x
Filter:
Filters applied
- HRCR Rare Diseases Article Collection
- Congenital heart diseaseRemove Congenital heart disease filter
Publication Date
Please choose a date range between 2021 and 2022.
Author
- Assar, Manish D1
- Chaloupecký, Václav Jr1
- Dall'Aglio, Pietro Bernardo1
- Faber, Thomas1
- Gebauer, Roman1
- Habash, Fuad1
- Higuchi, Shuntaro1
- Hilgendorf, Ingo1
- Hosoda, Junya1
- Ishikawa, Toshiyuki1
- Iwata, Shuko1
- Janoušek, Jan1
- Jäckel, Markus1
- Kale, Parag1
- Kawamura, Yuichiro1
- Khairy, Paul1
- Koubský, Karel1
- Kovanda, Jan1
- Lemieux, Ariane1
- Matsumoto, Katsumi1
- Mondésert, Blandine1
- Mongeon, François-Pierre1
- Nakagawa, Keita1
- Nitta, Manabu1
- Patlolla, S Shiva1
Keyword
- Catheter ablation2
- Heart failure2
- Accessory pathway ablation1
- Atrial fibrillation1
- Atrial tachycardia1
- Atrioventricular block1
- Biventricular pacing1
- Cardiac resynchronization therapy1
- Cone repair1
- Cor triatriatum sinister1
- Cryoablation1
- Device reimplantation1
- Dextrocardia1
- Ebstein's anomaly1
- Eisenmenger syndrome1
- Elderly patient1
- Intracardiac shunt1
- Leadless pacemaker1
- Leadless pacing1
- Multidetector computed tomography1
- Mustard operation1
- Pulmonary vein isolation1
- Right ventricular cardiac resynchronization therapy1
- Situs inversus totalis1
HRCR Rare Diseases Article Collection

Read case reports pertaining to rare diseases
6 Results
- Case ReportOpen Access
A case of successful catheter ablation for biatrial reentrant tachycardia after a Mustard operation for dextro-transposition of the great arteries
HeartRhythm Case ReportsVol. 9Issue 3p140–143Published online: December 5, 2022- Yuka Taguchi
- Katsumi Matsumoto
- Morio Shoda
- Manabu Nitta
- Junya Hosoda
- Toshiyuki Ishikawa
Cited in Scopus: 0Mustard and Senning operations are atrial switch techniques for dextro-transposition of the great arteries (d-TGA) that have been mainly performed during a period from the 1960s to the mid-1980s. - Case ReportOpen Access
Electrophysiology and surgery intertwined in complex treatment of Ebstein’s anomaly in childhood
HeartRhythm Case ReportsVol. 9Issue 1p17–22Published online: September 30, 2022- Václav Chaloupecký Jr.
- Roman Gebauer
- Jan Kovanda
- Karel Koubský
- Ioana Sus
- Jan Janoušek
Cited in Scopus: 0Ebstein’s anomaly, a rare and highly variable congenital heart defect,1 still presents a treatment challenge. The currently used cone repair of the tricuspid valve has carried favorable results in suitable patients.2 Arrhythmogenic substrates including accessory pathways3,4 and right bundle branch block5 associated with electromechanical ventricular dyssynchrony present additional therapeutic targets. We present a patient with Ebstein’s anomaly of tricuspid valve and Wolff-Parkinson-White syndrome in whom joint electrophysiological and surgical interventions were used to address all major disease components. - Case ReportOpen Access
The man in the mirror: Biventricular device implantation in a patient with dextrocardia with situs inversus totalis
HeartRhythm Case ReportsVol. 8Issue 11p790–792Published online: September 6, 2022- Ariane Lemieux
- S. Shiva Patlolla
- Fuad Habash
- Detlef Wencker
- Parag Kale
- Jeffrey M. Schussler
- and others
Cited in Scopus: 0The population of individuals with adult congenital heart disease is expanding as advances in surgical and medical management allow patients to live into adulthood. Consequently, these patients are developing other cardiovascular diseases, such as arrhythmias and heart failure, later in life. Procedures involving congenital anatomic variations are becoming more commonplace, and operators must become familiar with them. One such congenital abnormality, dextrocardia, involves the reversal of the base–apex axis of the heart caudally and to the right. - Case ReportOpen Access
Catheter ablation for persistent atrial fibrillation in an elderly patient with cor triatriatum sinister
HeartRhythm Case ReportsVol. 8Issue 9p639–642Published online: July 1, 2022- Shuko Iwata
- Masaru Yamaki
- Keita Nakagawa
- Shuntaro Higuchi
- Hirotsuka Sakai
- Yuichiro Kawamura
Cited in Scopus: 0Cor triatriatum sinister (CTS) accounts for <0.1% of all congenital heart diseases. It is a condition in which the fibromuscular membrane divides the left atrium (LA) into 2 chambers.1 The superior and posterior chambers receive the pulmonary veins, and the inferior and anterior chambers are connected to the left atrial appendage and mitral orifice.2 Pathophysiologically, CTS is similar to mitral stenosis,3 and the symptoms are correlated with pulmonary venous congestion and pressure loading at the right side of the heart. - Case ReportOpen Access
First reported implantation of a VDD leadless pacemaker and a subcutaneous defibrillator in a patient with congenitally corrected transposition of the great arteries
HeartRhythm Case ReportsVol. 8Issue 7p505–508Published online: April 23, 2022- Luca Trolese
- Pietro Bernardo Dall’Aglio
- Thomas Faber
- Johannes Steinfurt
- Markus Jäckel
- Ingo Hilgendorf
Cited in Scopus: 0Entirely subcutaneous implantable cardioverter-defibrillators (S-ICD™ system; Boston Scientific Corp, Marlborough, MA) provide effective defibrillation and reduce the risk of infection or lead-related problems.1–3 S-ICD systems may be a valid alternative to transvenous implantable cardioverter-defibrillator (ICD) in patients in whom bradycardia pacing or cardiac resynchronization therapy (CRT) is not required.4,5 The Micra™ AV Transcatheter Pacing System (Medtronic Inc, Minneapolis, MN) is a recently approved leadless pacemaker enabling atrioventricular (AV) synchronized pacing, which may, in theory, compensate the S-ICD’s inability to pace. - Case ReportOpen Access
Leadless atrioventricular synchronous pacing in Eisenmenger syndrome
HeartRhythm Case ReportsVol. 7Issue 8p538–541Published online: May 5, 2021- Paul Khairy
- Blandine Mondésert
- François-Pierre Mongeon
- Nancy Poirier
- Bernard Thibault
Cited in Scopus: 1Eisenmenger syndrome is at the extreme end of the phenotypic spectrum of pulmonary arterial hypertension associated with congenital heart disease. Over time, a large nonrestrictive left-to-right shunt provokes progressive pulmonary vascular disease that results in the shunt becoming bidirectional or reversing direction (ie, right-to-left). When the need for pacing arises, transvenous leads are generally considered contraindicated owing to a prohibitively high risk of paradoxical thromboembolism.