Opiods in Anesthesia
Transcript of Opiods in Anesthesia
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Opioids in anesthesiaOpium derived from dried juice of
poppy plant which contains over 20
plant alkaloids.including morphineand codiene.
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NARCOTIC AGONISTS
Site of Action *Opioid receptors are predominantly located
in the:
1-Brain stem (amygdala,corpus
striatum,periaqueductal gray matter and
medulla)
2-spinal cord (substantia gelatinosa).
3- GIT
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They act on 3 types of receptors: *
1. Mu receptors:analgesia,respiratorydepression,euophoria,and physical
dependence. 2.Kappa
receptors:analgesia,sedation,respiratorydepression,miosis.
3.Segma :dysphoria,hallucination,tachypnea,tachycardia.
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PHARMACOKINETICS -Rapied distribution through the body
following IV injection.
-It is metabolised by the liver and the majority
of the inactive metabolites are excreted
unchanged in the urine.
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PHARMACODYNAMICS
CNS: Opioids sedate through interfering with
sensory perception of painful stimuli.
**large doses produce unconsciousness but
they are generally incapable of producinganesthesia and it can not guarantee totalamnesia.
It may produce nausia & emesis throughstimulation of the chemoreceptor triggerzone.
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RESPIRATORY They result in dose related depression of
respiratory rate and minute volume.but
increase the tidal volume which will lead to a
slow deep respiration.Reversed by Naloxone
adminstration.
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CVS Opioids have litle myocardial depressant effect even
when adminstrated in high doses.
Supplementation with either N2O or Benzodiazepinesmy depress cardiac output.
They decrease systemic vascular resistance either bydecreasing sympathetic outflow or by releasinghistamine ( as Morphine) which producesvasodilatation & decrease SVR.
Synthetic opioids are less likely to release histamine.
They lead to bradycardia by stimulation vagal nucleusin the brain stem.
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GIT *Narcotics slow GI mobility and may result in
constipation or post operative ileus.
**increases biliary tract tone which may lead
to biliary colic eith patients with bile stones.
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OTHERS ***Increases the bladder sphincters tone.
And urine retention
***Anaphylactic
reactions,bronchospasm,chest wall regidity
and pruritis.
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FENTANYL & MORPHINE Fentanyl is the most commonly used during
induction of anesthesia due to its rapied
onset(highly lipid solubility)and predictable
duration of action about 30 minutes
**Morphine is used in the preioperative
period to provide long lasting analgesia.and it
should be adminstrated slowlyat a rate< 5mg/min to avoid excessive histamine release.
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Low doseAnalgesic
dose
Potency
Ratio
0.05-0.2mg/kg10 mg1Morphine
0.5-3 mic
g/kg
100
mcg
100Fentanyl
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NARCOTIC ANTAGONISTS NALOXONE:
It competes at the mu,delta,kappa andsigma receptors.
Peak effect 1-2 minutes. Duration of action 30-60 min.
Indicated in perioperative surgical
patientsnwith excessive sedation orrespiratory sedationnsecondary toopioids.
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Given in small incremental doses.
High doses of naloxone will result in sudden
reversal of analgesiac effects leading to abrupt
tachycardia,pulmonary edema,arrythmias and
cardiac arrest.
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