FREQUENCY AND COMPLICATION OF SERUM IRON OVERLOAD IN TRANSFUSION DEPENDENT PATIENT

Main Article Content

Wajeeha Rahman
Ansa kalsoom rehman
Hira arooj
Gulshan munir
Seema gul hussain
Aftab Nazir
Farhana jabeen shah

Keywords

serum iron overload, transfusion, hemoglobin, thalassemia

Abstract

Introduction: The aim of the current study was to determine the frequency and complications of serum iron overload in transfusion-dependent patients with an aim to assess the prevalence of iron overload and identify associated complications.


Methods: The current study adopted cross-sectional and observational research design. The data was collected the transfusion-dependent patients who were receiving regular treatment at the Hayatabad Medical Complex (HMC), Peshawar. A sample of 151 patients who were dependent on transfusion was collected through convenient sampling technique. Information on the duration and frequency of blood transfusions, the frequency of serum ferritin level monitoring, and recent ferritin levels, and complications experienced by the patient due to iron overload were collected through structured questionnaire. Statistical analysis, including demographic, descriptive, chi-square and cross-tabulation was conducted through SPSS.


Results: The analysis of 151 transfusion-dependent patients revealed that liver enlargement (29.8%) and fatigue (23.2%) are the most common complications of iron overload. Results also shows that majority of patients (43.0%) have moderate serum iron overload while iron Chelation Therapy is the most commonly administered treatment, particularly for patients with severe iron overload (75%). Patients generally start experiencing complications between 10 and 30 years of age. The demographic data indicate a predominance of thalassemia and a fairly balanced gender distribution among the study participants.


Conclusion: Regular monitoring of serum ferritin levels and related issues is crucial for early diagnosis and treatment. Patients need to be educated about the risks of iron overload and the need of sticking to their treatment plans.

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References

1. Cacciotti, C. and U. Athale, Transfusion-related iron overload in children with leukemia. Journal of Pediatric Hematology/Oncology, 2021. 43(1): p. 18-23.
2. Chan, K.C., et al., Pulmonary function in patients with transfusion-dependent thalassemia and its associations with iron overload. Scientific Reports, 2023. 13(1): p. 3674.
3. DivakarJose, R.R., C. Delhikumar, and G. Ram Kumar, Efficacy and safety of combined oral chelation with deferiprone and deferasirox on iron overload in transfusion dependent children with thalassemia–A Prospective Observational Study. Indian Journal of Pediatrics, 2021. 88: p. 330-335.
4. Kapure, A., BLOOD TRANSFUSION COMPLICATIONS PREVALENCE PARAMETRIC CAUSES FOR STRESS OF DISEASE AND MANGEMENT OF TRANSFUSION DEPENDENT THALASSEMIA: A NARRATIVE REVIEW. 2020.
5. Karimi, M., et al., Prevalence and severity of Coronavirus disease 2019 (COVID-19) in Transfusion Dependent and Non-Transfusion Dependent β-thalassemia patients and effects of associated comorbidities: an Iranian nationwide study. Acta Bio Medica: Atenei Parmensis, 2020. 91(3): p. e2020007.
6. Padeniya, P., et al., Frequency of Hereditary Hemochromatosis Gene (HFE) Variants in Sri Lankan Transfusion-Dependent Beta-Thalassemia Patients and Their Association With the Serum Ferritin Level. Frontiers in Pediatrics, 2022. 10: p. 890989.
7. Pinto, V.M. and G.L. Forni, Management of iron overload in beta-thalassemia patients: clinical practice update based on case series. International Journal of Molecular Sciences, 2020. 21(22): p. 8771.
8. Piperno, A., S. Pelucchi, and R. Mariani, Inherited iron overload disorders. Translational gastroenterology and hepatology, 2020. 5.
9. Verma, G., et al., Clinical, Hematological Profile and Status of Iron Overload in Children with Transfusion Dependent Thalassemia: A Study from Rural Northern India.
10. Bauduer, F. and H. Recanzone, Transfusional iron overload in patients with myelodysplastic syndromes: A 10-year retrospective survey from a French general hospital. Transfusion Clinique et Biologique, 2020. 27(3): p. 128-132.
11. Bauduer, F. and H. Recanzone, Transfusional iron overload in heavily transfused patients: Real-life data from a 10-year retrospective study of 611 cases managed in a French general hospital. Transfusion Clinique et Biologique, 2022. 29(3): p. 236-242.
12. Cattoni, A., et al., Iron Overload Following Hematopoietic Stem Cell Transplantation: Prevalence, Severity, and Management in Children and Adolescents with Malignant and Nonmalignant Diseases. Transplantation and Cellular Therapy, 2023. 29(4): p. 271. e1-271. e12.
13. Fianza, P.I., et al., Iron Overload in Transfusion‐Dependent Indonesian Thalassemic Patients. Anemia, 2021. 2021(1): p. 5581831.
14. Franke, G.-N., et al., Iron overload and its impact on outcome of patients with hematological diseases. Molecular Aspects of Medicine, 2020. 75: p. 100868.
15. Kurban, L.A., et al., Optimized serum ferritin prediction of iron overload in transfusion-dependent thalassemia: likelihood ratio and age-adjustment approach. Annals of Saudi medicine, 2023. 43(2): p. 90-96.
16. Rotha, K.T., Iron Overload Complication in Thalassemia Patients. Indian Journal of Forensic Medicine & Toxicology, 2020. 14(2).
17. Soliman, A.T., et al., Blood transfusion and iron overload in patients with Sickle Cell Disease (SCD): Personal experience and a short update of diabetes mellitus occurrence. Acta Bio Medica: Atenei Parmensis, 2022. 93(4).
18. Tat, L.K., L.S. Lin, and G.A. Sim, Prevalence of endocrine complications in transfusion dependent thalassemia in Hospital Pulau Pinang: A pilot study. Med J Malay, 2020. 75(1): p. 33-37.

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