Abstract:
Objective: To assess the quality of life among beta-thalassemic major children in a tertiary care setting.
Method: The cross-sectional descriptive study was conducted at the Federal Government Hospital, Islamabad, Pakistan,
from October to December, 2020, and comprised beta-thalassemic major children aged 7-13 years. Socio-demographic
information was collected using a questionnaire, while the quality of life was assessed using a pretested tool with Cronbach’s
alpha value 0.855. The data was analysed using SPSS 25.
Results: Of the 87 subjects, 47(54%) were males and 40(46%) were females. The overall mean age was 10.71±1.99 years.
The mean quality of scale score was 50.24±18.88. Poor quality of life was found among 33(37.9%) children. The quality of
life had significant association with age 7-9 years, male gender and blood transfusion frequency 2 or more (p<0.05). The
adjusted odds were also significant with age and blood transfusion frequency (p<0.05). The overall mean score was
significantly related within age groups and frequency of blood transfusion (p<0.05), whereas physical and emotional
domains were significant with age (p<0.05), while the four domains of physical, psychological, social and educational were
associated with frequency of blood transfusion (p<0.05).
Conclusion: Quality of life among thalassemic children was found to be considerably low. The physical and emotional
domains need to be focussed upon for improving the quality of life. Measures should be taken to avoid the increased need
of blood transfusions through treatment compliance.
