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An Electronic Alert System for In-Hospital Acute Kidney Injury

Not Applicable
Completed
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
Inclusion Criteria
  • Adults >=18 years
  • Admitted to the Hospital of the University of Pennsylvania for greater than 24 hours.
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Exclusion Criteria
  • 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
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
AlertAlertText 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
NameTimeMethod
Dialysis Within 7 DaysFrom 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.

Death7 days of randomization
Relative Maximum Change in Creatinine7 days of randomization
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hospital of the University of Pennsylvania

🇺🇸

Phiadelphia, Pennsylvania, United States

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