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Early single clinical experience with the new Figulla ASD Occluder for

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dc.contributor.author Cansel, M
dc.contributor.author Pekdemir, H
dc.contributor.author Yagmur, J
dc.contributor.author Tasolar, H
dc.contributor.author Ermis, N
dc.contributor.author Kurtoglu, E
dc.contributor.author Acikgoz, N
dc.contributor.author Atas, H
dc.contributor.author Ozdemir, R
dc.date.accessioned 2022-10-19T07:42:33Z
dc.date.available 2022-10-19T07:42:33Z
dc.date.issued 2011
dc.identifier.uri http://hdl.handle.net/11616/81425
dc.description.abstract Background. Recently, the Occlutech Figulla ASD Occluder (FSO) has been introduced for transcatheter closure of atrial septal defects. This device can be used for transcatheter closure of small as well as large atrial septal defects.
dc.description.abstract Aims. To evaluate the feasibility and short-term results of transcatheter closure of secundum type atrial septal defects using the FSO device in adult patients.
dc.description.abstract Methods. Seventy-four consecutive adult patients were referred for transcatheter closure of secundum large atrial septal defects ("stretched" diameter > 20 mm and/or invasive pulmonary/systemic flow [Qp/Qs] ratio > 1.5) using the FSO device.
dc.description.abstract Results. The FSO device was successfully implanted in 68 patients (mean +/- SD [range] age: 31.8 +/- 12.3 [17-64] years; weight: 71.5 +/- 18.4 [49-98] kg). All patients had right atrial and ventricular volume overload with a mean Qp/Qs ratio of 2.5 +/- 0.6 (range 1.5-3.8). Mean atrial septal defect diameter was 22.3 +/- 4.8 (range 12-33) mm and the size of the implanted FSO was 24.1 +/- 4.9 (range 12-36) mm. Two patients had trivial (jet width <1 mm in diameter) residual shunts and one patient had a small (1-2 mm) residual shunt. There were no moderate or severe residual shunts. No device embolization or other serious complication occurred during either the procedure or the follow-up.
dc.description.abstract Conclusion. The present study found that transcatheter closure of isolated secundum atrial septal defects using the novel design of the FSO device was safe, effective, and had an excellent outcome during the 6 month follow-up period. (C) 2011 Elsevier Masson SAS. All rights reserved.
dc.description.abstract C1 [Cansel, Mehmet; Pekdemir, Hasan; Yagmur, Julide; Tasolar, Hakan; Ermis, Necip; Kurtoglu, Ertugrul; Acikgoz, Nusret; Atas, Halil; Ozdemir, Ramazan] Inonu Univ, Fac Med, TR-44100 Malatya, Turkey.
dc.source ARCHIVES OF CARDIOVASCULAR DISEASES
dc.title Early single clinical experience with the new Figulla ASD Occluder for
dc.title transcatheter closure of atrial septal defect in adults


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