Evaluation of chromogenic factor IX assays by automated protocols

被引:15
作者
Kershaw, G. W. [1 ,2 ]
Dissanayake, K. [1 ]
Chen, V. M. [2 ,3 ]
Khoo, T. -L. [1 ]
机构
[1] Royal Prince Alfred Hosp, Inst Haematol, Camperdown, NSW, Australia
[2] Univ Sydney, Anzac Res Inst, Sydney, NSW, Australia
[3] Concord Repatriat Gen Hosp, Dept Haematol, Concord, NSW, Australia
关键词
chromogenic; factor IX; haemophilia B; reference interval; reproducibility; spike recovery; MODIFIED FACTOR-VIII; ONE-STAGE; CLOTTING ASSAY; HEMOPHILIA-B; DISCREPANCIES; RECOMBINANT; FVIII; DIAGNOSIS; PRODUCTS;
D O I
10.1111/hae.13446
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionChromogenic substrate assays (CSA) to measure Factor IX (FIX) have recently become commercially available. However, information on their performance characteristics and use in diagnostic haemostasis laboratories remains limited. AimTo evaluate the Hyphen Biomed (Hyphen) and Rossix FIX CSAs on fully automated coagulation analysers and compare them to the FIX one-stage assay (OSA). This study was conducted in a tertiary referral haemostasis laboratory associated with a haemophilia treatment centre. MethodsAutomated CSA protocols were adapted to the Sysmex CS2500 (CS2500) and Diagnostica Stago STA-R (STA-R) analysers. Samples assayed were from healthy volunteers, haemophilia B patients and FIX deficient plasma spiked with either plasma derived, recombinant or extended half-life FIX products. ResultsReference intervals for Hyphen and Rossix assays were 73 IU/dL to 164 IU/dL and 73 IU/dL to 168 IU/dL, respectively, on the CS2500 analyser; and 84 IU/dL to 165 IU/dL for the Rossix assay on the STA-R. Repeatability across all method/analyser combinations resulted in CVs ranging from 0.8% to 5.4%. Between run reproducibility gave CVs <6.7% for all method/analyser combinations. In spiked samples, FIX recoveries were mostly within an acceptable limit of 10025% for BeneFIX((R)), Rixubis((R)) and Alprolix((R)) with some differences between CSAs. ConclusionBoth commercial factor FIX CSA kits can be adapted for Stago and Sysmex automated coagulation analysers. Reagent cost and workflow practices will need to be considered. These assays are potentially more consistent than OSA in measurement of replacement FIX products in haemophilia B patients.
引用
收藏
页码:492 / 501
页数:10
相关论文
共 22 条
[1]   MEASUREMENT IN MEDICINE - THE ANALYSIS OF METHOD COMPARISON STUDIES [J].
ALTMAN, DG ;
BLAND, JM .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES D-THE STATISTICIAN, 1983, 32 (03) :307-317
[2]  
[Anonymous], 2017, BEN COAG FACT 9 REC
[3]   Insights from factor IX activation studies with chromogenic assays: implications of disparate product results [J].
Barrowcliffe, T. W. .
HAEMOPHILIA, 2010, 16 :9-12
[4]   Standardization of FVIII & FIX assays [J].
Barrowcliffe, TW .
HAEMOPHILIA, 2003, 9 (04) :397-402
[5]   Measuring factor IX activity of nonacog beta pegol with commercially available one-stage clotting and chromogenic assay kits: a two-center study [J].
Bowyer, A. E. ;
Hillarp, A. ;
Ezban, M. ;
Persson, P. ;
Kitchen, S. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2016, 14 (07) :1428-1435
[6]   Accuracy of FVIII:C assay by one-stage method can be improved using hemophilic plasma as diluent [J].
Cinotti, S ;
Paladino, E ;
Morfini, M .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (04) :828-833
[7]  
Gray E, 2016, HAEMOPHILIA, V22, P70
[8]   Discrepancies between the one-stage clotting assay and the chromogenic assay in haemophilia B [J].
Kihlberg, K. ;
Strandberg, K. ;
Rosen, S. ;
Ljung, R. ;
Astermark, J. .
HAEMOPHILIA, 2017, 23 (04) :620-627
[9]   Recombinant to modified factor VIII and factor IX - chromogenic and one-stage assays issues [J].
Kitchen, S. ;
Kershaw, G. ;
Tiefenbacher, S. .
HAEMOPHILIA, 2016, 22 :72-77
[10]   A computer-based model to assess costs associated with the use of factor VIII and factor IX one-stage and chromogenic activity assays [J].
Kitchen, S. ;
Blakemore, J. ;
Friedman, K. D. ;
Hart, D. P. ;
Ko, R. H. ;
Perry, D. ;
Platton, S. ;
Tan-Castillo, D. ;
Young, G. ;
Luddington, R. J. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2016, 14 (04) :757-764