Zobrazeno 1 - 10
of 55
pro vyhledávání: '"LQTS, Long QT syndrome"'
Publikováno v:
JACC: Case Reports. 4:438-442
We describe the case of a young woman with a dual-chamber implantable cardioverter-defibrillator for long-QT syndrome who was referred to our emergency department (Cardiovascular Research Centre of Aalst, Belgium) because of an "arrhythmic storm" cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d235f1af5c3413f98ca72d84294915
https://doi.org/10.1016/j.jaccas.2021.12.013
https://doi.org/10.1016/j.jaccas.2021.12.013
Autor:
Maully J. Shah, Michael J. Silka, Jennifer N. Avari Silva, Seshadri Balaji, Cheyenne M. Beach, Monica N. Benjamin, Charles I. Berul, Bryan Cannon, Frank Cecchin, Mitchell I. Cohen, Aarti S. Dalal, Brynn E. Dechert, Anne Foster, Roman Gebauer, M. Cecilia Gonzalez Corcia, Prince J. Kannankeril, Peter P. Karpawich, Jeffery J. Kim, Mani Ram Krishna, Peter Kubuš, Martin J. LaPage, Douglas Y. Mah, Lindsey Malloy-Walton, Aya Miyazaki, Kara S. Motonaga, Mary C. Niu, Melissa Olen, Thomas Paul, Eric Rosenthal, Elizabeth V. Saarel, Massimo Stefano Silvetti, Elizabeth A. Stephenson, Reina B. Tan, John Triedman, Nicholas H. Von Bergen, Philip L. Wackel, Philip M. Chang, Fabrizio Drago, Anne M. Dubin, Susan P. Etheridge, Apichai Kongpatanayothin, Jose Manuel Moltedo, Ashish A. Nabar, George F. Van Hare
Publikováno v:
Indian Pacing and Electrophysiology Journal
In view of the increasing complexity of both cardiovascular implantable electronic devices (CIEDs) and patients in the current era, practice guidelines, by necessity, have become increasingly specific. This document is an expert consensus statement t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64af7d2de6924889f62c150f5b6bfb98
https://doi.org/10.1016/j.ipej.2021.07.005
https://doi.org/10.1016/j.ipej.2021.07.005
Publikováno v:
JACC Case Reports
We report a case series of 4 patients with transient marked QTc prolongation and ventricular arrhythmias in the setting of inflammation with very high ferritin levels. Three patients were positive for coronavirus disease-2019. In the setting of an ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb122917628354bf0cc058573d7355ec
http://europepmc.org/articles/PMC8314122
http://europepmc.org/articles/PMC8314122
Publikováno v:
Indian Pacing and Electrophysiology Journal
Indian Pacing and Electrophysiology Journal, Vol 21, Iss 3, Pp 186-190 (2021)
Indian Pacing and Electrophysiology Journal, Vol 21, Iss 3, Pp 186-190 (2021)
Congenital long QT syndrome [LQTS] is a channelopathy characterized by QT prolongation and polymorphic VT. LQTS however need not be a purely electrical disease. Defects in ion channels may cause myocardial architectural disruption leading to ventricu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a58c302ef959dad6763d93d3f1a9fa56
https://doi.org/10.1016/j.ipej.2021.03.001
https://doi.org/10.1016/j.ipej.2021.03.001
Autor:
Sanjaya Gupta, Rahul Myadam
Publikováno v:
JACC: Case Reports, Vol 3, Iss 3, Pp 504-507 (2021)
JACC Case Reports
JACC Case Reports
A 26-year-old woman with recurrent unexplained syncope in the postpartum period was diagnosed with long QT syndrome type 2. Traditional implantation of defibrillator using fluoroscopy became contraindicated after she again became pregnant prior to de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fe28fbfaef56d0ba8e66cb8b86d9b7d
https://doi.org/10.1016/j.jaccas.2020.12.038
https://doi.org/10.1016/j.jaccas.2020.12.038
Autor:
Xin-Hui Zhang, Hong-Min Liu, Yongfang Yao, Li-Ying Ma, Xue-Jian Feng, Qin Shangshang, Tingting Yu, Bing Zhao, De-Quan Yu, Xiaoling Zhang, Ying Liu
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 11, Iss 1, Pp 203-221 (2021)
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B
New Delhi metallo-β-lactamase-1 (NDM-1) is capable of hydrolyzing nearly all β-lactam antibiotics, posing an emerging threat to public health. There are currently less effective treatment options for treating NDM-1 positive “superbug”, and no p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c44e2471539ae24953ab00f10282f4be
http://www.sciencedirect.com/science/article/pii/S2211383520306316
http://www.sciencedirect.com/science/article/pii/S2211383520306316
Autor:
Evdoxia J Apostolopoulos, Helen Melita, Antonis A. Manolis, Antonis S. Manolis, Theodora A Manolis, Despoina Papatheou
Publikováno v:
Trends in Cardiovascular Medicine
Highlights • Serious cardiac arrhythmias may be the consequence of direct effects of COVID-19 infection, but also the outcome of the deleterious effects of systemic illness and the adverse proarrhythmic reactions to drugs employed in the treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e75a21209bb74e6199b08057de45aa0
https://doi.org/10.1016/j.tcm.2020.08.002
https://doi.org/10.1016/j.tcm.2020.08.002
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 2, Iss 8, Pp 1178-1181 (2020)
JACC: Case Reports, Vol 2, Iss 8, Pp 1178-1181 (2020)
Catecholaminergic polymorphic ventricular tachycardia is a genetic disorder that causes ventricular tachyarrhythmias via increased release of intracellular calcium. The standard diagnostic measure is an exercise stress test that reveals ventricular e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ea46ef533bee796918cb911b75d0cc8
http://europepmc.org/articles/PMC8311990
http://europepmc.org/articles/PMC8311990
Publikováno v:
JACC: Case Reports, Vol 2, Iss 6, Pp 930-934 (2020)
JACC Case Reports
JACC Case Reports
We report an unusual case of a patient with hypertrophic obstructive cardiomyopathy, anomalous aortic origin of a coronary artery, obesity hypoventilation syndrome, and acquired long QT syndrome who was able to defy the odds of sudden cardiac death i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22a6d8ad669737921022bf2c06d07e4f
https://doi.org/10.1016/j.jaccas.2020.04.046
https://doi.org/10.1016/j.jaccas.2020.04.046
Autor:
Silvia Magnani, Frank Cecchin, Steven Fowler, Linda Borneman, Marina Cerrone, Lior Jankelson, Larry A. Chinitz, Reina Tan
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 2, Iss 4, Pp 591-594 (2020)
JACC: Case Reports, Vol 2, Iss 4, Pp 591-594 (2020)
Implantable loop recorders (ILRs) can be a valuable tool in monitoring patients with inherited arrhythmia. This paper reports on a family with long QT syndrome (type 2 [LQT2]) in which a pseudopolymorphic wide complex tachycardia detected by ILR was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::742b6b1027508d018012396653954e9c
http://europepmc.org/articles/PMC8298547
http://europepmc.org/articles/PMC8298547