TY - JOUR
T1 - Red blood cell transfusion in acute brain injury subtypes
T2 - An observational cohort study
AU - Moman, Rajat N.
AU - Kor, Daryl J.
AU - Chandran, Arun
AU - Hanson, Andrew C.
AU - Schroeder, Darrell R.
AU - Rabinstein, Alejandro A.
AU - Warner, Matthew A.
N1 - Funding Information:
This study was made possible by funding from the Mayo Clinic Department of Anesthesiology and Perioperative Medicine and the Critical Care Integrated Multidisciplinary Practice , Rochester, Minnesota. In addition, this study was supported by an NIH R01 grant ( HL121232 ) to Dr. Kor and by CTSA grant number KL2 TR002379 to Dr. Warner from the National Center for Advancing Translational Sciences (NCATS). The manuscript has been read and approved by all authors. There are no actual or potential conflicts of interest capable of influencing the judgement on the part of any author.
Publisher Copyright:
© 2018
PY - 2019/4
Y1 - 2019/4
N2 - Purpose: Optimal red blood cell (RBC) transfusion thresholds in acute brain injury (ABI) are poorly defined. Materials and methods: We conducted a retrospective cohort study of adult patients with ABI and moderate anemia (Hb 7–10 g/dL) in a neurological intensive care unit (ICU) at an academic medical center between 2008 and 2015. Transfused and non-transfused patients were matched based on age, ABI subtype, pre-transfusion hemoglobin, and ICU length of stay (LOS) at the time of RBC transfusion. Multivariable regression analyses were performed to assess the relationship between RBC transfusion and hospital LOS, hospital mortality, ICU LOS, ICU mortality, and 24 h change in sequential organ failure assessment (SOFA) scores. Results: 2638 patients met inclusion criteria, with 225 (8.5%) receiving RBC transfusion. Acute ischemic stroke was the most prevalent ABI diagnosis (43.3%) then intracranial hemorrhage (25.6%), subarachnoid hemorrhage (16.5%), and traumatic brain injury (TBI) (14.6%). In multivariable analyses, RBC transfusion was associated with longer hospital and ICU LOS, and higher SOFA scores. Each ABI subtype had similar results, except for TBI which showed no difference in hospital LOS. Mortality was not significantly different. Conclusions: In moderately anemic patients with ABI, RBC transfusion was associated with longer hospital and ICU LOS. Prospective investigations are necessary to further assess these relationships.
AB - Purpose: Optimal red blood cell (RBC) transfusion thresholds in acute brain injury (ABI) are poorly defined. Materials and methods: We conducted a retrospective cohort study of adult patients with ABI and moderate anemia (Hb 7–10 g/dL) in a neurological intensive care unit (ICU) at an academic medical center between 2008 and 2015. Transfused and non-transfused patients were matched based on age, ABI subtype, pre-transfusion hemoglobin, and ICU length of stay (LOS) at the time of RBC transfusion. Multivariable regression analyses were performed to assess the relationship between RBC transfusion and hospital LOS, hospital mortality, ICU LOS, ICU mortality, and 24 h change in sequential organ failure assessment (SOFA) scores. Results: 2638 patients met inclusion criteria, with 225 (8.5%) receiving RBC transfusion. Acute ischemic stroke was the most prevalent ABI diagnosis (43.3%) then intracranial hemorrhage (25.6%), subarachnoid hemorrhage (16.5%), and traumatic brain injury (TBI) (14.6%). In multivariable analyses, RBC transfusion was associated with longer hospital and ICU LOS, and higher SOFA scores. Each ABI subtype had similar results, except for TBI which showed no difference in hospital LOS. Mortality was not significantly different. Conclusions: In moderately anemic patients with ABI, RBC transfusion was associated with longer hospital and ICU LOS. Prospective investigations are necessary to further assess these relationships.
KW - Acute brain injury
KW - Anemia
KW - Length of stay
KW - Mortality
KW - Red blood cell transfusion
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U2 - 10.1016/j.jcrc.2018.11.006
DO - 10.1016/j.jcrc.2018.11.006
M3 - Article
C2 - 30471560
AN - SCOPUS:85056828518
SN - 0883-9441
VL - 50
SP - 44
EP - 49
JO - Seminars in Anesthesia
JF - Seminars in Anesthesia
ER -