Literature DB >> 23546724

Nijmegen-Bethesda assay to measure factor VIII inhibitors.

Elizabeth Duncan1, Margaret Collecutt, Alison Street.   

Abstract

Hemophilia A is an inherited bleeding disorder caused by a deficiency of factor VIII coagulant activity (FVIII:C). Patients are treated with infusions of either plasma-derived or recombinant factor VIII. However, some patients develop inhibitory antibodies (inhibitors) to infused factor VIII which render it ineffective. The original Bethesda method was developed to standardize measurement of inhibitors in a factor VIII neutralization assay. One Bethesda unit is defined as that amount of inhibitor that results in 50% residual FVIII:C activity of a defined test mixture. In the Nijmegen modification of the original Bethesda method, the pH and the protein concentration of the test mixture is further standardized. As a result, the FVIII:C in the test mixture is less prone to artifactual deterioration and the test has improved specificity. Even with a standardized procedure a number of factors can affect the performance of the test and it is important for laboratory staff to be aware of their impact on the result outcome.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23546724     DOI: 10.1007/978-1-62703-339-8_24

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  8 in total

1.  Improved coagulation and haemostasis in haemophilia with inhibitors by combinations of superFactor Va and Factor VIIa.

Authors:  Vikas Bhat; Annette von Drygalski; Andrew J Gale; John H Griffin; Laurent O Mosnier
Journal:  Thromb Haemost       Date:  2015-10-15       Impact factor: 5.249

Review 2.  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

3.  Detailed analysis of anti-emicizumab antibody decreasing drug efficacy, using plasma samples from a patient with hemophilia A.

Authors:  Makoto Kaneda; Ryohei Kawasaki; Naoki Matsumoto; Hiroto Abe; Yoshihito Tashiro; Yuta Inokuchi; Hideyuki Yasuno; Mariko Sasaki-Noguchi; Tetsuhiro Soeda; Yasushi Yoshimura; Toshiaki Oka
Journal:  J Thromb Haemost       Date:  2021-09-28       Impact factor: 16.036

4.  The prevalence of factor VIII and IX inhibitors among Saudi patients with hemophilia: Results from the Saudi national hemophilia screening program.

Authors:  Tarek Owaidah; Abdulkareem Al Momen; Hazzaa Alzahrani; Abdulrahman Almusa; Fawaz Alkasim; Ahmed Tarawah; Randa Al Nouno; Fatima Al Batniji; Fahad Alothman; Ali Alomari; Saud Abu-Herbish; Mahmoud Abu-Riash; Khawar Siddiqui; Mansor Ahmed; S Y Mohamed; Mahasen Saleh
Journal:  Medicine (Baltimore)       Date:  2017-01       Impact factor: 1.889

5.  Autoimmune Acquired Factor XIII Deficiency: A Case Report.

Authors:  Ana Marco; Pascual Marco
Journal:  J Blood Med       Date:  2021-02-09

6.  Acquired haemophilia in patients with malignant disease: A case report.

Authors:  Veronika Krašek; Aleša Kotnik; Hana Zavrtanik; Jasna Klen; Samo Zver
Journal:  World J Clin Cases       Date:  2021-04-06       Impact factor: 1.337

7.  Diagnosis and Management of Acquired Hemophilia A: Case Reports and a Literature Review.

Authors:  Ikhwan Rinaldi; Findy Prasetyawaty; Siti Fazlines; Kevin Winston; Yusuf Aji Samudera Nurrobi; Jessica Leoni; Ilham Hidayat Restu Tulus Maha; Satrio Wicaksono; Abdillah Yasir Wicaksono; Averina Octaxena Aslani; Rizkania Ikhsani
Journal:  Case Rep Med       Date:  2021-09-14

8.  Plasma-derived FVIII/VWF complex shows higher protection against inhibitors than isolated FVIII after infusion in haemophilic patients: A translational study.

Authors:  Maria Isabel Bravo; Alba Pérez; Aida Raventós; Salvador Grancha; Juan Ignacio Jorquera; Nora Viviana Butta; Maria Teresa Álvarez-Román; Montserrat Costa; Todd Willis; Victor Jiménez-Yuste
Journal:  Haemophilia       Date:  2022-06-02       Impact factor: 4.263

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.