Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Project Grant

Centre hospitalier de l'Université de Montréal (CHUM)

$248,626.00

Proactive prescription-based fluid management vs usual care in critically ill patients on Kidney Replacement Therapy

EF 2021-22

Résumé
Individuals with critical illness requiring intensive care frequently develop severe acute kidney injury. Unfortunately, short-term death occurs in up to 40% of patients who develop this condition. An abrupt reduction of the ability of the kidneys to produce urine almost always results in fluid accumulation. Considerable evidence suggests that fluid accumulation may impair the function of multiple organs and lead to major complications and increase the risk of death. Kidney replacement therapy enables the removal of fluid in this setting. However, rapid fluid removal may also harm individuals when it results in significant instability. It is therefore urgent to determine what is the best strategy for these patients. This clinical trial proposes to use a proactive approach aimed to avoid fluid accumulation to effectively and safely optimize fluid removal in a critically ill patient with acute kidney injury on kidney replacement therapy. The aim of this pilot study is to enroll 125 individuals to determine whether a larger would be possible to perform. In half of the participants, fluid removal prescription will follow a pre-specified and regularly updated template while fluid removal in the other half will be prescribed according to usual care. The proactive fluid removal strategy will continue until 14 days after enrollment. Participants will be followed until 90 days to assess whether the intervention is safe, whether it is associated with important events, and to determine its impact on the use of healthcare resources. The proposed study is the first step to perform a large-scale definitive study to determine if a proactive fluid management strategy aiming at limiting fluid accumulation is able to improve chances of survival in critically ill adults with severe acute kidney injury. This question is a priority considering the high mortality rate in this population.
Programme
Project Grant
Emplacement
Quebec, Canada
Type de bénéficiaire
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
451345
Name
Beaubien-Souligny William
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Clinical
Prcname2
Clinical Investigation - C: Digestive, Endocrine and Excretory Systems
Projecttitle
Proactive prescription-based fluid management vs usual care in critically ill patients on Kidney Replacement Therapy
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$248,626
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Acute Kidney Injury; Critical Illness; Fluid Hemeostasis; Non-Pharmacologic Intervention; Organ Failure; Pragmatic Trial; Renal Replacement Therapy
Abstract
Individuals with critical illness requiring intensive care frequently develop severe acute kidney injury. Unfortunately, short-term death occurs in up to 40% of patients who develop this condition. An abrupt reduction of the ability of the kidneys to produce urine almost always results in fluid accumulation. Considerable evidence suggests that fluid accumulation may impair the function of multiple organs and lead to major complications and increase the risk of death. Kidney replacement therapy enables the removal of fluid in this setting. However, rapid fluid removal may also harm individuals when it results in significant instability. It is therefore urgent to determine what is the best strategy for these patients. This clinical trial proposes to use a proactive approach aimed to avoid fluid accumulation to effectively and safely optimize fluid removal in a critically ill patient with acute kidney injury on kidney replacement therapy. The aim of this pilot study is to enroll 125 individuals to determine whether a larger would be possible to perform. In half of the participants, fluid removal prescription will follow a pre-specified and regularly updated template while fluid removal in the other half will be prescribed according to usual care. The proactive fluid removal strategy will continue until 14 days after enrollment. Participants will be followed until 90 days to assess whether the intervention is safe, whether it is associated with important events, and to determine its impact on the use of healthcare resources. The proposed study is the first step to perform a large-scale definitive study to determine if a proactive fluid management strategy aiming at limiting fluid accumulation is able to improve chances of survival in critically ill adults with severe acute kidney injury. This question is a priority considering the high mortality rate in this population.
Competitiondate
202109
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Beaubien-Souligny, William; Bagshaw, Sean M; Wald, Ron
Approvedterm
2 ans 0 mois
Cihrcontribution2
~ $248,626~ $0~