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. 2026 Mar 16;31(17):107414. doi: 10.1016/j.jaccas.2026.107414

Fundamental Anatomy and its Impact on Clinical Practice

Bachmann's Bundle and Interatrial Conduction (Part I-III)

David González-Casal a, Adrian Baranchuk b, Damián Sánchez-Quintana c, José-Ángel Cabrera a,∗
PMCID: PMC13130930  PMID: 41837930

Abstract

Architecture and Vascular Substrate of Bachmann's Bundle: Bachmann's bundle (BB) is the most prominent and consistent muscular bridge between the right and left atria, which constitutes the dominant anatomical substrate for physiological interatrial conduction. Located in the subepicardial anterior atrial region along the interatrial groove, BB establishes atrial continuity by bridging infolded atrial walls rather than the true septum. Architecturally, it is not separated by a fibrous sheath; instead, it is defined by a highly ordered, predominantly parallel cardiomyocyte alignment that favors longitudinal impulse propagation and creates a preferential conduction pathway. Its arterial supply arises from branches of the sinus node artery, most commonly originating from the right coronary artery, though left-sided and dual supplies are also documented. In structurally diseased hearts, chronic ischemia and fibrotic remodeling may compromise BB integrity, contributing to interatrial conduction delay or block. Guest Insight on Clinical Impact—The Interatrial Conduction Block: Clinically, fibrotic involvement of the Bachmann region underlies interatrial block, which can redirect activation through inferior pathways (eg, via the coronary sinus) with retrograde left atrial activation and provides an electrical substrate for atrial fibrillation. Interatrial block is identifiable on the 12-lead electrocardiogram by P-wave prolongation and characteristic morphological changes.

Take-Home Message

BB represents a structurally distinct, subepicardial anterior interatrial myocardial bridge whose tightly aggregated cardiomyocytes are arranged in a predominantly parallel fashion, enabling preferential impulse propagation between both atria.

Key words: electrocardiogram, electrophysiology, supraventricular arrhythmias

Graphical Abstract

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Architecture and Vascular Substrate of Bachmann's Bundle

Interatrial conduction in the human heart relies on a complex 3-dimensional organization of atrial myocardium, within which Bachmann's bundle (BB) represents the most prominent and consistent muscular bridge between the right and left atria (Figure 1).

Figure 1.

Figure 1

Bachmann's Bundle and Transverse Pericardial Sinus

(A) Dissection performed by removing the epicardium from the anterior interatrial groove and the walls of the left atrium. This preparation demonstrates how individual working atrial cardiomyocytes are aggregated in a parallel fashion within the atrial walls, particularly within Bachmann's bundle (white dashed lines), thereby facilitating preferential conduction. Dorsally and superiorly, extending toward the roof of the left atrium, the septopulmonary bundle is identified beneath the epicardium (red dashed lines). The spatial intersection and continuity between these 2 muscular systems contribute to the 3-dimensional complexity of left atrial myoarchitecture. (B) Dissection obtained after removal of the epicardium from the roof of the left atrium and the anterior walls of both atria. The aggregated working atrial cardiomyocytes forming Bachmann's bundle provide a direct muscular pathway from the anterior wall adjacent to the superior caval vein to the anterior wall of the left atrium, just posterior to the transverse sinus. LPVs = left pulmonary veins; LSPV = left superior pulmonary vein; RIPV = right inferior pulmonary vein; RSPV = right superior pulmonary vein; SCV = superior caval vein.

The concept of a preferential muscular connection between the atria emerged at the beginning of the 20th century, when careful anatomical observations challenged the prevailing view that interatrial continuity was confined to septal structures.1 A decisive step toward functional interpretation followed with the work of Jean George Bachmann, who explored the temporal relationships of atrial activation and proposed that a distinct myocardial band with orderly fiber alignment could facilitate rapid interatrial impulse transmission.2 Subsequent experimental and anatomical investigations consolidated this concept, establishing BB as the most substantial interatrial muscular connection and the dominant anatomical substrate for physiological interatrial conduction.3, 4, 5 High-density 3-dimensional atrial mapping studies indicate that, in addition to the preferential anterior routes, interatrial conduction can occasionally proceed through less well-defined posterior pathways located in Waterston's groove, probably involving the posterior interatrial folds or the margins of the oval fossa. Notably, a posterior sinus node breakout without conduction delay at the junction with the terminal crest favors posterior propagation through these interatrial structures.6

BB occupies the subepicardial plane of the anterior atrial region, running along the anterior aspect of the interatrial groove, an infolding of the atrial walls containing epicardial fibrofatty tissue. Because the true interatrial septum is confined to the region of the oval fossa and its immediate margins, BB establishes atrial continuity by bridging infolded atrial walls.7

When examined from the epicardial aspect, particularly after exposure of the transverse pericardial sinus, BB appears as a broad myocardial band running transversely and approximately parallel to the atrioventricular junction (Video 1, Figure 1). BB positioned beneath, or posterior to, the proximal ascending aorta and above the atrial chambers occupies a strategic 3-dimensional interface between intracardiac musculature and extracardiac anatomical landmarks. BB exhibits a trapezoidal configuration with marked interindividual variability in size and prominence. The superior margin is consistently longer than the inferior margin, whereas the central portion related to the interatrial groove forms a relatively thick and tall muscular plate.7

At the architectural level, BB lacks a fibrous sheath segregating it from the surrounding atrial myocardium. It is more accurately defined by a highly ordered, parallel alignment of atrial cardiomyocytes, in contrast to the heterogeneous and intersecting cardiomyocyte orientations of adjacent atrial walls (Video 1, Figure 2).7,8 This organization favors longitudinal impulse propagation, establishing a preferential pathway for interatrial activation.

Figure 2.

Figure 2

Muscular Architecture of Bachmann's Bundle

(A) Histologic section through both atrial chambers at the level of the superior cavoatrial junction. The terminal crest is seen continuing anterior to the orifice of the superior caval vein, with cardiomyocytes aggregated in a parallel arrangement and extending into the left atrial wall as Bachmann's bundle. (B) Dissection obtained by removing the epicardium from the roof and walls of both atria and oriented identically to panel (A). The preparation demonstrates cardiomyocytes aggregated in a parallel fashion, continuing into the left atrial wall as Bachmann's bundle. (C) Higher magnification of the histologic section shown in panel (A) at the level of Bachmann's bundle. (D) Higher magnification of the dissection shown in panel (B) at the level of Bachmann's bundle. LAA = left atrial appendage; LIPV = left inferior pulmonary vein; LSPV = left superior pulmonary vein; RAA = right atrial appendage; RIPV = right inferior pulmonary vein; RSPV = right superior pulmonary vein; SCV = superior caval vein.

The arterial supply of BB consistently derives from branches of the sinus node artery (Video 1). In most hearts, this vessel originates from the right coronary artery (55% of cases), whereas a substantial proportion receive supply from a left-sided sinus node artery arising from the circumflex artery (45% of cases); dual arterial supply is less common but well documented (5% of cases) (Figure 3).9 Advanced imaging studies have demonstrated that in hearts with structural disease, BB may become difficult to delineate, even though fine arterial branches persist within its expected anatomical territory. These observations support the concept that chronic ischemia and fibrotic remodeling may preferentially affect the bundle, alter its structural integrity, and contribute to interatrial conduction delay or block.9,10

Figure 3.

Figure 3

The Arterial Supply of Bachmann's Bundle

(A) Dissection of the sinus node artery showing its origin from the right coronary artery and its course anterior to the superior caval vein (precaval), toward the terminal groove of His. The artery courses within the region of Bachmann's bundle, positioning itself toward the neck of the left atrial appendage. (B) Dissection of the sinus node artery originating from the circumflex artery (highlighted in red). The artery courses through Bachmann's bundle and reaches the terminal groove of His anterior to the superior caval vein (precaval). White arrow indicates precaval course of the sinus nodal artery. Red arrow indicates sinus nodal artery within the region of Bachmann's bundle. LAA = left atrial appendage; LIPV = left inferior pulmonary vein; LSPV = left superior pulmonary vein; RIPV = right inferior pulmonary vein; RSPV = right superior pulmonary vein; SCV = superior caval vein.

In this context, the combined myocardial architecture and vascular supply of BB define the structural substrate for preferential interatrial conduction and provide the necessary foundation for a focused analysis of its rightward and leftward extensions, which will be addressed separately.

Guest Insight on Clinical Impact: The Interatrial Conduction Block

The diagnosis of interatrial block (IAB) indicates a delay of conduction between the right and left atria. This alteration of conduction is the result of fibrotic areas across the Bachmann region, and classic cardiovascular risk factors (such as hypertension and diabetes) may predispose to the replacement of normal atrial tissue by fibrotic tissue.10, 11, 12

The delay in conduction between the atria through the Bachmann region may force interatrial conduction by the region of the coronary sinus, activating the left atrium in a retrograde manner (inferior-to-superior) (Figure 4). This is the electrical substrate for atrial fibrillation (AF), which, in addition to the anatomical substrate (fibrotic tissue), is the perfect scenario for AF trigger and maintenance.11, 12, 13 Several studies have confirmed that IAB is an electrocardiographic predictor of AF.13 In addition, sex-related differences in the electrical remodeling of BB have been observed in patients with AF.14

Figure 4.

Figure 4

Bachmann's Bundle and ECG Correlates of Interatrial Conduction Block

(A) Surface ECG illustrating interatrial conduction block (IAB). Prolongation of the P-wave duration (>120 milliseconds) and characteristic morphological changes are shown, including a biphasic (positive-negative) P-wave morphology in the inferior leads, consistent with advanced IAB. The schematic representation illustrates delayed conduction through the Bachmann region, with redirection of interatrial activation toward inferior pathways, resulting in retrograde (inferior-to-superior) activation of the left atrium via the coronary sinus region. (B) Anatomical specimen demonstrating the structural substrate of interatrial conduction. Bachmann's bundle is identified as a distinct subepicardial myocardial bridge located along the anterior interatrial groove, connecting the right and left atria above the oval fossa. The relationships with adjacent landmarks, including the terminal crest, coronary sinus, inferior caval vein, mitral valve, and left atrial chamber, are shown, emphasizing how fibrotic involvement of this region may disrupt preferential interatrial conduction and promote the electrophysiological substrate for atrial fibrillation. AVN = atrioventricular node; ECG = electrocardiogram; SN = sinus node.

The surface 12-lead electrocardiogram is critical for the proper diagnosis of IAB. The 2 major changes in comparison to the normal P-wave are duration and morphology.11

  • 1.

    A P-wave duration longer than 120 milliseconds indicates IAB.11

  • 2.
    An alteration of the P-wave morphology may present 2 distinctive characteristics:
    • a.
      A positive P-wave with a “notch” in the superior aspect (also known as “P-mitrale”) indicating “partial IAB” or
    • b.
      A biphasic P-wave (positive-negative) indicating “advanced” IAB.11

A less frequent condition is the alternation of normal P-wave with “partial” or “advanced” IAB, which is considered “intermittent” IAB (or second-degree IAB), and it requires a fixed P-P interval.12

Currently, the concept of “atypical” advanced IAB has been accepted in the literature, and modifications of the morphology (ie, “triphasic” P-wave—positive-negative-positive) or the duration (ie, advanced IAB with a P-wave duration of < 120 milliseconds) are the most common atypical forms.

Funding Support and Author Disclosures

The authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Take-Home Messages

  • •

    Bachmann's bundle represents a structurally distinct, subepicardial anterior interatrial myocardial bridge composed of tightly aggregated cardiomyocytes arranged in a predominantly parallel fashion, forming a continuous muscular framework between both atria that enables preferential impulse propagation.

  • •

    Fibrotic involvement of this region disrupts this orderly architecture, leading to interatrial conduction block, redirection of atrial activation through inferior pathways with retrograde left atrial activation, and the creation of a critical electrophysiological substrate for atrial fibrillation with clear clinical implications identifiable on the surface electrocardiogram.

Footnotes

The authors attest they are in compliance with human studies committees and animal welfare regulations of the authors’ institutions and Food and Drug Administration guidelines, including patient consent where appropriate. For more information, visit the Author Center.

Appendix

For a supplemental video, please see the online version of this paper.

Appendix

Video 1

Structure and Arterial Supply of Bachmann's Bundle

Download video file (76.3MB, mp4)

References

  • 1.Lewis T., Meakins J., White P.D. The excitatory process in the dog’s heart. Part I. The auricles. Phil Trans Roy Soc Lond. 1914;205:375–426. [Google Scholar]
  • 2.Bachmann G. The interauricular time interval. Am J Physiol. 1916;41:309–320. [Google Scholar]
  • 3.Ho S.Y., Anderson R.H., Sánchez-Quintana D. Atrial structure and fibres: morphological basis of atrial conduction. Cardiovasc Res. 2002;54(2):325–336. doi: 10.1016/s0008-6363(02)00226-2. [DOI] [PubMed] [Google Scholar]
  • 4.van Campenhout M.J., Yaksh A., Kik C., et al. Bachmann's bundle: a key player in the development of atrial fibrillation? Circ Arrhythm Electrophysiol. 2013;6(5):1041–1046. doi: 10.1161/CIRCEP.113.000758. [DOI] [PubMed] [Google Scholar]
  • 5.Bayes de Luna A., Cladellas M., Oter R., et al. Interatrial conduction block and retrograde activation of the left atrium and paroxysmal supraventricular tachyarrhythmia. Eur Heart J. 1988;9:1112–1118. doi: 10.1093/oxfordjournals.eurheartj.a062407. [DOI] [PubMed] [Google Scholar]
  • 6.Anderson R.H., Sutton R., Sánchez-Quintana D. Bachmann's bundle: how anatomists and electrophysiologists see it. Heart Rhythm. 2025;22(11):e1077–e1081. doi: 10.1016/j.hrthm.2025.04.064. [DOI] [PubMed] [Google Scholar]
  • 7.Pambrun T., Derval N., Duchateau J., et al. Sinus node exit, crista terminalis conduction, interatrial connection, and wavefront collision: key features of human atrial activation in sinus rhythm. Heart Rhythm. 2022;19(5):701–709. doi: 10.1016/j.hrthm.2022.01.016. [DOI] [PubMed] [Google Scholar]
  • 8.Ho S.Y., Sanchez-Quintana D., Cabrera J.A., Anderson R.H. Anatomy of the left atrium: implications for radiofrequency ablation of atrial fibrillation. J Cardiovasc Electrophysiol. 1999;10(11):1525–1533. doi: 10.1111/j.1540-8167.1999.tb00211.x. [DOI] [PubMed] [Google Scholar]
  • 9.Saremi F., Channual S., Krishnan S., et al. Bachmann bundle and its arterial supply: imaging with multidetector CT — implications for interatrial conduction abnormalities and arrhythmias. Radiology. 2008;248:447–457. doi: 10.1148/radiol.2482071908. [DOI] [PubMed] [Google Scholar]
  • 10.Guerra J.M., Vilahur G., Bayés de Luna A., et al. Interatrial block can occur in the absence of left atrial enlargement: new experimental model. Pacing Clin Electrophysiol. 2020;43(4):427–429. doi: 10.1111/pace.13895. [DOI] [PubMed] [Google Scholar]
  • 11.Conde D., Seoane L., Gysel M., Mitrione S., Bayes de Luna A., Baranchuk A. Bayés’ syndrome: the association between interatrial block and supraventricular arrhythmias. Expert Rev Cardiovasc Ther. 2015;13(5):541–550. doi: 10.1586/14779072.2015.1037283. [DOI] [PubMed] [Google Scholar]
  • 12.Bayes de Luna A., Baranchuk A., Pulido C.N., et al. Second-degree interatrial block: brief review and concept. Ann Noninv Electrocardiol. 2018;23(6) doi: 10.1111/anec.12583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Martínez-Sellés M., Elosua R., Ibarrola M., et al. Advanced interatrial block and P-wave duration are associated with atrial fibrillation and stroke in older adults with heart disease: the BAYES registry. Europace. 2020;22(7):1001–1008. doi: 10.1093/europace/euaa114. [DOI] [PubMed] [Google Scholar]
  • 14.Freriks A.I., de Kruijf N.L.M., van Schie M.S., et al. Men and women’s hearts don’t beat the same: epicardial mapping of Bachmann’s bundle. Neth Heart J. 2025;33:421–428. doi: 10.1007/s12471-025-02001-x. [DOI] [PMC free article] [PubMed] [Google Scholar]

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Supplementary Materials

Video 1

Structure and Arterial Supply of Bachmann's Bundle

Download video file (76.3MB, mp4)

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