Emergency drugs used in anaesthesia

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KRISTINA PRADHAN INTERN

description

5 drugs majorly used by anaesthesia department with their basic pharmcology and how it is prepared.

Transcript of Emergency drugs used in anaesthesia

Page 1: Emergency drugs used in anaesthesia

KRISTINA PRADHAN

INTERN

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EMERGENCY DRUGS

ATROPINE

ADRENALINE

MEPHENTERMINE

EPHEDRINE

XYLOCARD

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ATROPINE

CLASS: ANTICHOLIGERNIC DRUGS.

BACKGROUND: A tertiary amine belladonna alkaloid, has a high affinity for muscarinic receptors.

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ATROPINEMOA: binds competitively, preventing acetylcholine from binding to those sites Atropine acts both centrally and peripherally.

Duration of action: Its general actions last about 4 hours except when placed topically in the eye, where the action may last for days

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ORGAN ACTION THERAPEUTIC USE

EYE Dilation of pupils(MYDRIASIS)Blurring of near vision(CYCLOPLEGIA); Dry eye

Ophthalmic: permits themeasurement of refractive errors without interference by the accommodative capacity of the eye. Shorter-acting antimuscarinics (cyclopentolante andtropicamide) have largely replaced atropine due to prolonged mydriasis.

GASTROINTESTINAL AntispasmodicGastric motility is reduced, hydrochloric acid production is not significantly affected

URINARY BLADDER Reduce hypermotility states of urinary bladder.

Occasionally used in enuresis among children.

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ORGAN ACTION THERAPEUTIC USE

Heart low doses—bradycardia. (due to central activation of vagal efferent outflow--result from blockade of the M1 receptors on the inhibitory prejunctional (or presynaptic) neurons-- permitting increased acetylcholinerelease.Higher doses-- M2

receptors on the SA nodeare blocked-- and the cardiac rate increases . (requires at least 1 mg of atropine)

Bradycardia and partial heart block

Secretions Sweat gland; salivary gland; lacrimal gland: Drying effect.

Antisecretory.

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ATROPINISATION IN OP POISONING

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ATROPINISATION- Start with 0.05mg/kg in children

0.6-2mg i.v. , repeat 10-25 min.

Until atropinisation obtained.; Tachycardia

D' s "

Delirium (disorientation)

Drowsiness

Dilated pupils (The mydriasis along with cyclopegia causes blurring of vision)

Dryness of mouth

Dry, hot skin

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ADVERSE EFFECTS

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PREPARATIONAvailable( ampule): 1ml=0.6mgDose: 0.01-0.02mg/kgBradyarythmia : 0.04mg/kgOnset: 1-2 minDuration of Action: 20-30 min(i.v)2-3 hrs (i.m.)

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ADRENALINE

Class :Direct acting sympathomimetic drugs.

It interact with both alpha and beta receptors.

At low dose , beta effect ( vasodilatation) on vascular system predominant.

At high dose , alpha effect (vasoconstriction) are strongest

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MODE OF ACTION

Increase contractility of myocardium( Inotropic Effect , beta1 action)Increase HR( Choronotropic Effect ,beta 1 action)So, Increase In CO leads to Increase BP

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ADRENALINEINDICATION ADVERSE EFFECTS CONTRAINDICATION

BRONCHOSPASM CNS EFFECTS: ANXIETY,HEADACHE, TENSION, TREMOR.

HYPERTHYROIDISM:INCREASED ADRENERGICRECEPTOR ON VASCULATURE—HYPERSENSITIVE RESPONSE

ANAPHYLACTIC SHOCK HEMORRHAGE: MARKED ELEVATIONOF BP—CEREBRAL HEMORRHAGE

COCAINE: PREVENT RE-UPTAKE OF CATECHOLAMINES—LONGER PERIOD OF TIME.

GLAUCOMA(2%) PULMONARY EDEMA

IN ANESTHETICS : TO INCREASE DURATION OF LOCAL

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DOSINGIn cardiac arrest

1 mg (10 mL 1:10,000 solution)

IV push every 3 to 5 minutes.

If this fails, higher doses of epinephrine (up to 0.2mg/kg) are acceptable but not recommended (there is growing evidence that it may be harmful)

In anaphylaxis: 3-5mcg/kg

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PREPARATION

Available in Ampule at concentration: 1mg/ml(1:1000)Preparation:

100mcg/ml10mcg/ml

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MEPHENTERAMINEClass: Sympathomimetic ( Mixed action adrenergic

agonist)

Mechanism of action: - Acts indirectly by releasing norepinephrine from its

storage sites and directly by exerting a slight effect on alpha and beta-1 receptors and a moderate effect on beta-2 receptors mediating vasodilation. Causes increased CO; also elicits slight CNS effects.

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INDICATION AND DOSINGINDICATION DOSING

Hypotension due to anesthesia IV, Adults: 30-45 mg; 30-mg doses may be repeated as required; or, IV infusion, Adults and children: 0.1% (1 mg/mL) mephentermine in D5W with the rate of infusion and duration dependent on response. IV, Pediatric: 0.4 mg/kg (12 mg/m2) as a single dose.Prophylaxis of hypotension in spinal anesthesia.IM, Adults: 30-45 mg 10-20 min before anesthesia. IM, Pediatric: 0.4 mg/kg (12 mg/m2) as a single dose.

Haemorrhage (only as emergency treatment until blood or blood substitutes can be given).

Not recommended, but IV infusion of 0.1% in D5W may maintain BP until blood volume is replaced.

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PREPARATION

Available: 1ml=30mgPreparation: 1ml+4ml NS= 6mg/ml

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EPHEDRINE

Class: Sympathomimetic ( Mixed action adrenergic agonist)

Action: longer duration of action; excellent oral absorption and penetrates into cns.

Elimination: unchanged in urine.

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EPHEDRINEMechanism of action:

Stimulates both alpha-and beta-receptors, causing increased heart rate, enhanced cardiac output and increased BP.

Raises systolic and diastolic blood pressure by vasoconstriction and cardiac stimulation.

Also causes bronchodilation but is less effective than epinephrine.

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DOSING AND PHARMACOKINETICS

Onset:30-60secDuration of action:

60minAvailable:

1ml=30mgDOSAGE: 3-6 mg

I.V.

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SOME COMMON SIDE EFFECTS OF ADRENERGIC AGONISTS.

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XYLOCARD Class: Antiarrhythmics class I B

Mechanism of action:

Sodium channel blocker : It acts by passing through the nerve membrane to attach or block the sodium conducting ion channels thereby inhibiting the nerve impulses.

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ONSET OF ACTION:45-90 SECONDS

DOSING: INDICATION:

DURATION: 10-20 MINS 1.5-2MG/KG FOLLOWED BY INFUSION AT A RATE OF 1-4 MG/MIN.

VENTRICULARTACHYARRYTHMIA.

AVAILABLE AS LOXICARD:2% : 1ML=20MG

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REFERENCEhttp://depts.washington.edu/opchild/images/ach.jpg-

http://www.lifehugger.com/moc/828/Atropinization_signs_symptoms

http://www.healthdigest.org/topics/category/1403-mephentermine-sulfate-dosage-interactions-side-effects-how-to-use-MEPHERTERMINE DOSING.

LIPPINCOTT PHARMACOLOGY

AJAY YADAV- SHORT TEXTBOOK OF ANAESTHESIA.