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Published in: Acta Neurochirurgica 6/2023

Open Access 27-04-2023 | Endoscopy | Original Article

Safety and technical efficacy of early minimally invasive endoscopy-guided surgery for intracerebral haemorrhage: the Dutch Intracerebral haemorrhage Surgery Trial pilot study

Authors: Lotte Sondag, Floris H.B.M. Schreuder, Sjoert A.H. Pegge, Jonathan M. Coutinho, Diederik W.J. Dippel, Paula M. Janssen, W. Peter Vandertop, Hieronymus D. Boogaarts, Ruben Dammers, Catharina J.M. Klijn, On behalf of the Dutch ICH Surgery Trial Study Group, part of the CONTRAST consortium

Published in: Acta Neurochirurgica | Issue 6/2023

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Abstract

Background

Previous randomised controlled trials could not demonstrate that surgical evacuation of intracerebral haemorrhage (ICH) improves functional outcome. Increasing evidence suggests that minimally invasive surgery may be beneficial, in particular when performed early after symptom onset. The aim of this study was to investigate safety and technical efficacy of early minimally invasive endoscopy-guided surgery in patients with spontaneous supratentorial ICH.

Methods

The Dutch Intracerebral Haemorrhage Surgery Trial pilot study was a prospective intervention study with blinded outcome assessment in three neurosurgical centres in the Netherlands. We included adult patients with spontaneous supratentorial ICH ≥10mL and National Institute of Health Stroke Scale (NIHSS) score ≥2 for minimally invasive endoscopy-guided surgery within 8 h after symptom onset in addition to medical management. Primary safety outcome was death or increase in NIHSS ≥4 points at 24 h. Secondary safety outcomes were procedure-related serious adverse events (SAEs) within 7 days and death within 30 days. Primary technical efficacy outcome was ICH volume reduction (%) at 24 h.

Results

We included 40 patients (median age 61 years; IQR 51–67; 28 men). Median baseline NIHSS was 19.5 (IQR 13.3–22.0) and median ICH volume 47.7mL (IQR 29.4–72.0). Six patients had a primary safety outcome, of whom two already deteriorated before surgery and one died within 24 h. Sixteen other SAEs were reported within 7 days in 11 patients (of whom two patients that already had a primary safety outcome), none device related. In total, four (10%) patients died within 30 days. Median ICH volume reduction at 24 h was 78% (IQR 50–89) and median postoperative ICH volume 10.5mL (IQR 5.1–23.8).

Conclusions

Minimally invasive endoscopy-guided surgery within 8 h after symptom onset for supratentorial ICH appears to be safe and can effectively reduce ICH volume. Randomised controlled trials are needed to determine whether this intervention also improves functional outcome.

Trial registration

Clinicaltrials.​gov: NCT03608423, August 1st, 2018.
Appendix
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Metadata
Title
Safety and technical efficacy of early minimally invasive endoscopy-guided surgery for intracerebral haemorrhage: the Dutch Intracerebral haemorrhage Surgery Trial pilot study
Authors
Lotte Sondag
Floris H.B.M. Schreuder
Sjoert A.H. Pegge
Jonathan M. Coutinho
Diederik W.J. Dippel
Paula M. Janssen
W. Peter Vandertop
Hieronymus D. Boogaarts
Ruben Dammers
Catharina J.M. Klijn
On behalf of the Dutch ICH Surgery Trial Study Group, part of the CONTRAST consortium
Publication date
27-04-2023
Publisher
Springer Vienna
Keyword
Endoscopy
Published in
Acta Neurochirurgica / Issue 6/2023
Print ISSN: 0001-6268
Electronic ISSN: 0942-0940
DOI
https://doi.org/10.1007/s00701-023-05599-2

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