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MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD

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Presentation on theme: "MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD"— Presentation transcript:

1 MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD www.anaesthesia.co.inanaesthesia.co.in@gmail.com

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3 Normal sinus rhythm Impulse formation beginning in the sinus node Impulse formation beginning in the sinus node At frequencies between 60 to 100 per minute At frequencies between 60 to 100 per minute P is always upright in I, II and aVF and inverted in aVR P is always upright in I, II and aVF and inverted in aVR Though rhythm is regular, minor variation in PP interval exists & longest and shortest PP differ< 0.16 except in sinus arrhythmia Though rhythm is regular, minor variation in PP interval exists & longest and shortest PP differ< 0.16 except in sinus arrhythmia

4 Normal sinus rhythm Every P is followed by a QRS complex Every P is followed by a QRS complex Every QRS is preceded by a P wave Every QRS is preceded by a P wave P and its following QRS is separated by fairly regular PR interval P and its following QRS is separated by fairly regular PR interval TO BE VERY PRECISE P AND QRS ARE IN SIMPLE HARMONY TO BE VERY PRECISE P AND QRS ARE IN SIMPLE HARMONY

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6 NORMAL ECG

7 When the rhythm deviates from the above said normalcy it is called ARRHYTHMIA When the rhythm deviates from the above said normalcy it is called ARRHYTHMIA Broadly it is classified as brady and tachy arrhythmia Broadly it is classified as brady and tachy arrhythmia Arrhythmogenesis may be due various causes Arrhythmogenesis may be due various causes

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9 Some arrhythmias are considered MALIGNANT Some arrhythmias are considered MALIGNANT Because if not properly and immediately treated, it can be LETHAL to the sufferer Because if not properly and immediately treated, it can be LETHAL to the sufferer This is important in understanding the concept of SUDDEN CARDIAC DEATH This is important in understanding the concept of SUDDEN CARDIAC DEATH

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11 SUDDEN CARDIAC DEATH

12 Anatomy of the conduction system

13 Sinus node- Sinus node- –RCA (55-60%) –left circumflex (40-45%)artery AV node- AV node- –RCA (85-90%) –left circumflex (10-15%) artery

14 ACUTE RVMI+IWMI

15 Anatomy of conduction system The conduction system is densely innervated by The conduction system is densely innervated by –Cholinergic fibers- parasympathetic –Adrenergic fibers- sympathetic This is important in understanding This is important in understanding –variability of cardiac function with autonomic influence –effect of parasympathetic stimulation in terminating arrhythmias

16 BRADYARRHYTHMIAS Sinus nodal Sinus nodal  Sinus bradycardia  Sinus arrhythmia  Sinus pause/arrest  Sinoatrial exit block  Sick sinus syndrome AV nodal blocks AV nodal blocks  First degree  Second degree(MOBITZ type 1 and 2)  Complete heart block

17 SINUS ARREST

18 SICK SINUS SYNDROME

19 ATRIO VENTRICULAR BLOCK I degree -conduction time prolonged: all impulses are conducted I degree -conduction time prolonged: all impulses are conducted II degree -2 forms II degree -2 forms oMobitz type I (WENCKEBACH)- progressive lengthening of conduction time until an impulse is failed to be conducted oMobitz type II- occasional or repetitive sudden block in conduction without prior measurable lengthening of conduction time Complete or III degree -no impulses are conducted Complete or III degree -no impulses are conducted

20 FIRST DEGREE AV BLOCK

21 FIRST DEGREE HB

22 IWMI+FIRST AV BLOCK

23 2:1 AV BLOCK

24 COMPLETE AV BLOCK Occurs when no atrial activity is conducted to the ventricles Occurs when no atrial activity is conducted to the ventricles So atria and ventricles are controlled by independent pacemakers So atria and ventricles are controlled by independent pacemakers One type of complete AV dissociation One type of complete AV dissociation Ventricular focus is usually just below the site of block Ventricular focus is usually just below the site of block If focus near HIS bundle the rhythm is more stable If focus near HIS bundle the rhythm is more stable

25 CHB can occur at various levels CHB can occur at various levels –AV Node-usually congenital-40-60 bpm –Bundle of HIS –Purkinje sys-usually acquired-

26 COMP HEART BLOCK

27 COMP HB

28 CHB

29 CHB

30 IWMI+CHB

31 APPROACH TO TACHYCARDIA

32 ATRIAL FLUTTER F waves: rapid regular undulations F waves: rapid regular undulations SAW TOOTH APPEARANCE Atrial rate:250-350 bpm Atrial rate:250-350 bpm Rate & regularity of ventricles: variable and depend on AV conduction sequence Rate & regularity of ventricles: variable and depend on AV conduction sequence QRS may be normal or abnormal as a result of preexisting intraventricular conduction defect or aberrancy QRS may be normal or abnormal as a result of preexisting intraventricular conduction defect or aberrancy

33 ATRIAL FLUTTER

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37 SVT VS VT

38 Differentiating a VT from SVT can be difficult at times Differentiating a VT from SVT can be difficult at times Golden rule in ER Golden rule in ER ANY WIDE QRS TACHYCARDIA IS VENTRICULAR TACHYCARDIA UNTIL PROVED OTHERWISE ESP`LY WHEN THE PATIENT HAS A STRUCTURAL HEART DISEASE

39 Diagnosis of VT Arises distal to the bifurcation of the HIS bundle Arises distal to the bifurcation of the HIS bundle Diagnosis is by the occurrence of a series of 3 or more consecutive, abnormally shaped PVCs whose duration exceeds 120 ms, with ST-T vector pointing opposite the major QRS deflection Diagnosis is by the occurrence of a series of 3 or more consecutive, abnormally shaped PVCs whose duration exceeds 120 ms, with ST-T vector pointing opposite the major QRS deflection

40 VENTRICULAR ECTOPICS

41 RR can be exceedingly regular or can vary RR can be exceedingly regular or can vary Atrial activity can be independent of ventricular activity or can be depolarized retrograde (VA association) Atrial activity can be independent of ventricular activity or can be depolarized retrograde (VA association)

42 Fusion beats and capture beats provide the maximum support for the diagnosis of VT Fusion beats and capture beats provide the maximum support for the diagnosis of VT FUSION BEATS-activation of ventricles from 2 foci FUSION BEATS-activation of ventricles from 2 foci CAPTURE BEATS- capture of the ventricle by supraventricular rhythmwith normal confguration of the captured QRS at intrvl shorter than tachycardia in question- indicates origin of impulse is supraventricular CAPTURE BEATS- capture of the ventricle by supraventricular rhythmwith normal confguration of the captured QRS at intrvl shorter than tachycardia in question- indicates origin of impulse is supraventricular

43 FUSION AND CAPTURE BEATS FUSION AND CAPTURE BEATS

44 QRS contours can be QRS contours can be –Unchanging (MONOMORPHIC) –Vary randomly (POLY OR PLEOMORPHIC) –Vary repetitively (TORSADES DE PONTES) –Vary in alternative cplxs (BIDIRECTIONAL)

45 MONOMORPHIC VT

46 POLYMORPHIC VT

47 TORSADES DE POINTES

48 TYPES OF VT VT can be SUSTAINED- lasting longer than 30 seconds or requiring termination due to hemodynamic collapse SUSTAINED- lasting longer than 30 seconds or requiring termination due to hemodynamic collapse NON SUSTAINED- stops spontaneously within 30 seconds NON SUSTAINED- stops spontaneously within 30 seconds

49 NON-SUSTAINED VT

50 SUSTAINED VT

51 HYPER ACUTE EXT ALMI

52 DIGITALIS EFFECT

53 PROLONGED QT(U) INTERVAL

54 Ventricular flutter & fibrillation Represent severe derangement of heart beat that usually terminate fatally within 3-5 mts if corrective measures are not undertaken promptly. Represent severe derangement of heart beat that usually terminate fatally within 3-5 mts if corrective measures are not undertaken promptly.

55 VENTRICULAR FLUTTER Manifested as sine wave in appearance Manifested as sine wave in appearance Regular large oscillations occurring at a rate of 150-300(usually 200)/min Regular large oscillations occurring at a rate of 150-300(usually 200)/min

56 VENTRICULAR FLUTTER

57 VENTRICULAR FIBRILLATION Irregular undulations of varying contour & amplitude Irregular undulations of varying contour & amplitude Distinct QRS, ST or T are absent Distinct QRS, ST or T are absent Fine amplitude fibrillatory waves (0.2mV) with prolonged VF: worse prognosis: confused with asystole Fine amplitude fibrillatory waves (0.2mV) with prolonged VF: worse prognosis: confused with asystole

58 VENTRICULAR FIBRILLATION

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