Respiratory Failure Clinical Trial
Official title:
Examination of the Impact of Better Surveillance and Communication of Patient Deterioration on Patient Related Outcomes (VitalCare - Guardian Version 2)
A hospitals manual method of patient monitoring will be implemented in an automated system and supported by an early patient deterioration detection for timely escalation. The purpose of this study is to assess if clinical outcomes of patients in Acute Care are significantly improved by such a system.
The purpose of this study is to assess if the Philips IntelliVue Guardian Solution (IGS)
with all its components can significantly improve clinical outcomes for deteriorating
patients on a general medical ward prior and after referral to the hospitals' Acute Care
Team (ACT). Further, to provide evidence that the Philips IGS assists to increase the
efficiency of a hospital's Early Warning Scoring process (afferent and efferent arm of the
escalation system).
The introduction of such an intelligent automated system offers a unique opportunity to
address the breakdown in the chain of prevention by strengthening the reliability of
calls-for-help to responders through a technical solution with the potential for a more
timely escalation where appropriate.
In this study the hospital's Standard of Care protocol for the monitoring of vital signs
(including timing, vital signs collected and escalation instructions) will be implemented in
a commercially available intelligent automatic monitoring and notification system. No
investigational procedures or devices are associated with this protocol.
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Observational Model: Cohort, Time Perspective: Prospective
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