Sudden cardiac death causes: Difference between revisions

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| [[VT]], [[VF]] (75%), [[bradycardia]], [[asystole]](25%) || Mechanism of [[VT]]: [[bundle branch reentry tachycardia]], terminal event: [[asystole]], [[electromechanical dissociation]] in advanced [[LV]] dysfunction || [[Ventricular tachycardia]], [[Ventricular fibrillation]]|| [[ECG]] in [[normal sinus rhythm]] [[T waves]] inversion in V1-V3, complete, incomplete [[RBBB]], epsilone wave ( terminal notch on [[QRS]] complex), [[VT]] is [[LBBB]] contour||  ||[[Atrial arrhythmias]] (43%), [[QRS]] prolongation (mean 132ms) || [[Torsadepoints]], [[ECG]] findings: abnormal Twaves contour, Twaves alternance, [[sinus bradycardia]]|| ||[[RV]] outflow tract [[VT]] is [[LBBB]] contour, inferior axis, Termination with [[vagal]] maneuver such as [[adenosine]]. [[LVOT VT]] or fasciculated [[VT]] is [[RBBB]] contour with left axis deviation, originated from left posterior septum, Termination with [[calcium channel blocker]]|| [[SCD]]  in the presence of [[polymorphic VT]] and  even normal [[LV]] function without [[torsadepoints]]. Termination of cathecolaminergic polymorphic [[VT]] ([[CPVT]]) with [[betablocker]],||[[Ealy repolarization]] abnormality in inferior lateral leads, No response to [[betablocker]] in the presence of ideopathic [[VF]] or short coupled of [[torsades de points]] ||
| [[VT]], [[VF]] (75%), [[bradycardia]], [[asystole]](25%) || Mechanism of [[VT]]: [[bundle branch reentry tachycardia]], terminal event: [[asystole]], [[electromechanical dissociation]] in advanced [[LV]] dysfunction || [[Ventricular tachycardia]], [[Ventricular fibrillation]]|| [[ECG]] in [[normal sinus rhythm]] [[T waves]] inversion in V1-V3, complete, incomplete [[RBBB]], epsilone wave ( terminal notch on [[QRS]] complex), [[VT]] is [[LBBB]] contour||  ||[[Atrial arrhythmias]] (43%), [[QRS]] prolongation (mean 132ms) || [[Torsadepoints]], [[ECG]] findings: abnormal Twaves contour, Twaves alternance, [[sinus bradycardia]]|| ||[[RV]] outflow tract [[VT]] is [[LBBB]] contour, inferior axis, Termination with [[vagal]] maneuver such as [[adenosine]]. [[LVOT VT]] or fasciculated [[VT]] is [[RBBB]] contour with left axis deviation, originated from left posterior septum, Termination with [[calcium channel blocker]]|| [[SCD]]  in the presence of [[polymorphic VT]] and  even normal [[LV]] function without [[torsadepoints]]. Termination of cathecolaminergic polymorphic [[VT]] ([[CPVT]]) with [[betablocker]]||[[Ealy repolarization]] abnormality in inferior lateral leads, No response to [[betablocker]] in the presence of ideopathic [[VF]] or short coupled of [[torsades de points]] ||
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Revision as of 05:52, 10 March 2021

Sudden cardiac death Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Sara Zand, M.D.[2]

Overview

Sudden cardiac arrest may be caused by coronary artery abnormality such as coronary atherosclerosis, acute MI, coronary artery embolism, coronary arteritis , hypertrophy of myocardium such as HCM, hypertensive heart disease, primary or secondary pulmonary hypertension , myocardial disease such as ischemic cardiomyopathy, non-ischemic cardiomyopathy, myocarditis ,valvular heart disease such as aortic stenosis, aortic insufficiency, mitral valve prolapse, endocarditis , congenital heart disease such as congenital septal defect with eisenmenger physiology , abnormality in conducting system such as Wolf-Parkinson-White syndrome , electrical instability such as (CPVT, LQTS)

Causes

Sudden cardiac arrest may be caused by :

Causes of acquired Long QT syndrome include the following

Causes of Sudden Death Including Sudden Cardiac Death by Organ System

Cardiovascular

Amyloid cardiopathy, Congestive heart failure, Ventricular rupture,

Hypoxia, Coronary thrombosis, Coronary vasospasm, Coronary artery aneurysm, Prinzmetal's variant angina ,

  • Pericardial

Cardiac tamponade,

Asymmetric septal hypertrophy , ST Elevation Myocardial Infarction, Dilated cardiomyopathy, Giant cell myocarditis , Hypertrophic cardiomyopathy, Kugel-Stoloff syndrome , Myocardial infarction, Myocarditis, Rupture of the papillary muscles,

  • Endocardial/Valvular

Mitral valve prolapse, Valvular aortic stenosis/insufficiency, Mitral valve disruption, Endocarditis, Prosthetic valve dysfunction,

Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Brugada syndrome, Jervell and Lange-Nielsen Syndrome, Prolonged Q-T Interval Syndrome, Multifocal ventricular premature beats , Naxos disease , Romano-Ward syndrome , Sick sinus syndrome, Short QT syndrome , Sinus node disease, Stokes-Adams Syndrome, Sudden Arrhythmia Death Syndrome, Wolf-Parkinson-White syndrome,

Acute aortic insufficiency, Acute coronary syndrome, Aortic dissection, Aortic stenosis, Aorto-ventricular tunnel, Arteritis, Coronary artery disease, Coronary arteries - congenital malformation , Ruptured abdominal aortic aneurysm,

  • Congenital/Developmental

Congenital aortic or pulmonary valve stenosis, Congenital septal defect with eisenmenger physiology, Congenital heart block , Congenital Long QT syndrome, Noncompaction Cardiomyopathy, Sudden Infant Death Syndrome, Uhl anomaly

Snake bite

No underlying causes
  • Drug Side Effect
Agalsidase beta, Articaine, caspofungin acetate, Clozapine, cytomegalovirus immune globulin, Drug allergy, drug overdose, Dornase Alfa, ferumoxytol, Flucytosine, galsulfase, Iodixanol, laronidase, Lincomycin Hydrochloride, Polidocanol, Potassium bicarbonate, pramipexole, prednisolone, Ramucirumab, Calcium gluconate, Dextran, Tiagabine
No underlying causes

Diabetic ketoacidosis - typically from undiagnosed diabetes, Thyrotoxicosis,

  • Environmental
Hypothermia,
  • Gastroenterologic

Appendicitis, Gastrointestinal bleeding, Retroperitoneal bleed,

Brugada syndrome, 3-methylglutaconic aciduria, type 1, Familial dilated cardiomyopathy , Familial hypertrophic cardiomyopathy 1, Hyperbilirubinemia transient, familial neonatal, Marfan syndrome , Timothy syndrome

No underlying causes
  • Iatrogenic
Transfusion reaction

Flu mainly in the elderly, infants, infirm or chronically ill, Neurocysticercosis , Lyme disease

No underlying causes

Apoplexy, Encephalitis, Intracranial hemmorhage, Meningitis, Stroke, Subarachnoid hemorrhage,

3-methylglutaconic aciduria, type 1, Alpha-ketoglutarate dehydrogenase deficiency , Food allergy

Amniotic fluid syndrome , Childbirth hemorrhage,

Atrial myxoma, familial

No underlying causes
  • Overdose / Toxicity

Opioid overdose , Oxycontin overdose, Pain killer overdose , Sleeping pill overdose

No underlying causes

Hypercapnia, Pickwickian Syndrome, Pulmonary embolism, Tension pneumothorax, Status asthmaticus

Hypercalcemia, Hypokalemia, Hyperkalemia,

Amyloidosis, Anaphylaxis, Myasthenia gravis, Sarcoidosis,

No underlying causes

Commotio cordis, Homicide, Motor Vehicle accident

No underlying causes
  • Miscellaneous

Shock, Asphyxia, Insect bite Sepsis syndrome, Shock



Cardiac causes of sudden death

Non cardiac causes of sudden death:

Diffential diagnosis of sudden cardiac death

[6][7][8][9][10][11][12][13][14][15][16][17][18]


Differentiating diagnosis of sudden cardiac death Coronary Artery Disease Ideopathic dilated cardiomyopathy Hypertrophic cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy Valvular Heart Disease Congenital Heart Disease Long QT syndrome WPW syndrome Ideopathic monomorphic VT Polymorphic VT Ideopathic VF Sudden unexpected nocturnal death (Lai-Lai, sleep death, Laos Pukkuri
Incidence 80% 10% 1% 2% 1% to 5% in native valves, 0.2%–0.9% in prosthesis 0.04% 0.05% 0.1% Rare 0.15% 5% 0.001%
Mechanism Atherosclerosis in coronary arteries: 3 vessels disease in 40-86% patients with stenosis > 75%, MI < 50%, Qwave MI < 25%, recent coronary thrombosis 15-64% , healed infarct>50% in autopsy or survivors of SCD, Non atherosclerotic changes including coronary emboli, coronary arthritis, coronary dissection in few cases Myocardial stretch, neuroendocrine factors, electrolyte abnormality, proarrhythmic effect of antiarrhythmic drugs, excessive activation of sympathetic and renin angiotensin system Arrhythmia, abrupt hemodynamic deterioration, ischemia Fatty and fibrofatty myocardial infiltration, patchy myocarditis, apoptosis of left ventricle, left ventricular septum (50-67%), right ventricular inflow, outflow tract and apex( triangle of dysplasia) Arrhythmia, prosthetic valve dysfunction, Coexisting CAD SCD is late presentation after surgical repair of complex congenital heart disease such as Eisenmenger syndrome,transposition of the great arteries (atrial switch or congenitally corrected), Fontan circulations. Prolongation of repolarization, early after depolarization In 10% of WPW patients, SCD is first presentation. Development of VF in the presence of rapid conduction of AF to the ventricle through accessory pathway Normal structure of the heart, Originated from RV outflow tract (more common), or LV outflow tract. SCD is rare Initiation of arrhythmia with coupled premature complex, in the presence of acquired or congenital Long QT interval or ischemia, sporadic or familiar Normal structure of the heart with high incidence of recurrence of VF or cardiac arrest or syncope (30%) without ICD implantation Unknown
Risk factors of SCD Plaque, fissure, hemorrhage, thrombosis in coronary arteries Frequent episodes of non sustain VT, syncope Family history of SCD, recurrent syncope, sustained VT, history of SCA, massive LVH, multiple episodes of non sustained VT Asymptomatic aotric valve disease is low risk for SCD. Risk factors of SCD in MVP: myxomatous degeneration of the valve, coexisting mitral regurgitation, LV dysfunction Risk factors of SCD in TOF: QRS prolongation, dilated RV Incidence of cardiac event in LQTS1, LQTS2> LQTS3 Lethality of cardiac event in LQTS3 > LQTS1, LQTS2 Predictors of VF: AF with shortest interval between ventricle beats less than 250 msec Cathecolamine release after stressful emotional or physical event Young, male sex, southeast asian ethnicity
Arrhythmia VT, VF (75%), bradycardia, asystole(25%) Mechanism of VT: bundle branch reentry tachycardia, terminal event: asystole, electromechanical dissociation in advanced LV dysfunction Ventricular tachycardia, Ventricular fibrillation ECG in normal sinus rhythm T waves inversion in V1-V3, complete, incomplete RBBB, epsilone wave ( terminal notch on QRS complex), VT is LBBB contour Atrial arrhythmias (43%), QRS prolongation (mean 132ms) Torsadepoints, ECG findings: abnormal Twaves contour, Twaves alternance, sinus bradycardia RV outflow tract VT is LBBB contour, inferior axis, Termination with vagal maneuver such as adenosine. LVOT VT or fasciculated VT is RBBB contour with left axis deviation, originated from left posterior septum, Termination with calcium channel blocker SCD in the presence of polymorphic VT and even normal LV function without torsadepoints. Termination of cathecolaminergic polymorphic VT (CPVT) with betablocker Ealy repolarization abnormality in inferior lateral leads, No response to betablocker in the presence of ideopathic VF or short coupled of torsades de points

References

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  2. Eisenberg MS, Mengert TJ (2001). "Cardiac resuscitation". N. Engl. J. Med. 344 (17): 1304–13. PMID 11320390. Unknown parameter |month= ignored (help)
  3. . doi:10.1080/2F20961790.2019.1595352. Missing or empty |title= (help)
  4. 4.0 4.1 Basso, Cristina; Perazzolo Marra, Martina; Rizzo, Stefania; De Lazzari, Manuel; Giorgi, Benedetta; Cipriani, Alberto; Frigo, Anna Chiara; Rigato, Ilaria; Migliore, Federico; Pilichou, Kalliopi; Bertaglia, Emanuele; Cacciavillani, Luisa; Bauce, Barbara; Corrado, Domenico; Thiene, Gaetano; Iliceto, Sabino (2015). "Arrhythmic Mitral Valve Prolapse and Sudden Cardiac Death". Circulation. 132 (7): 556–566. doi:10.1161/CIRCULATIONAHA.115.016291. ISSN 0009-7322.
  5. Yap, Sing-Chien; Harris, Louise (2014). "Sudden cardiac death in adults with congenital heart disease". Expert Review of Cardiovascular Therapy. 7 (12): 1605–1620. doi:10.1586/erc.09.153. ISSN 1477-9072.
  6. Moore, Benjamin; Yu, Christopher; Kotchetkova, Irina; Cordina, Rachael; Celermajer, David S. (2018). "Incidence and clinical characteristics of sudden cardiac death in adult congenital heart disease". International Journal of Cardiology. 254: 101–106. doi:10.1016/j.ijcard.2017.11.117. ISSN 0167-5273.
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  9. Yamashina, Y.; Yagi, T.; Namekawa, A.; Ishida, A.; Sato, H.; Nakagawa, T.; Sakuramoto, M.; Sato, E.; Yambe, T. (2011). "Prevalence and characteristics of idiopathic right ventricular outflow tract arrhythmias associated with J-waves". Europace. 13 (12): 1774–1780. doi:10.1093/europace/eur256. ISSN 1099-5129.
  10. Henriques de Gouveia R, Corte Real Gonçalves F (2019). "Sudden cardiac death and valvular pathology". Forensic Sci Res. 4 (3): 280–286. doi:10.1080/20961790.2019.1595351. PMC 6713097 Check |pmc= value (help). PMID 31489394. Vancouver style error: initials (help)
  11. Israel CW (2014). "Mechanisms of sudden cardiac death". Indian Heart J. 66 Suppl 1: S10–7. doi:10.1016/j.ihj.2014.01.005. PMC 4237287. PMID 24568819.
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  18. Viskin S (May 2017). "Idiopathic Polymorphic Ventricular Tachycardia: a "Benign Disease" with a Touch of Bad Luck?". Korean Circ J. 47 (3): 299–306. doi:10.4070/kcj.2016.0303. PMC 5449521. PMID 28567077.