<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(2)</volume><submitter>Sularz A</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Intracardiac echocardiography (ICE) is an alternative to transesophageal echocardiography to guide left atrial appendage occlusion (LAAO). However, 2-dimensional ICE has important limitations that hinder its adoption in routine practice.&lt;h4>Objectives&lt;/h4>This prospective multicenter study (NCT04569734) investigated the feasibility and safety of ICE-guided LAAO with Watchman FLX using a novel 3-dimensional ICE catheter (VeriSight Pro, Philips).&lt;h4>Methods&lt;/h4>A total of 100 patients undergoing LAAO with the Watchman FLX device were recruited. All cases were performed under moderate sedation. A simplified 2 orthogonal view ICE imaging protocol was adopted to assess PASS (position, anchoring, sizing, and sealing) criteria. The feasibility endpoint was successful implantation of the FLX device and adequate seal (peri-device leak &lt;5 mm) at 45 days. The safety endpoint was the incidence of major complications at 7 and 45 days. Physician experience and imaging quality scores were collected (1 = lowest, 5 = highest).&lt;h4>Results&lt;/h4>The mean age was 77.0 ± 8.1 years, and 39 (39%) were women. CHA&lt;sub>2&lt;/sub>DS&lt;sub>2&lt;/sub>-VASc score was 4.8 ± 1.5 and HAS-BLED score was 3.2 ± 1.1. Total procedural time was 54 ± 25 minutes. Mean contrast volume was 41 ± 46 ml, with no contrast used in 16 patients. The feasibility endpoint was achieved in 95 patients (95%); 4 patients were not implanted due to unsuitable anatomy, and 1 patient had a leak >5 mm at 45 days. There was 1 periprocedural stroke and 2 gastrointestinal bleeds requiring transfusion at 7 days with no other major complications. Physicians' rating of overall ICE imaging quality was 4.6 ± 0.6.&lt;h4>Conclusions&lt;/h4>The novel 3-dimensional ICE VeriSight Pro Probe can safely and effectively guide LAAO with Watchman FLX using a simplified imaging protocol.</pubmed_abstract><journal>JACC. Advances</journal><pagination>101570</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11782859</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety and Feasibility of 3D Intracardiac Echocardiography in Guiding Left Atrial Appendage Occlusion With WATCHMAN FLX.</pubmed_title><pmcid>PMC11782859</pmcid><pubmed_authors>Sularz A</pubmed_authors><pubmed_authors>Chavez Ponce A</pubmed_authors><pubmed_authors>Doshi SK</pubmed_authors><pubmed_authors>Al-Abcha A</pubmed_authors><pubmed_authors>Simard T</pubmed_authors><pubmed_authors>Killu AM</pubmed_authors><pubmed_authors>Alkhouli M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and Feasibility of 3D Intracardiac Echocardiography in Guiding Left Atrial Appendage Occlusion With WATCHMAN FLX.</name><description>&lt;h4>Background&lt;/h4>Intracardiac echocardiography (ICE) is an alternative to transesophageal echocardiography to guide left atrial appendage occlusion (LAAO). However, 2-dimensional ICE has important limitations that hinder its adoption in routine practice.&lt;h4>Objectives&lt;/h4>This prospective multicenter study (NCT04569734) investigated the feasibility and safety of ICE-guided LAAO with Watchman FLX using a novel 3-dimensional ICE catheter (VeriSight Pro, Philips).&lt;h4>Methods&lt;/h4>A total of 100 patients undergoing LAAO with the Watchman FLX device were recruited. All cases were performed under moderate sedation. A simplified 2 orthogonal view ICE imaging protocol was adopted to assess PASS (position, anchoring, sizing, and sealing) criteria. The feasibility endpoint was successful implantation of the FLX device and adequate seal (peri-device leak &lt;5 mm) at 45 days. The safety endpoint was the incidence of major complications at 7 and 45 days. Physician experience and imaging quality scores were collected (1 = lowest, 5 = highest).&lt;h4>Results&lt;/h4>The mean age was 77.0 ± 8.1 years, and 39 (39%) were women. CHA&lt;sub>2&lt;/sub>DS&lt;sub>2&lt;/sub>-VASc score was 4.8 ± 1.5 and HAS-BLED score was 3.2 ± 1.1. Total procedural time was 54 ± 25 minutes. Mean contrast volume was 41 ± 46 ml, with no contrast used in 16 patients. The feasibility endpoint was achieved in 95 patients (95%); 4 patients were not implanted due to unsuitable anatomy, and 1 patient had a leak >5 mm at 45 days. There was 1 periprocedural stroke and 2 gastrointestinal bleeds requiring transfusion at 7 days with no other major complications. Physicians' rating of overall ICE imaging quality was 4.6 ± 0.6.&lt;h4>Conclusions&lt;/h4>The novel 3-dimensional ICE VeriSight Pro Probe can safely and effectively guide LAAO with Watchman FLX using a simplified imaging protocol.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-05-26T03:08:32.12Z</modification><creation>2025-04-03T23:26:39.21Z</creation></dates><accession>S-EPMC11782859</accession><cross_references><pubmed>39898347</pubmed><doi>10.1016/j.jacadv.2024.101570</doi></cross_references></HashMap>