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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