Baxter International Inc. has announced 510(k) clearance of the PrisMax system and the integrated TherMax blood warmer, the company’s next-generation platform for continuous renal replacement therapy (CRRT) and therapeutic plasma exchange (TPE).
Designed with real-world input from more than 650 healthcare providers around the world, Baxter says the PrisMax system offers innovative technology to help simplify therapy delivery, while providing hospitals the flexibility to meet the unique demands of the ICU.
Building on Baxter’s Prismaflex technology, currently used by hospitals in more than 90 countries, the PrisMax system is used to treat patients with acute kidney injury (AKI) and select autoimmune diseases.
PrisMax includes new digital health features that allow hospitals to connect the system to electronic medical record (EMR) platforms. This enables straightforward integration of information from PrisMax to the EMR, allowing ICU nurses to spend less time manually documenting treatment data, while reducing the risk of transcription errors. PrisMax also features TrueVue Analytics, Baxter’s proprietary data and analytics platform. Hospitals can use TrueVue Analytics tools to evaluate data aggregated at the hospital level and assess the quality and effectiveness of their CRRT programs.
The TherMax blood warmer, which is used exclusively with the PrisMax system, is an important component for extracorporeal CRRT to warm the blood prior to returning to the body, helping keep the patient’s body temperature at a normal level.