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CHAPTER 104 Broad Q R S Tachycardia - Dilemma in Diagnosis B. Majumdar, A. Kumar, P. Ranjan, S. Mondal Introduction Wide QRS Complex tachycardia (WCT) a common arrhythmia with important therapeutic and prognostic implication and often present a diagnostic challenge. When confronted with a tachycardia having a broad QRS complex, it is important to be able to differentiate between a supraventricular (SVT) and a ventricular tachycardia (VT). Medication given for the treatment of SVT may be harmful to a patient with a ventricular tachycardia (VT). Familiarity with the electrocardiogram(ECG) sign allowing the diagnosis of a VT is therefore essential. ECG not only help to diagnose type of arrhythmia but also its etiology and its site of origin. Both these aspects are important in decision making about the prognostic significance of the WCT and correct treatment. Definition Wide QRS complex tachycardia may be defined as tachycardia irrespective of site of origin having QRS duration of < 120 msec. Ventricular tachycardia is defined as three or more consecutive ventricular beats with a rate of 100 beat/min or more. It is defined nonsustained if it lasts less than 30 seconds and sustained if lasts more than 30 sec or requires therapeutic intervention for termination. It can originate anywhere below the AV node, including the His bundle, bundle branch, fascicles, Purkinje fibers, and ventricular tissue. Supraventricular tachycardia can be defined as any tachycardia using the normal AV conduction system for ventricular excitation, with tachycardia originating in the atria or AV node and requiring the AV node for its maintenance. Etiology Under normal circumstances, activation through the His bundle depolarizes both ventricles simultaneously through the bundle branches and the specialized Purkinje network. This process of depolarization normally takes 80–120 msec. Prolongation of QRS duration occurs in the two under mentioned condition 1. Sequentially rather than simultaneous ventricular activation seen in Bundle branch block Ventricular tachycardia Accessory pathway (WPW synd).

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CHAPTER

104Broad Q R S Tachycardia - Dilemma in DiagnosisB. Majumdar, A. Kumar, P. Ranjan, S. Mondal

Introduction Wide QRS Complex tachycardia (WCT) acommon arrhythmia with important therapeutic and prognostic implication and often present a diagnostic challenge. When confronted with a tachycardia having a broad QRS complex, it is important to be able to differentiate between a supraventricular (SVT) and a ventricular tachycardia (VT). Medication given for the treatment of SVT may be harmful to a patient with a ventricular tachycardia (VT). Familiarity with theelectrocardiogram(ECG)signallowingthediagnosisofaVTisthereforeessential.ECGnot only help to diagnose type of arrhythmia but also its etiology and its site of origin. Both these aspects are important in decision making about the prognostic significance of the WCT andcorrect treatment.

Definition• WideQRScomplextachycardiamaybedefined

as tachycardia irrespective of site of origin having QRS duration of < 120 msec.

• Ventricular tachycardia is defined as threeor more consecutive ventricular beats with a rate of 100 beat/min or more. It is defined nonsustained if it lasts less than 30 seconds and sustained if lasts more than 30 sec or requires

therapeutic intervention for termination. It can originate anywhere below the AV node, including the His bundle, bundle branch, fascicles, Purkinje fibers, and ventricular tissue.

• Supraventricular tachycardia can be definedas any tachycardia using the normal AV conduction system for ventricular excitation, with tachycardia originating in the atria or AV node and requiring the AV node for its maintenance.

EtiologyUnder normal circumstances, activation through the His bundle depolarizes both ventricles simultaneously through the bundle branches and the specialized Purkinje network. This process of depolarization normally takes 80–120 msec. Prolongation of QRS duration occurs in the two under mentioned condition

1. Sequentially rather than simultaneous ventricular activation

seen in

• Bundlebranchblock

• Ventriculartachycardia

• Accessorypathway(WPWsynd).

784 Medicine Update 2008 Vol. 18

2. ConductionabnormalityoverH.P.Mpathway(His- Purkinje – myocardium)

seen in

• Ischemia

• Drug(Procainamide)

• Electrolyteimbalance(Hyperkalemia)

ClassificationThe wide complex tachycardia (WCT) can bedivided in two broad group depending on regularity of the arrhythmia as depicted in Table-1

This classification has one important aspect during dilemma while dealing WCT is that, thediagnostic bolus of adenosine should never be trieduponWCTwithirregularrhythmbecauseifit is given in patient having accessory pathway, the rhythm of SVT may degenerate in ventricular fibrillation that may be fatal.

Approach to PatientTheECGandhemodynamicstatusofthepatientis the prime guide for the management of a patient withWCT.Whentimeavailableandhemodynamicstatus allows, history should be elicited as it gives clue regarding diagnosis as well as etiology hence should not be omitted when confronting wide QRS complex tachycardia.

A. History

Risk Factor: Presence of structural heart disease especially coronary artery disease and previous

myocardial infarction or congestive heart failure strongly suggests for VT.2 In > 98% of patients with previous myocardial infarction, the cause ofWCTisVT,whereasonly7%ofpatientswithSVT have this history.1

Duration: It is some help and when it has been present for more than 3 years, any SVT is more likely3

B. Physical Examination

AV Dissociation: Dissociation between atrial and ventricular activity during tachycardia is a hallmark of VT and the clinical sign of AV dissociation should be looked during physical examination, which are as follows. • Cannonawaves4

• Variablefirstheartsound4

• Changesinsystolicbloodpressure4

Vagal Maneuvers : Carotid sinus massageleading to termination of tachycardia suggests that AV node is a critical link in the tachycardia circuit and favor diagnosis of SVT.

C. Chest Radiograph

Presence of cardiomegaly or evidence of prior cardiovascular surgery strongly favors the diagnosis of VT because it implies underlying structural heart disease.

D. Electrocardiogram

Evaluation of 12-lead & rhythm strip is most importantstepindeterminingetiologyofWCT.The following points should be given utmost importancewhilegoingthroughtheECG

1. AV Dissociation

• Demonstration of atrio-ventricular dissociation during tachycardia is suggestive of VT.

• But AV dissociation is present in only 60 – 75% of patient, while 25% VT patients demonstrate ventriculo–atrial conduction (VA conduction)especially at slow VT rate.5

Table 1Wide QRS tachycardia with regular rhythm

• Ventriculartachycardia

• SupraventricularTachycardiawithBBB

• AntidromicAVre-entryTachycardia

Wide QRS tachycardia with irregular rhythm

Torsades de pointes•

LBBB with AF or AFL with Variable block•

WPW with AF or AFL with variable block•

BBB – Bundle branch block; AF – Atrial Fibrillation; AFL – Atrial Flutter

785Broad Q R S Tachycardia - Dilemma in Diagnosis

• Capturebeatsandfusionbeatsmaybeseen in the presence of AV dissociation which occur when a dissociated p wave totally (capture) or partially (fusion) activates the ventricle in advance of the next VT cycle.

2. QRS Axis

• Asignificant shift in axis during tachycardia is suggestive of VT.

• Mean QRS axis within normal rangefavor SVT.

• Extreme LAD (Lt. Axis deviation) orExtreme RAD or northwest axis seldom seen in conditions other than VT.

• NothelpfulwhenWCTisduetoaccessorypathway

4. QRSConcordance.

• VToriginatingfromapexhassuperioraxis while that of originating from base has inferior axis.

• RBBBshapedWCTwithsuperioraxisandLBBB shapedWCTwith inferioraxis strongly suggest VT.

3. QRS Duration

• QRS duration more that 0.14 sec inRBBBmorphologyWCTandmorethan0.16 sec in LBBB morphology WCTargues for a VT.5

• QRS duration is very wide whenarrhythmia originate from lateral free wall leading to sequential activation of ventricle, while duration is small when it has its origin in or close to intraventricular septum.

• Whenallprecordial leadsshoweithernegative or positive QRS complexes are called negative or positive concordance respectively.

• NegativeconcordanceisdiagnosticofVTarising from antero–apical region.

II

I

I

IIIII II

VT origin infero-apical→ Frontal QRS axis ↑

VT origin antero-apical→ Frontal QRS axis ↓

II

I

III

VT origin for from interventricular septum→ sequential ventricular activation→ wide QRS

400 msec

II

I

IIIVT origin close to interventricular septum→ more stimultaneous ventricularactivation → more narrow QRS

PosteriorPosterior

AnteriorAnterior

V6

V1 V1

V6LV LVRV RV

786 Medicine Update 2008 Vol. 18

• Positive concordance is seen in VToriginating from postero-basal left ventricle, or SVT due to left posterior accessory pathway.

5. QRS Narrowing During Tachycardia

• When during tachycardia the QRS is more narrower than during sinus rhythm a VT should be diagnosed. Because wide QRS during sinus rhythm is due to sequential activation become narrower during tachycardia can only be explained by a ventricular origin close to the intraventricular septum and more simultaneous activation of the two ventricles.

• WheninV6R:Sratio<1orQSpatternis suggestive of VT.

Left bundle branch Block pattern: (predominantly negative in V1)

• Initial positive QRS with positivitymeasuring more than 0.03 seconds favor VT.

• SlurringornotchingofdownslopeofSwave

• When the V6 shows QR or QS issuggestive of VT.

6. QRS Morphology

Right bundle branch Block Pattern: - (predominantly positive in V1)

• Triphasiccomplexorbiphasicwithr<R’ in V1 lead favor SVT.

• AmonophasicorQRpatterninV1leadfavours VT

Lead V 1-2

QR

QRQS RS**

MonophasicR

AND Lead V 6

LBBB - like QRS (predominantly negative in lead V )1

RS interval > 100 msec (onset of R to nadir of S) in any precordial lead.

7. Ventricular Activation Velocity Ratio (Vi/Vt):-

An index of slow conduction at the beginning and at the end of the QRS complex obtained by measuring voltage in millivolt on the ECG tracing the impulse traveledvertically during initial 40 m sec (Vi) and the terminal 40 sec(Vt) of bi or multiphasic QRS complex, in any lead having initial ventricular activation most rapid.

A B

I

II

III

I

II

III

avr

avl

avf

avr

avl

avf

V1

V2

V3

V4

V5

V6

V1

V2

V3

V4

V5

V6

Tachycardia QRS smaller than QRS during sinus rhythm. On the leftsinus rhythm is present with a very wide QRS because of anterolateralmyocardial information and the pronounced delay in left ventricular activation. On the right a VT arising on the right side of the interventricular septum result in moresimultaneous activation of the right and left ventricle than during sinus rhythmand therefore a smaller QRS complex.

400 msec

AND Lead V6 QS

QR Monophasic RA: > 30 ms FAVOURS VTB: NOTCHING, SLURRING FAVOURS VTC: > 70 ms FAVOURS VT

C

B

A

V1 and V2

787Broad Q R S Tachycardia - Dilemma in Diagnosis

• Aratioof>1suggestiveofSVT

• A ratio of < 1 is highly suggestive ofVT

6. Diagnostic CriteriaMost commonly used diagnostic criteria for diagnosing SVT over VT in clinical parlance is Brugada criteria.

It has sensitivity of 99% and specificity of 97%

Yes Step I R S WAVE

No Step II R S INTERVAL Yes

100m sec

No

Step III Evidence of AV dissociation Yes

No

Step IV Morphological criteria of VT Yes No

Brugada criteria for broad QRS Tachycardia.

WIDE QRS TACHYCARDIA

SUPRAVENTRICULAR TACHYCARDIA

V E NT R I C U LAR TACH Y C R D I A

A recently published new algorithm for diagnosing ventricular tachycardia by Verecrie et alusingVi/Vtratio is thatduringWCTdue toSVT, the activation of septum should be invariably rapid and the intraventricular conduction delay causing the wide QRS complex occurs in the mid to terminalpartof theQRS.WhileduringWCTdue to VT, however, an initial slower muscle to muscle spread of activation occurs until the impulse reaches the His-purkinje system, after which the rest of myocardium is more rapidly activated and hence Vi /Vt will be greater than < 1.

Value and limitation of E.C.G. finding in diagnosing Broad QRS tachycardia

• AVdissociationsuggestsVT,butVAconductionmay be present during VT.

• A QRS width of > 160 ms suggests VT, butneed to rule out:

• Pre–existentBBB(especiallyLBBB)

• SVTwithAVconductionoveranAP

• Use of drugs slowing intraventricularconduction (flecainide).

Keep in mind – VT arising close to or in the intraventricular conduction system may have a width of < 140 ms

• Leftaxisdeviation(totheleftof-30suggestsVT, but is not helpful in:

• LBBBshapedQRS

• SVTwithconductionoverarightsidedorposteroseptal AP

• SVTduringuseofclass1Cdrugs

• Right axis deviation (to the right of + 90) suggests VT in LBBB shaped QRS

• Concordant pattern in precordial leads suggests VT, but positive concordance may occur during SVT with AV conduction over a left posterior AP

• R nadir S > 100 ms in one or more precordial leads suggests VT, but may be found in:

• SVT on drugs slowing intraventricularconduction

• SVTwithAVconductionoveranAP

• Pre–existenceBBB(especiallyLBBB)

• QR complexes during VT suggests previousmyocardial infarction as etiology

Wide QRS Tachycardiayes

Step I Av dissociation Present

No

yesStep II

Step III

Step IV

Initial R wave in aVR present

Noyes

QRS morphology unlike RBBB OR FB

No

No

yesVi/Vt Ratio < 1

Supraventricular tachycardia

VENTRICULAR

TACHYCARDIA

788 Medicine Update 2008 Vol. 18

References1. Akhtar M, Shenasa M , Jazayeri M, et al: Wide QRS

Tachycardia, reappraisal of a common clinical problem. Ann Intern Med 1933. 109:905 – 912.

2. Baerman JM; Morady F, Dicar 10 LA, et al: differentiation of Ventricular tachycardia from Supraventricular tachycardia with aberration ; Value of the clinical history. Ann Emerg Med 1987. 16 : 40 – 43.

3. Andrics E, Brugada P, Brugada J, et al: A practical approach to the diagnosis of a tachycardia with a wide QRS complex. In podrid PJ; Cowey PR(eds) : Cardiac Arrhythmias :Mechanism , diagnosis and management . Baltimore , William

& Wilkins 1995:7 PP b 1022 – 1038.

4. Harvey WP, Ronan JAS; Bedside diagnosis of arrhythmias. Prog cardiovasc Dis 1966: 8 : 419 – 45.

5. Wellens HJJ, Bar FWHM, Lie Ki. The value of electrocardiogram in differential diagnosis of tachycardia with widened QRS complex Am J Med 1978 : 64 : 27 – 33

6. Andras Vere ckei, Gabor Durag; Gabors, et al . Application of a new alogorithm in the diagnosis of wide QRS tachycardia Euro Heart 2007 : 28, 589 – 600

7. BrugadaP; BrugadaM et al . A new approach to the differential diagnosis of regular tachycardia with wide QRS complex . Circulation 1991 : 83 : 1649 – 1659.