Milrinone

Milrinone

Mechanism of action

Inhibitor of cAMP phosphodiesterase III isoenzyme -> decrease the hydrolysis of cAMP
Increase of cAMP leads to:
-> increase in adenyl cyclase
-> increase protein kinases
-> increased phosphorylation of proteins -
> net influx of Ca2+ into muscle

Milrinone effect = ‘inodilator’ -> inotropy -> vascular and bronchial muscle relaxation inotropy + decreased SVR -> increased SV

Milrinone might be used in patients on b-blockers and with b-adrenoceptor downregulation (as occurs in chronic CHF)

Milrinone lowers pulmonary vascular resistance (PVR).

Milrinone is not recommenden in patients with myocardial infarction => increases mortality.

Indications and dose

Side-effects

Hypotension

Arrhythmias (less than dobutamine)

Headache

Pharmacokinetics

Onset: 5-15 minutes

Metabolism: Hepatic

Half-life of elimination: 2.5 hours

Excretion: Urine

Directions for administration

For intravenous infusion dilute in 500 ml of 5% glucose or 0.9% sodium chloride. 

Medicinal forms

1 vial = 10 mg in 10 ml

References

  1. https://bnf.nice.org.uk/drugs/milrinone/ 
  2. https://litfl.com/milrinone/ 
  3. https://www.uptodate.com/contents/milrinone-drug-information?search=milrinone&source=panel_search_result&selectedTitle=1~72&usage_type=panel&kp_tab=drug_general&display_rank=1