EPTIS
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Quantitative Faecal Hb (FHb)

[Quantitative Faecal Hb (FHb)]

EPTIS factsheet 1177234 | Last revision 2024-09-24 | URL: https://www.eptis.bam.de/pts1177234 https://www.eptis.bam.de/pts1177234

PT provider
PT provider Weqas Weqas
Based in United Kingdom
Language(s)
Remarks Faecal immunochemical tests (FIT) are designed to detect small amounts of blood in stool samples (faecal occult blood) using antibodies specific to human haemoglobin (Hb). These tests are recommended by NICE to guide referrals for suspected colorectal cancer in symptomatic patients. [DG 30 – quantitative faecal immunochemical tests to guide referral for colorectal cancer in primary care] and in NICE guideline [NG12: Suspected cancer: recognition and referral]. FIT is also recommended by the UK National Screening Committee and has replaced gFOBT as part of the testing strategy for the UK Bowel Cancer Screening Programmes. The base material is organic material which closely mirrors the basic constituents of human faeces to which a known quantity of Hb (as human whole blood) is added. Material at a range of Hb concentrations is prepared to cover the pathological and analytical range for FIT including samples at or near the clinical cut-off of 10 ug Hb /g used for symptomatic testing pathways and the higher cut offs used in asymptomatic population screening programmes. The homogeneous material is dispensed aseptically into buffered vials specific to each instrument manufacturer. The three samples per distribution is designed to assess laboratory and method performance, including linearity, bias, and within batch imprecision. Key Features: - Material closely mirrors the basic constituents of human faeces. - FIT samples are pre loaded into buffered collection tubes specific to each instrument. - Covers the pathological and analytical range for quantitative FIT automated analysers. - Samples challenging clinically relevant cut-offs for symptomatic testing pathways. For more information: https://www.weqas.com/services/eqa/quantitative-faecal-hb-fhb/ or contact@weqas.com
Keywords
Product groups Health care / medical devices
Testing fields Medical analysis
Technical details
Test item Tested property Testing method
Organic material spiked with human whole blood Quantitative FIT Routine testing methods (recommended)
Aims of the PT scheme
Target group of participants To assess performance of laboratories undertaking FIT as part of the diagnostic investigation of colorectal cancer in symptomatic patients and in the assessment of specialist centres using FIT for the asymptomatic population screening for colorectal cancer.
Linked to specific legislation / standards Accreditation by UKAS based on ISO/IEC 17043.
Additional, subsidiary aims validation of testing methods
Number of participants
Accredited or otherwise reviewed by a 3rd party

Accredited by UKAS on the basis of ISO/IEC 17043 for part of the parameters

Operation is commissioned / requested by
Fees and frequency
Participation fee https://www.weqas.com/participantzone/subscription-charges/
Regularly operated Yes (Frequency: Monthly. Samples: 3. )
Year of first operation 2015
Contact details of the PT provider
Provider Contact person
Weqas
Unit 6, Parc Ty Glas
CF14 5DU Cardiff
United Kingdom

Phone: 44 (0) 2920 314750
Fax:
Web: http://www.weqas.com http://www.weqas.com
Laura Lloyd-Lewis
Phone: 44 (0) 29218 32884
Fax:
Email: laura.lloyd-lewis@wales.nhs.uk laura.lloyd-lewis@wales.nhs.uk
If you find any mistakes please contact the responsible EPTIS coordinator in United Kingdom, Mr Savvas Xystouris. Mr Savvas Xystouris.
Any questions or problems? Please contact us at eptis@bam.de.
Application version: 1.23-SNAPSHOT.20230502124635-7925ae379a631fc1ececff45d2921c8db38877d5