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Prevention of heart disease by subcutaneous desferoxamine in patients with thalassaemia major

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Abstract Background: Cardiac siderosis from transfused iron remains the major cause of death in thalassaemia major, despite iron chelation therapy with desferrioxamine. Aims: Our aim was to determine the nature and extent of cardiac involvement and its relationship to desferrioxamine use in a group with thalassaemia major. Methods: We reviewed 76 patients with thalassaemia major and performed multiple logistic regression to analyse factors affecting cardiac involvement. Factors studied included: patient sex, age, haemoglobin, serum ferritin, total transfusions, liver iron, duration of desferrioxamine use, electrocardiograms, echocardiograms and compliance to desferrioxamine treatment. Results: Thirty‐seven patients developed heart disease. They were older (p < 0.001), began desferrioxamine later (p < 0.001), had more liver iron (p= 0.014), higher serum ferritin levels (p= 0.023) and received more blood (p = 0.018). Compared to those with optimal compliance the odds of developing heart disease were increased 10.7 times in fair compilers (p <0.001) and 5.1 times in poor compilers (p= 0.016). However, there was no significant difference between those with fair and poor compliance. After multivariate analysis only compliance (p= 0.02) and age at desferrioxamine onset (p= 0.004) remained significant. Compliance was inversely related to liver iron (p< 0.001), serum ferritin (p< 0.001) and age at desferrioxamine commencement (p< 0.001). Conclusions: We conclude that late commencement of desferrioxamine and noncompliance are associated with greater iron loading and an increased riskof heart disease. (Aust NZ J Med 1993; 23: 656–661.)
Title: Prevention of heart disease by subcutaneous desferoxamine in patients with thalassaemia major
Description:
Abstract Background: Cardiac siderosis from transfused iron remains the major cause of death in thalassaemia major, despite iron chelation therapy with desferrioxamine.
Aims: Our aim was to determine the nature and extent of cardiac involvement and its relationship to desferrioxamine use in a group with thalassaemia major.
Methods: We reviewed 76 patients with thalassaemia major and performed multiple logistic regression to analyse factors affecting cardiac involvement.
Factors studied included: patient sex, age, haemoglobin, serum ferritin, total transfusions, liver iron, duration of desferrioxamine use, electrocardiograms, echocardiograms and compliance to desferrioxamine treatment.
Results: Thirty‐seven patients developed heart disease.
They were older (p < 0.
001), began desferrioxamine later (p < 0.
001), had more liver iron (p= 0.
014), higher serum ferritin levels (p= 0.
023) and received more blood (p = 0.
018).
Compared to those with optimal compliance the odds of developing heart disease were increased 10.
7 times in fair compilers (p <0.
001) and 5.
1 times in poor compilers (p= 0.
016).
However, there was no significant difference between those with fair and poor compliance.
After multivariate analysis only compliance (p= 0.
02) and age at desferrioxamine onset (p= 0.
004) remained significant.
Compliance was inversely related to liver iron (p< 0.
001), serum ferritin (p< 0.
001) and age at desferrioxamine commencement (p< 0.
001).
Conclusions: We conclude that late commencement of desferrioxamine and noncompliance are associated with greater iron loading and an increased riskof heart disease.
(Aust NZ J Med 1993; 23: 656–661.
).

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