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Rigshospitalet - en del af Københavns Universitetshospital
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Familial Evaluation in Idiopathic Ventricular Fibrillation: Diagnostic Yield and Significance of J-Wave Syndromes

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

DOI

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  • Greg J Mellor
  • Lennart J Blom
  • Sanne A Groeneveld
  • Bo G Winkel
  • Bode Ensam
  • Johannes Bargehr
  • Bianca van Rees
  • Chiara Scrocco
  • Ingrid P C Krapels
  • Paul G A Volders
  • Jacob Tfelt-Hansen
  • Andrew D Krahn
  • Rutger J Hassink
  • Elijah R Behr
Vis graf over relationer

Background - Familial cascade screening is well established in patients with heritable cardiac disease and in cases of Sudden Arrhythmic Death Syndrome (SADS). The clinical benefit of family screening in idiopathic ventricular fibrillation (IVF) is unknown. Methods - Patients with IVF were identified from national and institutional registries. All underwent systematic and comprehensive clinical evaluation to exclude identifiable causes of cardiac arrest with a minimum requirement of ECG, cardiac (echocardiogram and/or MRI) and coronary imaging, exercise ECG and sodium channel blocker (SCB) provocation. Additional investigations including genetic testing were performed at the physician's discretion. First-degree relatives who were assessed with at least a 12-lead ECG were included in the final cohort. Results of additional investigations, performed at the physician's discretion, were also recorded. Results were coded as normal, abnormal or minor findings. Results - We identified 201 first-degree relatives of 96 IVF patients. In addition to a 12 lead ECG, echocardiography was performed in 159 (79%) and ≥ 1 additional investigation in 162 (80%) relatives. An inherited arrhythmia syndrome was diagnosed in 5 (3%) individuals from 4 (4%) families. Two relatives hosted the DPP6 risk haplotype identified in a single proband, one of whom received a primary prevention ICD. In three separate families an asymptomatic parent of the IVF proband developed a type 1 Brugada ECG pattern during SCB provocation. All were managed with lifestyle measures only. The Early Repolarisation ECG pattern (ER) was present in 16% probands and was more common in relatives in those families than those where the proband did not have ER (25% vs. 8%, p=0.04). Conclusions - The yield of family screening in relatives of IVF probands is low when the proband is comprehensively investigated. The significance of J wave syndromes in relatives and the role for systematic SCB provocation are, however, uncertain and require further research.

OriginalsprogEngelsk
Artikelnummere009089
TidsskriftCirculation. Arrhythmia and Electrophysiology
Vol/bind14
Udgave nummer3
Sider (fra-til)296-305
Antal sider10
ISSN1941-3149
DOI
StatusUdgivet - mar. 2021

ID: 62373184