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Screening for arrhythmogenic heart disease in school age children-a pilot study

Title: Screening for arrhythmogenic heart disease in school age children-a pilot study
Authors: Bagkaki, A; Parthenakis, F; Chlouverakis, G; Anastasakis, A; Papagiannis, I; Germanakis, I
Source: European Journal of Preventive Cardiology ; volume 31, issue Supplement_1 ; ISSN 2047-4873 2047-4881
Publisher Information: Oxford University Press (OUP)
Publication Year: 2024
Description: Introduction There is a relative lack of data regarding efficacy of cardiovascular (CV) screening programs including ECG when applied in young children, for early detection of unrecognized genetic conditions associated with high risk for sudden cardiac death (SCD). Purpose We evaluated the performance of a CV screening program, including 12-lead ECG recording, when applied in selected populations of Mediterranean children. Methods A CV screening program for primary schools, approved by Ministry of Health, was applied in a sample of primary schools of a Mediterranean island, in geographical isolated areas with reported increased SCD incidence. Participation was voluntary following parental consent. After completion of a standardized history questionnaire by parents, children underwent clinical evaluation and 12-lead ECG recording, at local health stations. A stepwise referral pattern was established, including pediatric cardiology evaluation and molecular DNA confirmatory testing, whenever the possibility of inherited arrhythmogenic CV disease was increased. Results 929 primary school children, (462 male, 467 female), median age 8,5 (range 5,5 -11,5 yrs) have been evaluated during eight years (2014-22). 52 children (5,6%) had an indication for further diagnostic or lifestyle modification for CV risk factors, including ECG abnormalities (n=16, 1.7%), abnormal heart auscultation (n=21, 2.2%), hypertension (n=10, 1%) and positive 1st degree family history of SCD (n= 5, 0.5%). ECG abnormalities included WPW (n=1, 0.1%), VES (n=4, 0.4%), probable LVH (n=2), abnormal QRS axis (n=7 ) and QTc prolongation (n=2, 0.2%) both boys, with QTc 475 and QTc 490. Children with ECG abnormalities underwent further evaluation including ambulatory ECG monitoring and regular follow up. Family ECG screening was positive in one child with prolonged QTc (490ms, wide T wave), regarding his father (QTc=460) and one sister (QTc=490). Further molecular DNA testing was negative in the first child, while it revealed a novel KCNH2 ...
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/eurjpc/zwae175.028
Availability: https://doi.org/10.1093/eurjpc/zwae175.028; https://academic.oup.com/eurjpc/article-pdf/31/Supplement_1/zwae175.028/58220469/zwae175.028.pdf
Rights: https://academic.oup.com/pages/standard-publication-reuse-rights
Accession Number: edsbas.3ED0626D
Database: BASE