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Fluid Chloride and AKI in Cardiopulmonary Bypass

The Impact of Low Chloride Containing Fluids on Acute Kidney Injury After Cardiopulmonary Bypass as Assayed by Urinary [TIMP2*IGFBP7]

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02668952
Enrollment
30
Registered
2016-01-29
Start date
2016-01-31
Completion date
2018-02-28
Last updated
2018-05-14

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

Conditions

Acute Kidney Injury

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.

Interventions

Sponsors

University of New Mexico
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Change in [TIMP2]*[IGFBP7] BiomarkerBaseline and postoperatively at 24 hoursThe 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

MeasureTime frameDescription
Serum Chloride Level at 24 Hours1 daySerum chloride ion measurement at 24 hours postoperatively
Proportion of Patients With Need for DialysisOne weekClinically-determined need for dialysis prior to discharge from hospital
Serum Creatinine Level at 24 Hours1 daySerum creatinine measurement at 24 hours
Serum Creatinine Level at 48 Hours2 daysSerum creatinine level 48 hours postoperatively
Serum Chloride at 48 Hours2 daysSerum chloride measurement at 48 hours postoperatively
Postoperative Arterial pHOne dayArterial pH, measured 24 hours after surgery

Countries

United States

Participant flow

Participants by arm

ArmCount
Normal Saline Group
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. 0.9% Normal Saline (0.9% Sodium Chloride) injection
16
Isolyte Group
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. Isolyte S injection
14
Total30

Baseline characteristics

CharacteristicIsolyte GroupTotalNormal Saline Group
Age, Continuous62.8 years
STANDARD_DEVIATION 9.4
64.1 years
STANDARD_DEVIATION 10.2
65.3 years
STANDARD_DEVIATION 11
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United States
14 Participants30 Participants16 Participants
Serum chloride106 mmol/L
STANDARD_DEVIATION 3.4
107 mmol/L
STANDARD_DEVIATION 3.2
108 mmol/L
STANDARD_DEVIATION 3.1
Serum creatinine0.88 mg/dL
STANDARD_DEVIATION 0.14
0.91 mg/dL
STANDARD_DEVIATION 0.16
0.93 mg/dL
STANDARD_DEVIATION 0.18
Sex: Female, Male
Female
8 Participants14 Participants6 Participants
Sex: Female, Male
Male
6 Participants16 Participants10 Participants
[TIMP2] x [IGFBP7]0.116 (ng/mL)^2/1000
STANDARD_DEVIATION 0.138
0.108 (ng/mL)^2/1000
STANDARD_DEVIATION 0.115
0.101 (ng/mL)^2/1000
STANDARD_DEVIATION 0.096

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 160 / 14
other
Total, other adverse events
0 / 160 / 14
serious
Total, serious adverse events
0 / 160 / 14

Outcome results

Primary

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

Time frame: Baseline and postoperatively at 24 hours

ArmMeasureValue (MEAN)Dispersion
Normal Saline GroupChange in [TIMP2]*[IGFBP7] Biomarker0.015 (ng/mL)^2/1000Standard Deviation 0.125
Isolyte GroupChange in [TIMP2]*[IGFBP7] Biomarker0.009 (ng/mL)^2/1000Standard Deviation 0.148
Secondary

Postoperative Arterial pH

Arterial pH, measured 24 hours after surgery

Time frame: One day

ArmMeasureValue (MEAN)Dispersion
Normal Saline GroupPostoperative Arterial pH7.38 pHStandard Deviation 0.03
Isolyte GroupPostoperative Arterial pH7.41 pHStandard Deviation 0.05
Secondary

Proportion of Patients With Need for Dialysis

Clinically-determined need for dialysis prior to discharge from hospital

Time frame: One week

ArmMeasureValue (NUMBER)
Normal Saline GroupProportion of Patients With Need for Dialysis0 percentage of patients
Isolyte GroupProportion of Patients With Need for Dialysis0 percentage of patients
Secondary

Serum Chloride at 48 Hours

Serum chloride measurement at 48 hours postoperatively

Time frame: 2 days

ArmMeasureValue (MEAN)Dispersion
Normal Saline GroupSerum Chloride at 48 Hours107 mmol/LStandard Deviation 4.6
Isolyte GroupSerum Chloride at 48 Hours104 mmol/LStandard Deviation 3
Secondary

Serum Chloride Level at 24 Hours

Serum chloride ion measurement at 24 hours postoperatively

Time frame: 1 day

ArmMeasureValue (MEAN)Dispersion
Normal Saline GroupSerum Chloride Level at 24 Hours110 mmol/LStandard Deviation 3
Isolyte GroupSerum Chloride Level at 24 Hours106 mmol/LStandard Deviation 3.1
Secondary

Serum Creatinine Level at 24 Hours

Serum creatinine measurement at 24 hours

Time frame: 1 day

ArmMeasureValue (MEAN)Dispersion
Normal Saline GroupSerum Creatinine Level at 24 Hours0.85 mg/dLStandard Deviation 0.24
Isolyte GroupSerum Creatinine Level at 24 Hours0.80 mg/dLStandard Deviation 0.16
Secondary

Serum Creatinine Level at 48 Hours

Serum creatinine level 48 hours postoperatively

Time frame: 2 days

ArmMeasureValue (MEAN)Dispersion
Normal Saline GroupSerum Creatinine Level at 48 Hours0.91 mg/dLStandard Deviation 0.31
Isolyte GroupSerum Creatinine Level at 48 Hours0.74 mg/dLStandard Deviation 0.14

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