Abstract
While hypertransfusion and subcutaneous iron chelation therapy have increased longevity of patients with beta-thalassemia (thal) major, endocrinopathies have become more common and impair the quality of their lives. Additionally, subcutaneous iron chelation therapy is an uncomfortable experience and can prevent patients from regular compliance with iron chelation therapy. We compared the efficacy of oral deferiprone (L1) to subcutaneous desferrioxamine (DFO) chelation therapy for the prevention of major endocrinopathies (growth hormone insufficiency, diabetes mellitus and gonadal dysfunction) among patients with beta-thal major to see if we could offer these patients an easier and more painless way to reduce their body iron load and related endocrine complications.
Publication types
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Comparative Study
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Controlled Clinical Trial
MeSH terms
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Administration, Oral
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Adolescent
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Adult
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Chelation Therapy / methods*
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Child
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Combined Modality Therapy
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Deferiprone
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Deferoxamine / administration & dosage
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Deferoxamine / therapeutic use*
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Diabetes Mellitus / etiology
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Diabetes Mellitus / prevention & control
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Dwarfism, Pituitary / etiology
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Dwarfism, Pituitary / prevention & control
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Endocrine System Diseases / etiology
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Endocrine System Diseases / prevention & control*
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Female
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Human Growth Hormone / deficiency
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Humans
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Hypogonadism / etiology
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Hypogonadism / prevention & control
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Infusions, Parenteral
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Iron Chelating Agents / administration & dosage
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Iron Chelating Agents / therapeutic use*
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Iron Overload / drug therapy*
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Iron Overload / etiology
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Male
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Patient Compliance
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Puberty, Delayed / etiology
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Puberty, Delayed / prevention & control
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Pyridones / administration & dosage
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Pyridones / therapeutic use*
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Subcutaneous Tissue
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Transfusion Reaction
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beta-Thalassemia / complications
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beta-Thalassemia / drug therapy*
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beta-Thalassemia / therapy
Substances
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Iron Chelating Agents
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Pyridones
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Human Growth Hormone
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Deferiprone
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Deferoxamine