TY - JOUR
T1 - Postoperative 20% albumin vs standard care and acute kidney injury after high-risk cardiac surgery (ALBICS)
T2 - study protocol for a randomised trial
AU - Balachandran, Mayurathan
AU - Banneheke, Piyusha
AU - Pakavakis, Adrian
AU - Al-Bassam, Wisam
AU - Sarode, Vineet
AU - Rowland, Michael
AU - Shehabi, Yahya
N1 - Funding Information:
The authors would like to acknowledge the contributions of all ALBICS investigators: Monash Medical Centre: Mayurathan Balachandran, Piyusha Banneheke, Adrian Pakavakis, Wisam Al-Bassam, Dhiraj Bhatia, Julian Smith, Yahya Shehabi University Hospital Geelong: Michael Rowland, Xiao Bo Zhang, Cheng Hon Yap, Marita Turner, Kathleen DenDryver, Neil Orford Cabrini Hospital: Vineet Sarode, Shannon Simpson Prince of Wales Hospital (public and private): Yahya Shehabi, David Bihari, David Collins The full protocol, participant-level dataset and statistical code will be available in accordance with Monash University data sharing protocols.
Publisher Copyright:
© 2021, The Author(s).
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/12
Y1 - 2021/12
N2 - Background: Acute kidney injury (AKI) is a common complication of cardiac surgery. Factors such as cardiopulmonary bypass, aortic cross-clamping and surgical stress may precipitate renal hypoperfusion and ischaemia, inflammation and oxidative stress are associated with development of AKI. Albumin’s pharmacological properties and widespread availability have the potential to mitigate these factors. However, the effect of albumin on cardiac surgery-associated AKI is unknown. Objective: To evaluate the impact of postoperative 20% albumin infusion on kidney function after high-risk cardiac surgery. Methods: We designed an open-label, multicentre, randomised controlled trial—the ALBICS study (ALBumin Infusion and acute kidney injury following Cardiac Surgery). A total of 590 patients undergoing high-risk cardiac surgery (combined procedure or estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m2) will be enrolled into the study and randomly allocated to receive a postoperative 20% albumin infusion or standard care in a 1:1 ratio, stratified by centre and baseline renal function. The study fluid will be administered upon arrival in intensive care for 15 h. Patients will be followed up until 28 days after surgery or until discharge from the hospital. The primary outcome is the proportion of patients who develop AKI in both groups. Secondary outcomes to be measured are proportions of AKI stage II and III, 28-day mortality, mechanical ventilation time and length of stay in intensive care and hospital. Conclusion: This trial aims to determine if a postoperative infusion of concentrated albumin reduces the risk of AKI following high-risk cardiac surgery. Trial registration: Australian New Zealand Clinical Trials Registry ACTRN12619001355167. Registered on 03 October 2019—retrospectively registered. https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=378383.
AB - Background: Acute kidney injury (AKI) is a common complication of cardiac surgery. Factors such as cardiopulmonary bypass, aortic cross-clamping and surgical stress may precipitate renal hypoperfusion and ischaemia, inflammation and oxidative stress are associated with development of AKI. Albumin’s pharmacological properties and widespread availability have the potential to mitigate these factors. However, the effect of albumin on cardiac surgery-associated AKI is unknown. Objective: To evaluate the impact of postoperative 20% albumin infusion on kidney function after high-risk cardiac surgery. Methods: We designed an open-label, multicentre, randomised controlled trial—the ALBICS study (ALBumin Infusion and acute kidney injury following Cardiac Surgery). A total of 590 patients undergoing high-risk cardiac surgery (combined procedure or estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m2) will be enrolled into the study and randomly allocated to receive a postoperative 20% albumin infusion or standard care in a 1:1 ratio, stratified by centre and baseline renal function. The study fluid will be administered upon arrival in intensive care for 15 h. Patients will be followed up until 28 days after surgery or until discharge from the hospital. The primary outcome is the proportion of patients who develop AKI in both groups. Secondary outcomes to be measured are proportions of AKI stage II and III, 28-day mortality, mechanical ventilation time and length of stay in intensive care and hospital. Conclusion: This trial aims to determine if a postoperative infusion of concentrated albumin reduces the risk of AKI following high-risk cardiac surgery. Trial registration: Australian New Zealand Clinical Trials Registry ACTRN12619001355167. Registered on 03 October 2019—retrospectively registered. https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=378383.
KW - Acute kidney injury
KW - Albumin
KW - Cardiac surgery
KW - Intensive care
UR - http://www.scopus.com/inward/record.url?scp=85113267623&partnerID=8YFLogxK
U2 - 10.1186/s13063-021-05519-8
DO - 10.1186/s13063-021-05519-8
M3 - Article
C2 - 34419128
AN - SCOPUS:85113267623
SN - 1745-6215
VL - 22
JO - Trials
JF - Trials
IS - 1
M1 - 558
ER -