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Blood transfusion therapy for β-thalassemia major and hemoglobin E β-thalassemia: adequacy, trends, and determinants in Sri Lanka.

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dc.contributor.author Mettananda, S.
dc.contributor.author Pathiraja, H.
dc.contributor.author Peiris, R.
dc.contributor.author Wickramarathne, N.
dc.contributor.author Bandara, D.
dc.contributor.author de Silva, U.
dc.contributor.author Mettananda, C.
dc.contributor.author Premawardhena, A.
dc.date.accessioned 2019-02-21T07:04:29Z
dc.date.available 2019-02-21T07:04:29Z
dc.date.issued 2019
dc.identifier.citation Pediatric Blood and Cancer.2019: e27643 en_US
dc.identifier.issn 1545-5009 (Print)
dc.identifier.issn 1545-5017 (Electronic)
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/19972
dc.description Indexed in Medline en_US
dc.description.abstract BACKGROUND: Regular blood transfusion therapy still remains the cornerstone in the management of β-thalassemia. Although recommendations are clear for patients with β-thalassemia major, uniform transfusion guidelines are lacking for patients with hemoglobin E β-thalassemia. In this study, we aim to describe the adequacy, trends, and determinants of blood transfusion therapy in a large cohort of pediatric patients with β-thalassemia major and hemoglobin E β-thalassemia. METHODS/PROCEDURE: This cross-sectional study was performed among all regularly transfused patents with β-thalassemia aged 2 to 18 years attending three large thalassemia centers in Sri Lanka. Data were collected using an interviewer-administered questionnaire, perusal of clinical records, and physical examination of patients by trained doctors. RESULTS: A total of 328 patients (male 47%) were recruited; 83% had β-thalassemia major, whereas 16% had hemoglobin E β-thalassemia. Sixty-one percent of patients had low pretransfusion hemoglobin levels (< 9.0 g/dL) despite receiving high transfusion volumes (> 200 mL/kg/year) by a majority (56%). Median pretransfusion hemoglobin was significantly lower in patients with hemoglobin E β-thalassemia compared with β-thalassemia major (P < 0.001); however, there was no difference in requirement for high transfusion volumes over 200 mL/kg/year in both groups (P = 0.14). Hepatomegaly and splenomegaly were more common in hemoglobin E β-thalassemia and were associated with lower pretransfusion hemoglobin. Transfusion requirements were higher among patients with hepatitis C and in those who are underweight. CONCLUSIONS: Over 60% of regularly transfused patients with β-thalassemia have low pretransfusion hemoglobin levels despite receiving large transfusion volumes. Patients with hemoglobin E β-thalassemia are undertransfused and specific recommendations should be developed to guide transfusions in these patients. en_US
dc.language.iso en en_US
dc.publisher John Wiley en_US
dc.subject Hemoglobinopathies en_US
dc.title Blood transfusion therapy for β-thalassemia major and hemoglobin E β-thalassemia: adequacy, trends, and determinants in Sri Lanka. en_US
dc.type Article en_US


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