Incidence and Natural History of Pediatric Large Vessel Occlusion Stroke: A Population Study.


Journal

JAMA neurology
ISSN: 2168-6157
Titre abrégé: JAMA Neurol
Pays: United States
ID NLM: 101589536

Informations de publication

Date de publication:
01 05 2022
Historique:
pubmed: 29 3 2022
medline: 12 5 2022
entrez: 28 3 2022
Statut: ppublish

Résumé

The incidence and natural history of large vessel occlusion (LVO) stroke in children is largely unknown. These knowledge gaps limit the uptake of reperfusion therapies and reduce the efficiency of pediatric acute stroke pathways. To determine the incidence and natural history of pediatric LVO stroke. This retrospective population-based cohort study was conducted between January 2010 and December 2019, with a mean (SD) follow-up of 37.0 (28.8) months. Admissions from all pediatric hospitals in the state of New South Wales, Australia, with a final diagnosis of arterial ischemic stroke (AIS) in patients 1 month to younger than 17 years were included. A total of 85 of 251 identified cases were excluded based on selection criteria. Data were analyzed from July 2020 to June 2021. One-third of patients with LVO received mechanical thrombectomy with or without intravenous thrombolysis while the remainder were treated conservatively. The primary outcome was the pediatric modified Rankin Scale (ped-mRS) score 3 months after stroke. Ordinal logistic regression was used to compare non-LVO, LVO without thrombectomy, and LVO with thrombectomy groups. Of 161 included patients, 56 (34.8%) were female, and the mean (SD) age was 6.1 (5.4) years. A total of 166 AIS admissions were studied, and clinical follow-up was available for 164 of 166 admissions. LVO was present in 39 admissions (23.5%). The incidence of LVO stroke was 0.24 per 100 000 patients per year (95% CI, 0.13-0.35). Patients with LVO who did not receive thrombectomy (n = 26) had poor neurological outcomes, with 19 (73.1%) experiencing moderate to severe disability or death (ped-mRS score of 3 to 6) at 3 months (6 of 12 patients receiving thrombectomy [50.0%]; 25 of 38 patients with LVO [65.8%]). Patients with LVO without thrombectomy had significantly worse clinical outcomes than patients with non-LVO at 3 months (odds ratio, 3.64; 95% CI, 1.68-7.87; P = .001). Most patients with LVO presented within time windows suitable for thrombectomy (27 of 39 [69.2%] within 6 hours; 35 of 39 [89.7%] within 24 hours). In this population-based cohort study, the natural history of pediatric patients with LVO stroke treated conservatively was poor, with most experiencing lifelong disability or death. Nearly 90% of pediatric patients with LVO presented within time windows suitable for thrombectomy.

Identifiants

pubmed: 35344005
pii: 2790530
doi: 10.1001/jamaneurol.2022.0323
pmc: PMC8961400
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

488-497

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Auteurs

Kartik D Bhatia (KD)

Department of Medical Imaging, Children's Hospital at Westmead, Westmead, Australia.
Children's Hospital at Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Westmead, Australia.
Faculty of Medicine, Macquarie University, Sydney, Australia.

Romain Briest (R)

Department of Neurology, Sydney Children's Hospital, Randwick, Sydney, Australia.

Robert Goetti (R)

Department of Medical Imaging, Children's Hospital at Westmead, Westmead, Australia.

Richard Webster (R)

Children's Hospital at Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Westmead, Australia.
T.Y. Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia.

Christopher Troedson (C)

Children's Hospital at Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Westmead, Australia.
T.Y. Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia.

Russell C Dale (RC)

Children's Hospital at Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Westmead, Australia.
T.Y. Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia.

Prakash Muthusami (P)

Division of Image-Guided Therapy, Department of Radiology, Hospital for Sick Children, Toronto, Ontario, Canada.

Christina Miteff (C)

Department of Neurology, John Hunter Children's Hospital, New Lambton Heights, Australia.

Ferdinand Miteff (F)

Department of Neurology, John Hunter Hospital, New Lambton Heights, Australia.

John Worthington (J)

Department of Neurology, Royal Prince Alfred Hospital, Camperdown, Australia.

Kylie Tastula (K)

Department of Neurology, Royal Prince Alfred Hospital, Camperdown, Australia.

Timothy Ang (T)

Department of Neurology, Royal Prince Alfred Hospital, Camperdown, Australia.

Ian Andrews (I)

Department of Neurology, Sydney Children's Hospital, Randwick, Sydney, Australia.
School of Women's and Children's Health, Faculty of Medicine, University of New South Wales, Randwick, Australia.

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