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55 Cards in this Set
- Front
- Back
Majority of drugs used for analgesia
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-opioids
-NSAIDs -Local Anesthetics |
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Analgesic drugs with no regional effects
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-NSAIDs
-Acetaminophen -Antiepileptics |
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Opioids
-use |
-most effective for most types of pain especially acute pain
|
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Opioids
-characterized by |
-analgesia without loss of proprioception or conciousness
|
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Opioids
-response depends on |
-opioid used (drug)
-species being treated -age and gender of the patient -condition or type of pain being treated (acute, chronic, somatic, visceral, neuropathic) -individual animal (genetics) |
|
Opioids
-analgesic effects |
-directly inhibit/modulate ascending transmission of nociceptive information from the spinal cord dorsal horn
-activate pain control circuits that descend from the midbrain to the spinal cord dorsal horn |
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Opioids
-non-analgesic effects |
-depression of respiratory center ----> decreased minute volume and increased arterial CO2
-increased GI tract tone with decreased peristalsis -Vagally mediated decreases in HR -Nausea and vomiting -effected thermoregulation -cough suppression -increased ADH ---> dec. urine production -histamine release (some opioids) -Excitement and dysphoria |
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Opioids
-vagally mediated decreases in heart rate are most evident with |
-potent mu agonists
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Opioids
-nausea and vomiting less likely in |
-partial agonists or mu antagonists
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Opioids
-effects on thermoregulation |
-hyperthermia in cats administered hydromorphone
-mild decreased temperature due to set point change |
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Opioids
-drugs that can cause histamine release |
-morphine
-meperidine |
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Opioids
-species susceptible to excitement and dysphoria |
-cats
-horses (Boxwalking) |
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Questions to ask for choosing an opioid
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-What type of pain will be treated?
-How would you rate the intensity or degrees of pain that is occurring or will occur? -How will the drug be given? -What will the treatment interval be? -Are there specific side-effects that you wish to avoid? -What species is being treated |
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Types of pain that may be treated with opioids
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-most frequently acute pain from surgery or trauma
-cancer pain may progress to where treatment with opioids is necessary -acute exacerbation of chronic disease (IVDD, osteoarthritis) |
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Specific opioid side effects that you may want to avoid
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-avoid vomiting with an esophageal foreign body
-hypethermia due to hydromorphone -decreased GI motility in horses |
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Opioids
-considerations for cats |
-high doses of mu agonists can cause dysphoria
-hyperthermia from hydromorphone |
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Opioids
-considerations for horses |
-possible increased locomotor activity and GI motility
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Opioids to use when there are concerns of locomotor and GI side-effects in horses
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-Kappa agonists, mu antagonists (Butorphanol)
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Opioids
-Ruminant concerns |
-GI motility
-rumen atony |
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Opioids
-avian concerns |
-kappa agonists may have better analgesia than mu agonists (unknown)
|
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Opioids
-main mu agonists |
-morphine
-hydromorphone -methadone -fentanyl |
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Opioids
-main partial mu agonists |
-buprenorphine
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Opioids
-main kappa agonists, mu antagonists |
-butorphanol
|
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Opioids
-main antagonists |
-naloxone
|
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Methadone
-duration |
2-6 hrs
-longer duration clinically than morphine |
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Methadone
-MOA |
-NMDA receptor antagonism
|
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Methadone
-pros |
-effective analgesic in horses with minimal excitatory effects
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Methadone
-cons |
-expensive
|
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Tramadol
-main MOA |
-inhibition of reuptake of norepinephrine and serotonin
|
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Most commonly used opioid in veterinary practice
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-morphine
|
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Morphine to use epidurally
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-must be preservative free
|
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Reason to use morphine epidurally
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-most water soluble opioid = longer duration of effect
|
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Epidural morphine
-pros |
-long duration of action (18-24 hrs)
-segmental analgesia (less sedation and behavioral effects) -good analgesia with no effect on proprioception or motor function |
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Epidural morphine
-cons |
-requires technical expertise
-increased cost -need to shave the area over the lumbosacral spine (aesthetics, slow to grow back) -potential side effects |
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Epidural morphine
-potential side effects |
-urinary retention
-pruritis -nausea and vomiting if the epidural is administered in awake animals -delayed respiratory depression in people |
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Major excitatory neurotransmitter in the CNS
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-Glutamate
|
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Glutamate receptors
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-AMPA
-Kainate -NMDA****** |
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Glutamate receptor with the biggest effect on nociception
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-NMDA
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How do NMDA receptors differ from the other glutamate receptors?
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-high calcium permeability
-magnesium blockade at resting membrane potential -may require glycine (co-agonist) for activation |
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NMDA receptor
-structure |
-heterotetrameric assembly of different subunits
NMDA receptors don't all look alike -mammals have 4 subunits of 2 receptors -some cells have a 3rd subunit for glycine -several isoforms of each subunit |
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NMDA
-variance in subunit composition due to |
-location in the nervous system
-age of the animal |
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NMDA
-reason for varied subunit composition |
-varied functions of a receptor
|
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NMDA at resting membrane potentials
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-inactive due to a blockade of extracellular magnesium even in the presence of glutamate
|
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How to activate an NMDA receptor
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--glutamate need to be released to bind to the receptor
-postsynaptic membrane needs to be depolarized to remove the magnesium blockade -NMDA mediated calcium influx then activates a series of signaling molecules within postsynaptic cells |
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NMDA receptor function on nociception
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-pivotal role in excitatory synaptic transmission and plasticity, including various brain processes such as memory ----> hallucination
-receptors are expressed in pain pathways from the periphery to the brain (critical role for triggering neuropathic pain) |
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Synaptic pasticity
-define |
-ability of the synapse between two neurons to change in strength in response to either use or disuse
|
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NMDA
-where are all subunits expressed |
-dorsal horn
|
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Method of possibly causing analgesia with fewer side effects
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-designing specific NMDA antagonists to target a specific receptor subunit
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NMDA antagonist drugs
-nonspecific |
-amantidine
-ketamine -phencyclidine -nitrous oxide -dextromethorphan -memantine -methadone -tramadol |
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NMDA antagonist drugs
-NR2B antagonist (specific) |
-ifenprodil
|
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Ketamine
-use |
-adjunct when treating chronic or neuropathic pain
-lower dose for analgesia than for anesthesia -often used in surgery for procedures where substantial pain was present prior to the procedure -adjunct analgesia for burn patients -possibly effective for treating central sensitization |
|
Ketamine
-route of administration |
-CRI (must use)
|
|
Ketamine
-surgeries where use may be indicated |
-total ear canal ablation
-limb amputation due to tremors -severe trauma |
|
Burn patient
-analgesic treatment |
Fentanyl CRI
-remained tachycardic -hunched up in cage Ketamine -seems more comfortable -eats small amounts Fluid and antibiotic therapy Wound debridement (distal limb nerve blocks) -off fentanyl -buprenorphine -continue ketamine -discontinue ketamine |
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NMDA anatagonist drugs
-drugs used to some success |
-amantidine
-dextromethorphan *cause anxiety and restlessness |