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Nephrologist Follow-up Versus Usual Care After an Acute Kidney Injury Hospitalization (FUSION)

Primary Purpose

Acute Kidney Injury, Chronic Kidney Disease

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
AKI Follow-up Clinic
Sponsored by
Unity Health Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Kidney Injury focused on measuring Acute kidney injury, Chronic kidney disease, Quality improvement

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 yrs
  • Kidney Disease Improving Global Outcomes (KDIGO) stage 2 AKI and above (including need for dialysis)

Exclusion Criteria:

  • Kidney transplant recipients
  • Outpatient baseline eGFR under 30mL/min/1.73m2 (by CKD-EPI equation); ignore if baseline serum creatinine is unavailable
  • Patients discharged from hospital with a persistent requirement for renal replacement therapy
  • Clinical diagnosis or suspicion of: glomerulonephritis, vasculitis with kidney involvement, hemolytic-uremic syndrome, polycystic kidney disease, myeloma cast nephropathy
  • Pregnancy
  • Residence at a nursing home facility (rehabilitation and retirement home patients should not be excluded)
  • Palliation as primary goal of care (defined as life expectancy ≤ six months or followed by a palliative care physician)
  • Patients with previously established and ongoing nephrology follow-up (defined as ≥ one outpatient appointment with a nephrologist in the previous 12 months)

Sites / Locations

  • Mount Sinai Hospital
  • St. Michael's Hospital
  • Sunnybrook Health Sciences Centre
  • University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

AKI Follow-up Clinic

Usual Care

Arm Description

Participants randomized to this arm will be referred to the AKI Follow-up Clinic where they will see a nephrologist who will coordinate follow-up care. The target appointment date is within 30 days of hospital discharge. Routine laboratory investigations will be performed at minimum every three months. Additional in-person visits with a nephrologist at the AKI Follow-up Clinic will be determined at the local sites based upon the participant's clinical status. If in-person visits at 12, 24, and/or 36 weeks are not necessary given the patient's clinical status, they may be replaced with a telephone visit

Participants randomized to this arm will have a letter outlining their AKI diagnosis mailed to their family physician. Participants may still be referred to a nephrologist by their inpatient or outpatient healthcare provider, but these participants will not have access to the AKI Follow-up Clinic. Rather, they will proceed through the standard local nephrology referral pathway. In addition, all usual care participants will be contacted via telephone by study staff every three months to assess their clinical condition and ensure study engagement. All usual care participants will be offered a nephrologist assessment and/or bloodwork one year after randomization to determine if ongoing nephrology care is indicated based upon the same criteria applied to AKI Follow-up Clinic participants.

Outcomes

Primary Outcome Measures

Proportion with a major adverse kidney event
Composite of chronic dialysis, chronic kidney disease progression, or death

Secondary Outcome Measures

Proportion with a major adverse kidney event
Composite of chronic dialysis, chronic kidney disease progression, or death
Proportion deceased
Proportion who require chronic dialysis
one outpatient dialysis treatment at any time after randomization
Proportion with chronic kidney disease progression using CKD-EPI eGFR equation
Time to major adverse kidney event
Composite of chronic dialysis, chronic kidney disease progression, or death
Time to death
Time to chronic dialysis
one outpatient dialysis treatment at any time after randomization
Time to CKD progression using CKD-EPI eGFR equation
Proportion with a major adverse cardiac event
Defined as a hospitalization or emergency department visit for stroke, congestive heart failure, myocardial infarction, or cardiac revascularization procedure
Proportion who experience a stroke
Hospitalization or emergency department visit for stroke
Proportion who experience a congestive heart failure episode
Hospitalization or emergency department visit for congestive heart failure
Proportion who undergo a cardiac revascularization procedure
Hospitalization or emergency department visit for a cardiac revascularization procedure
Proportion who experience a myocardial infarction
Hospitalization or emergency department visit for myocardial infarction
Time to first rehospitalization
Defined as the first readmission to hospital for any reason
Time to first emergency department visit
Defined as the first emergency department visit for any reason
Time to first acute kidney injury episode post-randomization using KDIGO serum creatinine criteria
Number of acute kidney injury episodes post-randomization using KDIGO serum creatinine criteria
Change in quality-of-life as measured by EuroQol-5D-5L instrument

Full Information

First Posted
June 18, 2015
Last Updated
April 17, 2018
Sponsor
Unity Health Toronto
Collaborators
Sunnybrook Health Sciences Centre, University Health Network, Toronto, Mount Sinai Hospital, Canada
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1. Study Identification

Unique Protocol Identification Number
NCT02483039
Brief Title
Nephrologist Follow-up Versus Usual Care After an Acute Kidney Injury Hospitalization
Acronym
FUSION
Official Title
Nephrologist Follow-up Versus Usual Care After an Acute Kidney Injury Hospitalization (FUSION): Vanguard Phase of a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
July 2018 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Unity Health Toronto
Collaborators
Sunnybrook Health Sciences Centre, University Health Network, Toronto, Mount Sinai Hospital, Canada

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective is to evaluate the impact of an AKI Follow-up Clinic on major adverse kidney events (MAKE) in comparison to hospitalized patients surviving an episode of AKI who are not exposed to the AKI Follow-up Clinic intervention.
Detailed Description
Survivors of acute kidney injury (AKI) are at increased risk of chronic kidney disease (CKD) and death, but have inconsistent follow-up care. Our team has developed and tested a model to deliver structured follow-up kidney care (the AKI Follow-up Clinic) that is feasible and sustainable, with standardized assessments based upon clinical practice guidelines that are transferable to any setting. This study will randomize patients with Kidney Disease Improving Global Outcomes (KDIGO) stage 2-3 AKI to the AKI Follow-up Clinic or usual care (control group). The usual care group will have a letter outlining their AKI diagnosis mailed to their family physician; the usual care group may still be referred to a nephrologist by their healthcare provider if desired, but these participants will not have access to the AKI Follow-up Clinic pathways. The primary outcome is development of a major adverse kidney event (MAKE), a composite of death, chronic dialysis, and estimated glomerular filtration rate (eGFR) decline. Outcomes will be ascertained after one year of follow-up, which is when AKI Follow-up Clinic patients are transitioned back to their family doctor or general nephrologist based upon pre-specified graduation criteria. Participants will also be followed using local hospital electronic resources and the Institute for Clinical Evaluative Sciences (ICES) administrative databases in order to assess the long-term impact of early nephrologist follow-up on AKI outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury, Chronic Kidney Disease
Keywords
Acute kidney injury, Chronic kidney disease, Quality improvement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
AKI Follow-up Clinic
Arm Type
Experimental
Arm Description
Participants randomized to this arm will be referred to the AKI Follow-up Clinic where they will see a nephrologist who will coordinate follow-up care. The target appointment date is within 30 days of hospital discharge. Routine laboratory investigations will be performed at minimum every three months. Additional in-person visits with a nephrologist at the AKI Follow-up Clinic will be determined at the local sites based upon the participant's clinical status. If in-person visits at 12, 24, and/or 36 weeks are not necessary given the patient's clinical status, they may be replaced with a telephone visit
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Participants randomized to this arm will have a letter outlining their AKI diagnosis mailed to their family physician. Participants may still be referred to a nephrologist by their inpatient or outpatient healthcare provider, but these participants will not have access to the AKI Follow-up Clinic. Rather, they will proceed through the standard local nephrology referral pathway. In addition, all usual care participants will be contacted via telephone by study staff every three months to assess their clinical condition and ensure study engagement. All usual care participants will be offered a nephrologist assessment and/or bloodwork one year after randomization to determine if ongoing nephrology care is indicated based upon the same criteria applied to AKI Follow-up Clinic participants.
Intervention Type
Behavioral
Intervention Name(s)
AKI Follow-up Clinic
Intervention Description
Participants randomized to this arm will be referred to the AKI Follow-up Clinic where they will see a nephrologist who will coordinate follow-up care. At the AKI Follow-up Clinic, assessment forms that were developed during the pilot study at St. Michael's Hospital may be used, but this decision will be left to individual sites. Routine laboratory investigations will be performed at minimum every three months.
Primary Outcome Measure Information:
Title
Proportion with a major adverse kidney event
Description
Composite of chronic dialysis, chronic kidney disease progression, or death
Time Frame
1 year after randomization
Secondary Outcome Measure Information:
Title
Proportion with a major adverse kidney event
Description
Composite of chronic dialysis, chronic kidney disease progression, or death
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Proportion deceased
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Proportion who require chronic dialysis
Description
one outpatient dialysis treatment at any time after randomization
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Proportion with chronic kidney disease progression using CKD-EPI eGFR equation
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Time to major adverse kidney event
Description
Composite of chronic dialysis, chronic kidney disease progression, or death
Time Frame
5 years following randomization
Title
Time to death
Time Frame
5 years following randomization
Title
Time to chronic dialysis
Description
one outpatient dialysis treatment at any time after randomization
Time Frame
5 years following randomization
Title
Time to CKD progression using CKD-EPI eGFR equation
Time Frame
5 years following randomization
Title
Proportion with a major adverse cardiac event
Description
Defined as a hospitalization or emergency department visit for stroke, congestive heart failure, myocardial infarction, or cardiac revascularization procedure
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Proportion who experience a stroke
Description
Hospitalization or emergency department visit for stroke
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Proportion who experience a congestive heart failure episode
Description
Hospitalization or emergency department visit for congestive heart failure
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Proportion who undergo a cardiac revascularization procedure
Description
Hospitalization or emergency department visit for a cardiac revascularization procedure
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Proportion who experience a myocardial infarction
Description
Hospitalization or emergency department visit for myocardial infarction
Time Frame
30, 90, 365 days, and 5 years following randomization
Title
Time to first rehospitalization
Description
Defined as the first readmission to hospital for any reason
Time Frame
5 years following randomization
Title
Time to first emergency department visit
Description
Defined as the first emergency department visit for any reason
Time Frame
5 years post-randomization
Title
Time to first acute kidney injury episode post-randomization using KDIGO serum creatinine criteria
Time Frame
5 years post-randomization
Title
Number of acute kidney injury episodes post-randomization using KDIGO serum creatinine criteria
Time Frame
5 years post-randomization
Title
Change in quality-of-life as measured by EuroQol-5D-5L instrument
Time Frame
1 year post-randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 yrs Kidney Disease Improving Global Outcomes (KDIGO) stage 2 AKI and above (including need for dialysis) Exclusion Criteria: Kidney transplant recipients Outpatient baseline eGFR under 30mL/min/1.73m2 (by CKD-EPI equation); ignore if baseline serum creatinine is unavailable Patients discharged from hospital with a persistent requirement for renal replacement therapy Clinical diagnosis or suspicion of: glomerulonephritis, vasculitis with kidney involvement, hemolytic-uremic syndrome, polycystic kidney disease, myeloma cast nephropathy Pregnancy Residence at a nursing home facility (rehabilitation and retirement home patients should not be excluded) Palliation as primary goal of care (defined as life expectancy ≤ six months or followed by a palliative care physician) Patients with previously established and ongoing nephrology follow-up (defined as ≥ one outpatient appointment with a nephrologist in the previous 12 months)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ron Wald, MDCM, MPH
Organizational Affiliation
Unity Health Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
33731806
Citation
Robinson C, Hessey E, Nunes S, Dorais M, Chanchlani R, Lacroix J, Jouvet P, Phan V, Zappitelli M. Acute kidney injury in the pediatric intensive care unit: outpatient follow-up. Pediatr Res. 2022 Jan;91(1):209-217. doi: 10.1038/s41390-021-01414-9. Epub 2021 Mar 17.
Results Reference
derived

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Nephrologist Follow-up Versus Usual Care After an Acute Kidney Injury Hospitalization

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