Hemodynamics, fluids & transfusion

Strategies for discontinuing vasopressin and norepinephrine during the recovery phase of shock: a single-center retrospective study

J Intensive CarePublished Retrospective cohort study

Authors' conclusion

In patients recovering from shock who received both arginine vasopressin and norepinephrine, discontinuing arginine vasopressin first was not associated with a higher risk of hypotension.

Study context

Population
ICU patients with shock who received both arginine vasopressin and norepinephrine, August 2017 to March 2024analysed
Participants
524 patients
Exposure
AVP-first vs NE-first
  • AVP-firstn = 293
  • NE-firstn = 231reference
Outcome
Incidence of hypotension (MAP < 60 mmHg requiring a ≥ 25% increase in the remaining vasopressor, reinstitution of the stopped agent, or a bolus of ≥ 500 mL crystalloid or 25 g albumin)
Follow-up
Within 24 h of vasopressor cessation
Methodological detailssingle-centre, propensity-score overlap weighting
  • Single-centre
  • Propensity-score overlap weighting

Main finding

As reported in the abstract

Hypotension within 24 h of vasopressor cessation · 24 h

Incidence of hypotension after overlap weighting, not significantly different

19% vs 21%

Observational data: associations, not effects.

Further findings

Hypotension (unadjusted) — NE-first
26%

Hypotension, septic shock subgroup (n = 267, weighted)

No significant difference between groups

Original publication

Strategies for discontinuing vasopressin and norepinephrine during the recovery phase of shock: a single-center retrospective study. J Intensive Care. Published 30 September 2025. doi:10.1186/s40560-025-00823-w

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