Modified Pulmonary Artery to Left Atrium Bypass as Bridge to Lung Transplantation in Pulmonary Artery Hypertension

2015 ◽  
Vol 63 (S 01) ◽  
Author(s):  
N. Patil ◽  
A. Weymann ◽  
A. Sabashnikov ◽  
A.-F. Popov ◽  
A. Simon
Keyword(s):  
Pulmonary Artery ◽  
Lung Transplantation ◽  
Left Atrium ◽  
Pulmonary Artery Hypertension

scholarly journals Lung transplantation in six patients with idiopathic pulmonary artery hypertension

2021 ◽  
Vol 35 (1) ◽  
pp. S13-S13
Author(s):  
Hyeonhwa Kim ◽  
Dongkwan Kim ◽  
Sehoon Choi ◽  
Geundong Lee ◽  
Dongkyu Oh ◽  
...  
Keyword(s):  
Pulmonary Artery ◽  
Lung Transplantation ◽  
Pulmonary Artery Hypertension

Extracorporeal life support during and after bilateral sequential lung transplantation in patients with pulmonary artery hypertension

2020 ◽  
Vol 44 (6) ◽  
pp. 628-637 ◽  
Author(s):  
Andrea Dell’Amore ◽  
Alessio Campisi ◽  
Stefano Congiu ◽  
Sara Mazzarra ◽  
Saverio Pastore ◽  
...  
Keyword(s):  
Pulmonary Artery ◽  
Lung Transplantation ◽  
Life Support ◽  
Extracorporeal Life Support ◽  
Pulmonary Artery Hypertension

scholarly journals Idopathic Pulmonary Hypertension Mimicking Pulmonary Veno-Occlusive Disease – A Case Report.

2016 ◽  
Vol 01 (03) ◽  
pp. 029-032
Author(s):  
K. Prasad ◽  
A. Kumar
Keyword(s):  
Pulmonary Hypertension ◽  
Case Report ◽  
Pulmonary Artery ◽  
Lung Transplantation ◽  
Treatment Options ◽  
Pulmonary Artery Hypertension ◽  
Occlusive Disease ◽  
Idiopathic Pulmonary Hypertension ◽  
Worse Prognosis

AbstractPVOD is rare cause of pulmonary artery hypertension which is associated with worse prognosis and limited treatment options apart from lung transplantation. Differentiating IPAH patients from PVOD is sometimes difficult relying on catheterization data alone. But differentiation between these two diseases is important as there are many evolved treatment options for IPAH. Here we are reporting a case of IPAH where catheterization data shows conflicting results which on further evaluation diagnosis confirmed as idiopathic pulmonary hypertension.

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