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Europace Advance Access originally published online on September 5, 2008
Europace 2008 10(10):1205-1211; doi:10.1093/europace/eun249
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2008. For permissions please email: journals.permissions@oxfordjournals.org


CLINICAL RESEARCH

Entrainment from the para-Hisian region for differentiating atrioventricular node reentrant tachycardia from orthodromic atrioventricular reentrant tachycardia

Jordi Pérez-Rodon1, Victor Bazan1,*, Jordi Bruguera-Cortada1, Sergi Mojal-García2, Josep M. Manresa-Domínguez2 and Julio Martí-Almor1

1 Electrophysiology Unit, Cardiology Department, Hospital del Mar, IMAS, 25 Passeig Marítim, 08003 Barcelona, Spain; 2 Parc de Recerca Biomèdica, 88 Doctor Aiguader, 08003 Barcelona, Spain

Manuscript submitted 24 May 2008. Accepted after revision 14 August 2008.

* Corresponding author. Tel: +34 93248 34 89; fax: +34 93 248 34 89. E-mail address: vbazan{at}imas.imim.es


    Abstract
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Conclusions
 References
 
Aims: The difference between the stimulus-atrial and ventriculo-atrial intervals (SA–VA) and between the post-pacing interval and the tachycardia cycle length (PPI–TCL) during entrainment from the right ventricular apex distinguishes atrioventricular node reentrant (AVNRT) from orthodromic atrioventricular reentrant tachycardia (AVRT). We hypothesized that these features still apply when entrainment is performed from the para-Hisian region.

Methods and results: Forty-seven supraventricular tachycardias (34 AVNRT/13 AVRT) were included. The SA–VA and PPI–TCL were obtained in all patients by using two right-sided diagnostic catheters. In 24 of them, these measurements were also performed upon His-bundle capture during entrainment. A paced QRS widening of ≥40 ms during entrainment, when compared with the tachycardia QRS width, identified absence of His-bundle capture, P < 0.001. A SA–VA >75 ms distinguished AVNRT from AVRT, P < 0.001 (sensitivity/specificity 97%/100%). A PPI–TCL >100 ms was diagnostic of AVNRT, P < 0.001 (sensitivity/specificity 97%/92%). Upon His-bundle capture, the SA–VA and PPI–TCL shortened in AVNRT (121 ± 23 to 66 ± 24 ms; 139 ± 30 to 85 ± 31 ms, respectively, P < 0.001) and no longer differentiated AVNRT from AVRT.

Conclusion: Para-Hisian entrainment without His-bundle capture distinguishes AVNRT from AVRT with the advantage of using only two diagnostic catheters.

Key Words: Entrainment, His bundle, Atrioventricular node reentrant tachycardia, Orthodromic atrioventricular reentrant tachycardia, Accessory pathway


    Introduction
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Conclusions
 References
 
Pacing from the right ventricular apex (RV) is an essential electrophysiological maneuver to differentiate atrioventricular node reentrant (AVNRT) from orthodromic atrioventricular reentrant tachycardia (AVRT).1Go–6Go Entrainment from the RV apex establishes the relative conduction time from the pacing site to the reentrant circuit, longer in AVNRT than in AVRT. As a result, a difference between the stimulus-atrial and the ventriculo-atrial intervals (SA–VA) of >85 ms, and between the post-pacing interval and the tachycardia cycle length (PPI–TCL) of >110–115 ms favours AVNRT as the tachycardia mechanism.3Go–4Go

The endocardial activation of the anteroseptal basal RV (para-Hisian region) starts 20–25 ms after the activation of the RV apex, in the absence of an accessory pathway (AP) with anterograde conduction capacities.7Go Inversely, during entrainment from the para-Hisian region, the pacing site, although anatomically close, is electrically away from the tachycardia circuit in AVNRT patients, since ventricular activation travels towards the RV apex to engage the Purkinje network before reaching the AV node retrogradely. This principle may enhance the distinction between AVNRT and AVRT when entrainment is performed from the para-Hisian region. During entrainment or resetting from the His-bundle area, a >40 ms increase of the SA interval ({Delta}SA) upon loss of His-bundle capture favours AVNRT as the tachycardia mechanism.8Go Noteworthy, varying the energy output during pacing for the achievement of loss of His-bundle capture may result in several degrees of local ventricular capture, His-bundle capture, and ‘pure’ His capture.9Go Therefore, a precise identification of RV and RV plus His-bundle capture during para-Hisian entrainment appears obligatory, and is still lacking.

We hypothesized that established criteria differentiating AVNRT from AVRT (i.e. SA–VA and PPI-TCL) still apply when entrainment is performed from the para-Hisian region, with the advantage of using only two right-sided diagnostic catheters. We further aimed to determine the role of His-bundle capture during tachycardia entrainment as a critical factor for these electrophysiological features to have value.


    Methods
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Conclusions
 References
 
Patient population
Fifty-five consecutive patients (30 female, mean age 49 ± 17 years) referred for electrophysiological study (EPS) and ablation of documented supraventricular tachycardia (SVT) or Preexcitation Syndrome were considered for inclusion. All patients gave written informed consent in accordance to our institutional guidelines. All but one had a single SVT mechanism, the remaining presenting with both AVRT and typical AVNRT. Patients in whom SVT could not be induced during the EPS or with atrial tachycardia were excluded, as well as those SVT that could not be entrained from the para-Hisian region.

Study protocol
The EPS was performed in the fasting state under conscious sedation. Two 6-French quadripolar catheters (interelectrode spacing 5 mm, C.R. Bard Inc., Murray Hill, NJ, USA) were inserted into the right femoral vein and advanced into the high right atrium (HRA) and the His bundle/proximal right bundle branch (HB–RB) area. Careful attention was given to minimize the atrial signal in the HB–RB catheter in order to ensure that the atrium was not captured during pacing, maintaining a HV interval of >30 ms in the absence of QRS aberrancy.1Go The surface ECG leads and bipolar intracardiac electrograms (filtered between 30 and 500 Hz) were recorded in the Lab Pro (C.R. Bard Inc., NJ, USA) system and analysed offline for the study analysis. Electronic calipers allowing 1 ms resolution were used at screen velocity of 100 mm/s for all measurements. Measurements were performed by two non-independent observers, and included in the data base after agreement between them. In case of disagreement, a third independent observer was used. The SVT mechanism was confirmed by established electrophysiological criteria and by elimination of the tachycardia after ablation plus inability to reinduce SVT with programmed stimulation within an observation period of 30 min.1Go–3Go,10Go During this period, ventricular stimulation and/or adenosine infusion were performed in order to rule out the presence of remaining retrograde pathways suitable of ablative therapy. Additional diagnostic catheters (essentially a coronary sinus catheter) were placed if considered necessary for guiding the ablation procedure, but not to elucidate the SVT mechanism.

The EPS was performed in a stepwise fashion. After para-Hisian pacing was performed, SVT induction was attempted under atrial programmed stimulation. Para-Hisian entrainment was then performed. The identification of two degrees of QRS widening were attempted during para-Hisian entrainment by varying the energy output, similar to para-Hisian pacing.

Para-Hisian pacing and entrainment
Para-Hisian pacing (sinus rhythm)
In the first 15 patients, the QRS width during para-Hisian pacing was compared with the tachycardia QRS width (considered the reference QRS complex), in order to quantify the QRS widening associated to the loss of HB–RB capture.9Go This would allow us to establish the degree of QRS widening during RV pacing and RV plus HB–RB pacing, thus establishing a cut-off value above which the HB–RB might not be captured. This cut-off value would permit us to group as presumable RV or RV/His-bundle capture the measurements performed during SVT entrainment subsequently. The QRS width in sinus rhythm was not used as a reference because of the presence of preexcitation in some patients.

Para-Hisian entrainment
Entrainment was attempted with and without HB–RB capture by pacing at 10–30 ms shorter than the TCL and was confirmed when the atrial cycle length accelerated to the pacing cycle length maintaining the same atrial sequence between the His and the HRA catheters, the tachycardia ongoing after pacing was discontinued.3Go The following intervals were measured: (i) the TCL and the VA (between the onset of the QRS and the HRA electrogram); (ii) the A–A and the atrial sequence between the HB–RB and HRA catheters during overdrive pacing (in order to ensure para-Hisian entrainment); (iii) the SA (from the last stimulus to last entrained atrial depolarization in the HRA) and the PPI (from the last stimulus to the first RV electrogram in the first return beat); and (iv) the QRS width during tachycardia (QRStach) and in the last entrained beat during presumable RV (QRSentr RV) or RV/HB–RB capture (QRSentr RV/HB–RB).

Statistical analysis
A test of normality was performed if considered necessary. Continuous variables (expressed as mean±SD) were analysed using the Student t-test for independent or repeated measures as appropriate. Categorical variables were compared using {chi}2 or Fisher’s exact test as appropriate. A P-value of <0.05 was considered statistically significant.


    Results
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Conclusions
 References
 
Nine of the 55 patients were excluded from the analysis because entrainment could not be performed for the following reasons: the tachycardia was not sustained (four patients), was repeatedly interrupted by ventricular pacing (four patients) or was haemodynamically not tolerated (one patient). As a result, 46 patients and 47 SVTs were included in the study analysis. Thirty-four patients presented with the slow–fast typical form of AVNRT and 13 with AVRT, 10 of which using a left free wall AP (LFWAP), 1 right posteroseptal, 1 left posteroseptal, and 1 para-Hisian. Five out of the 13 AVRT were using a concealed AP, and the remaining 8 presented with an AP with anterograde conduction properties. Only three patients had structural heart disease, consisting of moderate mitral regurgitation (one patient), ischaemic (one patient), and non-ischaemic (one patient) cardiomyopathy. The ablation was successful in all cases except one AVNRT patient, in whom the tachycardia was still inducible under isoproterenol infusion after ablation, but with no clinical recurrences. During a mean follow-up period of 8 ± 3 months no tachycardia recurrences were documented among our patient population.

Para-Hisian pacing (sinus rhythm)
Results are presented in Table 1. The QRS width during tachycardia was 89 ± 12 ms (range 78–120 ms), 142 ± 12 ms during RV pacing (range 124–166 ms), and 116 ± 12 ms during RV/HB–RB pacing (range 96–148 ms). When compared with the QRS width in tachycardia, the QRS was significantly longer upon both RV capture and RV/HB–RB capture, P < 0.001. The QRS widening was significantly greater during RV capture as opposed to RV/HB–RB capture, P < 0.001. Of note, a cut-off value of ≥40 ms for the QRS widening (when compared with the tachycardia QRS) reached highest discriminatory power to differentiate between RV and RV/HB–RB capture during para-Hisian pacing, P < 0.001, with sensitivity of 93%, specificity of 94%, positive predictive value of 100%, and negative predictive value of 94% (Figure 1).


Figure 1
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Figure 1 QRS widening during para-Hisian pacing and entrainment. The 12-lead ECG is used to compare the QRS width during sinus rhythm (A) and supraventricular tachycardia (B), with the QRS width during para-Hisian pacing (C) and entrainment with (D) and without (E) His bundle capture. A ≥40 ms of QRS widening is associated to the loss of His-bundle capture during para-Hisian pacing and entrainment.

 


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Table 1 Para-Hisian pacing to identify the loss of His-bundle capture

 
Para-Hisian entrainment
Patients with AVNRT presented with a shorter VA than during AVRT (46 ± 24 vs. 136 ± 49 ms, respectively, P < 0.001). No significant differences in the SVT cycle length were observed (350 ± 74 vs. 327 ± 73 ms, P = 0.3).

QRS width during entrainment
The QRSentr RV was significantly longer than the QRSentr RV/HB–RB: 147 ± 19 ms (range 120–202 ms) vs. 117 ± 21 ms (range 74–160 ms), respectively, P < 0.001. Similarly, the {Delta}QRSentr RV (QRSentr RV–QRStach) was longer than the {Delta}QRSentr RV/HB–RB (QRSentr RV/HB–RB–QRStach): 60 ± 13 ms (range 40–98 ms) vs. 30 ± 13 ms (range 2–58 ms), respectively, P < 0.001. All patients had a {Delta}QRSentr RV of ≥40 ms. All but two patients had a {Delta}QRSentr RV/HB–RB of ≤40 ms. These two cases were included as RV/HB–RB entrainment because an increase in the {Delta}QRSentr-tach was observed from 58 to 76 ms and 56 to 98 ms, respectively, during entrainment at lower energy output. As a result, the proposed cut-off value of ≥40 ms indeed identified absence of HB–RB capture in the overall analysis, P < 0.001, with sensitivity of 100%, specificity of 87%, positive predictive value of 89%, and negative predictive value of 100%.

Entrainment without His-bundle capture
Entrainment without HB–RB capture (presumable RV capture) was performed in all patients (Table 2). The SA–VA and the PPI–TCL values were significantly longer in AVNRT patients as opposed to AVRT: 121 ± 23 vs. 49 ± 19 ms and 139 ± 30 vs. 75 ± 25 ms, respectively, P < 0.001 (Figures 2 and 3). All but one patient with AVNRT and none with AVRT presented with an SA–VA difference of >75 ms. All but one patient with AVNRT and none except one with AVRT presented with a PPI–TCL difference of >100 ms. Thus, a cut-off value of >75 ms for the SA–VA and >100 ms for the PPI–TCL distinguished AVNRT from AVRT, P < 0.001, with a sensitivity of 97 and 97%, specificity of 100 and 92%, positive predictive value of 100 and 97%, and negative predictive value of 93 and 92%, respectively (Figure 4). When analysed separately, significantly shorter SA–VA and PPI–TCL were observed during AVRT using a septal AP (only three cases) when compared with AVNRT (31 ± 27 vs. 121 ± 23 ms, P < 0.001; 49 ± 36 vs. 139 ± 30 ms, P < 0.001, respectively) with no overlap between patients.


Figure 2
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Figure 2 Entrainment of orthodromic atrioventricular tachycardia from the para-Hisian region. Entrainment without (A) and with (B) His-bundle capture during AVRT is represented. The acceleration of the atrial cycle length (A–A) to the pacing cycle length (S1) and resuming the tachycardia after pacing confirms entrainment has been accomplished. The stimulus-atrial (SA) interval is measured from the last pacing stimulus to the last entrained high right atrial (HRA) electrogram. The post-pacing interval (PPI) is measured from the last pacing stimulus to the return cycle RV electrogram. RV capture (A): SA–VA = 250–180 ms = 70 (<75) ms; PPI–TCL = 410–320=90 (<100) ms. RV/HB–RB capture (B): SA–VA = 210–180 ms = 30 ms; PPI–TCL = 390–320 ms = 70 ms. QRS measurements: {Delta}QRSentr RV (QRSentr RV–QRS tach) = 145–80 = 65 (>40) ms and {Delta}QRSentr RV/HB–RB (QRSentr RV/HB–RB–QRStach): 115–80 = 35 (<40) ms. HRAd, high right atrium distal; HRAp, high right atrium proximal; HBd, His-bundle distal; HBp, His-bundle proximal; TCL, tachycardia cycle length; VA, ventriculo-atrial interval. {Delta}QRSentr RV = QRS entr RV–QRS tach = QRS width during entrainment without HB–RB capture minus QRS width in tachycardia. {Delta}QRSentr RV/HB–RB = QRSentr RV/HB–RB–QRStach = QRS width during entrainment with HB–RB capture minus QRS width in tachycardia.

 


Figure 3
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Figure 3 Entrainment of atrioventricular node reentrant tachycardia from the para-Hisian region. Tachycardia entrainment without (A) and with (B) His-bundle capture is represented. The ventriculo-atrial (VA) interval and tachycardia cycle length (TCL) are measured immediately before entrainment. The stimulus-atrial (SA) interval is measured from the last pacing stimulus to the last entrained high right atrium (HRA) electrogram. The post-pacing interval (PPI) is measured from the last pacing stimulus to the return cycle RV electrogram. The SA–VA and PPI–TCL are measured upon RV or RV/HB–RB capture. RV capture (A): SA–VA = 170–40 ms = 130 ms (>75 ms); PPI–TCL = 540–350 ms = 190 ms (>100 ms). RV/HB–RB capture (B): SA–VA = 105–40 ms = 65 ms; PPI–TCL = 400–330 ms = 70 ms. QRS measurements: {Delta}QRS entr RV = QRSentr RV–QRStach = 135–80=55 (>40) ms and {Delta}QRSentr RV/HB–RB = QRSentr RV/HB–RB–QRStach = 105–80 = 25 (<40) ms. HRAd, high right atrium distal; HRAp, high right atrium proximal; HBd, His-bundle distal; HBp, His-bundle proximal. {Delta}QRS entr RV = QRS entr RV–QRS tach = QRS width during entrainment without His-bundle capture minus QRS width in tachycardia. {Delta}QRS entr RV/HB–RB = QRS entr RV/HB–RB–QRS tach = QRS width during entrainment with His-bundle capture minus QRS width in tachycardia.

 


Figure 4
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Figure 4 The SA–VA and PPI–TCL cut-off values to distinguish between AVNRT and AVRT. The individual values and mean values±SD of the stimulus-atrial–ventriculoatrial (SA–VA) and post-pacing interval–tachycardia cycle length (PPI–TCL) are represented. The line drawn at 75 ms for the SA–VA and 100 ms for the PPI–TCL represents the discriminatory value distinguishing AVNRT from AVRT patients, P < 0.001.

 


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Table 2 Tachycardia entrainment from the para-Hisian region without His-bundle capture

 
Entrainment with His-bundle capture
Entrainment with His-bundle capture was performed in 24 patients (Table 3). The SA and PPI significantly shortened in AVNRT patients upon RV/HB–RB capture, when compared with RV capture: 114 ± 31 vs. 165 ± 35 ms, P < 0.001; and 428 ± 81 vs. 493 ± 92 ms, P = 0.012, respectively. As a result, the SA–VA and PPI–TCL values shortened: 66 ± 24 vs. 121 ± 23 ms; and 85 ± 31 vs. 139 ± 30 ms, respectively, P < 0.001. As for AVRT patients, the SA–VA and PPI–TCL did not significantly shorten upon His-bundle capture: 35 ± 22 vs. 49 ± 19 ms, P = 0.204; and 55 ± 32 vs. 75 ± 25 ms, P = 0.172, respectively. Although the SA–VA value was still longer in AVNRT as opposed to AVRT patients (66 ± 24 vs. 35 ± 22 ms, P = 0.016), the important overlap between the two groups precluded for the definition of a discriminatory cut-off value confirming AVNRT as the tachycardia mechanism. Similarly, the PPI–TCL value no longer distinguished AVNRT from AVRT upon His-bundle capture during tachycardia entrainment: 85 ± 31 vs. 55 ± 32 ms, P = 0.074.


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Table 3 Tachycardia entrainment from the para-Hisian region with His-bundle capture

 

    Discussion
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Conclusions
 References
 
Major findings
Our study demonstrates that para-Hisian entrainment without His-bundle capture distinguishes AVNRT from AVRT. A SA–VA difference of >75 ms and PPI–TCL of >100 ms mostly identify AVNRT as the tachycardia mechanism, P < 0.001. This study first quantifies the degree of QRS widening when compared with the tachycardia QRS to determine the absence of His-bundle capture during para-Hisian entrainment ({Delta}QRSentr RV–tach of ≥40 ms). Importantly, these electrophysiological features do not apply when the His bundle is captured ({Delta}QRS entr–tach<40 ms), and thus a precise identification of the absence of HB–RB capture appears compelling. At high-energy output (His-bundle capture), retrograde atrial activation proceeds directly over the AV node in AVNRT patients, avoiding the necessity of engaging the Purkinje network distally in the RV apex before reaching the AV junction. As a result, the SA–VA and PPI–TCL intervals shorten during AVNRT and no longer distinguish AVNRT from AVRT.

These maneuvers were performed by using only two right-sided diagnostic catheters with its subsequent cost-effectiveness and clinical benefits.11Go However, it is suggested that additional diagnostic catheters should be positioned if considered necessary to confirm the SVT mechanism, especially when several retrograde pathways are suspected, and for guiding the ablation procedure.

Previous studies
Reddy et al.8Go described the para-Hisian entrainment as a novel maneuver to differentiate AVNRT from AVRT. Unlike para-Hisian pacing (sinus rhythm), para-Hisian entrainment confirms either the AV node or an AP as the retrograde limb of the tachycardia circuit.10Go In this study, a >40 ms increase in the SA interval ({Delta}SA) upon the loss of HB–RB capture was associated to AVNRT. Our study contributes to precisely identify the loss of His-bundle capture during para-Hisian entrainment on the basis of the paced QRS widening, and additionally includes the SA–VA and PPI–TCL values as useful features to differentiate AVNRT from AVRT from the para-Hisian region.

The obtained cut-off values for the SA–VA and the PPI–TCL favouring AVNRT in the present study are lower than those obtained during entrainment from the RV apex.3Go,4Go The inclusion of patients with atypical AVNRT (fast–slow), with decremental retrograde conduction properties, could have contributed to the longer mean SA–VA and PPI–TCL values obtained in AVNRT patients, and the higher cut-off values for the SA–VA and PPI–TCL, when compared with our study.3Go Of note, the para-Hisian region is electrically further away than the RV apex from the AVNRT circuit, and closer to the atrio-ventricular annulae, where APs are found, including LFWAP, in which fast conduction through the interventricular septum may be responsible for the shorter SA and PPI intervals obtained.7Go This also may have played a role in the lower cut-off values for the SA–VA and PPI–TCL observed and also in the almost absence of overlap in SA–VA values between AVNRT and AVRT using a LFWAP in comparison with other studies in which entrainment or resetting is performed from the RV apex.4Go,5Go

Study limitations
In this study, a limited number of AVRT, especially those using a septal AP, were included. However, this fact did not preclude for the identification of SA–VA and PPI–TCL highly specific cut-off values distinguishing AVRT from AVNRT. Although the number of AVRT patients in whom entrainment was performed with HB–RB capture is limited, we believe retrograde conduction over an AP should not be significantly affected by whether the His bundle is captured or not during entrainment, and thus the inclusion of additional AVRT patients with HB–RB entrainment should not modify our results.7Go,10Go Our AVRT population is mainly representative of patients with non-septal APs, and the validation of the SA–VA and PPI–TCL cut-off values for patients with septal APs, although statistically enough in our analysis may need further investigation.

The analysis of the QRS widening to determine absence of His-bundle capture during para-Hisian pacing was not performed in a separated cohort of patients and may appear statistically redundant. Nevertheless, in the overall analysis the obtained cut-off value was confirmed as valuable for identifying absence of HB–RB capture equally with a high discriminatory power.

The measurement of the QRS widening during para-Hisian pacing and entrainment to identify absence of His-bundle capture may be limited by the presence of overlap among patients. As a result, an absolute value of the QRS width during RV or RV/HB–RB pacing cannot be determined by this study. Regardless, we believe the proposed cut-off value of ≥40 ms related to the tachycardia QRS width is a reasonable reference to distinguish the absence of His-bundle capture during para-Hisian pacing/entrainment.

The QRS aberrancy during tachycardia may limit the assessment of RV vs. RV/HB–RB capture during para-Hisian entrainment. Among our population, five patients presented with transitory bundle branch block during SVT, but measurements could be performed without QRS aberrancy in all patients.

Measurements were performed by two non-independent observers, and therefore interobserver variability was not analysed in this study.

The assessment of tachycardia entrainment by using two right-sided diagnostic catheters may have limitations. The EPS included the investigation of additional retrograde pathways after ablation, and the favourable outcome of ablative therapy observed in our population appears to validate the SVT differential diagnosis performed during our study protocol.

Our criteria have not been validated in patients with AVRT using APs with decremental properties, neither in patients with atypical AVNRT. Whether the described electrophysiological features apply to these patients remains unclear.


    Conclusions
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Conclusions
 References
 
Para-Hisian entrainment without His-bundle capture distinguishes AVNRT from AVRT. An SA–VA of >75 ms and PPI–TCL of >100 ms is highly specific of AVNRT. The absence of His-bundle capture during entrainment is defined by a ≥40 ms increase in the QRS width, when compared with the tachycardia QRS. This maneuver can be performed with the use of only two right-sided diagnostic catheters.

Conflict of interest: none declared.


    References
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Conclusions
 References
 
[1] Josephson ME. Clinical Cardiac Electrophysiology: Techniques and Interpretations. (2002) 3rd ed. Philadelphia: Lippincott Williams & Wilkins. 168–271.

[2] Knight BP, Ebinger M, Oral H, Kim MH, Sticherling C, Pelosi F, et al. Diagnostic value of tachycardia features and pacing maneuvers during paroxysmal supraventricular tachycardia. J Am Coll Cardiol (2000) 36:574–82.[Abstract/Free Full Text]

[3] Michaud GF, Tada H, Chough S, Baker R, Wasmer K, Sticherling C, et al. Differentiation of atypical atrioventricular node re-entrant tachycardia from orthodromic reciprocating tachycardia using a septal accessory pathway by the response to ventricular pacing. J Am Coll Cardiol (2001) 38:1163–7.[Abstract/Free Full Text]

[4] González-Torrecilla E, Arenal A, Atienza F, Osca J, García-Fernández J, Puchol A, et al. First postpacing interval after tachycardia entrainment with correction for atrioventricular node delay: a simple maneuver for differential diagnosis of atrioventricular nodal reentrant tachycardias versus orthodromic reciprocating tachycardias. Heart Rhythm (2006) 3:674–9.[CrossRef][Web of Science][Medline]

[5] Crozier I, Wafa S, Ward D, Camm J. Diagnostic value of comparison of ventriculoatrial interval during junctional tachycardia and right ventricular apical pacing. Pacing Clin Electrophysiol (1989) 12:942–53.[CrossRef][Medline]

[6] Ormaetxe JM, Almendral J, Arenal A, Martínez-Alday JD, Pastor A, Villacastín JP, et al. Ventricular fusion during resetting and entrainment of orthodromic supraventricular tachycardia involving septal accessory pathways. Implications for the differential diagnosis with atrioventricular nodal reentry. Circulation (1993) 88:2623–31.[Abstract/Free Full Text]

[7] Durrer D, van Dam RT, Freud GE, Janse MJ, Meijler FL, Arzbaecher RC. Total excitation of the isolated human heart. Circulation (1970) 41:899–912.[Abstract/Free Full Text]

[8] Reddy VY, Jongnarangsin K, Albert CM, Sabbour H, Keane D, Mela T, et al. Para-Hisian entrainment: a novel pacing maneuver to differentiate orthodromic atrioventricular reentrant tachycardia from atrioventricular nodal reentrant tachycardia. J Cardiovasc Electrophysiol (2003) 14:1321–8.[CrossRef][Web of Science][Medline]

[9] Takatsuki S, Mitamura H, Tanimoto K, Fukuda Y, Ieda M, Miyoshi S, et al. Clinical implications of ‘pure’ hisian pacing in addition to para-Hisian pacing for the diagnosis of supraventricular tachycardia. Heart Rhythm (2006) 3:1412–8.[CrossRef][Web of Science][Medline]

[10] Hirao K, Otomo K, Wang X, Beckman KJ, McClelland JH, Widman L, et al. Para-Hisian pacing. A new method for differentiating retrograde conduction over an accessory AV pathway from conduction over the AV node. Circulation (1996) 94:1027–35.[Abstract/Free Full Text]

[11] Heidbüchel H, Ector H, Adams J, Van de Werf F. Use of only a regular diagnostic His-bundle catheter for both fast and reproducible ‘para-Hisian pacing’ and stable right ventricular pacing. J Cardiovasc Electrophysiol (1997) 8:1121–32.[Web of Science][Medline]


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