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Verfasst von:Kaski, Juan Pablo [VerfasserIn]   i
 Norrish, Gabrielle [VerfasserIn]   i
 Gimeno Blanes, Juan Ramon [VerfasserIn]   i
 Charron, Philippe [VerfasserIn]   i
 Elliott, Perry [VerfasserIn]   i
 Tavazzi, Luigi [VerfasserIn]   i
 Tendera, Michal [VerfasserIn]   i
 Laroche, Cécile [VerfasserIn]   i
 Maggioni, Aldo P. [VerfasserIn]   i
 Baban, Anwar [VerfasserIn]   i
 Khraiche, Diala [VerfasserIn]   i
 Ziolkowska, Lidia [VerfasserIn]   i
 Limongelli, Giuseppe [VerfasserIn]   i
 Ojala, Tiina [VerfasserIn]   i
 Gorenflo, Matthias [VerfasserIn]   i
 Anastasakis, Aris [VerfasserIn]   i
 Mostafa, Shaimaa [VerfasserIn]   i
 Caforio, Alida L. P. [VerfasserIn]   i
 Arnold, Raoul [VerfasserIn]   i
 Uhl, Sebastian [VerfasserIn]   i
 Ziesenitz, Victoria C. [VerfasserIn]   i
 Rösch, Eva [VerfasserIn]   i
Titel:Cardiomyopathies in children and adolescents
Titelzusatz:aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry
Verf.angabe:Juan Pablo Kaski, Gabrielle Norrish, Juan Ramon Gimeno Blanes, Philippe Charron, Perry Elliott, Luigi Tavazzi, Michal Tendera, Cécile Laroche, Aldo P. Maggioni, Anwar Baban, Diala Khraiche, Lidia Ziolkowska, Giuseppe Limongelli, Tiina Ojala, Matthias Gorenflo, Aris Anastasakis, Shaimaa Mostafa, and Alida L.P. Caforio, on behalf of the EORP Paediatric Cardiomyopathy Registry Investigators
E-Jahr:2024
Jahr:21 April 2024
Umfang:12 S.
Illustrationen:Illustrationen
Fussnoten:EORP Paediatric Cardiomyopathy Registry Investigators: Belarus: Minsk: S. Komissarova, N. Chakova, S. Niyazova, Egypt: Benha: S. Mostafa, Finland: Helsinki: J. Pihkala, T. Ojala, A. Hiippala, T. Jarvinen, France: Paris: D. Bonnet, D. Khraiche, I. Szezepanski, Germany: Heidelberg: M. Gorenflo, R. Arnold, S. Uhl, V. Ziesenitz, A. Jung, E. Roesch, Great Britain: Glasgow: M. Ilina, London: J.P. Kaski, G. Norrish, E. Field, Greece: Athens: A. Anastasakis, K. Ritsatos, V. Vlagkouli, Athens: S. Rammos, G. Kourelis, G. Vagenakis, Athens: G. Papadopoulos, A. Giannakopoulou, E. Karanasios, P. Papachristou, G. Servos, Italy: Bologna: E. Biagini, A. Corsini, C. Gagliardi, M. Graziosi, A. Milandri, L. Ragni, S. Palmieri, Naples: R. Calabro, G. Pacileo, M.G. Russo, G. Limongelli, M. Caiazza, A. Cirillo, G. Del Giorno, A. Esposito, S. Tramonte, F. Valente, R. Gravino, T. Marrazzo, D. Masarone, V. Pazzanese, A. Rea, M. Rubino, Rome: F. Drago, A. Baban, Trieste: G. Sinagra, C. Carriere, M. Merlo, F. Ramani, M. Bobbo, B. Dagata, Lithuania: Kaunas: A. Kavoliuniene, A. Krivickiene, E. Tamuleviciute-Prasciene, M. Viezelis, Netherlands: Utrecht: F.W. Asselbergs, N. De Jonge, J.H. Kirkels, J. Van Der Heijden, L. Van Laake, A. Sammani, Nigeria: Lagos: J. Ajuluchukwu, A. Olusegun-Joseph, E. Ekure, Poland: Warsaw: G. Brzezinska-Rajszys, L. Ziolkowska, A. Boruc, E. Plodzien, Russian Federation: Moscow: E. Zaklyazminskaya, S. Dzemeshkevich, E. Kolbasova, N. Kotlukova, V. Rusinova, Spain: Barcelona: A. Cequier, J. Salazar-Mendiguchia, J. Gonzalez, N. Manito, Madrid: P. Garcia-Pavia, A. Briceno, M. Cobo-Marcos, F. Dominguez, Murcia: J.R. Gimeno Blanes, F.J. Castro, C. Munoz Esparza, M. Sabater Molina, M. Sorli García, D. Lopez Cuenca, Salamanca: P.L. Sanchez Fernandez, E. Villacorta, B. Plata, C. Avila, L. Bravo, E. Diaz-Pelaez, M. Gallego-Delgado, L. Garcia-Cuenllas, Seville: J.E. Lopez-Haldon, E.M. Cantero Perez, M.L. Pena Pena ; Gesehen am 10.09.2024
Titel Quelle:Enthalten in: European heart journal
Ort Quelle:Oxford : Oxford University Press, 1980
Jahr Quelle:2024
Band/Heft Quelle:45(2024), 16 vom: Apr., Seite 1443-1454
ISSN Quelle:1522-9645
Abstract:Childhood-onset cardiomyopathies are rare and poorly characterized. This study examined the baseline characteristics and 1-year follow-up of children with cardiomyopathy in the first European Cardiomyopathy Registry.Prospective data were collected on individuals aged 1-<18 years enrolled in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis long-term registry (June 2014-December 2016).A total of 633 individuals aged ≤18 years with hypertrophic [HCM; n = 388 (61.3%)], dilated [DCM; n = 206 (32.5%)], restrictive [RCM; n = 28 (4.4%)], and arrhythmogenic right ventricular cardiomyopathy [ARVC; n = 11 (1.7%)] were enrolled by 23 referral centres in 14 countries. Median age at diagnosis was 4.0 [interquartile range (IQR) 0-10] years, and there was a male predominance [n = 372 (58.8%)] across all subtypes, with the exception of DCM diagnosed <10 years of age; 621 (98.1%) patients were receiving cardiac medication and 80 (12.6%) had an implantable cardioverter-defibrillator. A total of 253 patients (253/535, 47.3%) had familial disease. Genetic testing was performed in 414 (67.8%) patients with a pathogenic or likely pathogenic variant reported in 250 (60.4%). Rare disease phenocopies were reported in 177 patients (28.0%) and were most frequent in patients under 10 years [142 (30.9%) vs. 35 (19.6%); P = .003]. Over a median follow-up of 12.5 months (IQR 11.3-15.3 months), 18 patients (3.3%) died [HCM n = 9 (2.6%), DCM n = 5 (3.0%), RCM n = 4 (16.0%)]. Heart failure events were most frequent in RCM patients (36.0%).The findings confirm the heterogeneous aetiology of childhood cardiomyopathies and show a high frequency of familial disease. Outcomes differed by cardiomyopathy subtype, highlighting a need for disease-specific evaluation and treatment.
DOI:doi:10.1093/eurheartj/ehae109
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1093/eurheartj/ehae109
 Volltext: https://academic.oup.com/eurheartj/article/45/16/1443/7617193
 DOI: https://doi.org/10.1093/eurheartj/ehae109
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1902274199
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