AKI-CHERUB: Study of the Prediction of Acute Kidney Injury in Children Using Risk Stratification and Biomarkers

Sponsor
Children's Hospital Medical Center, Cincinnati (Other)
Overall Status
Completed
CT.gov ID
NCT01735162
Collaborator
(none)
184
1
24
7.7

Study Details

Study Description

Brief Summary

Acute kidney injury (AKI) is a common clinical event with severe consequences. In the pediatric intensive care unit (PICU), AKI occurs in almost 10% of all patients and evidence suggests that children are dying not just with AKI, but from AKI. Unfortunately, the treatment for AKI is limited to a great extent by delayed diagnosis. Reliance on markers of kidney injury that change only when significant damage has already occurred has rendered potential therapies ineffective. For this reason, identification of new markers of AKI that change early in the course of injury is paramount. While new AKI biomarkers have been identified, their performance in the general PICU population is variable. The investigators recently proposed the concept of 'renal angina' as a way to risk stratify patients in the ICU for AKI risk. In the AKI-CHERUB study, the investigators propose to study renal angina in PICU patients alone and in combination with urinary biomarkers for AKI prediction. The investigators hypothesize that renal angina will increase the predictive precision of urinary biomarkers for AKI.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Reliance on serum creatinine and urine output for diagnosis of acute kidney injury (AKI) has limited the ability of potential therapeutic measures to be effective. The investigators' recent proposition of the renal angina construct aims to improve and expedite AKI diagnosis through use of risk stratification. An apt parallel is the profound outcome change that has been effected in acute coronary syndrome through targeted troponin measurements in patients with both risk factors and clinical symptoms of coronary ischemia. Novel AKI biomarkers will struggle to gain widespread use until their performance in patients of varying degrees of AKI risk can be balanced with their cost and availability. The investigators hypothesize risk stratification using renal angina (ANG) identifies children at-risk vs. not at-risk for AKI, focusing subsequent biomarker measurement to "rule out" AKI only in children with ANG, increasing biomarker predictive precision. This study is significant because it represents the next step in the vertical integration of AKI biomarkers into routine clinical practice to guide their use rationally. The identification of at-risk patients to guide appropriate biomarker use is high-impact because it will make implementation of preventive and supportive therapies for AKI more effective; data from this study would serve to provide the indications to the Food and Drug Administration (FDA) for biomarker use in critically ill children. The study is innovative because it is the first prospective attempt to study the predictive performance of biomarkers AKI in the PICU population using ANG stratification. The investigators will observe all children admitted to the PICU with an expected length of stay

    48 hours. Urine will be collected from these children and levels of neutrophil gelatinase associated lipocalin (NGAL), interleukin-18 (IL-18), liver-fatty acid binding protein (l-FABP), and kidney injury molecule-1 (KIM-1) will be measured. Renal angina will be assessed at time of admission. Primary outcome will be presence of AKI (as measured by Kidney Diseases Improving Global Outcome (KDIGO) Class 2 or greater) at hospital day 3.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    184 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Prospective Study of Acute Kidney Injury in Critically Ill Children Predicted by Renal Angina and Urinary Biomarkers
    Study Start Date :
    Oct 1, 2012
    Actual Primary Completion Date :
    May 1, 2013
    Actual Study Completion Date :
    Oct 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Very high risk

    Very high risk PICU patients are on mechanical ventilation and at least one inotrope or vasopressor at time of admission

    High Risk

    High risk PICU patients have a history of transplantation (solid organ or bone marrow)

    Moderate risk

    Moderate risk PICU patients are all other admissions to the ICU (may have either mechanical ventilation or inotropy/vasopressor use but not both). Cannot have a history of transplant. Minimum expected stay 48 hours.

    Outcome Measures

    Primary Outcome Measures

    1. Acute kidney injury [At day 3 of PICU admission]

      Development of AKI by KDIGO Stage 2 criteria (Creatinine > 200% baseline)

    Secondary Outcome Measures

    1. PICU length of stay [60 days]

      Observational assessment of duration of length of stay in PICU from time of renal angina assessment

    Other Outcome Measures

    1. Mortality [60 day]

      Incidence of death within 60 days of ICU admission

    2. Renal replacement therapy [During ICU stay]

      We will use a dichotomization (yes/no) of whether renal replacement therapy was used in each patient until ICU discharge or death, whichever came first, followed up to 60 days

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Minimum stay 48 hours

    • Indwelling urinary catheter

    Exclusion Criteria:
    • History of renal disease

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cincinnati Children's Hospital Medical Center Cincinnati Ohio United States 45229

    Sponsors and Collaborators

    • Children's Hospital Medical Center, Cincinnati

    Investigators

    • Principal Investigator: Stuart Goldstein, MD, Children's Hospital Medical Center, Cincinnati

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Rajit Basu, MD, F.A.A.P., Director, Center for Acute Care Nephrology, Children's Hospital Medical Center, Cincinnati
    ClinicalTrials.gov Identifier:
    NCT01735162
    Other Study ID Numbers:
    • CIN001-AKI-CHERUB
    First Posted:
    Nov 28, 2012
    Last Update Posted:
    Feb 3, 2015
    Last Verified:
    Feb 1, 2015
    Keywords provided by Rajit Basu, MD, F.A.A.P., Director, Center for Acute Care Nephrology, Children's Hospital Medical Center, Cincinnati
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 3, 2015