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2005, Number 4

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Arch Cardiol Mex 2005; 75 (4)

Patent ductus arteriosus closure with a NIT-Occluded device. Experience with 13 cases

Munayer CJE, Aldana PT, Lázaro CJL, San Luis MR, Ramírez RH, Amaya HA, Carpio HJC
Full text How to cite this article

Language: Spanish
References: 9
Page: 408-412
PDF size: 86.84 Kb.


Key words:

Nit-Occlud device, Percutaneous closure, Nitinol.

ABSTRACT

We report our experience with the percutaneous closure of patent ductus arteriosus with a Nit-Occlud device made of Nitinol (Nickel-Titanium alloy) in 13 patients; 10 women and 3 men, average age of 23.2 ± 21.1 years. Average diameters were 3.8 ± 0.8 mm and the morphologies, according to Krichenko’s classification, were 10 type A, 2 type E, and 1 type C. The device was selected according to the aortic ampule and the narrowest part of the ductus. We implanted 8 occluders of 11 x 6 mm, 4 of 9 x 6 mm, and 1 of 7 x 6 mm. In three patients (25%) total occlusion was observed 15 minutes after implantation, in seven (54%) a trivial leak was observed, and in only two patients (16.6%) was the leak moderate to severe. In on patient, the occluder migrate to the pulmonary artery trunk and was successfully removed percutaneously; the patient was subjected then to surgical closure. Echocardiography follow-up 24 h later showed total occlusion in nine patients (69%). Six months after the procedure, two patient presented trivial leak (15%). One patient developed an endocarditic infection and died. We concluded that this occluder might be useful for this pathology, but further studies must be done.


REFERENCES

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Arch Cardiol Mex. 2005;75