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A Retrospective Study to Evaluate the Predictability of Abnormal Arterial Blood Gas Measurements Through Novel Observations of Continuous Trends in Electronically Measured Respiratory Rate in a Mixed Cohort of Respiratory Compromised Patients

Conditions
Respiratory Failure
Pneumonia
COVID-19
Pulmonary Disease
Community-acquired Pneumonia
COPD
Interventions
Device: RespiraSense
Registration Number
NCT05384314
Lead Sponsor
Beaumont Hospital
Brief Summary

A retrospective study to evaluate the predictability of abnormal arterial blood gas measurements through novel observations of continuous trends in electronically measured respiratory in a mixed cohort of respiratory compromised patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
322
Inclusion Criteria
  • Respiratory condition is the primary admission diagnosis
Exclusion Criteria
  • Pregnant patients in their 2nd or 3rd trimester

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Respiratory Compromised GeneralRespiraSensePatients admitted with Pneumonia, COPD, COVID, to be included
COPDRespiraSensePatients admitted with COPD as the primary admission.
Primary Outcome Measures
NameTimeMethod
Positive Predictive Value/Precision (PPV)12 months

Positive Predictive Value/Precision (PPV) of an elevated RespiraSense monitoring Respiratory Rate (RR) for an abnormal ABG - for a single disease state (COPD)

Secondary Outcome Measures
NameTimeMethod
PPV of an elevated RR for an abnormal ABG - for a mix of disease states12 months

PPV of an elevated RR for an abnormal ABG - for a mix of disease states, all of which fall under Respiratory Failure

Trial Locations

Locations (1)

Beaumont Hospital

🇮🇪

Dublin, Ireland

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