Retrospective Review of Mechanically Ventilated Patients Using a Continuous Data Collection System.

Completed

• Conditions: Mechanical Ventilation; Acute Respiratory Distress Syndrome; Hypoxic Respiratory Failure

• Registration Number: NCT02184208
• Lead Sponsor: Boston Children's Hospital

Brief Summary

Today, the electronic medical record, microprocessor mechanical ventilators, and physiologic monitoring are under-utilized when translating research into decision support. Current medical informatic capabilities can be leveraged to calculate trends in measured parameters to initiate a paradigm shift in critical care from reaction-based treatment to proactive and plausibly preventative care. Therefore, the purpose of this study is to develop baseline understanding of our practice and how data collection utilizing a newly implemented system called T3. We would like to retrospectively review mechanically ventilated patients in which we have collected continuous data to test a newly developed analytic platform. Additionally we would like to compare these results to our standards of practice established by clinical practice guidelines.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-01-17
• Study First Submitted: 2014-07-02
• Study First Submitted QC: 2014-07-03
• Study First Posted: 2014-07-09
• Primary Completion: 2016-12-30
• Study Completion: 2017-01-09
• Results First Submitted: 2017-01-30
• Status Verified: 2017-07
• Results First Submitted QC: 2017-07-18
• Last Update Submitted: 2017-07-18
• Results First Posted: 2018-02-05
• Last Update Posted: 2018-02-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 278

Inclusion Criteria

• Patient selection will be determined by available data collected in the T3 system. We estimate 50 patients in which mechanical ventilator data has been collected utilizing the limited intellibridge modules (4 systems currently available to collect ventilator data).

Exclusion Criteria

• Patient not connected to T3 data collection system.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Successful Extubation	Within 24 hours of extubation	Successful extubation without the use of noninvasive ventilation or requiring reintubation

Trial Locations

Locations (1)

Boston Children's Hospital; 🇺🇸 Boston, Massachusetts, United States