Evidence map›Paper›PMID 41930115›Full record

ArticleFrontiers in medicine2026

Evolution of therapy for autoimmune diseases in pregnancy: a retrospective study from 2000 to 2023.

Cristina Garufi, Francesca Rizzo, Viviana Matys, Ester Garufi, Angela Botta, Valerio Andreozzi, Silvia Salvi, Tullio Ghi, Sara De Carolis

Abstract read
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Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Cristina Garufi *Department of Internal Clinical Sciences, Anesthesiology and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.
Francesca Rizzo *Department of Women and Child Health, Women Health Area, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
Viviana MatysDepartment of Maternal, Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.
Ester GarufiDepartment of Anesthesiology and Intensive Care Medicine, Catholic University of the Sacred Heart, Rome, Italy.
Angela BottaDepartment of Women and Child Health, Women Health Area, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
Valerio AndreozziDepartment of Orthopaedics, Sapienza University of Rome, Rome, Italy.
Silvia SalviDepartment of Women and Child Health, Women Health Area, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
Tullio GhiDepartment of Women and Child Health, Women Health Area, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
Sara De CarolisDepartment of Women and Child Health, Women Health Area, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Treatment options for rheumatic diseases in pregnancy have consistently changed over the years. The most common therapies for autoimmune diseases during pregnancy include low-dose aspirin (LDA), low-molecular-weight heparin (LMWH), steroids, and hydroxychloroquine (HCQ). Therapy choice is based on obstetrical history, presence of antiphospholipid antibodies, and disease severity and refractoriness. Over the years, we have observed a decrease in glucocorticoid administration and an increase in HCQ administration. Glucocorticoid therapy during pregnancy can increase the risk of premature rupture of membranes and intrauterine growth restriction. In mothers, it is correlated with gestational hypertension, diabetes, osteoporosis, and infections. HCQ appears safe in pregnancy for fetal development and growth; it may improve pregnancy outcomes and reduce the risk of preeclampsia and autoimmune disease flares. Methods: We conducted a retrospective study of 266 pregnant women affected by autoimmune diseases (systemic lupus erythematosus, antiphospholipid syndrome, Sjogren's Syndrome, connective tissue disease) referred to our center from 2000 to 2023. Results: We observed substantial stability in LDA use, ranging from 100% in 2000-2003 to 96% in 2020-2023 (mean 88%; p 0.54). Regarding LMWH, we observed a modest but consistent increase, starting from 25% in 2000-2003 to 61% in 2020-2023 (mean 50%; Conclusion: These changes in therapy reflect increased knowledge in autoimmune diseases during pregnancy, with a more consistent number of women able to have and carry a pregnancy despite their disease severity. Over the years, our center had offered the best therapeutic management to achieve a good obstetrical outcome and minimize the incidence of obstetrical complications.

Indexed as

autoimmune diseasescorticosteroidshydroxychloroquinelow-doseaspirinlow-molecular-weight heparinpregnancy

Identifiers

PMID41930115
PMCPMC13038967

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