Is the Detection of Factor IX Inhibitors in Hemophilia B Orphan than Factor VIII Inhibitors in Hemophilia A? A Concise, Systematic Review

Author:

Mansouritorghabeh Hassan1ORCID,Mohades Seyedeh T.2ORCID

Affiliation:

1. Immunology Research Center, Inflammation and Inflammatory Diseases Division, Mashhad University of Medical Sciences, Mashhad, Iran

2. Department of Hematology, Razavi Hospital, Mashhad, Iran

Abstract

Objective: Development of inhibitors in hemophilia A and B comprise significant challenge for patients, hematologists, and health provider systems. It has recommended by the World Federation of Hemophilia (WFH) to check inhibitors every 3-4 months. The incidence of inhibitor in hemophilia B is lower than hemophilia A. Here, it tried to unravel whether the detection of inhibitors in hemophilia B neglected compared to hemophilia A or not? Methods: A comprehensive review carried out using six international and local medical search engines on published contributions about inhibitors in hemophilia A and B in Iran. Results: From 699 titles, 12 relevant papers were selected. The mean of factor VIII inhibitors in hemophilia A was 14.8%. The mean of factor IX inhibitors in hemophilia B was 6%. The minimum and maximum reported percentages of factor VIII inhibitors were 4% and 19.6%, while the minimum and maximum of reported percentages of factor IX inhibitors were 0% and 11.8%, respectively. The inhibitors in hemophilia A had reported in 6 papers. One paper had covered the inhibitors in hemophilia B. There were five papers on inhibitors in both hemophilia A and B. The comparison between the reported patients showed that 3020 patients with hemophilia A and 314 patients with hemophilia B had studied. Conclusion: Consistent with the lower frequency of hemophilia B and the lower development of inhibitors in hemophilia B compared to hemophilia A, it was concluded that hemophilia B had not neglected in Iran. It seems to be rational that each country, check rates of detection of inhibitors in hemophilia B to identify whether it has neglected or not.

Publisher

Bentham Science Publishers Ltd.

Subject

Cardiology and Cardiovascular Medicine,Pharmacology,Hematology,Molecular Medicine,General Medicine

Reference34 articles.

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2. Mancuso M.E.; Fasulo M.R.; Thrombin generation assay as a laboratory monitoring tool during bypassing therapy in patients with hemophilia and inhibitors.Semin Thromb Hemost; Thieme Medical Publishers, 2016,42,030-035

3. Franchini M.; Mannucci P.M.; The safety of pharmacologic options for the treatment of persons with hemophilia. Expert Opin Drug Saf 2016,15(10),1391-1400

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5. Tabriznia-Tabrizi S.; Gholampour M.; Mansouritorghabeh H.; A close insight to factor VIII inhibitor in the congenital hemophilia A. Expert Rev Hematol 2016,9(9),903-913

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