Measuring factor VIII activity in patients with severe haemophilia A treated with extended half-life concentrates – comparison of selected assay results
																	
									Authors:
											M.- Prudková						1 3; 											P. Smejkal						1,3; 											D. Chytrá						1,3; 											J. Zavřelová						1,3; 											G.- Romanová						1 3; 											M. Penka						1,2; 											A. Buliková						1,2										
				
									Authors‘ workplace:
											Oddělení klinické hematologie, FN Brno
						1; 											Interní hematologická a onkologická klinika LF MU a FN Brno
						2; 											Katedra laboratorních metod, LF MU, Brno
						3										
				
									Published in:
					Transfuze Hematol. dnes,30, 2024, No. 4, p. 243-252.
					
				
									Category:
					Original Papers
					
				
									doi:
					
						https://doi.org/10.48095/cctahd2024prolekare.cz16
					
							
Overview
Introduction: Optimal substitutional treatment includes measuring FVIII activity (FVIII: C) using the one-stage clotting assay (OSA) or chromogenic substrate assay (CSA). However, with the advent of FVIII concentrates with an extended half-life, discrepancies between methods have increased due to modifications of the FVIII molecule. Aim: Evaluation of OSA and CSA discrepancy in patients treated with extended half--life FVIII concentrates. Method: FVIII: C measurement by OSA with reagents Cephascreen® (Diagnostica Stago) and Pathromtin® SL (Siemens Healthineers) and by CSA BIOPHENTM FVIII: C (Hyphen BioMed) in patients treated with efmoroctocog alfa, rurioctocog alfa pegol, turoctocog alfa pegol and damoctocog alfa pegol. Results: The results of both methods correlated well for efmoroctocog alfa, the differences being up to 21%. The results of rurioctocog alfa pegol in the range of 15–200% were slightly lower using OSA with both reagents, on average by 11% and 18%, while the results up to 10% were higher using OSA with an average difference of 54% for Cephascreen® and up to 75% for Pathromtin® SL. The results of turoctocog alfa pegol were lower using OSA in the range of 15–200%, on average by 36% and 25%. The samples with FVIII: C above 10% of damoctocog alfa pegol were slightly higher using OSA (Cephascreen® by 18%), but samples up to 10% were significantly higher, with Cephascreen® on average by 91% and by 100% with Pathromtin® SL. Conclusions: OSA Cephascreen® or Pathromtin® SL and CSA Hyphen correlate excellently in the case of efmoroctocog alfa. Of the other concentrates, the results correlate excellently in the case of rurioctocog alfa pegol (only Cephascreen®) and damoctocog alfa pegol, and only for FVIII: C > 10%.
Keywords:
haemophilia A – FVIII activity – EHL concentrates
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Haematology Internal medicine Clinical oncologyArticle was published in
Transfusion and Haematology Today
					2024 Issue 4
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