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Indications for Pressor and Why

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... increase in SVR, and also can stimulate receptors, thus causing tachycardia ... with pulseless ventricular tachycardia and ventricular fibrillation, aystole ... – PowerPoint PPT presentation

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Title: Indications for Pressor and Why


1
Indications for Pressor and Why?
  • Taimur Khan

2
Vasopressors
  • Dopamine
  • Norepinephrine
  • Phenylephrine
  • Epinephrine
  • Dobutamine
  • Amrinone/Milrinone

3
Dopamine
  • At low doses dopamine receptor activation and
    renal, mesenteric, cerebral circulations
    increased dose usually set at 3 µg/kg/min
  • At doses between 4-7 µg/kg/min, ß stimulation and
    augmentattion of cardiac output occurs
  • At doses above 8 µg/kg/min, progressive
    vasoconstriction is dominant feature
  • Pressor effects are milder as compared to
    Norepinephrine and Phenylephrine, can be
    initially used for pressure support but if no
    response present switch to more potent pressors

4
Norepinephrine
  • Mainly an a receptor agonist theat promotes
    widespread vasoconstriction
  • In cases of hypotension refractory to dopamine,
    it can be added as a second agent
  • Dose dependent increase in SVR, and also can
    stimulate ß receptors, thus causing tachycardia
  • Cardiac output increased only at low doses
  • Range of dose 2-12 µg/min usual dosage rate 2-4
    µg/min

5
Phenylephrine
  • Primarily a- receptor agonist and causing
    peripheral vasoconstriction
  • Some ß effects can occur at higher doses
  • Primary effects, include peripheral
    vasoconstriction with resultant increase in
    diastolic and systolic blood pressures, small
    decreases in cardiac output and an increase in
    circulation time. A reflex bradycardia can occur
  • May be a good choice when tachyarrhythmias limit
    therapy with other vasopressors.

6
Epinephrine
  • Primarily ß receptor agonist at low doses and an
    a receptor agonist at high dose
  • Vasopressor range 0.01 0.1 µg/kg/min
  • Uses include cardiac arrest associated with
    pulseless ventricular tachycardia and ventricular
    fibrillation, aystole and pulseless electrical
    activity
  • Not recommended as first line agent for routine
    management of low cardiac output or circulatory
    shock

7
Dobutamine
  • Primarily a ß1- receptor agonist (cardiac
    stimulation), but also a mild ß-2 effect
    (vasodialtrion)
  • Dose dependent increase in Stroke volume (SV),
    accompanied by decrease in cardiac filling
    pressures
  • Increase in SV also accompained with decrease in
    systemic vascular resistance (SVR) (baroreceptor
    medicated) thus arterial BP remains unchanged.
  • Effective on both right and left sided heart
    failure
  • Dosage can range from 5-15 µg/kg/min. Between 4-7
    µg/kg/min, ß receptor stimulation and
    augmentation of cardiac output occurs
  • Not indicated for monotherapy in patients with
    cardiogenic shock

8
Amrinone/Milrinone
  • Phosphodiestrase inhibitor that has both positive
    ionotropic and vasodilator actions
  • Combined actions of amrinone produce and increase
    in cardiac stroke output without increase in
    cardiac stoke work
  • Unlike dobutamine, the actions are not attenuated
    by ß receptor antagonists
  • Can be effective as single agent for low output
    states due to systolic hear failure however
    mostly used as a second agent that is added to
    dobutamine in cases of refractory heart failure
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