Association Between Hospital-Documented Atrial Fibrillation and Central Retinal Artery Occlusion.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
04 2023
Historique:
medline: 29 3 2023
pubmed: 3 2 2023
entrez: 2 2 2023
Statut: ppublish

Résumé

Carotid stenosis is thought to be the primary risk factor for central retinal artery occlusion (CRAO); however, it is not known whether atrial fibrillation (AF)-a cardiac arrhythmia that underlies over 25% of cerebral ischemic strokes-predisposes patients to CRAO. A retrospective, observational, cohort study was performed using data from the State Inpatient Databases and State Emergency Department Databases from New York (2006-2015), California (2003-2011), and Florida (2005-2015) to determine the association between AF and CRAO. The primary exposure was hospital-documented AF. The primary end point was hospital-documented CRAO, defined as having an Of 39 834 885 patients included in the study, 2 723 842 (median age, 72.7 years; 48.5% women) had AF documented during the exposure window. The median follow-up duration was 6 years and 1 month. Patients with AF were older, more likely to be of non-Hispanic White race/ethnicity, and had a higher burden of cardiovascular comorbidities compared with patients without AF. The cumulative incidence of CRAO determined prospectively after exclusions was 8.69 per 100 000 at risk in those with AF and 2.39 per 100 000 at risk in those without AF over the study period. Before adjustment, AF was associated with higher risk of CRAO (hazard ratio, 2.55 [95% CI, 2.15-3.03]). However, after adjustment for demographics, state, and cardiovascular comorbidities, there was an inverse association between AF and risk of CRAO (adjusted hazard ratio, 0.72 [95% CI, 0.60-0.87]). These findings were robust in our prespecified sensitivity analyses. By contrast, positive control outcomes of embolic and ischemic stroke showed an expected strong relationship between AF and risk of stroke. We found an inverse association between AF and CRAO in a large, representative study of hospitalized patients; however, this cohort did not ascertain AF or CRAO occurring outside of hospital or emergency department settings.

Sections du résumé

BACKGROUND
Carotid stenosis is thought to be the primary risk factor for central retinal artery occlusion (CRAO); however, it is not known whether atrial fibrillation (AF)-a cardiac arrhythmia that underlies over 25% of cerebral ischemic strokes-predisposes patients to CRAO.
METHODS
A retrospective, observational, cohort study was performed using data from the State Inpatient Databases and State Emergency Department Databases from New York (2006-2015), California (2003-2011), and Florida (2005-2015) to determine the association between AF and CRAO. The primary exposure was hospital-documented AF. The primary end point was hospital-documented CRAO, defined as having an
RESULTS
Of 39 834 885 patients included in the study, 2 723 842 (median age, 72.7 years; 48.5% women) had AF documented during the exposure window. The median follow-up duration was 6 years and 1 month. Patients with AF were older, more likely to be of non-Hispanic White race/ethnicity, and had a higher burden of cardiovascular comorbidities compared with patients without AF. The cumulative incidence of CRAO determined prospectively after exclusions was 8.69 per 100 000 at risk in those with AF and 2.39 per 100 000 at risk in those without AF over the study period. Before adjustment, AF was associated with higher risk of CRAO (hazard ratio, 2.55 [95% CI, 2.15-3.03]). However, after adjustment for demographics, state, and cardiovascular comorbidities, there was an inverse association between AF and risk of CRAO (adjusted hazard ratio, 0.72 [95% CI, 0.60-0.87]). These findings were robust in our prespecified sensitivity analyses. By contrast, positive control outcomes of embolic and ischemic stroke showed an expected strong relationship between AF and risk of stroke.
CONCLUSIONS
We found an inverse association between AF and CRAO in a large, representative study of hospitalized patients; however, this cohort did not ascertain AF or CRAO occurring outside of hospital or emergency department settings.

Identifiants

pubmed: 36729390
doi: 10.1161/STROKEAHA.122.042292
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

983-991

Subventions

Organisme : NEI NIH HHS
ID : P30 EY006360
Pays : United States

Auteurs

Jay B Lusk (JB)

Duke University School of Medicine, Durham, NC (J.B.L., A.S.).

Ailin Song (A)

Duke University School of Medicine, Durham, NC (J.B.L., A.S.).

Shakthi Unnithan (S)

Department of Biostatistics and Bioinformatics (S.U., H.R.A.-K.), Duke University School of Medicine, Durham, NC.

Hussein R Al-Khalidi (HR)

Department of Biostatistics and Bioinformatics (S.U., H.R.A.-K.), Duke University School of Medicine, Durham, NC.

Alen Delic (A)

Department of Neurology, University of Utah, Salt Lake City (A.D.).

Adam de Havenon (A)

Department of Neurology, Yale University School of Medicine, New Haven, CT (A.d.H.).

Valérie Biousse (V)

Departments of Ophthalmology (V.B.), Emory University School of Medicine, Atlanta, GA.
Neurology (V.B.), Emory University School of Medicine, Atlanta, GA.

Matthew Schrag (M)

Department of Neurology, Vanderbilt University School of Medicine, Nashville, TN (M.S.).

Sven Poli (S)

Department of Neurology and Stroke (S.P.), University of Tübingen, Germany.
Hertie Institute for Clinical Brain Research (S.P.), University of Tübingen, Germany.

Jonathan P Piccini (JP)

Department of Medicine (J.P.P.), Duke University School of Medicine, Durham, NC.
Duke Clinical Research Institute, Durham, NC (J.P.P., E.C.O., B.M.G.).

Ying Xian (Y)

Department of Neurology, University of Texas-Southwestern Medical Center, Dallas (Y.X.).

Emily C O'Brien (EC)

Department of Neurology (E.C.O., B.M.G.), Duke University School of Medicine, Durham, NC.
Duke Clinical Research Institute, Durham, NC (J.P.P., E.C.O., B.M.G.).
Department of Population Health Sciences, Duke University, Durham, NC (E.C.O.).

Brian Mac Grory (B)

Department of Neurology (E.C.O., B.M.G.), Duke University School of Medicine, Durham, NC.
Duke Clinical Research Institute, Durham, NC (J.P.P., E.C.O., B.M.G.).

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