Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kristen N. Brown"'
Autor:
Kristen N. Brown, MD, Kyle Gronbeck, MD, Ayesha Azmeen, MBBS, Aleem Siddique, MBBS, Ronald Zolty, MD, PhD, James N. Sullivan, MD
Publikováno v:
JACC: Case Reports, Vol 7, Iss , Pp 101716- (2023)
1,1-Difluoroethane (DFE) cardiomyopathy results from the direct inhalation of toxic halogenated hydrocarbons. We present a case series of acute DFE cardiomyopathy illustrating the typical presentation of severe DFE cardiomyopathy along with a detaile
Externí odkaz:
https://doaj.org/article/23b64236fdc740cfb656eea5ad8d63e4
Publikováno v:
European Heart Journal - Case Reports. 7
Background ST elevation myocardial infarction (STEMI) has traditionally been a relative contraindication for the utilization of rotational atherectomy (RA). However, in severely calcified lesions, RA may be necessary to facilitate stent delivery. Cas
Publikováno v:
Journal of visualized experiments : JoVE. (185)
Right ventricular (RV) shock, classically characterized by elevated central venous pressure (CVP) with normal to low pulmonary artery (PA) and pulmonary capillary wedge pressures (PCWP), remains a significant cause of morbidity and mortality worldwid
Publikováno v:
Journal of the Society for Cardiovascular Angiography & Interventions. 1:100402
Publikováno v:
World Journal of Cardiology
BACKGROUND The prevalence of left atrial appendage (LAA) thrombus detection by transesophageal echocardiogram (TEE) in patients with non-valvular atrial fibrillation (AF) anticoagulated with apixaban is not well defined and identification of addition
Publikováno v:
Chest. 156:A673
Autor:
Gurpreet Johal, Jason Wen, Stuart Cavalieri, Joe B. Calkins, Kristen N. Brown, Jonathan Hanson
Publikováno v:
Journal of the American College of Cardiology. 73:2873
A bifid sternum (BS) is a rare congenital anomaly generally diagnosed as asymptomatic at birth and surgically corrected during the first month of life. It is extremely rare for a patient with BS to be diagnosed later in life. We present a rare case o
CONGENITAL LONG QT SYNDROME TYPE 2: THE CASE OF A MISDIAGNOSED ARRHYTHMIA AND A NEAR FALL FROM DEATH
Publikováno v:
Journal of the American College of Cardiology. 73:2929
Long QT Syndrome-2 (LQT2) is a rare congenital disorder of ventricular myocardial repolarization due to heterozygous mutations in the alpha subunit of the rapid rectifier potassium channel of HERG and MiRP1 genes resulting in slowing of cardiac potas
Publikováno v:
Journal of the American College of Cardiology. 71:A297
The prevalence of left atrial cavity (LAC) and left atrial appendage (LAA) thrombus in patients prescribed warfarin for non-valvular atrial fibrillation (AF) is 1.1-1.9%. A similar prevalence is reported in patients treated with Dabigatran (1.2-1.8%)
Publikováno v:
Journal of the American College of Cardiology. 71:A2356
Chronic anthracycline induced cardiotoxicity (AIC) is a type 1 chemotherapeutic cardiotoxicity characterized by irreversible myocyte destruction and necrosis. Although rare, acute AIC is characterized by a transient decline in left ventricular ejecti