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Use of Ketamine for Pain Management in Hospice Care

August 30, 2019

This document is for informational and educational purposes only and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified health care provider.  All information contained in this document is protected by copyright and remains the property of ProCare HospiceCare.  All rights reserved.


Ketamine shows promise as an effective option for hospice patients who have pain that does not fully respond to increasing doses of opioids. However, in all instances, this treatment option should be discussed and approved by the patient’s medical provider. It may be especially useful for neuropathic pain that does not respond fully to usual pain regimens that may include, opioids, NSAIDS, certain antidepressants, anticonvulsants, and gabapentinoids. Ketamine appears to be synergistic with opioids in patients who no longer have an analgesic response to high doses of opioids.  It is also reported to be opioid-sparing and appears to play a role in opioid potentiation. Keep in mind the use of ketamine for pain is off-label and it can be very complex to dose, so coordination with the patient’s medical provide is critical.


Contraindications, side effects, and monitoring parameters are listed in Table 1. If needed, a ProCare pharmacist can provide information to facilitate your decision about whether or not ketamine would be appropriate.

*Relative contraindications (may not apply to hospice patients). Evaluate risks vs. benefits of using in a hospice patient.


**Less likely with oral administration of ketamine than with infusions.


*** Ketamine does not suppress respiration, but can cause a reversal of opioid tolerance and opioid potentiation, which may suppress respiration if the opioid dose has not been reduced appropriately.



Ketamine is soluble in water and lipids and has many routes of administration. It can be given intravenous, subcutaneous, intramuscular, oral, sublingual, nasal, rectal, topical, and epidural. Dosing via the oral, sublingual, intravenous, and subcutaneous routes are most commonly used for pain and will be reviewed further.

Ketamine dosing is complex. Concurrent opioid adjustments are generally also needed. Oral or sublingual administration of ketamine is preferred. Ketamine infusions can be used, but are best reserved in an inpatient setting, and should not exceed a specified max, in order to avoid anesthesia. See table 2.

When able, patients on continuous infusions of ketamine can be converted to oral ketamine. The conversion range is 1-3:1 IV:PO. If the patient has only been on the ketamine infusion for a few days, use a conversion range of 1:1. Give the total daily oral dose in three divided doses. Generally, a taper off infusion while starting oral medication is recommended. For the first 24 hours, continue parenteral ketamine at 50% or original rate. If possible, reduce parenteral ketamine to 25% of original rate on day 2 before stopping the infusion. Titrate the oral dose by 10-25 mg/day every 3-4 days or by 20-30% every 3-4 days. If the patient experiences pain before next dose is due, consider shortening the dosing interval.


In summary, the advantages, disadvantages, and possible contraindications must be evaluated to determine if the patient is a candidate for ketamine. Some advantages of ketamine include that it is a non-opioid for pain, has no significant effect on pulmonary function, has many routes of administration and is cost-effective when compared to most other pain regimens. Disadvantages may include possible psychotomimetic effects (though not as likely with oral dosing), little data regarding long-term use, it must be compounded for oral or sublingual use, kept refrigerated, and is only good for seven days. Although not a first-line agent for pain, ketamine may provide another good option for patients that fail to fully respond to increasing opioid doses and other adjuvants for pain management, provided the patient’s physician confirms the alternate treatment protocol.


Written by: Karen Bruestle-Wallace, Pharm D, BCGP



References:

  1. Li, L. and Vlidides, P. (2016). Ketamine: 50 Years of Modulating the Mind. Frontiers in Human Neuroscience, 10(612), DOI: 10.3389/fnhum.2016.00612
  2. Ketamine. (2019, March 1). Retrieved from http://www.cesar.umd.edu/cesar/drugs/ketamine.asp
  3. Anderson, L. (2018, Nov. 5). Ketamine Abuse. Retrieved from https://www.drugs.com/illicit/ketamine.html
  4. Lexi-Comp OnlineTM, Lexi-Drugs Online TM, Hudson, Ohio: Lexi-Comp, Inc.; Accessed: June 2018
  5. Ingraham, P. (2018, Nov 21). The 3 Basic Types of Pain Nociceptive, neuropathic and “other” (and then some more”. Retrieved from https://www.painscience.com/articles/pain-types.php
  6. ProCare HospiceCare, (2016). Ketamine Use-Quick Guide. (brochure). Gainesville, GA: ProCare HospiceCare.
  7. Clark, J. (1995). Effective Treatment of Severe Cancer Pain of the Head Using Low-Dose Ketamine in an Opioid-Tolerant Patient. Journal of Pain and Symptom Management, 10(4), 310-314.
  8. Rigo, F. K., Trevisan, G., Godoy, M., Rossato, M., Dalmolin, G., Silva, M.,…Ferreira, J. (2017). Management of Neuropathic Chronic


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Renal impairment is relatively common in both the elderly and hospice patients, and it can affect the way medications act in the body in several ways. Most commonly, it results in decreased clearance of renally-excreted medications, leading to accumulation of the drug and/or its metabolites and subsequent adverse or toxic effects. The absorption of oral medications may be reduced in patients with renal impairment due to increased gastric pH and gut wall edema. Uremia caused by renal impairment can increase sensitivity to medications that act on the central nervous system (CNS), as well as increase the risk of hyperkalemia due to potassium-sparing drugs. In addition, uremia can enhance the potential for NSAID-induced edema or GI bleeding. Renal impairment can also lead to edema or ascites, cachexia, dehydration, decreased albumin levels and binding capacity, and decreased tissue binding, all of which can impact the effects of medications. To compensate for these renal impairment-induced changes in drug disposition, the typical actions taken regarding medication administration are to decrease the dose, increase the dosing interval, or a combination of the two. The action that would be recommended depends on the drug and its specific characteristics. There are many medications that require dose adjustment in renal impairment, but here we’ll be discussing just those that are most often seen in hospice. The goal is to make you aware of these common medications (and categories) that often need dose adjustment so they trigger a mental alert for possible follow-up if they are ordered for your patients with decreased renal function. Opioids: Many opioids can accumulate in renal impairment as the parent drug and/or metabolites. Tramadol has a maximum daily dose in all patients, but in patients with a creatinine clearance (CrCL) less than 30 mL/minute, this maximum dose is reduced to 200 mg per day and the dosing interval should be extended to every 12 hours. Morphine renal dose reductions start with a CrCL less than 60 mL/minute, with possible extension of the dosing interval at this point as well. It is typically recommended to start considering alternatives to morphine in patients with a CrCL less than 30 mL/minute, and to avoid it altogether in patients with a CrCL less than 15 mL/minute. At end of life, the benefits of morphine can sometimes outweigh the risks. Because the presentation of renal accumulation-based adverse effects may be delayed, morphine can be used even in severe renal impairment or renal failure when the prognosis is hours to days, or in dialysis patients when death is imminent. Typically, oxycodone and hydromorphone are considered preferred alternatives to morphine in patients with significant renal impairment, although they both have metabolites that can accumulate in renal failure. As a result, the dose of oxycodone should be reduced and the dosing interval increased in patients with a CrCL less than 60 mL/minute, and oxycodone extended-release products should usually be avoided in patients with a CrCL less than 30 mL/minute. Hydromorphone dose reduction is also recommended when CrCL is less than 60 mL/minute; further dose reduction and extension of the dosing interval is recommended for hydromorphone when CrCL is less than 30 mL/minute. Although hydrocodone and its active metabolites may accumulate in renal impairment, there are no dose reductions for hydrocodone/acetaminophen according to the manufacturer’s labeling. Hydrocodone extended-release products (Hysingla ER®, Zohydro ER®) are rarely used in hospice, but dose reductions are recommended in patients with moderate to severe renal impairment. Methadone and fentanyl patch are considered among the safest opioids in renal impairment because they do not have active metabolites. However, renal impairment can still alter how fentanyl moves in the body, so dose reduction is recommended in patients with a CrCL of 50 mL/minute or less. For methadone, dose reduction is not recommended until very severe renal impairment (CrCL less than 10 mL/minute). No dose reductions are recommended for buprenorphine at any degree of renal impairment, and it is generally considered safe in this population. NSAIDs: Examples of NSAIDs that are commonly used in hospice include ibuprofen (Advil®, Motrin®), naproxen (Aleve®), and meloxicam (Mobic®), and as mentioned previously, there are some concerns regarding the use of NSAIDs in renal impairment. According to the Kidney Disease: Improving Global Outcomes (KDIGO) 2012 Clinical Practice Guideline, prolonged therapy with NSAIDs is not recommended if GFR is less than 60 mL/minute/1.73m² , and NSAIDs should typically be avoided in patients with a GFR less than 30 mL/minute/1.73m². As a general rule, NSAIDs should be used at the lowest effective dose for the shortest time possible in patients with renal impairment. In addition, NSAIDs should be avoided in patients with a high risk for developing acute kidney injury (e.g. volume depleted, elderly, and/or taking other nephrotoxic medications), and should be discontinued if acute kidney injury occurs during use. Antimicrobials: Many antimicrobials require dose reduction and/or extension of the dosing interval in renal impairment. Specific dosing recommendations depend on the antimicrobial in question and the type of infection being treated. When used for multiple doses, the dose of the antifungal fluconazole (Diflucan®) should be reduced in patients with a CrCL of 50 mL/minute or less. Examples of antibiotics commonly used in hospice that need dose adjustment include: sulfamethoxazole/trimethoprim (Bactrim®); fluoroquinolone antibiotics, including ciprofloxacin (Cipro®) and levofloxacin (Levaquin®); certain penicillin antibiotics, such as amoxicillin and amoxicillin/clavulanate (Augmentin®); and some cephalosporins, including cephalexin (Keflex®) and cefdinir (Omnicef®). Nitrofurantoin (Macrobid®, Macrodantin®) also has significant concerns in renal impairment. According to the manufacturer’s prescribing information, it is contraindicated in anuria, oliguria, or significant renal impairment (defined as a CrCL less than 60 mL/minute or clinically significant elevated serum creatinine). However, limited data suggest it is safe and effective for short-term use in patients with a CrCL of 30 to 60 mL/minute, although there appears to be an increased risk of pulmonary adverse events when eGFR is less than 50 mL/minute. In any case, nitrofurantoin should be avoided altogether in patients with a CrCL less than 30 mL/minute, due to the risk of pulmonary toxicity, hepatotoxicity, and peripheral neuropathy. Renal impairment can affect drug disposition in several ways, often increasing the risk of adverse and toxic effects. Whenever you have a patient with renal impairment, evaluate whether they are taking medications that may be cause for concern and require dose adjustment, and remember that hospice clinicians, pharmacists, and drug information resources can help by providing specific renal dosing recommendations. By Joelle K. Potts RPh, PharmD, BCGP REFERENCES: Aging and Kidney Disease. National Kidney Foundation. Available at: https://www.kidney.org/news/monthly/wkd_aging [accessed 8/8/2022] Aronoff GR, Bennett WM, Berns JS, Brier ME, Kasbekar N, Mueller BA, et al. Drug Prescribing in Renal Failure: Dosing Guidelines for Adults and Children. 5th American College of Physicians, Philadelphia, PA; 2007. Renal Impairment. Chapter in: Palliative Care Formulary, 7th Edition (PCF7). Wilcock A, Howard P, Charlesworth S, Eds. Pharmaceutical Press, London, UK. Chapter 17, added April 2017; 715-35. Drug monographs. Lexcomp Online, Lexi-Drugs Online. Waltham, MA: UpToDate, Inc. https://online.lexi.com. O’Connor NR, Corcoran AM. End-stage renal disease: symptom management and advance care planning. Am Fam Physician. 2012; 85(7): 705-10. Kidney Disease: Improving Global Outcomes (KDIGO). KDIGO 2012 clinical practice guideline for the evaluation and management of chronic kidney disease. Kidney International Supplements. Jan 2013; 3(1). Available at: www.kidney-international.org Macrobid® Prescribing Information. Proctor and Gamble Pharmaceuticals, Inc. Cincinnati, OH. Revised Jan 2009. Available at: https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020064s019lbl.pdf [accessed 6/13/2022] Macrodantin® Prescribing Information. Almatica Pharma Inc. Pine Brook, NJ. Revised Mar 2013. Available at: https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/016620s072lbl.pdf [accessed 6/13/2022] 2019 American Geriatrics Society Beers Criteria® Update Expert Panel. American Geriatrics Society 2019 updated Beers Criteria® for potentially inappropriate medication use in older adults. JAGS. 2019; 00: 1-21
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