ASAM Provider Guide

National Practice Guideline for the Treatment of Opioid Use Disorder - 2020 Update

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25 Î MAJOR REVISION – The addition of a short-acting full agonist opioid to the patient's regular dose of buprenorphine can be effective for the management of severe acute pain in supervised settings, such as during hospitalization. • The dose of additional full agonist opioid analgesic prescribed is anticipated to be higher than the typical dose necessary to achieve adequate analgesia in opioid- naïve individuals. • Because of a lack of evidence, the committee was unable to come to consensus on whether this adjunct treatment can be safely prescribed in ambulatory care settings. Î MAJOR REVISION – Discontinuation of methadone or buprenorphine before surgery is NOT required. • Higher-potency intravenous full agonist opioids can be used perioperatively for analgesia. Î Decisions related to discontinuing or adjusting the dose of buprenorphine prior to a planned surgery should be made on an individual basis through consultation between the surgical and anesthesia teams and the addiction treatment provider when possible. Î MAJOR REVISION – If it is decided that buprenorphine or methadone should be discontinued before a planned surgery, this may occur the day before or the day of surgery, based on surgical and anesthesia team recommendations. • Higher-potency intravenous full agonist opioids can be used perioperatively for analgesia. • Methadone or buprenorphine can be resumed post-operatively when the need for full opioid agonist analgesia has resolved, with additional considerations for post- operative pain management as described for acute pain above. • The initial dose and titration should typically be determined by the prescriber. • In general, pre-surgery daily doses of these medications can be resumed if they were withheld for less than 2–3 days. Î Patients on naltrexone may not respond to opioid analgesics in the usual manner. Therefore, it is recommended that mild pain be treated with non-opioid analgesics, and moderate to severe pain be treated with higher potency NSAIDs (e.g., ketorolac) on a short-term basis. Î Oral naltrexone should be discontinued 72 hours before surgery and extended-release injectable naltrexone should be discontinued 30 days before an anticipated surgery. (Reinitiation of naltrexone should follow the guidance on p. 12 of this pocket guide.) Î NEW – Naltrexone's blockade of the mu opioid receptor can often be overcome when necessary with high potency full agonist opioids. • In these instances, patients should be closely monitored in an emergency department or hospital setting.

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