A Perspective on the Quality of Life of Hemophilia A Patients in Romania—A Study on 100 Patients

0Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Hemophilia A is an X-linked coagulopathy, where there is a deficit in the production of the coagulation factor VIII. Even though there is a higher incidence of hemophilia A than of hemophilia B, it is still considered a rare disease, as its incidence is of 1 in 10,000 people born. We have applied three questionnaires regarding quality of life: Haem-A-QoL, Haemo-SYM and EQ-5D-5L to 101 adult patients with hemophilia A, which were separated into two groups: on-demand and prophylactic treatment. The results showed a relatively young lot, with medium and high education, but with a sedentary lifestyle and are pensioners. They also seem to have moderate mobility issues but, overall, a good quality of life. The quality of life in our studied lot is relatively good, but a more diverse lot is advised.

Cite

CITATION STYLE

APA

Guran, C., Ioniţă, H. M., Haţegan, M. G., Ioniţă, I., Trăilă, A., & Ilie, A. M. (2022). A Perspective on the Quality of Life of Hemophilia A Patients in Romania—A Study on 100 Patients. Journal of Vascular Diseases, 1(2), 105–112. https://doi.org/10.3390/jvd1020012

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free