Association between red blood cell transfusion and adverse clinical outcomes is Independent of cardiac history: a multicenter observational InPUT study analysis
Status In-Process Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
PubMed
41413913
PubMed Central
PMC12713240
DOI
10.1186/s13054-025-05745-5
PII: 10.1186/s13054-025-05745-5
Knihovny.cz E-zdroje
- Klíčová slova
- Critical care, Heart failure, Intensive care units, Red blood cell transfusion,
- Publikační typ
- časopisecké články MeSH
PURPOSE: Red-blood-cell (RBC) transfusion is one of the most frequent interventions in critical care patients. While patients with acute cardiac conditions are more likely to receive transfusions at higher haemoglobin thresholds than other critically ill patients, data on RBC transfusion practice for critically ill patients with pre-existing cardiac conditions are scarce. METHODS: Using the International Point-Prevalence Study of Intensive-Care Unit Transfusion Practices cohort, weighted logistic regression investigated the association between the RBC units transfused and the primary composite outcome of 28-day mortality, new-onset acute kidney injury or ventilatory weaning failure. Interactions with cardiac history (acute coronary syndrome and/or heart failure) were tested. RESULTS: Cardiac history was present in 746 of 3643 patients (20%) and 894 of 3643 (25%) received at least one RBC unit. Transfusion rates were similar in patients with and without cardiac history (25% vs. 24%; p = 0.51). Among transfused patients, median nadir haemoglobin during ICU stay was slightly higher in those with cardiac history (7.6 g/dL vs. 7.4 g/dL respectively; p = 0.007), whereas stated haemoglobin transfusion threshold did not statistically differ (8.5 g/dL vs. 8.0 g/dL; p = 0.11). Each additional RBC unit increased the odds of the composite outcome in the whole cohort (2.18, 95% CI 1.85–2.56, p < 0.0001), without interaction with cardiac history (p = 0.44). CONCLUSIONS: RBC transfusion was commonly and similarly prescribed in critically ill patients with or without cardiac history. Each additional unit was associated with a worse outcome with no evidence of differential effect due to cardiac history. TRIAL REGISTRATION: NL9049 (Dutch Trial Register), registered on 16 November 2020. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-025-05745-5.
Department of Anesthesia and Intensive Care Military Medical Academy Belgrade Belgrade Serbia
Department of Anesthesiology Aga Khan University Hospital Nairobi Kenya
Department of Anesthesiology and Intensive Care IRCCS Humanitas Research Hospital Milan Italy
Department of Anesthesiology University Medical Center Groningen Groningen the Netherlands
Department of Cardiothoracic Surgery European Interbalkan Medical Center Thessaloniki Greece
Department of Clinical Medicine University of Copenhagen Copenhagen Denmark
Department of Clinical Science and Education Karolinska Institutet SödersjukhusetStockholm Sweden
Department of Critical Care Asgar Ali Hospital Dhaka Bangladesh
Department of Intensive Care Adults Erasmus MC University Medical Centers Rotterdam the Netherlands
Department of Intensive Care Amsterdam University Medical Centers Amsterdam the Netherlands
Department of Intensive Care Pontificia Universidad Católica de Chile Santiago Chile
Faculty of Medicine University of Tripoli Tripoli Libya
FHU PROMICE DMU Parabola APHP Nord Paris France
Intensive Care Service Hospital Universitario La Paz Madrid Spain
Médecine Intensive Réanimation CHU de Brest Université de Bretagne Occidentale Brest France
Medical Faculty Ljubljana University of Ljubljana General Teaching Hospital Celje Ljubljana Slovenia
Nuffield Department of Clinical Neurosciences University of Oxford Oxford UK
School of Public Health and Preventive Medicine Monash University Melbourne Australia
Unidad de Cuidados Intensivos Hospital Vicente Corral Moscoso Cuenca Ecuador
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