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Efficacy and safety of gastrodin in preventing postoperative delirium following cardiac surgery: a randomized placebo controlled clinical trial.

Critical care (London, England)2025-03-12PubMed
Total: 84.0Innovation: 8Impact: 8Rigor: 9Citation: 8

Summary

In a double-blind RCT of 155 CABG patients, gastrodin infusion (600 mg twice daily through POD6) reduced postoperative delirium incidence from 35.9% to 19.5% and increased odds of hospital discharge without drug-related adverse events. POCD incidence was low and similar between groups.

Key Findings

  • Postoperative delirium incidence reduced to 19.5% with gastrodin versus 35.9% with placebo (RR 0.54, 95% CI 0.32–0.93).
  • No increase in adverse events; none were drug related (9.1% vs 14.1%).
  • Greater odds of discharge in the gastrodin group (subhazard ratio 1.20, 95% CI 1.00–1.84).

Clinical Implications

Gastrodin infusion may be considered as a prophylactic adjunct for delirium in CABG patients pending replication, with monitoring protocols and inclusion in multimodal delirium prevention bundles.

Why It Matters

This is one of the first adequately blinded RCTs to show a pharmacological reduction in postoperative delirium after cardiac surgery, a high-impact outcome lacking effective prophylaxis.

Limitations

  • Single-country, single drug regimen; generalizability beyond CABG ± valve surgery is uncertain.
  • Sample size modest; POCD outcomes were rare, limiting power for cognitive endpoints.

Future Directions

Multicenter, larger RCTs across cardiac and non-cardiac surgeries, dose–response assessments, mechanistic studies (GABAergic/anti-inflammatory pathways), and health economic evaluations.

Study Information

Study Type
RCT
Research Domain
Prevention
Evidence Level
I - Randomized, double-blind, placebo-controlled trial
Study Design
OTHER