Stay ahead of critical moments:
Find out how at ISICEM 2022

We are excited to see you live and in person at the International Symposium on Intensive Care and Emergency Medicine (ISICEM) in Brussels, Belgium

Demands on clinicians in the ICU to make the right clinical decisions at the right time are higher than ever. Visit our booth to learn how we’ve harnessed the power of machine learning and connected technologies to help you stay ahead of critical moments. Don’t miss our informative symposium, educational resources and Demo Box.

What to see at ISICEM 2022

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Visit our booth

Stop by our booth to visit with the Edwards team and demo the latest innovations.

Visit our booth

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Lunch Symposium

Patient safety in the ICU: How AI innovation helps prevent hemodynamic instability

Tuesday, March 22
12:30-13:30 CET
Brussels Convention Center:
Silver Hall

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Workshop/Demo Box

Improving patient safety with advanced hemodynamic monitoring in the ICU

Dr. D. Veelo and Prof. A. Vlaar

Thursday, March 24
15:10-15:40 CET
Brussels Convention Center:
Exhibition Hall, Box 1

Lunch Symposium

Patient safety in the ICU:

How AI innovation helps prevent
hemodynamic instability

Tuesday, March 22
12:30-13:30 CET
Brussels Convention Center: Silver Hall

Patient safety in the ICU

Hypotension as an important risk
factor in critically ill patients:
Time to reflect

Patient safety in the ICU

Treatment improvement with AI:
Time to invest

Patient safety in the ICU

Hypotension management in the ICU:
Time to change

Patient safety in the ICU

Discover more advanced hemodynamic monitoring solutions

HemoSphere advanced monitoring
platform

HemoSphere advanced monitoring platform

The only modular hemodynamic monitoring platform to offer full-range cuff, sensor and catheter compatibility and first-of-its-kind predictive decision support software, HemoSphere advanced monitoring platform enables proactive, individualized patient management.

Explore HemoSphere advanced monitoring platform

Acumen IQ cuff and Acumen HPI software

Acumen Hypotension Prediction Index (HPI) software

Acumen HPI software detects hemodynamic instability and substantially reduces intraoperative hypotension when used in surgical patients who require hemodynamic monitoring during non-cardiac surgery.

A recent study demonstrated a 57% reduction in duration of intraoperative hypotension.*1

*Single arm, multicenter, prospective-to-historical control where patients received arterial line monitoring

Discover Acumen HPI software

ForeSight tissue oximetry system

ForeSight tissue oximetry system

The ForeSight system delivers absolute StO2 values that – when used in combination with the full hemodynamic insights delivered by the HemoSphere advanced monitoring platform – enable you to confidently recognize and address cerebral desaturations.

Explore the ForeSight system

Edwards clinical education

Hemodynamic education empowering
clinical advancement

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.

See all resources

clinical education

Can't attend ISICEM 2022?

Stay up to date with the latest in advanced hemodynamic monitoring and see how intelligent solutions can transform your practice. Contact us to get in touch with an Edwards representative.

Do you have feedback about our products? Click here

References
  1. U.S. Food and Drug Administration. 2021. K203224 510k Summary, Acumen Hypotension Prediction Index, viewed August 24, 2021. https://www.accessdata. fda.gov/cdrh_docs/pdf20/K203224.pdf.

For professional use

For professional use

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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