Tunneled Dialysis Catheters Versus Non-tunneled Dialysis Catheters as First-line for Renal Replacement Therapy in the ICU (BACKDOOR)
Primary Purpose
Acute Kidney Injury
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Tunneled versus non-tunneled dialysis catheter insertion
Sponsored by
About this trial
This is an interventional treatment trial for Acute Kidney Injury focused on measuring Renal replacement therapy
Eligibility Criteria
Inclusion Criteria:
All adult patients in the BWH ICUs with an incident AKI requiring renal replacement therapy
Exclusion Criteria:
- Clinical instability requiring bedside catheter placement
- INR >2.0 or other significant coagulopathy
- Pending blood cultures within 48 hours or active bacteremia
- Urgency of line placement warranting placement within 6 hours.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Tunneled dialysis catheter
Non-tunneled dialysis catheter
Arm Description
In this arm, patients will be randomized to undergo tunneled dialysis catheter insertion.
In this arm, patients will be randomized to undergo non-tunneled dialysis catheter insertion.
Outcomes
Primary Outcome Measures
Rate of complications
Composite outcome including rate of infection and thrombosis. The incidence of both of these adverse events will be added together to give a composite rate of complications.
Secondary Outcome Measures
Dialysis venous access pressure
Median venous access pressure
Dialysis arterial access pressure
Median arterial access pressure
Dialysis blood flow rate
Median blood flow rate
Feasibility of tunneled catheter placement for AKI
Time to catheter placement
Cost of dialysis access placement for AKI
Cost of dialysis catheter placement
Full Information
NCT ID
NCT03496935
First Posted
March 28, 2018
Last Updated
April 11, 2018
Sponsor
Brigham and Women's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03496935
Brief Title
Tunneled Dialysis Catheters Versus Non-tunneled Dialysis Catheters as First-line for Renal Replacement Therapy in the ICU
Acronym
BACKDOOR
Official Title
A Randomized Controlled Trial of Tunneled Dialysis Catheters Versus Non-tunneled Dialysis Catheters for Renal Replacement Therapy in the ICU
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2018 (Anticipated)
Primary Completion Date
July 1, 2020 (Anticipated)
Study Completion Date
September 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators propose a randomized controlled trial to examine whether tunneled dialysis catheters should be first-line for acute kidney injury requiring renal replacement therapy (AKI-RRT) in the critical care setting, barring any clinical contraindications, compared to non-tunneled access. This randomized controlled trial will include patients admitted to an intensive care unit (ICU) at Brigham and Women's Hospital (BWH). The investigators will randomize all eligible consented incident patients with AKI requiring renal replacement therapy either to tunneled dialysis catheter or non-tunneled dialysis catheter placement. The inclusion criteria encompasses all adult patients in the BWH ICUs with an incident AKI requiring renal replacement therapy. The investigators' hypothesis is that the rate of overall complications is lower with tunneled dialysis catheters compared to non-tunneled catheters.
Detailed Description
Acute kidney injury (AKI) is defined by an abrupt decrease in kidney function resulting in the retention of urea and other nitrogenous waste products and in the dysregulation of extracellular volume and electrolytes. AKI is common, harmful and potentially treatable.
Despite decades of research, renal replacement therapy (RRT) in the form of dialysis remains the primary therapy to treat AKI and its complications. Due to convenience of scheduling and distribution of expertise, non-tunneled dialysis catheters have generally been the first-line source of vascular access for patients requiring acute dialysis for AKI in the ICU setting. However, there is evidence that tunneled dialysis catheters are associated with improved outcomes compared to non-tunneled dialysis catheters.
The investigators for this proposed trial performed an observational study at Brigham and Women's Hospital in 2016 comparing outcomes from temporary dialysis catheter versus tunneled dialysis catheter use for renal replacement therapy in the ICU.12 They found that there was a significant increase in median venous and arterial access pressure between temporary dialysis catheters and tunneled dialysis catheters for patients on CVVH with an increased rate ratio of interruptions and decreased blood flow rates for temporary dialysis catheters compared to tunneled dialysis catheters
The investigators now propose a prospective randomized controlled trial to examine whether tunneled dialysis catheters should be first-line for AKI-RRT in the critical care setting, barring any clinical contraindications, compared to non-tunneled access. This RCT will include patients admitted to an ICU at Brigham and Women's Hospital. The investigators will randomize all eligible consented incident patients with AKI requiring renal replacement therapy either to tunneled dialysis catheter or non-tunneled dialysis catheter placement. The inclusion criteria encompasses all adult patients in the BWH ICUs with an incident AKI requiring renal replacement therapy. Exclusion criteria will include 1) clinical instability requiring bedside catheter placement; 2) international normalized ratio (INR) >2.0 or other significant coagulopathy; 3) pending blood cultures within 48 hours or active bacteremia; or 4) urgency of line placement warranting placement within 6 hours. To avoid bias introduced by operator performance, the same group of interventional nephrologists will be utilized to place the catheters in both arms of the trial. The investigators' hypothesis is that the rate of overall complications is lower with tunneled dialysis catheters compared to non-tunneled catheters. Other secondary outcomes of interest include dialysis delivery parameters including access pressures and blood flow rates. The investigators also plan to assessing the feasibility of tunneled dialysis catheter placement for AKI, by capturing data on time to placement, resource utilization and cost. The proposal challenges a common clinical practice; placement of non-tunneled catheters for RRT initiation, which is not evidence-based, to determine if tunneled catheters can improve outcomes for patients compared to usual care.
The investigators will identify all patients with AKI requiring vascular access by reviewing inpatient renal consult patient lists and electronic orders for intermittent hemodialysis (IHD) or continuous renal replacement therapy (CRRT) initiation. Data will be prospectively collected on demographics, comorbidities, laboratory data, and microbiology results on a daily basis. Data will also be abstracted from procedure notes to identify procedural complications. Similarly, CVVH and IHD data (blood flow rates, venous and arterial pressures, total time of RRT per session, and number of interruptions during RRT) will be gathered prospectively on a daily basis from RRT flowsheets and RRT nursing notes. Patients will be followed throughout the entirety of the hospitalization until hospital discharge or death.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
Keywords
Renal replacement therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
102 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Tunneled dialysis catheter
Arm Type
Active Comparator
Arm Description
In this arm, patients will be randomized to undergo tunneled dialysis catheter insertion.
Arm Title
Non-tunneled dialysis catheter
Arm Type
Active Comparator
Arm Description
In this arm, patients will be randomized to undergo non-tunneled dialysis catheter insertion.
Intervention Type
Device
Intervention Name(s)
Tunneled versus non-tunneled dialysis catheter insertion
Intervention Description
The study participants will be randomized either to tunneled or non-tunneled dialysis catheter insertion to commence renal replacement therapy for an acute kidney injury requiring either continuous or intermittent dialysis in the ICU.
Primary Outcome Measure Information:
Title
Rate of complications
Description
Composite outcome including rate of infection and thrombosis. The incidence of both of these adverse events will be added together to give a composite rate of complications.
Time Frame
Up to 60 days
Secondary Outcome Measure Information:
Title
Dialysis venous access pressure
Description
Median venous access pressure
Time Frame
Up to 60 days
Title
Dialysis arterial access pressure
Description
Median arterial access pressure
Time Frame
Up to 60 days
Title
Dialysis blood flow rate
Description
Median blood flow rate
Time Frame
Up to 60 days
Title
Feasibility of tunneled catheter placement for AKI
Description
Time to catheter placement
Time Frame
Up to 60 days
Title
Cost of dialysis access placement for AKI
Description
Cost of dialysis catheter placement
Time Frame
Up to 60 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All adult patients in the BWH ICUs with an incident AKI requiring renal replacement therapy
Exclusion Criteria:
Clinical instability requiring bedside catheter placement
INR >2.0 or other significant coagulopathy
Pending blood cultures within 48 hours or active bacteremia
Urgency of line placement warranting placement within 6 hours.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yvelynne P Kelly, M.D. MSc.
Phone
857-350-0573
Email
ypkelly@bwh.harvard.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mallika Mendu, M.D. MBA.
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34519356
Citation
Tsujimoto Y, Miki S, Shimada H, Tsujimoto H, Yasuda H, Kataoka Y, Fujii T. Non-pharmacological interventions for preventing clotting of extracorporeal circuits during continuous renal replacement therapy. Cochrane Database Syst Rev. 2021 Sep 14;9(9):CD013330. doi: 10.1002/14651858.CD013330.pub2.
Results Reference
derived
Learn more about this trial
Tunneled Dialysis Catheters Versus Non-tunneled Dialysis Catheters as First-line for Renal Replacement Therapy in the ICU
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