Evidence map›Paper›PMID 42210517›Full record

ArticleActa obstetricia et gynecologica Scandinavica2026

Cardiovascular outcomes for Australian women with rheumatic heart disease during pregnancy: A retrospective linked data analysis, 2002-2017.

Ingrid Stacey, Mohammed Junaid, Holger W Unger, Geraldine Vaughan, Ye'elah Berman, Vicki Wade, Lee Nedkoff, James Marangou, Judith M Katzenellenbogen

Abstract read
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 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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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Ingrid StaceyCardiovascular Epidemiology Research Centre, University of Western Australia, Perth, Western Australia, Australia.ORCID https://orcid.org/0000-0002-3032-6031
Mohammed JunaidDental School and Oral Health Centre of Western Australia, University of Western Australia, Nedlands, Western Australia, Australia.ORCID https://orcid.org/0000-0002-2027-4231
Holger W UngerDepartment of Obstetrics and Gynaecology, Royal Darwin Hospital, Tiwi, Northern Territory, Australia.ORCID https://orcid.org/0000-0001-6347-536X
Geraldine VaughanSchool of Health, Medical and Applied Sciences, CQ University, Rockhampton, Queensland, Australia.ORCID https://orcid.org/0000-0002-0132-9946
Ye'elah BermanMedical School, Division of Obstetrics and Gynaecology, University of Western Australia, Perth, Western Australia, Australia.ORCID https://orcid.org/0000-0002-5632-2602
Vicki WadeMenzies School of Health Research, Charles Darwin University, Casuarina, Northern Territory, Australia.ORCID https://orcid.org/0000-0002-0554-0255
Lee NedkoffCardiovascular Epidemiology Research Centre, University of Western Australia, Perth, Western Australia, Australia.ORCID https://orcid.org/0000-0002-3970-625X
James MarangouMenzies School of Health Research, Charles Darwin University, Casuarina, Northern Territory, Australia.ORCID https://orcid.org/0000-0002-8688-506X
Judith M KatzenellenbogenCardiovascular Epidemiology Research Centre, University of Western Australia, Perth, Western Australia, Australia.ORCID https://orcid.org/0000-0001-5287-5819

Funding

National Health and Medical Research Council 1146525National Heart Foundation of Australia 108106National Heart Foundation of Australia 110335
6 · The paper itself

Abstract

introductionRheumatic heart disease (RHD) is the acquired autoimmune heart valve damage resulting from untreated infection with the Streptococcus pyogenes bacterium, which affects people experiencing socioeconomic disadvantage globally. This study measured RHD-associated major adverse cardiovascular events (MACE) and the increased risk associated with pregnancy among women diagnosed with RHD. MATERIAL AND

methodsPopulation-level analysis of all births to women with RHD in four Australian jurisdictions was conducted, which covered 71% of the total population and 88% of the Aboriginal and Torres Strait Islander population (a group who experience some of the highest RHD rates reported globally). A retrospective cohort study using linked RHD register and midwives, hospital, and death data collections was designed. Females with at least one birth record aged 12-44 years, whose first RHD diagnosis occurred prior to 20 weeks' gestation and age < 35 years, were identified during 2002-2017. Survival methods (incorporating mixed effects and time-varying covariates) estimated proportions and hazard ratios. Probability of hospitalization for new RHD-associated MACE was measured for pulmonary hypertension secondary to left heart disease, heart failure, valvular surgery, stroke, infective endocarditis, atrial fibrillation, acute pulmonary edema, cardiomyopathy, and/or death.

resultsWe identified 558 pregnancies in women with uncomplicated RHD (345 women) and 88 pregnancies in women with complicated RHD (60 women). During pregnancy, 4.5% of women with uncomplicated RHD and 31.8% of women with complicated RHD experienced new RHD-associated MACE. Risk of RHD-associated MACE was three- to six-fold higher during periods of pregnancy (compared with non-pregnancy) and did not differ by RHD stage.

conclusionsAfter 20 weeks of gestation, women with RHD experienced RHD-associated MACE outcomes at frequencies that were contingent upon RHD stage at 20 weeks of gestation. Awareness of RHD status before 20 weeks of gestation, especially in regions where RHD is endemic, is critical for ensuring women's cardiovascular health in pregnancy and beyond.

Indexed as

Pregnancy Complications, CardiovascularRheumatic Heart DiseaseAdolescentAdultAustraliaFemaleHumansPregnancyPregnancy OutcomeRetrospective StudiesYoung AdultAboriginal and Torres Strait IslanderAustraliacardiovascular diseasecohort studylinked datapregnancyrheumatic heart disease

Identifiers

PMID42210517
PMCPMC13356470

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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.