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Effect on neonatal outcomes of maintenance of maternal blood pressure targets with noradrenaline after spinal anaesthesia for caesarean delivery: a multicentre, randomised, controlled trial.

Anaesthesia2026-02-27PubMed
Total: 82.5Innovation: 7Impact: 0Rigor: 0Citation: 0

Summary

In 1183 women randomized to systolic blood pressure targets of 90% vs 80% of baseline using noradrenaline, mean umbilical artery pH was similar, but neonatal acidaemia (pH < 7.2) was less frequent in the 90% group. Maternal hypotension, severe hypotension, and nausea/vomiting were also significantly reduced with the higher target, at the expense of more noradrenaline boluses.

Key Findings

  • Neonatal acidaemia (umbilical artery pH < 7.2) was lower with SBP-90% vs SBP-80% (0.5% vs 2.2%; p=0.020).
  • Maternal hypotension (<80% baseline) and severe hypotension (<60% baseline) were significantly less frequent with the 90% target.
  • Nausea/vomiting was reduced with SBP-90% (9.8% vs 18.4%; p<0.001), though more noradrenaline boluses were required.

Clinical Implications

Target maternal systolic blood pressure above 90% of baseline with noradrenaline boluses during cesarean under spinal anesthesia to reduce neonatal acidaemia and maternal hypotension/nausea. Protocols should specify frequent monitoring and proactive dosing.

Why It Matters

Defines a pragmatic blood pressure target during cesarean spinal anesthesia with clear maternal and neonatal benefits, informing vasopressor titration protocols.

Limitations

  • Primary endpoint (mean umbilical artery pH) was similar; rare events may limit power for neonatal outcomes.
  • Short-term peridelivery outcomes only; generalizability to other vasopressors or infusion strategies is uncertain.

Future Directions

Evaluate continuous infusion strategies, individualized baselines, and longer-term neonatal neurodevelopmental outcomes; compare noradrenaline with phenylephrine in similar target-based protocols.

Study Information

Study Type
RCT
Research Domain
Treatment
Evidence Level
I - Randomized controlled trial providing highest-level interventional evidence.
Study Design
OTHER