Evidence map›Paper›PMID 38943224›Full record

ArticleActa obstetricia et gynecologica Scandinavica2024

Pregnancy outcomes in patients with systemic lupus erythematosus compared to a high-risk tertiary cohort and to standard population from the Austrian birth registry.

Klara Rosta, Florian Heinzl, Valerie Kuczwara, Stefanie Schindler, Veronica Falcone, Anja Catic, Marina Riedmann, Hermann Leitner, Elisabeth Simader, Valentin Ritschl and 4 more

Abstract readComparative Study
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. 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

14 authors.

Klara RostaDepartment of Obstetrics and Gynecology, Clinical Division of Gynecological Endocrinology and Reproductive Medicine, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-3502-3734
Florian HeinzlDepartment of Obstetrics and Gynecology, Clinical Division of Gynecological Endocrinology and Reproductive Medicine, Medical University of Vienna, Vienna, Austria.
Valerie KuczwaraDepartment of Obstetrics and Gynecology, Clinical Division of Gynecological Endocrinology and Reproductive Medicine, Medical University of Vienna, Vienna, Austria.ORCID 0009-0008-1633-1767
Stefanie SchindlerDepartment of Obstetrics and Gynecology, Clinical Division of Gynecological Endocrinology and Reproductive Medicine, Medical University of Vienna, Vienna, Austria.
Veronica FalconeDepartment of Obstetrics and Gynecology, Clinical Division of Gynecological Endocrinology and Reproductive Medicine, Medical University of Vienna, Vienna, Austria.
Anja CaticDepartment of Obstetrics and Gynecology, Clinical Division of Gynecological Endocrinology and Reproductive Medicine, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-1065-5313
Marina RiedmannDepartment of Clinical Epidemiology, Tyrolean Federal Institute for Integrated Care, Tirol Kliniken GmbH, Innsbruck, Austria.
Hermann LeitnerDepartment of Clinical Epidemiology, Tyrolean Federal Institute for Integrated Care, Tirol Kliniken GmbH, Innsbruck, Austria.
Elisabeth SimaderDepartment of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
Valentin RitschlCenter for Medical Data Science, Institute for Outcomes Research, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-8763-8215
Tanja StammCenter for Medical Data Science, Institute for Outcomes Research, Medical University of Vienna, Vienna, Austria.
Alexandra SzlatinayDepartment of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
Peter MandlDepartment of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
Antonia Mazzucato-PuchnerDepartment of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.

Funding

Erasmus Plus COHRICE 2021-1-HU01-KA220-HED-000027613PfizerUCB
6 · The paper itself

Abstract

introductionWomen with systemic lupus erythematosus (SLE) have a higher risk for fetal and maternal complications. We aimed to investigate maternal and fetal complications in pregnant women with SLE compared to a high-risk pregnancy cohort (HR) from a tertiary university center and a standard-risk general population (SR) from the Austrian Birth Registry. MATERIAL AND

methodsIn this retrospective data analysis, we compared the incidence of fetal/neonatal and maternal complications of pregnancies and deliveries of women with SLE to age, body mass index and delivery date-matched high-risk pregnancies from the same department, a progressive tertiary obstetric center and to a group of women, who represent pregnancies with standard obstetric risk from the Austrian Birth Registry.

resultsOne hundred women with SLE were compared to 300 women with high-risk pregnancies and 207 039 women with standard-risk pregnancies. The incidence of composite maternal complications (preeclampsia, Hemolysis, Elevated Liver enzymes and Low Platelets [HELLP] syndrome, pregnancy-related hypertension, gestational diabetes mellitus, maternal death, thromboembolic events) was significantly higher in the SLE as compared to the SR group (28% vs. 6.28% SLE vs. SR, p = 0.001). There was no difference between the SLE and the HR groups (28% vs. 29.6% SLE vs. HR group, p = 0.80). The incidence of composite fetal complications (preterm birth before 37 weeks of gestation, stillbirths, birthweight less than 2500 g, fetal growth restriction, large for gestational age, admission to neonatal intensive care unit, 5-min Apgar <7) was also higher in the SLE than in the SR group (55% vs. 25.54% SLE vs. SR p < 0.001) while the higher incidence of adverse fetal outcome was detected in the HR than in the SLE group (55% vs. 75% SLE vs. HR group, p = 0.0005).

conclusionsAlthough composite fetal risk is higher in the SLE group than in the general population, it is still significantly lower as compared to high-risk pregnant women at a tertiary obstetric center. Prepregnancy counseling of women with SLE should put fetal and maternal risk in perspective, not only in relation to healthy, low risk cohorts, but also compared to mixed HR populations.

Indexed as

Lupus Erythematosus, SystemicPregnancy ComplicationsPregnancy OutcomeRegistriesAdultAustriaFemaleHumansIncidenceInfant, NewbornPregnancyPregnancy, High-RiskRetrospective Studiesbirth registryhigh‐risk pregnancyobstetric risksystemic lupus erythematosus

Identifiers

PMID38943224
PMCPMC11324932

What OpenQuestion holds

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Registered trials

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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.