Patients assessed as low risk with Framingham Risk Scores but who also had Endothelia Dysfunction, suffered 300% more adverse cardiac events over a 7 year period than those with low risk but normal endothelia function.
EndoPATâ„¢ is the leading medical device for noninvasive endothelial function assessment. It is FDA-cleared, CE-marked and used in preeminent clinical institutions, research centers and Pharmaceutical clinical phase studies in over 40 countries.
Some of the features that make Endo-PAT appealing are its ease of use, user-independence and immediate, automatically calculated test results. It provides clinicians with a reliable and reproducible index of endothelial function in a 15-minute, office-based test.
It is incorporated into numerous multi-center and population-based studies such as the Framingham Heart Study. Research using Endo-PAT has yielded more than 100 articles in peer-reviewed journals and abstracts. It is becoming widely recognized as the standard method for endothelial function assessment.

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