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Identification of Critical Slowing of Conduction Using Unipolar Atrial Voltage and Fractionation Mapping.
Ye, Ziliang; Ramdat Misier, Nawin L; van Schie, Mathijs S; Xiang, Hongxian; Knops, Paul; Kluin, Jolanda; Taverne, Yannick J H J; de Groot, Natasja M S.
Afiliação
  • Ye Z; Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Ramdat Misier NL; Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.
  • van Schie MS; Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Xiang H; Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Knops P; Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Kluin J; Department of Cardiothoracic Surgery, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Taverne YJHJ; Department of Cardiothoracic Surgery, Erasmus Medical Center, Rotterdam, the Netherlands.
  • de Groot NMS; Department of Cardiology, Erasmus Medical Center, Rotterdam, the Netherlands; Department of Microelectronics, Signal Processing Systems, Faculty of Electrical Engineering, Mathematics and Computer Sciences, Delft University of Technology, Delft, the Netherlands. Electronic address: n.m.s.degroot@era
Article em En | MEDLINE | ID: mdl-39023486
ABSTRACT

BACKGROUND:

Ablation strategies targeting fractionated or low-voltage potentials have been widely used in patients with persistent types of atrial fibrillation (AF). However, recent studies have questioned their role in effectively representing sites of conduction slowing, and thus arrhythmogenic substrates.

OBJECTIVES:

The authors studied the relationship between local conduction velocity (CV) and the occurrence of fractionated and/or low-voltage potentials in order to identify areas with critically slowing of conduction.

METHODS:

Intraoperative epicardial mapping was performed during sinus rhythm. Unipolar potentials with an amplitude <1.0 mV were initially classified as low-voltage and potentials with ≥3 deflections as fractionation. A range of thresholds were also explored. Local CV was computed using discrete velocity vectors.

RESULTS:

A total of 319 patients were included. Fractionated, low-voltage potentials were rare, accounting for only 0.36% (Q1-Q3 0.15%-0.78%) of all atrial sites. Local CV at sites with fractionated, low-voltage potentials (46.0 cm/s [Q1-Q3 22.6-72.7 cm/s]) was lowest compared with sites with either low-voltage, nonfractionated potentials (64.5 cm/s [Q1-Q3 34.8-99.4 cm/s]) or fractionated, high-voltage potentials (65.9 cm/s [Q1-Q3 41.7-92.8 cm/s]; P < 0.001). Slow conduction areas (CV <50 cm/s) could be most accurately identified by using a low voltage threshold (<1 mV) and a minimum of 3 deflections (positive predictive value 54.2%-70.7%), although the overall sensitivity remained low (0.1%-1.9%).

CONCLUSIONS:

Sites with fractionated, low-voltage potentials have substantially slower local CV compared with sites with either low-voltage, nonfractionated potentials or fractionated, high-voltage potentials. However, the strong inverse relationship between the positive predictive value and sensitivity of a combined voltage and fractionation threshold for slowed conduction is likely to complicate the use of these signal-based ablation approaches in AF patients.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article