Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/53109
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dc.contributor.authorLoh J.B.-E.-
dc.contributor.authorWellard C.-
dc.contributor.authorHaysom H.E.-
dc.contributor.authorSparrow R.L.-
dc.contributor.authorWood E.M.-
dc.contributor.authorMcQuilten Z.K.-
dc.date.accessioned2025-01-20T00:25:12Z-
dc.date.available2025-01-20T00:25:12Z-
dc.date.copyright2025-
dc.date.issued2025-01-08en
dc.identifier.citationTransfusion. (no pagination), 2025. Date of Publication: 2025.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/53109-
dc.description.abstractBackground: The provision of ABO-incompatible fresh frozen plasma (FFP) in massive transfusion (MT) has become accepted to conserve AB FFP stock. There is an evidence gap in non-trauma settings. We compare characteristics of patients who received ABO-compatible or ABO-incompatible FFP during an MT episode due to any cause of critical bleeding, and assess the impact of incompatible FFP transfusion on inhospital mortality. Method(s): Using the Australian and New Zealand Massive Transfusion Registry, data were extracted for patients aged >=18 years who received an MT (defined as >=5 red cell units in 4 h) between April 2011 and October 2018. Incompatible FFP was defined as transfusion of >=1 unit of FFP with a bidirectional or minor ABO-mismatch in the first 24 h from MT initiation. Result(s): A total of 7340 patients from 28 hospitals were included. Seventy-seven (1%) patients received incompatible FFP (26 trauma, 51 non-trauma). Those who had incompatible FFP received a median of seven units of FFP, compared to those who only received compatible FFP receiving five units, p =.005. A total of 226 units of incompatible FFP were provided overall. Incompatible FFP provision was not independently associated with inhospital mortality in MT (HR of 1.40 [95% CI 0.84-2.26, p =.2]). Variables independently associated with inhospital mortality included increased FFP volume in the first 24 h, age, Charlson Comorbidity Index score, and lower pre-transfusion fibrinogen and peri-transfusion pH values. Conclusion(s): Transfusion of incompatible FFP in MT in our cohort was not independently associated with higher inhospital mortality, although the number of patients who received incompatible FFP was small.Copyright © 2024 AABB.-
dc.publisherJohn Wiley and Sons Inc-
dc.relation.ispartofTransfusion-
dc.subject.meshbleeding-
dc.titleOutcomes of massive transfusion recipients administered abo-incompatible fresh frozen plasma.-
dc.typeArticle-
dc.identifier.affiliationHaematology-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional, or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1111/trf.18070-
dc.publisher.placeUnited States-
dc.identifier.pubmedid39739303-
dc.identifier.institution(Loh, Wellard, Haysom, Sparrow, Wood, McQuilten) Transfusion Research Unit, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia-
dc.identifier.institution(Loh, Wood, McQuilten) Department of Haematology, Monash Health, Melbourne, VIC, Australia-
dc.identifier.institution(McQuilten) Department of Haematology, Alfred Health, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Loh, Wood, McQuilten) Department of Haematology, Monash Health, Melbourne, VIC, Australia-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptHaematology-
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