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Utility and acceptability of remote 6-lead electrocardiographic monitoring in children with inherited cardiac conditions.
Lawley, Claire Margaret; Luczak-Wozniak, Katarzyna; Chung, Sheng-Chia; Field, Ella; Barnes, Annabelle; Starling, Luke; Cervi, Elena; Kaski, Juan Pablo.
Afiliação
  • Lawley CM; Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Luczak-Wozniak K; The University of Sydney Children's Hospital Westmead Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
  • Chung SC; Centre for Paediatric Inherited and Rare Cardiovascular Disease, Institute of Cardiovascular Sciences, University College London, London, UK.
  • Field E; Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Barnes A; Department of Pediatric Cardiology and General Pediatrics, Medical University of Warsaw, Warszawa, Poland.
  • Starling L; Centre for Paediatric Inherited and Rare Cardiovascular Disease, Institute of Cardiovascular Sciences, University College London, London, UK.
  • Cervi E; Health Data Research UK, Institute of Health Informatics, University College London, London, UK.
  • Kaski JP; Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Arch Dis Child ; 109(9): 742-747, 2024 Aug 16.
Article em En | MEDLINE | ID: mdl-38849195
ABSTRACT

OBJECTIVE:

This pilot study sought to investigate the utility and acceptability of the KardiaMobile 6-lead ECG (KM6LECG) as a tool for remote monitoring in children with inherited cardiac conditions.

DESIGN:

A single-centre prospective cohort study. Children underwent standard clinical evaluation including a 12-lead ECG and a KM6LECG in the clinic. Participants recorded KM6LECGs monthly at home for 3 months. Families completed a questionnaire on their experience.

SETTING:

Great Ormond Street Hospital Centre for Inherited Cardiovascular Diseases.

PARTICIPANTS:

64 children 22 with hypertrophic cardiomyopathy (HCM); 22 with long QT syndrome and 20 unaffected siblings (controls). MAIN OUTCOME

MEASURES:

Comparison of data extracted from the clinic 12-lead ECG and supervised KM6LECG, and the supervised and unsupervised KM6LECG recording.

RESULTS:

Of 64 children (35% female, mean age 12 years), 58 had a baseline 12-lead ECG and appropriate baseline KM6LECG. In children with HCM, abnormalities in ventricular depolarisation/repolarisation in the limb leads of the 12-lead ECG were reliably reproduced. From the whole cohort, there was a strong positive correlation between the corrected QT interval from the 12-lead ECG and baseline KM6LECG (intraclass correlation coefficient=0.839) and baseline KM6LECG with an unsupervised KM6LECG (intraclass correlation coefficient=0.736). Suspected 'lead' misplacement impacted 18% of unsupervised recordings. Overall, the acceptability of the KM6LECG to families was good.

CONCLUSIONS:

The KM6LECG provides an accurate tool for assessing some ECG abnormalities associated with paediatric inherited cardiovascular disease and may provide a useful at-home adjunct to face-to-face clinical care of children requiring ECG assessment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do QT Longo Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Arch Dis Child Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do QT Longo Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Arch Dis Child Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Reino Unido