Post traumatic cerebral sinovenous thrombosis in children: A retrospective and multicenter study.


Journal

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
ISSN: 1532-2130
Titre abrégé: Eur J Paediatr Neurol
Pays: England
ID NLM: 9715169

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 25 05 2022
revised: 26 12 2022
accepted: 17 01 2023
medline: 11 4 2023
pubmed: 7 2 2023
entrez: 6 2 2023
Statut: ppublish

Résumé

Cerebral sinovenous thrombosis (CSVT) is a rare but life-threatening condition in the pediatric population and there is no pediatric guidelines regarding anticoagulation for post traumatic CSVT. This study aims to describe a cohort of children with post traumatic CSVT and the use of anticoagulant therapy in this population. A multicenter retrospective study. Patients admitted with post traumatic CSVT in the six participating Pediatric Intensive Care Unit were included. Overall, 29 patients (median age 8.2 years [IQR 4.8-14.6], n = 22 (76%) males) were included in the study (Table 1). CSVT was observed within the first 24 h after admission for a half of the patients (n = 14, 50%). Anticoagulation was initiated in 18 patients (62%). No patient received thrombolytic therapy or endovascular treatment. The presence of epidural hematoma was associated with the absence of anticoagulation (n = 0 versus n = 10, p = 0.003). One patient (3%) died of extracranial injury (not related with adverse event of anticoagulation) and in survivors, median Pediatric Overall Performance Category Outcome (POPC) score at discharge from PICU was 2 [IQR 2-4] (i.e., mild disability). Regarding the outcomes of patients, we found no association according to the anticoagulation status (p = 1). Overall, 23 patients (79%) had a follow-up cerebral imaging with a median delay of 42 days [IQR 6-63] after admission. CSVT was still seen in 9 patients (31%). We found no difference regarding the persistence of CSVT between patients according to the anticoagulation status (p = 0.36). The median duration of anticoagulant treatment was 58 days [IQR 44-91] and one patient (3%) experienced adverse event related to anticoagulation. There were minimal adverse events in patients with post traumatic CSVT treated with therapeutic anticoagulation. However, the effect of anticoagulation on outcomes needs to be confirmed in further studies.

Identifiants

pubmed: 36746017
pii: S1090-3798(23)00009-0
doi: 10.1016/j.ejpn.2023.01.009
pii:
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12-15

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no conflict of interest to declare.

Auteurs

Helena Roth (H)

Pediatric Intensive Care Unit, Grenoble-Alpes University Hospital, 38000, Grenoble, France. Electronic address: hroth@chu-grenoble.fr.

Roman Ränsch (R)

Pediatric Intensive Care Unit, Grenoble-Alpes University Hospital, 38000, Grenoble, France. Electronic address: rransch@chu-grenoble.fr.

Manoelle Kossorotoff (M)

French Centre for Paediatric Stroke, Pediatric Neurology Department, Necker-Enfants Maladies University Hospital, Assistance Publique Hôpitaux de Paris, 75015, Paris, France. Electronic address: manoelle.kossorotoff@aphp.fr.

Adela Chahine (A)

Pediatric Intensive Care Unit, Toulouse University Hospital, 31000, Toulouse, France. Electronic address: Chahine.a@chu-toulouse.fr.

Olivier Tirel (O)

Pediatric Intensive Care Unit, Rennes University Hospital, 35000, Rennes, France. Electronic address: Olivier.tirel@chu-rennes.fr.

David Brossier (D)

Pediatric Intensive Care Unit, Caen University Hospital, 14000, Caen, France; Université Caen Normandie, Medical School, Caen, F-14000, France. Electronic address: brossier-d@chu-caen.fr.

Isabelle Wroblewski (I)

Pediatric Intensive Care Unit, Grenoble-Alpes University Hospital, 38000, Grenoble, France. Electronic address: iwroblewski@chu-grenoble.Fr.

Gilles Orliaguet (G)

Department of Pediatric Anaesthesia and Intensive Care, Necker University Hospital, AP-HP, Centre - Université Paris Cité, France; EA 7323 Université de Paris "Pharmacologie et évaluation des Thérapeutiques Chez L'enfant et La Femme Enceinte", Paris, France. Electronic address: gilles.orliaguet@aphp.fr.

Stéphane Chabrier (S)

French Centre for Paediatric Stroke, Pediatric Physical and Rehabilitation Medicine Department, Saint-Etienne University Hospital, 42000, Saint-Etienne, France. Electronic address: stephane.chabrier@chu-st-etienne.fr.

Guillaume Mortamet (G)

Pediatric Intensive Care Unit, Grenoble-Alpes University Hospital, 38000, Grenoble, France; Univ. Grenoble-Alpes, 38000, Grenoble, France. Electronic address: gmortamet@chu-grenoble.fr.

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Classifications MeSH