DEMONSTRATION PROJECT TO REFINE, AUTOMATE AND TEST A NOVEL EMERGENCY DEPARTMENT TRIGGER TOOL
Project Number5R18HS025052-03
Contact PI/Project LeaderGRIFFEY, RICHARD T
Awardee OrganizationWASHINGTON UNIVERSITY
Description
Abstract Text
Abstract
The overarching aim of this 3-year project is to develop a trigger tool (EDTT) specifically tailored for detecting
and characterizing adverse events in the emergency department (ED). Trigger tools such as those pioneered
by the Institute for Healthcare Improvement (IHI) have outperformed traditional methods for detecting and
characterizing patient harm in other clinical settings, to the point that they have been featured by the Agency
for Healthcare Research and Quality as “the premier measurement strategy for patient safety.” The need for an
EDTT adapted for use in ED is especially salient given: (i) that current ED surveillance methods are outdated
and often inefficient; (ii) that EDs now account for 1/3 of all acute care visits, nearly 50% of hospital admissions
in the US and are a major source of care for minority and vulnerable populations; and (iii), that numerous
factors such as increasing acuity, limited data for decision making, time pressures and hospital crowding and
boarding create an environment with a high potential for adverse events (AEs). In developing the EDTT, we will
build on the results of a prior multicenter preliminary study in which we identified candidate triggers. In
selecting these triggers, we balanced expected content with ease of application to electronic health records.
We will first test and optimize the EDTT (refining trigger selection, eliminating poorly performing ones) on 2,400
randomly selected ED visit records, using dual independent review. This “gold standard” sample will be used,
following a slight delay to allow for data accrual, to develop a computerized version of the EDTT. Then we will
validate the optimized, automated EDTT on an independent random sample of up to 20,000 charts, in order to
identify 6,000 records with triggers. We will review all of these records for the presence of AEs. Analyses will
focus on yield (roughly, ability to detect AEs), reliability, and associations with patient characteristics. This will
provide a new standard for detection of harm in the ED setting, establish a baseline against which to measure
improvement efforts and help direct resources for improving patient safety and quality. Our consultants come
from several institutions nationwide, so that our work will always maintain a view toward multisite
implementation and testing.
Public Health Relevance Statement
Project Narrative
This project proposes a novel method for detecting and characterizing adverse events in the emergency
department to allow an assessment of the effectiveness of quality improvement efforts. Current processes
prove inadequate. The need for improved methodology is critical, given the evolving role of the emergency
department in the health care system.
No Sub Projects information available for 5R18HS025052-03
Publications
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Outcomes
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Clinical Studies
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History
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