[186] Pain Management

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113 Terms

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Mild
NCCN classification rating of 1 - 3 corresponds to --- pain
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Moderate
NCCN classification rating of 4 - 7 corresponds to --- pain
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Severe
NCCN classification rating of 8 - 10 corresponds to --- pain
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Numerical Rating Scale
Rating scale where Px are asked to rate the pain from 0 to 10
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Numerical Rating Scale
Type of rating scale where exact numerical range of each level of pain is unclear
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Verbal Rating scale
Type of rating scale that provides a clear ranking of pain
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Visual Analog Scale
Type of rating scale where Px are asked to make along the line the level of pain they are experiencing
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Face Scale
Type of rating scale where different number assignments are used; severe pain is 5 instead of 10
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NCCN Classification
Standard way of classifying pain intensity
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Analgesia, Activities, Adverse Events, Aberrant Drug Taking, Affect
Optimize pain treatment outcomes in these give dimensions (5As)
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Analgesia
Determine dimension (5As): Optimizing pain relief
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Activities
Determine dimension (5As): Optimizing psychosocial functioning
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Adverse events
Determine dimension (5As): minimize possible AEs
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Aberrant Drug Taking
Determine dimension (5As): should be managed to avoid possible addiction-related outcomes
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Aberrant Drug Taking
Indicator of drug misuse and/or abuse
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Affect
Determine dimension (5As): refers to the emotional component of the pain; pertains to the relationship between pain and mood
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Non-opioids, adjuvant therapies
These should be given to manage mild pain unless Px is contraindicated due to AE or potential drug interactions
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short-acting opioids
This may be added to non-opioids and adjuvant therapies as needed to manage moderate pain
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30 - 50%
short-acting opioids are titrated with the goal of increasing the daily dose by --- every day
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long-acting opiods
These may be considered if the Px consistently requires 3-4 doses of short-acting opioids for managing moderate pain
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regular schedule, rescue dose
For persistent moderate pain, you may initiate --- of opioid with *---* as needed
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Opioids
These are used to manage severe pain
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Hospital, inpatient admission
For severe pain, -- or -- may be done to achieve patient-specific goals for comfort and function
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Mild
Determine intensity of pain based on treatment given:

non-opioid +/- adjuvant analgesics
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Moderate
Determine intensity of pain based on treatment given:

non-opioids +/- adjuvant therapies +/- weak opioids
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Severe
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

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short half-life, standard staring DOC

PO preferred
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Hydromorphone
Pure; Mu receptor agonist, weak delta receptor agonist

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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

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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

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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

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Possible AE: Torsades de pointes, QTc prolongation
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Oxycodone
Pure; Mu, kappa, and delta receptor agonist

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similar analgesic and AE to morphine

short half-life
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Hydrocodone
Pure; Mu and delta receptor agonist

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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

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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

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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

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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

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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

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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

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has risk for hepatotoxicity and renal impairment

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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

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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
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Hormonal therapy, chemotherapy, corticosteroids, radioisotopes
Treatments that may be considered if Px has diffuse bone pain without oncologic emergency
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Local RT, nerve block, vertebral augmentation, radiofrequency ablation
Treatments that may be considered if Px has local bone pain without oncologic emergency
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Surgical intervention
If bowel obstruction is due to cancer, this treatment should be considered.
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Corticosteroids, metoclopramide
If px has partial bowel obstruction, these medical management may be considered
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Bowel rest, nasogastric suction, percutaneous gastrostomy drainage, corticosteroids, H2 blockers, anticholinergics, ocreotide
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

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pain comes and goes but is chronic

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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)

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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
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Codeine, morphine, hydromorphone, hydrocodone, oxymorphone
used in caution for Px with fluctuating renal function

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metabolites of these drugs may accumulate