Evidence map›Paper›PMID 35971629›Full record

ArticleAlcoholism, clinical and experimental research2022

The prevalence of fetal alcohol spectrum disorders in rural communities in South Africa: A third regional sample of child characteristics and maternal risk factors.

Philip A May, Marlene M de Vries, Anna-Susan Marais, Wendy O Kalberg, David Buckley, Julie M Hasken, Omar Abdul-Rahman, Luther K Robinson, Melanie A Manning, Soraya Seedat and 2 more

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
11.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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  12. Substance and alcohol use in pregnant women attending antenatal care at a tertiary hospital in Johannesburg, South Africa.The South African journal of psychiatry : SAJP : the journal of the Society of Psychiatrists of South Africa · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 2 countries.

Philip A MayNutrition Research Institute, The University of North Carolina at Chapel Hill, Kannapolis, North Carolina, USA.ORCID 0000-0003-1939-8701
Marlene M de VriesFaculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Anna-Susan MaraisFaculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Wendy O KalbergCenter on Alcoholism, Substance Abuse and Addictions, The University of New Mexico, Albuquerque, New Mexico, USA.
David BuckleyCenter on Alcoholism, Substance Abuse and Addictions, The University of New Mexico, Albuquerque, New Mexico, USA.
Julie M HaskenNutrition Research Institute, The University of North Carolina at Chapel Hill, Kannapolis, North Carolina, USA.
Omar Abdul-RahmanDepartment of Genetic Medicine, Munroe-Meyer Institute, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Luther K RobinsonDepartment of Pediatrics, State University of New York, Buffalo, New York, USA.
Melanie A ManningDepartment of Pathology and Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
Soraya SeedatFaculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Charles D H ParryFaculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
H Eugene HoymeFaculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Stellenbosch University · ZAUniversity of New Mexico · USUniversity of North Carolina at Chapel Hill · USNebraska Medical Center · USSanford Health · USSouth African Medical Research Council · ZAStanford University · USUniversity at Buffalo, State University of New York · US

Funding

Trajectory of Fetal Alcohol Spectrum Disorders (FASD) Across the Lifespan: Continuing Prevention and Longitudinal EpidemiologyU01AA015134 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MAY, PHILIP ALAN · 2009 to 2018
$7.8M
Trajectory of Fetal Alcohol Spectrum Disorders (FASD) Across the Lifespan: Continuing Prevention and Longitudinal EpidemiologyR01AA015134 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MAY, PHILIP ALAN · 2006 to 2022
$4.5M
NIAAA NIH HHS R01 AA015134NIAAA NIH HHS U01 AA015134
6 · The paper itself

Abstract

backgroundThis study is the ninth cross-sectional community study of fetal alcohol spectrum disorders (FASD) conducted by the multidisciplinary Fetal Alcohol Syndrome Epidemiology Research team in the Western Cape Province of South Africa. It is the third comprehensive study of FASD in a rural, agricultural region of South Africa.

methodsPopulation-based, active case ascertainment methods were employed among a school-based cohort to assess child physical and neurobehavioral traits, and maternal risk factor interviews were conducted to identify all children with FASD to determine its prevalence.

resultsConsent was obtained for 76.7% of 1158 children attending first grade in the region's public schools. Case-control results are presented for 95 with fetal alcohol syndrome (FAS), 64 with partial fetal alcohol syndrome (PFAS), 77 with alcohol-related neurodevelopmental disorder (ARND), 2 with alcohol-related birth defects (ARBD), and 213 randomly-selected controls. Four techniques estimating FASD prevalence from in-person examinations and testing yielded a range of total FASD prevalence of 206-366 per 1000. The final weighted, estimated prevalence of FAS was 104.5 per 1000, PFAS was 77.7 per 1000, ARND was 125.2 per 1000, and total FASD prevalence was 310 per 1000 (95% CI = 283.4-336.7). Expressed as a percentage, 31% had FASD. Although the rate of total FASD remained steady over 9 years, the proportion of children within the FASD group has changed significantly: FAS trended down and ARND trended up. A detailed evaluation is presented of the specific child physical and neurobehavioral traits integral to assessing the full continuum of FASD. The diagnosis of a child with FASD was significantly associated with maternal proximal risk factors such as: co-morbid prenatal use of alcohol and tobacco (OR = 19.1); maternal drinking of two (OR = 5.9), three (OR = 5.9), four (OR = 38.3), or more alcoholic drinks per drinking day; and drinking in the first trimester (OR = 8.4), first and second trimesters (OR = 17.7), or throughout pregnancy (OR = 18.6). Distal maternal risk factors included the following: slight or small physical status (height, weight, and head circumference), lower BMI, less formal education, late recognition of pregnancy, and higher gravidity, parity, and older age during the index pregnancy.

conclusionThe prevalence of FASD remained a significant problem in this region, but the severity of physical traits and anomalies within the continuum of FASD is trending downwards.

Indexed as

Fetal Alcohol Spectrum DisordersFluorocarbonsAlcohol DrinkingChildCross-Sectional StudiesFemaleHumansPregnancyPrevalenceRisk FactorsRural PopulationSouth AfricaFluorocarbonschild traits of FASDfetal alcohol spectrum disorders (FASD)maternal risk for FASDprenatal alcohol useprevalenceSouth Africa

Identifiers

PMID35971629
PMCPMC9588757
OpenAlexW4291941986

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.