TY - JOUR
T1 - Baseline Characteristics and Representativeness of Participants in the BEST-Fluids Trial
T2 - A Randomized Trial of Balanced Crystalloid Solution Versus Saline in Deceased Donor Kidney Transplantation
AU - Collins, Michael G.
AU - Fahim, Magid A.
AU - Pascoe, Elaine M.
AU - Hawley, Carmel M.
AU - Johnson, David W.
AU - Varghese, Julie
AU - Hickey, Laura E.
AU - Clayton, Philip A.
AU - Gill, John S.
AU - Dansie, Kathryn B.
AU - McConnochie, Rachael C.
AU - Vergara, Liza A.
AU - Kiriwandeniya, Charani
AU - Reidlinger, Donna
AU - Mount, Peter F.
AU - Weinberg, Laurence
AU - McArthur, Colin J.
AU - Toby Coates, P.
AU - Endre, Zoltan H.
AU - Goodman, David
AU - Howard, Kirsten
AU - Howell, Martin
AU - Jamboti, Jagadish S.
AU - Kanellis, John
AU - Laurence, Jerome M.
AU - Lim, Wai H.
AU - McTaggart, Steven J.
AU - O'Connell, Philip J.
AU - Pilmore, Helen L.
AU - Wong, Germaine
AU - Chadban, Steven J.
N1 - Funding Information:
The BEST-Fluids trial was funded by an Australian Government Medical Research Future Fund (MRFF) Rare Cancers, Rare Diseases and Unmet Needs Grant 2018 (APP ID 1152390); a Health Research Council of New Zealand Project Grant 2017 (17/414); Better Evidence And Translation in Chronic Kidney Disease (BEAT-CKD) grants in 2016 and 2017 (allocated from NHMRC Program Grant 2014—CIA Craig APP ID 1092957); and Royal Australasian College of Physicians/Jacquot Research Establishment Fellowship Grants in 2017 and 2018. The manufacturer of Plasma-Lyte 148, Baxter Healthcare (Deerfield, IL), supported the trial by providing in-kind support via a Baxter Investigator-Initiated Research Grant (Medication Delivery) 2017 to provide 930 boxes of trial fluid.
Funding Information:
The BEST-Fluids trial was funded by an Australian Government Medical Research Future Fund (MRFF) Rare Cancers, Rare Diseases and Unmet Needs Grant 2018 (APP ID 1152390); a Health Research Council of New Zealand Project Grant 2017 (17/414); Better Evidence And Translation in Chronic Kidney Disease (BEAT-CKD) grants in 2016 and 2017 (allocated from NHMRC Program Grant 2014—CIA Craig APP ID 1092957); and Royal Australasian College of Physicians/Jacquot Research Establishment Fellowship Grants in 2017 and 2018. The manufacturer of Plasma-Lyte 148, Baxter Healthcare (Deerfield, IL), supported the trial by providing in-kind support via a Baxter Investigator-Initiated Research Grant (Medication Delivery) 2017 to provide 930 boxes of trial fluid. Additional fluids required to complete the trial (380 boxes) were purchased under standard commercial agreements from Baxter Healthcare Pty Ltd (Australia). The funders had no role in (1) the conception, design, or conduct of the study; (2) the collection, management, analysis, interpretation, or presentation of data; or (3) the preparation or approval of the article or the decision to submit the article for publication.
Publisher Copyright:
© 2022 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.
PY - 2022/11/4
Y1 - 2022/11/4
N2 - Background. 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.
AB - Background. 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.
UR - http://www.scopus.com/inward/record.url?scp=85141970901&partnerID=8YFLogxK
U2 - 10.1097/TXD.0000000000001399
DO - 10.1097/TXD.0000000000001399
M3 - Article
C2 - 36479278
AN - SCOPUS:85141970901
SN - 2373-8731
VL - 8
JO - Transplantation Direct
JF - Transplantation Direct
IS - 12
M1 - e1399
ER -