Neuropathic Pain Flashcards

1
Q

what does gabapentin targget

A

calcium channel (central sensitization)

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2
Q

what do TCAs target

A

NE/serotonin receptor

disinhibition

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3
Q

what so SNRIs target

A

NE, serotonin (disinhibition)

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4
Q

what does lidocaine target

A

sodium channels (peripheral)

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5
Q

efficacy of neuropathic pain meds

A

not a lot of eveidednce
very few comparative trials suggest similarity
dont look at the NNT poor studies behind them
can consider them all the same and pick based on the patient

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6
Q

should we use opioids

A

very low eficacy and lots of dependence and abuse so no

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7
Q

is tramadol an exception

A

besides opioid receptor agonist its also inhibits NE and serotonin reuptake
lower abuse potential but still not that great

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8
Q

what do we know about functioning

A

insufficient evidence regarding quality of life but we can assess this in our patients

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9
Q

TCA side effects

A

constipation, dry mouth
weight gain
orthostatic hypotension
sedation

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10
Q

TCA cautions

A

elderly, dementia, glaucoma, urinary retention, cardiac disease

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11
Q

gabapentin and pregabalin SE

A

dizzy
sedation
peripheral edema

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12
Q

gabapentin cautions

A

elderly
edema
fall risk
abuse potential

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13
Q

SNRI SE

A

nausea - goes away with time
increased BP
dizziness

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14
Q

SNRI cautions

A

hypertension

biploar

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15
Q

tramadol SE

A

nausea
constipation
sedation
dizziness

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16
Q

tramadol cautions

A

opioid dependence
addiction risk
seizure risk

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17
Q

3 options worth a trial but just warn patient that most experience side effects

A

TCA
gabapentin
SNRI

18
Q

non pharms

A
meditation 
psychosocial 
CBT 
music
exercise? - good for other stuff 
heat and ice
19
Q

dosing trial for TCA

A

start 10-25 HS to 50-100HS

max 150

20
Q

dosing trial for gabepentin

A

start at 300mg/day then 300-900TID

max 1200TID - max dose just see a plateau and increase in SE

21
Q

dosing trial for pregabalin

A

start 75 BID then 150-300 BID

22
Q

dosing trial for duloxetine

A

start 30 mg then go up to 60mg

23
Q

dosing trial for venlafaine

A

37.5daily

then up to 150-225 daily

24
Q

how long is an adequate trial of meds

A

once reach the low end of the usual effective dose then 2-4 weeks

25
Q

onset for pain meds

A

1 week

26
Q

ways to incease dose

A

fast: increase 50-100% every 3 days
slow: increase 50-100% every week

27
Q

why do we start low and go slow

A

no rush
not worth risking harm to the patient
side effects may result in a loss of a viable option
higher doses have a low likelihood of resulting in greater benefit

28
Q

drugs to use if patient has depression or anxiety

A

TCA - but we tend not to use doses as high as in depression

SNRI

29
Q

drugs to use if patient has insomnia

A

gabapentin

TcA

30
Q

drug to use if patient has osteoarthritis

A

duloxetine

tramadol

31
Q

drug to use if patient has migraines

A

TCA

32
Q

monitoring timeline

A

1 week to se how their doing, side effects

2-4 weeks for efficacy: pain level and functioning

33
Q

if patient sees no benefit try

A

increase dose if not at upper dose

it at upper dose stop and switch

34
Q

if patient experiencing some benfit from med try

A

continue and maybe increase the dose or add another agent

35
Q

if side effects not tolerable try

A

if there was a benefit at a lower dose decrease the dose and add another agent
or stop and switch

36
Q

if med tolerable and effective reassess for ongoing need in

A

3 months

37
Q

should we use combination therapy

A

not a lot of evidence

may be beneficial to have ttwo diff moa?

38
Q

which two do we absolutely not combine

A

gabapentin + opioid

NNT = NNH

39
Q

lidocaine advantages

A

immediate onset

min systemic absorption

40
Q

capsaicin recommendation

A

doesnt work

burning just cuases a distraction

41
Q

topical option if very resistant to all treatments

A

ketamine

42
Q

patient counseling points

A

benefit
onset
side effects
cost/coverage