TY - JOUR
T1 - Forced diuresis with matched hydration during transcatheter aortic valve implantation for Reducing Acute Kidney Injury
T2 - A randomized, sham-controlled study (REDUCE-AKI)
AU - Arbel, Yaron
AU - Ben-Assa, Eyal
AU - Puzhevsky, Daniela
AU - Litmanowicz, Batia
AU - Galli, Naama
AU - Chorin, Ehud
AU - Halkin, Amir
AU - Sadeh, Ben
AU - Konigstein, Maayan
AU - Bassat, Orit Kliuk Ben
AU - Steinvil, Arie
AU - Bazan, Samuel
AU - Banai, Shmuel
AU - Finkelstein, Ariel
N1 - Publisher Copyright:
© 2019 Published on behalf of the European Society of Cardiology. All rights reserved.
PY - 2019/10/7
Y1 - 2019/10/7
N2 - Aims: Acute kidney injury (AKI) is a common complication following transcatheter aortic valve implantation (TAVI) and is associated with increased risk for short- and long-term mortality. In patients undergoing percutaneous coronary intervention (PCI), forced diuresis with matched hydration has been shown to reduce the incidence of AKI by ∼50%. The aim of the present study was to evaluate whether forced diuresis with matched intravenous hydration reduces AKI in patients undergoing TAVI. Methods and results: Reducing Acute Kidney Injury (REDUCE-AKI) was a single-centre, prospective, randomized, double-blind sham-controlled clinical trial, designed to examine the effect of an automated matched saline infusion with urine output for the prevention of AKI in patients undergoing TAVI. A total of 136 TAVI patients were randomized, 68 in each group. Mean age was 83.9 ± 5 years and 41.2% were males. There were no differences in baseline characteristics between the two groups. The rate of AKI was not statistically different between the groups (25% in the active group vs. 19.1% in the sham group, P = 0.408). There was a significant increase in long-term mortality in the active group (27.9% vs. 13. 2% HR 3.744, 95% CI 1.51-9.28; P = 0.004). The study was terminated prematurely by the Data Safety Monitoring Board for futility and a possible signal of harm. Conclusions: Unlike in PCI, forced diuresis with matched hydration does not prevent AKI in patients undergoing TAVI, and might be associated with increased long-term mortality. Future studies should focus on understanding the mechanisms behind these findings. Clinicaltrials.gov registration: NCT01866800, 30 April 2013.
AB - Aims: Acute kidney injury (AKI) is a common complication following transcatheter aortic valve implantation (TAVI) and is associated with increased risk for short- and long-term mortality. In patients undergoing percutaneous coronary intervention (PCI), forced diuresis with matched hydration has been shown to reduce the incidence of AKI by ∼50%. The aim of the present study was to evaluate whether forced diuresis with matched intravenous hydration reduces AKI in patients undergoing TAVI. Methods and results: Reducing Acute Kidney Injury (REDUCE-AKI) was a single-centre, prospective, randomized, double-blind sham-controlled clinical trial, designed to examine the effect of an automated matched saline infusion with urine output for the prevention of AKI in patients undergoing TAVI. A total of 136 TAVI patients were randomized, 68 in each group. Mean age was 83.9 ± 5 years and 41.2% were males. There were no differences in baseline characteristics between the two groups. The rate of AKI was not statistically different between the groups (25% in the active group vs. 19.1% in the sham group, P = 0.408). There was a significant increase in long-term mortality in the active group (27.9% vs. 13. 2% HR 3.744, 95% CI 1.51-9.28; P = 0.004). The study was terminated prematurely by the Data Safety Monitoring Board for futility and a possible signal of harm. Conclusions: Unlike in PCI, forced diuresis with matched hydration does not prevent AKI in patients undergoing TAVI, and might be associated with increased long-term mortality. Future studies should focus on understanding the mechanisms behind these findings. Clinicaltrials.gov registration: NCT01866800, 30 April 2013.
KW - AKI
KW - Complications
KW - Contrast
KW - TAVI
KW - TAVR
UR - http://www.scopus.com/inward/record.url?scp=85072994071&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehz343
DO - 10.1093/eurheartj/ehz343
M3 - Article
C2 - 31120108
AN - SCOPUS:85072994071
SN - 0195-668X
VL - 40
SP - 3169
EP - 3178
JO - European Heart Journal
JF - European Heart Journal
IS - 38
ER -