Atlas Contents

The AV Conduction Axis for Permanent Pacing

1. A continuous axis within a changing tissue environment

The atrioventricular conduction axis is a continuous system of specialized cardiomyocytes. It begins with the compact atrioventricular node, continues through the penetrating, non-branching, and branching portions of the His bundle, and divides into the right and left bundle branches before reaching the Purkinje network. The familiar names identify segments of one axis rather than separate anatomical structures. What changes along its course is the relationship of the specialized cardiomyocytes to working myocardium and to the fibrous tissues that provide electrical insulation [1–4].

The compact node occupies the apex of the inferior pyramidal space. It receives transitional cardiomyocytes and inferior nodal extensions from the atrial myocardium. The decisive anatomical transition to the penetrating bundle occurs where the axis loses its last atrial myocardial connection and becomes insulated by the central fibrous body. Cellular appearance alone does not define this boundary. This distinction is important for pacing: a lead positioned inferiorly within the triangle of Koch may stimulate atrial myocardium, nodal inputs, or the non-insulated nodal axis, whereas effective His-bundle pacing requires capture of the insulated or immediately adjacent His bundle [2–5].

The right atrial landmarks are the tendon of Todaro, coronary sinus ostium, hinge of the septal tricuspid leaflet, membranous septum, and the crest of the muscular ventricular septum. They are surface guides to a deeper three-dimensional structure. The triangle of Koch is therefore not a flat map of the conduction system. It is the right atrial surface of the inferior pyramidal space; the compact node lies within its apex, and the axis turns superiorly and anteriorly toward the central fibrous body. Differences in the size of the inferior pyramidal space, the position of the tricuspid hinge, and the depth of the septal crest alter the relationship between an apparently identical catheter or lead position and the conduction tissue beneath it [3–6].

2. The central fibrous body and membranous septum

The central fibrous body is a region of fibrous continuity joining the aortic and atrioventricular junctions. It includes the right fibrous trigone and is continuous with the membranous septum and the fibrous tissues supporting the aortic root. It should not be reduced to a single discrete trigone. The atrioventricular conduction axis passes through this fibrous complex, which separates it from atrial and ventricular working myocardium except at defined proximal and distal connections [2,4,7].

The membranous septum is a small but clinically prominent component of this complex. The hinge of the septal tricuspid leaflet divides it into an atrioventricular component, separating right atrium from left ventricle, and an interventricular component between the ventricles. Their relative dimensions vary markedly. In some hearts the membranous septum is broad and readily recognized; in others it is short or predominantly atrioventricular. Its inferior border is related to the crest of the muscular ventricular septum, while the aortic root lies superiorly and leftward. Because the penetrating and branching axis courses along this changing boundary, the membranous septum is a useful landmark but not a complete representation of the His bundle [4,7–9].

Fluoroscopy does not show the membranous septum directly. The summit of the ventricular septum, the tricuspid valvar hinge, contrast within the aortic root, and electrograms recorded from the His region are used as surrogates. Computed tomography can display the fibrous septal region and its relation to the aortic annular plane, but it still cannot routinely trace the entire conduction axis. A sound implantation strategy therefore combines anatomical landmarks with electrical evidence rather than assuming that one radiographic point contains the His bundle.

3. The penetrating His bundle

The penetrating His bundle is the segment that enters the central fibrous body after the compact node has lost its final atrial myocardial connection. It passes superiorly and anteriorly from the apex of the inferior pyramidal space, adjacent to the membranous septum and the crest of the muscular ventricular septum. Once surrounded by fibrous tissue, it is insulated from ordinary myocardium. Distally it continues as the non-branching His bundle before giving rise to the branching component and the bundle branches. The length assigned to each segment depends on whether insulation, gross position, or origin of the first bundle-branch ramifications is used as the boundary; the underlying axis remains continuous [2–4].

Its arrangement is highly variable. Serial histology and gross reconstructions show that the bundle may run along the lower border of the membranous septum, remain more deeply embedded within the fibrous tissues, or become exposed on the crest or left aspect of the muscular septum. The three patterns popularized by Kawashima and Sasaki provide a useful visual framework: a relatively subendocardial bundle, a bundle separated from the endocardium by a thin myocardial layer, and a deeper intramyocardial course. These are configurations within a continuum, not rigid categories [5,10,11].

This variability helps explain why His-bundle pacing is straightforward in some patients and difficult in others. A superficially placed axis may produce a sharp His potential and be captured at relatively low output. A deeper or more extensively insulated axis may require a different lead orientation, greater penetration, or higher output. The largest His potential does not invariably identify the best long-term pacing site: fixation, sensing, threshold, atrial signal, and the relation to the tricuspid leaflet must also be considered. Conversely, failure to record a conspicuous His signal does not prove that the bundle is distant; catheter orientation and fibrous insulation can attenuate the local electrogram [5,6,10].

The penetrating bundle lies close to tissues that should not be injured unnecessarily. Proximally, excessive trauma or energy can affect the compact node and create atrioventricular block. Distally, injury can involve the branching bundle or proximal bundle branches. The adjacent septal tricuspid leaflet can interfere with lead stability, and lead passage across the valve can affect leaflet mobility. The aortic root is leftward and superior, while the atrioventricular nodal artery approaches the compact nodal region through the inferior pyramidal space. These relations support a controlled anatomical approach rather than repeated blind penetration at the His recording zone.

4. His-bundle pacing: target and interpretation

Permanent His-bundle pacing seeks to recruit the native His–Purkinje system proximal to or within a site of conduction disease. The target commonly lies at the superior aspect of the triangle of Koch near the septal tricuspid hinge and membranous septum. However, the successful point may be atrial, at the hinge, or ventricular in apparent fluoroscopic location because the penetrating and non-branching axis crosses these anatomical levels obliquely. An atrial electrogram at the pacing site is therefore not unexpected, and its size depends on the position of the lead relative to the last atrial connections and the leaflet hinge [5,6,12].

Selective His capture activates the His bundle without simultaneous capture of adjacent working myocardium, producing an isoelectric interval between the pacing stimulus and ventricular activation. Non-selective capture recruits both His tissue and adjacent myocardium, creating a local myocardial component while preserving rapid activation through the conduction system. These responses are electrophysiological expressions of lead–tissue geometry, insulation, output, and local excitability; neither should be judged from QRS appearance alone. Output-dependent transitions, changes in activation time, and correction of bundle-branch block provide stronger evidence of conduction-system recruitment [12,13].

Threshold may rise when the lead contacts predominantly fibrous tissue or when the bundle is deep. Sensing can be limited by small ventricular signals or large atrial signals. The narrow target and variable bundle course also explain why small changes in lead position can alter capture. Anatomical success is therefore not merely placement beside a recorded His potential. It is stable contact with an accessible segment of the axis that provides acceptable electrical performance without compromising atrioventricular conduction or valvar function.

5. The left bundle branch

The left bundle branch arises from the left side of the branching His bundle beneath the membranous septum and spreads over the left ventricular aspect of the muscular septum. It should not be represented as a thin cable that simply divides into two isolated fascicles. In many hearts its proximal origin is broad, and its specialized cardiomyocytes form a subendocardial network with anterior, posterior, and septal radiations connected to the Purkinje system. The shape and relative prominence of these radiations vary considerably between individuals [2,3,14–17].

Proximally, the left bundle may descend as a compact sheet or ribbon before widening. Some ramifications arise close to the lower border of the membranous septum; others emerge more distally along the smooth left septal surface. The anterior radiation generally courses toward the anterosuperior papillary region, the posterior radiation toward the posteroinferior septum and papillary region, and septal ramifications spread through the midseptal territory. These directional descriptions are useful, but the extensive interconnections contradict a rigid bifascicular model. In the atlas, the branch is best shown as a variable three-dimensional network [14–17].

Histologically, left-bundle cardiomyocytes may be separated from working ventricular myocardium by connective tissue, but the thickness and completeness of this insulation are not uniform. The branch itself also varies in thickness and depth. In some regions it is immediately subendocardial; elsewhere it is covered by endocardium, connective tissue, or a layer of working myocardium. These features influence whether a pacing lead records a discrete conduction potential and whether current first captures local septal myocardium, specialized tissue, or both. Similar fluoroscopic depths can therefore produce different electrical transitions [14,15,18].

The branch lies on the left side of the septum, while implantation usually begins from the right ventricular septal surface. The lead must cross right ventricular endocardium and a variable thickness of muscular septum before approaching the subendocardial left-bundle network. The target is consequently a volume, not a visible line. Septal thickness, obliquity of the lead, local trabeculation, and the position of proximal left-bundle radiations determine whether the helix reaches an effective site.

6. Left bundle branch area pacing

Left bundle branch area pacing encompasses direct capture of the left bundle or its ramifications and deep septal pacing in their vicinity. The usual right-sided entry region is below the membranous septum and distal to the His-bundle target, often guided by the tricuspid annulus, His recording, septal fluoroscopic orientation, and paced QRS pattern. Attitudinally, this is an anterosuperior to midseptal approach whose exact level varies with the anatomy of the aortic root, membranous septum, and muscular septal crest [14,18–20].

Lead advancement through the septum is monitored by impedance, electrograms, paced morphology, activation time, and imaging or contrast when used. A left-bundle potential can support proximity but is neither invariably present nor by itself proof of capture. More persuasive evidence includes output-dependent transition between non-selective and selective conduction-system capture, stable and short left ventricular activation time at different outputs, and characteristic changes during programmed stimulation. These criteria translate tissue recruitment; they should not be replaced by a single morphological sign [13,18–20].

Anatomy also defines complications. A lead that remains shallow may provide only right ventricular septal myocardial pacing. Excessive advancement may perforate into the left ventricular cavity or damage the left septal endocardium. Septal coronary arterial branches and veins are variably distributed and cannot be assumed absent from the trajectory. A septal haematoma, coronary injury, thromboembolic exposure of a perforating lead, or delayed loss of capture are uncommon but anatomically plausible. The safest procedure balances the desire for conduction-system capture with stable fixation and an adequate residual margin from the left ventricular cavity [18–20].

7. Choosing and documenting the anatomical target

His-bundle pacing and left bundle branch area pacing recruit different portions of the same axis. His pacing is the most proximal strategy and can preserve physiological activation when the distal system is intact, but its narrow and variably insulated target may yield higher thresholds or lower sensing amplitudes. Left bundle branch area pacing uses a broader distal network and often offers robust sensing and thresholds, but requires transseptal lead penetration and may activate the right ventricle partly through working myocardium. The choice is clinical as well as anatomical and depends on the level of conduction disease, septal anatomy, ventricular function, and the desired resynchronization effect [12,13,18–20].

Reports should distinguish the intended region, observed electrical criteria, and final evidence of capture. “His region,” “deep septal,” “left bundle branch area,” and proven selective or non-selective capture are not interchangeable labels. Fluoroscopic projection should be stated in attitudinal terms, and when computed tomography or echocardiography is available, lead depth and relation to the membranous and muscular septum should be documented. Precise language allows anatomy, electrical behaviour, and outcomes to be compared across studies.

Key Anatomical Messages

Anatomical focus

Practical implication

Continuity

The compact AV node, His bundle, bundle branches, and Purkinje network form one continuous conduction axis.

Penetrating His

Fibrous insulation and its variable depth—not a single fluoroscopic point—define accessibility for His-bundle pacing.

Membranous septum

A useful surface and imaging landmark, but an incomplete surrogate for the entire His–Purkinje axis.

Left bundle

A broad, variably insulated subendocardial network with anterior, posterior, and septal radiations.

Capture

Electrical transitions and activation timing must be interpreted together with lead–tissue anatomy.

Safety

Respect the tricuspid valve, septal thickness, left ventricular cavity, and variable septal vessels.

References

  1. Anderson RH, Yanni J, Boyett MR, Chandler NJ, Dobrzynski H. The anatomy of the cardiac conduction system. Clin Anat. 2009;22:99–113. doi:10.1002/ca.20700.
  2. Padala SK, Cabrera JA, Ellenbogen KA. Anatomy of the cardiac conduction system. Pacing Clin Electrophysiol. 2021;44:15–25. doi:10.1111/pace.14107.
  3. Sánchez-Quintana D, Anderson RH, Tretter JT, et al. Anatomy of the conduction tissues 100 years on: what have we learned? Heart. 2022;108:1430–1437.
  4. Sánchez-Quintana D, Cabrera JA, Anderson RH. The clinical anatomy of the atrioventricular conduction axis. Europace. 2024;26:euae048. doi:10.1093/europace/euae048.
  5. Cabrera JA, Anderson RH, Macías Y, et al. Variable arrangement of the atrioventricular conduction axis within the triangle of Koch: implications for permanent His bundle pacing. JACC Clin Electrophysiol. 2020;6:362–377. doi:10.1016/j.jacep.2019.12.004.
  6. Cabrera JA, Anderson RH, Porta-Sánchez A, et al. The atrioventricular conduction axis and its implications for permanent pacing. Arrhythm Electrophysiol Rev. 2021;10:181–189. doi:10.15420/aer.2021.32.
  7. de Almeida MC, Sánchez-Quintana D, Anderson RH. The membranous septum revisited: a glimpse of our anatomical past. Clin Anat. 2021;34:178–186. doi:10.1002/ca.23599.
  8. Macías Y, Tretter JT, Sánchez-Quintana D, et al. The atrioventricular conduction axis and the aortic root—inferences for transcatheter replacement of the aortic valve. Clin Anat. 2022;35:143–154. doi:10.1002/ca.23793.
  9. Anderson RH, Sánchez-Quintana D, Spicer DE, et al. Revisiting the atrioventricular conduction axis for the 21st century. Arrhythm Electrophysiol Rev. 2024;13:e20. doi:10.15420/aer.2024.15.
  10. Kawashima T, Sasaki H. Gross anatomy of the human cardiac conduction system with comparative morphological and developmental implications for human application. Ann Anat. 2011;193:1–12. doi:10.1016/j.aanat.2010.11.002.
  11. Massing GK, James TN. Anatomical configuration of the His bundle and bundle branches in the human heart. Circulation. 1976;53:609–621. doi:10.1161/01.CIR.53.4.609.
  12. Bressi E, Grieco D, Čurila K, et al. Pacing of the specialized His–Purkinje conduction system: “back to the future”. Eur Heart J Suppl. 2023;25:C234–C241. doi:10.1093/eurheartjsupp/suad047.
  13. Burri H, Jastrzębski M, Cano Ó, et al. EHRA clinical consensus statement on conduction system pacing implantation. Europace. 2023;25:1208–1236. doi:10.1093/europace/euad043.
  14. Cabrera JA, Porta-Sánchez A, Tung R, Sánchez-Quintana D. Tracking down the anatomy of the left bundle branch to optimize left bundle branch pacing. JACC Case Rep. 2020;2:750–755. doi:10.1016/j.jaccas.2020.04.004.
  15. Cabrera JA, González-Casal D, Curila K, et al. Left bundle branch pacing: histology, the key to understand different responses. JACC Clin Electrophysiol. 2025;11:1659–1666. doi:10.1016/j.jacep.2025.03.007.
  16. Demoulin JC, Kulbertus HE. Histopathological examination of concept of left hemiblock. Br Heart J. 1972;34:807–814. doi:10.1136/hrt.34.8.807.
  17. Zuin M, Vijayaraman P, Abuin G, et al. Anatomical considerations for left bundle branch area pacing. Heart Rhythm. 2026. doi:10.1016/j.hrthm.2026.05.013.
  18. Imnadze G, Abdin A, Biffi M, et al. Left bundle branch area pacing: anatomical and physiological features made easy. Eur Heart J Open. 2026;6:oeag081. doi:10.1093/ehjopen/oeag081.

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