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Updated: May 26, 2026

Drug-Induced Sleep Endoscopy (DISE) with Target Controlled Infusion (TCI) and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
Adverse event reporting tool to standardize the reporting and tracking of adverse events during procedural sedation:
K P Mason1, Keira P Mason, S M Green
1Department of Anesthesiology, Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, USA. keira.mason@childrens.harvard.edu
Abstract:
Currently, there are no established definitions or terminology for sedation-related adverse events (AEs). With clear terminology and definitions, sedation events may be accurately identified and tracked, providing a benchmark for defining the occurrence of AEs, ranging from minimal to severe. This terminology could apply to sedation performed in any location and by any provider. We present a consensus document from the International Sedation Task Force (ISTF) of the World Society of Intravenous Anaesthesia (World SIVA). The ISTF is composed of adult and paediatric sedation practitioners from multiple disciplines throughout the world.
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