Elsevier

Heart Rhythm

Volume 18, Issue 7, July 2021, Pages 1057-1063
Heart Rhythm

Clinical
Atrial Fibrillation
Significance of manifest localized staining during ethanol infusion into the vein of Marshall

https://doi.org/10.1016/j.hrthm.2021.03.023Get rights and content

Background

Localized staining due to venule injury is attributable to ethanol infusion into the vein of Marshall (Et-VOM).

Objective

The purpose of this study was to investigate adverse outcomes of localized staining during Et-VOM in patients undergoing ablation for atrial fibrillation.

Methods

Two hundred four patients (age 64 ± 10 years; 153 male) were sorted based on the aspect of localized staining. Staining of atrial myocardium that spread uniformly along the VOM vascular tree following selective VOM venography was considered normal, in contrast to predominantly localized staining that spread concentrically from a focal point due to vascular injury. Outcomes between the 2 groups were compared.

Results

Localized staining was observed in 27% of patients. No patients developed clinically significant pericardial effusions during Et-VOM; however, 7 patients developed pericardial effusions on the first postprocedural day (3.6% in patients with vs 3.4% in patients without localized staining). No significant difference was found in achievement of acute mitral isthmus (MI) block (96% vs 98%) and size of the endocardial low-voltage area (8.5 ± 4.1 cm2 vs 9.3 ± 5.3 cm2) in patients with and without localized staining, respectively. Long-term follow-up was not impacted by localized staining. Freedom from recurrent atrial tachyarrhythmias (66% vs 76%) and durability of MI block (57% vs 54%) were not significantly different with and without localized staining. There were no cases of rehospitalization for pericarditis, chronic pericardial effusion, or heart failure.

Conclusion

In our study, localized staining was frequent but was not associated with clinically relevant impact or disadvantages.

Introduction

Creating conduction block at the mitral isthmus (MI) with endocardial radiofrequency catheter ablation (RFCA) by connecting the mitral annulus to the ostium of the left inferior pulmonary vein (PV) is an effective treatment of persistent atrial fibrillation (AF) and perimitral flutter.1,2 However, achieving bidirectional MI block is technically challenging and carries a risk of complications.1 To overcome these difficulties, chemical ablation by ethanol infusion into the vein of Marshall (Et-VOM) has been developed.3,4

The vein of Marshall (VOM) is anatomically linked to the MI and is an embryonic remnant of the left superior vena cava. It contains epicardial muscular bundles that connect left atrial (LA) myocardium to coronary sinus (CS) musculature—connections that have been implicated in the maintenance of atrial tachyarrhythmia (ATa).5, 6, 7, 8 Et-VOM is designed to ablate these epicardial muscular bundles as well as portions of the LA myocardium, thus facilitating MI block.6,9, 10, 11, 12 Recently, the VENUS (Vein of Marshall Ethanol iNfusion in Untreated perSistent Atrial Fibrillation) trial demonstrated the advantage of adjunctive Et-VOM over RFCA alone in reducing recurrent AF at 1 year in patients undergoing ablation for persistent AF.12

Localized staining commonly occurs during Et-VOM, presumably caused by injury to VOM venules, and is visualized as leakage of contrast medium from a focal point of origin. This aspect may prompt operators to discontinue the procedure, as the risk for cardiac tamponade may increase with the vascular lesion.13 However, despite the high incidence of localized staining, few reports have described this potential complication and its clinical significance. We sought to examine whether manifest localized staining during Et-VOM was associated with adverse outcomes and to describe its management in patients undergoing de novo ablation for persistent AF.

Section snippets

Study population

Consecutive patients with drug-resistant persistent AF who underwent de novo RFCA with Et-VOM at our institute between December 2017 and April 2020 were included in the study. All patients provided informed consent. The study complied with the Declaration of Helsinki and was approved by the Institutional Review Board of the University of Bordeaux.

General principles

All procedures were performed with patients under conscious sedation with midazolam and morphine. Antiarrhythmic drugs were discontinued >5 half-lives

Patient characteristics

Two hundred twenty-two consecutive patients with persistent AF were included in the study. Et-VOM was attempted in all patients. In 11 patients, Et-VOM could not be performed because of absence of VOM in 8; failure of VOM cannulation in 2; and persistent left superior vena cava in 1. In 6 patients, Et-VOM was prematurely terminated because of CS dissection during CS venography. One patient had cardiac tamponade that occurred during right PV isolation and was excluded from this analysis. In

Discussion

The main findings of this study are that localized staining (1) is frequent, being observed in almost one-third of patients; (2) does not carry extra risks such as pericardial effusions; and (3) does not impact the efficacy of Et-VOM based on rate of MI block, size of endocardial LVAs, risk of recurrent ATa, or durability of MI block in redo patients.

Conclusion

Localized staining was observed in 27% of patients undergoing Et-VOM but without clinical impact on safety or efficacy.

References (20)

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Cited by (4)

Funding sources: Dr Ramirez is supported by a Canadian Institutes of Health Research Banting Postdoctoral Fellowship. Dr Krisai is supported by the University of Basel, the Mach-Gaensslen Foundation, and the Bangerter-Rhyner Foundation. Disclosures: Drs Pambrun, Duchateau, Sacher, and Derval received modest consulting fees and speaking honoraria from Biosense Webster. Drs Derval, Sacher, and Jaïs received modest speaking honoraria from Boston Scientific. All other authors have reported that they have no relationship relevant to the contents of this paper to disclose.

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