Evidence map›Paper›PMID 38198446›Full record

ArticlePloS one2024

Trends in harmful drug exposure during pregnancy in France between 2013 and 2019: A nationwide cohort study.

Margaux Louchet, Mathis Collier, Nathanaël Beeker, Laurent Mandelbrot, Jeanne Sibiude, Laurent Chouchana, Jean Marc Treluyer

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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

7 authors.

Margaux LouchetUPR7323 "Pharmacology and Drug Evaluatioán in Children and Pregnant Women", Université Paris Cité, Paris, Île-de-France, France.ORCID 0000-0001-5589-3174
Mathis CollierUPR7323 "Pharmacology and Drug Evaluatioán in Children and Pregnant Women", Université Paris Cité, Paris, Île-de-France, France.
Nathanaël BeekerUPR7323 "Pharmacology and Drug Evaluatioán in Children and Pregnant Women", Université Paris Cité, Paris, Île-de-France, France.
Laurent MandelbrotDepartment of Obstetrics and Gynecology, Louis Mourier Hospital, Assistance Publique-Hôpitaux de Paris, Paris, Île-de-France, France.ORCID 0000-0002-5883-7597
Jeanne SibiudeDepartment of Obstetrics and Gynecology, Louis Mourier Hospital, Assistance Publique-Hôpitaux de Paris, Paris, Île-de-France, France.
Laurent ChouchanaUPR7323 "Pharmacology and Drug Evaluatioán in Children and Pregnant Women", Université Paris Cité, Paris, Île-de-France, France.ORCID 0000-0002-9626-3571
Jean Marc TreluyerUPR7323 "Pharmacology and Drug Evaluatioán in Children and Pregnant Women", Université Paris Cité, Paris, Île-de-France, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDescribe the trends of exposure to harmful drugs during pregnancy over recent years in France.

designNationwide cohort study.

settingThe French National administrative health Data System (SNDS). POPULATION: Pregnancies starting between 2013 and 2019 and outcomes corresponding to live births, medical terminations of pregnancy, and stillbirths.

methodsEach pregnancy was divided into a preconceptional period of 90 days before conception and three trimesters from conception to birth. Harmful drugs were defined according to their risks to the fetus: teratogenicity or fetotoxicity. Exposure was defined using the critical period during pregnancy for each type of harmful drug: preconceptional period or first trimester for teratogenic drugs and second or third trimesters for fetotoxic drugs.

main outcome measuresPrevalence of pregnancies exposed to at least one harmful drug.

resultsAmong 5,253,284 pregnancies, 204,402 (389 per 10,000) pregnancies were exposed to at least one harmful drug during the critical periods: 48,326 (92 per 10,000) pregnancies were exposed to teratogenic drugs during the preconceptional period or the first trimester, and 155,514 (299 per 10,000) pregnancies were exposed to fetotoxic drugs during the second or third trimesters. Teratogenic drugs were mainly retinoids for topical use (44 per 10,000 pregnancies), antiepileptics (13 per 10,000 pregnancies) and statins (13 per 10,000 pregnancies). Fetotoxic drugs were mainly non-steroidal anti-inflammatory drugs (NSAIDs), for systemic (128 per 10,000 pregnancies) and topical use (122 per 10,000 pregnancies). Exposure to teratogenic drugs decreased from the preconceptional period to the first trimester. Exposure to fetotoxic drugs decreased from the second to the third trimester. Between 2013 and 2019, we found a decrease in harmful drug exposure overall, mainly for topical and systemic NSAIDs and for topical retinoids.

conclusionsIn this nationwide study, about one in 25 pregnancies was exposed to at least one harmful drug, mainly NSAIDs and topical retinoids. Although the prevalence of harmful drug exposure decreased over the study period, NSAID exposure in the second and third trimester remains of concern.

Indexed as

AnticonvulsantsAnti-Inflammatory Agents, Non-SteroidalCohort StudiesFemaleFranceHumansPregnancyRetinoidsTeratogensAnticonvulsantsAnti-Inflammatory Agents, Non-SteroidalRetinoidsTeratogens

Identifiers

PMID38198446
PMCPMC10781191

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