Hostname: page-component-848d4c4894-5nwft Total loading time: 0 Render date: 2024-05-22T09:52:06.890Z Has data issue: false hasContentIssue false

The differential diagnosis of primary electrical diseases from seizures in childhood

Published online by Cambridge University Press:  13 January 2010

Alban-Elouen Baruteau*
Affiliation:
CHU Rennes, Service de Cardiologie et Maladies Vasculaires, Rennes, F-35000, France Université de Rennes 1, LTSI, Rennes, F-35000, France INSERM, CIC-IT 804, Rennes, F-35000, France INSERM, U915, Nantes, F-44000, France
Julien Baruteau
Affiliation:
Assistance Publique – Hôpitaux de Paris, Hôpital Robert Debré, Service de Neurologie Pédiatrique et des Maladies Héréditaires du Métabolisme, Paris, F-75000, France CHU Toulouse, Service d’Hépato-Gastro-Entérologie Pédiatrique et des Maladies Héréditaires du Métabolisme, Toulouse, F-31000, France
Philippe Mabo
Affiliation:
CHU Rennes, Service de Cardiologie et Maladies Vasculaires, Rennes, F-35000, France Université de Rennes 1, LTSI, Rennes, F-35000, France INSERM, CIC-IT 804, Rennes, F-35000, France INSERM, U642, Rennes, F-35000, France
*
Correspondence to: Alban-Elouen Baruteau, MD, Département de Cardiologie et Maladies Vasculaires, Centre Cardio-pneumologique, Hôpital Pontchaillou, Centre Hospitalier Universitaire de Rennes, 2 rue Henri Le Guilloux, 35033 Rennes cedex, France. Tel: (+33)299282525; Fax: (+33)299282510; E-mail: alban.baruteau@wanadoo.fr
Rights & Permissions [Opens in a new window]

Abstract

Type
Letter to the Editor
Copyright
Copyright © Cambridge University Press 2010

Dear Sir,

The recent diagnosis of a catecholaminergic polymorphic ventricular tachycardia in a young boy, considered for several years as epileptic, and whose sister died suddenly after a long history of refractory anti-epileptic, has encouraged us to write this letter. Cardiac channelopathies appear to be often underdiagnosed, especially during childhood. We focus here on their relevance to seizures in children, and the importance of considering and investigating them as a differential diagnosis from epilepsy.

Clinical data supports the notion that those suffering from epilepsy have a two- to three-fold increase of premature death than those without epilepsy. The most common mode of sudden and unexpected death, in fact, is epilepsy. The pathophysiology of this happening in epileptics remains obscure, but cardiac arrhythmias are likely to play a role during seizures.Reference Stollberger and Finsterer1

Cardiac channelopathies, principally represented by the congenital long QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia, are a group of inherited primary electrical diseases predisposing to sudden cardiac death by ventricular arrhythmias occuring in structurally normal hearts.Reference Lehnart, Ackerman and Benson2 They are sometimes misdiagnosed as epilepsy, especially during childhood, as arrhythmia-related syncope can lead to convulsions.

Evidence supporting the possible misdiagnosis of long QT syndrome as epilepsy is now well documented.Reference Ghosh and Agarwala3Reference Maccormick, McAlister and Crawford6 Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia can also present as seizures in childhood. Primary electrical diseases, however, remain underdiagnosed. When properly diagnosed, anti-arrhythmic treatment can efficiently prevent sudden cardiac death, while familial screening can lead to early diagnosis of asymptomatic relatives. That is why investigations of seizures in a child should include a 12-lead electrocardiogram at rest, and also during exercise should the seizures occur in an adrenergic context, such as exercise, emotion, or stress.

Brugada syndrome is characterized by a elevation of the ST segments in the right precordial leads, and carries a predisposition to sudden cardiac death, particularly in children and young adults. Its affects from 1 to 5 per 10,000 inhabitants worldwide.Reference Antzelevitch, Brugada and Borggrefe7 Ventricular arrhythmias typically occur at rest, especially while sleeping.Reference Antzelevitch, Brugada and Borggrefe7 Fever represents the most important precipitating factor for arrhythmic events in children, and life-threatening arrhythmias can masquerade as febrile seizures.Reference Probst, Denjoy and Meregalli8, Reference Skinner, Chung and Nel9 It has been diagnosed in patients with a history of drug-resistant seizures.Reference Fauchier, Babuty and Cosnay10, Reference Girard, Cadena and Acharya11

Catecholaminergic polymorphic ventricular tachycardia is characterized by stress-induced ventricular tachyarrhythmias, and usually occurs during childhood. If untreated, the estimated mortality is from one-third to one-half of those afflicted before the age of 30 years.Reference Francis, Sankar, Nair and Priori12, Reference Leenhardt, Lucet, Denjoy, Grau, Ngoc and Coumel13 The resting electrocardiogram is normal. Diagnosis is through the exercise electrocardiogram, which shows a typical bidirectionnal ventricular tachycardia.Reference Francis, Sankar, Nair and Priori12, Reference Liu, Ruan and Priori14 Family history is positive in three-quarters of cases, and almost half of the afflicted children are initially considered to be epileptic, and are often treated as such for several times without control of attacks.Reference Celiker, Erdogan, Karagoz and Ozer15

Long QT syndrome, Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia should all be investigated, therefore, as part of the differential diagnosis of paediatric seizures. A family history of seizures is not indicative of epilepsy, as it can be due to misdiagnosed inherited arrythmias. We submit, therefore, that a cardiological assessment of presumed epileptic children should always be considered, especially in case of drug-refractory seizures, and in case of a family history of seizures or sudden death.

References

1.Stollberger, C, Finsterer, J. Cardiorespiratory findings in sudden unexplained/unexpected death in epilepsy (SUDEP). Epilepsy Res 2004; 59: 5160.CrossRefGoogle ScholarPubMed
2.Lehnart, SE, Ackerman, MJ, Benson, DW Jr, et al. Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function. Circulation 2007; 116: 23252345.CrossRefGoogle ScholarPubMed
3.Ghosh, A, Agarwala, BN. Torsades de Pointes in a child. Pediatr Cardiol 2009; 30: 553554.CrossRefGoogle ScholarPubMed
4.Johnson, JN, Hofman, N, Haglund, CM, Cascino, GD, Wilde, AA, Ackerman, MJ. Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy. Neurology 2009; 72: 224231.CrossRefGoogle Scholar
5.Levine, E, Rosero, SZ, Budzikowski, AS, Moss, AJ, Zareba, W, Daubert, JP. Congenital long QT syndrome: considerations for primary care physicians. Cleve Clin J Med 2008; 75: 591600.CrossRefGoogle ScholarPubMed
6.Maccormick, JM, McAlister, H, Crawford, J, et al. Misdiagnosis of long QT syndrome as epilepsy at first presentation. Ann Emerg Med 2009, Mar 10 [Epub ahead of print].CrossRefGoogle ScholarPubMed
7.Antzelevitch, C, Brugada, P, Borggrefe, M, et al. Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005; 111: 659670.CrossRefGoogle ScholarPubMed
8.Probst, V, Denjoy, I, Meregalli, PG, et al. Clinical aspects and prognosis of Brugada syndrome in children. Circulation 2007; 115: 20422048.CrossRefGoogle ScholarPubMed
9.Skinner, JR, Chung, SK, Nel, CA, et al. Brugada syndrome masquerading as febrile seizures. Pediatrics 2007; 119: e1206e1211.CrossRefGoogle ScholarPubMed
10.Fauchier, L, Babuty, D, Cosnay, P. Epilepsy, Brugada syndrome and the risk of sudden unexpected death. J Neurol 2000; 247: 643644.CrossRefGoogle ScholarPubMed
11.Girard, S, Cadena, A, Acharya, Y. Woman with Brugada syndrome and epilepsy: a unifying diagnosis? South Med J 2008; 101: 11501153.CrossRefGoogle ScholarPubMed
12.Francis, J, Sankar, V, Nair, VK, Priori, SG. Catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm 2005; 2: 550554.CrossRefGoogle ScholarPubMed
13.Leenhardt, A, Lucet, V, Denjoy, I, Grau, F, Ngoc, DD, Coumel, P. Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients. Circulation 1995; 91: 15121519.CrossRefGoogle ScholarPubMed
14.Liu, N, Ruan, Y, Priori, SG. Catecholaminergic polymorphic ventricular tachycardia. Prog Cardiovasc Dis 2008; 51: 2330.CrossRefGoogle ScholarPubMed
15.Celiker, A, Erdogan, I, Karagoz, T, Ozer, S. Clinical experiences of patients with catecholaminergic polymorphic ventricular tachycardia. Cardiol Young 2009; 19: 4552.CrossRefGoogle ScholarPubMed