Left Ventricular Outflow Tract Gradient Is Associated With Coronary Artery Obstruction in Children With Williams-Beuren Syndrome.
Williams-Beuren syndrome
coronary obstruction
transthoracic echocardiogram
Journal
Journal of cardiothoracic and vascular anesthesia
ISSN: 1532-8422
Titre abrégé: J Cardiothorac Vasc Anesth
Pays: United States
ID NLM: 9110208
Informations de publication
Date de publication:
12 2021
12 2021
Historique:
received:
28
11
2020
revised:
24
12
2020
accepted:
28
12
2020
pubmed:
23
1
2021
medline:
8
1
2022
entrez:
22
1
2021
Statut:
ppublish
Résumé
Patients with Williams-Beuren syndrome are associated with a high risk of hemodynamic collapse during sedation and/or anesthesia, presumably due to occult coronary obstruction. The objective of this study was to determine the association between transthoracic echocardiogram findings and the presence of coronary obstruction to examine if coronary obstruction can be predicted by transthoracic echocardiogram before anesthesia. Retrospective data analysis of patients with Williams-Beuren syndrome who underwent transthoracic echocardiogram, cardiac catheterization, and/or surgical interventions to determine the correlation between echocardiogram findings and the presence of coronary obstruction determined by cardiac catheterization and/or surgery. Single-center university teaching hospital. The study included 49 patients with Williams-Beuren syndrome who underwent transthoracic echocardiogram, cardiac catheterization, and/or surgical interventions. The only variable associated with coronary artery obstruction was the maximum instantaneous gradient (MIG) across the left ventricular outflow tract (LVOT) on a transthoracic echocardiogram. LVOT MIG ≥ 75 mmHg as the optimal cutoff value was associated with coronary artery obstruction (area under the curve 0.659, odds ratio 6.71, 95% CI 1.31-34.35, p = 0.022). LVOT gradient can serve as a good predictor of the presence of coronary obstruction in patients with Williams-Beuren syndrome.
Identifiants
pubmed: 33478883
pii: S1053-0770(20)31397-5
doi: 10.1053/j.jvca.2020.12.050
pmc: PMC9327879
mid: NIHMS1823861
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3677-3680Subventions
Organisme : NHLBI NIH HHS
ID : T32 HL007572
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.
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