Macroscopic lesions of maternal and fetal vascular malperfusion in stillborn placentas: Diagnosis in the absence of microscopic histopathological examination.
Fetal vascular malperfusion
Macroscopic evaluation
Maternal vascular malperfusion
Stillbirth
Journal
Placenta
ISSN: 1532-3102
Titre abrégé: Placenta
Pays: Netherlands
ID NLM: 8006349
Informations de publication
Date de publication:
07 09 2023
07 09 2023
Historique:
received:
11
04
2023
revised:
06
06
2023
accepted:
27
07
2023
pmc-release:
07
09
2024
medline:
15
9
2023
pubmed:
4
8
2023
entrez:
3
8
2023
Statut:
ppublish
Résumé
Lesions of maternal vascular malperfusion (MVM) and fetal vascular malperfusion (FVM) are common in placentas associated with both stillbirth and live birth. The objective of this study was to identify lesions present more commonly in stillborn placentas and those most indicative of MVM and FVM without microscopic pathologic evaluation. Data were derived from the Stillbirth Collaborative Research Network. Lesions were identified according to standard protocols published previously and categorized as either MVM or FVM according to the Amsterdam Placental Workshop Group Consensus Statement and macroscopic "umbilical cord at risk" findings. Multivariate logistic regression was used to determine the odds of stillbirth with macroscopic findings of MVM or FVM. 595 stillbirths and 1,305 live births were analyzed. FVM lesions (85.2%) were marginally more common (though not statistically different) in stillbirths compared to MVM lesions (81.3%). Macroscopic findings of both MVM and FVM were more common in stillbirths versus livebirths (p < 0.001). Odds ratios of macroscopic MVM and FVM lesions for stillbirth, adjusted for gestational age at delivery, maternal race (minority), ethnicity (Hispanic), age, and history of hypertension or diabetes, were 1.48 (95% CI 1.30-1.69) and 1.34 (95% CI 1.18-1.53), respectively. Macroscopic features of MVM and FVM are associated with higher odds of stillbirth versus live birth even when controlled for gestational age and maternal factors, which may be a useful clue in determining the pathophysiology of these events. This information is also useful for pathologists when microscopic examination is not available.
Identifiants
pubmed: 37536149
pii: S0143-4004(23)00453-8
doi: 10.1016/j.placenta.2023.07.296
pmc: PMC10530266
mid: NIHMS1923000
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
60-65Subventions
Organisme : NICHD NIH HHS
ID : U10 HD045953
Pays : United States
Organisme : NICHD NIH HHS
ID : U01 HD045954
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045925
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045952
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045955
Pays : United States
Organisme : NICHD NIH HHS
ID : U10 HD045944
Pays : United States
Informations de copyright
Copyright © 2023 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this article.
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