Impact of the size of the lesion in prenatal neural tube defect repair on imaging, neurosurgical and motor outcomes: a retrospective cohort study.


Journal

BJOG : an international journal of obstetrics and gynaecology
ISSN: 1471-0528
Titre abrégé: BJOG
Pays: England
ID NLM: 100935741

Informations de publication

Date de publication:
Jan 2021
Historique:
accepted: 28 04 2020
pubmed: 15 5 2020
medline: 5 3 2021
entrez: 15 5 2020
Statut: ppublish

Résumé

(1) To compare brain findings between large and non-large neural tube defect (NTD); (2) to evaluate the impact of large lesion on the surgical parameters; (3) to study any associations between the size of the lesions and brain findings 6 weeks postoperatively and neurological short-term outcomes. Retrospective cohort study. Texas Children's Hospital, between 2011 and 2018. Patients who underwent prenatal NTD repair. Large lesion was defined when the lesion's surface was >75th centile of our cohorts' lesions. Time of referral: ventriculomegaly and anatomical level of the lesion; surgery: duration and need for relaxing incisions. 6 weeks postoperative: hindbrain herniation (HBH) and ventriculomegaly. After delivery: dehiscence, need for hydrocephalus treatment and motor function. A total of 99 patients were included, 25 of whom presented with large lesions. Type of lesion and ventriculomegaly were comparable between individuals with large and non-large lesions. Individuals with large lesions were associated with increased need for relaxing incisions by 5.4 times (95% CI 1.3-23.2, P = 0.02). Six weeks postoperatively, having a large lesion decreased by ten times the likelihood of having a postoperative reversal of HBH (odds ratio = 0.1, 95% CI 0.1-0.4, P < 0.01). At birth, larger lesions increased the risk for repair dehiscence by 6.1 times (95% CI 1.6-22.5, P < 0.01) and the risk of dehiscence or leakage of cerebrospinal fluid at birth by 5.5 times (95% CI 1.6-18.9, P < 0.01). Prenatal repair of patients with large NTD presents a lower proportion of HBH reversal 6 weeks after the surgery, a higher risk of dehiscence and a higher need for postnatal repair. Evaluation of the size of fetal NTD can predict adverse neurological outcomes after prenatal NTD repair.

Identifiants

pubmed: 32406575
doi: 10.1111/1471-0528.16316
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

392-399

Subventions

Organisme : O'quinn foundation
Organisme : fondren foundation
Organisme : Tramuto foundation
Organisme : Sterling-Turner Foundation

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 Royal College of Obstetricians and Gynaecologists.

Références

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Auteurs

R Corroenne (R)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

K H Zhu (KH)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

E Johnson (E)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

R Johnson (R)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

W E Whitehead (WE)

Department of Neurosurgery, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

J Espinoza (J)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

J Castillo (J)

Department of Pediatrics, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

H Castillo (H)

Department of Pediatrics, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

G Orman (G)

E. B. Singleton Department of Pediatric Radiology, Texas Children's Hospital & Department of Radiology, Baylor College of Medicine, Houston, Texas, USA.

Tagm Huisman (T)

E. B. Singleton Department of Pediatric Radiology, Texas Children's Hospital & Department of Radiology, Baylor College of Medicine, Houston, Texas, USA.

A R Mehollin-Ray (AR)

E. B. Singleton Department of Pediatric Radiology, Texas Children's Hospital & Department of Radiology, Baylor College of Medicine, Houston, Texas, USA.

A A Shamshirsaz (AA)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

A A Nassr (AA)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

M A Belfort (MA)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

M Sanz Cortes (M)

Department of Obstetrics and Gynecology, Texas Children's Hospital & Baylor College of Medicine, Houston, Texas, USA.

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