Cardiac arrhythmias in adult patients with congental heart disease

Author:

Wiktor Dominika1,Mazurek Michał2,Średniawa Beata3,Jędrzejczyk-Patej Ewa2

Affiliation:

1. Studenckie Koło Naukowe przy Katedrze Kardiologii, Wrodzonych Wad Serca i Elektroterapii, Śląski Uniwersytet Medyczny w Katowicach, Wydział Nauk Medycznych w Zabrzu

2. Oddział Kliniczny Kardiologii, Katedry Kardiologii, Wrodzonych Wad Serca i Elektroterapii, Śląskie Centrum Chorób Serca w Zabrzu

3. Katedra Kardiologii, Wrodzonych Wad Serca i Elektroterapii, Oddział Kliniczny Kardiologii, Śląski Uniwersytet Medyczny w Katowicach, Wydział Nauk Medycznych w Zabrzu, Śląskie Centrum Chorób Serca w Zabrzu

Abstract

Congenital Heart Disease (CHD) is an anatomical and functional abnormality in the structure of the heart and/or large vessels that occurs since birth. This is diagnosed in 8-10 children out of 1,000 live born in the world. Every year about 3,000 newborns are born with CHD in Poland. The development of medicine enables the long-term survival of patients with CHD, followed by an increase in the number of adult patients being treated for CHD complications, including arrhythmias. Arrhythmias contribute to decreased quality of life, increased morbidity, and mortality among adults with congenital heart disease. The following article discusses diagnostic and therapeutic procedures in subjects with CHD and arrhythmias.

Publisher

Index Copernicus

Reference28 articles.

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4. Khairy P, FRCPC, Van Hare GF, et al. 2014. PACES/HRS Expert Consensus Statement on the Recognitionand Management of Arrhythmias inAdult Congenital Heart Disease: developed inpartnership between the Pediatric and CongenitalElectrophysiology Society (PACES) and the HeartRhythm Society (HRS). Endorsed by the governingbodies of PACES, HRS, the American Collegeof Cardiology (ACC), the American Heart Association(AHA), the European Heart RhythmAssociation (EHRA), the Canadian Heart RhythmSociety (CHRS), and the International Societyfor Adult Congenital Heart Disease (ISACHD).Heart Rhythm 11 (10): e102-65. doi: 10.1016/j.hrthm.2014.05.009.

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