Michael Barbella, Managing Editor04.23.24
FIRE1 has completed patient enrollment in the U.S. Early Feasibility Study (FUTURE-HF2) of its FIRE1 System for remote heart failure monitoring. The FIRE1 System reportedly is the first device designed to directly measure a patient’s volume status by measuring the inferior vena cava (the body's largest vein where most fluid is stored) to better manage heart failure.
The FIRE1 study encompassed 15 patients treated at five U.S. centers, including Austin Heart Central at the Heart Hospital of Austin, NewYork-Presbyterian/Columbia University Irving Medical Center, Duke University Medical Center, Rochester General Hospital, and The Ohio State University Wexner Medical Center.
“Fluid build-up is challenging to accurately measure today and results in unnecessary hospital admissions due to fluid overload that was not caught early enough to be managed in the home,” said Dr. Nir Uriel, director of advanced heart failure and cardiac transplantation at NewYork-Presbyterian, principal study investigator, professor of medicine in the Division of Cardiology at Columbia University Vagelos College of Physicians and Surgeons, and adjunct professor of medicine in the Greenberg Division of Cardiology at Weill Cornell Medicine. “We are encouraged by our experience using the FIRE1 system and excited about the prospect of heart failure management becoming easier and more effective for both patients and for the clinical team.”
FIRE1 aims to enable patients to monitor and control fluid volume themselves with a device at home. Fluid overload is a classic clinical feature of heart failure, which affects more than 6 million people in the United States and is the most common cause of hospitalization for those aged 65 and over. Current technologies do not directly measure fluid volume where it is primarily stored (the inferior vena cava), resulting in lagging measurements that do not identify fluid overload early enough to manage outside of the hospital. The FIRE1 system is a small, minimally invasive implantable sensor designed to accurately identify fluid build-up earlier, when it can be more easily managed by the patient and their physician without a hospital visit.
“It is gratifying to see the physician interest in our novel technology that earlier studies suggest should be a more sensitive measure than pressure in monitoring heart failure,” FIRE1 President/CEO Conor Hanley stated. “We look forward to sharing the results of this study with the clinical community and conducting larger studies to validate the performance of the FIRE1 device. By enabling patients to better manage their fluid load, we hope to unload the burden on emergency rooms, helping hospitals focus on the most urgent patients who need immediate care rather than on acute management of heart failure.”
Headquartered in Dublin, Ireland, FIRE1 is a connected medical device solutions company. Its investors include Andera Partners, Gilde Healthcare, Gimv, the Ireland Strategic Investment Fund, Lightstone Ventures, Medtronic, New Enterprise Associates, Novo Holdings and Seventure. FIRE1 is led by an experienced medical devices team working closely with researchers, clinicians, patients, and payers to reduce the burden of heart failure.
The FIRE1 study encompassed 15 patients treated at five U.S. centers, including Austin Heart Central at the Heart Hospital of Austin, NewYork-Presbyterian/Columbia University Irving Medical Center, Duke University Medical Center, Rochester General Hospital, and The Ohio State University Wexner Medical Center.
“Fluid build-up is challenging to accurately measure today and results in unnecessary hospital admissions due to fluid overload that was not caught early enough to be managed in the home,” said Dr. Nir Uriel, director of advanced heart failure and cardiac transplantation at NewYork-Presbyterian, principal study investigator, professor of medicine in the Division of Cardiology at Columbia University Vagelos College of Physicians and Surgeons, and adjunct professor of medicine in the Greenberg Division of Cardiology at Weill Cornell Medicine. “We are encouraged by our experience using the FIRE1 system and excited about the prospect of heart failure management becoming easier and more effective for both patients and for the clinical team.”
FIRE1 aims to enable patients to monitor and control fluid volume themselves with a device at home. Fluid overload is a classic clinical feature of heart failure, which affects more than 6 million people in the United States and is the most common cause of hospitalization for those aged 65 and over. Current technologies do not directly measure fluid volume where it is primarily stored (the inferior vena cava), resulting in lagging measurements that do not identify fluid overload early enough to manage outside of the hospital. The FIRE1 system is a small, minimally invasive implantable sensor designed to accurately identify fluid build-up earlier, when it can be more easily managed by the patient and their physician without a hospital visit.
“It is gratifying to see the physician interest in our novel technology that earlier studies suggest should be a more sensitive measure than pressure in monitoring heart failure,” FIRE1 President/CEO Conor Hanley stated. “We look forward to sharing the results of this study with the clinical community and conducting larger studies to validate the performance of the FIRE1 device. By enabling patients to better manage their fluid load, we hope to unload the burden on emergency rooms, helping hospitals focus on the most urgent patients who need immediate care rather than on acute management of heart failure.”
Headquartered in Dublin, Ireland, FIRE1 is a connected medical device solutions company. Its investors include Andera Partners, Gilde Healthcare, Gimv, the Ireland Strategic Investment Fund, Lightstone Ventures, Medtronic, New Enterprise Associates, Novo Holdings and Seventure. FIRE1 is led by an experienced medical devices team working closely with researchers, clinicians, patients, and payers to reduce the burden of heart failure.