Objective-To report the total UK multicentre experience of a novel art
erial occlusion device (Duct Occlud pfm). Design-Descriptive study of
selected non-randomised paediatric patients with a variety of aortopul
monary connections. Setting-Five UK tertiary referral centres for cong
enital heart disease. Patients and methods-Between March 1994 and Febr
uary 1995, 57 children aged 2 weeks to 14 years (median 50 months) und
erwent attempted closure of their aortopulmonary connection. Fifty one
had persistent arterial ducts and 9 of them had had a Rashkind umbrel
la device implanted. Five patients had superfluous modified Blalock-Ta
ussig shunts (mBTS). in one there was also a native major aortopulmona
ry collateral artery (MAPCA). Another patient had a native major aorto
pulmonary connection (APC). Transcatheter occlusion was attempted in a
ll cases through a 4 F delivery catheter. Results-Devices were success
fully deployed in 49/57 (86%) patients. Seven of 51 cases with persist
ent arterial ducts were judged too large for the device and a Rashkind
umbrella was used. 40 (91%) of the 43 in whom the detachable coil dev
ice was used had complete occlusion at 24 hours on colour flow Doppler
echocardiography. Devices were successfully deployed in all 6 remaini
ng patients (4 mBTS, 1 mBTS + MAPCA, and 1 APC). Embolisation of a dev
ice occurred on 4 occasions. Two devices were not retrieved but caused
no apparent clinical problems. Conclusion-This novel detachable coil
type occlusion system compares favourably with other methods of transc
atheter occlusion of native, residual, or surgically created aortopulm
onary shunts. The delivery system allows its use in small children.