Liberal transfusion strategy to prevent mortality and anaemia-associated, ischaemic events in elderly non-cardiac surgical patients – the study design of the LIBERAL-Trial
Patrick Meybohm,
Simone Lindau,
Sascha Treskatsch,
Roland Francis,
Claudia Spies,
Markus Velten,
Maria Wittmann,
Erdem Gueresir,
Christian Stoppe,
Ana Kowark,
Mark Coburn,
Sixten Selleng,
Marcel Baschin,
Gregor Jenichen,
Melanie Meersch,
Thomas Ermert,
Alexander Zarbock,
Peter Kranke,
Markus Kredel,
Antonia Helf,
Rita Laufenberg-Feldmann,
Marion Ferner,
Eva Wittenmeier,
Karl-Heinz Gürtler,
Peter Kienbaum,
Marcel Gama de Abreu,
Michael Sander,
Michael Bauer,
Timo Seyfried,
Matthias Gruenewald,
Suma Choorapoikayil,
Markus M. Mueller,
Erhard Seifried,
Oana Brosteanu,
Holger Bogatsch,
Dirk Hasenclever,
Kai Zacharowski,
LIBERAL Collaboration Group
Affiliations
Patrick Meybohm
Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt
Simone Lindau
Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt
Sascha Treskatsch
Department of Anesthesiology, Operative Intensive Care Medicine, Berlin Institute of Health, Charité – Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, Campus Charite Mitte, Campus Virchow Klinikum, Campus Benjamin Franklin, Charité
Roland Francis
Department of Anesthesiology, Operative Intensive Care Medicine, Berlin Institute of Health, Charité – Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, Campus Charite Mitte, Campus Virchow Klinikum, Campus Benjamin Franklin, Charité
Claudia Spies
Department of Anesthesiology, Operative Intensive Care Medicine, Berlin Institute of Health, Charité – Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, Campus Charite Mitte, Campus Virchow Klinikum, Campus Benjamin Franklin, Charité
Markus Velten
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Bonn
Maria Wittmann
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Bonn
Erdem Gueresir
Department of Neurosurgery, University Hospital Bonn
Christian Stoppe
Department of Intensive Care Medicine, RWTH University Aachen
Ana Kowark
Department of Anesthesiology, RWTH University Aachen
Mark Coburn
Department of Anesthesiology, RWTH University Aachen
Sixten Selleng
Department of Anesthesiology, University Hospital Greifswald
Marcel Baschin
Department of Anesthesiology, University Hospital Greifswald
Gregor Jenichen
Department of Anesthesiology, University Hospital Greifswald
Melanie Meersch
Department of Anaesthesiology, Intensive Care and Pain Therapy, University Hospital Münster
Thomas Ermert
Department of Anaesthesiology, Intensive Care and Pain Therapy, University Hospital Münster
Alexander Zarbock
Department of Anaesthesiology, Intensive Care and Pain Therapy, University Hospital Münster
Peter Kranke
Department of Anaesthesia and Critical Care, University Hospital of Würzburg
Markus Kredel
Department of Anaesthesia and Critical Care, University Hospital of Würzburg
Antonia Helf
Department of Anaesthesia and Critical Care, University Hospital of Würzburg
Rita Laufenberg-Feldmann
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Mainz
Marion Ferner
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Mainz
Eva Wittenmeier
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Mainz
Karl-Heinz Gürtler
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Augsburg
Peter Kienbaum
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Düsseldorf
Marcel Gama de Abreu
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Dresden
Michael Sander
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Giessen-Marburg
Michael Bauer
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Jena
Timo Seyfried
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Regensburg
Matthias Gruenewald
Department of Anaesthesiology and Intensive Care Medicine, University Hospital Schleswig-Holstein, Campus Kiel
Suma Choorapoikayil
Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt
Markus M. Mueller
Institute for Transfusion Medicine and Immunohaematology Frankfurt/ Main, German Red Cross Blood Transfusion Service Baden-Wuerttemberg – Hessen
Erhard Seifried
Institute for Transfusion Medicine and Immunohaematology Frankfurt/ Main, German Red Cross Blood Transfusion Service Baden-Wuerttemberg – Hessen
Oana Brosteanu
Clinical Trial Centre Leipzig, University Leipzig
Holger Bogatsch
Clinical Trial Centre Leipzig, University Leipzig
Dirk Hasenclever
Institute for Medical Informatics, Statistics and Epidemiology, University Leipzig
Kai Zacharowski
Department of Anaesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt
Abstract Background Perioperative anaemia leads to impaired oxygen supply with a risk of vital organ ischaemia. In healthy and fit individuals, anaemia can be compensated by several mechanisms. Elderly patients, however, have less compensatory mechanisms because of multiple co-morbidities and age-related decline of functional reserves. The purpose of the study is to evaluate whether elderly surgical patients may benefit from a liberal red blood cell (RBC) transfusion strategy compared to a restrictive transfusion strategy. Methods The LIBERAL Trial is a prospective, randomized, multicentre, controlled clinical phase IV trial randomising 2470 elderly (≥ 70 years) patients undergoing intermediate- or high-risk non-cardiac surgery. Registered patients will be randomised only if Haemoglobin (Hb) reaches ≤9 g/dl during surgery or within 3 days after surgery either to the LIBERAL group (transfusion of a single RBC unit when Hb ≤ 9 g/dl with a target range for the post-transfusion Hb level of 9–10.5 g/dl) or the RESTRICTIVE group (transfusion of a single RBC unit when Hb ≤ 7.5 g/dl with a target range for the post-transfusion Hb level of 7.5–9 g/dl). The intervention per patient will be followed until hospital discharge or up to 30 days after surgery, whichever occurs first. The primary efficacy outcome is defined as a composite of all-cause mortality, acute myocardial infarction, acute ischaemic stroke, acute kidney injury (stage III), acute mesenteric ischaemia and acute peripheral vascular ischaemia within 90 days after surgery. Infections requiring iv antibiotics with re-hospitalisation are assessed as important secondary endpoint. The primary endpoint will be analysed by logistic regression adjusting for age, cancer surgery (y/n), type of surgery (intermediate- or high-risk), and incorporating centres as random effect. Discussion The LIBERAL-Trial will evaluate whether a liberal transfusion strategy reduces the occurrence of major adverse events after non-cardiac surgery in the geriatric population compared to a restrictive strategy within 90 days after surgery. Trial registration ClinicalTrials.gov (identifier: NCT03369210).