Results 51 to 60 of about 3,671 (165)

Differing impacts of cardiac implantable electronic device leads on tricuspid regurgitation

Journal of Arrhythmia, Volume 41, Issue 4, August 2025.
This study evaluates the impact of different CIED lead types (ICD, RV‐PM, His‐PM) on the progression of tricuspid regurgitation (TR). The effect of CIED leads on TR grade represents a spectrum related to the type of lead traversing the tricuspid valve.
Sophie A. Leon, Melissa Austin, Nayeem Nasher, Daler Rahimov, Faizaan Siddique, Chitra Parikh, Danial Ahmad, Vakhtang Tchantchaleishvili, Behzad B. Pavri   +8 more
wiley   +1 more source

Miocardiopatia arritmogénica do ventrículo direito. Contribuição de diferentes técnicas de eletrocardiografia

Revista Portuguesa de Cardiologia, 2014
Resumo: A miocardiopatia arritmogénica do ventrículo direito – também denominada de displasia arritmogénica do ventrículo direito – é uma patologia em que se verifica a substituição do miocárdio por tecido fibroso ou fibroadiposo predominantemente no ...
Davide Moreira, Anne Delgado, Bruno Marmelo, Emanuel Correia, Pedro Gama, João Pipa, Luís Nunes, Oliveira Santos   +7 more
doaj   +1 more source

Butorphanol or a Combination of Ketamine and Xylazine Do Not Interfere With Arrhythmogenic Parameters in Agoutis (Dasyprocta prymnolopha) Obtained Through High‐Resolution Electrocardiogram

Journal of Experimental Zoology Part A: Ecological and Integrative Physiology, Volume 343, Issue 6, Page 693-702, July 2025.
ABSTRACT Introduction/Objectives: Agoutis is a medium‐sized wild rodent with potential for use as an experimental model. This study aimed to evaluate physiological parameters of arrhythmogenesis in this species, by HR‐ECG and VCG techniques, under physical and pharmacological containment (ketamine‐xylazine and butorphanol). Materials and methods: Eight
Charlys Rhands Coelho de Moura, Hermínio José da Rocha Neto, Regina Lucia dos Santos Silva, Nayla Maria da Silva Rezende Amorim, José Lindenberg Rocha Sarmento, Miguel Ferreira Cavalcante Filho, Wanderson Gabriel Gomes de Melo, Dayseanny de Oliveira Bezerra, Maria Acelina Martins Carvalho, Napoleão Martins Argolo Neto   +9 more
wiley   +1 more source

A rare presentation of spontaneous ventricular tachycardia in young adult

Heart India, 2017
Arrhythmogenic right ventricular dysplasia (ARVD) is a common cause of sudden cardiac death in young adults. It is a disease that has a wide spectrum of presentation.
Ram Narayan, Mansoor C Abdulla, Jemshad Alungal   +2 more
doaj   +1 more source

Troponin May Lie: Recognizing an Atypical Case of Wellens Syndrome

Clinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT Wellens syndrome is associated with a critical coronary artery stenosis and an impending extensive myocardial infarction. Despite having chest pain, both ECG and troponin can be misleading. It is crucial to recognize this syndrome to allow urgent revascularization. Failure to recognize and noninvasive stress tests were shown to be detrimental.
Juthipong Benjanuwattra, Cristian Castillo‐Rodriguez, Manisha Das, Shaheer Zulfiqar, Imran Arif   +4 more
wiley   +1 more source

Kocher-Debre-Semelaigne syndrome with arrhythmogenic right ventricular cardiomyopathy: A hitherto unrecognized association

Indian Journal of Endocrinology and Metabolism, 2012
Kocher-Debre-Semelaigne (KDS) syndrome is a rare form of hypothyroid myopathy, with associated hypertrophy of muscles. Although cardiac manifestations of hypothyroidism are well known, reports of cardiac involvement in KDS have only described the ...
Nagaraja Moorthy, Sudeep Kumar, Preeti Dabadghao, Aditya Kapoor   +3 more
doaj   +1 more source

Arrhythmogenic Right Ventricular Cardiomyopathy in Children: A Systematic Review

Diagnostics
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited disease characterized by the progressive replacement of the normal myocardium by fibroadipocytic tissue.
Stefana Maria Moisa, Elena Lia Spoiala, Eliza Cinteza, Radu Vatasescu, Lacramioara Ionela Butnariu, Crischentian Brinza, Alexandru Burlacu   +6 more
doaj   +1 more source

Naxos disease: from the origin to today

Orphanet Journal of Rare Diseases, 2018
Naxos disease, first described by Dr. Nikos Protonotarios and colleagues on the island of Naxos, Greece, is a special form of arrhythmogenic right ventricular dysplasia (ARVD).
Guo-Liang Li, Ardan M. Saguner, Guy H. Fontaine   +2 more
doaj   +1 more source

An atypical case report of an arrhythmogenic cardiomyopathy in a 70-years-old patient with suggestive left ventricular signs

Radiology Case Reports
Arrhythmogenic dysplasia of the right ventricule (ARVC), actually known as arrhythmogenic cardiomyopathy (ACM) is a rare genetic condition caused by the replacement of the normal right ventricular myocardium with fibrofatty tissue.
ikram Tahani, MD, oumayma Hattab, MD, Nabila ismaili, PhD, Noha el ouafi, PhD   +3 more
doaj   +1 more source

Varied Presentation of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C): A Case Series. [PDF]

Cureus, 2023
Mishra D, Shankar O, Aggarwal V.
europepmc   +1 more source