Clinical profile of transfusion-dependent thalassemia major children with reference to serum ferritin and liver function: A prospective observational study

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DOI:

https://doi.org/10.3126/ajms.v14i11.56668

Keywords:

Serum ferritin; Liver function; Growth pattern; Iron overload; Blood transfusions; Pediatric population

Abstract

Background: Thalassemia major is a genetic disorder characterized by severe anemia and the need for lifelong blood transfusions.

Aims and Objectives: The aim of this study was to investigate the clinical profile of transfusion-dependent thalassemia major children with reference to serum ferritin levels and liver function.

Materials and Methods: A prospective observational study included 100 children aged 1–12 years with beta-thalassemia major, who were receiving blood transfusions. Clinical data, including growth parameters, serum ferritin levels, and liver function tests, were collected. Descriptive and inferential statistical analyses were performed.

Results: The study population predominantly consisted of children aged 1–5 years (54%) and males (51%). Hindu children accounted for 85% of the participants. Most children were diagnosed with thalassemia major before the age of 1 year (84%) and were diagnosed through Hb electrophoresis (77%). The majority of children received blood transfusions every 15–30 days (49%). Pre-transfusion hemoglobin levels ranged from <5 g/dL to 8.0 g/dL, while post-transfusion levels ranged from 7.1 g/dL to 10.1 g/dL. Liver function tests indicated the mean values for total serum bilirubin (0.81±0.2), direct bilirubin (0.34±0.10), indirect bilirubin (0.49±0.10), aspartate transaminase (47.22±11.06), alanine transaminase (45.45±8.97), alkaline phosphatase (97.74±4.39), total proteins (6.28±0.29), and serum albumin (3.72±0.2). No significant changes were observed in growth parameters over the 18-month study period.

Conclusion: This study provides insights into the clinical profile of children with transfusion-dependent thalassemia major, emphasizing the significance of early diagnosis, regular transfusions, and monitoring of serum ferritin levels and liver function.

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Published

2023-11-01

How to Cite

Chiluka Sudhakar, Blessy Prabhu Priyanka S, Shanmuga Sundaram M, & Rajashekar K. (2023). Clinical profile of transfusion-dependent thalassemia major children with reference to serum ferritin and liver function: A prospective observational study. Asian Journal of Medical Sciences, 14(11), 260–265. https://doi.org/10.3126/ajms.v14i11.56668

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Section

Original Articles