Evidence map›Paper›PMID 42696279›Full record

ArticleJAMA network open2026

Perioperative Management of Anticoagulation in Patients With Mechanical Heart Valves.

Gabriella Hrubesz, Vincent Chan, Yan Xu, Nicola Potere, Marcel Miron-Celis, Jean Connors, Jerrold H Levy, Deborah M Siegal, James Douketis, Grégoire Le Gal and 2 more

Abstract read
In one paragraph

Article in JAMA network open, 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

12 authors.

Gabriella HrubeszDepartment of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Vincent ChanCardiac Surgery at The University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
Yan XuDepartment of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Nicola PotereDepartment of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Marcel Miron-CelisAnalytics, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Jean ConnorsDivision of Cancer Hematology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Jerrold H LevyDepartment of Anesthesiology, Critical Care, and Surgery, Duke University School of Medicine, Durham, North Carolina.
Deborah M SiegalDepartment of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
James DouketisDepartment of Medicine, McMaster University, Hamilton, Ontario, Canada.
Grégoire Le GalDepartment of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Marc CarrierDepartment of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Joseph R ShawDepartment of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Perioperative interruption of vitamin K antagonist (VKA) therapy in patients with mechanical heart valves (MHVs) is complex, and contemporary data to inform management are limited. Objectives: To describe perioperative anticoagulation management and to estimate 30-day risks of arterial thromboembolism (ATE) and bleeding after VKA interruption in adults with left-sided MHVs. Design, Setting, and Participants: This retrospective cohort study included consecutive adult patients (aged ≥18 years) with left-sided aortic, mitral, or dual MHVs undergoing planned invasive procedures requiring VKA interruption from January 1, 2016, to December 31, 2023, with 30-day follow-up. The study was conducted at the thrombosis clinic at The Ottawa Hospital in Ontario, Canada. Exposure: Planned invasive procedure requiring temporary interruption of VKA therapy. Main Outcomes and Measures: Primary outcomes were 30-day postoperative ATE and major bleeding. Secondary outcomes included clinically relevant nonmajor bleeding (CRNMB) and all-cause mortality. Major bleeding and CRNMB were defined according to the International Society on Thrombosis and Hemostasis. Results: The cohort included 373 patients (median [IQR] age, 67 [60-73] years; 217 [58.2%] male) contributing 613 interruptions. Therapeutic-dose bridging was used preoperatively in 516 interruptions (84.2%) and postoperatively in 193 (31.5%) (99 of 215 [46.0%] in mitral or dual MHV vs 94 of 398 [23.6%] in aortic MHV interruptions). Patients with mitral or dual (vs aortic) valve position and prior thromboembolism had higher estimated odds of receiving postoperative therapeutic-dose bridging (mitral or dual vs aortic: adjusted odds ratio [aOR], 2.90; 95% CI, 1.91-4.41; prior thromboembolism: aOR, 1.91; 95% CI, 1.05-3.46). Estimated 30-day risks of ATE and major bleeding were 1.5% (95% CI, 0.8%-2.8%) and 2.1% (95% CI, 1.2%-3.6%), respectively. Clinically relevant bleeding (composite of major bleeding and CRNMB) occurred in 3.9% (95% CI, 2.6%-5.8%) of interruptions. Three deaths occurred (0.5%; 95% CI, 0.2%-1.5%), 1 attributed to fatal ischemic stroke. Omission of postoperative bridging was associated with higher estimated ATE risk (4.9% vs 0.9%; subdistribution hazard ratio [sHR], 5.30; 95% CI, 1.45-19.40; P = .01); this finding was no longer statistically significant in landmark analysis (sHR, 3.26; 95% CI, 0.62-17.21). Conclusions and Relevance: In this retrospective cohort study, patients with MHVs experienced clinically meaningful risks of perioperative ATE and bleeding. These data do not establish a causal protective effect of postoperative bridging. However, omitting bridging in patients with MHVs was associated with a higher estimated risk of ATE in exploratory analyses and should be approached cautiously, pending stronger evidence from representative cohorts.

Indexed as

AnticoagulantsHeart Valve ProsthesisPerioperative CareThromboembolismAgedAnticoagulation BridgeFemaleHemorrhageHumansMaleMiddle AgedOntarioRetrospective StudiesTreatment InterruptionVitamin KAnticoagulantsVitamin K

Identifiers

PMID42696279
PMCPMC13545669

What OpenQuestion holds

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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.