Quality of life in patients with transfusion-dependent thalassemia after hematopoietic SCT
| Autor: | Amanda Sio-Peng Mok, Alan Ks Chiang, Daniel K. L. Cheuk, Gcf Chan, Shau-Yin Ha, Acw Lee, Yu-Lung Lau |
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| Rok vydání: | 2008 |
| Předmět: |
Adult
Male Hemolytic anemia Pediatrics medicine.medical_specialty Adolescent Thalassemia Acquired immunodeficiency syndrome (AIDS) Quality of life Surveys and Questionnaires Internal medicine medicine Humans Transplantation Homologous Sibling Child Transplantation Hematology business.industry Hematopoietic Stem Cell Transplantation medicine.disease humanities Hemoglobinopathy El Niño Child Preschool Quality of Life Female business |
| Zdroj: | Bone Marrow Transplantation. 42:319-327 |
| ISSN: | 1476-5365 0268-3369 |
| Popis: | In this cross-sectional study, we compared the quality of life (QOL) in transfusion-dependent thalassemic patients who survived matched sibling hematopoietic SCT (HSCT, n=24) with patients treated conventionally with transfusion and iron chelation (n=74). WHOQOL-BREF(HK) and PedsQL questionnaires were administered to patients aged >18 years and 5–12 years, respectively. Patients aged 12–18 years received both questionnaires. WHOQOL-BREF(HK) revealed post transplant patients rated overall health better than those treated conventionally (score 3.67 vs 3.06, P=0.01). They are less dependent on medical aids (3.87 vs 2.96, P=0.006), having higher activity level (4.00 vs 3.36, P=0.026) and better personal relationships (4.13 vs 3.69, P=0.014). Physical health domain score was better (75.20 vs 63.94, P=0.007). These differences remained significant after adjustment for comorbidities. PedsQL revealed post transplant patients rated better for running (3.53 vs 2.72, P=0.001) and sports (3.20 vs 2.64, P=0.038), even after adjustment for comorbidities, but were less satisfied for school absence to attend hospital (2.53 vs 3.29, P=0.03). Post transplant patients were significantly more likely to consider marriage (100 vs 75.7%, P=0.033), but not childbearing (66.7 vs 51.4%, P=0.28). In conclusion, transplanted thalassemic patients enjoy better QOL, mainly in physical health, compared with conventionally treated patients. This information is important to patients considering HSCT. |
| Databáze: | OpenAIRE |
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