Literature DB >> 29884997

Shifting Landscape of Hemophilia Therapy: Implications for Current Clinical Laboratory Coagulation Assays.

Hanny Al-Samkari1,2, Stacy E Croteau3,2.   

Abstract

Clinical coagulation assays are an integral part of diagnosing and managing patients with hemophilia; however, in this new era of bioengineered factor products and non-factor 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. This article is protected by copyright. All rights reserved.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  Coagulation Factor Replacement therapies; Hemophilia; chromogenic substrate assay; extended half-life products; one stage clotting assay

Year:  2018        PMID: 29884997     DOI: 10.1002/ajh.25153

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  5 in total

Review 1.  Consensus recommendations on appropriate coagulation tests during emicizumab administration in Saudi Arabia.

Authors:  Tarek Owaidah; Abdulakareem Almomen; Ahmed Tarawah; Ashraf Warsi; Fawaz Alkasim; Hazzaa Alzahrani; Mahassen Saleh; Ohoud Kashari; Wasil Jastaniah
Journal:  Am J Blood Res       Date:  2022-06-20

2.  Intrinsic differences between FVIIIa mimetic bispecific antibodies and FVIII prevent assignment of FVIII-equivalence.

Authors:  Nina C Leksa; Maria M Aleman; Allison G Goodman; Deana Rabinovich; Robert Peters; Joe Salas
Journal:  J Thromb Haemost       Date:  2019-04-26       Impact factor: 5.824

3.  External qualification of the Web-Accessible Population Pharmacokinetic Service-Hemophilia (WAPPS-Hemo) models for octocog alfa using real patient data.

Authors:  Pierre Chelle; Dagmar Hajducek; Mohammed Mahdi; Stuart Young; Alfonso Iorio; Josh Silvertown; Andrea Edginton
Journal:  Res Pract Thromb Haemost       Date:  2021-11-02

4.  Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy.

Authors:  Yuki Hatayama; Toru Motokura; Yuzuru Hosoda; Sayaka Suzuki; Hiroya Namba; Konami Kato; Nao Kojima; Takuya Horie; Takuya Iwamoto; Noriko Yamashita; Hitomi Ichikawa; Tetsuya Fukuda
Journal:  Clin Appl Thromb Hemost       Date:  2022 Jan-Dec       Impact factor: 2.389

5.  Does difference between label and actual potency of factor VIII concentrate affect pharmacokinetic-guided dosing of replacement therapy in haemophilia A?

Authors:  Tine M H J Goedhart; Laura H Bukkems; Iris van Moort; Colin C Spence; Michel C Zwaan; Moniek P M de Maat; Ron A A Mathôt; Marjon H Cnossen
Journal:  Haemophilia       Date:  2022-05-08       Impact factor: 4.263

  5 in total

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