Which Psychosocial Factors are Related to Chelation Adherence in Thalassemia? A Systematic Review
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.485080
Reference28 articles.
1. Iron-Chelating Therapy and the Treatment of Thalassemia
2. Family care-giving and chronic illness: how parents cope with a child with a sickle cell disorder or thalassaemia
3. Development of Tridentate Iron Chelators: From Desferrithiocin to ICL670
4. Prospective evaluation of patient-reported outcomes during treatment with deferasirox or deferoxamine for iron overload in patients with β-thalassemia
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1. Promoting Adherence to Iron Chelation Treatment in Beta-Thalassemia Patients;Patient Preference and Adherence;2022-06
2. Quality of Life and Burden of Disease in Italian Patients with Transfusion-Dependent Beta-Thalassemia;Journal of Clinical Medicine;2021-12-21
3. Non-compliance to iron chelation therapy in patients with transfusion-dependent thalassaemia;Pediatric Hematology Oncology Journal;2021-12
4. Concordance with comprehensive iron assessment, hepatitis A vaccination, and hepatitis B vaccination recommendations among patients with sickle cell disease and thalassaemia receiving chronic transfusions: an analysis from the Centers for Disease Control haemoglobinopathy blood safety project;British Journal of Haematology;2021-08-24
5. Patient Perspective on Iron Chelation Therapy: Barriers and Facilitators of Medication Adherence;Journal of Patient Experience;2021-01-01
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