Evidence map›Paper›PMID 35562676›Full record

ArticleBMC medical research methodology2022

Minimizing sample bias due to stigmatized behaviours: the representativeness of participants in a cohort study of alcohol in pregnancy.

David Tappin, Daniel Mackay, Lucy Reynolds, Niamh Fitzgerald

Abstract read
In one paragraph

Article in BMC medical research methodology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

4 authors.

David TappinSection of Child Health, College of Medical, Veterinary & Life Sciences, Wolfson Medical School Building, University of Glasgow, 31, Shawhill Road, Glasgow, Scotland, G41 3RW, UK. david.tappin@glasgow.ac.uk.
Daniel MackayInstitute of Health and Wellbeing, Public Health, University of Glasgow, 1 Lilybank Gardens, Glasgow, Scotland, G12 8RZ, UK.
Lucy ReynoldsNHS Greater Glasgow & Clyde Health Board, Community Child Health, Children's Services, Woodside Health and Care Centre, 891 Garscube Road, Glasgow, G20 7ER, UK.
Niamh FitzgeraldInstitute for Social Marketing & Health, Faculty of Health Sciences & Sport, University of Stirling, Stirling, FK9 4LA, UK.

Funding

Medical Research Council MR/S037519/1
6 · The paper itself

Abstract

backgroundStigmatized behaviours are often underreported, especially in pregnancy, making them challenging to address. The Alcohol and Child Development Study (ACDS) seeks to inform prevention of foetal alcohol harm, linking self-report as well as a maternal blood alcohol biomarker with child developmental outcomes. Samples were requested using passive, generic consent. The success of this approach at minimizing bias is presented comparing characteristics of women who provided samples to those who did not.

methodsAll pregnant women in the study city were sent a Patient Information Sheet (PIS) with their first NHS obstetric appointment letter. The PIS informed them that the NHS would like to take an extra blood sample for research purposes, unless they opted out. Neither the women nor the midwives were informed that the samples might be tested for an alcohol biomarker. This paper examines the extent to which women who provided the extra sample were representative of women where no sample was provided, in terms of routinely collected information: age; body mass index; area-based deprivation; previous pregnancies, abortions and caesarians; smoking status and carbon monoxide level; self-reported alcohol use, gestation and birth weight of their baby. Chi-square and Mann-Whitney U tests were used to compare groups.

results3436 (85%) of the 4049 pregnant women who attended their appointment provided the extra sample. Women who did not were significantly younger (p < 0.001), more materially deprived (p < 0.001), and less likely to be considered for intervention based on self-reported alcohol use (p < 0.001). There were no significant differences between the two groups on other routine data.

conclusionsThe use of passive consent without disclosure of the specific research focus resulted in a high level of sample provision. There was no evidence that study blinding was breached, and women who provided a sample were more likely to report alcohol consumption. Passive consent to draw additional blood for research purposes at routine antenatal venipuncture reduced sampling bias compared to asking women to give blood for an alcohol study. This methodology may be useful for other stigmatised behaviours.

Indexed as

Alcohol DrinkingChild DevelopmentSmokingSmoking CessationCohort StudiesFemaleHumansInfant, NewbornPregnancyPregnant PeopleClinical markersCohort studyData collectionDemographyEpidemiologyEthics of informed consent

Identifiers

PMID35562676
PMCPMC9107203

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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.