Impact of a Data-driven Monitor Alarm Reduction Strategy Implemented in Safety Huddles
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Hospitalization
- Sponsor
- Children's Hospital of Philadelphia
- Enrollment
- 77280
- Locations
- 1
- Primary Endpoint
- Change from baseline in the unit-wide rate of alarms per patient-day at 44 weeks
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
This is a pragmatic, paired, cluster-randomized controlled trial evaluating the impact of a safety huddle-based intervention on physiologic monitor alarm rates on pediatric inpatient units.
Detailed Description
Hospital physiologic monitors can alert clinicians to early signs of physiologic deterioration, and thus have great potential to be life-saving. However, monitors generate frequent alarms, most of which are non-actionable. When clinicians become overburdened with alarms, they begin to exhibit alarm fatigue: responding more slowly to alarms or ignoring alarms entirely. In this protocol the investigators outline the methods they will use to evaluate the impact of a safety huddle-based intervention on physiologic monitor alarm rates using a pragmatic, paired, cluster-randomized controlled trial with the intervention delivered at the unit level. This work is considered quality improvement research, and some of the approaches described in this protocol are from the field of quality improvement. Currently, at most hospitals data like this on the numbers of alarms that patients generate are only available to researchers with the software tools needed to interrogate and record data from the monitor network. The goal of this proposal is to bring this data to the safety huddles occurring daily on inpatient units in an accessible format to help teams make informed decisions about monitoring and minimize the potential of harm from alarm fatigue.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Change from baseline in the unit-wide rate of alarms per patient-day at 44 weeks
Time Frame: Baseline and 44 weeks
Secondary Outcomes
- Pre-post huddle patient-level difference in differences of alarm rates(The 24 hours before a safety huddle opportunity versus the 24 hours before a safety huddle opportunity)
- Implementation outcomes(Within 4 hours after the huddle intervention occurred)