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International point prevalence study of Intensive Care Unit transfusion practices-Pilot study in the Netherlands

Authors :
H. Schoechl
Simon Oczkowski
Jens Meier
M. Y. Alders
Matthias Müller
Anders Perner
Cécile Aubron
Gavin J. Murphy
M. Lance
Timothy S. Walsh
Maurizio Cecconi
Joanna C. Dionne
N. Nielsen
R. van Bruggen
Thomas Scheeren
Aarne Feldheiser
B. Hunt
S. de Bruin
Jacques Duranteau
Alexander P.J. Vlaar
M. Antonelli
Jan Bakker
Dirk de Korte
Graduate School
ACS - Pulmonary hypertension & thrombosis
AII - Inflammatory diseases
Human Genetics
Amsterdam Reproduction & Development (AR&D)
Landsteiner Laboratory
ACS - Microcirculation
Intensive Care Medicine
Intensive Care
Critical care, Anesthesiology, Peri-operative and Emergency medicine (CAPE)
Vascular Ageing Programme (VAP)
Clinical Genetics
Amsterdam Reproduction & Development
Source :
Transfusion clinique et biologique, 26(4), 202-208. Elsevier Masson, Transfusion Clinique et Biologique, 26(4), 202-208. Elsevier Masson, Transfusion clinique et biologique, 26(4), 202-208. ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Publication Year :
2019
Publisher :
Elsevier Masson, 2019.

Abstract

Background. - Anaemia and coagulopathy are common issues in critically ill patients. Transfusion can be lifesaving, however, is associated with potential life threatening adverse events. As an international transfusion guideline for this specific patient population is lacking, we hypothesize that a high heterogeneity in transfusion practices exists. In this pilot-study we assessed transfusion practice in a university hospital in the Netherlands and tested the feasibility of this protocol for an international multi-centre study.Methods. - A prospective single centre cohort study was conducted. For seven days all consecutive non-readmitted patients to the adult Intensive Care Unit (ICU) were included and followed for 28 days. Patients were prospectively followed until ICU discharge or up to day 28. Patient outcome data was collected at day 28. Workload for this study protocol was scored in hours and missing data.Results. - In total, 48 patients were included, needed in total three hours patient to include and collect all data, with 1.6% missing data showing the feasibility of the data acquisition. Six (12.5%) patients received red blood cells (RBCs), three patients (6.3%) received platelet concentrates, and two (4.2%) patients received plasma units. In total eight (16.7%) patients were transfused with one or more blood products. Median pre- and post-transfusion haemoglobin (Hb) levels were 7.6 (6.7-7.7) g/dL and 8.1 (7.6-8.7) g/dL, respectively.Conclusion. - In this pilot-study we proved the feasibility of our protocol and observed in this small population a restrictive transfusion practice for all blood products. (C) 2019 Societe francaise de transfusion sanguine (SFTS). Published by Elsevier Masson SAS. All rights reserved.

Details

ISSN :
12467820
Volume :
26
Issue :
4
Database :
OpenAIRE
Journal :
Transfusion Clinique et Biologique
Accession number :
edsair.doi.dedup.....5a6c069bb80cb5116911a6dd2335e85d