Liberal versus restrictive transfusion strategies in subarachnoid hemorrhage: a secondary analysis of the TRAIN study.
Summary
In a pre-planned secondary analysis of SAH patients within the TRAIN RCT, a liberal transfusion threshold (Hb <9 g/dL) did not significantly reduce unfavorable outcomes at 180 days versus a restrictive threshold (Hb <7 g/dL) in unadjusted analyses. However, liberal strategy was associated with less cerebral ischemia and, after adjustment, with a lower risk of unfavorable outcome.
Key Findings
- Randomized comparison within TRAIN: liberal (Hb <9 g/dL) vs restrictive (Hb <7 g/dL) transfusion in 190 SAH patients.
- Unfavorable outcome at 180 days: RR 0.87 (95% CI 0.71–1.04) for liberal vs restrictive (not statistically significant).
- Cerebral ischemia significantly lower with liberal strategy: RR 0.63 (95% CI 0.41–0.97).
- Adjusted analysis associated liberal randomization with lower risk of unfavorable outcome: RR 0.83 (95% CI 0.70–0.99).
Clinical Implications
For neuroanesthesiology and neurocritical care, considering a more liberal transfusion threshold may reduce cerebral ischemia risk in SAH. Patient blood management protocols could individualize thresholds, especially in patients at high risk of delayed cerebral ischemia.
Why It Matters
Transfusion thresholds in SAH are clinically controversial. This analysis provides randomized evidence suggesting potential benefits of a higher Hb target in reducing cerebral ischemia.
Limitations
- Secondary analysis; potential for residual confounding despite adjustment.
- Liberal group was older; imbalances may influence outcomes.
- Trial not primarily powered for SAH subgroup alone.
Future Directions
A definitive SAH-specific RCT comparing transfusion thresholds with cerebral ischemia and functional outcomes as co-primary endpoints is warranted; mechanistic monitoring (e.g., brain tissue oxygenation) could guide individualized thresholds.
Study Information
- Study Type
- RCT
- Research Domain
- Treatment
- Evidence Level
- II - Pre-planned secondary analysis within a randomized controlled trial.
- Study Design
- OTHER