Health-related quality of life and associated factors among children with Transfusion-dependent β-thalassaemia: a cross-sectional study in Guangxi Province

被引:0
作者
Qiao, Jingyi [1 ,2 ]
Luo, Bingxing [1 ,2 ]
Ming, Jian [1 ,2 ]
Zhang, Xinhua [3 ]
Weng, Junling [1 ,2 ]
Deng, Qingwen [1 ,2 ]
Zhou, Shanyan [1 ,2 ]
Chen, Yingyao [1 ,2 ]
机构
[1] Fudan Univ, Sch Publ Hlth, Shanghai, Peoples R China
[2] Fudan Univ, Natl Hlth Commiss, Key Lab Hlth Technol Assessment, Shanghai, Peoples R China
[3] 923rd Hosp Peoples Liberat Army, Dept Hematol, Nanning, Guangxi, Peoples R China
关键词
Transfusion-dependent thalassaemia; Health-related quality of life; Patient-reported outcomes; TranQoL;
D O I
10.1186/s12955-024-02307-1
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background Transfusion-dependent beta-thalassemia (TDT) is a severe inherited disorder. Without regular treatment, patients with TDT experience complications that can significantly shorten life expectancy and severely impact both their quality of life and that of their families. The condition has attracted significant attention in global health discussions. Due to the challenges of blood supply shortages, the high costs of iron chelation therapy, and hematopoietic stem cell transplantation (HSCT), TDT presents a serious health risk to patients and imposes a substantial burden on families and society. However, research on the health-related quality of life (HRQoL) of thalassemia patients in China remains limited. This study evaluated the factors affecting the HRQoL of these patients, with the goal of developing strategies to improve their quality of life. Methods In this cross-sectional study, children with TDT were recruited from five treatment centers in Guangxi, a province with a high prevalence of thalassemia in China. Structured questionnaires were employed to gather relevant data on sociodemographic variables, disease characteristics, treatments, and associated costs. The HRQoL was assessed using the Transfusion-Dependent Quality of Life (TranQoL) questionnaire, with a proxy version for patients aged 0-11 years and a child version for those aged 12-18 years. Results The study included 418 participants, yielding an overall TranQoL score of 60.6 +/- 16.3 among thalassemia patients. Multiple linear regression analysis revealed a negative correlation (P < 0.05) between overall TranQoL scores and several factors: increasing patient age, the presence of multiple thalassemia patients within a family, and undergoing HSCT. Conversely, adherence to regular treatment was positively correlated with higher TranQoL scores (P < 0.05). Conclusion The study demonstrates that HRQoL among Chinese patients with TDT is at a low level. Age, treatment adherence, family support, and socioeconomic status were identified as key determinants influencing HRQoL. It is essential to further enhance and optimize health insurance policies and medical services to support comprehensive treatment strategies for these patients.
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共 34 条
[1]   Factors Impacting Quality of Life in Thalassemia Patients; Results from the Intercontinenthal Collaborative Study [J].
Amid, Ali ;
Leroux, Rebecca ;
Merelles-Pulcini, Manuela ;
Yassobi, Saeed ;
Saliba, Antoine N. ;
Ward, Richard ;
Karimi, Mehran ;
Taher, Ali T. ;
Klaassen, Robert J. ;
Kirby-Allen, Melanie .
BLOOD, 2016, 128 (22)
[2]   Health-related quality of life (HRQoL) in beta-thalassemia major (β-TM) patients assessed by 36-item short form health survey (SF-36): a meta-analysis [J].
Arian, Mahdieh ;
Mirmohammadkhani, Majid ;
Ghorbani, Raheb ;
Soleimani, Mohsen .
QUALITY OF LIFE RESEARCH, 2019, 28 (02) :321-334
[3]  
Beijing AngelMom Charity Foundation China Philanthropy Research Institute, 2020, Blue Book of Thalassemia in China: Survey Report on the Prevention and Treatment of Thalassemia in China, V1st
[4]   Quality of life among beta-thalassemic major children presenting at Federal Government Hospital Islamabad, Pakistan [J].
Bukhari, Gul Mehar Javaid .
JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION, 2022, 72 (11) :2241-2244
[5]   Prospective Assessment of Health-Related Quality of Life in Pediatric Patients with Beta-Thalassemia following Hematopoietic Stem Cell Transplantation [J].
Caocci, Giovanni ;
Efficace, Fabio ;
Ciotti, Francesca ;
Roncarolo, Maria Grazia ;
Vacca, Adriana ;
Piras, Eugenia ;
Littera, Roberto ;
Markous, Raji Suleiman Dawood ;
Collins, Gary Stephen ;
Ciceri, Fabio ;
Mandelli, Franco ;
Marktel, Sarah ;
La Nasa, Giorgio .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2011, 17 (06) :861-866
[6]   Quality of life in patients with β-thalassemia: A prospective study of transfusion-dependent and non-transfusion-dependent patients in Greece, Italy, Lebanon, and Thailand [J].
Cappellini, Maria Domenica ;
Kattamis, Antonis ;
Viprakasit, Vip ;
Sutcharitchan, Pranee ;
Pariseau, Joseph ;
Laadem, Abderrahmane ;
Jessent-Ciaravino, Valerie ;
Taher, Ali .
AMERICAN JOURNAL OF HEMATOLOGY, 2019, 94 (10) :E261-E264
[7]  
Cappellini MD, 2021, Guidelines for the Management of Transfusion Dependent Thalassaemia (4th edition-Version 2.0), V4th
[8]   Quality of life in patients with transfusion-dependent thalassemia after hematopoietic SCT [J].
Cheuk, D. K. L. ;
Mok, A. S. P. ;
Lee, A. C. W. ;
Chiang, A. K. S. ;
Ha, S. Y. ;
Lau, Y. L. ;
Chan, G. C. F. .
BONE MARROW TRANSPLANTATION, 2008, 42 (05) :319-327
[9]  
Choudhury Nabajyoti, 2011, Asian J Transfus Sci, V5, P117, DOI 10.4103/0973-6247.83234
[10]   Thalassemia patients in transfussion dependent period and after hematopoietic stem cell transplantation: how are the psychiatric status and life quality of these patients? (Assesment of patients with beta-thalassemia and in patients who underwent HSCT) [J].
Cikili-Uytun, Merve ;
Eroglu, Mehtap ;
Ertem, Mehmet ;
Ileri, Dilber Talia ;
Ince, Elif ;
Guenay Kilic, Birim .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2023, 40 (07) :617-628