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MALIGNANT ARRHYTHMIAS: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD DR.SIVAKUMAR ARDHANARI MD www.anaesthesia.co.in [email protected]
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MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Dec 16, 2015

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Page 1: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

MALIGNANT ARRHYTHMIAS:MALIGNANT ARRHYTHMIAS:ECG IDENTIFICATIONECG IDENTIFICATION

DR.SIVAKUMAR ARDHANARI DR.SIVAKUMAR ARDHANARI MDMD

www.anaesthesia.co.in [email protected]

Page 2: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.
Page 3: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Normal sinus rhythmNormal sinus rhythm

Impulse formation beginning in the Impulse formation beginning in the sinus nodesinus node

At frequencies between 60 to 100 per At frequencies between 60 to 100 per minuteminute

P is always upright in I, II and aVF and P is always upright in I, II and aVF and inverted in aVRinverted in aVR

Though rhythm is regular, minor Though rhythm is regular, minor variation in PP interval exists & variation in PP interval exists & longest and shortest PP differ< 0.16 longest and shortest PP differ< 0.16 except in sinus arrhythmiaexcept in sinus arrhythmia

Page 4: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Normal sinus rhythmNormal sinus rhythm

Every P is followed by a QRS complexEvery P is followed by a QRS complex Every QRS is preceded by a P waveEvery QRS is preceded by a P wave P and its following QRS is separated P and its following QRS is separated

by fairly regular PR intervalby fairly regular PR interval TO BE VERY PRECISE P AND QRS ARE TO BE VERY PRECISE P AND QRS ARE

IN SIMPLE HARMONYIN SIMPLE HARMONY

Page 5: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.
Page 6: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

NORMAL ECGNORMAL ECG

Page 7: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

When the rhythm deviates from the When the rhythm deviates from the above said normalcy it is called above said normalcy it is called ARRHYTHMIAARRHYTHMIA

Broadly it is classified as brady and Broadly it is classified as brady and tachy arrhythmiatachy arrhythmia

Arrhythmogenesis may be due Arrhythmogenesis may be due various causesvarious causes

Page 8: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.
Page 9: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Some arrhythmias are considered Some arrhythmias are considered MALIGNANT MALIGNANT

Because if not properly and Because if not properly and immediately treated, it can be immediately treated, it can be LETHAL to the suffererLETHAL to the sufferer

This is important in understanding This is important in understanding the concept of SUDDEN CARDIAC the concept of SUDDEN CARDIAC DEATHDEATH

Page 10: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.
Page 11: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

SUDDEN CARDIAC DEATHSUDDEN CARDIAC DEATH

Page 12: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Anatomy of the conduction Anatomy of the conduction systemsystem

Page 13: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Anatomy of the conduction Anatomy of the conduction systemsystem

Sinus node- Sinus node- – RCA (55-60%) RCA (55-60%) – left circumflex (40-45%)arteryleft circumflex (40-45%)artery

AV node-AV node-– RCA (85-90%) RCA (85-90%) – left circumflex (10-15%) arteryleft circumflex (10-15%) artery

Page 14: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

ACUTE RVMI+IWMIACUTE RVMI+IWMI

Page 15: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Anatomy of conduction Anatomy of conduction systemsystem

The conduction system is densely The conduction system is densely innervated byinnervated by – Cholinergic fibers- parasympathetic Cholinergic fibers- parasympathetic – Adrenergic fibers- sympatheticAdrenergic fibers- sympathetic

This is important in understanding This is important in understanding – variability of cardiac function with variability of cardiac function with

autonomic influence autonomic influence – effect of parasympathetic stimulation in effect of parasympathetic stimulation in

terminating arrhythmiasterminating arrhythmias

Page 16: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

BRADYARRHYTHMIASBRADYARRHYTHMIAS Sinus nodalSinus nodal

Sinus bradycardiaSinus bradycardia Sinus arrhythmiaSinus arrhythmia Sinus pause/arrestSinus pause/arrest Sinoatrial exit blockSinoatrial exit block Sick sinus syndromeSick sinus syndrome

AV nodal blocksAV nodal blocks First degreeFirst degree Second degree(MOBITZ type 1 and 2)Second degree(MOBITZ type 1 and 2) Complete heart blockComplete heart block

Page 17: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

SINUS ARRESTSINUS ARREST

Page 18: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

SICK SINUS SYNDROMESICK SINUS SYNDROME

Page 19: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

ATRIO VENTRICULAR BLOCKATRIO VENTRICULAR BLOCK I degree I degree -conduction time prolonged: all impulses -conduction time prolonged: all impulses

are conductedare conducted

II degreeII degree -2 forms -2 forms

o Mobitz type I (WENCKEBACH)-Mobitz type I (WENCKEBACH)- progressive lengthening of progressive lengthening of conduction time until an impulse is failed to be conductedconduction time until an impulse is failed to be conducted

o Mobitz type II-Mobitz type II- occasional or repetitive sudden block in occasional or repetitive sudden block in conduction without prior measurable lengthening of conduction without prior measurable lengthening of conduction timeconduction time

Complete or III degreeComplete or III degree -no impulses are conducted -no impulses are conducted

Page 20: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

FIRST DEGREE AV BLOCKFIRST DEGREE AV BLOCK

Page 21: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

FIRST DEGREE HBFIRST DEGREE HB

Page 22: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

IWMI+FIRST AV BLOCKIWMI+FIRST AV BLOCK

Page 23: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

2:1 AV BLOCK2:1 AV BLOCK

Page 24: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

COMPLETE AV BLOCKCOMPLETE AV BLOCK

Occurs when no atrial activity is Occurs when no atrial activity is conducted to the ventriclesconducted to the ventricles

So atria and ventricles are controlled So atria and ventricles are controlled by independent pacemakersby independent pacemakers

One type of complete AV dissociationOne type of complete AV dissociation Ventricular focus is usually just below Ventricular focus is usually just below

the site of blockthe site of block If focus near HIS bundle the rhythm If focus near HIS bundle the rhythm

is more stableis more stable

Page 25: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

CHB can occur at various levelsCHB can occur at various levels– AV Node-usually congenital-40-60 AV Node-usually congenital-40-60

bpmbpm– Bundle of HISBundle of HIS– Purkinje sys-usually acquired-Purkinje sys-usually acquired-

Page 26: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

COMP HEART BLOCKCOMP HEART BLOCK

Page 27: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

COMP HBCOMP HB

Page 28: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

CHBCHB

Page 29: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

CHBCHB

Page 30: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

IWMI+CHBIWMI+CHB

Page 31: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

APPROACH TO APPROACH TO TACHYCARDIATACHYCARDIA

Page 32: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

ATRIAL FLUTTERATRIAL FLUTTER

F waves: rapid regular undulationsF waves: rapid regular undulations

SAW TOOTH APPEARANCESAW TOOTH APPEARANCE Atrial rate:250-350 bpmAtrial rate:250-350 bpm Rate & regularity of ventricles: variable Rate & regularity of ventricles: variable

and depend on AV conduction and depend on AV conduction sequencesequence

QRS may be normal or abnormal as a QRS may be normal or abnormal as a result of preexisting intraventricular result of preexisting intraventricular conduction defect or aberrancyconduction defect or aberrancy

Page 33: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

ATRIAL FLUTTERATRIAL FLUTTER

Page 34: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

ATRIAL FLUTTERATRIAL FLUTTER

Page 35: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

ATRIAL FLUTTERATRIAL FLUTTER

Page 36: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.
Page 37: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

SVT VS VTSVT VS VT

Page 38: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Differentiating a VT from SVT can be Differentiating a VT from SVT can be difficult at timesdifficult at times

Golden rule in ER Golden rule in ER

ANY WIDE QRS TACHYCARDIA IS ANY WIDE QRS TACHYCARDIA IS VENTRICULAR TACHYCARDIA VENTRICULAR TACHYCARDIA UNTIL PROVED OTHERWISE UNTIL PROVED OTHERWISE ESP`LY WHEN THE PATIENT HAS ESP`LY WHEN THE PATIENT HAS A STRUCTURAL HEART DISEASEA STRUCTURAL HEART DISEASE

Page 39: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Diagnosis of VTDiagnosis of VT

Arises distal to the bifurcation of the Arises distal to the bifurcation of the HIS bundleHIS bundle

Diagnosis is by the occurrence of a Diagnosis is by the occurrence of a series of 3 or more consecutive, series of 3 or more consecutive, abnormally shaped PVCs whose abnormally shaped PVCs whose duration exceeds 120 ms, with ST-T duration exceeds 120 ms, with ST-T vector pointing opposite the major vector pointing opposite the major QRS deflectionQRS deflection

Page 40: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

VENTRICULAR ECTOPICSVENTRICULAR ECTOPICS

Page 41: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

RR can be exceedingly regular or can RR can be exceedingly regular or can varyvary

Atrial activity can be independent of Atrial activity can be independent of ventricular activity or can be ventricular activity or can be depolarized retrograde (VA depolarized retrograde (VA association)association)

Page 42: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Fusion beats and capture beats provide the Fusion beats and capture beats provide the maximum support for the diagnosis of VTmaximum support for the diagnosis of VT

FUSION BEATS-activation of ventricles from FUSION BEATS-activation of ventricles from 2 foci2 foci

CAPTURE BEATS- capture of the ventricle CAPTURE BEATS- capture of the ventricle by supraventricular rhythmwith normal by supraventricular rhythmwith normal confguration of the captured QRS at intrvl confguration of the captured QRS at intrvl shorter than tachycardia in question- shorter than tachycardia in question- indicates origin of impulse is indicates origin of impulse is supraventricularsupraventricular

Page 43: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

FUSION AND CAPTURE FUSION AND CAPTURE BEATSBEATS

Page 44: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

QRS contours can be QRS contours can be – Unchanging (MONOMORPHIC)Unchanging (MONOMORPHIC)– Vary randomly (POLY OR PLEOMORPHIC)Vary randomly (POLY OR PLEOMORPHIC)– Vary repetitively (TORSADES DE Vary repetitively (TORSADES DE

PONTES)PONTES)– Vary in alternative cplxs Vary in alternative cplxs

(BIDIRECTIONAL)(BIDIRECTIONAL)

Page 45: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

MONOMORPHIC VTMONOMORPHIC VT

Page 46: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

POLYMORPHIC VTPOLYMORPHIC VT

Page 47: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

TORSADES DE POINTESTORSADES DE POINTES

Page 48: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

TYPES OF VTTYPES OF VT

VT can beVT can be SUSTAINED- lasting longer than 30 SUSTAINED- lasting longer than 30

seconds or requiring termination due seconds or requiring termination due to hemodynamic collapseto hemodynamic collapse

NON SUSTAINED- stops NON SUSTAINED- stops spontaneously within 30 secondsspontaneously within 30 seconds

Page 49: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

NON-SUSTAINED VTNON-SUSTAINED VT

Page 50: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

SUSTAINED VTSUSTAINED VT

Page 51: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

HYPER ACUTE EXT ALMIHYPER ACUTE EXT ALMI

Page 52: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

DIGITALIS EFFECTDIGITALIS EFFECT

Page 53: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

PROLONGED QT(U) PROLONGED QT(U) INTERVALINTERVAL

Page 54: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

Ventricular flutter & Ventricular flutter & fibrillationfibrillation

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

Page 55: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

VENTRICULAR FLUTTERVENTRICULAR FLUTTER

Manifested as sine wave in Manifested as sine wave in appearanceappearance

Regular large oscillations occurring Regular large oscillations occurring at a rate of 150-300(usually 200)/minat a rate of 150-300(usually 200)/min

Page 56: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

VENTRICULAR FLUTTERVENTRICULAR FLUTTER

Page 57: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

VENTRICULAR FIBRILLATIONVENTRICULAR FIBRILLATION

Irregular undulations of varying Irregular undulations of varying contour & amplitudecontour & amplitude

Distinct QRS, ST or T are absentDistinct QRS, ST or T are absent Fine amplitude fibrillatory waves Fine amplitude fibrillatory waves

(0.2mV) with prolonged VF: worse (0.2mV) with prolonged VF: worse prognosis: confused with asystoleprognosis: confused with asystole

Page 58: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.

VENTRICULAR FIBRILLATIONVENTRICULAR FIBRILLATION

Page 59: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.
Page 60: MALIGNANT ARRHYTHMIAS: ECG IDENTIFICATION DR.SIVAKUMAR ARDHANARI MD @gmail.com.