Key result
Intracardiac echocardiography-guided left atrial appendage occlusion showed equivalent technical success rate (RR 1.01, 95% CI 1.00–1.02, P=0.24) and comparable complication risk (RR 0.94, 95% CI 0.82–1.09, P=0.43) compared to transesophageal echocardiography guidance in patients with atrial fibrillation.
Why the study?
Differences in safety, efficacy, and economics between ICE and TEE-guided LAAO needed systematic evaluation to provide an evidence-based rationale for image-guided modality selection.
Does intracardiac echocardiography (ICE) improve technical success and safety compared to transesophageal echocardiography (TEE) in patients with atrial fibrillation undergoing left atrial appendage occlusion?
Systematic Review
Yes
Does intracardiac echocardiography (ICE) improve technical success and safety compared to transesophageal echocardiography (TEE) in patients with atrial fibrillation undergoing left atrial appendage occlusion?
Effect estimate: RR 1.01 (95% CI 95% CI 1.00–1.02)
p-value: p=0.24
ICE and TEE provide equivalent technical success and safety for LAAO, but ICE may improve operational efficiency in younger patients and specific device subgroups.
Objective To systematically evaluate the differences in safety, efficacy, and economics between intracardiac ultrasound (ICE) and transesophageal echocardiography (TEE)-guided LAAO (LAAO), and to provide an evidence-based rationale for the selection of clinical image-guided modalities. Methods PubMed, Embase, Cochrane Library, Web of Science and Wanfang databases were searched to include randomized controlled trials and observational studies comparing ICE with TEE-guided LAAO, strictly following PRISMA guidelines. Two investigators independently screened the literature, extracted data and assessed the risk of bias (ROBINS-I and Cochrane tools). Meta-analysis was performed using RevMan 5.4.1, and the outcome indicators included technical success, procedure time, contrast dose, fluoroscopy time, complications, and economic parameters, and subgroup analyses were performed to explore the effects of factors such as patient characteristics and instrument type. Results A total of 16 studies were included.There was no significant difference between ICE and TEE in terms of technical success (RR = 1.01,95% CI 1.00–1.02, P = 0.24) and total risk of physical complications (RR = 0.94,95% CI 0.82–1.09, P = 0.43). Subgroup analysis showed: Operative efficiency ICE significantly reduced operative time in the subgroups of single-center studies (MD = −7.28 min, 95% CI: −9.46 to −5.10, P < 0.001), with AcuNav catheter (MD = −3.21 min, 95% CI: −6.20 to −0.19, P = 0.04), and patients aged <75 years (MD = −15.89 min, 95% CI: −18.95 to −12.82, P < 0.001); the use of multi-seal devices was associated with a significant reduction in contrast agent volume (MD = −21.69 mL, 95% CI: −31.44 to −11.94, P < 0.001). Disease characteristics In the subgroup with a hypertension proportion <90%, ICE shortened both operative time (MD = −12.00 min, 95% CI: −15.08 to −8.92, P < 0.001) and fluoroscopic time (MD = −9.32 min, 95% CI: −14.26 to −4.37, P = 0.003); however, operative time was prolonged in the ICE group for patients with a proportion of paroxysmal atrial fibrillation ≥50% (MD = 14.20 min, 95% CI: 7.60–20.80, P < 0.001). Economics ICE reduced professional/anesthesia-related costs (MD = -$2,654, P < 0.001) but increased hospitalization costs by approximately 17.8%, with notable geographic heterogeneity in total costs (comparable in the United States, but potentially higher for ICE in China based on existing cost structures). Sensitivity analyses showed good stability of the results, with heterogeneity (I 2 > 90%) mainly stemming from differences in study design and device type. Conclusion The core clinical outcomes (success and safety) of ICE and TEE in LAAO are equivalent, but operational efficiency is moderated by patient age, LV morphology, and device design. ICE is recommended for young, anatomically simple patients at high risk for anesthesia, and individualized decision-making needs to be optimized with team experience and health economic assessment. Future multicenter RCTs and cost-utility analyses are needed to validate long-term benefits. Systematic Review Registration PROSPERO CRD42024626272.
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Luo et al. (2026) conducted a systematic review in Patients with atrial fibrillation undergoing left atrial appendage occlusion (LAAO) guided by intracardiac echocardiography (ICE) or transesophageal echocardiography (TEE). Intracardiac echocardiography (ICE)-guided left atrial appendage occlusion vs. Transesophageal echocardiography (TEE)-guided left atrial appendage occlusion was evaluated on Technical success rate of left atrial appendage occlusion (successful device implantation without device-related complications) (RR 1.01, 95% CI 95% CI 1.00–1.02, p=0.24). Intracardiac echocardiography-guided left atrial appendage occlusion showed equivalent technical success rate (RR 1.01, 95% CI 1.00–1.02, P=0.24) and comparable complication risk (RR 0.94, 95% CI 0.82–1.09, P=0.43) compared to transesophageal echocardiography guidance in patients with atrial fibrillation.
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