Maternal and infant outcomes in pregnancies of women with axial spondyloarthritis compared with matched controls: results from nationwide health insurance data.


Journal

RMD open
ISSN: 2056-5933
Titre abrégé: RMD Open
Pays: England
ID NLM: 101662038

Informations de publication

Date de publication:
07 2022
Historique:
received: 07 12 2021
accepted: 04 05 2022
entrez: 15 7 2022
pubmed: 16 7 2022
medline: 20 7 2022
Statut: ppublish

Résumé

To investigate pregnancy outcomes in women with axial spondyloarthritis (axSpA) under different pharmacological treatments in comparison with matched controls. Using health insurance data from 2006 to 2019, pregnancy outcomes of women with axSpA were compared with those of age-matched and calendar year-matched controls without axSpA. Women with axSpA were further stratified by treatment prior to delivery and pregnancy outcomes compared. Adjusted ORs (aORs) with 95% CIs were calculated using generalised estimating equation analyses. A total of 1021 pregnancy outcomes in patients with axSpA were identified (928 deliveries, 80 abortions, 13 ectopic pregnancies) and compared with 10 210 pregnancy outcomes in controls (9488 deliveries, 615 abortions, 147 ectopic pregnancies). Compared with controls, women with axSpA showed higher odds of elective caesarean section (aOR 1.52; 1.25 to 1.85).Among women with axSpA, the risk of preterm birth was higher under non-steroidal anti-inflammatory drugs (NSAIDs) treatment (aOR 2.22; 1.09 to 4.52) than without any anti-inflammatory treatment. The risks of preterm birth (aOR 4.01; 1.93 to 8.34) and small-for-gestational-age (aOR 3.22; 1.34 to 7.73) were increased under NSAIDs treatment in combination with conventional synthetic disease-modifying anti-rheumatic drugs (DMARDs), steroids or analgesics. Non-significant increased risks of small-for-gestational-age (aOR 1.68; 0.43 to 6.57) and preterm birth (aOR 1.56; 0.51 to 4.83) were found under biological DMARDs. Women with axSpA have significantly increased odds of caesarean section compared with matched controls. Risks of preterm birth and small-for-gestational-age vary by type of anti-inflammatory treatment.

Identifiants

pubmed: 35840311
pii: rmdopen-2021-002146
doi: 10.1136/rmdopen-2021-002146
pmc: PMC9295643
pii:
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Antirheumatic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: XB has received honoraria for talks, advisory boards, paid consultancies, and grants for studies from AbbVie, Amgen, Bristol-Myers Squibb, Celltrion, Celgene, Chugai, Gilead, Janssen, Lilly, MSD, Novartis, Pfizer, Sandoz, UCB. AS has received speaking fees from Bristol-Myers Squibb, Celltrion, MSD, Pfizer and Roche. UM is an employee of BARMER. AZ has received speaking fees from AbbVie, Janssen, Pfizer, Roche and Sanofi-Aventis.

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Auteurs

Imke Redeker (I)

Epidemiology and Health Services Research, German Rheumatism Research Centre, Berlin, Berlin, Germany Redeker.imke@gmail.com.

Anja Strangfeld (A)

Epidemiology and Health Services Research, German Rheumatism Research Centre, Berlin, Berlin, Germany.

Johanna Callhoff (J)

Epidemiology and Health Services Research, German Rheumatism Research Centre, Berlin, Berlin, Germany.

Ursula Marschall (U)

BARMER Institute for Health Systems Research, BARMER Statutory Health Insurance, Wuppertal, Germany.

Angela Zink (A)

Epidemiology and Health Services Research, German Rheumatism Research Centre, Berlin, Berlin, Germany.

Xenofon Baraliakos (X)

Internal Medicine and Rheumatology, Ruhr University Bochum, Bochum, Germany.

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Classifications MeSH