Skip to content

Strategy for Uptake of Processes for Recognizing and Responding to Acute Kidney Injury

Strategy for Uptake of Processes for Recognizing and Responding to Acute Kidney Injury

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03564314
Acronym
SUPPORT AKI
Enrollment
2135
Registered
2018-06-20
Start date
2018-03-13
Completion date
2020-12-31
Last updated
2023-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury

Keywords

Acute kidney injury, Major surgery, Clinical decision support

Brief summary

Acute kidney injury (AKI) is common and costly complication of major surgery. AKI can lead to prolonged hospitalization and a higher likelihood of dialysis, chronic kidney disease and death. However, AKI can be reversed when recognized early, by ensuring that patients receive adequate fluids and medications that worsen kidney function or cause toxicity are avoided or appropriately prescribed. Past research suggests that AKI in surgical settings can be missed early in its onset, leading to delayed intervention and progression to more severe stages. The purpose of this project is to implement clinical decision support for early recognition and management of AKI on surgical units in Alberta hospitals, and to determine whether the initiative leads to improvements in the quality of care for AKI, length of hospital stay for patients, and costs to the healthcare system.

Detailed description

Overview: Cluster-randomized stepped-wedge trial to evaluate the impact of implementing a clinical decision support initiative for early recognition and management of hospital-acquired AKI. Study Population: Adult patients hospitalized on surgical units in Alberta who develop acute kidney injury will be eligible if not already receiving dialysis. Intervention: The multidimensional clinical decision support intervention consists of: (1) electronic and non-computerized tools for early recognition of AKI, (2) educational program for clinical staff, (3) decision support resources and guidance for the management of AKI and consultation with specialists. Study Design: Using a stepped-wedge design, eight general and vascular surgery unit clusters in Calgary (Foothills Medical Centre, Peter Lougheed Centre) and Edmonton (University of Alberta Hospital, Grey Nuns Community Hospital), Alberta will be randomly ordered to be sequentially introduced to the clinical decision support intervention. The pre-implementation period will include all patients admitted to the participating hospital units in the year before the random timing of introduction of the initiative on each participating unit. The post-implementation study cohort will include patients admitted in the year after the random timing of introduction of the initiative on each unit. Analysis of processes of care and outcomes will focus on patients on these units who develop AKI during the pre- and post-implementation time periods (i.e. are eligible to receive care under the AKI decision support initiative). Additionally, health care providers (e.g. physicians, nursing staff, pharmacists) who have direct experience with the clinical decision support tools and processes will be invited to participate in the surveys and interviews pre- and post-implementation.

Interventions

OTHERSUPPORT AKI Clinical Decision Support

Surgical units will receive a multidimensional clinical decision support intervention consisting of: (1) electronic and non-computerized tools to alert for early recognition of AKI, (2) educational program for physicians and nursing staff, (3) decision support tools with guidance on fluid therapies, medication management, investigations for AKI, and consultation with specialists.

Sponsors

Alberta Health services
CollaboratorOTHER
University of Alberta
CollaboratorOTHER
Covenant Health, Canada
CollaboratorOTHER
University of Calgary
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients (18 years of age and older) who develop hospital-acquired acute kidney injury on identified general and vascular surgery units in Alberta

Exclusion criteria

* Hospitalized on non-surgical units * Receiving dialysis prior to admission on surgery unit

Design outcomes

Primary

MeasureTime frameDescription
Progression of AKIFrom date of AKI onset to discharge from hospital, assessed up to 30 daysIncidence of progression of AKI to higher AKI stage (including progression to dialysis or death)

Secondary

MeasureTime frameDescription
Resource use for AKIDuration of index hospital admission, assessed up to 30 daysMean total health care costs of hospital care during the index admission
Time to initial response to AKIFrom AKI onset up to 48 hours following AKI onsetTime from AKI onset to clinical response with fluid or medication management intervention
Volume intervention (change in fluid or diuretic order) for AKIWithin 48 hours following AKI onsetNew or modified intravenous fluid or diuretic order
Length of AKI hospital stay, daysFrom date of AKI onset to discharge from hospital, assessed up to 30 daysMean length of hospital stay from acute kidney injury to discharge
Medical consultation for AKIWithin 7 days of AKI onsetConsultation with nephrology or general internal medicine
Change in estimated Glomerular Filtration Rate (eGFR)From most recent baseline eGFR measurement prior to AKI onset to eGFR measurement closest to 3 months after AKI onsetThe difference in eGFR from baseline to 3 months after development of AKI
MortalityWithin 30 days of AKI onsetAll cause mortality
Adverse medication exposureWithin 48 hours following AKI onsetDose modification or suspension or a medication that may cause AKI or that is cleared by the kidney

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026