Week 3 Opiods Flashcards
Morphine
low oral to parenteral ratio b/c high 1st pass metabolism- low analgesic effect- give parenterally; relieves breathing difficulty caused by pulmonary edema w/ LT ventricular heart failure; decreases: anxiety, cardiac load, venous load; 4-5 hours
Fentanyl
strong opiod agonist- low O/P ratio- P450 metablism
Codeine (Dextromethorphan)
partial mu opioid agonist- high O/P ratio- metabolized into morphine-then its effective- CYP2D6 metabolized; acts by reducing the cough reflex when given @ doses that will not cause analgesia- Dextromethorphan has less addictive properties & less constipation; 3-4 hours
Hydrocodone
Partial mu opioid agonist- medium O/P ratio; give orally-reasonable analgesic action; 4-6 hours
Oxycodone
partial mu opioid agonist; medium o/p ratio; 3-4 hours
Pt who has tolerance to opioids cant overcome these side effects
miosis and constipation
Morphine & Oxycodone
chronic & severe pain, not best for sharp, intermittent pain- hospice care: fixed-interval admin w/ reg dose
Fentanyl
transdermal patch given over long periods if slow GI transit occurs from oral sustained release; buccal for short breakthrough pain; decrease respiratory rate; opioid choice for adjunct anesthesia; used before anesthesia & surgery for sedative, anxiety reducing & analgesic properties; used if a need exists to minimize the risk of cardiovascular depression; 1-1.5 hours
Methadone
synthetic w/ equi-anelgesic potency to morphine
maintenance in rehab programs; withdrawal symptoms less severe; 4-6 hours
Meperidine
less severe respiratory depression, constipation, biliary colic & urinary retention
strong anti-muscarinic effects- tachycardia is a contraindication; used to prevent shivering- actions on Alpha-2 adrenoceptor subtypes; 2-4 hours
Codeine & Hydrocodone
Partial agonists; pathological cough suppression; often combined w/ other drugs like aspirin or acetaminophen; can antagonize strong agonists
Loperamide or Diphenoxylate
peripheral neuropathic pain; action @ at mu opioid receptors while lacking CNS effects; used for diarrhea- has selective actions in the GI tract- poor solubility properties thus useful for parenteral routes
Tramadol
very weak opioid agonist; inhibits serotonin & norepinephrine reuptake; treatment for chronic pain
Buprenorphine + naloxone
maintenance for heroin addicts; long lasting- avoids 1st pass metabolism; kappa antagonist & partial mu agonist- resistant to naloxone reversal; 4-8 hours
Butorphanol
kappa opioid agaonist & partial mu agonist; greater sedation than nalbuphine & buprenorphine; treats severe pain- migraine or labor; not reversed w/ naloxone if overdose; 3-4 hours