Cardiac stasis imaging, stroke, and silent brain infarcts in patients with nonischemic dilated cardiomyopathy

dc.contributor.authorRodríguez González, Elena
dc.contributor.authorGonzález Mansilla, Ana
dc.contributor.authorEspinosa, Mª Ángeles
dc.contributor.authorMombiela, Teresa
dc.contributor.authorGuzmán De Villoria, Juan A.
dc.contributor.authorBorja, María Guadalupe
dc.contributor.authorDíaz Otero, Fernando
dc.contributor.authorGómez de Antonio, Rubén
dc.contributor.authorFernández García, Pilar
dc.contributor.authorFernández Ávila, Ana I.
dc.contributor.authorPascual Izquierdo, María Cristina
dc.contributor.authorÁlamo, Juan C. del
dc.contributor.authorBermejo Thomas, Francisco Javier
dc.date.accessioned2025-01-27T08:52:39Z
dc.date.available2025-01-27T08:52:39Z
dc.date.issued2024-06-07
dc.description.abstractCardioembolic stroke is one of the most devastating complications of nonischemic dilated cardiomyopathy (NIDCM). However, in clinical trials of primary prevention, the benefits of anticoagulation are hampered by the risk of bleeding. Indices of cardiac blood stasis may account for the risk of stroke and be useful to individualize primary prevention treatments. We performed a cross-sectional study in patients with NIDCM and no history of atrial fibrillation (AF) from two sources: 1) a prospective enrollment of unselected patients with left ventricular (LV) ejection fraction <45% and 2) a retrospective identification of patients with a history of previous cardioembolic neurological event. The primary end point integrated a history of ischemic stroke or the presence intraventricular thrombus, or a silent brain infarction (SBI) by imaging. From echocardiography, we calculated blood flow inside the LV, its residence time (TR) maps, and its derived stasis indices. Of the 89 recruited patients, 18 showed a positive end point, 9 had a history of stroke or transient ischemic attack (TIA) and 9 were diagnosed with SBIs in the brain imaging. Averaged TR, ̅𝑇R,  performed well to identify the primary end point [AUC (95% CI) = 0.75 (0.61–0.89), P = 0.001]. When accounting only for identifying a history of stroke or TIA, AUC for ̅𝑇R was 0.92 (0.85–1.00) with odds ratio = 7.2 (2.3–22.3) per cycle, P < 0.001. These results suggest that in patients with NIDCM in sinus rhythm, stasis imaging derived from echocardiography may account for the burden of stroke.
dc.description.departmentDepto. de Medicina
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.sponsorshipSociedad Española de Cardiología
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.sponsorshipUnión Europea
dc.description.statuspub
dc.identifier.citationRodríguez-González, E., Martinez-Legazpi, P., González-Mansilla, A., Espinosa, M. Á., Mombiela, T., Guzmán De-Villoria, J. A., ... & Bermejo, J. (2024). Cardiac stasis imaging, stroke, and silent brain infarcts in patients with nonischemic dilated cardiomyopathy. American Journal of Physiology-Heart and Circulatory Physiology, 327(2), H446-H453.
dc.identifier.doi10.1152/ajpheart.00245.2024
dc.identifier.essn1522-1539
dc.identifier.issn0363-6135
dc.identifier.officialurlhttps://doi.org/10.1152/ajpheart.00245.2024
dc.identifier.relatedurlhttps://journals.physiology.org/doi/full/10.1152/ajpheart.00245.2024
dc.identifier.urihttps://hdl.handle.net/20.500.14352/116162
dc.issue.number2
dc.journal.titleAmerican Journal of Physiology-Heart and Circulatory Physiology
dc.language.isoeng
dc.page.finalH453
dc.page.initialH446
dc.publisherAmerican Physiological Society
dc.relation.projectIDPACER-1 PI21/00274
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu616.12
dc.subject.keywordblood stasis
dc.subject.keywordcardioembolism
dc.subject.keywordechocardiography
dc.subject.keywordheart failure
dc.subject.keywordischemic stroke
dc.subject.ucmMedicina
dc.subject.unesco32 Ciencias Médicas
dc.titleCardiac stasis imaging, stroke, and silent brain infarcts in patients with nonischemic dilated cardiomyopathy
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number327
dspace.entity.typePublication
relation.isAuthorOfPublication0f947fa4-a6fa-4d51-8b6c-051e96afbd0b
relation.isAuthorOfPublicationf26c9740-9da8-4361-a7d8-542983191a93
relation.isAuthorOfPublication.latestForDiscoveryf26c9740-9da8-4361-a7d8-542983191a93

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