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Ethicon Endo-Surgery SEDASYS(R) System Receives Regulatory Approval in Canada and CE Mark in European Union
Date:5/3/2010

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  • "Level of Sedation and Patient/Clinician Satisfaction" (Date of Presentation: May 3) – the study demonstrated patients who underwent routine colonoscopy and EGD procedures were satisfied with minimal-to-moderate sedation and their satisfaction did not increase as the level of sedation deepened. Consistent with the pivotal study, the clinicians were more satisfied with the procedures that involved propofol sedation delivered with the SEDASYS® System compared to the procedures in which patients were sedated with the current standard of care drugs.
  • "A Novel Patient Responsiveness Monitor for Minimal/Moderate Sedation" (Date of Presentation: May 5) – the study showed that the SEDASYS® System's automated responsiveness monitor (ARM) is able to reliably assess a patient's level of sedation and notify a clinician when a transition from moderate to deep sedation may occur. The SEDASYS® System, with the ARM, enabled the clinician to maintain patients at minimal-to-moderate sedation, reducing episodes of deep sedation and general anesthesia.

  • About Colorectal Cancer

    Colorectal cancer, also known as colon cancer, is one of the deadliest and most expensive diseases to treat. Colon cancer is the second-leading cause of cancer-related deaths in Canada(i) and the third-leading cause of cancer death in the European Union.(ii) It is also the third-leading cause of cancer death in the United States, afflicting nearly 150,000 new patients each year, and claiming the lives of nearly 50,000 more.(iii)

    Regular screening tests – such as colonoscopy – are the most effective way to detect abnormal and potentially precancerous growths in the colon or rectum. While there has bee
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    SOURCE Ethicon Endo-Surgery
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