Neuroimaging selection for thrombectomy in pediatric stroke: a single-center experience.


Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 21 02 2019
revised: 04 04 2019
accepted: 09 04 2019
pubmed: 18 5 2019
medline: 27 11 2019
entrez: 18 5 2019
Statut: ppublish

Résumé

The extended time window for endovascular therapy in adult stroke represents an opportunity for stroke treatment in children for whom diagnosis may be delayed. However, selection criteria for pediatric thrombectomy has not been defined. We performed a retrospective cohort study of patients aged <18 years presenting within 24 hours of acute large vessel occlusion. Patient consent was waived by our institutional IRB. Patient data derived from our institutional stroke database was compared between patients with good and poor outcome using Fisher's exact test, t-test, or Mann-Whitney U-test. Twelve children were included: 8/12 (66.7%) were female, mean age 9.7±5.0 years, median National Institutes of Health Stroke Scale (NIHSS) 11.5 (IQR 10-14). Stroke etiology was cardioembolic in 75%, dissection in 16.7%, and cryptogenic in 8.3%. For 2/5 with perfusion imaging, Tmax >4 s appeared to better correlate with NIHSS. Nine patients (75%) were treated: seven underwent thrombectomy alone; one received IV alteplase and thrombectomy, and one received IV alteplase alone. Favorable outcome was achieved in 78% of treated patients versus 0% of untreated patients (P=0.018). All untreated patients had poor outcome, with death (n=2) or severe disability (n=1) at follow-up. Among treated patients, older children (12.8±2.9 vs 4.2±5.0 years, P=0.014) and children presenting as outpatient (100% vs 0%, P=0.028) appeared to have better outcomes. Perfusion imaging is feasible in pediatric stroke and may help identify salvageable tissue in extended time windows, though penumbral thresholds may differ from adult values. Further studies are needed to define criteria for thrombectomy in this unique population.

Sections du résumé

BACKGROUND BACKGROUND
The extended time window for endovascular therapy in adult stroke represents an opportunity for stroke treatment in children for whom diagnosis may be delayed. However, selection criteria for pediatric thrombectomy has not been defined.
METHODS METHODS
We performed a retrospective cohort study of patients aged <18 years presenting within 24 hours of acute large vessel occlusion. Patient consent was waived by our institutional IRB. Patient data derived from our institutional stroke database was compared between patients with good and poor outcome using Fisher's exact test, t-test, or Mann-Whitney U-test.
RESULTS RESULTS
Twelve children were included: 8/12 (66.7%) were female, mean age 9.7±5.0 years, median National Institutes of Health Stroke Scale (NIHSS) 11.5 (IQR 10-14). Stroke etiology was cardioembolic in 75%, dissection in 16.7%, and cryptogenic in 8.3%. For 2/5 with perfusion imaging, Tmax >4 s appeared to better correlate with NIHSS. Nine patients (75%) were treated: seven underwent thrombectomy alone; one received IV alteplase and thrombectomy, and one received IV alteplase alone. Favorable outcome was achieved in 78% of treated patients versus 0% of untreated patients (P=0.018). All untreated patients had poor outcome, with death (n=2) or severe disability (n=1) at follow-up. Among treated patients, older children (12.8±2.9 vs 4.2±5.0 years, P=0.014) and children presenting as outpatient (100% vs 0%, P=0.028) appeared to have better outcomes.
CONCLUSIONS CONCLUSIONS
Perfusion imaging is feasible in pediatric stroke and may help identify salvageable tissue in extended time windows, though penumbral thresholds may differ from adult values. Further studies are needed to define criteria for thrombectomy in this unique population.

Identifiants

pubmed: 31097548
pii: neurintsurg-2019-014862
doi: 10.1136/neurintsurg-2019-014862
doi:

Substances chimiques

Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

940-946

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: GWA: Ownership Interest; Significant; iSchemaView. Consultant/Advisory Board; Significant; iSchemaView, Medtronic.

Auteurs

Sarah Lee (S)

Stanford Stroke Center, Department of Neurology & Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Division of Child Neurology, Department of Neurology & Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.

Jeremy J Heit (JJ)

Department of Radiology, Division of Neuroimaging & Neurointervention, Stanford University School of Medicine, Stanford, CA, USA.

Gregory W Albers (GW)

Stanford Stroke Center, Department of Neurology & Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.

Max Wintermark (M)

Department of Radiology, Division of Neuroimaging & Neurointervention, Stanford University School of Medicine, Stanford, CA, USA.

Bin Jiang (B)

Department of Radiology, Division of Neuroimaging & Neurointervention, Stanford University School of Medicine, Stanford, CA, USA.

Eric Bernier (E)

Stanford Stroke Center, Department of Neurology & Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.

Nancy J Fischbein (NJ)

Department of Radiology, Division of Neuroimaging & Neurointervention, Stanford University School of Medicine, Stanford, CA, USA.

Michael Mlynash (M)

Stanford Stroke Center, Department of Neurology & Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.

Michael P Marks (MP)

Department of Radiology, Division of Neuroimaging & Neurointervention, Stanford University School of Medicine, Stanford, CA, USA.

Huy M Do (HM)

Department of Radiology, Division of Neuroimaging & Neurointervention, Stanford University School of Medicine, Stanford, CA, USA.
Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA, USA.

Robert L Dodd (RL)

Department of Radiology, Division of Neuroimaging & Neurointervention, Stanford University School of Medicine, Stanford, CA, USA.
Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA, USA.

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Classifications MeSH