Reprieve Cardiovascular is a medical device company developing an intelligent automated fluid management system for treating acute decompensated heart failure (ADHF). Their flagship product, the Reprieve System, aims to personalize decongestion management by monitoring physiological parameters like urine output and delivering personalized diuretic dosing and fluid replacement. This approach intends to safely and efficiently remove excess fluid, improve patient outcomes, and prevent hospital readmissions.
ADHF, caused by rapid fluid volume overload, affects over 6.7 million Americans. Over one million patients are admitted annually in the US with a primary heart failure diagnosis, averaging hospital stays exceeding five days. Nearly one in four patients are readmitted within 30 days, and approximately half within six months, to re-treat fluid overload. The Reprieve System offers a potential solution to this costly issue by providing physicians and care teams real-time visibility and control over the decongestion process.
In 2022, Reprieve initiated the FASTR Trial, a pilot study comparing their system's efficacy to standard diuretic therapy for ADHF patients. The company has raised USD 42 million in Series A financing in February 2024 to advance clinical programs, including the ongoing FASTR Trial and an upcoming pivotal trial. Reprieve Cardiovascular is a privately held company headquartered in Milford, Massachusetts.
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