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Updated: Jan 19, 2026

Subdural Soft Electrocorticography ECoG Array Implantation and Long-Term Cortical Recording in Minipigs
Published on: March 31, 2023
Prospective randomized placebo-controlled double-blind clinical study of adjuvant dexamethasone with surgery for
K Mebberson1, M Colditz1, L A G Marshman2
1Department of Neurosurgery, The Townsville Hospital, Douglas, Townsville 4810, Queensland, Australia.
Insights
This study suggests dexamethasone (DX) may reduce chronic subdural hematoma (CSDH) recurrence after surgery. Adjuvant DX with post-operative drainage appears safe and effective in preventing CSDH return.
Area of Science:
- Neurosurgery
- Clinical Trials
- Pharmacology
Background:
- Chronic subdural hematoma (CSDH) recurrence after surgery ranges from 3-30%.
- Post-operative subdural drainage is the only proven adjuvant to decrease CSDH recurrence rate (RR).
- Corticosteroids, like dexamethasone (DX), have been explored for conservative management and surgical adjuncts.
Purpose of the Study:
- To present an interim analysis of the first prospective randomized placebo-controlled trial (PRPCT) evaluating adjuvant dexamethasone (DX) on CSDH recurrence and outcomes.
- To assess the safety and efficacy of adjuvant DX in patients undergoing CSDH evacuation with post-operative drainage.
Main Methods:
- A prospective randomized placebo-controlled trial (PRPCT) was conducted with participants randomized to placebo or a 2-week reducing DX regimen.
- All participants underwent CSDH evacuation and post-operative subdural drainage.
- Outcomes including recurrence rate (RR), post-operative mortality (POMT), morbidity (POMB), length of stay (LOS), and modified Rankin Score (mRS) were assessed.
Main Results:
- Interim analysis (n=47) showed no recurrences in the DX group versus 20.83% in the placebo group (P=0.049).
- No significant differences were observed between groups for POMT, POMB, LOS, mRS, or adverse events.
- The study suggests adjuvant DX with post-operative drainage is safe and may significantly decrease CSDH recurrences.
Conclusions:
- This interim analysis of the first PRPCT suggests adjuvant dexamethasone (DX) is safe and potentially reduces CSDH recurrence when used with post-operative drainage.
- A larger sample size (n≈89) may be needed to confirm a 12.5% between-group difference in recurrence.
- Future research could explore longer durations of adjuvant DX therapy.
Abstract:
Most chronic subdural haematomas (CSDH) are successfully treated neurosurgically. However, operative recurrences occur with a frequency 3-30%, consume resources and potentially prolong length-of stay (LOS). The only adjuvant factor proven to significantly decrease CSDH recurrence rate (RR) is post-operative subdural drainage. Corticosteroids have been used to conservatively manage CSDH. One non-randomised study also compared dexamethasone (DX) as an adjunct to surgery without post-operative drainage: whilst a null effect was observed, the 'surgery-alone' group consisted of only n = 13. We present an interim analysis of the first registered prospective randomised placebo-controlled trial (PRPCT) of adjuvant DX on RR and outcome after CSDH surgery with post-operative drainage. Participants were randomised to either placebo or a reducing DX regime over 2 weeks, with CSDH evacuation and post-operative drainage. Post-operative mortality (POMT) and RR were determined at 30 days and 6 months; modified Rankin Score (mRS) at discharge and 6 months. Post-operative morbidity (POMB) and adverse events (AEs) were determined at 30 days. Interim analysis at approximately 50% estimated sample size was performed (n = 47). Recurrences were not observed with DX: only with placebo (0/23 [0%] v 5/24 [20.83%], P = 0.049). There was no significant between-group differences in POMT, POMB, LOS, mRS or AEs. CONCLUSIONS: In this first registered PRPCT, interim analysis suggested that adjuvant DX with post-operative drainage is both safe and may significantly decrease recurrences. A 12.5% point between-groups difference may be reasonable to power a final sample size of approximately n = 89. Future studies could consider adjuvant DX for longer than the arbitrarily-chosen 2 weeks.
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