Incidence of pre-eclampsia: effect of deprivation.


Journal

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
ISSN: 1469-0705
Titre abrégé: Ultrasound Obstet Gynecol
Pays: England
ID NLM: 9108340

Informations de publication

Date de publication:
01 2023
Historique:
revised: 12 09 2022
received: 22 08 2022
accepted: 13 09 2022
pubmed: 1 10 2022
medline: 6 1 2023
entrez: 30 9 2022
Statut: ppublish

Résumé

To examine the relationship between the English index of multiple deprivation (IMD) and the incidence of pre-eclampsia (PE), evaluate the distribution of IMD in a cohort of ethnically diverse pregnant women in South East England and assess whether IMD improves the prediction of PE compared with that provided by the 'history-only' competing-risks model (based on maternal characteristics and medical history). This was a prospective, observational study of 159 125 women with a singleton pregnancy who attended their first routine hospital visit at 11 + 0 to 13 + 6 weeks' gestation in two maternity hospitals in the UK. The inclusion criteria were delivery at ≥ 24 weeks' gestation of babies without major abnormality. Participants completed a questionnaire on demographic characteristics and obstetric and medical history, which was then reviewed by a doctor together with the woman. Patients were asked to self-identify as white, black, South Asian, East Asian or mixed race. IMD was used as a measure of socioeconomic status, which takes into account income, employment, education, skills and training, health and disability, crime, barriers to housing and services, and living environment. Each neighborhood is ranked according to their level of deprivation relative to that of other areas into one of five equal groups, with Quintile 1 containing the 20% most deprived areas and Quintile 5 containing the 20% least deprived areas. IMD was assigned based on a woman's postcode. Risk factors for PE and its incidence were assessed across IMD using chi-square test or t-test, as appropriate. The relationship between IMD and gestational age at delivery with PE was evaluated by fitting parametric survival models for IMD alone, IMD combined with race and IMD combined with the Fetal Medicine Foundation history-only competing-risks model. The incidence of PE (n = 4088, 2.6%) increased progressively across IMD quintiles, from 2.0% in Quintile 5 (least deprived) to 3.0% in Quintile 1 (most deprived). Compared with white women and those in other racial groups, black women had a higher incidence of PE (4.8%), were less often in IMD Quintiles 4 and 5, and were more often in IMD Quintiles 1 and 2. None of the IMD quintiles improved the prediction of PE compared with that provided by the history-only competing-risks model (which includes race). The history-only competing-risks model with vs without IMD had a similar detection rate for delivery with PE at < 37 weeks' gestation (44.1% (95% CI, 41.1-47.2%) vs 43.9% (95% CI, 40.1-47.0%)) and at any gestational age (35.2% (95% CI, 33.8-36.7%) vs 35.1% (95% CI, 33.7-36.6%)), at a 10% screen-positive rate. The incidence of PE is higher in women living in the most deprived areas in South East England and in black women (vs those of other racial groups), who also live in areas of higher deprivation. However, in screening for PE, inclusion of IMD does not improve the prediction of PE provided by race and other maternal characteristics and elements of medical history. © 2022 International Society of Ultrasound in Obstetrics and Gynecology.

Identifiants

pubmed: 36178775
doi: 10.1002/uog.26084
doi:

Substances chimiques

Biomarkers 0
Placenta Growth Factor 144589-93-5

Types de publication

Observational Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

26-32

Subventions

Organisme : Fetal Medicine Foundation
ID : Grant/Award Number: 1037116

Informations de copyright

© 2022 International Society of Ultrasound in Obstetrics and Gynecology.

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Auteurs

A Arechvo (A)

Fetal Medicine Research Institute, King's College Hospital, London, UK.
Department of Obstetrics and Gynecology, Institute of Clinical Sciences Lund, Lund University, Lund, Sweden.

A Wright (A)

Institute of Health Research, University of Exeter, Exeter, UK.

A Syngelaki (A)

Fetal Medicine Research Institute, King's College Hospital, London, UK.

P von Dadelszen (P)

Institute of Women and Children's Health, School of Life Course and Population Sciences, King's College London, London, UK.

L A Magee (LA)

Institute of Women and Children's Health, School of Life Course and Population Sciences, King's College London, London, UK.

R Akolekar (R)

Fetal Medicine Unit, Medway Maritime Hospital, Gillingham, UK.
Institute of Medical Sciences, Canterbury Christ Church University, Chatham, UK.

D Wright (D)

Department of Obstetrics and Gynecology, Institute of Clinical Sciences Lund, Lund University, Lund, Sweden.

K H Nicolaides (KH)

Fetal Medicine Research Institute, King's College Hospital, London, UK.

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