[HTML][HTML] A cost-utility and budget impact analysis of allogeneic hematopoietic stem cell transplantation for severe thalassemic patients in Thailand
P Leelahavarong, U Chaikledkaew, S Hongeng… - BMC health services …, 2010 - Springer
Background Hematopoietic stem cell transplantation (HSCT) is the only curative treatment
available to severe thalassemic patients. The treatment, however, is very costly, particularly …
available to severe thalassemic patients. The treatment, however, is very costly, particularly …
[HTML][HTML] Cost utility analysis of reduced intensity hematopoietic stem cell transplantation in adolescence and young adult with severe thalassemia compared to …
R Sruamsiri, N Chaiyakunapruk, S Pakakasama… - BMC health services …, 2013 - Springer
Background Hematopoieticic stem cell transplantation is the only therapeutic option that can
cure thalassemia disease. Reduced intensity hematopoietic stem cell transplantation (RI …
cure thalassemia disease. Reduced intensity hematopoietic stem cell transplantation (RI …
[HTML][HTML] Cost effectiveness of hematopoietic stem cell transplantation compared with transfusion chelation for treatment of thalassemia major
Hematopoietic stem cell transplantation (HSCT) is the only cure for thalassemia major (TM),
which inflicts a significant 1-time cost. Hence, it is important to explore the cost effectiveness …
which inflicts a significant 1-time cost. Hence, it is important to explore the cost effectiveness …
[HTML][HTML] Hematopoietic cell transplantation for thalassemia: a global perspective BMT tandem meeting 2013
PA Mehta, LB Faulkner - Biology of Blood and Marrow Transplantation, 2013 - Elsevier
Hematopoietic cell transplantation (HCT) remains the sole available curative option for
patients with β-thalassemia major. Expanded and improved supportive therapies for …
patients with β-thalassemia major. Expanded and improved supportive therapies for …
[HTML][HTML] Economic burden in the management of transfusion-dependent thalassaemia patients in Malaysia from a societal perspective
AA Shafie, JHY Wong, HM Ibrahim… - Orphanet Journal of …, 2021 - Springer
Background Transfusion-dependent thalassaemia (TDT) is a hereditary blood disorder in
which blood transfusion is the mainstay treatment to prolong survival and improve quality of …
which blood transfusion is the mainstay treatment to prolong survival and improve quality of …
[HTML][HTML] Healthcare resource utilization and direct costs of transfusion-dependent thalassemia patients in Dubai, United Arab Emirates: a retrospective cost-of-illness …
S Alshamsi, S Hamidi, HO Narci - BMC health services research, 2022 - Springer
Background Patients with transfusion-dependent thalassemia (TDT) require lifelong blood
transfusions and iron chelation therapy. Thus, patients afflicted with TDT often have to …
transfusions and iron chelation therapy. Thus, patients afflicted with TDT often have to …
[HTML][HTML] Low-cost matched sibling bone marrow transplant for standard-risk thalassemia in a limited-resource setting
S Ramprakash, R Agarwal, R Dhanya… - Pediatric Hematology …, 2017 - Elsevier
Thalassemias are the most common inherited genetic disorder in India and a major public
health burden with bone marrow transplant (BMT) considered the only established curative …
health burden with bone marrow transplant (BMT) considered the only established curative …
Financial burden of national health insurance for treating patients with transfusion-dependent thalassemia in Taiwan
The thalassemias are a heterogeneous group of inherited hypochromic anemias of varying
severity. The mainstay of supportive treatment is regular blood transfusion accompanied by …
severity. The mainstay of supportive treatment is regular blood transfusion accompanied by …
[HTML][HTML] Health state utilities associated with treatment for transfusion-dependent β-thalassemia
LS Matza, LC Paramore, KD Stewart, H Karn… - The European Journal of …, 2020 - Springer
Objectives Transfusion-dependent β-thalassemia (TDT) is a genetic disease that affects
production of red blood cells. Conventional treatment involves regular red blood cell …
production of red blood cells. Conventional treatment involves regular red blood cell …
Innovative curative treatment of beta thalassemia: cost-efficacy analysis of gene therapy versus allogenic hematopoietic stem-cell transplantation
S Coquerelle, M Ghardallou, S Rais, P Taupin… - Human gene …, 2019 - liebertpub.com
Seventy-five percent of patients with beta thalassemia (β-thalassemia) do not have human
leukocyte antigen–matched siblings and until recently had no access to a curative treatment …
leukocyte antigen–matched siblings and until recently had no access to a curative treatment …