Fetal growth restriction as the initial finding of preeclampsia is a clinical predictor of maternal and neonatal prognoses: a single-center retrospective study.

Adverse pregnancy outcomes Cesarean section Eclampsia Fetal growth restriction Hypertensive disorder of pregnancy New ISSHP criteria Nonreassuring fetal status Preeclampsia Pregnancy complications

Journal

BMC pregnancy and childbirth
ISSN: 1471-2393
Titre abrégé: BMC Pregnancy Childbirth
Pays: England
ID NLM: 100967799

Informations de publication

Date de publication:
06 Oct 2021
Historique:
received: 15 01 2021
accepted: 23 09 2021
entrez: 7 10 2021
pubmed: 8 10 2021
medline: 11 1 2022
Statut: epublish

Résumé

Preeclampsia (PE) is a hypertensive disorder specific to pregnancy that can cause severe maternal-neonatal complications. The International Society for the Study of Hypertension in Pregnancy revised the PE criteria in 2018; a PE diagnosis can be established in the absence of proteinuria when organ or uteroplacental dysfunction occurs. The initial findings of PE (IFsPE) at the first diagnosis can vary considerably across patients. However, the impacts of different IFsPE on patient prognoses have not been reported. Thus, we investigate the predictors of pregnancy complications and adverse pregnancy outcomes based on IFsPE according to the new criteria. This retrospective study included 3729 women who delivered at our hospital between 2015 and 2019. All women were reclassified based on the new PE criteria and divided into three groups based on the IFsPE: Classification 1 (C-1), proteinuria (classical criteria); Classification 2 (C-2), damage to other maternal organs; and Classification 3 (C-3), uteroplacental dysfunction. Pregnancy complications and adverse pregnancy outcomes were assessed and compared among the three groups. In total, 104 women with PE were included. Of those, 42 (40.4%), 28 (26.9%), and 34 (32.7%) were assigned to C-1, C-2, and C-3 groups, respectively. No significant differences in maternal characteristics were detected among the three groups, except for gestational age at PE diagnosis (C-1, 35.5 ± 3.0 weeks; C-2, 35.2 ± 3.6 weeks; C-3, 31.6 ± 4.6 weeks, p <  0.01). The rates of premature birth at < 37 weeks of gestation, fetal growth restriction (FGR), and neonatal acidosis were significantly higher in the C-3 group compared to the C-1 and C-2 groups. Additionally, the composite adverse pregnancy outcomes of the C-3 group compared with C-1 and C-2 represented a significantly higher number of patients. PE patients with uteroplacental dysfunction as IFsPE had the most unfavorable prognoses for premature birth, FGR, acidosis, and composite adverse pregnancy outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Preeclampsia (PE) is a hypertensive disorder specific to pregnancy that can cause severe maternal-neonatal complications. The International Society for the Study of Hypertension in Pregnancy revised the PE criteria in 2018; a PE diagnosis can be established in the absence of proteinuria when organ or uteroplacental dysfunction occurs. The initial findings of PE (IFsPE) at the first diagnosis can vary considerably across patients. However, the impacts of different IFsPE on patient prognoses have not been reported. Thus, we investigate the predictors of pregnancy complications and adverse pregnancy outcomes based on IFsPE according to the new criteria.
METHODS METHODS
This retrospective study included 3729 women who delivered at our hospital between 2015 and 2019. All women were reclassified based on the new PE criteria and divided into three groups based on the IFsPE: Classification 1 (C-1), proteinuria (classical criteria); Classification 2 (C-2), damage to other maternal organs; and Classification 3 (C-3), uteroplacental dysfunction. Pregnancy complications and adverse pregnancy outcomes were assessed and compared among the three groups.
RESULTS RESULTS
In total, 104 women with PE were included. Of those, 42 (40.4%), 28 (26.9%), and 34 (32.7%) were assigned to C-1, C-2, and C-3 groups, respectively. No significant differences in maternal characteristics were detected among the three groups, except for gestational age at PE diagnosis (C-1, 35.5 ± 3.0 weeks; C-2, 35.2 ± 3.6 weeks; C-3, 31.6 ± 4.6 weeks, p <  0.01). The rates of premature birth at < 37 weeks of gestation, fetal growth restriction (FGR), and neonatal acidosis were significantly higher in the C-3 group compared to the C-1 and C-2 groups. Additionally, the composite adverse pregnancy outcomes of the C-3 group compared with C-1 and C-2 represented a significantly higher number of patients.
CONCLUSIONS CONCLUSIONS
PE patients with uteroplacental dysfunction as IFsPE had the most unfavorable prognoses for premature birth, FGR, acidosis, and composite adverse pregnancy outcomes.

Identifiants

pubmed: 34615491
doi: 10.1186/s12884-021-04152-2
pii: 10.1186/s12884-021-04152-2
pmc: PMC8495959
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

678

Informations de copyright

© 2021. The Author(s).

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Auteurs

Masaya Takahashi (M)

Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Tomioka 2-1-1, Urayasu City, Chiba, 279-0021, Japan.

Shintaro Makino (S)

Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Tomioka 2-1-1, Urayasu City, Chiba, 279-0021, Japan. shintaro@juntendo.ac.jp.

Kyoko Oguma (K)

Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Tomioka 2-1-1, Urayasu City, Chiba, 279-0021, Japan.

Haruka Imai (H)

Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Tomioka 2-1-1, Urayasu City, Chiba, 279-0021, Japan.

Ai Takamizu (A)

Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Tomioka 2-1-1, Urayasu City, Chiba, 279-0021, Japan.

Akari Koizumi (A)

Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Tomioka 2-1-1, Urayasu City, Chiba, 279-0021, Japan.

Koyo Yoshida (K)

Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Tomioka 2-1-1, Urayasu City, Chiba, 279-0021, Japan.

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