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Blood transfusion therapy for β-thalassemia major and hemoglobin E β-thalassemia: Adequacy, trends, and determinants in Sri Lanka.
- Source :
-
Pediatric blood & cancer [Pediatr Blood Cancer] 2019 May; Vol. 66 (5), pp. e27643. Date of Electronic Publication: 2019 Jan 29. - Publication Year :
- 2019
-
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.<br />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.<br />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.<br />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.<br /> (© 2019 Wiley Periodicals, Inc.)
- Subjects :
- Adolescent
Blood Transfusion statistics & numerical data
Child
Child, Preschool
Cross-Sectional Studies
Female
Follow-Up Studies
Hepatomegaly epidemiology
Humans
Incidence
Male
Splenomegaly epidemiology
Sri Lanka epidemiology
Blood Transfusion methods
Blood Transfusion trends
Hemoglobin E metabolism
beta-Thalassemia classification
beta-Thalassemia therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1545-5017
- Volume :
- 66
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Pediatric blood & cancer
- Publication Type :
- Academic Journal
- Accession number :
- 30697927
- Full Text :
- https://doi.org/10.1002/pbc.27643