Cardiac Transplantation
Cardiac transplantation is the treatment
of choice for otherwise healthy patients with end-stage heart disease so severe
that they are unlikely to survive the next 6–12 months. The procedure is
generally asso-ciated with 80–90% postoperative survival at 1 year and 60–90%
survival at 5 years. Transplantation improves the quality of life and most
patients are able to resume a relatively normal lifestyle. Unfortunately, the
number of cardiac transplants performed is limited by the supply of donor
hearts, which are obtained from brain-dead patients, most commonly following
intracranial hemorrhage or head trauma.Patients with intractable heart failure
have an ejection fraction of less than 20% and fall into NYHA functional class
IV and heart failure class D. For most
patients, the pri-mary diagnosis is cardiomyopathy. Intractable heart failure
may be the result of a severe con-genital lesion, ischemic cardiomyopathy,
viral cardiomyopathy, peripartum cardiomyopathy, a failed prior
transplantation, or valvular heart dis-ease. Medical therapy should include the
standard drugs used for heart failure, including angioten-sin-converting enzyme
inhibitors (or angiotensin receptor blockers, or both) and β blockade
(usu-ally with carvedilol). Other drugs may include diuretics, vasodilators,
and even oral inotropes; oral anticoagulation with warfarin may also be
necessary. Patients may not be able to survive without intravenous inotropes
while awaiting transplantation. Intraaortic balloon counterpulsa-tion, an LVAD,
or even a total mechanical heart may also be necessary.
Transplant candidates must not have
suffered extensive end-organ damage or have other major systemic illnesses.
Reversible renal and hepatic dysfunction are common because of chronic
hypo-perfusion and venous congestion. PVR must be normal or at least responsive
to oxygen or vasodi-lators. Irreversible pulmonary vascular disease is usually
associated with a PVR of more than 6–8 Wood units (1 Wood unit = 80 dyn·s·cm–5), and is a contraindication to orthotopic cardiac
transplan-tation because right ventricular failure is a major cause of early
postoperative mortality. Patients with long-standing pulmonary hypertension
may, however, be candidates for combined heart–lung transplantation.
Tissue cross-matching is generally not
per-formed. Donor–recipient compatibility is based on size, ABO blood-group
typing, and cytomegalovirus serology. Donor organs from patients with hepatitis
B or C or HIV infections are excluded.
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