Ligament of Marshall ablation for persistent atrial fibrillation.
Konstantinos VlachosNicolas DervalThomas PambrunJosselin DuchateauClaire A MartinGeorge BazoukisAntonio FronteraMasateru TakigawaTakashi NakashimaMichael EfremidisKonstantinos P LetsasFelix BourierClémentine AndréPhilipp KrisaiF Daniel RamirezTsukasa KamakuraTakamitsu TakagiYosuke NakataniRomain TixierRemi ChauvelNicolas WelteTakeshi KitamuraGhassen ChnitiFrédéric SacherPierre JaïsMichel HaïssaguerreMélèze HociniPublished in: Pacing and clinical electrophysiology : PACE (2021)
Beyond pulmonary vein isolation, the two main additional strategies: Cox-Maze procedure or targeting of electrical signatures (focal bursts, rotational activities, meandering wavelets), remain controversial. High-density mapping of these arrhythmias has demonstrated firstly that a patchy lesion set is highly proarrhythmogenic, favoring macro-re-entry through conduction slowing and providing pivots for localized re-entry. Secondly, discrete anatomical structures such as the Vein or Ligament of Marshall (VOM/LOM) and the coronary sinus (CS) have epicardial muscular bundles that are more frequently involved in re-entry than previously thought. The Marshall Bundle can be ablated at any point along its course from the mid-to-distal coronary sinus to the left atrial appendage. If necessary, the VOM may be directly ablated using ethanol infusion to eliminate PV contributions and produce conduction block across the mistral isthmus. Ethanol ablation of the VOM, supplemented with RF ablation, may be more effective in producing conduction block at the mitral isthmus than repeat RF ablation alone.
Keyphrases
- catheter ablation
- left atrial appendage
- atrial fibrillation
- high density
- left atrial
- coronary artery disease
- coronary artery
- radiofrequency ablation
- minimally invasive
- high resolution
- mitral valve
- heart failure
- left ventricular
- oral anticoagulants
- low dose
- aortic stenosis
- mass spectrometry
- gene expression
- drug delivery