Takeaway
- For patients experiencing trauma-related haemorrhagic shock, low-dose supplementation with arginine vasopressin (AVP) leads to a reduced need for blood products and no more complications than placebo.
- Commentary:
- “This finding refutes the dogma that pressor therapy should never be initiated in patients with hypotension or bleeding and that the answer is volume.”
- Warns that targeting specific mean arterial pressure (MAP) may mean result is artifact.
- Suggests deep venous thrombosis (DVT) finding is likely a statistical anomaly.
Why this matters
- Aggressive fluid resuscitation and transfusions in this setting can cause complications.
Key results
- AVP use vs placebo:
- 1.00 L less blood product (95% CI, −2.03 to 0.00 L; P=.03).
- Fewer DVTs: 20% vs 39% (P=.05).
- Similar lengths of stay, overall complications, mortality.
- On per-protocol analysis, AVP led to use of fewer blood products and fewer DVTs.
Study design
- Randomised, double-blind placebo-controlled AVERT Shock trial(n=100).
- Adults receiving ≥6 units of blood products were randomly assigned to receive bolus+infusion of AVP vs placebo.
- Study infusion and pressors titrated to maintain MAP at ≥65 mmHg.
- Outcomes: volume of transfused blood products within 48 hours.
- Funding: Supported by National Trauma Institute and Army awards to researchers.
Limitations
- Small, single-centre study.
References
References