2013
DOI: 10.1016/j.rec.2012.04.017
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Immediate and One-year Results in 35 Consecutive Patients After Closure of Left Atrial Appendage With the Amplatzer Cardiac Plug

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Cited by 46 publications
(51 citation statements)
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References 27 publications
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“…The procedural success (97%) and complication (8%) rates in this study are similar to that of published registries using the same devices but performed under general anaesthesia and TEE guidance [17][18][19][20][21] or conscious sedation and right-sided ICE guidance. 11 Two deaths occurred in the follow-up period.…”
Section: Discussionsupporting
confidence: 84%
See 1 more Smart Citation
“…The procedural success (97%) and complication (8%) rates in this study are similar to that of published registries using the same devices but performed under general anaesthesia and TEE guidance [17][18][19][20][21] or conscious sedation and right-sided ICE guidance. 11 Two deaths occurred in the follow-up period.…”
Section: Discussionsupporting
confidence: 84%
“…Although these deaths were not procedure-or device-related, they underline the importance of careful patient selection and limitations of anticoagulation discontinuation. Mean procedural (103 minutes) time is comparable or slightly longer than the average of 63-92 minutes reported in other ACP registries, 17,19,22 however, because no general anaesthesia is required, the catheterization room turnover time is likely * Because device implantation failed in 1 patient, the final grade of occlusion was measured in 36 patients only. Furthermore, the angiographic grade of occlusion was only measured in 35 patients because 1 of the patients underwent device implantation without angiography because of severe anaphylactic reaction to iodinated contrast media.…”
Section: Discussionmentioning
confidence: 72%
“…The Plaato device was the first device designed specifically for endocardial appendage exclusion but is no longer under development due to financial considerations (40). Small retrospective studies support the efficacy and safety of the Amplatzer cardiac plug for appendage exclusion (41)(42)(43)(44). However, randomized data are not available, and a randomized clinical trial was designed but could not be conducted due to failure to obtain the investigational device exemption from the FDA (45).…”
Section: Future Directions In Appendage Exclusionmentioning
confidence: 99%
“…Initial registry data reflected the technical improvements with a reduction of the embolisation rate to approximately 2% across a wide range of observational studies [13,14,[23][24][25][26]. Pericardial effusion leading to cardiac tamponade requiring interventions occurred in about 2% as did neurological events.…”
Section: Amplatzer Device Familymentioning
confidence: 99%