Lesion size index-guided cavotricuspid isthmus linear ablation
Background The lesion size index (LSI) predicts radiofrequency (RF) ablation lesion size and is an established parameter for pulmonary vein isolation. However, the effectiveness and safety of LSI for cavotricuspid isthmus (CTI) linear ablation remain unclear. Methods This single-center retrospective...
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Published in | Journal of interventional cardiac electrophysiology Vol. 66; no. 2; pp. 485 - 492 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.03.2023
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Background
The lesion size index (LSI) predicts radiofrequency (RF) ablation lesion size and is an established parameter for pulmonary vein isolation. However, the effectiveness and safety of LSI for cavotricuspid isthmus (CTI) linear ablation remain unclear.
Methods
This single-center retrospective study included 50 of patients (67 ± 10 years, 68% male) who underwent
de novo
CTI linear ablation between July 2020 and December 2020. The LSI target was set at 5.0 and 4.0 for the anterior
2/3
and posterior
1/3
segments, respectively. Acute procedural parameters of ablation were evaluated.
Results
Acute bidirectional CTI block was achieved in all patients with an RF application time of 4.0 min (3.1–5.0 min), RF application number of 15 ± 7, and length of CTI of 36.9 ± 9.3 mm. First-pass bidirectional conduction block of the CTI was achieved in 39/50 (78%) patients. No major complications were observed. The contact force (CF) per application was significantly lower in the gap tag group than in the non-gap tag group (7 g [7–8 g] vs. 10 g [7–12 g],
P
= 0.0284).
Conclusions
LSI-guided CTI linear ablation is an effective and safe treatment approach. CF affects gap formation, even when the target LSI is the same. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1572-8595 1383-875X 1572-8595 |
DOI: | 10.1007/s10840-022-01360-4 |