Pain 4 Flashcards

1
Q

What are the steps in conducting an opioid trial?

A
  1. decide and document trial duration
  2. set and document functional goals (SMART)
  3. choose opioid and optimal dose
  4. implement with safer opioid prescribing principles, universal precautions, counselling about AEs
  5. reassess and measure opioid effectiveness
  6. monitor for adverse effects, medical complications, adherence, and risks
  7. end titration
  8. document the trial
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2
Q

What is considered a reasonable trial of opioids?

A

3-6 months

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3
Q

What is the lowest starting dose of an opioid for an opioid-naive patient?

A

5-10 MME/dose or a daily dosage of 20-30 MME/day

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4
Q

Which dosage form should we start with for opioids?

A

IR
consider transdermal buprenorphine for those who can afford it (less risk of respiratory depression, tolerance, opioid-induced hyperalgesia)

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5
Q

At what strength should we initiate an opioid?

A

start with low dose and then increase the dose in small quantities
-opioids produce a graded analgesic response
slow titration:
-avoids unnecessarily high doses
-reduces the risk of sedation and overdose as it ensures that a dose increase does not exceed the patients tolerance

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6
Q

What are the recommendations from Canadian Opioid Guidelines for choosing an opioid dose?

A

ideally restrict to < 50 MEQ/day
avoid higher than 90 MEQ/day
harms increase with doses > 50-90 MEQ
long-acting agents dosed on a scheduled basis considered more useful

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7
Q

What are some patient factors which further warrant starting opioids at lower doses?

A

increased age
decreased weight
sleep apnea
impaired renal or hepatic function
interacting drugs/concurrent CNS depressants
pulmonary disease or conditions that cause decreased pulmonary drive
seizures
risk of developing GI obstruction

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8
Q

What is the onset of opioids?

A

IV direct: 3-5 min
IV intermittent: 10-15 min
IM/SC: 10-15 min
oral: 15-30 min

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9
Q

How is an optimal dose reached for opioids?

A

with a balance of three factors:
1. effectiveness
-improved function or at least 30% decrease in pain intensity
2. plateauing
-effectiveness plateaus: increasing dose yields negligible benefit
3. adverse effects/risks
-adverse effects and risks are manageable

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10
Q

What is the issue with PRN opioids for breakthrough pain?

A

PRN opioid for breakthrough pain in CNCP can be problematic:
-patients may rely on PRN opioids
-leads to dose escalation without documented benefit on pain and function
better for patient to learn other coping strategies
PRN use may result in cycling of “pain-pain relief and subtle euphoria”

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11
Q

What are some important education pieces to provide with opioids?

A

possible functional benefits (limited in most cases)
adverse effects (common, increase over time)
drug interactions (increase of toxicity)
-may even consider deprescribing other drugs before opioid trial
importance of active, self-management strategies +/- ongoing exploration of non-opioid pharmacotherapy

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12
Q

How often should we follow up with a patient during an opioid trial?

A

q2-4 weeks
-repeat initial pain assessment questionnaires
-revisit co-created functional goals (objective improvements should be incremental, 30% subjective pain reduction=clinically significant)
-document!

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13
Q

What are some considerations to make before an opioid dose exceeds 90-200 MEQ/day?

A

has the pt shown appropriate opioid effectiveness in response to the dose increases to date?
is the diagnosis accurate?
is opioid considered effective for the patients diagnosis?
is further investigation and/or consultation required?
are non-opioid treatment options available?
is there an inadequately treated mental health disorder?

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14
Q

What are some medical complications of opioids?

A

neuroendocrine abnormalities
erectile dysfunction
sleep apnea
opioid-induced hyperalgesia

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15
Q

What are some extra precautions you could consider for a patient at high risk of opioid misuse?

A

ask the patient to bring their medication for pill counts and to explain any discrepancies
using screening tools to check for aberrant drug-related behaviours

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16
Q

What should be done if you suspect opioid use disorder?

A

assess and refer for treatment
-use precautions/tigher boundaries
treat both pain and OUD

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17
Q

When have we hit the “end” of an opioid trial?

A
  1. the “optimal” dose is attained
    -balance of effectiveness, plateauing, adverse effects/risk
  2. trial is considered a “failed” trial
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18
Q

What is a “failed” trial of opioids?

A

a) the patient experiences insufficient analgesia after 2-3 dose increases and/or unacceptable AEs and/or medical complications and/or risks are too high
b) there are indications of aberrant use and/or OUD
c) insufficient improvement in ability to function per SMART goals

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19
Q

What are some universal precautions that should be taken with opioids?

A

complete OUD screening with Opioid Risk Tool
one opioid prescriber, one pharmacy
urine drug screens (baseline, random q6mos)
limited quantities (total, part-fill, intervals)
lock box at home
random pill counts
treatment agreement (boundaries and rules)

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20
Q

What should we always have when starting an opioid?

A

an exit strategy

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21
Q

When do we consider tapering opioids?

A

when opioids taken > 1 week at regular intervals

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22
Q

What are some opioid taper precautions?

A

pregnancy
-severe, acute opioid withdrawal has been associated with premature labour and spontaneous abortion
unstable medical and psychiatric conditions can be worsened by anxiety associated with withdrawal
-tapering after long-term use may increase risk of overdose and mental health crises
if opioid use disorder
-may lead to accessing from unregulated sources

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23
Q

True or false: the approach to an opioid taper will be the same regardless if the person has been on short-term or long-term therapy

A

false
approach will differ for long-term vs short-term

24
Q

What are some symptoms of opioid withdrawal?

A

early (hrs-days)symptoms may include:
-anxiety, sweating, dilated pupils, brief increase in pain
late (days-weeks) symptoms may include:
-rapid breathing, yawning, tremor, piloerection, NV
prolonged (weeks to 6mo) symptoms may include:
-fatigue, malaise, psychological, bradycardia, low body temp

25
Q

What are some pharmacological options for management of opioid withdrawal?

A

physical withdrawal (sweating, anxiety, insomnia, nausea)
-clonidine
aches/pains/myalgias
-NSAIDs, acetaminophen
bowel function (diarrhea)
-loperamide
nausea/vomiting
-dimenhydrinate
anxiety/irritability/cramps/rhinorrhea/insomnia
-hydroxyzine
insomnia
-non drug and sleep hygiene measures
-trazodone
sweating
-oxybutynin

26
Q

What are indications to consider tapering an opioid?

A

the patient requests dosage reduction or d/c
pain improves and might indicate resolution of underlying cause
opioid therapy has not meaningfully reduced pain or improved function
the pt is receiving higher opioid dosages without receiving benefit
the pt experiences side effects that diminish QOL or function
evidence of opioid misuse
the pt experiences an overdose or other serious AEs or has warning signs of an impending event
the pt is using substances or has medical conditions that increase risk for AE

27
Q

What are the potential benefits to tapering an opioid?

A

lower risk of toxicity/overdose
less side effects and long-term complications
mood and energy improve
less perseveration on pain and opioid around the clock
may report improvements in mood and pain
-decreased withdrawal-mediated pain
-decreased hyperalgesia
-“reset pain threshold”
cost-saving

28
Q

What are some general considerations prior to an opioid taper?

A

determine what goal is reasonable
-dose reduction vs complete d/c
-overall goal is to improve function, reduce pain intensity
discuss that plan may be paused or reassessed if pain and/or function deteriorates or withdrawal symptoms persist
avoid making arbitrary dosing endpoints
understand that complete taper may take months-years

29
Q

What are the limitations of opioid guidelines?

A

limited evidence available to guide the design of tapering regimens
no evidence to guide specifics of tapering regimens for chronic pain patients
-must be individualized
gaps in literature remain regarding:
-tapering rate
-medication choice
-use of alpha-2 agonists to manage withdrawal

30
Q

Describe a brief overview of the adjustment strategies for opioids.

A

slow and gradual taper: decrease dose 5-10% q2-4wks
rapid taper: decrease dose 10-20% q1-3 days
rotating opioids; switch to alt opioid at 50-75% of current MEQ
cross-over rotation: decrease dose of one while upping new
transition to OAT: switch to methadone or buprenorphine/naloxone

31
Q

How much do we decrease an opioid dose by when doing a slow and gradual taper?

A

decrease dose by 5-10% q2-4 wks
-go slower as taper gets closer to finishing
-once at 1/3 original dose may slow taper down to 5% dose q4-8wks to improve success
-may need to change formulation for smaller doses

32
Q

How long does it take to perform a slow and gradual taper for an opioid?

A

may be completed in 1-6 months
-longer may be preferred (12-24mo) if long history of use or anxious/difficulty coping
-some allow 1 month of taper per year of opioid tx

33
Q

What is common with a slow and gradual opioid taper?

A

rebound or withdrawal pain
-may need to slow or temporarily pause taper
give time for pain to resolve (often 2 wks) before the next dose decrease

34
Q

How much do we decrease an opioid dose when performing a rapid taper?

A

decrease dose 10-20% q1-3 days

35
Q

How long does it take to complete a rapid opioid taper?

A

often completed in 1-2 weeks
-often in supervised setting

36
Q

What is common with a rapid opioid taper?

A

withdrawal symptoms are common
-use objective scales to monitor withdrawal (COWS, SOWS)
-supportive meds

37
Q

Which patients might it be a good idea to pursue a rapid opioid taper?

A

at very high risk of opioid harms
highly motivated to d/c their opioid quickly
on low doses of opioids for short period of time

38
Q

How do we rotate/switch opioids?

A

switch to an alt opioid at 50-75% of the current MEQ
after rotation, pause taper for ~1 month, allowing stabilization, then rotating again to a different opioid can be useful for some

39
Q

What are the advantages of rotating/switching opioids?

A

takes advantage of incomplete cross tolerance between opioids
gives a “head start” on the taper
can facilitate switching to an opioid that is easier to taper
can improve pain control +/- decrease opioid related AEs

40
Q

What are the suggested initial doses of new opioids when switching?

A

if previous dose was high (>200mg total daily MEQ)
-new dose: 50% or less of previous opioid
if previous dose was low (<200mg total daily MEQ)
-new dose: 75% of previous opioid

41
Q

Which opioid do we use for rotating?

A

review comorbidities & medication history
look for an ER product the person is not currently taking/has not taken previously

42
Q

What are the benefits of once-daily options?

A

decreased pill burden
increased adherence
maintain therapeutic level through the day
decreased psychological focus on opioids
decreased chance of using tomorrows supply

43
Q

Summarize the opioid conversions.

A

morphine:
-to convert to morphine: multiply by 1
-to convert from morphine: divide by 1
codeine:
-to convert to morphine: multiply by 0.15
-to convert from morphine: multiply by 6.67
oxycodone:
-to convert to morphine: multiply by 1.5
-to convert from morphine: multiply by 0.667
hydromorphone:
-to convert to morphine: multiply by 5
-to convert from morphine: multiply by 0.2

44
Q

What is the potency of parenteral opioids?

A

2x as potent as oral

45
Q

What is cross-over rotation?

A

simultaneously decreasing the dose of one opioid while up-titrating a new opioid
not a preferred approach as it can be confusing and risks the patient having two opioids

46
Q

What is a possible advantage of cross-over rotation?

A

reducing risk of withdrawal symptoms during rotation to new opioid

47
Q

What are endocannabinoids?

A

naturally produced by our body
-AEA
-2-AG

48
Q

What are phytocannabinoids?

A

come from a plant
-THC: euphoria, appetite, alter pain perception
-CBD: anti-infl, analgesic, anti-anxiety

49
Q

What are synthetic cannabinoids?

A

prescribed
-nabilone: synthetic THC
-nabiximol: whole plant extract

50
Q

What are the routes of admin for cannabinoids?

A

smoked, vaporized, oral, SL, topical, rectal
avoid inhaled products

51
Q

What are the short term effects of cannabinoids?

A

mostly linked to THC
dizziness, dry mouth, drowsiness, nausea
decreased learning, memory, psychomotor deficits
increased risk of motor vehicle accidents
increased risk of falls in the elderly
associated with psychosis
5-fold risk of MI within 1hr of smoking

52
Q

What are the effects with long-term use of cannabinoids?

A

cognitive impairment, decreased adolescent IQ
increased anxiety, depression, bipolar
down-regulation/desensitization of receptors with chronic high doses
dependence & withdrawal
cannabis use disorder
cannabis hyperemesis syndrome
increased LFTs

53
Q

What are some drug interactions of cannabinoids?

A

additive with CNS depressants and anticholinergics
involved in CYP 450 metabolism
-CBD may inhibit 3A4, 2D6, 2C19
-CBD substrate for 3A4, 2C19

54
Q

What is the strength of evidence of cannabinoids for pain?

A

could consider for refractory neuropathic pain
-unclear benefit
-tried 3 other agents
harms exceed benefits for OA and chronic LBP

55
Q

If we are going to try a cannabinoid for pain, which type would be preferred?

A

pharmaceutical cannabinoid > storefront cannabis
-nabilone, nabiximol