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Impact of targeted hypothermia in expanded-criteria organ donors on recipient kidney-graft function: study protocol for a multicentre randomised controlled trial (HYPOREME).

Authors :
Brulé N
Canet E
Péré M
Feuillet F
Hourmant M
Asehnoune K
Rozec B
Duveau A
Dube L
Pierrot M
Humbert S
Tirot P
Boyer JM
Martin-Lefevre L
Labadie F
Robert R
Benard T
Kerforne T
Thierry A
Lesieur O
Vincent JF
Lesouhaitier M
Larmet R
Vigneau C
Goepp A
Bouju P
Quentin C
Egreteau PY
Huet O
Renault A
Le Meur Y
Venhard JC
Buchler M
Michel O
Voellmy MH
Herve F
Schnell D
Courte A
Glotz D
Amrouche L
Hazzan M
Kamar N
Moal V
Bourenne J
Le Quintrec-Donnette M
Morelon E
Boulain T
Grimbert P
Heng AE
Merville P
Garin A
Hiesse C
Fermier B
Mousson C
Guyot-Colosio C
Bouvier N
Rerolle JP
Durrbach A
Drouin S
Caillard S
Frimat L
Girerd S
Albano L
Rostaing L
Bertrand D
Hertig A
Westeel PF
Montini F
Delpierre E
Dorez D
Alamartine E
Ouisse C
Sebille V
Reignier J
Source :
BMJ open [BMJ Open] 2022 Mar 28; Vol. 12 (3), pp. e052845. Date of Electronic Publication: 2022 Mar 28.
Publication Year :
2022

Abstract

Introduction: Expanded-criteria donors (ECDs) are used to reduce the shortage of kidneys for transplantation. However, kidneys from ECDs are associated with an increased risk of delayed graft function (DGF), a risk factor for allograft loss and mortality. HYPOREME will be a multicentre randomised controlled trial (RCT) comparing targeted hypothermia to normothermia in ECDs, in a country where the use of machine perfusion for organ storage is the standard of care. We hypothesise that hypothermia will decrease the incidence of DGF.<br />Methods and Analysis: HYPOREME is a multicentre RCT comparing the effect on kidney function in recipients of targeted hypothermia (34°C-35°C) and normothermia (36.5°C-37.5°C) in the ECDs. The temperature intervention starts from randomisation and is maintained until aortic clamping in the operating room. We aim to enrol 289 ECDs in order to analyse the kidney function of 516 recipients in the 53 participating centres. The primary outcome is the occurrence of DGF in kidney recipients, defined as a requirement for renal replacement therapy within 7 days after transplantation (not counting a single session for hyperkalemia during the first 24 hours). Secondary outcomes include the proportion of patients with individual organs transplanted in each group; the number of organs transplanted from each ECD and the vital status and kidney function of the recipients 7 days, 28 days, 3 months and 1 year after transplantation. An interim analysis is planned after the enrolment of 258 kidney recipients.<br />Ethics and Dissemination: The trial was approved by the ethics committee of the French Intensive Care Society (CE-SRLF-16-07) on 26 April 2016 and by the competent French authorities on 20 April 2016 (Comité de Protection des Personnes-TOURS-Région Centre-Ouest 1, registration #2016-S3). Findings will be published in peer-reviewed journals and presented during national and international scientific meetings.<br />Trial Registration Number: NCT03098706.<br />Competing Interests: Competing interests: EC received fees for lectures and conference talks and had travel and accommodation expenses related to attending scientific meetings covered by Gilead, Baxter and Sanofi-Genzyme.<br /> (© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)

Details

Language :
English
ISSN :
2044-6055
Volume :
12
Issue :
3
Database :
MEDLINE
Journal :
BMJ open
Publication Type :
Academic Journal
Accession number :
35351701
Full Text :
https://doi.org/10.1136/bmjopen-2021-052845