Analgesia Flashcards
Define hyperalgesia
A decrease in pain threshold/increase in perceived pain for a given noxious stimulus
Define appropriate pain
Pain while injury is still there
Define chronic/pathologic pain
Pain that extends beyond the healing process
Describe the effect of post-injury analgesia on post-injury hypersensitivity
- Analgesia will decrease hypersensitivity and pain
- Effects only last as long as analgesic action
- Once wears off, go back up to hypersensitivity that would have been present without analgesia
- Repeated doses until patient will no longer experience pain
Explain post-injury hypersensitivity
- Following injury, will have a hypersensitive period where contact to the site is painful
- Pain may continue after the injury has healed
Describe the effect of pre-emptive analgesia on post-injury hypersensitivity
- Analgesia is in effect at the time of injury (surgery)
- No hypersensitivity occurs after
- No chronic pain
What is IVRA and what is it used for?
- Intravenous regional anaesthesia
- Good for providing anaesthesia and analgesia in an area where it is needed, especially in cattle e.g. for claw removal
Name different classes of analgesic drugs and state whether they act peripherally or centrally
- Opioids (central)
- Alpha2 agonists (central)
- Local anaesthetics (peripheral)
- NSAIDs (peripheral)
Where can analgesic drugs act?
- May act at site of injury, decrease pain associated with inflammatory reaction
- May alter nerve conduction
- May modify transmission in dorsal horn
- May affect central component and emotional aspects of pain
Name the opioid receptors and state which is the most important
- Mu (most important)
- Delta
- Kappa
- Nociceptin
What is nociceptin?
A pro-nociceptive receptor
Name the opioids used in analgesia
- Morphine
- methadone
- pethidine
- Fentanyl
- Buprenorphine
- Butorphanol
Outline the key features of morphine (duration of action, routes of administration, licensing, effect on MAC/MIR)
- Most efficacious opioid at relieving pain
- Significantly reduces MAC and MIR
- Can be given PO, SC, IM, IV, CRI, epidural
- Duration of action approx 4 hours
- Not licensed, schedule 2 controlled drug
Outline the key features of methadone (site of action, administation, side effects, uses, licensing, duration of action)
- Action on NMDA receptor, involved in chronic pain
- Norepinephrine and serotoning reuptake inhibitor
- 4 hours duration of action
- Used as premed, sedative, introp, in recovery, CRI
- IV administration, poor oral availability
- Licensed for dogs and cats
Describe the key features of pethidine (duration of action, administration, licensing)
- Significant negative inotropic effects, increase heart rate with no cardiac output change
- Controlled drug Schedule 2, licensed for dogs, cats and horses
- Duration: 1.5hours
Describe the key features of fentanyl (uses, administration, drug schedule)
- Intraop as bolus, at induction with BZD
- IV, CRI, transdermal patches, spot ons
- Controlled drug, Schedule 2
Describe the key features of buprenorphine (administration, licensing, drug schedule, uses)
- High potency, lower efficacy
- Used for mild-moderate pain, good sedative, long duration of action
- IV administraiton, oral transmucosal route
- Peak effect after 45-60mins
- Licensed for dogs, cats, horses
- Schedule II drug but does not need recording
Describe the receptor affinity of buprenorphine
Partial agonist, strong affinity for mu, kappa antagonist
Describe the key features of butorphanol (adminstration, uses, licensing)
- Oral, IV
- Useful in combination with ACP for sedation of cardiac patients
- Antitussive
- Licensed fo rdogs, cats and horses
Describe the receptor actions of butorphanol
- Kappa agonist
- Mu antagonist
List potential unwanted effects of opioids
- CVS effects
- Pruritus
- Urinary retention
- Ileus
- Pancreatic duct
- Pyrexia
- Miosis
- Mydriasis
- Vomiting and nausea
Describe the receptor actions of morphine
- Full agonist
- Mu, delta and kappa receptors
What is the main side effect seen with morphine?
Vomiting
Describe the receptor action of methadone
- Full mu agonist
- Affinity for NMDA receptor