scholarly journals Noninvasive assessment of donor and native heart function after heterotopic heart transplantation

1988 ◽  
Vol 95 (1) ◽  
pp. 75-81 ◽  
Author(s):  
Margaret D. Allen ◽  
Corrie A. Naasz ◽  
Richard L. Popp ◽  
Sharon A. Hunt ◽  
Michael L. Goris ◽  
...  
2019 ◽  
Vol 46 (3) ◽  
pp. 199-202
Author(s):  
Elizabeth L. Godfrey ◽  
Michael L. Kueht ◽  
Abbas Rana ◽  
O.H. Frazier

Substantial technological advances in mechanical circulatory support have caused a shift in the management of end-stage heart failure. From the 1970s through the 1990s, heterotopic heart transplantation was routinely performed in patients in whom orthotopic transplantation was likely to fail. Heterotopic heart transplantation is now performed less often because modern mechanical circulatory assist devices are routinely used as bridges to orthotopic transplantation; regardless, the operation has helped numerous patients who would not otherwise have received adequate allografts. We describe the case of a man with idiopathic nonischemic cardiomyopathy who, at age 17, was given an ABO- and size-matched heterotopic allograft that was a complete human leukocyte antigen mismatch. The graft functioned normally for 20 years until the patient had a myocardial infarction that necessitated placement of a coronary artery stent. Subsequent treatments involved many interventions, including insertion of an intra-aortic balloon pump, medical therapy for heart failure, implantation of a total artificial heart, and, ultimately, orthotopic transplantation. To our knowledge, our patient is the longest surviving recipient of a heterotopic heart transplant, with a remarkable 25-year graft survival despite poor histocompatibility and an almost complete lack of native heart function. The strategies used for his treatment make him a living case study that can add valuable information to the history of cardiac support.


2011 ◽  
Vol 59 (S 01) ◽  
Author(s):  
J Sindermann ◽  
I Alejnik ◽  
J Hoffmann ◽  
S Klotz ◽  
A Löher ◽  
...  

2016 ◽  
Vol 37 (44) ◽  
pp. 3356-3356 ◽  
Author(s):  
Charles Roux ◽  
Shaida Varnous ◽  
Pascal Leprince ◽  
Philippe Cluzel

1995 ◽  
Vol 75 (5) ◽  
pp. 415-417 ◽  
Author(s):  
Richard P.W. Cowell ◽  
Jayne Morris-Thurgood ◽  
John G. Coghlan ◽  
Charles D.J. Ilsley ◽  
Andrew G. Mitchell ◽  
...  

1989 ◽  
Vol 98 (3) ◽  
pp. 457-459
Author(s):  
Albert de Roos ◽  
Joost Doornbos ◽  
Albert V.G. Bruschke ◽  
Ad. E. van Voorthuisen ◽  
Magdi Yacoub

Author(s):  
N. V. Grudinin ◽  
V. K. Bogdanov ◽  
M. G. Sharapov ◽  
N. S. Bunenkov ◽  
N. P. Mozheiko ◽  
...  

Peroxiredoxin 6 (Prdx6) is an antioxidant enzyme in the human body that performs a number of important functions in the cell. Prdx6 restores a wide range of peroxide substrates, thus playing a leading role in maintaining redox homeostasis in mammalian cells. In addition to peroxidase activity, Prdx6 has an activity of phospholipase A2, thus taking part in membrane phospholipid metabolism. Due to its peroxidase and phospholipase activity, Prdx6 participates in intracellular and intercellular signal transmission, thereby facilitating the initiation of regenerative processes in the cell, suppression of apoptosis and activation of cell proliferation. Given the functions performed, Prdx6 can effectively deal with oxidative stress caused by various factors, including ischemia-reperfusion injury. On an animal model of rat heterotopic heart transplantation, we showed the cardioprotective potential of exogenous recombinant Prdx6, introduced before transplantation and subsequent reperfusion injury of the heart. It has been demonstrated that exogenous Prdx6 effectively alleviates the severity of ischemia-reperfusion injury of the heart by 2–3 times, providing normalization of its structural and functional state during heterotopic transplantation. The use of recombinant Prdx6 can be an effective approach in preventing/alleviating ischemia-reperfusion injury of the heart, as well as in maintaining an isolated heart during transplantation.


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