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Cochrane Database of Systematic Reviews

Deferasirox for managing iron overload in people with thalassaemia

Overview of attention for article published in this source, February 2012
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Title
Deferasirox for managing iron overload in people with thalassaemia
Published by
John Wiley & Sons, Ltd, February 2012
DOI 10.1002/14651858.cd007476.pub2
Pubmed ID
Authors

Meerpohl, Joerg J, Antes, Gerd, Rücker, Gerta, Fleeman, Nigel, Motschall, Edith, Niemeyer, Charlotte M, Bassler, Dirk

Abstract

Thalassemia is a hereditary anaemia due to ineffective erythropoiesis. In particular, people with thalassaemia major develop secondary iron overload resulting from regular red blood cell transfusion. Iron chelation therapy is needed to prevent long-term complications.Both deferoxamine and deferiprone have been found to be efficacious. However, a systematic review of the effectiveness and safety of the new oral chelator deferasirox in people with thalassaemia is needed.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 92 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Indonesia 1 1%
France 1 1%
Unknown 90 98%

Demographic breakdown

Readers by professional status Count As %
Student > Master 16 17%
Researcher 14 15%
Student > Bachelor 12 13%
Student > Ph. D. Student 10 11%
Student > Postgraduate 9 10%
Other 20 22%
Unknown 11 12%
Readers by discipline Count As %
Medicine and Dentistry 45 49%
Nursing and Health Professions 11 12%
Psychology 5 5%
Agricultural and Biological Sciences 3 3%
Pharmacology, Toxicology and Pharmaceutical Science 3 3%
Other 8 9%
Unknown 17 18%