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Epinephrine / Adrenaline
 By Shamin Joshi
Its primarily a medication as well as hormone
Its an emergency drug
Its direct sympathomimetics drugs
Its 1st line drug used incardiac arrest
At low dose , beta effect (vasodilators ) on
vascular system predominant
At high dose , alpha effect ( vasoconstrictor )
are strongest
Chemical Structure
 molecular weight = 183.2.
 Epinephrine solution deteriorates rapidly
 On exposure to air or light, turning pink from
oxidation to adrenochrome and brown from
the formation of melanin.
Routes
 IV
 Intratracheal
 Continous infusion
 nebulisation
Metabolism
 Epinephrine is rapidly inactivated in the body and
is degraded by enzymes in the liver and other
tissues.
 The larger portion of injected doses is excreted in
the urine as inactivated compounds and the
remainder either partly unchanged or conjugated.
 The drug becomes fixed in the tissues and is
inactivated chiefly by enzymatic transformation to
metanephrine or normetanephrine either of
which is subsequently conjugated and excreted in
the urine in the form of sulfates and
glucuronides.
OrganEffects
 Heart - Increases heart rate
 Lungs - Increases respiratory rate
 Systemic- Vasoconstriction and vasodilation
 Liver - Stimulates glycogenolysis
 Systemic - Triggers lipolysis
 Systemic - Muscle contraction
Indication
 Anaphylactic shock
 Prolonged action of LA
 Cardiac arrest
 Bronchospasm
 Chronic orthostatic hypotension
 Topically , to stop bleeding
 Minimal dysfunction of brain
Dose
 La without adrenaline is 300mg or 4.4 mg/kg
 With adrenaline is 500mg or 7mg/kg
 Epineprine dilution of 1: 50000and 1: 100000
are considerably more effective
Epinephrine in lA
Advantage
 Prolongs duration of action of la by keeping them in
contact with nerve fibers
 Limits systemic absorption
 Decreasing possibility of systemic toxicity cause rate of
metabolism will match rate of absorption
 Decreases bleeding ( improves visualization )
Disadvantage
 Makes injection more painful
 Increase chances of local injury and necrosis
 May raise blood pressure and promote arrhymias
ADR
 Stinging
 Alergic lid rxn
 Systemic hypertension
 Arrythmia
 Throbbing headache ,
 Tremor
 Palpitation
 Teratogenic effects
Contraindication
 Severe hypertension
 Cardiac disease
 Thyrotoxicosis
Epinephrine

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Epinephrine

  • 1. Epinephrine / Adrenaline By Shamin Joshi
  • 2. Its primarily a medication as well as hormone Its an emergency drug Its direct sympathomimetics drugs Its 1st line drug used incardiac arrest At low dose , beta effect (vasodilators ) on vascular system predominant At high dose , alpha effect ( vasoconstrictor ) are strongest
  • 3. Chemical Structure molecular weight = 183.2. Epinephrine solution deteriorates rapidly On exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin.
  • 4. Routes IV Intratracheal Continous infusion nebulisation
  • 5. Metabolism Epinephrine is rapidly inactivated in the body and is degraded by enzymes in the liver and other tissues. The larger portion of injected doses is excreted in the urine as inactivated compounds and the remainder either partly unchanged or conjugated. The drug becomes fixed in the tissues and is inactivated chiefly by enzymatic transformation to metanephrine or normetanephrine either of which is subsequently conjugated and excreted in the urine in the form of sulfates and glucuronides.
  • 6. OrganEffects Heart - Increases heart rate Lungs - Increases respiratory rate Systemic- Vasoconstriction and vasodilation Liver - Stimulates glycogenolysis Systemic - Triggers lipolysis Systemic - Muscle contraction
  • 7. Indication Anaphylactic shock Prolonged action of LA Cardiac arrest Bronchospasm Chronic orthostatic hypotension Topically , to stop bleeding Minimal dysfunction of brain
  • 8. Dose La without adrenaline is 300mg or 4.4 mg/kg With adrenaline is 500mg or 7mg/kg Epineprine dilution of 1: 50000and 1: 100000 are considerably more effective
  • 9. Epinephrine in lA Advantage Prolongs duration of action of la by keeping them in contact with nerve fibers Limits systemic absorption Decreasing possibility of systemic toxicity cause rate of metabolism will match rate of absorption Decreases bleeding ( improves visualization ) Disadvantage Makes injection more painful Increase chances of local injury and necrosis May raise blood pressure and promote arrhymias
  • 10. ADR Stinging Alergic lid rxn Systemic hypertension Arrythmia Throbbing headache , Tremor Palpitation Teratogenic effects
  • 11. Contraindication Severe hypertension Cardiac disease Thyrotoxicosis