2020, Number 3
<< Back Next >>
Rev Hematol Mex 2020; 21 (3)
Assessment of the quality of life related to health in adolescents and adults with hemophilia attended in a rehabilitation unit
Espinosa-Maldonado EG, Torres-González R, Gibraltar-Conde A
Language: Spanish
References: 10
Page: 136-141
PDF size: 404.11 Kb.
ABSTRACT
Background: Hemophilia is a hereditary coagulation disorder linked to the X
chromosome, caused by the deficiency or dysfunction of factor VIII in hemophilia
type A and factor IX in hemophilia type B. Health-related quality of life focuses on the
evaluation by the individual of the limitations that, in different areas, have determined
the development of a disease and/or accident.
Objective: To determine the health-related quality of life in adolescents and adults
with hemophilia treated in a rehabilitation unit.
Material and Method: A cross-sectional, descriptive and observational study in
adolescents and adults with hemophilia who attended the North Physical Medicine
and Rehabilitation Unit, Mexico City was done from March to June 2019. The SF-12
questionnaire was applied and clinical and sociodemographic data were collected.
Results: Fourty-one men participated with an average age of 37 years with a range
of 14 to 68 years. The scores of the SF-12 questionnaire showed that these patients
had a mean health-related quality of life, being good in their mental component and
poor in the physical.
Conclusions: Health-related quality of life in the participants of this study was
categorized globally as mean.
REFERENCES
Peyvandi F, Garagiola I, Young G. The past and future of haemophilia: diagnosis, treatments, and its complications. Lancet 2016; 388(10040): 187-97. https://doi.org/10.1016/ S0140-6736(15)01123-X
Amador-Medina FL, Vargas-Ruiz G.. Hemofilia. Rev Med Inst Mex Seguro Soc 2013; 51(6): 638-43.
Vinaccia-Alpi S, Quiceno JM. Calidad de vida relacionada con la salud y enfermedad crónica: estudios colombianos. Psychol Av la Discip 2012; 6(1): 123-36.
Velarde-Jurado E, Avila-Figueroa C. Evaluación de la calidad de vida. Rev Salud Pública México 2002; 44(4): 349-61.
Miners A, Sabin C, Tolley K, Jenkinson C, Kind P, Lee C. Assessing health-related quality-of-life in individuals with haemophilia. Haemophilia 1999; 5: 378-85. doi: 10.1046/j.1365-2516.1999.00347.x
Osorio-Guzmán M, Olvera-González S, Bazán-Riverón GE, Gaitán-Fitch RC. Calidad de vida percibida por pacientes pediátricos con hemofilia y sus padres. Psicol y Salud 2016; 26(1): 15-23.
Fuenmayor-Castaño A, Jaramillo-Restrepo M, Salinas- Durán F. Calidad de vida en una población con hemofilia: Estudio de corte transversal en un centro de tratamiento de hemofilia. Rev Colomb Reumatol 2017; 24(1): 18-24. DOI: 10.1016/j.rcreu.2016.10.006
Poon J, Zhou Z, Doctor J, Wu J, Ullman M, Ross C, et al. Quality of life in haemophilia A: Hemophilia Utilization Group Study Va (HUGS-Va). Haemophilia 2012; 18(5): 699- 707. doi: 10.1111/j.1365-2516.2012.02791.x
Lindvall K, Von Mackensen S, Berntorp E. Quality of life in adult patients with haemophilia - a single centre experience from Sweden. Haemophilia 2012; 18(4): 527-31. doi: 10.1111/j.1365-2516.2012.02765.x
Carruyo-Vizcaíno C, Vizcaíno G, Carrizo E, Arteaga-Vizcaíno M, Sarmiento S, Viscaíno-Carruyo J. Actitud de los individuos adultos con hemofilia hacia su enfermedad. Invest Clin 2004; 45(3).