Skip to main content
Clinical Trials/NCT06065761
NCT06065761
Not yet recruiting
Not Applicable

Improving Risk Stratification of Emergency Department Patients With Acute Heart Failure: Building and Testing a Machine-learning Platform for Personalized, Accurate, Real-time Risk Prediction

Kaiser Permanente21 sites in 1 country17,459 target enrollmentOctober 1, 2024
ConditionsHeart Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Kaiser Permanente
Enrollment
17459
Locations
21
Primary Endpoint
Number of patients with serious adverse events
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The primary goal is to build and test a previously developed and validated risk model and clinical decision support tool embedded within the electronic health record to improve risk stratification of emergency department (ED) patients with acute heart failure (AHF).

Detailed Description

The study team will build an electronic health record-embedded clinical decision support tool using a recently developed risk prediction model that curates patient-specific data in real-time, accurately estimates short-term patient risk, and presents tailored clinical recommendations. This will be a regional implementation study in which the tool is turned on at 21 emergency departments (ED) across Kaiser Permanente Northern California (KPNC). The study team will validate risk predictions and study key clinical outcomes as part of this trial.

Registry
clinicaltrials.gov
Start Date
October 1, 2024
End Date
December 31, 2025
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult (≥18y) KPNC members treated in the ED for presumed acute heart failure

Exclusion Criteria

  • Children (\<18y).
  • Patients who left against medical advice or eloped prior to ED physician evaluation.

Outcomes

Primary Outcomes

Number of patients with serious adverse events

Time Frame: 30 days from index ED visit

Serious adverse events include mortality, cardiopulmonary resuscitation (CPR), intubation/ventilation, new end-stage renal disease (ESRD), balloon pump placement, or percutaneous coronary intervention (PCI)/coronary artery bypass grafting (CABG)

Number of patients with all-cause mortality

Time Frame: 30 days from index ED visit

Study Sites (21)

Loading locations...

Similar Trials