Results 11 to 20 of about 1,375 (122)

A Canadian Experience With a Percutaneous Microaxial Ventricular Assist Device in Children With Cardiogenic Shock. [PDF]

CJC Pediatr Congenit Heart Dis
Abstract Background The experience of a percutaneous microaxial (Impella) left ventricular assist device in children with cardiogenic shock is limited. The primary objective of this study was to review our institutional clinical outcomes of Impella use in children with cardiogenic shock.
Langanecha BD, Power A, Vanderlaan RD, Honjo O, Zaulan O, Maurich A, Chaturvedi R, Jeewa A.   +7 more
europepmc   +2 more sources

Administrative Databases: Friend or Foe in Paediatric Cardiomyopathy

CJC Pediatric &Congenital Heart Disease, Volume 2, Issue 6PB, Page 490-493, December 2023., 2023
Abstract Background Cardiomyopathy (CM) is a rare childhood disease associated with morbidity and mortality. Limited data exist on paediatric CM in Canada. Given the rare nature, single‐centre studies are not sufficiently powered to address important questions. Therefore, administrative health data may serve as a resource for the study of childhood CM.
Jennifer Conway, Olesya Barrett, Tara Pidborochynski, Katie Schroeder, Chentel Cunningham, Aamir Jeewa, Padma Kaul   +6 more
wiley   +1 more source

Automatic Prediction of Paediatric Cardiac Output From Echocardiograms Using Deep Learning Models

CJC Pediatric &Congenital Heart Disease, Volume 2, Issue 1, Page 12-19, February 2023., 2023
Graphical abstract Abstract Background Cardiac output (CO) perturbations are common and cause significant morbidity and mortality. Accurate CO assessment is crucial for guiding treatment in anaesthesia and critical care, but measurement is difficult, even for experts.
Steven Ufkes, Mael Zuercher, Lauren Erdman, Cameron Slorach, Luc Mertens, Katherine L. Taylor   +5 more
wiley   +1 more source

A Case of NAA10‐related Syndrome With Prolonged QTc Treated With a Subcutaneous Implantable Cardioverter Defibrillator After Ventricular Fibrillation

CJC Pediatric &Congenital Heart Disease, Volume 1, Issue 6, Page 270-273, December 2022., 2022
Abstract NAA10 is an enzyme involved in the N‐terminal acetylation of proteins. NAA10‐related syndrome is caused by a pathogenic variant of NAA10 on X chromosome, resulting in several phenotypes, including mental retardation, hypotonia, growth retardation, and various external malformations, with varying degrees of severity.
Yuta Mizuno, Yasuhiro Ichikawa, Shun Kawai, Takuya Wakamiya, Hiroaki Murakami, Kenji Kurosawa, Hideaki Ueda   +6 more
wiley   +1 more source

Sudden Cardiac Arrest in the Paediatric Population

CJC Pediatric &Congenital Heart Disease, Volume 1, Issue 2, Page 45-59, April 2022., 2022
Abstract Sudden cardiac arrest in the young is a rare event with a range of potential causes including cardiomyopathies, ion channelopathies, and autonomic nervous system dysfunction. Investigations into the cause involve a multidisciplinary team, including cardiologists, geneticists, and psychologists. In addition to a detailed medical history, family
Sonia Franciosi, Dominic J. Abrams, Jodie Ingles, Shubhayan Sanatani   +3 more
wiley   +1 more source

The aorto‐left ventricular tunnel from a fetal perspective: Original case series and literature review

Prenatal Diagnosis, Volume 42, Issue 2, Page 267-277, February 2022., 2022
Abstract Introduction Aorto‐left ventricular tunnel (ALVT) accounts for <0.1% of congenital heart defects. Evidence on the prognosis from a fetal perspective is limited. With this retrospective international case series, we provide information on the outcome of fetuses with ALVT.
Amber E. L. van Nisselrooij, Anita J. Moon‐Grady, Annette Wacker‐Gussmann, Viktor Tomek, Ivan Malčić, Agnieszka Grzyb, Anna Pavlova, Kalliopi Kazamia, Varsha Thakur, Elena Sinkovskaya, A. Derk Jan ten Harkel, Monique C. Haak   +11 more
wiley   +1 more source

Description de la Qualité de Vie des Patients Présentant une Cardiomyopathie Dilatée [PDF]

, 2020
But. – Décrire la qualité de vie de patients présentant une cardiomyopathie dilatée hospitalisés au service de Cardiologie de l’Hôpital Joseph Raseta Befelatanana.Patients et Méthodes. – Nous avons effectué une étude prospective descriptive, basée sur 31
Ritchy, RAMIANDRISOA Lahatriniavo, Benja, RAMILITIANA, Avisoa, RANDRIAMIHANGY Narindrarimanana, Lazasoa, ANDRIANASOLO Radonirina, Nirina, RABEARIVONY, Olivier, RAKOTO SEDSON Rado   +5 more
core   +1 more source

Cardiomyopathie du péripartum [PDF]

, 2018
La cardiomyopathie du péri-partum (CMP-PP) ou syndrome de Meadows, est une cardiomyopathie dilatée survenue pendant ou au décours d'une grossesse, définie par une insuffisance cardiaque avec une fraction d'éjection systolique du ventricule gauche ...
Drissi, Jihad, Dehayni, Mohamed, Kouach, Jaouad, Idri, Zakaria, Moussaoui, Driss   +4 more
core   +1 more source

Cardiomyopathie du péripartum : à propos d’une observation et revue de la littérature [PDF]

, 2016
La cardiomyopathie du péripartum ou cardiomyopathie gravidique primitive, est une entité rare et méconnue définie comme une insuffisance cardiaque systolique survenant le dernier mois de la grossesse ou les cinq premiers mois du postpartum en l'absence d'
Bouzerda, Abdelmajid
core   +1 more source

Cirrhotic Cardiomyopathy: Does it Contribute to Chronic Fatigue and Decreased Health‐Related Quality of Life in Cirrhosis?

Canadian Journal of Gastroenterology and Hepatology, Volume 17, Issue 9, Page 545-551, 2003., 2003
Diminished health‐related quality of life (HRQoL) and fatigue have been reported in patients with cirrhosis. The presence of cirrhotic cardiomyopathy and the attendant poor cardiac response to physical stress may affect HRQoL and contribute to fatigue in these patients. AIMS: To evaluate the contribution of cirrhotic cardiomyopathy to HRQoL and fatigue
Nigel Girgrah, Graham Reid, Shona MacKenzie, Florence Wong   +3 more
wiley   +1 more source