Health-Related Quality-of-Life Profile of Pediatric Patients with β Thalassemia after Hematopoietic Stem Cell Transplantation

被引:5
作者
Mulas, Olga [1 ]
Efficace, Fabio [2 ]
Orofino, Maria Grazia [3 ]
Piroddi, Antonio [3 ]
Piras, Eugenia [1 ]
Vacca, Adriana [1 ]
Barella, Susanna [4 ]
Costa, Alessandro [1 ]
Giesinger, Johannes M. [5 ]
La Nasa, Giorgio [1 ]
Caocci, Giovanni [1 ]
机构
[1] Univ Cagliari, Businco Hosp, Dept Med Sci & Publ Hlth, Hematol Unit, Cagliari 09124, Italy
[2] Italian Grp Adult Hematol Dis GIMEMA, Hlth Outcomes Res Unit, Data Ctr, I-00161 Rome, Italy
[3] Pediat Hosp Microcitem A Cao, Bone Marrow Transplant Ctr, I-09121 Cagliari, Italy
[4] Pediat Hosp Microcitemico A Cao, Pediat Clin, Thalassemia & Rare Dis, I-09121 Cagliari, Italy
[5] Med Univ Innsbruck, Univ Hosp Psychiat 2, A-6020 Innsbruck, Austria
关键词
thalassemia; bone marrow transplantation; health-related quality of life; BONE-MARROW-TRANSPLANTATION; TRANSFUSION; DISEASE; RELIABILITY; CHELATION; CHILDREN; CANCER; SCALE;
D O I
10.3390/jcm12186047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Matched hematopoietic stem cell transplantation (HSCT) is a feasible and curative treatment in pediatric patients with beta thalassemia major (beta-TM). However, little data are available regarding patients and their parents ' health-related quality of life (HRQoL) after the procedure. As such, we investigated the HRQoL of pediatric patients with beta-TMafter HSCT compared to that of patients treated with blood transfusions and iron chelation. The health-related quality of life of 43 beta-TM pediatric patients and 43 parents were evaluated using the Pediatric Quality of Life Inventory (PedsQL). A total of 25 patients underwent HSCT: 15 from a sibling and 10 from an HLA-matched donor. The median follow-up time from HSCT was 5 years (range 1-13 years). The mean ages at the survey were 10.1 years (range 5-15) and 9.6 years (range 5-15) for transfused and transplanted patients, respectively. A significant reduction inHRQoLwas reported in the group of transfused patients comparedwith that of patients transplanted in the following PedsQL domains: children ' s and parents ' physical functions, Delta = 15.4, p = 0.009 and Delta = 11.3, p = 0.002, respectively; children ' s and parents ' emotional functioning, Delta = 15.2, p = 0.026 and Delta = 15.2, p = 0.045, respectively; child ' s and parents ' school functioning, Delta = 25, p = 0.005 and Delta = 22.5, p = 0.011, respectively; total child and parents scores, Delta = 14.5, p = 0.004 and Delta = 13.2, p = 0.005, respectively. The results of a multivariable analysis showed that the HSCT procedure was significantly associated with a higher total child PedsQL score (adjusted mean difference = 15.3, p = 0.001) and a higher total parent PedsQL score (adjusted mean difference = 14.1, p = 0.006). We found no significant difference in the HRQoL measured after sibling or unrelated human leukocyte antigen (HLA)-matched HSCT. Finally, a significant positive correlation across all the PedsQL domains was found between the scores reported by the children and those reported by their parents. In conclusion, our study shows that HSCT in pediatric patients with fi-TMis associated with a good overall HRQoL profile. This information further supports physicians when counseling patients and their parents before the HSCT procedure.
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页数:13
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共 31 条
[1]   Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel [J].
Angelucci, Emanuele ;
Matthes-Martin, Susanne ;
Baronciani, Donatella ;
Bernaudin, Francoise ;
Bonanomi, Sonia ;
Cappellini, Maria Domenica ;
Dalle, Jean-Hugues ;
Di Bartolomeo, Paolo ;
Diaz de Heredia, Cristina ;
Dickerhoff, Roswitha ;
Giardini, Claudio ;
Gluckman, Eliane ;
Hussein, Ayad Achmed ;
Kamani, Naynesh ;
Minkov, Milen ;
Locatelli, Franco ;
Rocha, Vanderson ;
Sedlacek, Petr ;
Smiers, Frans ;
Thuret, Isabelle ;
Yaniv, Isaac ;
Cavazzana, Marina ;
Peters, Christina .
HAEMATOLOGICA, 2014, 99 (05) :811-820
[2]  
[Anonymous], Cure for Thalassemia Major-From Allogeneic Hematopoietic Stem Cell Transplantation to Gene Therapy
[3]   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
[4]   A systematic review of quality of life in sickle cell disease and thalassemia after stem cell transplant or gene therapy [J].
Badawy, Sherif M. ;
Beg, Usman ;
Liem, Robert, I ;
Chaudhury, Sonali ;
Thompson, Alexis A. .
BLOOD ADVANCES, 2021, 5 (02) :570-583
[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 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
[7]   Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease [J].
Ferraresi, Marta ;
Panzieri, Daniele Lello ;
Leoni, Simona ;
Cappellini, Maria Domenica ;
Kattamis, Antonis ;
Motta, Irene .
EUROPEAN JOURNAL OF PEDIATRICS, 2023, 182 (06) :2509-2519
[8]   Bone disease and skeletal complications in patients with β thalassemia major [J].
Haidar, Rachid ;
Musallam, Khaled M. ;
Taher, Ali T. .
BONE, 2011, 48 (03) :425-432
[9]   Comparison of Blood Transfusion Plus Chelation Therapy and Bone Marrow Transplantation in Patients with beta-Thalassemia: Application of SF-36, EQ-5D, and Visual Analogue Scale Measures [J].
Javanbakht, Mehdi ;
Keshtkaran, Ali ;
Shabaninejad, Hossien ;
Karami, Hassan ;
Zakerinia, Maryam ;
Delavari, Sajad .
INTERNATIONAL JOURNAL OF HEALTH POLICY AND MANAGEMENT, 2015, 4 (11) :733-740
[10]   Health-related quality of life (HRQL) in children with sickle cell disease and thalassemia following hematopoietic stem cell transplant (HSCT) [J].
Kelly, Michael J. ;
Pennarola, Brian W. ;
Rodday, Angie Mae ;
Parsons, Susan K. .
PEDIATRIC BLOOD & CANCER, 2012, 59 (04) :725-731