4.6 Article

Assessment of oxygen extraction rate changes following red blood cell transfusion in the intensive care unit: a protocol for a prospective observational non-interventional study

Journal

BMJ OPEN
Volume 13, Issue 8, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bmjopen-2023-074413

Keywords

Blood bank & transfusion medicine; Anaemia; Adult intensive & critical care

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This study aims to evaluate the oxygen extraction rate as a reliable indicator for blood transfusion in ICU patients and assess its effectiveness through clinical outcomes. Utilizing physiological indicators to guide blood transfusion decisions can expedite the decision-making process and minimize the risks of unnecessary transfusions.
Introduction Haemoglobin transfusion thresholds have been used in the intensive care unit (ICU) to guide red blood cell transfusion (RBCT) decisions. Recent research has also focused on physiological indicators of tissue oxygenation as trigger points for blood transfusion. This study aims to assess the oxygen extraction rate (O2ER) as a critical indicator of the oxygen delivery-consumption balance in tissues and investigate its potential as a reliable trigger for blood transfusion in ICU patients by analysing clinical outcomes. The utilisation of physiological indicators may expedite the decision-making process for RBCT in patients requiring immediate intervention, while simultaneously minimising the risks associated with unnecessary transfusions.Methods and analysis This prospective, single-centre, observational cohort study will include 65 ICU patients undergoing RBCT. We will evaluate essential markers such as arterial oxygen content, central venous oxygen content, arteriovenous oxygen difference, O2ER and near-infrared spectroscopy before and 15 min after transfusion. The primary outcome is the percentage increase in O2ER between the two groups relative to the initial O2ER level. Secondary outcomes will assess complications and patient outcomes in relation to baseline O2ER. A 90-day comprehensive follow-up period will be implemented for all enrolled patients.Ethics and dissemination This study has obtained ethics committee approval from the Izmir Katip Celebi University Non-Interventional Clinical Studies Institutional Review Board. Written informed consent will be obtained from all patients before their enrolment in the study. The findings will be disseminated through publication in peer-reviewed journals and presentation at national or international conferences.Trial registration number NCT05798130

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