Pain Assessment and Treatment Flashcards

1
Q

what pain meds inhibit perception?

A

inhibit perception
1. anesthetics
2. opioids
3. alpha 2 agonists
4. benzos
5. phenothiazines

inhibit transmission
1. local anesthetics
2. alpha 2 agonists
3. NMDA agonists

modulation of spinal pathway

inhibit transduction

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2
Q

describe opioids

A
  1. opioid receptors throughout body
  2. central and peripheral action
  3. peripherally prevent neurotransmitter release and nociceptor sensitization, esp if inflam present
  4. centrally, modulate afferent input onto substantia gelatinosa; blunt pain perception in cortical areas
  5. best used multimodally
  6. profound analgesia
  7. many adverse effects
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3
Q

describe the effects and uses of opioids

A

effects:
-analgesia
-sedation
-hypoventilation
-bradycardia
-vomiting
-cough suppression
-occasional dysphoria

  1. very good agents for use in young, old, debilitated, ill animals
  2. can be injectable, PO, transdermal patches
  3. controlled drugs
  4. antagonists available
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4
Q

describe tramadol

A
  1. synthetic opioid; atypical mu-agonist (adjuvant drug, not used in opioid category)
  2. MOA:
    -moderate mu agonist (5-10 times less than morphine), weak kappa agonist
    -decrease reuptake of norepinephrine and serotonin
  3. active metabolites: O-desmethyltramadol (active version)
    -very small amounts in dogs and horses = no work super well
  4. no respiratory depression, no tolerance
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5
Q

describe alpha 2 agonists

A
  1. in locus ceruleus, thalamus, cortex
    -sedation and supraspinal analgesia
  2. binding receptors in dorsal horn of the spinal cord = spinal analgesia
  3. prolong the duration of nerve blocks via inhibition of C-fibers
  4. effects:
    -sedation, analgesia, muscle relaxation
    -bradycardia (AV blocks), peripheral vasoconstriction (hypertension followed by hypotension), decreased CO
    -vomit, decreased GI motility
    -hyperglycemia
    -increased diuresis
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6
Q

describe NMDA agonists

A
  1. analgesic effect via 2 mechanisms
    -blockade of dorsal horn NMDA receptors to prevent central sensitization
    -activation of opioid receptors
  2. also has a local anesthetic effect, blocking action potentials along nociceptive axons
  3. generally administered as a bolus at induction of anesthesia
    -can be given as a CRI at sub-anesthetic doses
  4. also include: amantadine, gabapentin, methadone, nitrous oxide
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7
Q

describe NSAIDs

A
  1. act peripherally at sites of inflammation
    -block formation of prostaglandins and thromboxanes
  2. in spinal cord: block glutamate and substance P receptors
  3. side effects: gastro-enteric system, kidneys, platelets
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8
Q

describe NSAID MOA

A
  1. inhibit COX-1 and COX-2
  2. classified based on COX1 versus COX2 selectivity
  3. COX2 selective drugs have more anti-inflammatory effects
    -meloxicam, carprofen, the coxibs
    -may have less severe adverse effects
  4. COX1 selective drugs have more anti-thrombotic effects: aspirin, ketoprofen
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9
Q

describe corticosteroids

A
  1. act peripherally at sites of inflammation

2, block phospholipase A2 and formation of prostaglandins, thromboxanes, and leukotrienes

  1. side effects:
    -GI, kidneys, coagulation, hyperglycemia, Cushing’s, immunosuppression
    -not usually used to treat pain, used more to treat acute inflammation that will cause pain
    -NO COMBINE WITH NSAIDS = more side effects
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10
Q

describe local anesthetics

A
  1. block the transduction and transmission of nociception by blocking Na+ channels
  2. nociceptive impulse never reaches dorsal horn = spinal anesthesia
  3. can be used for local techniques
    -ring block, brachial plexus block, epidural
  4. IV lidocaine:
    -IV bolus and/or CRI
    –NO bupivicaine (cardiotoxic)
    –no lidocaine in cats (severe cardiovascular depression)
    -transdermal patch
  5. systemic administration: analgesic, anti-inflam, anti-arrhythmic, prokinetic, free-radical scavenger, reduced anesthetic requirements
  6. side effects: convulsion, coma, CV depression, cardio-resp arrest, neurotox, methemoglobinemia
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11
Q

what are adjuvants? (3)

A
  1. anticonvulsants
  2. NMDA-agonists
  3. tricyclic antidepressants
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12
Q

describe gabapentin

A
  1. MOA not well known but considered an anticonvulsant
    -increases synth and decreases reuptake of GABA
    -decreases synth of glutamate
    -Ca2+ channel block at spinal and supraspinal levels blocking central sensitization
    -may inhibit NMDA receptors
  2. side effects: drowsiness, GI (V/D, constipation)
  3. used most commonly for neuropathic pain
    -no evidence that it works on acute pain, may be helpful for chronic
  4. clinical use:
    -may be useful as an adjunct to a multimodal analgesic approach
    -may decrease incidence of chronic pain if used post-op
    -behavior modification in cats
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13
Q

describe amantadine

A
  1. NMDA receptor antagonist, may decrease central sensitization
  2. may enhance the effects of NSAIDs, gabapentin, and opioids
  3. clinical use:
    -may be useful as an adjunct to a multimodal analgesic approach
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14
Q

describe tricyclic antidepressants

A
  1. amitriptyline
  2. MOA:
    -decrease reuptake of norepi and serotonin
    -Na+ channel blockade
    -NMDA receptor antagonist
  3. clinical use:
    -may be useful as an adjunct to a multimodal analgesic approach, may be useful for neuropathic pain
  4. side effects:
    -low therapeutic index
    -sedation
    -anticholinergic effects: tachycardia, urinary retention, decreased GI motility
    -bradycardia
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