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Desferrioxamine mesylate for managing transfusional iron overload in people with transfusion‐dependent thalassaemia

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Abstract

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Background

Thalassaemia major is a genetic disease characterised by a reduced ability to produce haemoglobin. Management of the resulting anaemia is through transfusions of red blood cells.

Repeated transfusions results in excessive accumulation of iron in the body (iron overload), removal of which is achieved through iron chelation therapy. Desferrioxamine is the most widely used iron chelator. Substantial data have shown the beneficial effects of desferrioxamine. However, important questions exist about whether desferrioxamine is the best schedule for iron chelation therapy.

Objectives

To determine the effectiveness (dose and method of administration) of desferrioxamine in people with transfusion‐dependent thalassaemia.

Search methods

We searched the Cochrane Haemoglobinopathies Trials Register, MEDLINE, EMBASE, ZETOC, Current Controlled Trials and bibliographies of relevant publications. We also contacted the manufacturers of desferrioxamine and other iron chelators.

Date of last searches: April 2004.

Selection criteria

Randomised controlled trials comparing desferrioxamine with placebo; with another iron chelator; or comparing two schedules of desferrioxamine, in people with transfusion‐dependent thalassaemia.

Data collection and analysis

Four authors working independently, were involved in trial quality assessment and data extraction. Missing data were requested from the original investigators.

Main results

Eight trials involving 334 people (range 20 to 144 people) were included. One trial compared desferrioxamine with placebo, five compared desferrioxamine with another iron chelator (deferiprone) and two compared different schedules of desferrioxamine. Overall, few trials measured the same outcomes.

Compared to placebo, desferrioxamine significantly reduced iron overload. The number of deaths at 12 years follow up and evidence of reduced end‐organ damage was less for desferrioxamine than placebo. When desferrioxamine was compared to deferiprone or a different desferrioxamine schedule there were no statistically significant differences in measures of iron overload. Compliance was recorded by two trials. Compliance was less for desferrioxamine than deferiprone in one trial and of no difference in comparison with desferrioxamine and deferiprone combined with a second trial.

Adverse events were recorded in trials comparing desferrioxamine with other iron chelators. There was evidence of adverse events in all treatment groups. In one trial, adverse events were significantly less likely with desferrioxamine than deferiprone, relative risk 0.45 (95% confidence interval 0.24 to 0.84).

Assessment of the methodological quality of included trials was not possible, given the general absence of these data in the trials.

Authors' conclusions

We found no reason to change current treatment recommendations. However, considerable uncertainty continues to exist about the optimal schedule for desferrioxamine in people with transfusion‐dependent thalassaemia.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Plain language summary

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Desferrioxamine mesylate for managing excess iron levels in the blood in people with thalassaemia who depend on blood transfusions

Thalassaemia is a genetic disease. People with thalassaemia are not able to produce enough haemoglobin. Haemoglobin is the part of the blood which carries oxygen around the body. A lack of this leads to anaemia. Treatment with blood transfusions leads to high levels of iron in the body. Excess iron must be removed to prevent damage to major organs. This is done through iron chelation therapy: the most widely used drug is desferrioxamine. The review includes eight trials which compared desferrioxamine to placebo or another iron chelator or to different doses of desferrioxamine. The review found that desferrioxamine is better than no iron chelation. But the drug does have side effects in some people. One trial showed fewer adverse events with desferrioxamine than another iron chelator. The best dosage of desferrioxamine is still very uncertain. Further research should answer this question. We can not recommend any change in practice at this time.