2019
DOI: 10.1016/j.jcin.2019.02.003
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Incidence, Characterization, and Clinical Impact of Device-Related Thrombus Following Left Atrial Appendage Occlusion in the Prospective Global AMPLATZER Amulet Observational Study

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Cited by 73 publications
(49 citation statements)
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“…In 2019, Aminian reported the results of a global observational study on the occurrence of DRT after Amulet occluder implantation. In 1078 patients with AF implanted with the Amulet device, 17 patients had DRT by the 1‐year follow‐up, with an annual rate of 1.7%, and one patient had recurrent DRT 9 . In 2017, Lempereur et al summarized 30 studies including 1 randomized controlled trial and 29 multi‐center registration studies, single‐center reviews, or case reports.…”
Section: Incidence Of Drt In Real‐world Clinical Practicementioning
confidence: 99%
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“…In 2019, Aminian reported the results of a global observational study on the occurrence of DRT after Amulet occluder implantation. In 1078 patients with AF implanted with the Amulet device, 17 patients had DRT by the 1‐year follow‐up, with an annual rate of 1.7%, and one patient had recurrent DRT 9 . In 2017, Lempereur et al summarized 30 studies including 1 randomized controlled trial and 29 multi‐center registration studies, single‐center reviews, or case reports.…”
Section: Incidence Of Drt In Real‐world Clinical Practicementioning
confidence: 99%
“…The criteria included an echo density on the LA aspect of the device: (a) not explained by imaging artifacts; (b) inconsistent with normal healing/device incorporation; (c) visible in multiple TEE planes, (d) in contact with the WATCHMAN device; and (e) exhibiting independent motion 25 . The criteria of DRT in the Prospective Global AMPLATZER Amulet Observational Study were defined as an echocardiographic or computed tomography (CT) density on the LA aspect of the device: (a) not explained by imaging artifact; (b) inconsistent with normal healing; (c) visible in multiple TEE or CT planes; and (d) in contact with the device 9 . Saw et al reported their preliminary experience of using CT as an alternative to TEE for post‐procedural surveillance with the ACP device.…”
Section: Diagnosis Of Drtmentioning
confidence: 99%
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“…Few studies have investigated the ability of DOACs to prevent thrombosis in patients with implanted devices. The RE-ALIGN study compared dabigatran to warfarin in patients with mechanical heart valve prostheses, but the study was prematurely stopped due to excess of bleeding and thrombotic events [8]. More recently, the GALILEO trial of rivaroxaban after transcatheter aortic valve insertion was stopped early due to patient harm [9,10].…”
Section: Discussionmentioning
confidence: 99%
“…More recently, the GALILEO trial of rivaroxaban after transcatheter aortic valve insertion was stopped early due to patient harm [9,10]. It has been hypothesized that foreign artificial materials implanted in the heart, such as valve prostheses and possibly also occluder devices, may trigger the tissue pathway of coagulation on the artificial surface, a pathway that is unaffected by DOACs [8]. Such a mechanism could potentially lead to device thrombosis.…”
Section: Discussionmentioning
confidence: 99%