Bronchial compression by a patent ductus arteriosus associated with pulmonary atresia

1985 ◽  
Vol 144 (3) ◽  
pp. 535-540 ◽  
Author(s):  
RI Markowitz ◽  
JT Fahey ◽  
WE Hellenbrand ◽  
GS Kopf ◽  
P Rothstein
2012 ◽  
Vol 23 (2) ◽  
pp. 197-202 ◽  
Author(s):  
Mazeni Alwi ◽  
Rahmat R. Budi ◽  
Marhisham Che Mood ◽  
Ming C. Leong ◽  
Hasri Samion

AbstractObjectiveTo determine the feasibility and safety of the Conquest Pro wire as an alternative to radiofrequency wire for perforation of atretic pulmonary valve and subsequent balloon dilatation and patent ductus arteriosus stenting in patients with pulmonary atresia with intact ventricular septum.BackgroundRadiofrequency valvotomy and balloon dilatation has become the standard of care for pulmonary atresia with intact ventricular septum in many institutions today.MethodsWe report eight consecutive patients in whom we used the Conquest Pro coronary guidewire, a stiff wire normally reserved for revascularisation of coronary lesions with chronic total occlusion, for perforation of atretic pulmonary valve and subsequent balloon dilatation, and stenting of the patent ductus arteriosus.ResultsPerforation of atretic pulmonary valve was successful in seven out of eight cases. Radiofrequency valvotomy was employed after failure of perforation by the Conquest Pro wire in one case where the right ventricular outflow tract was broad based and tapered towards the pulmonary valve, and was heavily trabeculated. Failure of the Conquest Pro wire to perforate the pulmonary valve plate was mainly attributed by the failure to engage the wire at the correct position.ConclusionThe Conquest Pro wire for perforation and subsequent interventions in the more straightforward cases of pulmonary atresia with intact ventricular septum is effective and safe, simplifying the entire procedure. However, the radiofrequency generator and wires remain essential tools in the paediatric interventional catheter laboratory.


2013 ◽  
Vol 95 (6) ◽  
pp. e143-e145
Author(s):  
Gerard J. Fitzmaurice ◽  
David M. Coleman ◽  
Kevin P. Walsh ◽  
Paul Oslizlok ◽  
John D. Russell ◽  
...  

2008 ◽  
Vol 4 (2) ◽  
pp. 81-83 ◽  
Author(s):  
Yoichi Kawahira ◽  
Kyoichi Nishigaki ◽  
Hideto Ozawa ◽  
Tsugutoshi Suzuki

2015 ◽  
Vol 6 (4) ◽  
pp. 96-98
Author(s):  
Rema V Nair ◽  
Velayudhan Nair ◽  
RV Mookambika ◽  
RG Mohandas Rao ◽  
SN Somayaji

We report a case of multiple congenital anomalies in a female newborn infant, born to themother from a hill tribe. The Doppler echocardiography of the baby showed large atrial septaldefect amounting to single atrium, atretic left atrioventricular valve, large single right sidedventricle, aorta shifted to the left arising from single ventricle and diminutive hypoplasticleft ventricle. Right atrioventricular valve was normal forming single inlet into the ventricle.Pulmonary artery was small and hypoplastic and no antegrade fl ow was observed in it. Thepatient was diagnosed as having single ventricle, pulmonary atresia, patent ductus arteriosus(PDA) and major aortopulmonary collateral artery (MAPCA).DOI: http://dx.doi.org/10.3126/ajms.v6i4.7660Asian Journal of Medical Sciences Vol.6(4) 2015 96-98 


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