Long QT Syndrome
Long QT Syndrome (LQTS) produces prolonged ventricular repolarisation -> predisposes to malignant ventricular arrhythmias
Long QT Syndrome (LQTS) produces prolonged ventricular repolarisation -> predisposes to malignant ventricular arrhythmias
Left Ventricular Outflow Tract Obstruction (LVOTO) and systolic anterior motion (SAM) of the mitral valve
Junctional Ectopic Tachycardia: rare; congenital or post surgery for congenital heart disease; abnormal automaticity within the His bundle; high mortality rate (35%)
Implantable Cardioverter Defibrillators (ICDs): implantable device defibrillator +/- pacemaker (counter shock vector is from RV -> both SVC)
Hypertrophic cardiomyopathy (HCM) is one of the most common inherited cardiac disorders (affecting ~ 1 in 500 people) and is the number one cause of sudden cardiac death in young athletes. Annual mortality is estimated at 1-2 %.
Criteria for heart transplant recipient
Follath F, et al; Steering Committee and Investigators of the Levosimendan Infusion versus Dobutamine (LIDO) Study. Efficacy and safety of intravenous levosimendan compared with dobutamine in severe low-output heart failure (the LIDO study): a randomised double-blind trial. Lancet. 2002 Jul…
Heart Block and Conduction Abnormalities with first, second, third degree blocks; and fascicular blocks
nasal intubation may be performed blind or with fiberoptic assistance. Indicated when oral intubation is not feasible
Cardiac Output (CO) = Stroke Volume (SV) x Heart rate (HR) CO = SV x HR changes based on exercise, age and body size. normal adult = 5L/min Stroke Volume (SV) determined by: Preload Afterload Contractility
Cardiac Lesions and Severe Clinical Signs; valvular issues, cardiac anomalies and their murmurs
Biomarkers can potentially be used to detect and monitor a wide range of cardiac conditions in the critical care setting