Definitions
The anatomic basis of atrioventricular reentrant tachycardia (AVRT) is an abnormal connection ( accessory pathway [AP] ) between the atrial and ventricular myocardium. One limb of the reentrant circuit is the atrioventricular (AV) node and the other is the AP. On rare occasions the circuit includes two or more APs.
The term preexcitation refers to earlier activation of the ventricle by a wave front arising in the atrium than would be expected if conduction occurred via the normal atrioventricular conduction pathway.
Wolff-Parkinson-White (WPW) syndrome refers to the combination of preexcitation on an electrocardiogram and episodic tachycardias using the AP ( Fig. 15.1 ).
The AP is located along the mitral or tricuspid annulus, and during sinus rhythm a typical pattern with the following characteristics is present on the electrocardiogram (ECG): (1) short PR interval (≤120 ms), (2) slurred upstroke or downstroke of the QRS complex (“delta wave”), and (3) a widened QRS complex during sinus rhythm. However, WPW patients with a fasciculoventricular pathway have a QRS width 120 ms or less. , Occasionally, preexcitation may not be fully apparent because of fusion of wave fronts progressing through the AP and the normal conduction system ( Figs. 15.2 and 15.3 ). In most cases accessory pathways giving rise to the WPW pattern are seen in structurally normal hearts.
Electrophysiology and classification of accessory pathways
APs are single or multiple strands of myocardial cells that bypass the physiologic conduction system and directly connect atrial and ventricular myocardium. These AV connections are due to incomplete embryologic development of the AV annuli, without complete separation between the atria and ventricles. There are different types of APs. The most common ones connect the atrium and the ventricle along the mitral or tricuspid annulus. Approximately 60% are located along the mitral valve and are referred to as left free wall APs; 25% insert along the septal aspect of the mitral or tricuspid annulus; and approximately 15% insert along the right free wall. Because ventricular muscle is lacking in the proximity of the anterior leaflet of the mitral valve, left-sided APs are usually limited to the region of the mitral annulus at the attachment of the mural (posterior) leaflet. APs can be located in the superoparaseptal area in close proximity to the His bundle and AV node. Accessory pathways exhibit rapid conduction.
Concealed accessory pathways
Approximately 50% of APs conduct in both antegrade and retrograde directions, and the majority of the others conducted only in the retrograde direction are labeled as “concealed” because there is no evidence of preexcitation on the ECG. A small percentage conduct only in the anterograde direction. Concealed APs give rise only to orthodromic AVRT and occasionally have decremental properties. They are not associated with an increased risk of sudden cardiac death. No gender predilection is found, and these pathways tend to become clinically apparent at an earlier age than atrioventricular nodal reentrant tachycardia (AVNRT); however, significant overlap exists. Concealed APs are predominantly localized along the left free wall (65%) and less often at septal (30%) and right free wall locations. ,
Multiple accessory pathways
Multiple APs occur in up to 12% of patients with preexcitation and in up to 50% in patients with Ebstein anomaly. Characteristics suggestive of two or more APs are as follows:
- 1.
Delta wave pattern not typical of any single location.
- 2.
Changes in delta wave during atrial fibrillation or during right atrial versus coronary sinus (CS) pacing.
- 3.
Retrograde fusion during orthodromic AVRT.
- 4.
Changes in retrograde atrial activation sequence during orthodromic AVRT, either spontaneous or during radiofrequency (RF) ablation
Atypical accessory pathways
Atypical APs (previously called Mahaim fibers) are connections between the right atrium or the AV node (AVN) and the right ventricle into or close to the right bundle branch. Pathways with atypical characteristics can be atriofascicular, nodofascicular, or nodoventricular, depending on their proximal and distal insertions. , Left-sided atypical pathways have also been described but are extremely rare. They usually contain accessory nodal tissue, which results in decremental properties, and connect the atrium to the fascicles by crossing the lateral aspect of the tricuspid annulus, but posteroseptal locations can also be found in rare cases. Conduction is usually anterograde only, but concealed nodoventricular and nodofascicular fibers have also been described and may give rise to incessant tachycardias. , The baseline QRS of patients with atypical APs is normal or displays different degrees of manifest preexcitation with left bundle branch block morphology. Programmed or incremental atrial pacing results in manifest preexcitation when there has been sufficient delay in the AH interval. An increase in AV interval plus shortening of the HV interval and QRS widening is observed at shorter pacing cycle lengths. Atypical pathways can participate in antidromic AVRT ( Fig. 15.4 ).
Diagnosis
Patients present with symptoms of paroxysmal tachycardia or with preexcited AF. AVRT is the most common tachycardia associated with the WPW syndrome. WPW predisposes to development of AF, which may or may not be eliminated after ablation of the pathway. , It is more common in patients with WPW syndrome than in the general population and may be the presenting arrhythmia in affected patients.
Antegrade-conducting APs may produce a typical WPW pattern on the ECG or may be latent. Latent pathways, when conducting antegrade, may be revealed by infusion of adenosine, which not only that blocks the AV node but also facilitates AP conduction. A small percentage of APs are dependent on sympathetic activation and become manifest only during infusion of isoprenaline. In the presence of a WPW pattern, localization of the AP may be accomplished from the 12-lead ECG ( Figs. 15.5 and 15.6 ).
Orthodromic AVRT
Orthodromic AVRT refers to a reentrant tachycardia that uses the AV node–His bundle axis as the antegrade limb and the AP as the retrograde limp ( Figs. 15.7 and 15.8 ).
Orthodromic AVRT accounts for more than 90% of AVRTs and 20% to 30% of all sustained SVTs. , The rate usually is 170 to 220 beats per minute. During tachycardia, the QRS is narrow unless there is a functional or underlying bundle branch block. ST segment depression often is present and has been shown to usually not be due to myocardial ischemia. Ipsilateral bundle branch block during AVRT results in an increase in VA time, which can also increase the cycle length of the tachycardia, although no change in rate may also be seen because of a compensatory reduction in AH interval. A contralateral bundle branch block has no effect on the tachycardia, as it is not a part of the tachycardia circuit.
The differential diagnosis of narrow-QRS complex tachycardias is discussed in Chapter 10 . In certain cases of tachycardias with atypical characteristics, multiple pacing techniques are required to reach a diagnosis. Figs. 15.9 to 15.11 present a case of a narrow-QRS tachycardia with prolonged RP intervals that was easily induced by both atrial and ventricular pacing.
The tachycardia was interrupted by ventricular extrastimulation and an A-V response or with single ventricular extrastimuli that were not conducted to the atria, while His-synchronous ventricular extrastimuli failed to reset the tachycardia. Thus the differential diagnosis is between atypical AVNRT and AVRT because of a concealed midseptal accessory pathway. For differential diagnosis, entrainment by ventricular pacing attempted both from the RV apex and RV base was necessary. After entrainment maneuvers as indicated in Figs. 15.10 and 15.11 , an accessory pathway was mapped and ablated at the midseptal area near the His bundle.
Fig. 15.12 presents a rare case of an orthodromic AVRT caused by a concealed nodoventricular pathway and AV dissociation.