ArticleBMC blood disorders2010
Factors affecting health-related quality of life in Thai children with thalassemia.
Article in BMC blood disorders, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.
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Who cites it
43 citing papers in PubMed.
- Thalassaemia.Nature reviews. Disease primers · 2026Review
- Distinct patterns of health risk behaviours in adolescents with thalassaemia.Annals of medicine · 2025Article
- Article
- Effectiveness of educational intervention on quality of life in adults with thalassemia major: A quasi-experimental study based on PRECEDE model.Health science reports · 2024Article
- Health-Related Quality of Life of Adolescents With Non-transfusion-Dependent Thalassemia in Basrah, Iraq.Cureus · 2024Article
- Article
- Quality of life and thalassemia in India: A scoping review.Journal of family medicine and primary care · 2024Article
- Health-related quality of life among thalassemia patients in Bangladesh using the SF-36 questionnaire.Scientific reports · 2023Article
- Article
- Genotypic spectrum of α-thalassemia and β-thalassemia in newborns of the Li minority in Hainan province, China.Frontiers in pediatrics · 2023Article
- Predictors of health state utility values using SF-6D for Chinese adult patients with β-thalassemia major.Frontiers in public health · 2022Article
- EQ-5D-3L health state utility values in transfusion-dependent thalassemia patients in Malaysia: a cross-sectional assessment.Health and quality of life outcomes · 2021Article
- Quality of Life and Related Paraclinical Factors in Iranian Patients with Transfusion-Dependent Thalassemia.Journal of environmental and public health · 2021Article
- Oral Health Profiles and Related Quality of Life in Thalassemia Children in Relation to Iron Overload: A Cross-Sectional Study.International journal of environmental research and public health · 2020Article
- Predictors of Quality of Life in Transfusion-dependent Thalassemia Patients Based on the PRECEDE Model: A Structural Equation Modeling Approach.Journal of epidemiology and global health · 2020Article
- Care-Related Quality of Life of Caregivers of Beta-Thalassemia Major Children: An Epidemiological Study in Eastern India.Journal of epidemiology and global health · 2020Observational
- Health-related quality of life among children with transfusion-dependent thalassemia: A cross-sectional study in Malaysia.Health and quality of life outcomes · 2020Article
- Health-Related Quality of Life in Thai Children with Thalassemia as Evaluated by PedsQL and EQ-5D-Y: A Single-Center Experience.Mediterranean journal of hematology and infectious diseases · 2020Article
- Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study.Health and quality of life outcomes · 2019Article
- Quality of Life (QoL) and the Factors Affecting it in Transfusion-dependent Thalassemic Children.Indian journal of pediatrics · 2018Observational
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6 authors.
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Abstract
backgroundKnowledge 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.
methodsA 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.
resultsThe 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.
conclusionsTo 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.
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