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Fluid Chloride and AKI in Cardiopulmonary Bypass

Primary Purpose

Acute Kidney Injury

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
0.9% Normal Saline (0.9% Sodium Chloride) injection
Isolyte S injection
Sponsored by
University of New Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Kidney Injury

Eligibility Criteria

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

Inclusion Criteria:

  • Planned on- or off-pump cardiac surgery including: bypass grafting, valvular procedures, congenital defect correction, and thoracic aortic procedures or a combination of these procedures

Exclusion Criteria:

  • Emergency surgery
  • Pregnancy
  • Previous renal transplantation
  • Documented moderate to severe acute kidney injury prior to enrollment (e.g. RIFLE-I or RIFLE-F/KDIGO stage 2 or 3)
  • Patients already receiving dialysis (acute or chronic) or in imminent need of dialysis at time of enrollment
  • Chronic kidney disease without baseline serum creatinine value obtained within 6 months of enrollment

Sites / Locations

  • University of New Mexico Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Normal Saline group

Isolyte group

Arm Description

0.9% Normal Saline (0.9% Sodium Chloride) injection intravenously as needed. The amount administered (dosage, frequency, and duration) will be left to the clinical judgment of the attending physicians, and will follow usual patterns of use in cardiac surgery patients.

Isolyte S (B Braun, Irvine CA) injection intravenously as needed. The amount administered (dosage, frequency, and duration) will be left to the clinical judgment of the attending physicians, and will follow usual patterns of use in cardiac surgery patients. Isolyte S is a prepackaged solution containing sodium chloride 0.53%, sodium gluconate 0.5%, sodium acetate trihydrate 0.37%, potassium chloride 0.037%, and magnesium chloride hexahydrate 0.03% w/v.

Outcomes

Primary Outcome Measures

Change in [TIMP2]*[IGFBP7] Biomarker
The difference in the [TIMP2]*[IGFBP7] biomarker between the preoperative value and a repeated measurement at 24 hours postoperatively. Positive values represent increase; negative values represent decrease

Secondary Outcome Measures

Serum Creatinine Level at 24 Hours
Serum creatinine measurement at 24 hours
Serum Chloride Level at 24 Hours
Serum chloride ion measurement at 24 hours postoperatively
Proportion of Patients With Need for Dialysis
Clinically-determined need for dialysis prior to discharge from hospital
Postoperative Arterial pH
Arterial pH, measured 24 hours after surgery
Serum Creatinine Level at 48 Hours
Serum creatinine level 48 hours postoperatively
Serum Chloride at 48 Hours
Serum chloride measurement at 48 hours postoperatively

Full Information

First Posted
January 20, 2016
Last Updated
April 13, 2018
Sponsor
University of New Mexico
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1. Study Identification

Unique Protocol Identification Number
NCT02668952
Brief Title
Fluid Chloride and AKI in Cardiopulmonary Bypass
Official Title
The Impact of Low Chloride Containing Fluids on Acute Kidney Injury After Cardiopulmonary Bypass as Assayed by Urinary [TIMP2*IGFBP7]
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
January 2016 (Actual)
Primary Completion Date
February 4, 2017 (Actual)
Study Completion Date
February 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of New Mexico

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Acute kidney injury (AKI) is a potential complication of cardiac surgery. In animal models, excess exogenous Cl- ion in the bloodstream is associated with AKI. Normal saline IV fluid has higher levels of Cl- ion than the blood usually carries. An alternative IV fluid sold under the name Isolyte has lower Cl- ion levels. There is no literature comparing AKI outcomes in cardiac patients between patients receiving normal saline vs. Isolyte. The investigators propose to recruit and randomize 30 trial-completing cardiac surgery patients (up to 40 enrolled) into 2 study arms and compare renal outcomes.
Detailed Description
Acute kidney injury (AKI) is a potential complication for patients undergoing cardiac surgery. AKI in post-cardiac surgery patients is associated with adverse outcomes, such as prolonged intensive care and hospital stay, diminished quality of life, increased long-term mortality, and an increased risk of chronic kidney disease requiring dialysis. The mortality in cardiac surgery patients with AKI severe enough to require renal replacement therapy (RRT) can be as high as 60%. One of the putative agents associated with AKI in animal models receiving crystalloid fluids for resuscitative interventions is excess exogenous chloride ion (Cl-). As compared to non-Cl- containing solutions in animal models, excess Cl- appears to lead to a hyperchloremic metabolic acidosis, increased renal vascular resistance, reduced renal blood flow, and reduced glomerular filtration rate - all of which are injurious to kidney function. Historically, one of the most common balanced salt-solutions used in adult cardiac surgery has been 0.9% normal saline (NS), a crystalloid solution with 154 mmol/L of Cl-. This is much higher than physiologic plasma levels of 103 mmol/L. Isolyte, a less commonly used crystalloid solution, is much closer to physiologic levels at 98 mmol/L Cl-. In the context of cardiac surgery, there is no literature expressly comparing the effects of balanced crystalloid solution such as Isolyte versus NS on AKI incidence. There is a single trial examining a low-Cl- containing colloid solution in cardiac surgery that found less metabolic acidosis; however, AKI or markers of AKI were not measured outcomes in that lone trial, so it is not known whether low Cl- solution will have any effect on AKI risk in humans. AKI results from a series of extremely complex cellular and molecular pathways involving endothelial, epithelial, inflammatory, and interstitial cells. The gold standard for identification and classification of AKI is dependent on serial serum creatinine (Scr) measurements, but this measurement can be unreliable during acute changes in kidney function. Recent studies have shown that tissue inhibitor of metalloproteinase (TIMP-2) performs better than existing markers for predicting the development of moderate or severe AKI (Kidney Disease: Improving Global Outcomes [KDIGO] stage 2 or 3) within 12 hours of sample collection. To further enhance the sensitivity of utilizing TIMP-2, the investigators plan on also measuring urinary insulin-like growth factor-binding protein 7 (IGFBP7). Along with TIMP-2, IGFBP7 is also an inducer of G1 cell cycle arrest, a key mechanism implicated in AKI. This study will utilize the urinary [TIMP-2]*[IGFBP7] multiplicative product as a composite biomarker index to investigate the impact of intraoperative infusion of NS versus Isolyte on post-cardiac surgery renal function. This biomarker should identify patients at risk of imminent (within 12 hours) AKI KDIGO criteria. Patients presenting for cardiac surgery are already quite ill often with multiple comorbidities. Acute kidney injury in this population is associated with significant morbidity and mortality. The available literature indicates that a fairly simple intervention could plausibly reduce the incidence of AKI, but it has not yet been examined in humans. Generating an evidence basis for it will substantially improve the safety of patients who need cardiac surgery. This intervention to reduce AKI may also then be applied to the broader non-cardiac surgery population as well.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Normal Saline group
Arm Type
Active Comparator
Arm Description
0.9% Normal Saline (0.9% Sodium Chloride) injection intravenously as needed. The amount administered (dosage, frequency, and duration) will be left to the clinical judgment of the attending physicians, and will follow usual patterns of use in cardiac surgery patients.
Arm Title
Isolyte group
Arm Type
Experimental
Arm Description
Isolyte S (B Braun, Irvine CA) injection intravenously as needed. The amount administered (dosage, frequency, and duration) will be left to the clinical judgment of the attending physicians, and will follow usual patterns of use in cardiac surgery patients. Isolyte S is a prepackaged solution containing sodium chloride 0.53%, sodium gluconate 0.5%, sodium acetate trihydrate 0.37%, potassium chloride 0.037%, and magnesium chloride hexahydrate 0.03% w/v.
Intervention Type
Drug
Intervention Name(s)
0.9% Normal Saline (0.9% Sodium Chloride) injection
Intervention Type
Drug
Intervention Name(s)
Isolyte S injection
Primary Outcome Measure Information:
Title
Change in [TIMP2]*[IGFBP7] Biomarker
Description
The difference in the [TIMP2]*[IGFBP7] biomarker between the preoperative value and a repeated measurement at 24 hours postoperatively. Positive values represent increase; negative values represent decrease
Time Frame
Baseline and postoperatively at 24 hours
Secondary Outcome Measure Information:
Title
Serum Creatinine Level at 24 Hours
Description
Serum creatinine measurement at 24 hours
Time Frame
1 day
Title
Serum Chloride Level at 24 Hours
Description
Serum chloride ion measurement at 24 hours postoperatively
Time Frame
1 day
Title
Proportion of Patients With Need for Dialysis
Description
Clinically-determined need for dialysis prior to discharge from hospital
Time Frame
One week
Title
Postoperative Arterial pH
Description
Arterial pH, measured 24 hours after surgery
Time Frame
One day
Title
Serum Creatinine Level at 48 Hours
Description
Serum creatinine level 48 hours postoperatively
Time Frame
2 days
Title
Serum Chloride at 48 Hours
Description
Serum chloride measurement at 48 hours postoperatively
Time Frame
2 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Planned on- or off-pump cardiac surgery including: bypass grafting, valvular procedures, congenital defect correction, and thoracic aortic procedures or a combination of these procedures Exclusion Criteria: Emergency surgery Pregnancy Previous renal transplantation Documented moderate to severe acute kidney injury prior to enrollment (e.g. RIFLE-I or RIFLE-F/KDIGO stage 2 or 3) Patients already receiving dialysis (acute or chronic) or in imminent need of dialysis at time of enrollment Chronic kidney disease without baseline serum creatinine value obtained within 6 months of enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Neal S Gerstein, MD
Organizational Affiliation
University of New Mexico
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of New Mexico Hospital
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87106
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Upon publication of study results, qualified researchers may contact the PI for the deidentified dataset.

Learn more about this trial

Fluid Chloride and AKI in Cardiopulmonary Bypass

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