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	Topics 
	  - Definitions
  
        - Synonyms and related keyword: sudden arrest
 
        - Background
 
        - Pathophysiologic
 
        - Frequency
 
        - Mortality/Morbidity 
 
        - Race
 
        - Sex
 
        - Age
 
        - Epidemiology
 
        - Prevalence
 
        - Incidence
 
        - The causes of sudden death
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			The causes of sudden death hide subtopics
          
		 - Ischemic heart disease
         
		 - Ischemic heart disease
 
        - Hypertension
 
        - Heart failure
 
        - Pulmonar embolism
 
        - Dilated cardiomyopathy (DCM)
 
        - Hypertrophic cardiomyopathy (HCM)
 
        - Restrictive cardiomyopathy (RCM)
 
        - Arrhythmogenic right ventricular dysplasia(ARVD);
 
        - Infiltrative  cardiomyopathy
 
        - Glycogen storage disease
 
        - Isolated ventricular noncompaction (IVNC)
 
        - Cardiomyopathies due to defective energy  metabolism: Mitochondrial disease: Key Sayre,  medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency.
 
        - Carnitine deficiency
 
        - Endocardial Fibroelastosis
 
        - Chagas' disease
 
        - Myocarditis
 
        - Valvular disease:
 
          (a) Aortic stenosis. 
          (b) Aortic insufficiency /Aortic  dissection or aneurysmal rupture is the other major cause of out-of-hospital  nonarrhythmic cardiovascular death. Predisposing factors for aortic dissection: genetic deficiencies of collagen Marfan  syndrome, Ehlers-Danlos syndrome, and aortic cystic medial necrosis. 
          (c) Mitral valve prolapse (MVP). 
	    - Congenital heart disease: Congenital Coronary artery  anomalies, congenital aortic stenosis, cystic medial  necrosis, and sinus node artery obstruction. Tetralogy of Fallot after surgery,  Transposition of the great arteries, Fontan operation, Marfan syndrome, Eisenmenger  syndrome, congenital heart block, Ebstein anomaly, 
 
	        - Congenital Left Ventricular Aneurysms and diverticula’s 
 
	        - Kawasaki syndrome
 
	        - Long QT syndrome:
 
          
	        (a) Hereditary, idiopathic or  congenital long QT syndrome 
   (b) Acquired long QT syndrome 
	      
	        - Primary  pulmonary hypertension 
 
	        - Commotio  cordis (traumatic blow to the chest wall causing VT/VF)
 
	        - Congenital  short QT syndrome (SQTS)
 
	        - Wolff-Parkinson-White syndrome(WPWS)
 
	        - Primary  VT
 
	        - Brugada syndrome 
 
	        - Sudden unexpected nocturnal death syndrome (SUNDS)
 
	        - Mixed forms or  overlapping clinical phenotypes:
  
	       (a) Brugada syndrome and LQTS variant LQT3  
    (b) Brugada syndrome and Lenègre  disease  
   (c) Brugada syndrome and sinus node dysfunction  
	        - Progressive cardiac  conduction defect (PCCD)
 
	       (a) Lenègre  syndrome 
    (b) Lev syndrome 
	        - Idiopathic ventricular  fibrillation
 
	        - Sudden infant death syndrome (SIDS)
 
	        - Catecholaminergic polymorphic ventricular tachycardia( CPVT)
 
	        - Short coupled variant of torsade de  pointes, polymorphic ventricular tachycardia or truly torsade de pointe without long QT
 
	        - Bi-directional ventricular  tachycardia
 
	        - Beta2-adrenergic  receptor genetic variants: Right  ventricular outflow tract ventricular tachycardia 
 
	        - Lown-Ganong-Levine syndrome( LGLS)
 
	        - Cardiac sarcoidosis
 
	        - Recreational  drug abuse
 
	        - Sudden  death in hemodialysis patients
 
	        - Cardiac  tumors
 
	        - Giant cell coronary arteritis
 
	        - Beta2-adrenergic receptor  polymorphisms and sudden cardiac death
 
	        - After butane gas inhalation
 
	        - Neurological meningo-cerebral  causes: Brain  infarction
 
	        - Acute leukemias
 
	        - Obesity and the metabolic syndrome.
 
	        - Alergic causes
 
	        - Hematologic causes 
 
	        - Endocrinological cause
  
         
        - Clinical Testing
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			Clinical Testing hide subtopics
		
          - Value  of History Family history
           
            - Value of physical examination
 
            - Value of non invasive and invasive tests 
 
            - Electrocardiography  (ECG or EKG)
 
            - ECG with modified protocol
 
            - Vectorcardiography  (VCG)
 
            - Signal-Averaged  Electrocardiogram (SAECG) or High-Resolution Electrocardiography
 
            - Ambulatory  monitoring Ambulatory Electrocardiography Recorders or Long-Term  Electrocardiographic Recording
 
            - Intermitent  Recorders
 
            - Memory-Looping Event Monitoring;
 
            - Heart  Rate Variability from 24hours Holter  Recording (HRV)
 
            - QT Dispersion
 
            - Microvolt T-Wave Alternans (TWA)
 
            - Heart rate turbulence
 
            - T peak-Tend and T peak-Tend dispersion 
 
            - Ambulatory monitoring;
 
            - Exercise Stress Tests or Treadmill  Exercise Test
 
            - Cardiopulmonary Metabolic Exercise  Testing or Exercise Testing (CMET)
 
            - Body-Surface Potential Maps (BSPM)
 
            - Chest Roentgenogram or chest x-ray
 
            - Conventional Echocardiography or Trans-thoracic  Echocardiography (TTE): M-mode and Two-Dimensional and Doppler Echocardiography
 
            - Trans-Esophageal Echocardiography  or Biplanar transesophageal Echocardiography (TEE)
 
            - Three-Dimensional Echocardiography or Real-Time  Three-Dimensional (3D) Echocardiography (RT3DE)
 
            - Intracardiac  Ultrasound or Intracardiac Echocardiography (ICE)
 
            - Cardiac Magnetic Resonance Imaging or Nuclear Magnetic  Resonance (CMRI, MRI or NMR) and Delayed-Enhancement Magnetic Resonance Imaging (gadodiamide MDE-MRI)
 
            - Ultrafast Computed Tomography (UFCT) or Electron-Bean  Computed Tomography (EBCT);
 
            - Contrast Enhanced ECG gated Computed Tomography (CT)
 
            - Gallium-67 scintigraphy
 
            - Electrocardiographically (ECG)-gated multi-detector row  computed tomography (CT);
 
            - Radionuclide Angiography or Radionuclide  Ventriculography (RNV)
 
            - Genetic investigations
 
            - Plasma levels of brain natriuretic  peptide (BNP)
 
            - Estimation of EF by echocardiogram or other non-invasive  methods
 
            - Electrophysiologic study response to programmed electrical stimulation (PES) (INDUCTION)
 
            - Cardiac catheterization: ejection fraction
 
          
          - Endomyocardial biopsy (EMB)
 
		  - Postmortem  magnetic resonance imaging (PMMRI)
   
		  - Treatment
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			Treatment hide subtopics
		  
		    - Drugs
 
		    - Balloon angioplasty or  PTCA
 
		    - Antiarrhythmic medicine
 
		    - Implantable  cardioverter / defibrillator
 
		    - Implantable pacemaker
 
		    - Interventional procedures or surgery 
 
		    - Coronary  artery bypass surgery
 
		    - Left  ventricular reconstruction surgery (surgical removal of the infarcted or dead  area of heart tissue)
 
		    - Heart transplantation
 
		    
		  - Sudden death in athletes
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			Sudden death in athletes hide subtopics
			
		    - Causes:
 (a) In young (<35 years old) (b) In veterans(>35 years old) 
		      - Prevelence
 
		      - Screening: Value of historic, physical  examination, electrocardiographic features and others methodologies.
 
		      - The athlete at heart characteristic.
 
		      - Asthma deaths and the athlete. 
 
		      - Commotio cordis in  athlete.
 
		      - Trials 
 
		      - Guideline
 
		       
		     - The risk factors of SCD
 
			- Factors that can increase a person's risk of sudden cardiac arrest and SCD. The two leading risk factors include:
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			Factors that can increase a person's risk of sudden cardiac arrest and SCD. The two leading risk factors include: hide subtopics
			- Previous heart attack (75  percent of SCD cases are linked to a previous heart attack) -- A person’s risk  of SCD is higher during the first six months after a heart attack
 
                - Coronary artery disease  (80 percent of SCD cases are linked with this disease) Risk factors for  coronary artery disease include smoking, family history of cardiovascular  disease, high cholesterol or an enlarged heart.
 
                - Ejection fraction of less  than 40 percent, combined with ventricular tachycardia
 
                - Prior episode of sudden  cardiac arrest
 
                - Family history of sudden  cardiac arrest or SCD;
 
                - Personal or family  history of certain abnormal heart rhythms including long QT syndrome,  Wolff-Parkinson-White Syndrome, extremely low heart rates or heart block
 
                - Ventricular tachycardia  or ventricular fibrillation after a heart attack
 
                - History of congenital  heart defects or blood vessel abnormalities
 
                - History of syncope  (fainting episodes of unknown cause)
 
                - Heart failure: a  condition in which the heart’s pumping power is weaker than normal. Patients  with heart failure are 6 to 9 times more likely than the general population to  experience ventricular arrhythmias that can lead to sudden cardiac arrest.
 
                - Dilated cardiomyopathy  (cause of SCD in about 10 percent of the cases): a decrease in the heart’s  ability to pump blood due to an enlarged (dilated) and weakened left ventricle 
 
                - Hypertrophic  cardiomyopathy (a thickened heart muscle that especially affects the  ventricles) 
 
                - Significant changes in  blood levels of potassium and magnesium (from using diuretics, for example),  even if there is not organic heart disease 
 
                - Obesity
 
                - Diabetes
 
                - Recreational drug abuse
 
                - Taking drugs that are  “pro-arrhythmic” may increase the risk for life-threatening arrhythmias.
 
              
  
            - The treatment for sudden cardiac death
 
	   
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