MICU intern's survival guide vasopressors: Difference between revisions
Jump to navigation
Jump to search
Line 26: | Line 26: | ||
===Vasopressin=== | ===Vasopressin=== | ||
====Mechanism of action==== | ====Mechanism of action==== | ||
* Acts | * Acts by stimulating V (vasopressin) receptors in vascular and GI smooth muscles causing contraction. It also has anti-diuretics effect. | ||
====Indications==== | ====Indications==== | ||
* [[Septic shock]] - second line treatment for septic shock | * [[Septic shock]] - second line treatment for septic shock |
Revision as of 14:52, 28 December 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Norepinephrine
Mechanism of action
Acts on both alpha1 (vasoconstriction of blood vessels) and beta1 receptors (increases cardiac output).
Indications
- Septic shock
- Cardiogenic shock - Recent studies have shown that norepinephrine may be better than dopamine in cardiogenic shock due to a decreased risk of tachyarrhythmias.
- In cases where the type of shock is unclear, norepinephrine can be tried as a first line agent.
Doses
- 1-30 mcg/min.
Dopamine
Mechanism of action
- Acts on alpha1 (vasoconstriction of blood vessels), beta1 (increases cardiac output) and dopamine receptors (scattered throughout the body).
- Its action is dose dependent. At low doses it predominantly acts on cardiac receptors (1-10 mcg/min) with less vasoconstriction activities. At higher doses it has both vasoconstriction and cardiac activities.
Indications
- Cardiogenic shock
- Septic shock - second line treatment for septic shock
Side-effects
- Arrhythmogenic. Avoid in patients prone to arrhythmias.
- Doses
- 1-20 mcg/min.
Dobutamine
Vasopressin
Mechanism of action
- Acts by stimulating V (vasopressin) receptors in vascular and GI smooth muscles causing contraction. It also has anti-diuretics effect.
Indications
- Septic shock - second line treatment for septic shock