Haematologica
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Published online 15 April 2008
Haematologica, Vol 93, Issue 6, 917-920 doi:10.3324/haematol.12513
Copyright © 2008 by Ferrata Storti Foundation
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Brief Report

Onset of cardiac iron loading in pediatric patients with thalassemia major

John C. Wood1, Raffaella Origa2, Annalisa Agus2, Gildo Matta3, Thomas D. Coates1, Renzo Galanello2

1 Department of Pediatrics and Radiology, Childrens Hospital Los Angeles, Los Angeles, CA, USA;
2 Departimento di Scienze Biomediche e Biotecnologie, Ospedale Regionale Microcitemie, Universita di Cagliari, Italy and
3 Division of Radiology, Ospedale San Michele, Cagliari, Italy

Correspondence: John C. Wood, Division of Cardiology, Mailstop 34, Children's Hospital Los Angeles, 4650 Sunset Blvd., Los Angeles, CA, 90027, USA. E-mail:jwood{at}chla.usc.edu

ABSTRACT

We reviewed cardiac T2* assessments from 77 thalassemia major patients between the ages of 2.5 and 18 years to study optimal timing of cardiac iron screening by magnetic resonance imaging. No patient under 9.5 years of age showed detectable cardiac iron in contrast to 36% of patients between the ages of 15–18 years old, corresponding to an odds-ratio of 1.28 (28%) per year. All patients with cardiac iron had received at least 35 grams of transfusional iron. Liver iron and ferritin failed to predict cardiac iron loading. Initiation of cardiac magnetic resonance imaging assessment should be determined according to age and transfusional burden rather than indices of iron overload. When appropriate chelation therapy has been administered since birth, cardiac magnetic resonance imaging can be postponed until 8 years of age when anesthesia is not required. Patients with suboptimal chelation, increased transfusional requirements, or who have initiated transfusions later in life should be tested sooner.

Key words: thalassemia major, heart, MRI, iron overload, children.




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