L2 S. M. Benjamin and N. C. Barnes
end-stage cardiomyopathy
[3]
. 24-year old Denise Darvall, who had suffered irreversible brain
injury following a road traffic accident, served as a donor. The blood groups of both the donor
and recipient were matched for compatibility. As soon as the donor was pronounced brain
dead and her cardiac contractions had completely stopped, her chest was opened surgically and
cardiopulmonary bypass was initiated
[4]
. Hypothermia was used to bring down the myocardial
temperature to 16
◦
C. The recipient’s heart was surgically excised and the donor heart was
soon placed inside the thoracic cavity of the recipient. Arterial anastomosis was established.
Cardiopulmonary bypass was restarted and electrical cardioversion applied to the heart ensuring
effective and co-ordinated ventricular contractions. The graft ischaemic time was 21 min. The
immunosuppressive regime post-transplant consisted of local irradiation to the transplanted
heart, azathioprine and prednisolone to counter possible immunologic rejection. Prophylactic
actinomycin C was administered for 3 days
[5]
.
Despite utmost sterile precautions observed during and after the transplant, the recipient
contracted Pseudomonas and Klebsiella pneumonia. The success of the procedure appeared to
be short-lived with the recipient expiring 18 days following the transplant despite the use of the
appropriate antibiotics.
Soon afterwards, Adrian Kantrowitz conducted the second human heart transplant on an 18-day
old infant with Ebstein’s malformation
[6]
. The baby died 5 h later from cardiac failure and
respiratory acidosis. Dr Christian Barnard attempted his second cardiac transplant early in 1968
on Dr Philip Blaibert, a 46-year-old man diagnosed with refractory congestive cardiac failure, severe
coronary artery disease and large left ventricular aneurysm. This operation assumed importance in
terms of the longest recipient survival time achieved thus far. The recipient survived for nearly 18
months post transplant. Duly acclaimed as a potentially life-saving measure for end-stage cardiac
disease, heart transplants had enormous impact worldwide, but were financially and ethically
controversial; at the end of the day it is an operation which can only help 50% of the population
at best. Nevertheless by the end of 1968 an unprecedented number of nearly 100 such procedures
had been performed.
However, the success story of cardiac transplants was curbed by the apparent short-term
recipient survival outcomes. The picture was grim in this respect with a 1 year survival rate of
only 20%. This was attributed to poor matching between donor and recipient, combined with an
equally poor understanding of immunosuppression. Invariably, its popularity soon dwindled with
the result that only a handful of cardiac transplants were conducted in the 1970s.
But they continued to be performed at a steady pace under Dr Shumway at Stanford University.
During this time, new methods of early diagnosis of allograft rejection using endomyocardial
biopsies of the heart, and its subsequent treatment, contributed to vastly improving the 1 year
and 5 year post-operative survival rates to 63% and 39% respectively. However, it was the discove ry
of cyclosporin A, a new immunosuppressive agent, which brought about dramatic increments in
recipient survival times. The 1 year and 5 year survival rates post transplant jumped to over 80%
and 60% respectively. This sparked a resurgence of interest in cardiac transplantation in the 1980s.
The introduction of cyclosporin A offered the distinct advantage in being able to reduce risk of acute
rejection and infection during the early months following transplant. The use of OKT3 monoclonal
antibodies and rabbit-derived anti-thymocyte globulin also played an important role in decreasing
early rejection rates.
Since then, phenomenal advances have been made, particularly relating to immunosuppression.
Current immunosuppressive strategy post transplant consists of cyclosporin A, azathioprine and
steroids. Some groups have advocated weaning patients off steroids altogether, or maintenance
on alternate low-dose therapy to offset the side effects. Tacrolimus, a potent immunosuppressive
agent, has now replaced cyclosporin A in many protocols especially in patients with persistent
rejection after renal, lung and heart transplant who were initially treated with cyclosporin A.
Mycophenolate mofetil (MMF), another relatively new agent, has been used instead of azathioprine
in cases of recurrent allograft rejection. Antilymphocyte serum or monoclonal anti-T cell antibodies
are presently used for treatment of steroid resistant rejection or an induction therapy.
Statistics regarding heart transplants have been recorded by the International Society for Heart
and Lung Transplantation (ISHLT), which was founded in 1981. It has been responsible for
maintaining a transplant registry since 1983. Quarterly reports are published by the ISHLT based on
data collected from transplant centres worldwide. These data show that average recipient survival
1 year and 3 years post orthotopic heart transplants performed between 1998 and 2002 stand at
83.9% and 77.4% respectively. In North America they are 85.1% and 78.1%
[7]
, while in Europe they are
documented at 81.2% and 75.6% respectively
[8]
. Analysis of the data also shows graft ischaemic time
to be a major determinant of survival outcomes. The shorter the duration of ischaemia, the bet ter