Your browser doesn't support javascript.
loading
Baseline Characteristics and Representativeness of Participants in the BEST-Fluids Trial: A Randomized Trial of Balanced Crystalloid Solution Versus Saline in Deceased Donor Kidney Transplantation.
Collins, Michael G; Fahim, Magid A; Pascoe, Elaine M; Hawley, Carmel M; Johnson, David W; Varghese, Julie; Hickey, Laura E; Clayton, Philip A; Gill, John S; Dansie, Kathryn B; McConnochie, Rachael C; Vergara, Liza A; Kiriwandeniya, Charani; Reidlinger, Donna; Mount, Peter F; Weinberg, Laurence; McArthur, Colin J; Coates, P Toby; Endre, Zoltan H; Goodman, David; Howard, Kirsten; Howell, Martin; Jamboti, Jagadish S; Kanellis, John; Laurence, Jerome M; Lim, Wai H; McTaggart, Steven J; O'Connell, Philip J; Pilmore, Helen L; Wong, Germaine; Chadban, Steven J.
Affiliation
  • Collins MG; Central Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, Australia.
  • Fahim MA; Department of Renal Medicine, Auckland City Hospital, Auckland, New Zealand.
  • Pascoe EM; Faculty of Medical and Health Sciences, The University of Adelaide, Adelaide, Australia.
  • Hawley CM; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Johnson DW; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Varghese J; Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.
  • Hickey LE; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Clayton PA; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Gill JS; Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.
  • Dansie KB; Translational Research Institute, Brisbane, Queensland, Australia.
  • McConnochie RC; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Vergara LA; Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.
  • Kiriwandeniya C; Translational Research Institute, Brisbane, Queensland, Australia.
  • Reidlinger D; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Mount PF; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Weinberg L; Central Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, Australia.
  • McArthur CJ; Faculty of Medical and Health Sciences, The University of Adelaide, Adelaide, Australia.
  • Coates PT; Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, Australia.
  • Endre ZH; Division of Nephrology, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Goodman D; Faculty of Medical and Health Sciences, The University of Adelaide, Adelaide, Australia.
  • Howard K; Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, Australia.
  • Howell M; Department of Critical Care Medicine, Auckland City Hospital, Auckland, New Zealand.
  • Jamboti JS; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Kanellis J; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Laurence JM; Australasian Kidney Trials Network, The University of Queensland, Brisbane, Australia.
  • Lim WH; Department of Nephrology, Austin Health, Melbourne, Australia.
  • McTaggart SJ; Department of Medicine (Austin), The University of Melbourne, Parkville, Melbourne, Australia.
  • O'Connell PJ; Department of Anaesthesia, Austin Health, Melbourne, Australia.
  • Pilmore HL; The University of Melbourne, Department of Critical Care, Melbourne, Australia.
  • Wong G; Department of Critical Care Medicine, Auckland City Hospital, Auckland, New Zealand.
  • Chadban SJ; Central Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, Australia.
Transplant Direct ; 8(12): e1399, 2022 Dec.
Article in En | MEDLINE | ID: mdl-36479278
Delayed graft function (DGF) is a major complication of deceased donor kidney transplantation. Saline (0.9% sodium chloride) is a commonly used intravenous fluid in transplantation but may increase the risk of DGF because of its high chloride content. Better Evidence for Selecting Transplant Fluids (BEST-Fluids), a pragmatic, registry-based, double-blind, randomized trial, sought to determine whether using a balanced low-chloride crystalloid solution (Plasma-Lyte 148) instead of saline would reduce DGF. We sought to evaluate the generalizability of the trial cohort by reporting the baseline characteristics and representativeness of the trial participants in detail. Methods: We compared the characteristics of BEST-Fluids participants with those of a contemporary cohort of deceased donor kidney transplant recipients in Australia and New Zealand using data from the Australia and New Zealand Dialysis and Transplant Registry. To explore potential international differences, we compared trial participants with a cohort of transplant recipients in the United States using data from the Scientific Registry of Transplant Recipients. Results: During the trial recruitment period, 2373 deceased donor kidney transplants were performed in Australia and New Zealand; 2178 were eligible' and 808 were enrolled in BEST-Fluids. Overall, trial participants and nonparticipants were similar at baseline. Trial participants had more coronary artery disease (standardized difference [d] = 0.09; P = 0.03), longer dialysis duration (d = 0.18, P < 0.001), and fewer hypertensive (d = -0.11, P = 0.03) and circulatory death (d = -0.14, P < 0.01) donors than nonparticipants. Most key characteristics were similar between trial participants and US recipients, with moderate differences (|d| ≥ 0.2; all P < 0.001) in kidney failure cause, diabetes, dialysis duration, ischemic time, and several donor risk predictors, likely reflecting underlying population differences. Conclusions: BEST-Fluids participants had more comorbidities and received slightly fewer high-risk deceased donor kidneys but were otherwise representative of Australian and New Zealand transplant recipients and were generally similar to US recipients. The trial results should be broadly applicable to deceased donor kidney transplantation practice worldwide.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Transplant Direct Year: 2022 Document type: Article Affiliation country: Australia Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Transplant Direct Year: 2022 Document type: Article Affiliation country: Australia Country of publication: Estados Unidos