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Transcatheter closure of very large secundum atrial septal defects: long-term follow-up study
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Aims
To evaluate the efficacy and safety of transcatheter closure of very large secundum atrial septal defects (ASD) with long-term follow-up results.
Methods and results
From June, 2001 to June, 2008, 74 patients diagnosed as secundum atrial septal defect with a diameter more than 30 mm were enrolled in the study. Percutaneous closure of ASDs were attempted by using the Domestic Shanghai ASD-O guided by transthoracic echocardiography (TTE). For the group of the 74 patients, 68 of them are adults. The closure was successful in 71/74 patients (96%). The mean diameter of the device was 38.2±2.73 mm. During the follow-up, complete closure could be achieved in 100% of patients. 7 adverse events (9.9%) were reported. Most adverse events were categorised as minor and there was one major adverse events (1.4%).
Conclusion
Transcatheter device closure is an effective management option for patients with very large ASD. Serious complications were rare.
Title: Transcatheter closure of very large secundum atrial septal defects: long-term follow-up study
Description:
Aims
To evaluate the efficacy and safety of transcatheter closure of very large secundum atrial septal defects (ASD) with long-term follow-up results.
Methods and results
From June, 2001 to June, 2008, 74 patients diagnosed as secundum atrial septal defect with a diameter more than 30 mm were enrolled in the study.
Percutaneous closure of ASDs were attempted by using the Domestic Shanghai ASD-O guided by transthoracic echocardiography (TTE).
For the group of the 74 patients, 68 of them are adults.
The closure was successful in 71/74 patients (96%).
The mean diameter of the device was 38.
2±2.
73 mm.
During the follow-up, complete closure could be achieved in 100% of patients.
7 adverse events (9.
9%) were reported.
Most adverse events were categorised as minor and there was one major adverse events (1.
4%).
Conclusion
Transcatheter device closure is an effective management option for patients with very large ASD.
Serious complications were rare.
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