opioids Flashcards
Butorphanol
u antagonist and k agonist. thus reverses sedation and resp depression but still maintains analgesia.
(torbutrol, stadol, torbugesic - opioid agonist-antagonists)
Morphine
u agonist
-less lipid soluble (slower onset)
-dont give IV (histamine release and hypotension)
-some dysphoria
-6 metabolite has analgesic effect and 3 metabolite has excitatory effects
analgesia 4-6 hrs after IM
Oxymorphone
u agonist.
- no histamine release when IV
- good CV stability
- analgesia 2-4 hrs after IM
- least amount dysphoria
Hydromorphone
u agonist
- no hist release but some excitement (IV)
- good CV stability
- more sedation than oxymorphone
- analgesia 2-3 hrs IM (longer in cats)
- CHEAP
- dogs vomit, cats get dysphoria if not in pain (premed sit.)
- alot of resp depression
Fentanyl
- u agonist
- profound analgesia
- CRI, transdermal
- pronounced bradycardia (vagal) when IV (otherwise good CV stability)
Remifentanil
- u agonist
- ultra short acting-used as CRI and faster anesthetic recover
- bradycardia, hypotension, resp. depression and histamine release (all signif. amts)
- NON-HEPATIC METABOLISM (muscle and intestine) thus used for patients with liver disease
- very expensive
Butrophanol
u antagonist, k agonist
mild to moderate analgesi
-low doses partially reverse effects of pure agonist
-Torbugesic = brand
-1-4 duration for somatic pain, less for visceral and less for cats.
Buprenorphine
Partial u agonist, k antagonist (opp. to butrophenol)
- long duration (6-8 hrs)
- good lingual absorption
- diff. to reverse with naloxone
Tramadol
Weak u agonist (partial?)
-racemic mixture with 30 metabolites (11 are analgesic)(O-desmethyltramdol)
-OK for cats and horses
-serotonin and NE reuptake inhibitor (some alpha 2 action)
MULTIMODAL ANALGESIA!