Volume 44, Issue 3 pp. 619-625
ORIGINAL ARTICLE

External quality assessment for one-stage and chromogenic factor IX assays in samples containing Alprolix (rFIXFc) or Idelvion (rIX-FP) and evidence that UK National External Quality Assessment Scheme for blood coagulation samples are commutable with patient samples

Steve Kitchen

Corresponding Author

Steve Kitchen

Sheffield Haemophilia and Thrombosis Centre, Sheffield, UK

UK National External Quality Assessment Scheme for Blood Coagulation, Sheffield, UK

Correspondence

Dr Steve Kitchen, Department of Coagulation, Royal Hallamshire Hospital, Glossop Road, Sheffield S10 2JF, UK.

Email: [email protected]

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Annette Bowyer

Annette Bowyer

Sheffield Haemophilia and Thrombosis Centre, Sheffield, UK

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Anna Lowe

Anna Lowe

UK National External Quality Assessment Scheme for Blood Coagulation, Sheffield, UK

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Ian Jennings

Ian Jennings

UK National External Quality Assessment Scheme for Blood Coagulation, Sheffield, UK

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Isobel D. Walker

Isobel D. Walker

UK National External Quality Assessment Scheme for Blood Coagulation, Sheffield, UK

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First published: 17 January 2022

Funding information

No external funding was sought or received for this study.

Abstract

Introduction

There may be clinically relevant differences between results of different FIX assays in samples containing extended half life FIX concentrates requiring regular surveillance of assay results through proficiency testing exercises. Control materials used in proficiency testing must be commutable, that is have the same inter-assay properties as those demonstrated by authentic clinical samples when measured by different analytical methods.

Methods

We assessed relationships between results with different FIX assays and commutability of UK National External Quality Assessment Scheme (NEQAS) materials containing rIX-FP (Idelvion) or rFIXFc (Alprolix) by comparing results obtained using widely used one-stage and chromogenic assays during a proficiency testing exercise with results obtained when analysing a series of individual patient samples using the same assay systems. NEQAS samples prepared by addition of either Idelvion or Alprolix to FIX deficient plasma were sent to 76 haemophilia centres in Europe. A total of 18 Idelvion and 22 Alprolix patient samples were assayed in a single centre. Two chromogenic and two one-stage assays were compared.

Results

The pattern of results obtained for NEQAS samples and patient samples was similar. In all cases, the NEQAS sample data point was within the scatter of patient sample data in plots of patient sample results showing one-stage assay results using Synthasil or Actin FS plotted against chromogenic assay results with Biophen or Rox chromogenic FIX kits.

Conclusion

This indicates that the NEQAS samples containing Idelvion or Alprolix were commutable and therefore suitable for use in proficiency testing exercises.

CONFLICT OF INTEREST

AB and SK have received speaker fees from Sobi. Other authors have no competing interests.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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