Pharm
Milrinone
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Milrinone
, Primacor
See Also
Vasopressor
Amrinone
Indications
Refractory
NYHA Class
3 to 4
Systolic Dysfunction
Mechanism
Phosphodiesterase (PDE) inhibitor Type 3
Blocks breakdown of cyclic
Adenosine
monophosphate (cAMP) in
Myocardium
and vascular
Smooth Muscle
Sustains
Catecholamine
activity (even when B-adrenergic
Antagonist
s are present)
Ineffective when cellular cAMP is depleted
Activity
Strong inotropy with increased contractility
Derived from
Amrinone
, which is 20-30 times less potent than Milrinone
Increases
Stroke Volume
and ejection fraction
Increases sinus rate
Decreases
Afterload
by dilating arterioles
Decreases
Peripheral Vascular Resistance
Dosing
Adults
Load: 50 mcg/kg IV infused over 10 minutes
Maintenance
CrCl
>50 ml/min: 0.125 to 0.5 mcg/kg/min (up to 0.75 mcg/kg/min) titrated to effect
CrCl
41 to 50 ml/min: 0.43 mcg/kg/min
CrCl
31 to 40 ml/min: 0.38 mcg/kg/min
CrCl
21 to 30 ml/min: 0.33 mcg/kg/min
CrCl
11 to 20 ml/min: 0.28 mcg/kg/min
CrCl
6 to 10 ml/min: 0.23 mcg/kg/min
CrCl
<=5 ml/min: 0.2 mcg/kg/min
Dosing
Children
Load: 50 mcg/kg IV infused over 10 minutes
Maintenance: 0.5 to 1 mcg/kg/min titrated to effect
Pharmacokinetics
Half life: 1.5 hours
Adverse Effects
Hypotension
risk (avoid in
Hypovolemia
)
Ventricular
Arrhythmia
s
Monitor on telemetry during infusion
Safety
Pregnancy Category C
Unknown safety in
Lactation
Resources
Milrinone Injection Solution
https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=88f78780-399f-4780-be19-205739db1682
References
Olson (2020) Clinical
Pharmacology
, Medmaster Miami, p. 74-5
Hamilton (2020) Tarascon Pocket Pharmacopoeia
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