Strategies for Implementing Research in Practice and Policy in CKD
Dale Coghlan, Allison Jaure, Shilpanjali Jesudason, Jonathan C. Craig, Anastasia Hughes, Mia Abdy, Hayley Candler, Brydee Cashmore, Christopher E. Davies, Amanda Dominello, Chandana Guha, Carmel M. Hawley, Laura E. Hickey, Katharine Hegerty, Brooke M Huuskes, Amandi Hiyare Hewage, Georgina Irish, David W. Johnson, Dominic Keuskamp, Feruza Kholmurodova, Jasmin Mazis, Thida Maung Myint, Colm O’Reilly, Laura Nolan, Angela Rejuso, Amanda Sluiter, Jacqueline H. Stephens, David J. Tunnicliffe, Anita van Zwieten, Andrea K. Viecelli, Germaine Wong, Rebecca Wu, Nicole Scholes-Robertson,Background
Routine implementation of chronic kidney disease research into practice and policy is delayed, fragmented and inconsistent. This workshop aimed to identify strategies to strengthen the implementation of research findings into practice and policy from the perspectives of patients, their caregivers and health professionals.
Methods
A workshop was conducted with patients (n=18), caregivers (n=9) and health professionals (n=102) from Australia and New Zealand. Thirteen simultaneous breakout groups of 6–10 participants were held online and in-person to discuss strategies for implementing research findings into practice and policy in chronic kidney disease. Transcripts were thematically analyzed.
Results
Three interrelated strategies were identified.
Conclusions
Embedding these strategies may strengthen the routine translation of research evidence into practice and policy, ultimately improving care and outcomes for individuals with kidney disease.