An Electronic Alert System for In-Hospital Acute Kidney Injury
- Conditions
- Acute Kidney Injury
- Interventions
- Other: Alert
- Registration Number
- NCT01862419
- Lead Sponsor
- University of Pennsylvania
- Brief Summary
This study will randomize hospitalized patients with acute kidney injury (AKI) to usual care, or an electronic alert intervention. The electronic alert will be in the form of a text page that will be sent to the covering clinician and unit pharmacist once per patient with AKI at the time lab results are uploaded. The investigators hypothesize that such an alert will improve outcomes in these patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 2393
- Adults >=18 years
- Admitted to the Hospital of the University of Pennsylvania for greater than 24 hours.
- Dialysis order within 24 hours of admission
- Dialysis order prior to AKI onset
- Initial creatinine >=4.0mg/dl
- Prior admission in which patient was randomized.
- Nephrectomy during the admission
- Admission to hospice service
- Admission to observation status
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Alert Alert Text page sent to patient's covering provider and unit pharmacist informing them of the presence of AKI as detected by changes in serum creatinine.
- Primary Outcome Measures
Name Time Method Dialysis Within 7 Days From start of AKI to 7 days later This metric will be sequentially ranked. The provision of acute dialysis therapy will be ranked as a more severe outcome than the worst relative change in creatinine and death will be ranked as a more severe outcome than dialysis.
Death 7 days of randomization Relative Maximum Change in Creatinine 7 days of randomization
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hospital of the University of Pennsylvania
🇺🇸Phiadelphia, Pennsylvania, United States