Evidence map›Paper›PMID 41183806›Full record

ArticleACR open rheumatology2025

Tumor Necrosis Factor Inhibitors and Risk of Serious Infections in Pregnant Women With Chronic Inflammatory Diseases.

Leah K Flatman, Marie-Eve Beauchamp, Yvan St-Pierre, Isabelle Malhamé, Anick Bérard, Sasha Bernatsky, Évelyne Vinet

Abstract read
In one paragraph

Article in ACR open rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Leah K FlatmanMcGill University and McGill University Health Centre, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-3719-1248
Marie-Eve BeauchampMcGill University Health Centre, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0001-9488-0157
Yvan St-PierreMcGill University Health Centre, Montreal, Quebec, Canada.
Isabelle MalhaméMcGill University and McGill University Health Centre, Montreal, Quebec, Canada.
Anick BérardUniversity of Montreal and CHU Sainte-Justine, Montreal, Quebec, Canada, and Université Claude Bernard Lyon 1, Lyon, France.ORCID https://orcid.org/0000-0001-7535-5517
Sasha BernatskyMcGill University and McGill University Health Centre, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-9515-2802
Évelyne VinetMcGill University and McGill University Health Centre, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0001-7727-5879

Funding

Arthritis Society STAR-19-0597CIHR FRN-181503CIHR PJT-166075CIHR PJT-180634Fonds de Recherche du Québec - Santé
6 · The paper itself

Abstract

objectiveTumor necrosis factor inhibitors (TNFi) are used by over 20% of pregnant women with chronic inflammatory diseases, which could further impede immune function and increase the risk of infections that require hospitalization. We assessed the risk of serious infections during pregnancy and postpartum between women exposed and unexposed to TNFi with chronic inflammatory diseases.

methodsUsing MarketScan, we identified pregnant women with chronic inflammatory diseases and modeled TNFi exposure during pregnancy and postpartum as a time-varying variable. Cox proportional hazards models estimated adjusted hazard ratios (HRs) for TNFi and the risk of hospitalized infection.

resultsWe followed a total of 62,813 women who had 70,529 pregnancies and 69,412 births. Among these, 4,485 (7.1%) women were exposed to at least one TNFi prescription during pregnancy and 3,559 women during postpartum. Overall, 449 women were hospitalized for infection during pregnancy, including 31 pregnant women who were exposed to TNFi. During postpartum, 205 women had hospitalized infection, of which 17 women were TNFi-exposed. Compared with no TNFi exposure, TNFi treatment during pregnancy was associated with a HR of 1.39 (95% confidence interval [CI], 0.95-2.05) for serious infections, whereas the HR during postpartum was 1.22 (95% CI, 0.72-2.06).

conclusionIn this population-based study, we found no statistically significant association between TNFi exposure during pregnancy and serious infection risk. Although point estimates were higher for pregnant women exposed to TNFi, CIs were wide and included the null, indicating that an increased risk cannot be ruled out. Given the frequency of TNFi treatment for pregnant women, these results support continued investigation and may inform counseling regarding TNFi treatment during pregnancy and postpartum.

Identifiers

PMID41183806
PMCPMC12582638

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.