Sample1_PPT.pptx
PPTX presentation 6 MB Posted
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- 36C77624R0132
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This document is a PowerPoint presentation that provides training on the use of intravenous (IV) ketamine and lidocaine infusions for acute pain management. The presentation covers the mechanism of action, patient selection, dosing, adverse effects, and monitoring requirements for these therapies. Key points include:
The presentation describes how low-dose IV ketamine can provide analgesia, reduce hyperalgesia, potentiate opioid effects, and preserve respiratory function. It reviews appropriate patient selection, including contraindications and relative contraindications. Dosing recommendations are provided, along with sample order sets and monitoring parameters. The training also covers implementing these infusions at healthcare facilities and addressing potential obstacles.
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Text version
APSEP
Oluwatobi Hunter, DNP, PMGT-BC, AGACNP-BC January 23, 2024 Inpatient Infusions for Acute Pain
Navigation and coruses requirements Information provided by ILEAD How to Navigate the Course Course Completion and Bookmarking
Estimated Duration: 20 to 30 minutes
Completion Requirements Review each page of the module Pass the posttest with a score of 80% or better
By the end of the module, you will be able to:
Describe the mechanism of action for intravenous ketamine and intravenous lidocaine for acute pain.
Identify appropriate patient selection for intravenous infusions for acute pain.
Discuss the safety and monitoring of patients receiving intravenous infusions for acute pain.
Review opportunities and obstacles to implementing acute pain infusions.
We will review:
Topic One: Ketamine infusions for acute pain.
Topic Two: Lidocaine infusions for acute pain.
Topic Three: Implementing infusions for acute pain at your facility.
TOPIC ONE:
Intravenous Ketamine Infusions for Acute Pain
What is ketamine?
Introduced clinically in 1970 as a dissociative anesthetic
Subanesthetic (low-dose) intravenous ketamine is used for pain relief Mion, G. (2017). Eur. J. Anaesthesiol, 34(9), 571-575.
Gorlin, A. (2016). J. Anaesthesiol. Clin. Pharmacol, 32(2), 160–167.
Vadivelu, N. (2016). J. Anaesthesiol. Clin. Pharmacol, 32(3), 298-306.
Low-dose Ketamine Provides analgesia
Reduces hyperalgesia
Potentiates the analgesic effects of opioids
Opioid-spearing effects
Preserves respiratory function and airway reflexes
Ketamine Mechanism of Action Primary drug effect:
N-methyl-D-aspartate (NMDA) receptor inhibition
Secondary drug effects:
Opioid receptor agonist Anti-inflammatory effects Niesters. (2014). Br J Clin Pharmacol, 77(2), 357-367.
Vadivelu, N. (2016). J Anaesthesiol Clin Pharmacol, 32(3), 298-306.
NMDA Receptor Antagonism Ketamine binds non-competitively to the NMDP receptor
Reduces glutamate release
Blocks calcium influx to inhibit neurotransmission
Adapted from Lisek M. (2020). Int J Mol Sci, 21(21):8410.
Ketamine Pharmacology Niesters. (2014). Br J Clin Pharmacol, 77(2), 357-367.
Vadivelu, N. (2016). J Anaesthesiol Clin Pharmacol, 32(3), 298-306.
Dose-dependent analgesic, amnesic, and anesthetic effects
Highly lipophilic and rapidly crosses the blood-brain barrier
Half-life: 2-3 hours
Hepatically metabolized to active and inactive metabolites
Excreted in urine and stool
Schwenk, E. (2018). Reg Anesth Pain Med, 43(5), 456-466.
Laskowski, K. (2011) Can J Anesth, 58(10), 911-923.
Ketamine Indications
Acute pain associated with moderately to severely painful surgery (e.g., thoracic, major abdominal, or major orthopedic)
Opioid-experienced patients
Patients at risk for opioid-related adverse events (e.g., asthma, sleep apnea, home oxygen, substance misuse)
Non-operative patients with severe acute pain or palliative care refractory to multimodal analgesics
Ketamine Patient Selection Contraindications:
Ketamine hypersensitivity Uncontrolled hypertension Severe hepatic dysfunction Pregnancy Active psychosis Poorly controlled psychiatric disorder
Relative Contraindications:
Catecholamine depletion (e.g., sepsis) Psychiatric disorder with hallucinations or nightmares Elevated intracranial pressure Elevated intraocular pressure Cardiovascular disease for which elevated blood pressure may be dangerous Current or prior ketamine misuse
CRE_Ketamine_Infusion_for_the_Treatment_of_Intractable_Neuropathic_Pain.pdf (va.gov) Gorlin, A. (2016). J. Anaesthesiol. Clin. Pharmacol, 32(2), 160–167.
Niesters, N. (2014). Br. J. Clin. Pharmacol, 77(2), 357-367.
Adverse effects
| Ketamine n=35 n | ||
| (%)Placebo n=35n (%) | Placebo |
n=35
| n (%) | p value | |||
| Nausea | 17 (49) | 14 (40) | 0.47 | |
| Vomiting | 8 (23) | 8 (23) | 1.00 | |
| Pruritus | 12 (34) | 13 (37) | 0.80 | |
| Sedation | 18 (51) | 15 (43) | 0.47 | |
| Lightheadedness | 14 (40) | 5 (14) | 0.02 | |
| Vivid dreams | 13 (40) | 2 (6) | 0.001 |
Chumbley GM. (2019). Eur J Pain, 23(5):985-993.
Other Adverse Effects Cohen, S. (2018). Reg Anesth Pain Med, 43(5), 521-546.
Niesters, N. (2014). Br. J. Clin. Pharmacol, 77(2), 357-367.
CRE_Ketamine_Infusion_for_the_Treatment_of_Intractable_Neuropathic_Pain.pdf (va.gov)
Psychomimetic effects are dose-dependent Less common with doses under 30mg/hr Treat with alpha-2 agonists or benzodiazepines Excessive salivation Stop ketamine if patient is unable to protect airway Central sympathetic stimulation Hypertension and tachycardia Direct myocardial depression More common at anesthetic doses or catecholamine depletion Cystitis Associated with illicit use or chronic use
Avoid standing titration orders outside of critical care settings
Loading bolus at the start of the infusion must be administered by an anesthesia provider, or someone credentialed with the routine use of ketamine, followed by direct observation for at least 30 minutes
Follow your facility’s controlled substance policy and medication policy Hunter OO. (2023). J Am Assoc Nurse Pract, 35(2):98-103.
VHA Directive 1073 (1) Appendix E “Parameters for the Safe Administration of Ketamine for Non-Sedation Purposes” January 13, 2023
Ketamine Prescribing
Ketamine Dosing Recommendations Must use ideal body weight
Optional loading bolus: 0.2-0.5 mg/kg Not necessary if continuing intraoperative infusion
Initiate at 0.1-0.2 mg/kg/hr IBW
Titrate by 0.1 mg/kg/hr IBW based on analgesia and side effects Hunter OO. (2023). J Am Assoc Nurse Pract, 35(2):98-103.
VHA Directive 1073 (1) Appendix E “Parameters for the Safe Administration of Ketamine for Non-Sedation Purposes” January 13, 2023
Ketamine Dosing Recommendations cont.
Consider intraoperative dosing recommendations for enhanced recovery after surgery (ERAS) protocols
Consider setting a maximum infusion dose on medical-surgical units
Hunter OO. (2023). J Am Assoc Nurse Pract, 35(2):98-103.
VHA Directive 1073 (1) Appendix E “Parameters for the Safe Administration of Ketamine for Non-Sedation Purposes” January 13, 2023
IV Ketamine Sample Order Set Part 1
VA Palo Alto HCS
IV Ketamine Sample Order Set Part 2
VA Palo Alto HCS
Monitoring & Documentation Vital signs, pain score, and sedation scale:
At the start of the infusion At 15 minutes Every 1 hr for the first 4hrs Then if stable every 4hrs until discontinued Telemetry optional if dose < 0.5mg/kg/hr IBW
Frequency of monitoring should be facility-specific Hunter OO. (2023). J Am Assoc Nurse Pract, 35(2):98-103.
VHA Directive 1073 (1) Appendix E “Parameters for the Safe Administration of Ketamine for Non-Sedation Purposes” January 13, 2023
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