Angiotensin II for the Treatment of Vasodilatory Shock by ATHOS-3 trial


Methods

AII was started at 20 ng/kg/min and adjusted to 1.25-40 ng/kg. Study infusion was discontinued at 48 hour mark.

Results

  • Mean reduction of 0.03 ug/kg/h of background vasopressors and increase in MAP within 3 hours.
  • Mean improvement in CV SOFA score at 48 hours without improvement in total SOFA score.
  • No mortality difference. 1

Follow up

  • Numerous counterpoint. 2
  • Follow up study found improvement in 28 day survival, MAP, and rate of RRT liberation.3

Footnotes

  1. https://www.nejm.org/doi/10.1056/NEJMoa1704154

  2. https://emcrit.org/pulmcrit/angiotensin-ii/

  3. https://journals.lww.com/ccmjournal/Fulltext/2018/06000/Outcomes_in_Patients_with_Vasodilatory_Shock_and.15.aspx