Statistical analysis plan for a cluster-randomised trial assessing the effectiveness of implementation of a bedside evidence-based checklist for clinical management of brain-dead potential organ donors in intensive care units: DONORS (Donation Network to Optimise Organ Recovery Study)
Natalia Elis Giordani,
Caroline Cabral Robinson,
Glauco Adrieno Westphal,
Regis Goulart Rosa,
Daniel Sganzerla,
Alexandre Biasi Cavalcanti,
Flávia Ribeiro Machado,
Luciano Cesar Pontes Azevedo,
Fernando Augusto Bozza,
Cassiano Teixeira,
Joel de Andrade,
Cristiano Augusto Franke,
Cátia Moreira Guterres,
Itiana Cardoso Madalena,
Adriane Isabel Rohden,
Sabrina Souza da Silva,
Luiza Vitelo Andrighetto,
Gabriela Soares Rech,
Bruna dos Passos Gimenes,
Luciano Serpa Hammes,
Daniela Ferreira Salomão Pontes,
Maureen O. Meade,
Maicon Falavigna
Affiliations
Natalia Elis Giordani
Research Projects Office, Hospital Moinhos de Vento (HMV)
Caroline Cabral Robinson
Research Projects Office, Hospital Moinhos de Vento (HMV)
Glauco Adrieno Westphal
Research Projects Office, Hospital Moinhos de Vento (HMV)
Regis Goulart Rosa
Adult Intensive Care Unit, HMV
Daniel Sganzerla
Research Projects Office, Hospital Moinhos de Vento (HMV)
Alexandre Biasi Cavalcanti
Research Institute, Hospital do Coração (HCor)
Flávia Ribeiro Machado
Department of Anaesthesiology, Pain and Intensive Care, Universidade Federal de São Paulo (UNIFESP)
Luciano Cesar Pontes Azevedo
Intensive Care Unit, Hospital Sírio-Libanês
Fernando Augusto Bozza
Department of Critical Care and Postgraduate Programme in Translational Medicine, D’Or Institute for Research and Education
Cassiano Teixeira
Department of Internal Medicine and Postgraduate Programme in Rehabilitation Science, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA)
Joel de Andrade
Organ Procurement Organisation of Santa Catarina (OPO/SC)
Cristiano Augusto Franke
Adult Intensive Care Unit, Hospital de Clínicas de Porto Alegre (HCPA)
Cátia Moreira Guterres
Research Projects Office, Hospital Moinhos de Vento (HMV)
Itiana Cardoso Madalena
Research Projects Office, Hospital Moinhos de Vento (HMV)
Adriane Isabel Rohden
Research Projects Office, Hospital Moinhos de Vento (HMV)
Sabrina Souza da Silva
Research Projects Office, Hospital Moinhos de Vento (HMV)
Luiza Vitelo Andrighetto
Research Projects Office, Hospital Moinhos de Vento (HMV)
Gabriela Soares Rech
Research Projects Office, Hospital Moinhos de Vento (HMV)
Bruna dos Passos Gimenes
Research Projects Office, Hospital Moinhos de Vento (HMV)
Luciano Serpa Hammes
Office of the Superintendent, HMV
Daniela Ferreira Salomão Pontes
General Coordination Office of the National Transplant System, Ministério da Saúde
Maureen O. Meade
Department of Medicine and Department of Health Research Methods, Evidence and Impact, McMaster University
Maicon Falavigna
Research Projects Office, Hospital Moinhos de Vento (HMV)
Abstract Background The quality of clinical care of brain-dead potential organ donors may help reduce donor losses caused by irreversible or unreversed cardiac arrest and increase the number of organs donated. We sought to determine whether an evidence-based, goal-directed checklist for donor management in intensive care units (ICUs) can reduce donor losses to cardiac arrest. Methods/design The DONORS study is a multicentre, cluster-randomised controlled trial with a 1:1 allocation ratio designed to compare an intervention group (goal-directed checklist for brain-dead potential organ donor management) with a control group (standard ICU care). The primary outcome is loss of potential donors due to cardiac arrest. Secondary outcomes are the number of actual organ donors and the number of solid organs recovered per actual donor. Exploratory outcomes include the achievement of relevant clinical goals during the management of brain-dead potential organ donors. The present statistical analysis plan (SAP) describes all primary statistical procedures that will be used to evaluate the results and perform exploratory and sensitivity analyses of the trial. Discussion The SAP of the DONORS study aims to describe its analytic procedures, enhancing the transparency of the study. At the moment of SAP subsmission, 63 institutions have been randomised and were enrolling study participants. Thus, the analyses reported herein have been defined before the end of the study recruitment and database locking. Trial registration ClinicalTrials.gov, NCT03179020 . Registered on 7 June 2017.