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Practice Guidelines for the Prevention, Detection, and Management of Respiratory Depression Associated with Neuraxial Opioid Administration. Troy Tada, DO October 21, 2009. Overview.
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Practice Guidelines for the Prevention, Detection, and Management of Respiratory Depression Associated with Neuraxial Opioid Administration Troy Tada, DO October 21, 2009
Overview • This article was chosen to review the updated from previous ASA practice guidelines in 2007 for prevention, detection and management of respiratory depression associated with neuraxial opioid administration. • The updated includes new survey data and recommendation pertaining to monitoring for respiratory depression • The purpose of these guidelines are to improve patient safety and enhance quality of anesthetic care
Overview • These guidelines focus on the treatment of all patients receiving epidural or spinal opioids in inpatient or ambulatory settings • They do not apply to chronic or cancer pain, patients with preexisting implantable drug delivery systems
Overview • Surveys given to two groups: • Task Force-appointed expert consultants • ASA member
Overview • The 2009 guidelines includes more specific recommendations in 4 areas: • Identification of patients at increased risk of respiratory depression (specific recommendations for focused history and physical examination); • Preventive strategies for respiratory depression after neuraxial opioid depression (recommendations for noninvasive positive pressure ventilation, drug selection, and dose selection); • Detection of respiratory depression and management (recommendations for monitoring for adequacy of ventilation, oxygenation, and level of consciousness); • Management and treatment of respiratory depression when it occurs (recommendations for supplemental oxygen, reversal agents, and noninvasive positive pressure ventilation).
Guidelines: Prevention • Identify pts at increased risk • Focused H/P • Literature suggests certain pt or clinical characteristics • Obesity, OSA, neuromuscular disease • Prior opioid administration
Guidelines • Prevention • Noninvasive PPV: no agreement of its effectiveness • However, pts who already utilizes these devises are encouraged to bring their own equipment to the hospital • Single-injection VS Parenteral opioids • Both groups disagree that single injections increase the occurrence of RD when compared to parenteral • Single injection neuraxial opioids may be safely used in place of parenteral opioids without altering the risk of RD or hypoxemia
Guidelines: Drug selection • Prevention • Fentanyl-sufentanil VS morphine-hydromorphone • Single injection • Both groups agree that RD increase with morphine/hydromorphone • May be safely used in place of parenteral opioids without altering risk of RD or hypoxia • Continuous • Literature reports no difference in epidural adm. • However, ASA members agree that RD increase with morphine/hydromorphone • consultants are equivocal regarding this issue • Appropiate doses of continuous epidural fentanyl/sufentanil may be used in place of morphine/hydromorphone without increasing risk of RD
Guidelines: Drug selection • Prevention • Extended release morphine • Both groups equivocal regarding it increasing RD compared with either parenteral opioid or conventional epidural morphine • May be used in place of intravenous or conventional epidural morphine • Extended monitoring may be required
Guidelines: Drug selection • Prevention • Continuous epidural VS parenteral opioids • Meta-analysis of literature indicates less RD with continuous epidural • Both groups disagree that continuous epidural increase the occurrence of RD • Continuous epidurals preferred to parenteral for reducing the risk of RD
Guidelines: Drug selection • Prevention • Based on duration of action, morphine and hydromorphone should not be given to outpatient surgical patients
Guidelines: Dose selection • Prevention • Low VS high dose • Literature indicates RD reduced with low doses of single injections • However, no difference in RD or sedation when used in continuous epidural • Both groups strongly agrees RD increased with higher doses for intrathecal or epidural, in addition to continuous epidural • Recom: lowest efficacious dose should be administered to minimize RD • Neuraxial combined with parenteral • Literature is insufficient • Both groups strongly agree that it increases occurrence of RD • Recom: Parenteral opioids should be cautiously administered, requires increased monitoring (intensity, duration, methods)
Literature on Detection of RD • Literature: • Insufficient to examine the efficacy of pulse oximetry or ETCO2 monitoring to diagnose RD for pt receiving neuraxial opioids • Comparative studies show • Pulse oximetryeffective in detecting hypoxemia in pt receiving a variety of anesthetic techniques • ETCO2 monitoring is effecting in detecting hypercapnia for parenteral opioids • Insufficient regarding using pulse oximetry, EKG, or ventilation is associated with improved detection of RD or hypoxemia for patients with neuraxial opioid
Pulse Oximetry/ETCO2/Level of Consciousness • Both groups disagree that pulse oximetry monitoring is more likely to detect RD than are clinical signs. • Both groups agree that continuous pulse oximetry monitoring is more likely to detect RD than periodic pulse ox monitoring • Both agree that ETCO2 monitoring is more likely to detect hypercapnia and RD than clinical signs • Both agree that checking level of alertness will identify pts at increased risk of RD
Guidelines: Detection • Monitoring • All patients receiving neuraxial opioids should be monitored for adequacy of ventilation • RR • Depth or respiration • Oxygenation • Level of consciousness • In cases with concerning signs, it is acceptable to awaken a sleeping patient to assess level of consciousness
Guidelines: Detection • Detection: Single-Injection neuraxial • lipophilic opioid • Continual monitoring should be performed for the first 20 minutes after adm., followed by monitoring at least once/hour until 2 hours has passed • hydrophilic opioid • Monitoring should be performed for a minimum of 24 hours • First 12 hours: once per hour • Next 12 hours: once per 2 hours
Guidelines: Detection • Detection: Continuous infusion or PCEA • lipophilic /hydrophilic opioid • Monitoring should be performed during the entire time the infusion is in use • First 12 hours: Once per hour • Next 12 hours: once per 2 hours • After 24 hours: should be performed at least once every 4 hours • After discontinuation, monitoring should be dictated by the patient’s overall clinical condition and concurrent medications • Lipophilic opioid only • necessitates continual monitoring for the first 20 minutes
Guidelines: Detection • Detection: Sustained- or extended-release epidural morphine • First 12 hours: once per hour • Next 12 hours: once per 2 hours • After 24 hours: at least every 4 hours for a minimum of 48 hours
Guidelines: Management & Treatment • Supplemental O2: literature • Literature is insufficient to assess whether it will reduce the frequency or severity of hypoxia or hypoxemia • Literature does support use when non-neuraxial anes. Utilized
Guidelines: Management & Treatment • Supplemental O2: guidelines • Both groups agree on all three of following: • Should be available for any use of neuraxial opioids • Administer when, respiratory depression develops, hypoxemia, altered mental status • Routine use may increase duration of apneic episodes and hinder detection of atelectasis, transient apnea, and hypoventilation
Guidelines: Management & Treatment • Reversal agents • Literature: insufficient comparative studies to assess the efficacy with the use of naloxone or naltrexone • IV access should be established and/or maintained • Agents should be available • Administer when clinical signs of RD develop and initiate resuscitation
Guidelines: Management & Treatment • Non-invasive positive pressure ventilation • Should be considered for improving ventilation status • Should consider to utilize if frequent or severe airway obstruction or hypoxemia occurs during postoperative monitoring