Initial Experience in Adults with Complex Congenital Heart Disease Treated with Sacubitril/Valsartan for Heart Failure

2020 ◽  
Vol 39 (4) ◽  
pp. S238-S239
Author(s):  
T.L. Goodwin ◽  
C.R. Broda ◽  
A. Opina ◽  
W. Lam ◽  
P.R. Ermis
2020 ◽  
Vol 300 ◽  
pp. 137-140 ◽  
Author(s):  
Susanne J. Maurer ◽  
Claudia Pujol Salvador ◽  
Sandra Schiele ◽  
Alfred Hager ◽  
Peter Ewert ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-12 ◽  
Author(s):  
Christine H. Attenhofer Jost ◽  
Dörthe Schmidt ◽  
Michael Huebler ◽  
Christian Balmer ◽  
Georg Noll ◽  
...  

Due to impressive improvements in surgical repair options, even patients with complex congenital heart disease (CHD) may survive into adulthood and have a high risk of end-stage heart failure. Thus, the number of patients with CHD needing heart transplantation (HTx) has been increasing in the last decades. This paper summarizes the changing etiology of causes of death in heart failure in CHD. The main reasons, contraindications, and risks of heart transplantation in CHD are discussed and underlined with three case vignettes. Compared to HTx in acquired heart disease, HTx in CHD has an increased risk of perioperative death and rejection. However, outcome of HTx for complex CHD has improved over the past 20 years. Additionally, mechanical support options might decrease the waiting list mortality in the future. The number of patients needing heart-lung transplantation (especially for Eisenmenger’s syndrome) has decreased in the last years. Lung transplantation with intracardiac repair of a cardiac defect is another possibility especially for patients with interatrial shunts. Overall, HTx will remain an important treatment option for CHD in the near future.


2014 ◽  
Vol 10 (5) ◽  
pp. 387-395 ◽  
Author(s):  
Elaine Y. Lin ◽  
Hillel W. Cohen ◽  
Ami B. Bhatt ◽  
Ada Stefanescu ◽  
David Dudzinski ◽  
...  

2005 ◽  
Vol 15 (4) ◽  
pp. 434-436 ◽  
Author(s):  
Dursun Alehan ◽  
Omer Faruk Dogan

Ventricular noncompaction is a rare unclassified cardiomyopathy occurring because of arrest of the normal intrauterine compaction of the loose luminal component of the ventricular myocardium. There is limited data regarding its diagnosis and outcome in children. It is recognised, however, that right ventricular involvement is extremely rare. We report a case in which only the right ventricular myocardium was noncompacted, a situation which led to heart failure soon after birth.


2021 ◽  
Vol 9 ◽  
pp. 232470962110433
Author(s):  
Sofia Lakhdar ◽  
Chandan Buttar ◽  
Sameen Hassan ◽  
Most Sirajum Munira ◽  
Theo Trandafirescu

A 60-year-old woman presented to the emergency department with worsening shortness of breath and non-productive cough for 1 week, which was preceding a recent COVID-19 infection. At the time the patient thought this was part of the constellation of symptoms of COVID-19, so she stayed home until her symptoms worsened to the point of needing hospitalization. The patient was found to have a rare and complex congenital heart disease that led her to develop acute heart failure precipitated by COVID-19 pneumonia. Medical management and surgical repair were essential in this patient given the late presentation.


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