VASOPRESSORS and Inotropic Agents Flashcards

1
Q

Isoproterenol, predominant receptors

A

beta1- and beta2-adrenergic receptor

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2
Q

Isoproterenol, predominant action at receptors

A

beta1- and beta2-adrenergic receptor agonist

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3
Q

Inotrope/chronotrope/vasodilator

A

Isoproterenol (Chemical pacemaker)

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4
Q

Act as a chemical pacemaker?

A

Isoproterenol.

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5
Q

Isoproterenol Dosing (mcg/min AND mcg/kg/min)

A

5 to 20 mcg/minute OR 0.05 to 0.2 mcg/kg/minute

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6
Q

2 major things to know about Isoproterenol

A
  • Exacerbation of hypotension is likely due to dose-dependent vasodilation (via beta2 stimulation)
  • May cause arrhythmias
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7
Q

Milrinone class

A

Inotrope/vasodilator (phosphodiesterase inhibitor)

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8
Q

Milrinone Mechanism of action

A

(decreases rate of cyclic adenosine monophosphate [cAMP] degradation)

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9
Q

Milrinone major thing to know

A

Can get hypotension likely due to vasodilation (via phosphodiesterase inhibition); concurrent administration of a potent vasoconstrictor such as norepinephrine or vasopressin may be necessary

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10
Q

Milrinone DOSING (Bolus?)

A

0.375 to 0.75 mcg/kg/minute (a loading dose of 50 mcg/kg over ≥10 minutes may be administered, but is often omitted)

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11
Q

Dobutamine Predominant action

A

Inotrope/vasodilator/dose-dependent chronotropy (beta1- and beta2-adrenergic receptor agonist

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12
Q

Dobutamine acts on what receptors?

A

Beta 1 and Beta 2

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13
Q

Dobutamine dosing (mcg/kg/min) (mcg/min)

A

1 to 20 mcg/kg/minute

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14
Q

Dobutamine : 1 thing to know

A

Exacerbation of hypotension is possible due to dose-dependent vasodilation (via beta2 stimulation); concurrent administration of a potent vasoconstrictor such as norepinephrine or vasopressin may be necessary

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15
Q

Dopamine predominant action

A

Inotrope/vasopressor/dose-dependent chronotropy

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16
Q

Dopamine acts on what receptors ?

A

Dopaminergic, beta1-, beta2-, and alpha1-adrenergic receptor agonist

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17
Q

Dopamine dose

A

2 to 20 mcg/kg/minute

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18
Q

Dopamine effects effects across dose range:

A

Low doses have primarily dopaminergic effects at <3 mcg/kg/minute
Intermediate doses have primarily beta1- and beta2-adrenergic effects at 3 to 10 mcg/kg/minute
High doses have primarily alpha1-adrenergic effects >10 mcg/kg/minute

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19
Q

Dopamine low dose may exacerbate what?

A

Low doses may exacerbate hypotension via beta2 stimulation

High doses may cause vasoconstriction, adverse metabolic effects, and arrhythmias

20
Q

Dopamine high dose may exacerbate ?

A

vasoconstriction, adverse metabolic effects, and arrhythmias

21
Q

Vasopressin act on what receptors?

A

Vasopressin1 and Vasopressin2 receptor agonist

22
Q

Vasopressin bolus dosing

A

1 to 4 units

23
Q

Vasopressin infusion dosing

A

0.01 to 0.04 units/minute

24
Q

When is vasopressin dose > 0.04 units/minute indicated?

A

Doses >0.04 units/minute up to 0.1 units/minute are reserved for salvage therapy (ie, failure to achieve adequate BP goals with other vasopressor agents)¶

25
Q

Effective for treatment of hypotension refractory to administration of catecholamines or sympathomimetics such as ephedrine, phenylephrine, or norepinephrine

A

Vasopressin

26
Q

No direct effect on HR

A

Vasopressin

27
Q

PVR

A

Little effect on PVR; can cause splanchnic vasoconstriction

28
Q

Vasopressin and skin

A

Peripheral extravasation may cause skin necrosis

29
Q

Individual responses to dose-related effects are variable with

A

Vasopressin

30
Q

Epinephrine vasopressor receptors

A

Inotrope/chronotrope/vasopressor (alpha1-adrenergic receptor agonist; beta1- and beta2-adrenergic receptor agonist)

31
Q

Epinephrine initial dose and dosing if initial dose inadequate?

A

4 to 10 mcg initially; up to 100 mcg boluses may be used when initial response is inadequate

32
Q

Epinephrine infusion dose

A

1 to 100 mcg/minute OR 0.01 to 1 mcg/kg/minute

33
Q

Epinephrine changing effects across dose range:

A
  • Low doses have primarily beta2-adrenergic effects at 1 to 2 mcg/minute or 0.01 to 0.02 mcg/kg/minute
  • Intermediate doses have primarily beta1- and beta2-adrenergic effects at 2 to 10 mcg/minute or 0.02 to 0.1 mcg/kg/minute
  • High doses have primarily alpha1-adrenergic effects at 10 to 100 mcg/minute or 0.1 to 1 mcg/kg/minute
34
Q

First-line treatment for cardiac arrest and for anaphylaxis

A

Epinephrine

35
Q

May be administered IV, IM, or via an endotracheal tube in emergencies

A

Epinephrine

36
Q

Low doses of epinephrine cause

A

bronchodilatory effects and may cause arterial vasodilation and decreased BP

37
Q

Intermediate doses of epinephrine cause

A

Intermediate doses cause increases in HR and BP

38
Q

High doses of epinephrine cause

A

vasoconstriction, with possible severe hypertension and adverse metabolic effects

39
Q

Norepinephrine boluses

A

Inotrope/vasopressor (alpha1- and beta1-adrenergic receptor agonist) 4 to 8 mcg (may begin infusion if repeated bolus doses are necessary)

40
Q

Often selected as a first-line agent during non-cardiac surgery, particularly for treatment of most types of shock

A

Norepinephrine

41
Q

Norepinephrine vs phenylephrine potency

A

Norepinephrine 8 mcg is approximately equivalent in potency to phenylephrine 100 mcg

42
Q

Norepinephrine Dosing

A

1 to 20 mcg/minute OR 0.01 to 0.3 mcg/kg/minute

43
Q

Peripheral extravasation of a high concentration may/cause tissue damage

A

Norepinephrine

44
Q

Ephedrine 5 to 10 mg boluses N/A

A

Inotrope/chronotrope/vasopressor (alpha1​-adrenergic receptor agonist; beta1- and beta2-adrenergic receptor agonist)

45
Q

Ephedrine should be administered with extreme caution

A

Administered with extreme caution (eg, in small incremental doses of 2.5 mg) to patients using monoamine oxidase (MAO) inhibitors or methamphetamines since exaggerated hypertensive responses or life-threatening dysrhythmias may occur

46
Q

Ephedrine multiple doses

A

Tachyphylaxis may occur with multiple repeated doses due to indirect postsynaptic release of norepinephrine

47
Q

Cardiovascular effects of ephedrine and other drugs.

A

Cardiovascular effects attenuated by drugs that block ephedrine uptake into adrenergic nerves (eg, cocaine) or those that deplete norepinephrine reserves (eg, reserpine)