Risk factors for perinatal arterial ischaemic stroke: a large case-control study.


Journal

Developmental medicine and child neurology
ISSN: 1469-8749
Titre abrégé: Dev Med Child Neurol
Pays: England
ID NLM: 0006761

Informations de publication

Date de publication:
04 2020
Historique:
accepted: 02 08 2019
pubmed: 7 9 2019
medline: 7 7 2020
entrez: 7 9 2019
Statut: ppublish

Résumé

To identify maternal, obstetric, and neonatal risk factors related to perinatal arterial ischaemic stroke (PAIS) diagnosed within 28 days after birth and to understand the underlying pathophysiology. For case and control ascertainment, we used active surveillance in 345 paediatric hospitals and a population-based perinatal database for quality assurance of hospital care. We analysed complete cases of PAIS using logistic regression. Multivariate analysis was guided by a directed acyclic graph. After exclusion of records with missing data, we analysed 134 individuals with PAIS and 576 comparison individuals. In univariate analysis, male sex, preterm birth (<37wks gestational age), small for gestational age (SGA), low umbilical artery pH (<7.1), low 5-minute-Apgar score (<7), multiple pregnancies, hypoxia, intubation/mask ventilation, nulliparity, Caesarean section, vaginal-operative delivery, chorioamnionitis, and oligohydramnios were associated with an increased risk. Mutual adjustment yielded male sex (odds ratio [OR] 1.81; 95% confidence interval [CI] 1.20-2.73), multiple birth (OR 3.22; 95% CI 1.21-8.58), chorioamnionitis (OR 9.89; 95% CI 2.88-33.94), preterm birth (OR 1.86; 95% CI 1.01-3.43), and SGA (OR 3.05; 95% CI 1.76-5.28) as independent risk factors. We confirmed the increased risk in males and the role of chorioamnionitis and SGA for PAIS, pointing to the importance of inflammatory processes and fetal-placental insufficiency. Multiple birth and preterm birth were additional risk factors. Chorioamnionitis and small for gestational age (SGA) precede perinatal arterial ischaemic stroke (PAIS). Chorioamnionitis and SGA are independent risk factors for PAIS. Inflammatory processes and fetal-placental insufficiency are the likely underlying mechanisms. Multiple birth and preterm birth are additional risk factors.

Identifiants

pubmed: 31489622
doi: 10.1111/dmcn.14347
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

513-520

Subventions

Organisme : Friedrich-Baur-Stiftung
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Mac Keith Press.

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Auteurs

Anna-Lisa Sorg (AL)

Division of Pediatric Epidemiology, Institute of Social Pediatrics and Adolescent Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.

Rüdiger von Kries (R)

Division of Pediatric Epidemiology, Institute of Social Pediatrics and Adolescent Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.

Mathias Klemme (M)

Department of Neonatology, University Children's Hospital and Perinatal Center, Ludwig-Maximilians-Universität München, Munich, Germany.

Lucia Gerstl (L)

Department of Pediatric Neurology, University Children's Hospital, Ludwig-Maximilians-Universität München, Munich, Germany.

Raphael Weinberger (R)

Division of Pediatric Epidemiology, Institute of Social Pediatrics and Adolescent Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.

Andreas Beyerlein (A)

Institute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany.

Nicholas Lack (N)

Bavarian Quality Assurance for In-Patient Medical Care, Munich, Germany.

Ursula Felderhoff-Müser (U)

Department of Pediatrics I, Neonatology, University of Duisburg-Essen, Essen, Germany.

Mark Dzietko (M)

Department of Pediatrics I, Neonatology, University of Duisburg-Essen, Essen, Germany.

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