Sep 2026· International Journal of Research in Medical Sciences· 0 citations· 27 references
TL;DR
Tracking transfusion volume, serial ferritin, and chelation adherence may improve iron-overload monitoring in resource-constrained TDT care.
Abstract
Background: Regular red-cell transfusion is essential for patients with transfusion-dependent thalassemia (TDT) but causes progressive iron loading. Where MRI-based tissue iron assessment is not routinely available, serum ferritin remains a practical marker. This study evaluated the association between transfusion burden and serum ferritin in patients with TDT.
Methods: This cross-sectional study included 150 patients with TDT at Sirajganj Medical College Hospital, Bangladesh, from July 2025 to June 2026. Transfusion exposure, pre-transfusion hemoglobin, thalassemia phenotype, chelation adherence, splenectomy status, and serum ferritin were assessed. Associations were examined using Spearman correlation and multivariable linear and logistic regression.
Results: Mean age was 17.06±6.87 years; 60.7% were male. Median annual transfusion burden was 144.08 ml/kg/year (IQR 126.95–161.41) and median ferritin was 1965.00 ng/mL (IQR 1329.28–2723.51); 31.3% had ferritin ≥2500 ng/mL. Annual transfusion burden correlated positively with ferritin (coefficient=0.231, p=0.004). After adjustment, each additional 10 ml/kg/year was associated with 5.9% higher ferritin (B=0.057, 95% CI 0.030–0.083; p<0.001) and 27% higher odds of ferritin ≥2500 ng/mL (aOR 1.27, 95% CI 1.08–1.50; p=0.004). Poor chelation adherence was strongly associated with ferritin ≥2500 ng/mL (aOR 6.92, 95% CI 2.84–16.85; p<0.001).
Conclusions: Greater transfusion burden and poor chelation adherence were independently associated with higher serum ferritin. Tracking transfusion volume, serial ferritin, and chelation adherence may improve iron-overload monitoring in resource-constrained TDT care.
Background: Transfusion-dependent β-thalassemia major requires lifelong blood transfusions, resulting in iron overload and hepatic and renal complications. Serum ferritin is widely used as a surrogate marker of body iron stores. This study evaluated serum ferritin levels and their association with hepatic and renal fun...
Rahul Garg, Mandayal Jamatia, Ritesh Vishwakarma· International Journal of Res...· 0 citations
Background: Growth impairment and undernutrition remain important concerns in children with transfusion-dependent β-thalassemia (TDT). Regular transfusion improves anemia but is accompanied by progressive iron loading, making simultaneous assessment of growth, transfusion adequacy, and iron burden important. The object...
Aashna Gupta, Naman Jain, Gajender Singh et al.· Acta Medica International· 0 citations
Introduction: Patients with beta-thalassemia frequently experience iron overload due to hemolysis and repeated transfusions, with the liver being a primary site of iron deposition. Excess iron can cause oxidative stress and liver dysfunction, making hepatic markers crucial for monitoring iron toxicity. This study exami...
Syakira Fitri Aulia, Pradana Zaky Romadhon, S. Suryantoro et al.· Current Internal Medicine Re...· 0 citations
Background: Regular iron chelation therapy is critical to prevent iron overload complications in transfusion-dependent patients. However, adherence remains suboptimal, thalassaemia is one of the most common inherited hemoglobin disorders worldwide, with a particularly high burden in South and Southeast Asia.
Objectives...
Mehnaj Ashraf, S. Selim, Md. Salahuddin Shah et al.· Journal of Association of Cl...· 0 citations
Serum ferritin concentrations were significantly associated with several red cell indices, particularly MCH and MCV, while RDW-CV demonstrated the greatest ability to distinguish children with IDA from those with normal ferritin levels, and routine CBC parameters, especially RDW-CV, MCH, and MCV, may serve as practical...
Khadeejah M. A. al-Khurum· Razi Medical Journal· 0 citations
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