Is chronic histiocytic intervillositis a severe placental disease? A case-control study.


Journal

Placenta
ISSN: 1532-3102
Titre abrégé: Placenta
Pays: Netherlands
ID NLM: 8006349

Informations de publication

Date de publication:
02 2020
Historique:
received: 22 04 2019
revised: 27 12 2019
accepted: 28 12 2019
entrez: 17 3 2020
pubmed: 17 3 2020
medline: 9 2 2021
Statut: ppublish

Résumé

Chronic histiocytic intervillositis (CHI) is a placental disease that has been associated with unfavorable obstetric outcomes in small, noncomparative series. The objective was to measure the excess risk of adverse obstetric outcomes associated with the discovery of CHI after birth. Retrospective single-center case-control study from 2000 through 2016. The case patients had a CHI diagnosis after a pathology analysis of the placenta. Two types of controls were defined for each case: low-risk control women were those who gave birth in our hospital immediately before each case patient, and the high-risk controls were the next women after each case for whom microscopic examination of the placenta was indicated. We observed 111 cases of CHI during the study period. Compared with the 111 low-risk controls, the cases had a significantly higher frequency of late miscarriages (5.4 vs 0.0%, p < .03), small for gestational age (SGA) babies <3rd centile (70.4 vs 0.9%, p < .001, OR 140, 95% CI, 19.9-2800), and in utero deaths (35.1 vs 0.9%, p < .001, OR 59.6, 95% CI 8.5-1192), with significantly fewer children surviving to discharge (54.9 vs 99.1%, p < .001, OR 0.01, 95% CI, 0.00-0.08). All of these factors also differed significantly compared with the high-risk women (severe SGA: OR 3.7, 95% CI 1.9-7.0; in utero death: OR 4.1, 95% CI 1.9-8.7; children surviving to discharge: OR 0.27, 95% CI, 0.14-0.52). Even compared with high-risk pregnancies, CHI is a severe placental disease associated with a substantial excess rate of late miscarriages, severe SGA and in utero death.

Identifiants

pubmed: 32174304
pii: S0143-4004(19)30731-3
doi: 10.1016/j.placenta.2019.12.020
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

31-36

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors report no conflict of interest.

Auteurs

C Homatter (C)

Univ. Lille, CHU Lille, Hôpital Jeanne de Flandre, Pôle Femme Mère Nouveau-né, F-59000, Lille, France. Electronic address: celine.homatter@ghrmsa.fr.

M Stichelbout (M)

CHU Lille, Pôle de Pathologie, Centre de Biologie-Pathologie, F-59000, Lille, France.

L Devisme (L)

CHU Lille, Pôle de Pathologie, Centre de Biologie-Pathologie, F-59000, Lille, France.

A Chudzinski (A)

Maternité de Beaumont, Centre Hospitalier, F-59100, Roubaix, France.

V Debarge (V)

Univ. Lille, CHU Lille, Hôpital Jeanne de Flandre, Pôle Femme Mère Nouveau-né, F-59000, Lille, France; Univ. Lille, EA 4489, Environnement périnatal et croissance, F-59000, Lille, France.

C Garabedian (C)

Univ. Lille, CHU Lille, Hôpital Jeanne de Flandre, Pôle Femme Mère Nouveau-né, F-59000, Lille, France; Univ. Lille, EA 4489, Environnement périnatal et croissance, F-59000, Lille, France.

D Subtil (D)

Univ. Lille, CHU Lille, Hôpital Jeanne de Flandre, Pôle Femme Mère Nouveau-né, F-59000, Lille, France; Univ. Lille, EA 2694 Santé Publique, Epidémiologie et Qualité des Soins, F-59000, Lille, France.

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