Quality of life in transfusion dependent thalassemic children
نویسندگان
چکیده
منابع مشابه
Assessment of Pancreatic Iron Overload in Transfusion Dependent Thalassemic Patients
Advances in the management of transfusion dependent thalassemic patients have improved the survival of these patients. The most important consequence of repeated and frequent transfusions is iron accumulation in vital organs. The magnetic resonance imaging (MRI) is a non-invasive and valid technique for the estimation of iron stores. Despite multiple studies about cardiac and liver MRI T2*, the...
متن کاملAbnormal glucose tolerance in transfusion-dependent beta-thalassemic patients.
OBJECTIVE To study the prevalence of and risk factors for abnormal glucose tolerance in transfusion-dependent beta-thalassemic patients. RESEARCH DESIGN AND METHODS A total of 89 transfusion-dependent beta-thalassemic patients were interviewed. Diabetes was previously diagnosed in 14 of them. In the remaining 75 patients, 68 participated in an oral glucose tolerance test. Potential risk facto...
متن کاملZinc Status and its Correlation with Basic Parameters in Transfusion Dependent Thalassemic Patients: A Pakistani Perspective
Background: β-thalassemia is an autosomal hemoglobinopathy with inconsistent universal distribution. Among patients with thalassemia diverse non-siderotic complications distinctly influence the attribute of life, including zinc deficiency due to varied etiologies. The objective of the present study was to determine zinc levels in patients with β-thalassemia major and its correlation with mat...
متن کاملHealth-related quality of life in Thai thalassemic children treated with iron chelation.
Thalassemia is a chronic hereditary disease in which patients with severe disease present with anemia during their first year of life. In Thailand, stem cell transplantation is not an option for most patients. Supportive treatments, such as blood transfusions and iron chelation are used. Little data exists regarding the Health Related Quality of Life (HRQoL) of these patients. We conducted a st...
متن کاملPost transfusion purpura in a thalassemic child.
Post transfusion purpura (PTP) is a rare condition and only 200 cases have been reported so far. It is commonly seen in women, with a preponderance in the sixth and seventh decade. Majority of these cases have been observed in whites and the condition is rare among Asian patients(l). It has not yet been reported in children(2). PTP is characterized by the development of thrombocytopenia associa...
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ژورنال
عنوان ژورنال: Pediatric Hematology Oncology Journal
سال: 2019
ISSN: 2468-1245
DOI: 10.1016/j.phoj.2019.08.029