EPTIS
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POCT PROM

[POCT PROM]

EPTIS Ringversuch Nr. 1177173 | Letze Änderung 2024-09-24 | URL: https://www.eptis.bam.de/pts1177173 https://www.eptis.bam.de/pts1177173

Name des Anbieters
Name des Anbieters Weqas Weqas
Ansässig in United Kingdom
Sprache(n)
Anmerkungen Premature rupture of the membranes (PROM) at term occurs in 5 to 10% of pregnancies and pre-term PROM (PROM<37 weeks’ gestation) occurs in approximately a third of all premature births and is associated with significant neonatal morbidity and mortality. Without clear evidence of amniotic fluid loss observed by speculum examination, the diagnosis of PROM can be uncertain and complementary diagnostic tests are recommended [NG25]. Amniotic fluid specific biomarkers tests from PROM commercially available in the UK include insulin-like growth factor binding protein-1 (IGFBP-1 - Actim® PROM) and placental alpha microglobulin-1 (PAMG-1 - AmniSure®). IGFBP-1 is a 25kD protein synthesized in the decidual cells and foetal liver and is secreted into amniotic fluid. This programme covers the qualitative assessment of IGFBP-1. Purified human IGFBP-1 is added to an artificial amniotic fluid buffer base to produce a high positive base. The high positive base is further diluted with the negative base to create a series of samples spanning the analytical range. Each of the samples are distributed on 2-3 occasions to allow for the assessment of between batch variability. Two samples are distributed bi-monthly, providing 12 samples over the year. Key Features: - Liquid stable samples are supplied ready to use; no pre-analytical preparation is required. - Qualitative reporting available, with interpretations based on cut-offs of 25 ug/L. - Linear related panel distributed covering the clinically relevant range. - Programme assesses diagnostic accuracy at a range of concentrations including near the diagnostic threshold. For more information: https://www.weqas.com/services/poct-eqa/igfbp-1/ or contact@weqas.com For information on Fetal Fibronectin (fFN) and phIGFBP-1: https://www.weqas.com/services/poct-eqa/pre-term-labour-markers/ or contact@weqas.com
Klassifizierung
Produktgruppen Health care / medical devices
Prüfgebiete Medical analysis
Technische Einzelheiten
Prüfobjekt Prüfeigenschaft Prüfmethode
Synthetic Amniotic fluid containing semi-purified IGFBP-1 IGFBP-1 Routine testing methods (recommended)
Ringversuchsziele
Zielgruppe des Ringversuchs The programme assesses the diagnostic accuracy of the test, specificity and sensitivity at a range of IGFBP-1 concentrations including the diagnostic threshold.
Relevante Rechtsvorschriften oder Normen Accreditation by UKAS based on ISO/IEC 17043.
Weitere Ziele validation of testing methods
Teilnehmerzahl
Anbieter unabhängig überprüft (akkreditiert, benannt, anerkannt)

Akkreditiert durch UKAS auf der Grundlage von ISO/IEC 17043 nicht für alle Parameter

Die Durchführung des Ringversuchs ist in Auftrag gegeben durch
Kosten
Teilnahmegebühr https://www.weqas.com/participantzone/subscription-charges/
Regelmässig durchgeführt Ja (Frequency: Bimonthly. Samples: 2 x 1.0mL. )
Der Ringversuch wird durchgeführt seit 2013
Kontaktdaten des Anbieters
Anbieter Kontaktperson
Weqas
Unit 6, Parc Ty Glas
CF14 5DU Cardiff
United Kingdom

Telefon: 44 (0) 2920 314750
Fax:
Web: http://www.weqas.com http://www.weqas.com
Laura Lloyd-Lewis
Telefon: 44 (0) 29218 32884
Fax:
E-Mail: laura.lloyd-lewis@wales.nhs.uk laura.lloyd-lewis@wales.nhs.uk
Haben Sie einen Fehler entdeckt? Bitte wenden Sie sich an den zuständigen EPTIS Koordinator für United Kingdom, Mr Savvas Xystouris. Mr Savvas Xystouris.
Haben Sie Fragen? Senden Sie uns eine E-Mail: eptis@bam.de.
Anwendungsversion: 1.23-SNAPSHOT.20230502124635-7925ae379a631fc1ececff45d2921c8db38877d5