Evidence map›Paper›PMID 41815982›Full record

ArticleResearch and practice in thrombosis and haemostasis2026

Pregnancy outcomes in women with Von Willebrand disease: a statewide cohort study.

Ming Y Lim, G Bryce Christensen, George M Rodgers, Sara E Simonsen

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 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

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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

4 authors.

Ming Y LimDepartment of Internal Medicine, Division of Hematology and Hematologic Malignancies, Salt Lake City, Utah, USA.
G Bryce ChristensenUtah Population Database, Huntsman Cancer Institute, Salt Lake City, Utah, USA.
George M RodgersDepartment of Internal Medicine, Division of Hematology and Hematologic Malignancies, Salt Lake City, Utah, USA.
Sara E SimonsenUniversity of Utah College of Nursing, Salt Lake City, Utah, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Multiple studies conducted between 1990s and 2010s reported increased rates of postpartum hemorrhage (PPH) among women with von Willebrand disease (VWD), even with specialized peripartum care. Objective: To generate contemporary data on pregnancy outcomes among women with VWD using a statewide database, the Utah Population Database. Methods: We included women with a first live singleton birth at Intermountain Health or University of Utah facilities from January 1, 2008, to December 31, 2020. VWD cases were identified using a validated algorithm incorporating diagnosis codes, laboratory, and medication data. Each case was matched (∼1:20) to controls by maternal birth year and age at delivery. Pregnancy outcomes were obtained from Utah birth certificates; PPH became reportable in 2017. Mixed effects logistic regression was used to compare pregnancy outcomes between women with and without VWD for the full cohort (2008-2020) and a limited cohort (2017-2020). Results: We identified 120 women with VWD matched to 2356 controls for the full cohort. Compared with controls, women with VWD had higher odds of blood transfusion (adjusted odds ratio [aOR] 12.8, 95% CI, 4.11-40.1) and preterm birth (aOR 1.82; 95% CI, 1.04-3.20), after adjusting for ethnicity. In the limited cohort, VWD was not significantly associated with PPH (aOR 1.59, 95% CI, 0.36-6.95). Conclusion: Despite increased awareness, women with VWD continue to face a higher risk of adverse pregnancy outcomes compared to the general population.

Indexed as

outcomespregnancyvon Willebrand disease

Identifiers

PMID41815982
PMCPMC12974098

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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.