Etiometry, the leader in clinical decision-support software, announced today its IVCO2 Index was cleared by the Food and Drug Administration for use with neonatal ICU patients under 2kg, who are especially vulnerable to the effects of hypercapnia. This is Etiometry’s 9th FDA clearance and its second this year.
Etiometry’s IVCO2 Index integrates multiple data sources to provide an individualized assessment for ventilation-perfusion mismatch and detect the likelihood a patient will have a PaCO2 of greater than 50 mmHg in mechanically ventilated patients. It has been specifically designed to overcome the challenges of existing conventional monitoring, such as arterial blood gas testing and transcutaneous monitoring for tiny premature newborns.
Many NICU patients require ventilatory support and their conditions can change quickly. Vigilant monitoring for hypercapnia is critical for maximizing neurodevelopmental outcomes and preventing complications. Digital monitoring illuminates the patient's condition between routine blood gas testing, adding another layer of protection to prevent oversights that may lead to poor outcomes.
Etiometry will showcase all of its risk indices and ways the platform helps improve outcomes by informing escalation and de-escalation decision-making at the upcoming World Congress of Pediatric Cardiology and Cardiac Surgery in Washington, D.C. later this month. Etiometry also supported the submission of five abstracts for this event.
