A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives

Background: The Maldives has the highest prevalence of thalassemia in the world. However, there is little research done on the psychosocial aspects of this illness. Objectives: This study aimed to examine health related quality of life (HRQOL) among adolescents with beta-thalassemia major attendi...

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Main Authors: Mansoor, Shanooha, Othman, Zahiruddin, Othman, Azizah, Husain, Maruzairi
Format: Article
Language:English
Published: Japan International Cultural Exchange Foundation 2018
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Online Access:http://eprints.usm.my/45303/1/211-5Mansoor.pdf
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spelling my.usm.eprints.45303 http://eprints.usm.my/45303/ A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives Mansoor, Shanooha Othman, Zahiruddin Othman, Azizah Husain, Maruzairi RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry Background: The Maldives has the highest prevalence of thalassemia in the world. However, there is little research done on the psychosocial aspects of this illness. Objectives: This study aimed to examine health related quality of life (HRQOL) among adolescents with beta-thalassemia major attending the National Thalassemia and Other Hemoglobinopathies Centre (NTC), Maldives Blood Services, Maldives. Thus, appropriate recommendation could be proposed. Methods: A total of 81 adolescents (mean age 15.7 years) with beta-thalassemia major were engaged. HRQOL was assessed using the Pediatric Quality of Life Inventory (PedsQL). Other relevant information was gathered through interview or medical record. Results: The HRQOL was reduced. The mean for physical, emotional, social, school and psychosocial HRQOL was 80.50, 72.30, 88.18, 76.44, and 78.96, respectively. The total HRQOL was 79.50 and this was lower in females (75.29) compared to males (83.29). Ferritin levels of 1,001-2,499 μg/l and > 2,500 μg/l were noted in 34.2% and 53.9%, respectively. Good compliance was reported in 55% of participants. Conclusions: Adolescents with beta-thalassemia major in the Maldives have reduced HRQOL. The high ferritin level could reduce the HRQOL and hence an attempt should be made towards lowering ferritin and improving compliance to chelation treatments. The gender difference in HRQOL signifies the need for more attention to the female patients and for areas of improvement to be explored Japan International Cultural Exchange Foundation 2018-08 Article PeerReviewed application/pdf en http://eprints.usm.my/45303/1/211-5Mansoor.pdf Mansoor, Shanooha and Othman, Zahiruddin and Othman, Azizah and Husain, Maruzairi (2018) A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives. International Medical Journal, 25 (4). pp. 211-214. ISSN 1341-2051 http://www.seronjihou.co.jp/IMJ/backnumber-IMJ.html
institution Universiti Sains Malaysia
building Hamzah Sendut Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Sains Malaysia
content_source USM Institutional Repository
url_provider http://eprints.usm.my/
language English
topic RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
spellingShingle RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Mansoor, Shanooha
Othman, Zahiruddin
Othman, Azizah
Husain, Maruzairi
A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives
description Background: The Maldives has the highest prevalence of thalassemia in the world. However, there is little research done on the psychosocial aspects of this illness. Objectives: This study aimed to examine health related quality of life (HRQOL) among adolescents with beta-thalassemia major attending the National Thalassemia and Other Hemoglobinopathies Centre (NTC), Maldives Blood Services, Maldives. Thus, appropriate recommendation could be proposed. Methods: A total of 81 adolescents (mean age 15.7 years) with beta-thalassemia major were engaged. HRQOL was assessed using the Pediatric Quality of Life Inventory (PedsQL). Other relevant information was gathered through interview or medical record. Results: The HRQOL was reduced. The mean for physical, emotional, social, school and psychosocial HRQOL was 80.50, 72.30, 88.18, 76.44, and 78.96, respectively. The total HRQOL was 79.50 and this was lower in females (75.29) compared to males (83.29). Ferritin levels of 1,001-2,499 μg/l and > 2,500 μg/l were noted in 34.2% and 53.9%, respectively. Good compliance was reported in 55% of participants. Conclusions: Adolescents with beta-thalassemia major in the Maldives have reduced HRQOL. The high ferritin level could reduce the HRQOL and hence an attempt should be made towards lowering ferritin and improving compliance to chelation treatments. The gender difference in HRQOL signifies the need for more attention to the female patients and for areas of improvement to be explored
format Article
author Mansoor, Shanooha
Othman, Zahiruddin
Othman, Azizah
Husain, Maruzairi
author_facet Mansoor, Shanooha
Othman, Zahiruddin
Othman, Azizah
Husain, Maruzairi
author_sort Mansoor, Shanooha
title A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives
title_short A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives
title_full A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives
title_fullStr A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives
title_full_unstemmed A Descriptive Study on Quality of Life among Adolescents with Beta-Thalassemia Major in the Maldives
title_sort descriptive study on quality of life among adolescents with beta-thalassemia major in the maldives
publisher Japan International Cultural Exchange Foundation
publishDate 2018
url http://eprints.usm.my/45303/1/211-5Mansoor.pdf
http://eprints.usm.my/45303/
http://www.seronjihou.co.jp/IMJ/backnumber-IMJ.html
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