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PMID: 5956023 Published · ppublish English Journal Article

Iron chelation in haematomas at fracture sites.

Journal of clinical pathology ·Vol. 19 ·No. 4 ·1966-07-00 ·Pages 364-7

O'Shaughnessy MC, Brunström GM, Fielding J

Abstract

Previous work suggested that during the catabolism of haemoglobin a physico-chemical form of iron was released which was more readily chelatable by desferrioxamine than normal storage forms, as ferritin-haemosiderin. Desferrioxamine chelation was therefore investigated in five patients with major fractures in which haemoglobin catabolism is greatly enhanced by the red cell destruction which proceeds in the associated haematoma. Considerable increases in the amounts of iron mobilized by desferrioxamine were observed from the second day after injury. In severe interstitial haemorrhage, these values tended to increase until 10 to 20 days, and sometimes were as high as chelation values seen in haemochromatosis. These results are considered to support the hypothesis that a highly chelatable form of iron is found at some stage during haemoglobin catabolism.

MeSH Terms
Adult Deferoxamine/therapeutic use Female Fractures, Bone/complications Hematoma Hemoglobins/metabolism Humans Iron/blood Iron Chelating Agents/therapeutic use Male Middle Aged
Chemicals
Hemoglobins Iron Chelating Agents Iron Deferoxamine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
O'Shaughnessy M C
Brunström G M
Fielding J
References (8)
8 references, click to expand
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    J Clin Pathol. 1964 Jul;17:395-8 PMID: 14195624
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    J Clin Pathol. 1965 Jan;18:88-97 PMID: 14247711
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    Acta Endocrinol (Copenh). 1955 Oct;20(2):148-56 PMID: 13275245
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Article Info
Journal
Journal of clinical pathology
Abbr.
J Clin Pathol
ISSN
0021-9746
Published
1966-07-00
Pages
364-7
Language
English
Region
England
NLM ID
0376601
PMCID
PMC473285
Subset
IM
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