Congenital Heart Disease in Patients With Cleft Lip/Palate and Its Impact on Cleft Management.
cleft lip
cleft palate
congenital heart disease
genetic syndrome
Journal
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
ISSN: 1545-1569
Titre abrégé: Cleft Palate Craniofac J
Pays: United States
ID NLM: 9102566
Informations de publication
Date de publication:
08 2020
08 2020
Historique:
pubmed:
29
5
2020
medline:
17
3
2021
entrez:
29
5
2020
Statut:
ppublish
Résumé
To evaluate characteristics of congenital heart disease (CHD) in patients with cleft lip and/or palate (CL/P) and assess potential associations with cleft outcomes. Retrospective review of all patients with CL/P who underwent primary cleft treatment from 2009 to 2015. Children's Hospital Los Angeles, a tertiary hospital. Exclusion criteria included microform cleft lip diagnosis, international patients, and patients presenting for secondary repair or revision after primary repair at another institution. Patient demographics, prenatal and birth characteristics, CL/P characteristics, syndromic status, postoperative complications, and other outcomes were analyzed relative to CHD diagnoses and management. Patients with CL/P with (+CHD) were compared to those without (-CHD) CHD using χ Among 575 patients with CL/P, 83 (14.4%) had CHD. Congenital heart disease rates were significantly higher in patients with cleft palate (CP) compared to other cleft types (χ Congenital heart disease is known to be more prevalent in patients with CL/P. These data suggest the condition is particularly increased in patients with CP. Severe forms of CHD are diagnosed and treated prior to cleft care however postoperative fistula may be more common in patients with CHD. Therefore, careful attention is required for patient optimization and palatal flap dissection in patients with coexisting CHD and CL/P.
Identifiants
pubmed: 32462926
doi: 10.1177/1055665620924915
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM