Evidence map›Paper›PMID 37519103›Full record

ArticleEuropean journal of haematology2023

Estrogen-based hormonal therapy and the risk of thrombosis in COVID-19 patients.

Corinne LaVasseur, Rick Mathews, Jenny S H Wang, Kylee Martens, Hannah Stowe McMurry, Shira Peress, Jean Sabile, Thomas Kartika, Ileisa Oleson, Jamie O Lo and 3 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in European journal of haematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 24% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Effect of Pituitary-Target Gland Axis on RAAS in the Context of COVID-19.International journal of medical sciences · 2025
    Review
  3. Review
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

13 authors at 1 institution in 1 country.

Corinne LaVasseurDepartment of Internal Medicine, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0001-7038-8889
Rick MathewsDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0003-2723-5646
Jenny S H WangDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Kylee MartensDivision of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0001-5379-8202
Hannah Stowe McMurryDivision of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0002-5596-1285
Shira PeressDepartment of Internal Medicine, Oregon Health & Science University, Portland, Oregon, USA.
Jean SabileDivision of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0002-2433-4844
Thomas KartikaDivision of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon, USA.
Ileisa OlesonDepartment of Internal Medicine, Oregon Health & Science University, Portland, Oregon, USA.
Jamie O LoDepartment of Obstetrics and Gynecology, Oregon Health and Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0002-1934-1935
Thomas G DeLougheryDivision of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0002-5790-4700
Owen J T McCartyDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Joseph J ShatzelDepartment of Internal Medicine, Oregon Health & Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0001-9396-5976
Oregon Health & Science University · US

Funding

Characterization of Coagulation Factor-platelet Interactions: Role of FXIR01HL101972 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Owen J McCarty · 2010 to 2026
$8.5M
Contact Pathway Activation on Vascular DevicesR01HL144113 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI HINDS, MONICA T, MCCARTY, OWEN J · 2018 to 2025
$6.0M
Impact of maternal marijuana use on epigenetic regulation of offspring neurodevelopmentDP1DA056493 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Jamie Lo · 2022 to 2026
$2.6M
Evaluating the Safety and Efficacy of Targeting the Contact Pathway to Prevent Device Associated Thrombosis.R01HL151367 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SHATZEL, JOSEPH JAMES · 2020 to 2024
$1.5M
Role of glycosaminoglycans (GAGs) in deep vein thrombus formation and resolutionF30HL163918 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI MATHEWS, RICK · 2022 to 2025
$213k
NHLBI NIH HHS F30 HL163918NHLBI NIH HHS R01 HL101972NHLBI NIH HHS R01 HL144113NHLBI NIH HHS R01 HL151367NIDA NIH HHS DP1 DA056493
6 · The paper itself

Abstract

objectiveEstrogen-containing contraceptives and hormone replacement therapy are used commonly, however, the risks of venous and arterial thrombosis imparted by such medications during COVID-19 infection or other similar viral infections remain undescribed.

methodsTo assess the risk of venous and arterial thrombosis in patients receiving oral estrogen-containing therapy (ECT) with COVID-19 as compared to those receiving non-estrogen-based hormonal therapy, we conducted a multicenter cohort study of 991 patients with confirmed COVID-19 infection, 466 receiving estrogen-containing hormonal therapy, and 525 receiving progestin-only or topical therapy.

resultsThe use of estrogen-containing therapy was found to significantly increase the risk of venous thromboembolism (VTE) following COVID-19 diagnosis after controlling for age (HR 5.46 [95% CI 1.12-26.7, p = .036]). This risk was highest in patients over age 50, with 8.6% of patients receiving estrogen-containing therapy diagnosed with VTE compared to 0.9% of those receiving non-estrogen-based therapies (p = .026). The risk of arterial thrombosis was not significantly associated with oral estrogen use.

conclusionsThese results suggest that estrogen-containing therapy is associated with a significantly increased risk of VTE in COVID-19 patients, especially in older individuals. These findings may guide provider counseling and management of patients with COVID-19 on estrogen-containing therapy.

Indexed as

COVID-19ThrombosisVenous ThromboembolismAgedCohort StudiesCOVID-19 TestingEstrogensHormone Replacement TherapyHumansMiddle AgedRisk FactorsEstrogenscontraceptionCOVID-19estrogenhormonal therapythrombosis

Identifiers

PMID37519103
PMCPMC11019854
OpenAlexW4385400987

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.