Continuous vs. Intermittent Infusion Vancomycin
Study Details
Study Description
Brief Summary
Hospitalized adult participants prescribed vancomycin by their treating physician will be randomized to receive vancomycin via continuous or intermittent infusion and measures of kidney function and injury will be collected.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
All study participants regardless of participation status will have been prescribed vancomycin by a treating physician and received a dose per institutional standard of care. Participants will be randomized 1:1 in permuted blocks of 2, 4, or 6 to receive subsequent doses via continuous or intermittent infusion. Participants randomized to intermittent infusion will receive doses per standard of care at infusion rates of 1 gram per hour in every 8,-12, or -24 hour intervals, while participants randomized to continuous infusion will receive a total daily dose infused over a period of 24 hours.
Vancomycin concentration will not exceed 5mg/ml and will be infused via central (preferred) or peripheral administration. In order to ensure consistent dosing between study arms, a precision dosing platform will be used by the PI and team to determine total daily doses to best target an AUC of 500 mg x hr/L (range 400-600 mg x hr/L). A single vancomycin concentration will be obtained the following day with Bayesian-guided area-under-the-curve (AUC) monitoring (with dosing adjusted if needed) to ensure vancomycin exposure remains similar between infusion strategies. Both the initiation and discontinuation of vancomycin, as well as any additional therapeutic drug monitoring, will remain at the discretion of the primary clinical team.
Glomerular filtration rate (GFR) will be measured on the day of enrollment and day 3 by the administration of 5 ml iohexol (300 mgI/ml) with iohexol plasma concentrations obtained 1 and 4 hours following administration of iohexol. This change in measured GFR between the infusion strategies is the primary outcome of the study. Plasma and urinary markers of kidney function and injury will be obtained the day of enrollment (Day 0) and subsequent days (Days 2-3). If the participant remains on vancomycin 120 hours following enrollment, measured glomerular filtration rate (mGFR) and biomarkers will be assessed again.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Vancomycin continuous infusion Continuous infusion of Vancomycin |
Drug: Vancomycin Continuous Infusion
A precision drug dosing platform will be used to determine the empiric dosing regimen and the dosing parameter targeted will be an area-under-the-curve (AUC) of 500 mg⸱hr/L (range 400-600 mg⸱hr/L). The total daily dose is infused over a period of 24 hours.
Other Names:
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| Active Comparator: Vancomycin intermittent infusion Intermittent infusion of vancomycin |
Drug: Vancomycin Intermittent Infusion
A precision drug dosing platform will be used to determine the empiric dosing regimen and the dosing parameter targeted will be an area-under-the-curve (AUC) of 500 mg⸱hr/L (range 400-600 mg⸱hr/L). The dose is infused at rates of 1 gram per hour in every 8, -12, or -24 hour intervals.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Change in measured glomerular filtration rate (GFR) [Baseline (Day 0) and Day 3]
measured via the administration of a small dose of iohexol followed by the collection of blood samples
- Change in urinary Kidney Injury Molecule 1 (KIM-1) [Baseline (Day 0) and Day 3]
Measured by urine ELISA test as the change score
Secondary Outcome Measures
- Plasma cystatin C over time [Baseline up to 5 days]
Measured by urine ELISA test at baseline, 48-, and 72-hours following the first dose of vancomycin. Additional measure at 120 hours if the patient is prescribed vancomycin for 120 hours or more.
- Urine Clusterin over time [Baseline up to 5 days]
Measured by urine ELISA test at baseline, 48-, and 72-hours following the first dose of vancomycin. Additional measure at 120 hours if the patient is prescribed vancomycin for 120 hours or more.
- Urine Osteopotin over time [Baseline up to 5 days]
Measured by urine ELISA test at baseline, 48-, and 72-hours following the first dose of vancomycin. Additional measure at 120 hours if the patient is prescribed vancomycin for 120 hours or more.
- Urine Kidney Injury Molecule-1 (KIM-1) over time [Baseline up to 5 days]
Measured by urine ELISA test test at baseline, 48-, and 72-hours following the first dose of vancomycin. Additional measure at 120 hours if the patient is prescribed vancomycin for 120 hours or more.
- Change in Urine Kidney Injury Molecule-1 (KIM-1) [Baseline (Day 0) and Day 5]
Measured as the change score, only in the only in subset of patients prescribed 5 or more days of vancomycin
- Vancomycin Area-Under-the-Curve (AUC) target attainment [Day 1]
Defined as range 400-600 mgxhr/L. AUC assessed using one concentration Bayesian estimates.
- Acute Kidney Injury over time [Daily up to 10 days]
Using serum creatinine and urine output components of Kidney Disease: Improving Global Outcome (KIDGO) classification
- Phlebitis over time [Daily up to 7 days]
Monitored per standard of care, using phlebitis scores of 0 (no clinical symptoms) to 4. Documented scores above 0 will be classified as phlebitis.
- Infiltration over time [Daily up to 7 days]
Monitored per standard of care, using infiltration scores of 0 (no clinical symptoms) to 4. Documented scores above 0 will be classified as infiltration.
- Acute Kidney Disease [Until hospital discharge, up to 17 days]
measured per Acute Disease Quality Initiative (ADQI) criteria in a subset of participants where AKI does not resolve by 7 days
- Major Adverse Kidney Events [Until hospital discharge, up to 17 days]
Composite of death, requirement for kidney replacement therapy, or reduction of 25% from baseline estimated glomerular filtration rate.
- Change in measured glomerular filtration rate (GFR) [Baseline (Day 0) and Day 5]
measured via the administration of a small dose of iohexol followed by the collection of blood samples, only in the subset of patients receiving vancomycin for 5 days
Eligibility Criteria
Criteria
Inclusion Criteria:
-
≥ 18 years of age
-
Hospitalized at University of Kentucky on a medical service (internal medicine or medical intensive care)
-
Prescribed ≥ 2 doses of vancomycin per treating physician
-
Be able to provide written, informed consent, or have a legally authorized representative (LAR) responsible for their care able to provide written, informed consent.
Exclusion Criteria:
-
Chronic kidney disease (documented or prior to admission eGFR <60 ml/min/1.73m2 using non-race-based creatinine GFR equation)
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End stage kidney disease
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Stage 1 or higher AKI per Kidney Disease: Improving Global Outcomes (KDIGO) classification (serum creatinine increase ≥ 0.3 mg/dl or 1.5-1.9 times baseline; urine output < 0.5 ml/kg/hr for 6-12 hours)
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Receipt of vancomycin within the last 72 hours (not considering the loading dose)
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Allergy to iohexol
-
Uroepithelial tumors
-
Pregnancy
-
Prisoner
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Kentucky | Lexington | Kentucky | United States | 40506 |
Sponsors and Collaborators
- Alexander Flannery
- National Institute of Allergy and Infectious Diseases (NIAID)
Investigators
- Principal Investigator: Alexander H Flannery, PharmD, PhD, University of Kentucky
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 83412
- R21AI176298