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dc.contributor.authorMarwah, S.S.
dc.contributor.authorBlann, A.D.
dc.contributor.authorHarrison, P.
dc.contributor.authorLumley, M.A.
dc.contributor.authorWright, J.
dc.contributor.authorMcDowell, J.
dc.contributor.authorPhillips, Jonathan D.
dc.contributor.authorRea, C.
dc.contributor.authorBareford, D.
dc.date.accessioned2008-06-04T11:17:52Z
dc.date.available2008-06-04T11:17:52Z
dc.date.issued2002
dc.identifier.citationVox Sanguinis, 82(3): 122-126
dc.identifier.issn0042-9007
dc.identifier.pmid11952985
dc.identifier.doi10.1046/j.1423-0410.2002.00153.x
dc.identifier.urihttp://hdl.handle.net/2436/29473
dc.description.abstractBACKGROUND AND OBJECTIVES: Non-transferrin bound iron (NTBI) is associated with increased morbidity in a number of transfusion-dependent disease states such as the severe haemoglobinopathies. We hypothesized that this may be related to excess NTBI present in plasma-depleted red blood cell units that are free of clear haemolysis. MATERIALS AND METHODS: The level of NTBI was determined using the bleomycin assay in samples from 20 stored plasma-depleted red cell units, at approximate 5-day intervals up to day 33 after donation. Forty units of fresh-frozen plasma (FFP) and 40 units of platelet concentrates were used as negative controls, and samples from 12 units of FFP were also serially assessed. RESULTS: Median [interquartile range (IQR)] NTBI was 0 microm (0-0.35) in samples taken from units 3-10 days after donation. Thereafter, the levels of NTBI increased, becoming significant (median 3.05; IQR: 0.05-6.7 microm) 17-22 days after donation. After 30 days, NTBI was detectable in all red cell units. NTBI was undetectable in platelet concentrates and FFP. CONCLUSIONS: Increased levels of NTBI become detectable 17-22 days after donation and increase further with storage time. This excess NTBI may promote bacterial infection in iron-loaded individuals.
dc.language.isoen
dc.publisherWiley InterScience
dc.relation.urlhttp://www.ingentaconnect.com/content/bsc/vox/2002/00000082/00000003/art00003
dc.subjectBacterial contamination
dc.subjectFresh-frozen plasma
dc.subjectBlood Transfusion
dc.subjectNontransferrin bound iron (NTBI)
dc.subjectPlatelets
dc.subjectSAG-M
dc.subject.meshBacterial Infections
dc.subject.meshBlood Preservation
dc.subject.meshErythrocyte Transfusion
dc.subject.meshErythrocytes
dc.subject.meshHumans
dc.subject.meshIron Overload
dc.subject.meshPlasma Substitutes
dc.subject.meshTime Factors
dc.subject.meshTransferrin
dc.titleIncreased non-transferrin bound iron in plasma-depleted SAG-M red blood cell units.
dc.typeJournal article
dc.identifier.journalVox Sanguinis
html.description.abstractBACKGROUND AND OBJECTIVES: Non-transferrin bound iron (NTBI) is associated with increased morbidity in a number of transfusion-dependent disease states such as the severe haemoglobinopathies. We hypothesized that this may be related to excess NTBI present in plasma-depleted red blood cell units that are free of clear haemolysis. MATERIALS AND METHODS: The level of NTBI was determined using the bleomycin assay in samples from 20 stored plasma-depleted red cell units, at approximate 5-day intervals up to day 33 after donation. Forty units of fresh-frozen plasma (FFP) and 40 units of platelet concentrates were used as negative controls, and samples from 12 units of FFP were also serially assessed. RESULTS: Median [interquartile range (IQR)] NTBI was 0 microm (0-0.35) in samples taken from units 3-10 days after donation. Thereafter, the levels of NTBI increased, becoming significant (median 3.05; IQR: 0.05-6.7 microm) 17-22 days after donation. After 30 days, NTBI was detectable in all red cell units. NTBI was undetectable in platelet concentrates and FFP. CONCLUSIONS: Increased levels of NTBI become detectable 17-22 days after donation and increase further with storage time. This excess NTBI may promote bacterial infection in iron-loaded individuals.


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