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Clinical Application
Septic Shock
 Norepinephrine (Levophed)-
Alpha 1 and vasoconstriction
raise MAP causes reflex
bradycardia but Beta 1
counteracts this and improves
CO
 Phenylephrine (Neosynephrine)-
pure vasoconstriction
 2nd Line Agent: Vasopressin and
Epinephrine- may require
decreased need for other
vasopressors
Heart Failure
 Dopamine- dose dependent,
 Dobutamine
 2nd Line Agent: Milrinone-
phosphdiesterase inhibitor w/
similar effects as Dobutamine w/
lower incidence of dysrhythmias,
cannot be used if pt. is
hypotensive
Cardiogenic Shock
 Norepinephrine (Levophed)
 Dobutamine added after
establishing adequate perfusion
to increase contractility, HR, and
CO
Anaphylactic Shock
 Epinephrine
 2nd Line Agent: Vasopressin
Neurogenic Shock
 Phenylephrine (Neosynephrine)-
Hypotension
 Phenylephrine(Neosynephrine)-
post anesthesia
 Epinephrine- post CABG
References
Williamson AP, Seifen E, Lindemann JP,
Kennedy RH. WB4101- and CEC-sensitive
positive inotropic actions of phenylephrine
in rat cardiac muscle. Am J Physiol.
1994;266(6 Pt 2):H2462.
UCI Internal Medicine Residency Mini-
Lecture Series
http://www.texasheart.org/HIC/Topics/Me
ds/inotropic.cfm
http://chicago.medicine.uic.edu/UserFiles/S
ervers/Server_442934/Image/1.1/residentg
uides/final/icuguidebook.pdf
VASOPRESSORS AND
INOTROPES
VASOPRESSORS
AND
INOTROPES
By: Megan Heffernan
Background
Vasopressors
 Class of drugs that elevate
Mean Arterial Pressure (MAP)
by inducing vasoconstriction
 Indicated for decrease of >30
mmHg from baseline systolic
blood pressure or MAP <60
mmHg when either condition
results in end-organ
dysfunction secondary to
hypoperfusion
Inotropes
 Increase cardiac contractility
so that the heart can pump
more blood with fewer
heartbeats
Many drugs have both vasopressor
and inotropic effects
Pharmacological
Properties
Alpha 1 Adrenergic
 Effects Vascular wall →
Vasoconstriction
 Effects Heart → Increase duration of
contraction w/o increased
chronotropy
Beta Adrenergic
 Beta 1 → Effects Heart → Increase
inotropy and chronotropy
 Beta 2 → Effects b
 lood vessels → Vasodilation
Dopaminergic Effects
 Renal, Mesenteric, Coronary,
Cerebral → Vasodilation
 Subtype → Vasoconstriction
(through norepinephrine release)
Medication Receptor
Activity & Clinical
Effects
Phenylephrine (Neo)
 Alpha 1
 SVR increase, CO increase
 Minimal cardiac ino or chrono
Norepinephrine (Levo)
 Alpha 1 and Beta 1
 SVR increase, CO increase
Epinephrine (Adrenalin)
 Potent Beta 1, moderate beta 2
and alpha 1
 CO increase, SVR increase (low
dose), SVR increase (high dose)
Dopamine (Inotropin)
 Doses dependent (mcg/kg/min)
.5-2 = beta 1 and dopaminergic,
vasodilation
5-10 = beta 1, alpha 1,
dopaminergic, increase CO & SVR
>10 = alpha 1, beta 2,
dopaminergic, increase SVR
Dobutamine
 Beta 1 and 2
 Increase CO and decrease SVR,
reduce LV filling pressure
Isoproterenol (Isuprel)
 Potent Beta 1 and 2
 Increase CO, decrease SVR
 Indicated for hypotension from
bradycardia

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Vasopressor Brochure

  • 1. Clinical Application Septic Shock  Norepinephrine (Levophed)- Alpha 1 and vasoconstriction raise MAP causes reflex bradycardia but Beta 1 counteracts this and improves CO  Phenylephrine (Neosynephrine)- pure vasoconstriction  2nd Line Agent: Vasopressin and Epinephrine- may require decreased need for other vasopressors Heart Failure  Dopamine- dose dependent,  Dobutamine  2nd Line Agent: Milrinone- phosphdiesterase inhibitor w/ similar effects as Dobutamine w/ lower incidence of dysrhythmias, cannot be used if pt. is hypotensive Cardiogenic Shock  Norepinephrine (Levophed)  Dobutamine added after establishing adequate perfusion to increase contractility, HR, and CO Anaphylactic Shock  Epinephrine  2nd Line Agent: Vasopressin Neurogenic Shock  Phenylephrine (Neosynephrine)- Hypotension  Phenylephrine(Neosynephrine)- post anesthesia  Epinephrine- post CABG References Williamson AP, Seifen E, Lindemann JP, Kennedy RH. WB4101- and CEC-sensitive positive inotropic actions of phenylephrine in rat cardiac muscle. Am J Physiol. 1994;266(6 Pt 2):H2462. UCI Internal Medicine Residency Mini- Lecture Series http://www.texasheart.org/HIC/Topics/Me ds/inotropic.cfm http://chicago.medicine.uic.edu/UserFiles/S ervers/Server_442934/Image/1.1/residentg uides/final/icuguidebook.pdf VASOPRESSORS AND INOTROPES VASOPRESSORS AND INOTROPES By: Megan Heffernan
  • 2. Background Vasopressors  Class of drugs that elevate Mean Arterial Pressure (MAP) by inducing vasoconstriction  Indicated for decrease of >30 mmHg from baseline systolic blood pressure or MAP <60 mmHg when either condition results in end-organ dysfunction secondary to hypoperfusion Inotropes  Increase cardiac contractility so that the heart can pump more blood with fewer heartbeats Many drugs have both vasopressor and inotropic effects Pharmacological Properties Alpha 1 Adrenergic  Effects Vascular wall → Vasoconstriction  Effects Heart → Increase duration of contraction w/o increased chronotropy Beta Adrenergic  Beta 1 → Effects Heart → Increase inotropy and chronotropy  Beta 2 → Effects b  lood vessels → Vasodilation Dopaminergic Effects  Renal, Mesenteric, Coronary, Cerebral → Vasodilation  Subtype → Vasoconstriction (through norepinephrine release) Medication Receptor Activity & Clinical Effects Phenylephrine (Neo)  Alpha 1  SVR increase, CO increase  Minimal cardiac ino or chrono Norepinephrine (Levo)  Alpha 1 and Beta 1  SVR increase, CO increase Epinephrine (Adrenalin)  Potent Beta 1, moderate beta 2 and alpha 1  CO increase, SVR increase (low dose), SVR increase (high dose) Dopamine (Inotropin)  Doses dependent (mcg/kg/min) .5-2 = beta 1 and dopaminergic, vasodilation 5-10 = beta 1, alpha 1, dopaminergic, increase CO & SVR >10 = alpha 1, beta 2, dopaminergic, increase SVR Dobutamine  Beta 1 and 2  Increase CO and decrease SVR, reduce LV filling pressure Isoproterenol (Isuprel)  Potent Beta 1 and 2  Increase CO, decrease SVR  Indicated for hypotension from bradycardia