Circadia Health has received expedited Food and Drug Administration (FDA) clearance for Contactless Respiration Rate (CResp) monitoring systems amid the Covid-19 outbreak.
The platform saves patient lives by forecasting and eliminating respiratory complications through early warning scores and allowing timely clinician interventions.
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The C100 system uses proprietary radar Signal Analysis Technology (rSAT) and cloud-based software for the early detection of patient deterioration to accelerate clinical decision-making.
CRespis is accurate, reliable, easy-to-use and scalable for both continuous and spot-check monitoring of early patient deterioration signs such as respiratory rate.
It provides long-term respiration data to allow effective triage and ongoing care management.
In addition to CResp, the Circadia rSAT and artificial intelligence (AI)-powered algorithms provide monitoring of motion, presence and sleep quality, as well as ambient sound and light monitoring for detecting disturbances and coughing.
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By GlobalDataFurthermore, C100 is said to improve patient outcomes, as well as reduce readmissions and the risk of infection transmission from patient-to-patient and patient-to-clinician.
Circadia Health co-founder and CEO Fares Siddiqui said: “Our goal is to provide a frictionless solution to clinicians in order to help improve patient outcomes and reduce the cost of care.
“During this Covid-19 crisis, the FDA has recognised the life-saving potential of our technology. We are now able to deliver the most convenient and powerful method to monitor fragile patients both in-facility and remotely at home.”
The company noted that it will soon roll out the C100 system to help hospitals and skilled nursing facilities contain respiratory-related illnesses such as Covid-19, pneumonia, chronic obstructive pulmonary disease (COPD) exacerbations and other forms of respiratory failures.
