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Fetal Fibronectin

[Fetal Fibronectin]

EPTIS factsheet 1177150 | Last revision 2025-03-17 | URL: https://www.eptis.bam.de/pts1177150 https://www.eptis.bam.de/pts1177150

PT provider
PT provider Weqas Weqas
Based in United Kingdom
Language(s)
Remarks Preterm labour is defined as regular contractions of the uterus resulting in changes in the cervix that start before 37 weeks of pregnancy. Point of care (POC) biomarker tests PartoSure, Actim Partus and quantitative Rapid fetal fibronectin (fFN) are intended for use with other clinical information to assess the risk of preterm birth in women with symptoms of preterm labour who have intact amniotic membranes. fFN is an adhesive glycoprotein that holds the membranes of the uterus to the fetal membranes. After 35 weeks of pregnancy, it begins to break down naturally, and is detectable in vaginal secretions. A positive result indicates an increased risk of pre-term labour and is useful in aiding patient management. The negative predictive value (NPV) of the test at 10 ng/mL is quoted as 100%, with a NPV at 50 ng/mL of 99.2%. The manufacturers quote a cut-off of >50 ng/mL as a positive result; indicating the likelihood of a preterm birth within the following 14 days. Further information is provided in NICE guideline on preterm labour and birth {NG25} Weqas offers 3 separate programmes, one for qualitative and quantitative fFn and separate programmes for phIGFBP-1 and PAMG-1. Key Features: - Liquid stable samples supplied ready to use for fFN and phIGFBP-1; no pre-analytical preparation is required. - Qualitative and Quantitative reporting available. - Linear related panel distributed covering the clinically relevant range. - Programme assesses both site and device performance, including bias, within and between batch imprecision and linearity for quantitative analytes. - Diagnostic accuracy assessed for the qualitative analytes. - Scoring based on Milan Model 3 performance specification. For more information: https://www.weqas.com/services/poct-eqa/pre-term-labour-markers/ or contact@weqas.com For information on POCT PROM https://www.weqas.com/services/poct-eqa/igfbp-1/ or contact@weqas.com
Keywords
Product groups Health care / medical devices
Testing fields Medical analysis
Technical details
Test item Tested property Testing method
Synthetic Amniotic Fluid containing purified fFN, phIGFBP-1 or PAMG-1 Quantitative fFN Routine testing methods (recommended)
Qualitative fFN Routine testing methods (recommended)
phIGFBP-1 Routine testing methods (recommended)
PAMG-1 Routine testing methods (recommended)
Aims of the PT scheme
Target group of participants Programme assesses both site and device performance, including bias, within and between batch imprecision and linearity for quantitative analytes.
Linked to specific legislation / standards Accreditation by UKAS based on ISO/IEC 17043. *PAM-1 Pilot programme for 2025. Currently not accredited.
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 *PAM-1 Pilot programme for 2025. Currently not accredited.

Operation is commissioned / requested by
Fees and frequency
Participation fee https://www.weqas.com/participantzone/subscription-charges/
Regularly operated Yes (Frequency: Bimonthly. Samples: 2 x 1.0ml for phIGFBP-1, 2 x 0.5mL for fFN and PAMG-1. )
Year of first operation 2013
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