Study of Serum ferritin levels in β-Thalassemia major children
Journal Title: Pediatric Review: International Journal of Pediatric Research - Year 2018, Vol 5, Issue 6
Abstract
Background: Thalassemiais one of the most common inherited single-gene disorder in the world. Every year approximately 100,000 thalassemia major children are born all over the world, and there are about 65,000-67,000 β thalassemia major patients in India, with around 9,000-10,000 cases being added every year. Measurement of serum ferritin level can give idea regarding starting of Iron chelation therapy, which will reduce the concentration of serum ferritin and effective in preventing iron induced tissue injury and prolonging life expectancy. Method: This study was conducted on 60 children between 3 to 17 years, being regularly transfused at department of Pediatrics, Kamala Raja Hospital, Gajra Raja Medical College, Gwalior, for period of 1 year from 2011 to 2012, after taking the informed consent from the parents and explaining them the purpose of study. Detailed history weretaken and serum ferritin level weremeasured by ELISA based serum ferritin assay kit. Results: Serum ferritin level was found to be elevated in all the patients of beta thalassemia major with range from 1050 to 5029 μg/l and with a mean value of 3879μg/l. Out of 60 patients, 30 (50%) patients had serum ferritin level below 2000μg/l,20 (33.3%) patients had serum ferritin value between 2001 to 4000 μg/l and rest 10 (17.7%) patients had values above 4000 μg/l. Mean value of serum ferritin was found to be higher in patients who received frequent blood transfusion. Conclusion: Majority of the patients had very high ferritin levels, with a mean value of 3879 μg/l. 50% patients had serum ferritin levels more than 2000μg/l. This cut off value reflect either inadequate chelation therapy or non-affordability of parents to purchase oral chelation therapy.
Authors and Affiliations
Sunita Koreti, Bablu Kumar Gaur, Ghanshyam Das, Ajay Gaur
Neuroimaging in Japanese encephalitis and their correlation with clinical profile in pediatric patients
Introduction: Japanese encephalitis is a major public health problem in Indian subcontinent. Regardless of all advances in prompt diagnosis of JE, it may be difficult to differentiate JE from other viral encephalitis. Ai...
A rare case of Mitochondrial Fatty Acid Oxidation Defect- Systemic Primary Carnitine Deficiency
Systemic primary carnitine deficiency (SPCD) also known as, carnitine transporter deficiency (CTD) is an inborn error of fatty acid transport caused by a defect in the transporter responsible for moving carnitine across...
To study the Knowledge regarding immunization schedule among parents and the source of information regarding vaccination
Background: Immunization, the most cost-effective public health intervention, continues to be under-used. It is profoundly tragic that almost two million children still die each year from disease for which vaccines are a...
Study of neuro developmental outcome of hypoxic ischemic encephalopathy of less than one-year infant in a tertiary care institute
Introduction: Perinatal asphyxia can lead to hypoxic ischemic encephalopathy (HIE). The mortality due to hypoxic ischemic encephalopathy is as high as 28.8% and morbidity is 30% of surviving new-born due to hypoxic ische...
Spondylocostal Dysostosis with Sprengel Deformity: A Rare Association
Spondylocostal dysostosis (SCDO) refers to multiple segmentation defects of the vertebrae in combination with abnormalities of the ribs. Sprengel deformity is a congenital elevation of the scapula. Here, we would like to...