2018
DOI: 10.1007/s11845-018-1895-x
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Trans-catheter paravalvular leak closure: a single-centre experience

Abstract: Patients with PVL represent a high-risk patient cohort. Percutaneous PVL offers a safe alternative to surgical PVL repair and appears particularly effective in those patients who present primarily with HF.

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Cited by 8 publications
(6 citation statements)
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“…The average time applied in the cohort was close to two hours, which correlates well with the work by previous authors. [ 10 15 ] A number of techniques were utilized in the cohort, including rail road, buddy wire or sequential delivery of multiple occluders, and have become our preferred approach in recent times. Interposing a hydrophilic wire across the PVL while releasing the occluder prevented the need for recrossing the defect in patients requiring multiple devices reducing the procedural time significantly.…”
Section: Discussionmentioning
confidence: 99%
“…The average time applied in the cohort was close to two hours, which correlates well with the work by previous authors. [ 10 15 ] A number of techniques were utilized in the cohort, including rail road, buddy wire or sequential delivery of multiple occluders, and have become our preferred approach in recent times. Interposing a hydrophilic wire across the PVL while releasing the occluder prevented the need for recrossing the defect in patients requiring multiple devices reducing the procedural time significantly.…”
Section: Discussionmentioning
confidence: 99%
“…Open surgical redo valve surgery for patients with asymptomatic bioprosthetic aortic regurgitation and acceptable surgical risk is a Class IIa recommendation 12 . However, many patients with PVR are symptomatic on presentation or are higher risk surgical candidates which make redo sternotomy and open valve replacement less appealing 13‐15 ; furthermore, many patients do not want to undergo another major operation. Recent data has shown equivalent outcomes with transcatheter procedures compared to surgery even though the transcatheter patients had more comorbidities 16‐18 .…”
Section: Discussionmentioning
confidence: 99%
“…While a number of devices have European approval, there are currently no occluder devices approved by the United States Food and Drug Administration specifically to treat PVR 19 . The majority of data surrounding these self‐expanding occluder devices are from procedures treating a focal jet of PVR and have shown a high degree of success (>85%) and minimal rates (3.8%‐10%) of procedural complications 9,10,13,14,20‐22 . Devices available include the Amplatzer vascular occluders, Amplatzer duct occluders, Amplatzer septal occluders, and Occlutech Paravalvular Leak Devices, with selection of specific device tailored to the patient (Figure 3).…”
Section: Discussionmentioning
confidence: 99%
“…74,75 For HF symptoms, there is strong evidence that correlates lower-grade residual regurgitation with enhanced clinical outcomes, 74 and therefore, good clinical improvements are well reported in these patients. [76][77][78][79] However, there is sparse and conflicting data for improved haemolysis; only 16% of patients in a UK PVL registry 32 had documented haemolysis and follow up was limited. Further, only 35 of the 362 patients from 12 studies included in a systematic review by Millan et al 80 were haemolysis patients, and the wide confidence intervals used in this study obviate meaningful interpolations.…”
Section: Heart Failure and Haemolysismentioning
confidence: 99%