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.
1. Mansouritorghabeh H.; Clinical and laboratory approaches to hemophilia a. Iran J Med Sci 2015,40(3),194-205
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
4. Franchini M.; Mannucci P.M.; Hemophilia A in the third millennium. Blood Rev 2013,27(4),179-184
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
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献