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2000, Number 5

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Arch Cardiol Mex 2000; 70 (5)

Percutaneous oclussion of patent ductus arteriosus with Rashkind device

Munayer CJ, Maza JG, Aldana PT, San LMR, Ramírez RH, Lázaro CJL, Arias ML
Full text How to cite this article

Language: Spanish
References: 14
Page: 468-471
PDF size: 207.76 Kb.


Key words:

Rashkind device, Patent ductus arterious (PDA), Follow-up.

ABSTRACT

We present the results and follow up of ductus arteriosus closure with the Rashkind device. Sixty six devices were implanted in 63 patients, 41 women and 22 men, with a mean age of 8.2 years. We determined the diameter of the duct, the presence or absence of immediate residual leak at 3 months, 6 months, 1 year, and every year of follow-up by ecocardiography. The hemodynamic determinations showed: type A morphology in 49, type C in 7 and type E in 7; with a mean diameter of 4.2 ± 1.4 mm (range of 2.3 to 8.7mm) and a Qp/Qs 2.2 ± 1.5 (range 0.7 to 8.6). Fourty five 17 mm devices and 18 of 12 mm were used. The incidence of immediate residual leak was 65% (n-41); at 24 hrs. Post-procedure was 31.7% (n-20) and at one year 7.9% (n-5). Three patients with persistent leak had implantation of a second Rashkind device and one more patient an endovascular coil, the other patient is waiting for a second oclusor. Minor complications occurred in 15.8% (n-10). Results show an occlusion rate at 24 hrs of 68% and at one year of 92%; no patient presented migration of the device, hemolysis or obstruction of the pulmonary artery branches. We consider that occlusion of the ductus arteriosus with the Rashkind device is a safe and effective option for the treatment of this pathology.


REFERENCES

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Arch Cardiol Mex. 2000;70