Shifting landscape of hemophilia therapy: Implications for current clinical laboratory coagulation assays

被引:25
作者
Al-Samkari, Hanny [1 ,2 ]
Croteau, Stacy E. [2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Canc Ctr, Ctr Hematol, Boston, MA 02114 USA
[2] Harvard Med Sch, Boston, MA USA
[3] Boston Childrens Hosp, Boston Hemophilia Ctr, Boston, MA USA
关键词
FACTOR-VIII ACTIVITY; FC FUSION PROTEIN; RECOMBINANT FACTOR-IX; HUMAN DOSE TRIAL; ONE-STAGE ASSAY; THROMBIN GENERATION; BISPECIFIC ANTIBODY; PHARMACOKINETIC PROPERTIES; HEMOSTASIS LABORATORIES; CHROMOGENIC SUBSTRATE;
D O I
10.1002/ajh.25153
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Clinical coagulation assays are an integral part of diagnosing and managing patients with hemophilia; however, in this new era of bioengineered factor products and nonfactor therapeutics, problems have arisen with use of traditional coagulation tests for the quantification of several of these new products. Discussion over the use of one-stage clotting assays versus chromogenic substrate assays for clinical decision making and potency labeling has been ongoing for many years. Emerging factor concentrates have heightened concern over assay selection and availability. Emicizumab interferes with all aPTT based assays, rendering them unreliable and potentially falsely reassuring to the unaware provider. This review explores considerations for coagulation assays in the clinical setting and highlights how awareness of institutional coagulation assays and potential limitations have never been more critical for providers caring for patients with bleeding disorders.
引用
收藏
页码:1082 / 1090
页数:9
相关论文
共 73 条
[1]  
[Anonymous], 2017, HEML EM KXWH PACK IN
[2]   Factor VIII and thrombin generation assays: relevance to pharmacokinetic studies in haemophilia A [J].
Barrowcliffe, T. W. .
HAEMOPHILIA, 2006, 12 :23-29
[3]   Monitoring haemophilia severity and treatment: new or old laboratory tests? [J].
Barrowcliffe, TW .
HAEMOPHILIA, 2004, 10 :109-114
[4]   Discrepancies in potency assessment of recombinant FVIII concentrates [J].
Barrowcliffe, TW ;
Raut, S ;
Hubbard, AR .
HAEMOPHILIA, 1998, 4 (04) :634-640
[5]   Standardization of FVIII & FIX assays [J].
Barrowcliffe, TW .
HAEMOPHILIA, 2003, 9 (04) :397-402
[6]  
BARROWCLIFFE TW, 1993, THROMB HAEMOSTASIS, V70, P433
[7]   POTENCY OF HIGH-PURITY FACTOR-VIII CONCENTRATES [J].
BARROWCLIFFE, TW ;
WATTON, J ;
HARMAN, A ;
TUBBS, JE ;
KEMBALLCOOK, G .
LANCET, 1990, 336 (8707) :124-124
[8]   THE ASSAY OF ANTIHAEMOPHILIC-GLOBULIN ACTIVITY [J].
BIGGS, R ;
EVELING, J ;
RICHARDS, G .
BRITISH JOURNAL OF HAEMATOLOGY, 1955, 1 (01) :20-34
[9]   The coagulation laboratory monitoring of Afstyla single-chain FVIII concentrate [J].
Bowyer, A. ;
Key, N. ;
Dalton, D. ;
Kitchen, S. ;
Makris, M. .
HAEMOPHILIA, 2017, 23 (05) :e469-e470
[10]   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