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Category: Research

June 2025 | American Journal of Respiratory and Critical Care Medicine (AJRCCM) | Temporary Transvenous Diaphragm Neurostimulation for Weaning from Mechanical Ventilation (RESCUE-3)

May 2025 | Critical Care | Phrenic stimulation decreases brain injury biomarkers in sedated mechanically ventilated patients: preliminary observations

April 2025 | Cardiovascular Research Foundation THT | Diaphragm Neurostimulation to optimize Biventricular Performance during Invasive Mechanical Ventilation for Acute Respiratory Failure

November 2024 | Communications Medicine | Restoring brain connectivity by phrenic nerve stimulation in sedated and mechanically ventilated patients

October 2024 | Clinics in Chest Medicine | Lung and Diaphragm Protection During Mechanical Ventilation in Patients with Acute Respiratory Distress Syndrome

September 2024 | Journal of Applied Physiology | Transvenous Phrenic Nerve Stimulation Reduces Diaphragm Injury During Controlled Mechanical Ventilation In A Preclinical Model of ARDS

May 2024 | American Thoracic Society (ATS) Conference | Monitoring diaphragmatic effort during phrenic nerve stimulation based on changes in airway pressure-time product

May 2024 | American Thoracic Society (ATS) Conference | Phrenic nerve stimulation increases brain connectivity in deeply sedated mechanically ventilated moderate ARDS patients

March 2024 | International Symposium on Intensive Care & Emergency Medicine (ISICEM) | Greater brain activity and connectivity induced by phrenic nerve stimulation in moderate ARDS patients

March 2024 | Anesthesiology | An Initial Investigation of Diaphragm Neurostimulation in Patients with Acute Respiratory Distress Syndrome

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© 2024 Lungpacer Medical Inc. ®

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AEROPACE SYSTEM INDICATIONS FOR USE

The AeroPace System is indicated to improve weaning success – increase weaning, reduce ventilator days, and reduce reintubation – in patients ages 18 years or older on mechanical ventilation ≥ 96 hours and who have not weaned.

SAFETY INFORMATION

Do not use the AeroPace System with active implanted cardiac pacemakers, defibrillators, or other implantable electronics within proximity to the AeroPace Neurostimulation Catheter. The AeroPace System has not been clinically evaluated for safety with these implantable electronic devices.

Risks include those that may occur with the use of central venous catheters and the risks of nerve and diaphragm stimulation.  These may include the risks of infection, blood vessel damage, or cardiac effects that can occur with use of catheters.  Stimulation risks are rare and may include nerve injury or fatigue of the breathing muscle.

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CAUTION: The AeroNova System is limited by Federal law (United States) to investigational use. Used exclusively for clinical investigations.

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Lungpacer® Medical, AeroPace® System and AeroNova® System are registered trademarks of Lungpacer Medical.

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The AeroPace® System is approved by the United States Food and Drug Administration to improve weaning success in adult patients on mechanical ventilation at least 96 hours and who have not weaned. The AeroPace System is not approved in any other country.

The AeroNova® System is limited by Federal Law (United States)to investigational use. Used exclusively for clinical investigations.

Lungpacer is developing innovative new technologies. By visiting Lungpacer Medical’s website, you acknowledge that not all the technology cited has regulatory approval and clinical trials are ongoing for investigational devices. These clinical studies may show an increased benefit, no benefit, or an adverse benefit to the patient.

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