Key result
Occlunix septal occluder achieves ~98% procedural success for secundum ASD closure without device-related complications.
Why the study?
Does the Occlunix septal occluder safely and effectively close secundum atrial septal defects in patients undergoing catheter closure?
Observational (n=56)
No
Does the Occlunix septal occluder safely and effectively close secundum atrial septal defects in patients undergoing catheter closure?
The Occlunix septal occluder demonstrates excellent technical and procedural success for secundum ASD closure with no complications and potentially lower costs compared to conventional devices.
Answers are grounded in this paper and cite their sources.
Suggests the Occlunix device may be a feasible option for secundum.
The Occlunix® septal occluder (OSO) is a new generation double disk occluder device for catheter closure of the secundum atrial septal defect (ASD). Fifty-six consecutive patients who underwent ASD device closure with the OSO between February 2022 and April 2024 were evaluated in this single-center observational study. All procedures were done under transesophageal echocardiography guidance. The OSO was successfully deployed in all patients (technical success 100%). Fifty-five patients had complete closure of the intervened ASD after device closure (procedural success 98.2%). The sole patient with trivial intradevice shunt had complete seal of the defect at 1-month follow-up. There were no device related complications – cardiac, vascular or systemic. During the follow-up period of 32.2 ± 9.1 months, the device position was satisfactory in all, with no complications. The OSO was associated with lower procedural cost than one of the most used conventional ASD occluders used in the country.
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Sharath et al. (2026) conducted an observational in secundum atrial septal defect (n=56). Occlunix septal occluder was evaluated on procedural success (complete closure of the intervened ASD). The Occlunix septal occluder achieved 100% technical success and 98.2% procedural success for catheter closure of secundum atrial septal defects, with no device-related complications.
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