Acute Kidney Injury
Conditions
Keywords
Nephrotoxicity, Urinary biomarkers, Clusterin, monocyte chemoattractant protein-1 (MCP1), Beta-2 microglobulin (ß2MG), Anti-microbials, Calcineurin inhibitors
Brief summary
The study aims to perform real-time validation of the RenaFAST kit (a point-of-care test kit that quantifies three urinary proteins) in predicting acute kidney injury(AKI) among patients prescribed drug therapies of nephrotoxic potential. Based on the type and duration of drug therapy, a maximum of 5 time-point urine samples will be collected from consenting patients and a real-time biomarker analysis will be conducted using the RenaFAST kits.
Detailed description
All eligible patients who fulfill the inclusion and exclusion criteria will be approached for consent. The patients with the highest AKI risk (with all 3 urine biomarkers, Clusterin, monocyte chemoattractant protein-1 (MCP1), and Beta-2 microglobulin (ß2MG), above prediction threshold set by the study) will be identified. The nephrology consultants within the research team will perform a medical chart and physical review(where required) of these patients, noting potential actions to be taken in data collection forms. This will help in evaluating if indeed there are perceived interventions that could potentially be delivered in response to early prediction of AKI.
Interventions
DIAGNOSTIC_TESTAKI risk screening using RenaFAST POCT test kits
Based on the type and duration of drug therapy, a maximum of 5 time-point urine samples will be collected and real-time biomarker measurement will be done using the RenaFAST POCT kits. Additionally, Trefoil factor 3 (TFF3) biomarker levels will also be quantified using developed POCT kits. Patients with all 3 biomarker (Clusterin, MCP1 and ß2MG) levels higher than the study cut-off will be identified as high-risk for AKI. The nephrology consultants within the research team will perform a medical chart and physical review (where required) of these patients, detailing potential actions to be taken in research data collection forms. No actual intervention (other than a patient review) will be performed.
Sponsors
Agency for Science, Technology and Research
National University Hospital, Singapore
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE
Intervention model description
Single arm design. All eligible and consenting patients will have their time-point urine samples collected and biomarker levels measured.
Eligibility
Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* Patients who receive a projected ≥7 days of therapy of antimicrobials including aminoglycosides (i.e., gentamicin or amikacin), vancomycin, polymyxin, amphotericin and foscarnet. * Patients who receive a projected ≥7 days of Calcineurin inhibitors (cyclosporin, tacrolimus) * Patients who receive a projected ≥7 days of anti-virals (Cidofovir and Ganciclovir) * Patients who receive Anti-cancer drugs (Chemotherapy such as cisplatin, Ifosfamide, Methotrexate, Pemetrexed) or * Patients who receive Anti-cancer drugs (Immunotherapy such as immune checkpoint inhibitors as well as types of VGEF inhibitors that are associated with acute kidney injury)
Exclusion criteria
* Patients with AKI prior to therapy initiation. * Patients with baseline eGFR \< 15 mL/min/1.73m2 (stage 5 chronic kidney disease) * Patients admitted to intensive care unit at study baseline, as critical illness is a natural confounder to AKI * Females who are pregnant * Immediate post-kidney transplant recipients (initial 3 months following transplant).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Presence of an Acute kidney injury (AKI) event | Start date of drug therapy till one week post end date of drug therapy | AKI will be defined by the minimum stage 1 criterion in accordance to KDIGO AKI criteria: 1. Relative increase in serum creatinine of 1.5 times or higher, versus the baseline. 2. Absolute increase in serum creatinine of \> 26.5 μmol/L within 48 hours. Additionally, for those administered cisplatin, cases of severe hyponatremia needing hospitalization for severe dehydration and intravenous fluid-rescue will also be taken as an outcome measure of clinically-evident kidney injury and renal salt wasting. If the subject meets any one of the above 3 criteria, the patient will be recorded as having suffered an AKI event. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Severity of AKI event | From the date of AKI onset to date of peak AKI | Peak AKI severity will be determined by highest recorded serum creatinine levels of patient. |
| Number of AKI days till recovery | From the date of AKI onset to date of resolution of AKI | Number of days from the onset of AKI (as per aforementioned AKI criteria) to resolution of AKI (Defined as when serum creatinine levels reach baseline levels or no longer meet the AKI criterion, whichever is earlier) |
| Length of stay in hospital | From the date of admission to the date of discharge of patient from hospital, assessed up to 12months from date of consent | Duration of hospital stay will be determined based on admission and discharge dates of the patient, for the period relevant to study participation. |
| Number of patients requiring dialysis treatment for the AKI event | From the date of AKI onset to date of resolution of AKI | Whether patient required dialysis/CRRT for treatment of AKI event |
Countries
Singapore
Contacts
Primary ContactHorng-Ruey Dr Chua
Outcome results
None listed