29.11.2012 Views

THE OSTIA VENAE HEPATICAE AND THE RETHROHEPATIC ...

THE OSTIA VENAE HEPATICAE AND THE RETHROHEPATIC ...

THE OSTIA VENAE HEPATICAE AND THE RETHROHEPATIC ...

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

282<br />

INTERMEDIATE TERM FOLLOW-UP ON TRANSCA<strong>THE</strong>TER CLOSURE<br />

OF ATRIAL SEPTAL DEFECTS BY AMPLATZER TM SEPTAL OCCLUDER<br />

Kritvikrom Durongpisitkul, Jarupim Soongswang, Duangmanee Laohaprasitiporn, Apichart<br />

Nana.<br />

Division of Pediatric Cardiology, Department of Pediatrics. Faculty of Medicine, Siriraj Hospital,<br />

Mahidol University.<br />

Key words : ASD = Transcatheter closure of atrial septal defects<br />

Faculty of Medicine Siriraj Hospital<br />

(381)<br />

Background: Surgical repair of secundum atrial septal defects (ASD) is a safe procedure,<br />

however, it is associated with morbidity and thoracotomy scar. The Amplatzer TM Septal Occluder<br />

(ASO) is a new device designed for closure of ASD.<br />

Objective: We report our clinical experience with closure of ASD by using the ASO<br />

with intermediate term follow-up.<br />

Patients & Methods: Patients having ASD met established criteria for transcatheter<br />

closure were selected. Procedures were performed under general anesthesia. ASD was measured by<br />

transesophageal echocardiogram (TEE) and balloon occlusion method (stretched diameter). The ASO<br />

was chosen to be equal to ±1 mm of the stretched diameter. Device was advanced transvenously into a<br />

guiding sheath and deployed under fluroscopic and TEE guidance.<br />

Results : There were 26 patients with mean age of 17.2±15.9 years old (2 to 60) and<br />

mean weight of 22±37.5 kg (10.7 to 62.5). The mean ASD diameter measured by TEE was 18.3±5.2 mm.<br />

with stretched diameter of 22±7.5mm. Four patients who had ASD stretched diameter over 32 mm were<br />

excluded because of the larger size devices were not available. Device were deployed in 22 patients with<br />

size from 9 to 30 mm (median=22mm). Immediate after closure tiny residual shunt was observed at the<br />

core of the device in each case. At 24 hours only two patients had small (

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!