Transvenous closure of patent ductus arteriosus with Ivalon plugs - Multicenter experience with a new technique

Citation
R. Schrader et al., Transvenous closure of patent ductus arteriosus with Ivalon plugs - Multicenter experience with a new technique, INV RADIOL, 34(1), 1999, pp. 65-70
Citations number
29
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
INVESTIGATIVE RADIOLOGY
ISSN journal
00209996 → ACNP
Volume
34
Issue
1
Year of publication
1999
Pages
65 - 70
Database
ISI
SICI code
0020-9996(199901)34:1<65:TCOPDA>2.0.ZU;2-U
Abstract
RATIONALE AND OBJECTIVE. The authors assess the clinical efficacy of transv enous closure of patent ductus arteriosus (PDA) with a new plug consisting of Ivalon foam and a platinum/iridium frame with four aortic and two pulmon ary nitinol struts. The most widely used devices for transcatheter treatmen t of PDA (Porstmann plug, Rashkind umbrella, Botallo occluder, coils) have specific limitations inherent to their design (eg, transarterial approach, residual shunts, limited retrieval). METHODS. Between 1994 and 1997, PDA closure was attempted in 33 children an d 67 adolescents and adults in 7 clinical centers; PDA diameter was 2 to 11 mm, Plug diameter was 6 to 20 mm, and 8 to 16 F venous sheaths were used f or insertion. RESULTS. Placement was successful in 98% (with a single plug in 88%, and a second or third plug in 10%) and unsuccessful in 2%. Plugs were retrieved a fter malpositioning in 12 of 12 patients and after pulmonary embolization i n 2 of 3 patients. One patient underwent surgery for removal of an embolize d plug, Complete PDA closure was proved by aortography and color Doppler ec hocardiography in 85% (40 of 43 patients with a PDA 2-3.9 mm, 30 of 36 pati ents with a PDA 4-5.9 mm, and 15 of 21 patients with a PDA 6-11 mm), During a median follow-up interval of 16 months, there were no complications (inf ection, hemolysis, fracture, embolization). CONCLUSION. The new plug device can be used successfully in patients with a PDA diameter up to 11 mm, Further investigations are underway to determine the definite clinical value of this technique.