Congenital JET (junctional ectopic tachycardia) is a rare and often difficult to treat tachyarrhythmia in young infants. The addition of Ivabradine to standard Congenital JET therapy has been shown to improve arrhythmia control. However, Ivabradine has not been reported as a single drug in the control of congenital JET. We report a pre-term neonate in whom Ivabradine monotherapy was successful in treating congenital JET.
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http://dx.doi.org/10.4103/apc.apc_264_20 | DOI Listing |
Turk Kardiyol Dern Ars
December 2024
Department of Pediatric Cardiology, Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital, İstanbul, Türkiye.
Objective: Postoperative junctional ectopic tachycardia (JET) is usually a self-limiting condition; however, when combined with atrioventricular dissociation and postoperative ventricular dysfunction, it may increase morbidity and mortality. This study aimed to determine the overall incidence of JET following congenital heart surgery, to identify patient and procedure-related risk factors, and to evaluate the clinical impact of JET on outcomes.
Methods: The records of 2,814 patients who underwent cardiac surgery over a five-year period were reviewed retrospectively to identify those with JET.
Open Heart
October 2024
Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval, Québec, Québec, Canada
J Equine Vet Sci
November 2024
Department of Veterinary Medicine, University of Perugia, Via San Costanzo 4, Perugia, 06126, Italy.
A 16-year-old horse, 400 kg, male, Quarter horse gelding was examined for a cardiac murmur that had not been previously heard. Physical examination revealed a regularly irregular pulse and a grade III/VI, decrescendo, diastolic murmur with a point of maximum intensity over the left heart base. Base-apex standard electrocardiographic examination at rest showed sinus rhythm with second-degree atrio-ventricular blocks.
View Article and Find Full Text PDFJ Pediatr Urol
December 2024
Department of Paediatric Surgery, All India Institute of Medical Sciences (AIIMS), 7th floor, Paediatric Surgery Office, Mother and Child Block, New Delhi, 110029, India. Electronic address:
J Thorac Dis
July 2024
Department of Biomedical Sciences, Humanitas University, Milan, Italy.
Background And Objective: Primary and secondary chest wall tumors (bone, breast, and soft tissue), congenital defects, and chest wall osteoradionecrosis often require extensive full-thickness local excisions to guarantee safe oncological margins (in cases of tumors) and complex reconstruction to provide stabilization and good biomechanical results avoiding postoperative respiratory failure. Thus, a personalized approach is required when dealing with chest wall defects, and reconstruction is planned. This review summarizes failed chest wall reconstruction procedures, identifies causes of failure, and highlights principles for complex chest wall reconstruction post-failure.
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