Determine intensity of pain based on treatment given:
non-opioids may still be given +/- adjuvant therapies +/- strong opioids
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Non-opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Acetaminophen
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Non-opioid
\[Non-opioid/ Opioid/ Adjuvant\]
NSAIDS
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Morphine
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Fentanyl
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Hydrocodone
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Codeine
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Hydromorphone
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Oxycodone
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Oxymorphone
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Methadone
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Levorphanol
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Tramadol
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Opioid
\[Non-opioid/ Opioid/ Adjuvant\]
Tapentadol
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Adjuvant
\[Non-opioid/ Opioid/ Adjuvant\]
SSRIs, SNRIs, TCAs
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Adjuvant
\[Non-opioid/ Opioid/ Adjuvant\]
Gabapentin
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Adjuvant
\[Non-opioid/ Opioid/ Adjuvant\]
Pregabalin
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Adjuvant
\[Non-opioid/ Opioid/ Adjuvant\]
Corticosteroids
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Adjuvant
\[Non-opioid/ Opioid/ Adjuvant\]
Local anesthetics
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Adjuvant
\[Non-opioid/ Opioid/ Adjuvant\]
Lidocaine patches
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Mu
Which opioid receptor causes physical dependence, EUphoria, respiratory and cardiac depression, reduced gastrointestinal motility, sedation, and analgesia (CNS, most opioids)?
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Kappa
Which opioid receptor causes Miosis, DYsphoria, sedatino, and analgesia (PNS, some opioids)?
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Delta
Which opioid receptor causes antidepressant effects and analgesia (PNS, some opioids)?
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Morphine
Pure; Mu receptor agonist, weak kappa receptor agonist
\ short half-life, standard staring DOC
PO preferred
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Hydromorphone
Pure; Mu receptor agonist, weak delta receptor agonist
\ similar to morphine
short half-life
has a metabolite that may lead to opioid neurotoxicity
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Myoclonus, hyperalgesia, seizures
symptoms of opioid neurotoxicity
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Fentanyl
Pure; Mu receptor agonist
\ highly lipid-soluble
short half-life
may be administered parenteral, spinal, transdermal, transmucosal, buccal, and intranasal
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Fentanyl
ToC if px is unable to swallow
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Methadone
Pure; Mu receptor agonist, N-methyl-D-aspartate (NMDA) receptor antagonist
\ long half-life (8 - 120 hours)
high potency
harder to manage but similar potency and efficacy to morphine
should be monitored due to possible drug accumulation
Has varied equivalence dosing with morphine
\ Possible AE: Torsades de pointes, QTc prolongation
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Oxycodone
Pure; Mu, kappa, and delta receptor agonist
\ similar analgesic and AE to morphine
short half-life
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Hydrocodone
Pure; Mu and delta receptor agonist
\ Equipotent with oral morphine but data are not substantiated
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Oxymorphone
Primarily a mu-receptor agonist
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Codeine
Pure; weak Mu and delta receptor agonist with little direct analgesic effect
\ weak opioid
depends on CYP240, especially CYP2D6
exhibits CYP2D6 polymorphism
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Levorphanol
Pure; Mu, kappa, and delta receptor agonist and NMDA antagonist
\ short half-life
predictable metabolism
varied equivalent dosing with morphine
similar benefit to methadone, less prescribing complexities and AEs
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Buprenorphine
Partial; Mu receptor agonist
\ treating cancer pain in px with Renal Impairment
has ceiling analgesic activity
if administered with high dose opioids, may cause withdrawal symptoms
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Tramadol
Mixed mechanism; weak mu receptor agonist with some NorE and 5-HT3 reuptake inhibition
\ used in caution in Px taking TCAs, SSRIs, SNRIs, and MAOIs
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Tapentadol
Mixed mechanism; mu receptor analgesic with NorE reuptake inhibition
\ used in caution in Px taking TCAs, SSRIs, SNRIs, and MAOIs
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Acetaminophen
aka Paracetamol
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Acetaminophen
has analgesic and antipyretic activity WITHOUT anti-inflammatory
\ has risk for hepatotoxicity and renal impairment
\ Used with caution or not used at all with combination of opioid-acetaminophen products to prevent excess acetaminophen dosing
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3g
Acetaminophen limit according to NCCN recommendations
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NSAIDs
has antipyretic, analgesic, anti-platelet, and anti-inflammatory effects
\ addition of this drug class to opioids is said to be beneficial due to possibility of opioid dose reduction esp when sedation, cognitive function, or other CNS effects of opioids are burdensome
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Misoprostol, PPIs
Drugs used as prophylaxis for NSAID-induced peptic ulcers
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CHF, HTN
For patients that are of high risk for cardiac toxicities, NSAIDs should be discontinued if -- or -- worsens/develops.
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Warfarin, Heparin
If px is taking anticoagulants such as -- and -- with NSAIDs, there a significant increase in risk for bleeding complications → avoid Oral NSAIDs in prophylactic or therapeutic anticoagulation
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Diclofenac
If Px is taking anticoagulants instead of oral NSAIDS, use of -- gel or patch is more recommended.
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Adjuvant analgesics
refer to medication coadministered to enhance opioid analgesia and reduce AEs
helpful if Px experiences pain that is only partially responsive to opioids
helps to manage bone pain, neuropathic pain, and visceral pain; also helps reduce opioid requirement
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Gabapentin, Cryotherapy, Local anesthetic formulations, oral care protocols
Therapies to manage mucositis, pharyngitis, and esophagitis
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NSAIDs, Acetaminophen, steroids
Therapies to manage bone pain without oncologic emergency
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bisphosphonates, denosumab
bone-modifying agents that may be considered if Px has bone pain without oncologic emergency
Agents that could be considered for palliative management of bowel obstruction
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Scopolamine, hyoscyamine, glycopryrrolate
examples of anticholinergics used for palliative management of bowel obstruction (3)
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Corticosteroids
Nerve pain compression or inflammation, trial of -- may be considered
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Antidepressants, anticonvulsants, topical agents
Nerve pain compression or inflammation, trial of --, --, or may be considered
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referral
most appropriate action if px has refractory neuropathic pain which may be paired with the use of interventional strategies
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radiation, hormones, chemotherapy
For painful lesions that are unlikely to respond to antineoplastic therapies, may consider (3)
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Topical Lidocaine
examples of topical agent that may be used for neuropathic pain
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Neuropathic pain
type of pain that results from nerve damage or malfunctioning of the nervous system → may be due to the cancer itself or to the acute or chronic effects of cancer
\ pain comes and goes but is chronic
\ Sx: shooting, burning pain; tingling and numbness
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dronabinol, nabilone, cannabidiol
3 approved FDA cannabinoids
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Dronabinol, nabilone
tetrahydrocannabinol (THC or THC mimics)
\ used to treat refractory nausea and vomiting associated with cancer treatment.
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Cannabidiol
cannabinoid approved for treatment of seizures with rare forms of severe epilepsy
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Dronabinol
cannabinoid approved to treat anorexia and weight loss related to AIDS
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Marijuana
cannabinoid classified as a Schedule 1 substance → high potential for abuse, no current accepted medical use and lack of accepted safety
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Inhaled cannabis
Cannabinoid hyperemesis syndrome is most common for --
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Edible cannabis
Acute psychiatric symptoms, intoxication, and cardiovascular symptoms are most common for --
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Opioids
principle analgesic for moderate to severe pain → high risk for dependence
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10 - 20%
Dose reduction for Px with the following condition:
* never or rarely required breakthrough analgesic * completion of acute pain event * improvement of pain control through use of non-opioid pain management therapies * well controlled pain in the setting of stable disease
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10 - 25%
dose reduction for px experiencing unmanageable AEs and mild pain (1-3)
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50 - 75%
dose reduction for Px with significant safety issues (i.e. sedation due to sepsis)
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Opioid-induced hyperalgesia
considered when increasing opioid dose leads to worsening of pain → dose reduction or rotation with attention to other pain therapies
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Opioid-induced hyperalgesia
state of nociceptive sensitization caused by exposure to opioids; paradoxical response where px receiving tx for pain becomes more sensitive to certain painful stimuli C