Affiliation:
1. Department of Paediatrics, Clinical Sciences Lund Lund University Lund Sweden
2. Chilhood Cancer Center Skåne University Hospital Lund Sweden
3. The Paediatric Heart Center Skåne University Hospital Lund Sweden
4. Department of Paediatric Neurology Skåne University Hospital Lund Sweden
5. Wallenberg Centre Molecular Medicine and Division Molecular Haematology Lund University Lund Sweden
Abstract
AbstractAimBreath‐holding spells (BHS) are common in children, but evidence‐based clinical guidelines are lacking. We investigated a large population‐based cohort of BHS patients, to propose a refined description of typical BHS and guidelines for its management.MethodsIn a cross‐sectional retrospective study, patients diagnosed with BHS in Southern Sweden 2004–2018 were recruited. Disease characteristics and diagnostic data were collected from patient medical records.ResultsIn total, 519 patients, mean age at diagnosis 19.8 ± 13.8 months with equal gender distribution, were included. In 48.3%, BHS had already been diagnosed after one spell. During spells, 78.0% of patients were unresponsive. For 71.5%, atonic, tonic, tonic–clonic or myoclonic seizures were reported, and 78.0% of patients had a spell lasting less than 1 min. Electroencephalography was conducted in 30.4% and Electrocardiography in 45.1%. Six children (3.8%) had a pathological electroencephalogram, four of which had concomitant epilepsy and only 0.9% of children had electrocardiogram findings suggesting pathology, none showing long QT syndrome.ConclusionChildren with BHS were frequently subjected to unnecessary diagnostic interventions. We characterise a typical presentation of BHS and propose a management‐algorithm, which is expected to reduce unnecessary usage of electroencephalography and electrocardiography.
Funder
Knut och Alice Wallenbergs Stiftelse
Region Skåne
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Cited by
1 articles.
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1. Issue highlights;Acta Paediatrica;2024-01-11