Cargando…

Factors affecting health-related quality of life in Thai children with thalassemia

BACKGROUND: Knowledge of the factors associated with health-related quality of life (HRQOL) among patients with thalassemia is essential in developing more suitable clinical, counseling, and social support programs to improve treatment outcomes of these patients. In light of the limited research in...

Descripción completa

Detalles Bibliográficos
Autores principales: Thavorncharoensap, Montarat, Torcharus, Kitti, Nuchprayoon, Issarang, Riewpaiboon, Arthorn, Indaratna, Kaemthong, Ubol, Bang-on
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836992/
https://www.ncbi.nlm.nih.gov/pubmed/20180983
http://dx.doi.org/10.1186/1471-2326-10-1
_version_ 1782178754971303936
author Thavorncharoensap, Montarat
Torcharus, Kitti
Nuchprayoon, Issarang
Riewpaiboon, Arthorn
Indaratna, Kaemthong
Ubol, Bang-on
author_facet Thavorncharoensap, Montarat
Torcharus, Kitti
Nuchprayoon, Issarang
Riewpaiboon, Arthorn
Indaratna, Kaemthong
Ubol, Bang-on
author_sort Thavorncharoensap, Montarat
collection PubMed
description BACKGROUND: Knowledge of the factors associated with health-related quality of life (HRQOL) among patients with thalassemia is essential in developing more suitable clinical, counseling, and social support programs to improve treatment outcomes of these patients. In light of the limited research in this area, this study aims to examine factors associated with HRQOL among children and adolescents with thalassemia in Thailand. METHODS: A cross-sectional survey was conducted in three selected hospitals in Thailand during June to November 2006. PedsQL™ 4.0 Generic Core Scale (Thai version) was used to assess HRQOL in 315 thalassemia patients between 5 and 18 years of age. Other related clinical characteristics of the patients were collected via medical record review. RESULTS: The mean (SD) of the total summary score was 76.67 (11.40), while the means (SD) for the Physical Health Summary score and Psychosocial Health Summary score were 78.24 (14.77) and 75.54 (12.76), respectively. The school functioning subscale scored the lowest, with a mean of 67.89 (SD = 15.92). The following factors significantly affected the HRQOL of the patients: age; age at onset of anemia and age at first transfusion; pre-transfusion hemoglobin (Hb) level; receiving a blood transfusion during the previous three months; and disease severity. In addition, iron chelation therapy had a significant negative effect on HRQOL in the school functioning subscale. In contrast, serum ferritin level, frequency of blood transfusions per year, and gender were not significantly related to HRQOL among these patients. The results from multivariate analysis also confirmed these findings. CONCLUSIONS: To improve HRQOL of thalassemia patients, suitable programs aimed at providing psychosocial support and a link between the patient, school officials, the family and the physician are important, especially in terms of improving the school functioning score. The findings also confirmed the importance of maintaining a pre-transfusion Hb level of at least 9-10.5 g/dL. In addition, special care and attention should be given to patients with a severe condition, and those who are receiving subcutaneous iron chelation therapy.
format Text
id pubmed-2836992
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-28369922010-03-12 Factors affecting health-related quality of life in Thai children with thalassemia Thavorncharoensap, Montarat Torcharus, Kitti Nuchprayoon, Issarang Riewpaiboon, Arthorn Indaratna, Kaemthong Ubol, Bang-on BMC Blood Disord Research article BACKGROUND: Knowledge of the factors associated with health-related quality of life (HRQOL) among patients with thalassemia is essential in developing more suitable clinical, counseling, and social support programs to improve treatment outcomes of these patients. In light of the limited research in this area, this study aims to examine factors associated with HRQOL among children and adolescents with thalassemia in Thailand. METHODS: A cross-sectional survey was conducted in three selected hospitals in Thailand during June to November 2006. PedsQL™ 4.0 Generic Core Scale (Thai version) was used to assess HRQOL in 315 thalassemia patients between 5 and 18 years of age. Other related clinical characteristics of the patients were collected via medical record review. RESULTS: The mean (SD) of the total summary score was 76.67 (11.40), while the means (SD) for the Physical Health Summary score and Psychosocial Health Summary score were 78.24 (14.77) and 75.54 (12.76), respectively. The school functioning subscale scored the lowest, with a mean of 67.89 (SD = 15.92). The following factors significantly affected the HRQOL of the patients: age; age at onset of anemia and age at first transfusion; pre-transfusion hemoglobin (Hb) level; receiving a blood transfusion during the previous three months; and disease severity. In addition, iron chelation therapy had a significant negative effect on HRQOL in the school functioning subscale. In contrast, serum ferritin level, frequency of blood transfusions per year, and gender were not significantly related to HRQOL among these patients. The results from multivariate analysis also confirmed these findings. CONCLUSIONS: To improve HRQOL of thalassemia patients, suitable programs aimed at providing psychosocial support and a link between the patient, school officials, the family and the physician are important, especially in terms of improving the school functioning score. The findings also confirmed the importance of maintaining a pre-transfusion Hb level of at least 9-10.5 g/dL. In addition, special care and attention should be given to patients with a severe condition, and those who are receiving subcutaneous iron chelation therapy. BioMed Central 2010-01-21 /pmc/articles/PMC2836992/ /pubmed/20180983 http://dx.doi.org/10.1186/1471-2326-10-1 Text en Copyright ©2010 Thavorncharoensap et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Thavorncharoensap, Montarat
Torcharus, Kitti
Nuchprayoon, Issarang
Riewpaiboon, Arthorn
Indaratna, Kaemthong
Ubol, Bang-on
Factors affecting health-related quality of life in Thai children with thalassemia
title Factors affecting health-related quality of life in Thai children with thalassemia
title_full Factors affecting health-related quality of life in Thai children with thalassemia
title_fullStr Factors affecting health-related quality of life in Thai children with thalassemia
title_full_unstemmed Factors affecting health-related quality of life in Thai children with thalassemia
title_short Factors affecting health-related quality of life in Thai children with thalassemia
title_sort factors affecting health-related quality of life in thai children with thalassemia
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836992/
https://www.ncbi.nlm.nih.gov/pubmed/20180983
http://dx.doi.org/10.1186/1471-2326-10-1
work_keys_str_mv AT thavorncharoensapmontarat factorsaffectinghealthrelatedqualityoflifeinthaichildrenwiththalassemia
AT torcharuskitti factorsaffectinghealthrelatedqualityoflifeinthaichildrenwiththalassemia
AT nuchprayoonissarang factorsaffectinghealthrelatedqualityoflifeinthaichildrenwiththalassemia
AT riewpaiboonarthorn factorsaffectinghealthrelatedqualityoflifeinthaichildrenwiththalassemia
AT indaratnakaemthong factorsaffectinghealthrelatedqualityoflifeinthaichildrenwiththalassemia
AT ubolbangon factorsaffectinghealthrelatedqualityoflifeinthaichildrenwiththalassemia