• Dig. Dis. Sci. · May 2014

    Review

    SEDASYS(®), airway, oxygenation, and ventilation: anticipating and managing the challenges.

    • Basavana Gouda Goudra, Preet Mohinder Singh, and Vinay Chandrasekhara.
    • Department of Anesthesia and Intensive Care, Hospital of the University of Pennsylvania, Philadelphia, PA, USA, goudrab@uphs.upenn.edu.
    • Dig. Dis. Sci. 2014 May 1;59(5):920-7.

    AbstractIn May 2013, the FDA (Federal Drug Administration) approved SEDASYS(®), a device that enables non-anesthesia physicians to provide mild-to-moderate sedation to patients undergoing colonoscopy and esophagogastroduodenoscopy. SEDASYS(®) is the first among the devices being built to provide computer-assisted personalized sedation. Although the intention of this approval is to cut the anesthesia related expenses, it is likely to create new challenges to the users-both clinical and administrative-that might even increase the cost. Deep sedation is required frequently for a successful completion of the procedure, which poses unforeseen challenges. The present review aims to provide clear information to the users regarding pre-procedure assessment, possible sedation related complications and management options.

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