Population-based prevalence of congenital defects in a routine sentinel site-based surveillance system in the Western Cape, South Africa.


Journal

Birth defects research
ISSN: 2472-1727
Titre abrégé: Birth Defects Res
Pays: United States
ID NLM: 101701004

Informations de publication

Date de publication:
Aug 2024
Historique:
revised: 18 06 2024
received: 28 03 2024
accepted: 15 07 2024
medline: 9 8 2024
pubmed: 9 8 2024
entrez: 9 8 2024
Statut: ppublish

Résumé

Lack of data on the burden and scope of congenital disorders (CDs) in South Africa undermines resource allocation and limits the ability to detect signals from potentially teratogenic pregnancy exposures. We used routine electronic data in the Western Cape Pregnancy Exposure Registry (PER) to determine the overall and individual prevalence of CD identified on neonatal surface examination at birth in the Western Cape, South Africa, 2016-2022. CD was confirmed by record review. The contribution of late (≤24 months) and antenatal diagnoses was assessed. We compared demographic and obstetric characteristics between women with/without pregnancies affected by CD. Women with a viable pregnancy (>22 weeks gestation; birth weight ≥ 500 g) (n = 32,494) were included. Of 1106 potential CD identified, 56.1% were confirmed on folder review. When internal and minor CD were excluded the prevalence of major CD identified on surface examination at birth was 7.2/1000 births. When missed/late diagnoses on examination (16.8%) and ultrasound (6.8%) were included, the prevalence was 9.2/1000 births: 8.9/1000 livebirths and 21.5/1000 stillbirths. The PER did not detect 21.5% of major CD visible at birth. Older maternal age and diabetes mellitus were associated with an increased prevalence of CD. Women living with/without HIV (or the timing of antiretroviral therapy, before/after conception), hypertension or obesity did not significantly affect prevalence of CD. A surveillance system based on routine data successfully determined the prevalence of major CD identified on surface examination at birth at rates slightly higher than in equivalent studies. Overall rates, modeled at ~2%, are likely underestimated. Strengthening routine neonatal examination and clinical record-keeping could improve CD ascertainment.

Sections du résumé

BACKGROUND BACKGROUND
Lack of data on the burden and scope of congenital disorders (CDs) in South Africa undermines resource allocation and limits the ability to detect signals from potentially teratogenic pregnancy exposures.
METHODS METHODS
We used routine electronic data in the Western Cape Pregnancy Exposure Registry (PER) to determine the overall and individual prevalence of CD identified on neonatal surface examination at birth in the Western Cape, South Africa, 2016-2022. CD was confirmed by record review. The contribution of late (≤24 months) and antenatal diagnoses was assessed. We compared demographic and obstetric characteristics between women with/without pregnancies affected by CD.
RESULTS RESULTS
Women with a viable pregnancy (>22 weeks gestation; birth weight ≥ 500 g) (n = 32,494) were included. Of 1106 potential CD identified, 56.1% were confirmed on folder review. When internal and minor CD were excluded the prevalence of major CD identified on surface examination at birth was 7.2/1000 births. When missed/late diagnoses on examination (16.8%) and ultrasound (6.8%) were included, the prevalence was 9.2/1000 births: 8.9/1000 livebirths and 21.5/1000 stillbirths. The PER did not detect 21.5% of major CD visible at birth. Older maternal age and diabetes mellitus were associated with an increased prevalence of CD. Women living with/without HIV (or the timing of antiretroviral therapy, before/after conception), hypertension or obesity did not significantly affect prevalence of CD.
CONCLUSIONS CONCLUSIONS
A surveillance system based on routine data successfully determined the prevalence of major CD identified on surface examination at birth at rates slightly higher than in equivalent studies. Overall rates, modeled at ~2%, are likely underestimated. Strengthening routine neonatal examination and clinical record-keeping could improve CD ascertainment.

Identifiants

pubmed: 39118354
doi: 10.1002/bdr2.2388
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2388

Subventions

Organisme : US National Institutes of Health
ID : R01HD080465
Organisme : US National Institutes of Health
ID : U01AI069924
Organisme : US Centers for Disease Control and Prevention
ID : GH001934
Organisme : Bill & Melinda Gates Foundation
ID : INV-004508
Pays : United States

Informations de copyright

© 2024 The Author(s). Birth Defects Research published by Wiley Periodicals LLC.

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Auteurs

Emma Kalk (E)

Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Sub-Saharan African Congenital Anomalies Network, University of Cape Town, Cape Town, South Africa.

Alexa Heekes (A)

Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Health Intelligence Directorate, Western Cape Government Department of Health & Wellness, Cape Town, South Africa.

Diane Lavies (D)

Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Sub-Saharan African Congenital Anomalies Network, University of Cape Town, Cape Town, South Africa.

Lizel Jacobs (L)

Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Sub-Saharan African Congenital Anomalies Network, University of Cape Town, Cape Town, South Africa.

Careni Spencer (C)

Division of Human Genetics, Department of Medicine, University of Cape Town & Groote Schuur Hospital, Cape Town, South Africa.

Alison Boutall (A)

Department of Obstetrics & Gynaecology, University of Cape Town & Groote Schuur Hospital, Cape Town, South Africa.

Ayesha Osman (A)

Department of Obstetrics & Gynaecology, University of Cape Town & Groote Schuur Hospital, Cape Town, South Africa.

Chantal Stewart (C)

Department of Obstetrics & Gynaecology, University of Cape Town & Mowbray Maternity Hospital, Cape Town, South Africa.

Mary-Ann Davies (MA)

Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Health Intelligence Directorate, Western Cape Government Department of Health & Wellness, Cape Town, South Africa.

Anika van Niekerk (A)

Sub-Saharan African Congenital Anomalies Network, University of Cape Town, Cape Town, South Africa.
Department of Paediatrics & Child Health, University of Cape Town & Mowbray Maternity Hospital, Cape Town, South Africa.

Karen Fieggen (K)

Sub-Saharan African Congenital Anomalies Network, University of Cape Town, Cape Town, South Africa.
Division of Human Genetics, Department of Medicine, University of Cape Town & Groote Schuur Hospital, Cape Town, South Africa.

Andrew Boulle (A)

Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Health Intelligence Directorate, Western Cape Government Department of Health & Wellness, Cape Town, South Africa.

Ushma Mehta (U)

Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
Sub-Saharan African Congenital Anomalies Network, University of Cape Town, Cape Town, South Africa.

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