Acumen intelligent decision support suite delivers outstanding data-driven solutions to support you in ensuring adequate perfusion for your patients. The suite includes predictive hemodynamic management software, a sensor, as well as a retrospective analysis tool for reviewing patient perfusion.
The minimally-invasive Acumen IQ sensor unlocks the Acumen Hypotension Prediction Index (HPI) software and introduces intelligent decision support to the reliable and trusted foundation of the Edwards Arterial Pressure-Based Cardiac Output (APCO) algorithm.
Acumen IQ sensor connects to any existing radial arterial line and automatically updates advanced parameters every 20 seconds, reflecting rapid physiological changes in moderate- to high-risk surgery. Advanced hemodynamic parameters provided by the Acumen IQ sensor offer you continuous insight into your patient’s hemodynamic status.
Developed in partnership with clinicians, this first-of-its-kind predictive decision support software detects the likelihood of a patient trending towards a hypotensive event* before the event occurs, and provides you with insights to understand the root cause and inform a potential course of action for your patient.
Acumen Analytics software enables you to download and analyze your patient’s data retrospectively to a PC. Monitoring sessions, including demographic data, can be downloaded from the HemoSphere advanced monitoring platform or EV1000 clinical platform into Acumen Analytics software for organization and analysis. Patient identifiers are omitted from the collection of data.
With a long-term commitment to improving the quality of care for surgical and critical care patients through education, Edwards clinical education meets you no matter where you are in the learning process — with a continuum of resources and tools that continuously support you as you solve the clinical challenges facing you today, and in the future.
We are committed to providing your institution, clinicians and staff with a high level of customer service and support to ensure seamless product implementation and ongoing use:
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For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use (consult eifu.edwards.com where applicable).
Edwards Lifesciences devices placed on the European market meeting the essential requirements referred to in Article 3 of the Medical Device Directive 93/42/EEC bear the CE marking of conformity.
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