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HIL Serum Indices

[HIL Serum Indices]

EPTIS factsheet 1177186 | Last revision 2024-09-24 | URL: https://www.eptis.bam.de/pts1177186 https://www.eptis.bam.de/pts1177186

PT provider
PT provider Weqas Weqas
Based in United Kingdom
Language(s)
Remarks Most manufacturers now include Haemolytic / Icteric / Lipaemic (HIL) Indices as part of their testing repertoire as a means of identifying these interfering parameters. The three major sample interferences found to affect the accuracy and reliability of most laboratory results are haemoglobin, lipaemia and Icterus. The aim of the Weqas HIL Serum Indices programme is to assess: the ability of the analysers HIL indices test to identify the presence of these potential interference, to determine how laboratories deal with results where indices suggest that interferences are present and to promote the harmonisation of reporting. The programme provides 3 monthly samples containing either no interferant, bilirubin, haemoglobin, intralipid (surrogate marker of turbidity) or a mix of interferants at a range of concentrations. A batch is prepared every 6 months consisting of 14 serum pools: 3 haemolysed, 3 icteric, 3 intralipid, 4 mixed and 1 negative. A total of 18 samples are dispatched every 6 months, with some pools dispatched on more than one occasion. The target value is assigned from the calculated gravimetric addition of the interferant, supported by the quantitative analysis of bilirubin, haemoglobin and triglyceride (as an approximate verification of the concentration of intralipid). Both semi-quantitative and qualitative results are accommodated. Key Features: - Liquid stable samples are supplied ready to use; no pre-analytical preparation is required. - Quantitative and qualitative reporting available. - Full range of HIL indices covered; samples with individual and combined indices distributed to assess potential interferences. For more information: https://www.weqas.com/services/eqa/serum-indices/ or contact@weqas.com
Keywords
Product groups Health care / medical devices
Testing fields Medical analysis
Technical details
Test item Tested property Testing method
Off the clot human serum Semi-Quantitative Haemolysis Index Routine testing methods (recommended)
Semi-Quantitative Icterus Index Routine testing methods (recommended)
Semi-Quantitative Lipaemic Index Routine testing methods (recommended)
Qualitative Haemolysis Index Routine testing methods (recommended)
Qualitative Icterus Index Routine testing methods (recommended)
Qualitative Lipaemic Index Routine testing methods (recommended)
Aims of the PT scheme
Target group of participants The clinical usefulness of laboratory test results depends on performance evaluation and detection of errors including those that affect the integrity of the sample and presence of interferants in that sample.
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 x 1.0mL. )
Year of first operation 2016
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