Respiratory Knowledge Portal Application to Reduce Ventilator Associated Events, Ventilator Induced Lung Injury and Alarm Parameter Variance
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 875
- 试验地点
- 3
- 主要终点
- Number of participants with Ventilator-Associated Events
研究概览
简要总结
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:
- To collect quality metrics utilizing RKP from patients requiring mechanical ventilation over a 3-4-month period for a retrospective baseline analysis.
- 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.
- To determine a return on investment (ROI) for a software system like RKP.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Sequential
- 主要目的
- Health Services Research
- 盲法
- None
盲法说明
Monitoring 3-4 months prior to intervention or use of the software.
入排标准
- 年龄范围
- — 至 100 Years(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects requiring invasive mechanical ventilation.
- •Subjects is in one of the monitored Galveston campus ICUs.
排除标准
- •Is in an ICU not monitored by RKP.
- •Adults on high frequency ventilation (pediatric patients are NOT excluded).
- •Any patient requiring ECMO.
研究组 & 干预措施
Control
We will monitor without clinician use of the software.
Use of RKP
Use of RKP alerts to the standard of care.
干预措施: RKP Monitoring Software (Other)
结局指标
主要结局
Number of participants with Ventilator-Associated Events
时间窗: 3-4 months
次要结局
- Number of Ventilator Alarm Set Outside of Compliance(3-4 months)
- Duration of Days on mechanical ventilation(3-4 months)
