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1.
Catheter Cardiovasc Interv ; 85(3): 430-4, 2015 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-24905333

RESUMEN

Pulmonary arteriovenous malformations (PAVMs) are usually well-tolerated hemodynamically. Rarely, they cause severe neonatal cyanosis, requiring urgent treatment. We report the use of multiple transcatheter vascular occlusion devices to reduce right-to-left shunting in a neonate with multiple, large PAVMs.


Asunto(s)
Fístula Arteriovenosa/terapia , Cateterismo Cardíaco/instrumentación , Arteria Pulmonar/anomalías , Venas Pulmonares/anomalías , Fístula Arteriovenosa/complicaciones , Fístula Arteriovenosa/diagnóstico por imagen , Cianosis/diagnóstico , Cianosis/etiología , Humanos , Recién Nacido , Masculino , Arteria Pulmonar/diagnóstico por imagen , Venas Pulmonares/diagnóstico por imagen , Radiografía , Índice de Severidad de la Enfermedad , Resultado del Tratamiento
2.
Catheter Cardiovasc Interv ; 72(5): 691-5, 2008 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-18798238

RESUMEN

OBJECTIVES: We report the use of non-ferromagnetic embolization coils for transcatheter PDA closure. BACKGROUND: Transcatheter patent ductus arteriosus (PDA) closure has been performed for 40 years. A number of devices have been used with varying degrees of success. Gianturco embolization coils have been used frequently since 1992 with excellent results. These coils are a stainless steel alloy, and create an artifact when subsequent MRI imaging is performed. METHODS: Eight patients underwent right and left heart catheterization and transcatheter PDA closure. Angiography displayed a PDA with left to right shunting. The minimum PDA diameter was measured. An Inconel MReye coil was implanted using standard retrograde technique. A postimplant angiogram was performed. Evaluations were performed the following morning and after 2 months. RESULTS: The median age was 5.5 years, median weight was 24 kg. The PDA minimum diameter was 1.7 mm (range 1.4-2.4 mm), with a median Qp:Qs=1.33:1. In all patients, the PDA was completely immediately closed using one Inconel coil. Two patients also had a small aorto-pulmonary collateral vessel that was occluded using a separate Inconel coil. All patients had follow-up evaluation the following day; the PDA remained completely occluded and there was no obstruction of the pulmonary artery branches or descending aorta. Seven patients had subsequent follow-up and echocardiograms; the PDA remained completely occluded. There were no complications. CONCLUSION: The Inconel MReye coil is safe and effective for coil occlusion of small PDA and aorto-pulmonary vessels. Additional studies are needed to define the maximum vessel diameter for Inconel coil occlusion.


Asunto(s)
Aleaciones , Aorta , Cateterismo Cardíaco/instrumentación , Conducto Arterioso Permeable/terapia , Embolización Terapéutica/instrumentación , Arteria Pulmonar , Adolescente , Aorta/patología , Aorta/fisiopatología , Aortografía , Artefactos , Niño , Preescolar , Cineangiografía , Circulación Colateral , Angiografía Coronaria , Conducto Arterioso Permeable/patología , Conducto Arterioso Permeable/fisiopatología , Diseño de Equipo , Femenino , Humanos , Lactante , Imagen por Resonancia Magnética , Masculino , Arteria Pulmonar/patología , Arteria Pulmonar/fisiopatología , Circulación Pulmonar , Estudios Retrospectivos , Factores de Tiempo , Resultado del Tratamiento
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