TY - JOUR
T1 - Transcatheter occlusion of patent ductus arteriosus with a new detachable coil system (DuctOcclud)
T2 - A multicenter clinical trial
AU - Oho, Shinichi
AU - Ishizawa, Akira
AU - Koike, Kazuyuki
AU - Kobayashi, Toshiki
AU - Nakanishi, Toshio
AU - Momma, Kazuo
AU - Ino, Toshihiro
AU - Nishimoto, Kei
AU - Ohkubo, Mataichi
AU - Ono, Yasuo
AU - Kamiya, Tetsuro
AU - Akagi, Teiji
AU - Kato, Hirohisa
PY - 1998/7
Y1 - 1998/7
N2 - A multicenter clinical trial of DuctOcclud, a new detachable coil for transcatheter occlusion of patent ductus arteriosus (PDA), was conducted. DuctOcclud was used in 35 patients (12 male and 23 female)for transcatheter occlusion of PDA between January, 1996, and April, 1997. The age of the patients ranged from 0.5 to 27.2 years (median 7.6 years) and weight from 6.3 to 70.0 kg (median 23.0 kg). The smallest diameter of PDA was 2.0±0.7 mm (range 1.0-3.3 mm). Pulmonary-systemic flow ratio (Qp/Qs) was 1.3 ± 0.3 (range 1.0-2.2). The coils were successfully implanted in 32 (91%) patients. Of 31 patients who were followed 6 months after the procedure, 26 (84%) had no residual shunt and 5 (16%) had trivial residual shunt. One patient had infective endocarditis 1 month after the procedure but recovered completely. There were no incidences of coil embolization, hemolysis, late coil migration, or pulmonary artery stenosis. We conclude that DuctOcclud is a safe and effective device of transcatheter occlusion of PDA.
AB - A multicenter clinical trial of DuctOcclud, a new detachable coil for transcatheter occlusion of patent ductus arteriosus (PDA), was conducted. DuctOcclud was used in 35 patients (12 male and 23 female)for transcatheter occlusion of PDA between January, 1996, and April, 1997. The age of the patients ranged from 0.5 to 27.2 years (median 7.6 years) and weight from 6.3 to 70.0 kg (median 23.0 kg). The smallest diameter of PDA was 2.0±0.7 mm (range 1.0-3.3 mm). Pulmonary-systemic flow ratio (Qp/Qs) was 1.3 ± 0.3 (range 1.0-2.2). The coils were successfully implanted in 32 (91%) patients. Of 31 patients who were followed 6 months after the procedure, 26 (84%) had no residual shunt and 5 (16%) had trivial residual shunt. One patient had infective endocarditis 1 month after the procedure but recovered completely. There were no incidences of coil embolization, hemolysis, late coil migration, or pulmonary artery stenosis. We conclude that DuctOcclud is a safe and effective device of transcatheter occlusion of PDA.
KW - Detachable coil
KW - DuctOcclud
KW - Patent ductus arteriosus
KW - Transcatheter occlusion
UR - http://www.scopus.com/inward/record.url?scp=0031848579&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0031848579&partnerID=8YFLogxK
U2 - 10.1253/jcj.62.489
DO - 10.1253/jcj.62.489
M3 - Article
C2 - 9707004
AN - SCOPUS:0031848579
SN - 0047-1828
VL - 62
SP - 489
EP - 493
JO - JAPANESE CIRCULATION JOURNAL
JF - JAPANESE CIRCULATION JOURNAL
IS - 7
ER -