RecruitingNCT07410624

Augmented Renal Clearance in Neurocritical Care

Augmented Renal Clearance in Neurocritical Care Population: A Prospective Multicenter Study


Sponsor

University of Alberta

Enrollment

512 participants

Start Date

Oct 1, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

Stroke, severe brain injury, uncontrolled seizures and brain infections are the most common life-threatening neurological illnesses in the world with an estimated combined annual hospital management cost of up to 44 billion dollars. Seizures and infections are common complications following acute neurological illnesses and contribute significantly to poor outcomes if not promptly treated with appropriately dosed anti-seizure medications and antibiotics, respectively. Limited research suggested that many of those patients present with a phenomenon called augmented renal clearance (ARC) or, in other words, enhanced kidney function. ARC may have a significant influence on how medications are removed from the body potentially resulting in insufficient doses and treatment failure. Therefore, patients with ARC require higher medication doses; however, ARC is largely undetected using kidney assessment methods currently used in practice. In addition, it is not clear how medications should be dosed in those with ARC. The majority of ARC research has not focused on patients with life-threatening neurological illnesses. Thus, clinicians are likely under-dosing vital medications in those patients, and completely unaware. There is an immediate need to address the gap in knowledge. Therefore, this research aims to characterize the phenomenon of ARC in patients with life-threatening neurological illnesses through identifying the frequency, duration, contributing factors and clinical impact of ARC. Adult patients admitted to the neurosciences intensive care unit for life-threatening neurological illnesses will be enrolled in the study. Urine and blood samples wil be collected from participants to determine the presence of ARC and identify its contributing factors. In addition, blood samples will be collected from participants treated with select antibiotics and anti-seizure medications to determine their concentration and propose dose adjustment in those with ARC. This research is expected to improve the care of patients with life-threatening neurological illnesses through efficient identification and monitoring of patients exhibiting ARC facilitating timely medication dosage optimization. Furthermore, recommendations of optimal doses of commonly used medications in patients with ARC would improve the likelihood of treatment success with potential to improve patients' health and wellbeing.


Eligibility

Min Age: 18 YearsMax Age: 85 Years

Inclusion Criteria5

  • Age 18-85 years
  • Admitted to ICU at one of the participating sites
  • Diagnosis: SAH, TBI, ICH, meningitis, SE or ischemic stroke
  • Provision of informed consent
  • Foley catheter in place at time of consent (to facilitate urine collection)

Exclusion Criteria2

  • Incarceration
  • Anticipated ICU length of stay is \< 72 hours (insufficient time for monitoring)

Locations(3)

UK HealthCare

Lexington, Kentucky, United States

The Ohio State University Wexner Medical Center

Columbus, Ohio, United States

University of Alberta Hospital

Edmonton, Alberta, Canada

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NCT07410624


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