Respiratory Trials·org

Cardiology in critical care · Choice of vasopressor in shock

SOAP II randomised trial

Comparison of dopamine and norepinephrine in the treatment of shock

SOAP II trial design and results
Design Multicentre, blinded randomised controlled trial
Treatment Dopamine as first-line vasopressor
Control Noradrenaline as first-line vasopressor
Population 1679 patients with shock of any cause
Follow-up 12 months
Primary endpoint 28-day all-cause mortality
Result 858 patients received dopamine and 821 noradrenaline. There was no significant between-group difference in the rate of death at 28 days, but dopamine was associated with substantially more arrhythmic events, and with higher mortality in the prespecified cardiogenic shock subgroup.
Secondary endpoints Arrhythmic events, mortality by shock subtype, organ dysfunction

Although there was no significant difference in the rate of death between patients with shock who were treated with dopamine as the first-line vasopressor agent and those who were treated with norepinephrine, the use of dopamine was associated with a greater number of adverse events.

The trial authors, in the published abstract

How it has aged

Ended dopamine as a first-line vasopressor. The headline is neutral and the practice change came from the safety data and the cardiogenic shock subgroup — a case where secondary findings rightly outweighed a null primary result.

Publications

Comparison of dopamine and norepinephrine in the treatment of shock

De Backer D, Biston P, Devriendt J, et al. Comparison of dopamine and norepinephrine in the treatment of shock. N Engl J Med 2010 Mar 4;362(9):779-89.

  • No significant difference in 28-day mortality
  • Substantially more arrhythmic events with dopamine
  • Higher mortality with dopamine in the cardiogenic shock subgroup