Amniotic membrane and placental histopathological findings after open and fetoscopic prenatal neural tube defect repair.


Journal

Prenatal diagnosis
ISSN: 1097-0223
Titre abrégé: Prenat Diagn
Pays: England
ID NLM: 8106540

Informations de publication

Date de publication:
03 2019
Historique:
received: 14 09 2018
revised: 20 11 2018
accepted: 24 12 2018
pubmed: 5 1 2019
medline: 24 3 2020
entrez: 5 1 2019
Statut: ppublish

Résumé

To describe and compare placental and amniotic histology in women who underwent a fetoscopic myelomeningocele repair to those who underwent an open hysterotomy myelomeningocele repair. Also, we intended to compare findings from both prenatal repair groups to age-matched control pregnant patients. Placental and membrane histopathology from 43 prenatally repaired spina bifida cases (17 fetoscopic and 26 open) and 18 healthy controls were retrospectively assessed. Quantitative assessment of histopathology included apoptosis count and maternal and fetal underperfusion scores. Qualitative assessment included the detection of pigmented macrophages and/or signs of placental/amniotic inflammation. Associations between the duration of surgery or the duration of CO Fetoscopic surgery cases did not show significant differences in any of the studied parameters when compared against controls. No differences were detected either when compared with open repaired cases, except for lower proportion of pigmented laden macrophages in the fetoscopic group (11.8% vs 61.5%, P < 0.01). No associations between the duration of surgery or the duration of CO These preliminary results support the lack of detrimental effects of the use of heated and humidified CO

Identifiants

pubmed: 30609053
doi: 10.1002/pd.5414
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

269-279

Informations de copyright

© 2019 John Wiley & Sons, Ltd.

Auteurs

Magdalena Sanz Cortes (M)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

Eumenia Castro (E)

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

Dina Sharhan (D)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

Paola Torres (P)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

Mayel Yepez (M)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

Jimmy Espinoza (J)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

Alireza A Shamshirsaz (AA)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

Ahmed A Nassr (AA)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

Edwina Popek (E)

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

William Whitehead (W)

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

Michael A Belfort (MA)

Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine & Texas Children's Hospital, Houston, TX, USA.

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Classifications MeSH