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However, current research suggests that, for many individuals, these risks are manageable under the guidance of a qualified healthcare provider

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The study duration spanned 68 weeks, with most significant loss occurring during the first 16 weeks as the dose was gradually increased from starting levels

I would like to thank Karen Domino, M.D., chair of the ASAs Committee on Practice Parameters (CPP) and Girish Joshi, M.D., vice-chair of the CPP, as well as ASAs Task Force on Preoperative Fasting for their commitment to patient safety in developing this guidance. Initial reports have found that patients who have experienced GI side effects, such as nausea or vomiting, while taking GLP-1 agonists were more likely to have increased residual gastric contents

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