Purpose

Ventilator associated events (VAE) is a quality metric defined by 48 hours of stability followed by 48 hours of escalation of ventilator settings within the ICU. VAE have been associated with poor outcomes and increases the cost of care, yet is not easy to avoid. Operationalizing all the standards of care known to improve outcomes of those requiring mechanical ventilation in the critical care environment requires a comprehensive approach. ICU teams are encouraged to follow best practice protocols to help liberate and prevent VAEs. Yet, compliance with protocols in most ICUs is suboptimal for multiple reasons. With the advent of computerized mechanical ventilators capable of streaming data from breath to breath and biomedical integration systems (BMDI) such as Capsule (UTMB's BMDI system), software systems have been developed to help identify variances in the standard of care. Automation in near real-time ventilator data feedback has been shown to reduce the incidences of VAEs. This quality improvement project will leverage Vyaire's Respiratory Knowledge Portal (RKP) to collect and store meaningful data regarding ventilator-associated events (VAE), alarm policy compliance, ventilator weaning, and lung protective analytics. Goals: 1. To collect quality metrics utilizing RKP from patients requiring mechanical ventilation over a 3-4-month period for a retrospective baseline analysis. 2. Provide the RKP tool to the ICU team to determine if the use of RKP's webportal and Messenger Zebra phone app improves quality of mechanical ventilation and outcomes. 3. To determine a return on investment (ROI) for a software system like RKP.

Conditions

Eligibility

Eligible Ages
Under 100 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Subjects requiring invasive mechanical ventilation. 2. Subjects is in one of the monitored Galveston campus ICUs. 3. Ages 0-100

Exclusion Criteria

  1. Is in an ICU not monitored by RKP. 2. Adults on high frequency ventilation (pediatric patients are NOT excluded). 3. Any patient requiring ECMO.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Sequential Assignment
Primary Purpose
Health Services Research
Masking
None (Open Label)
Masking Description
Monitoring 3-4 months prior to intervention or use of the software.

Arm Groups

ArmDescriptionAssigned Intervention
No Intervention
Control
We will monitor without clinician use of the software.
Active Comparator
Use of RKP
Use of RKP alerts to the standard of care.
  • Other: RKP Monitoring Software
    Use of RKP alerting and monitoring software.

Recruiting Locations

University of Texas Medical Branch
Galveston, Texas 77555
Contact:
Brian K Walsh, PhD, RRT
409-772-9283
bkwalsh@utmb.edu

More Details

Status
Recruiting
Sponsor
The University of Texas Medical Branch, Galveston

Study Contact

Brian K Walsh, PhD, RRT
409-772-9283
bkwalsh@utmb.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.