gastroenterol
Pays: England
ID NLM: 101660690

Informations de publication

Date de publication:
2019
Historique:
received: 25 02 2019
revised: 28 03 2019
accepted: 01 04 2019
entrez: 6 7 2019
pubmed: 6 7 2019
medline: 6 7 2019
Statut: epublish

Résumé

To determine whether a faecal immunochemical test (FIT) for faecal haemoglobin concentration (f-Hb) can be safely implemented in primary care as a rule-out test for significant bowel disease (SBD) (colorectal cancer (CRC), higher risk adenoma (HRA) and inflammatory bowel disease (IBD)) when used as an adjunct to the clinical assessment of new bowel symptoms. Single-centre prospective cohort study of all patients who attended primary care and submitted a FIT in the first calendar year of the service beginning December 2015. f-Hb was estimated using HM-JACKarc (Kyowa Medex) with a clinical cut-off of ≥10 µg Hb/g faeces. Incident cases of CRC were verified via anonymised record linkage to the Scottish Cancer Registry. 5422 patients submitted 5660 FIT specimens, of which 5372 were analysed (positivity: 21.9%). 2848 patients were referred immediately to secondary care and three with f-Hb <10 µg/g presented acutely within days with obstructing CRC. 1447 completed colonoscopy in whom overall prevalence of SBD was 20.5% (95 CRC (6.6%), 133 HRA (9.2%) and 68 IBD (4.7%)); 6.6% in patients with f-Hb <10 µg/g vs 32.3% in patients with f-Hb ≥10 µg/g. One CRC was detected at CT colonoscopy. 2521 patients were not immediately referred (95.3% had f-Hb <10 µg/g) of which four (0.2%) later developed CRC. Record linkage identified no additional CRC cases within a follow-up period of 23-35 months. In primary care, measurement of f-Hb, in conjunction with clinical assessment, can safely and objectively determine a patient's risk of SBD.

Identifiants

pubmed: 31275586
doi: 10.1136/bmjgast-2019-000293
pii: bmjgast-2019-000293
pmc: PMC6577357
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e000293

Subventions

Organisme : Chief Scientist Office
ID : ASM/14/04
Pays : United Kingdom

Déclaration de conflit d'intérêts

Competing interests: CGF has undertaken paid consultancy with Immunostics, Ocean, NJ, USA, and Kyowa Medex, Tokyo, Japan, and has received support for attendance at conferences from Alpha Labs, Eastleigh, Hants, UK.

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Auteurs

Craig Mowat (C)

Department of Gastroenterology, Ninewells Hospital and Medical School, Dundee, UK.

Jayne Digby (J)

Centre for Research into Cancer Prevention and Screening, University of Dundee, Dundee, UK.

Judith A Strachan (JA)

Department of Blood Sciences, Ninewells Hospital and Medical School, Dundee, UK.

Rebecca McCann (R)

Department of Blood Sciences, Ninewells Hospital and Medical School, Dundee, UK.

Christopher Hall (C)

Health Informatics Centre, University of Dundee, Dundee, UK.

Duncan Heather (D)

Health Informatics Centre, University of Dundee, Dundee, UK.

Francis Carey (F)

Department of Pathology, Ninewells Hospital and Medical School, Dundee, UK.

Callum G Fraser (CG)

Centre for Research into Cancer Prevention and Screening, University of Dundee, Dundee, UK.

Robert J C Steele (RJC)

Centre for Research into Cancer Prevention and Screening, University of Dundee, Dundee, UK.

Classifications MeSH