TY - JOUR
T1 - Variation in Blood Transfusion and Coagulation Management in Traumatic Brain Injury at the Intensive Care Unit
T2 - A Survey in 66 Neurotrauma Centers Participating in the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury Study
AU - CENTER-TBI investigators and participants
AU - Huijben, Jilske A.
AU - Van Der Jagt, Mathieu
AU - Cnossen, Maryse C.
AU - Kruip, Marieke J.H.A.
AU - Haitsma, Iain K.
AU - Stocchetti, Nino
AU - Maas, Andrew I.R.
AU - Menon, David K.
AU - Ercole, Ari
AU - Maegele, Marc
AU - Stanworth, Simon J.
AU - Citerio, Giuseppe
AU - Polinder, Suzanne
AU - Steyerberg, Ewout W.
AU - Lingsma, Hester F.
A2 - Auslands, Kaspars
N1 - Funding Information:
The authors thank all clinical and research staff at the CENTERTBI sites for completing the provider profiling questionnaires. This work was supported by European Commission FP7 Framework Program 602150. Data used in preparation of this manuscript were obtained in the context of CENTER-TBI, a large collaborative project with the support of the European Commission 7th Framework program (602150). The funder had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Funding Information:
18Department of Neurosurgery, Radboud University Medical Center, Nijmegen, The Netherlands. 19Department of Neurosurgery, University of Szeged, Szeged, Hungary. 20Institute for Transfusion Medicine (ITM), Witten/Herdecke University, Cologne, Germany. 21Department of Neurocritical care, Innsbruck Medical University, Innsbruck, Austria. 22Deparment of Neurosurgery & Anesthesia & Intensive Care Medicine, Karolinska University Hospital, Stockholm, Sweden. 23NIHR Surgical Reconstruction and Microbiology Research Centre, Birmingham, United Kingdom. 24Intensive care Unit, CHU Poitiers, Poitiers, France. 25Anesthesie-Réanimation, Assistance Publique – Hopitaux de Paris, Paris, France 26Department of Anesthesia & ICU, AOU Città della Salute e della Scienza di Torino–Orthopedic and Trauma Center, Torino, Italy. 27Department of Anesthesiology & Intensive Care, S Raffaele University Hospital, Milan, Italy. 28Department of Neurosurgery, University Hospital Heidelberg, Heidelberg, Germany. 29Department of Neurology, Odense University Hospital, Odense, Denmark. 30Departments of Neuroscience and Nursing Science, Norwegian University of Science and Technology, Trondheim, Norway. 31Department of Anesthesiology & Intensive Care, University Hospital of Grenoble, Grenoble, France. 32BehaviourWorks Australia, Monash Sustainability Institute, Monash University, Clayton, Victoria, Australia. 33Department of Public Health, Faculty of Health Sciences and Social Work, Trnava University, Trnava, Slovakia. 34Department of Neurosurgery, Bagdasar-Arseni Emergency Clinical Hospital, Bucharest, Romania. 35Department of Neurosurgery, Umea University Hospital, Umea, Sweden. 36Department of Neurosurgery, University of Pecs and MTA-PTE Clinical Neuroscience MR Research Group and Janos Szentagothai Research Center, University of Pecs, Hungarian Brain Research Program, Pecs, Hungary. 37Department of Medical Psychology, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany. 38Neuro ICU, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy. 39Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia. 40Department of Neurosurgery, Hospital of Cruces, Bilbao, Spain. 41Intensive Care and Department of Pediatric Surgery, Erasmus Medical Center, Sophia Children’s Hospital, Rotterdam, The Netherlands. 42Department of Neurosurgery, Hospital Universitario 12 de Octubre, Madrid, Spain. 43Department of Neuroscience, Azienda Ospedaliera Università di Padova, Padova, Italy. 44NeuroIntensive Care, Azienda Ospedaliera San Gerardo di Monza, Monza, Italy. 45School of Medicine and Surgery, Università Milano Bicocca, Milano, Italy. 46Department of Public Health, Erasmus Medical Center–University Medical Center, Rotterdam, The Netherlands. 47Department of Anesthesiology, University Hospital of Aachen, Aachen, Germany. 48Department of Anesthesia & Neurointensive Care, Cambridge University Hospital NHS Foundation Trust, Cambridge, United Kingdom. 49School of Public Health & PM, Monash University and The Alfred Hospital, Melbourne, Victoria, Australia. 50Radiology/MRI department, MRC Cognition and Brain Sciences Unit, Cambridge, United Kingdom. 51Institute of Medical Psycholology and Medical Sociology, Universi-tätsmedizin Göttingen, Göttingen, Germany. 52Oxford University Hospitals NHS Trust, Oxford, United Kingdom. 53Department of Neurosurgery, University of Pecs and MTA-PTE Clinical Neuroscience MR Research Group and Janos Szentagothai Research Center, University of Pecs, Hungarian Brain Research Program (Grant No. KTIA 13 NAP-A-II/8), Pecs, Hungary. 54Brain Physics Lab, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Addenbrooke’s Hospital, Cambridge, United Kingdom 55Intensive Care Unit, CHR Citadelle, Liège, Belgium.
Funding Information:
This work was supported by European Commission FP7 Framework Program 602150.
Publisher Copyright:
© Copyright 2018, Mary Ann Liebert, Inc.
PY - 2018/1/15
Y1 - 2018/1/15
N2 - Our aim was to describe current approaches and to quantify variability between European intensive care units (ICUs) in patients with traumatic brain injury (TBI). Therefore, we conducted a provider profiling survey as part of the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) study. The ICU Questionnaire was sent to 68 centers from 20 countries across Europe and Israel. For this study, we used ICU questions focused on 1) hemoglobin target level (Hb-TL), 2) coagulation management, and 3) deep venous thromboembolism (DVT) prophylaxis. Seventy-eight participants, mostly intensivists and neurosurgeons of 66 centers, completed the ICU questionnaire. For ICU-patients, half of the centers (N = 34; 52%) had a defined Hb-TL in their protocol. For patients with TBI, 26 centers (41%) indicated an Hb-TL between 70 and 90 g/L and 38 centers (59%) above 90 g/L. To treat trauma-related hemostatic abnormalities, the use of fresh frozen plasma (N = 48; 73%) or platelets (N = 34; 52%) was most often reported, followed by the supplementation of vitamin K (N = 26; 39%). Most centers reported using DVT prophylaxis with anticoagulants frequently or always (N = 62; 94%). In the absence of hemorrhagic brain lesions, 14 centers (21%) delayed DVT prophylaxis until 72 h after trauma. If hemorrhagic brain lesions were present, the number of centers delaying DVT prophylaxis for 72 h increased to 29 (46%). Overall, a lack of consensus exists between European ICUs on blood transfusion and coagulation management. The results provide a baseline for the CENTER-TBI study, and the large between-center variation indicates multiple opportunities for comparative effectiveness research.
AB - Our aim was to describe current approaches and to quantify variability between European intensive care units (ICUs) in patients with traumatic brain injury (TBI). Therefore, we conducted a provider profiling survey as part of the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) study. The ICU Questionnaire was sent to 68 centers from 20 countries across Europe and Israel. For this study, we used ICU questions focused on 1) hemoglobin target level (Hb-TL), 2) coagulation management, and 3) deep venous thromboembolism (DVT) prophylaxis. Seventy-eight participants, mostly intensivists and neurosurgeons of 66 centers, completed the ICU questionnaire. For ICU-patients, half of the centers (N = 34; 52%) had a defined Hb-TL in their protocol. For patients with TBI, 26 centers (41%) indicated an Hb-TL between 70 and 90 g/L and 38 centers (59%) above 90 g/L. To treat trauma-related hemostatic abnormalities, the use of fresh frozen plasma (N = 48; 73%) or platelets (N = 34; 52%) was most often reported, followed by the supplementation of vitamin K (N = 26; 39%). Most centers reported using DVT prophylaxis with anticoagulants frequently or always (N = 62; 94%). In the absence of hemorrhagic brain lesions, 14 centers (21%) delayed DVT prophylaxis until 72 h after trauma. If hemorrhagic brain lesions were present, the number of centers delaying DVT prophylaxis for 72 h increased to 29 (46%). Overall, a lack of consensus exists between European ICUs on blood transfusion and coagulation management. The results provide a baseline for the CENTER-TBI study, and the large between-center variation indicates multiple opportunities for comparative effectiveness research.
KW - coagulopathy
KW - Europe
KW - intensive care unit
KW - transfusion
KW - traumatic brain injury
UR - http://www.scopus.com/inward/record.url?scp=85041043718&partnerID=8YFLogxK
U2 - 10.1089/neu.2017.5194
DO - 10.1089/neu.2017.5194
M3 - Article
C2 - 28825511
AN - SCOPUS:85041043718
SN - 0897-7151
VL - 35
SP - 323
EP - 332
JO - Journal of Neurotrauma
JF - Journal of Neurotrauma
IS - 2
ER -