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Propofol Sedation for ERCP Procedures: A Dilemna? Observations from an Anesthesia Perspective
Author(s) -
Davinder S. Garewal,
Pallavi Waikar
Publication year - 2012
Publication title -
diagnostic and therapeutic endoscopy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.158
H-Index - 24
eISSN - 1029-0516
pISSN - 1026-714X
DOI - 10.1155/2012/639190
Subject(s) - propofol , medicine , sedation , anesthesia , endoscopic retrograde cholangiopancreatography , hypoxemia , anesthetic , food and drug administration , intensive care medicine , surgery , medical emergency , pancreatitis
Propofol sedation for endoscopic retrograde cholangiopancreatography (ERCP) procedures is a popular current technique that has generated controversy in the medical field. Worldwide, both anesthetic and nonanesthetic personnel administer this form of sedation. Although the American and Canadian societies of gastroenterologists have endorsed the administration of propofol by nonanesthesia personnel, the US Food and Drug Administration (FDA) has not licensed its use in this manner. There is some evidence for the safe use of propofol by nonanesthetic personnel in patients undergoing endoscopy procedures, but there are few randomized trials addressing the safety and efficacy of propofol in patients undergoing ERCP procedures. A serious possible consequence of propofol sedation in patients is that it may result in rapid and unpredictable progression from deep sedation to general anesthesia, and skilled airway support may be required as a rescue measure. Potential complications following deep propofol sedation include hypoxemia and hypotension. Propofol sedation for ERCP procedures is an area of clinical practice where discussion and mutual cooperation between anesthesia and nonanesthesia personnel may enhance patient safety.

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