Author:
Westphal Glauco Adrieno,Robinson Caroline Cabral,Biasi Alexandre,Machado Flávia Ribeiro,Rosa Regis Goulart,Teixeira Cassiano,de Andrade Joel,Franke Cristiano Augusto,Azevedo Luciano Cesar Pontes,Bozza Fernando,Guterres Cátia Moreira,da Silva Daiana Barbosa,Sganzerla Daniel,do Prado Débora Zechmeister,Madalena Itiana Cardoso,Rohden Adriane Isabel,da Silva Sabrina Souza,Giordani Natalia Elis,Andrighetto Luiza Vitelo,Benck Patrícia Spessatto,Roman Fernando Roberto,de Melo Maria de Fátima Rodrigues Buarque,Pereira Thattyane Borba,Grion Cintia Magalhães Carvalho,Diniz Pedro Carvalho,Oliveira João Fernando Picollo,Mecatti Giovana Colozza,Alves Flávio André Cardona,Moraes Rafael Barberena,Nobre Vandack,Hammes Luciano Serpa,Meade Maureen O,Nothen Rosana Reis,Falavigna Maicon
Abstract
IntroductionThere is an increasing demand for multi-organ donors for organ transplantation programmes. This study protocol describes the Donation Network to Optimise Organ Recovery Study, a planned cluster randomised controlled trial that aims to evaluate the effectiveness of the implementation of an evidence-based, goal-directed checklist for brain-dead potential organ donor management in intensive care units (ICUs) in reducing the loss of potential donors due to cardiac arrest.Methods and analysisThe study will include ICUs of at least 60 Brazilian sites with an average of ≥10 annual notifications of valid potential organ donors. Hospitals will be randomly assigned (with a 1:1 allocation ratio) to the intervention group, which will involve the implementation of an evidence-based, goal-directed checklist for potential organ donor maintenance, or the control group, which will maintain the usual care practices of the ICU. Team members from all participating ICUs will receive training on how to conduct family interviews for organ donation. The primary outcome will be loss of potential donors due to cardiac arrest. Secondary outcomes will include the number of actual organ donors and the number of organs recovered per actual donor.Ethics and disseminationThe institutional review board (IRB) of the coordinating centre and of each participating site individually approved the study. We requested a waiver of informed consent for the IRB of each site. Study results will be disseminated to the general medical community through publications in peer-reviewed medical journals.Trial registration numberNCT03179020; Pre-results.
Funder
Brazilian Ministry of Health
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