Literature DB >> 9441155

[Heart transplantation--state of the art today].

B M Meiser1, W von Scheidt, M Weis, D Böhm, F Kur, J Koglin, H Reichenspurner, P Uberfuhr, B Reichart.   

Abstract

In spite of pharmacological progress, end stage congestive heart failure is still associated with a decrease in quality and expectation of life. Heart transplantation remains the last therapeutic option for these patients. While the one year survival rate has increased over the last few years up to 84%, a major problem remains the significant lack of donors. Therefore, the criteria for the selection of candidates for cardiac transplantation have to be kept quite tight: Evidence of poor outcome without transplantation is associated with ejection fractions below 20 to 25%, cardiac indices less than 2.01/min/m2, left ventricular filling pressure above 20 mm Hg and a enddiastolic diameter of > 80 mm. There are, however, also quite important functional parameters indicating the need for heart transplantation, e.g. the maximal oxygene uptake being less than 10 ml/kg/min or below 50% of the age-appropriate value. Elevated pulmonary vascular resistance above 4 to 5 Wood units without a significant decrease during application of prostaglandin derivatives or inhalation of NO represents a contraindication for orthotopic heart transplantation; alternatively, a heterotopic transplantation can be considered. Since there is a significant shortage of suitable donor organs, the donor criteria have been broadened, e. g. the accepted donor age was increased to 60 years. Based on these extended criteria, a careful donor evaluation including cardiac history, cardiac examination, ECG and echocardiogram has to be performed. Coronary angiography in older donors is suggested, but in many cases not possible due to circumstances. Further precondition for a good graft function is a sophisticated donor management until the time of explantation. Hypovolemia and hypocalemia, hypothermia, hypoxia and rapid lost of circulating triiodothyronine (T3) have to be detected and balanced. The cardioplegic solution used might not only have an impact on the immediate postoperative performance of the graft, but also on the long term outcome, particularly with regard to graft vessel disease. There are generally two types of solutions: Those with intracellular and those with extracellular electrolyte concentrations. In addition, the potassium concentration might be of some importance. Potassium seems to damage endothelial cells and trigger subsequent immunological reactions. Therefore, high potassium concentrations in the cardioplegic solution might correlate with the incidence of graft vessel disease during the long term follow-up. The surgical technique for orthotopic heart transplantation developed at the beginning of the sixties by Lower and Shumway has been used unchanged for the last 30 years. The only alteration recently introduced is the separate direct anastomosis of the pulmonary and systemic veins in order to improve the atrial function. Until recently the commonly employed immunosuppressive strategy after heart transplantation consisted of the standard drugs cyclosporin, azathioprin and prednisolon. Some transplant-units use additionally induction therapy with antibody preparations. Many centers, however, abolished this regimen due to significant short and long term side effects. Promising new, more specific antibodies (which are chimerized or humanised) could revive the induction concept. The most thoroughly tested novel immunosuppressive agent is tacrolimus (FK506). It has been demonstrated to be 10 to 100 times more potent than cyclosporin A in in vitro and in vivo models. It binds to a different binding protein (FK-binding-protein) than cyclosporin (cyclophilin), but has a similar mechanism of action inhibiting the expression of T-cell-activator genes for certain cytokines. First non-randomised studies after heart transplantation performed at the University of Pittsburgh revealed that significantly more tacrolimus than cyclosporin patients were free of rejection. In order to confirm these observations, we performed a prospective randomised controlled clin

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Year:  1997        PMID: 9441155     DOI: 10.1007/bf03044252

Source DB:  PubMed          Journal:  Herz        ISSN: 0340-9937            Impact factor:   1.443


  91 in total

1.  Contractility of the transplanted, denervated human heart.

Authors:  W von Scheidt; J Neudert; E Erdmann; B M Kemkes; J M Gokel; G Autenrieth
Journal:  Am Heart J       Date:  1991-05       Impact factor: 4.749

2.  Expression of major histocompatibility antigens and vascular adhesion molecules on human cardiac allografts preserved in University of Wisconsin solution.

Authors:  A Ardehali; H Laks; D C Drinkwater; N S Kato; L C Permut; P W Grant; A S Aharon; T A Drake
Journal:  J Heart Lung Transplant       Date:  1993 Nov-Dec       Impact factor: 10.247

3.  Does rapidity of development of transplant coronary artery disease portend a worse prognosis?

Authors:  S Z Gao; S A Hunt; J S Schroeder; E Alderman; I R Hill; E B Stinson
Journal:  J Heart Lung Transplant       Date:  1994 Nov-Dec       Impact factor: 10.247

4.  Single-center randomized trial comparing tacrolimus (FK506) and cyclosporine in the prevention of acute myocardial rejection.

Authors:  B M Meiser; P Uberfuhr; A Fuchs; D Schmidt; M Pfeiffer; D Paulus; C Schulze; S Wildhirt; W V Scheidt; C Angermann; V Klauss; S Martin; H Reichenspurner; E Kreuzer; B Reichart
Journal:  J Heart Lung Transplant       Date:  1998-08       Impact factor: 10.247

5.  Cytomegalovirus infection is associated with cardiac allograft rejection and atherosclerosis.

Authors:  M T Grattan; C E Moreno-Cabral; V A Starnes; P E Oyer; E B Stinson; N E Shumway
Journal:  JAMA       Date:  1989 Jun 23-30       Impact factor: 56.272

6.  Treatment of cutaneous T-cell lymphoma by extracorporeal photochemotherapy. Preliminary results.

Authors:  R Edelson; C Berger; F Gasparro; B Jegasothy; P Heald; B Wintroub; E Vonderheid; R Knobler; K Wolff; G Plewig
Journal:  N Engl J Med       Date:  1987-02-05       Impact factor: 91.245

Review 7.  Purine metabolism and immunosuppressive effects of mycophenolate mofetil (MMF).

Authors:  A C Allison; E M Eugui
Journal:  Clin Transplant       Date:  1996-02       Impact factor: 2.863

8.  Early endothelial dysfunction predicts the development of transplant coronary artery disease at 1 year posttransplant.

Authors:  S F Davis; A C Yeung; I T Meredith; F Charbonneau; P Ganz; A P Selwyn; T J Anderson
Journal:  Circulation       Date:  1996-02-01       Impact factor: 29.690

9.  Acetylcholine-induced constriction of angiographically normal coronary arteries is not time dependent in transplant recipients. Effects of stepwise infusion at 1, 6, 12 and more than 24 months after transplantation.

Authors:  A Nitenberg; C Benvenuti; E Aptecar; I Antony; P Deleuze; D Loisance; J P Cachera
Journal:  J Am Coll Cardiol       Date:  1993-07       Impact factor: 24.094

10.  The spectrum of coronary artery pathologic findings in human cardiac allografts.

Authors:  D E Johnson; S Z Gao; J S Schroeder; W M DeCampli; M E Billingham
Journal:  J Heart Transplant       Date:  1989 Sep-Oct
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