Opiates Flashcards
Fentanyl analgesic dose
As adjuvant to inhaled anesthesia
1-2mcg/kg analgesia
2-20 mcg/kg w/ inhaled anesthesia
Fentanyl dose as primary anesthetic
50-150 mcg/kg
Are opiods reliable as a sole anesthetic
Why?
No
Unreliable anmesia No muscle relaxation Post-op ventilatory depression Sympathetic breakthrough possible Absorbed by CBP circuits
Fentanyl analgesic effects go hand in hand with
Ventilatory depressant effects
Causes lead chest
Too rapid and too large fentanyl dose
Transdermal fentanyl delivers
75-100mcg/hg
Peaks 18 hours
Fentanyl lollipops deliver _____
Risk of
5-20 mcg/kg
Risk of PONV and hypoxemia
Sufentanil dose
0.2-0.6 mcg/kg w/ inhalation anesthesia
8-30 mcg/kg for cardiac
Remifentanil dose
Up to 1 mcg/kg bolus
0.5-2 mcg/kg/min infusions
Morphine dose
2-15 mg adult
0.1 mg/kg peds
Meperidine dose
0.5-1.5 mg/kg.
Shivering
Hydromorphone dose
- 25-2 mg adult
0. 01-0.04 mg/kg peds
Meperidine principle metabolite
Elimination 1/2 life of metabolite
Normeperidine
15 hours
Greater effect in elderly, malnourished, liver failure
Fentanyl has much greater volume of distribution than morphine due to
Greater lipid solubility
Unlike morphine Sufentanil has rapid penetration of
BBB
Enhanced neonate effect to Sufentanil due to
Lower plasma protein levels so less binding sites
Termination effect of Sufentanil due to
Redistribution to inactive tissues and metabolism
Remifentanil metabolism
Provides for
Hydrolysis at ester linkage
Short action
Precise titration
No cumulative effect
Rapid recovery
Recovery from Remifentanil infusion
5-10 minutes regardless of duration of infusion
Neuroaxial opiods (fentanyl/Sufentanil) work in part via
Systemic absorption
Absorbed into epidural fat and epidural space venous plexus
and CSF
Cephalad movement of opiods
Greater with less lipid soluble (morphine)
Follows CSF currents to brain
Opiods work by imitating
Endogenous opioids
Only what 2 types of opiods bind to receptors
Non-ionized
Levorotary
Opioid receptor activation decreases NTS transmission via
presynaptic NTS inhibition
Mos important opioid receptor in anesthesia
Mu
CNS sites of opioid analgesia
- ascending pain sensory pathways
-descending pain modulation pathway
- ascending
Nociceptive nerve endings
Spinal cord
Thalamus - descending
Mid brain
Medulla
First drug shown to bind to mu receptors
Morphine
First drug to attatch to kappa receptors
Ketocyclazocine
Mu receptor agonist given to
Decrease perception of pain
Ventilatory depression with mu receptor agonist occurs where
Nucleus of slitract, nucleus ambiguous, parabrachial nucleus
Kappa receptors are a mixed agonist/antagonist site causing
Some analgesia, less than mu
Dysphroia, sedation
Facilitate mu activities
Delta receptors