Heart transplantation in Chagas’ disease

Abstract

Among the several etiologies of heart failure, the chagasic myocardiopathy is considered the most aggressive. Once there is no treatment capable of reverting the disease evolution, the heart transplantation becomes the only option. We analyzed 107 patients with Chagas disease submitted to heart transplantation, aged between 11 and 62 years (42.7 ± 15.3 years). Patients with symptomatic megacolon and megaesophagus are automatically excluded from transplant programs due to a higher possibility of postoperative short and long term complications. The expectation of inferior results for the transplantation of chagasic patients in comparison with other myocardiopathies was not confirmed and, paradoxically, were found better survival rates. We noticed an immediate mortality rated in 17.7% (19 cases), whose main cause of death were: infection (6 cases, 31.5%), graft dysfunction (6 cases, 31.5%), rejection (4 cases 21,1%), sudden cardiopulmonary arrest (2 cases 10.5%) and ABO incompatibilities (1 case 5,3%). Late after transplant, 27 (25.2%) patients died, and the major causes were: rejection (6 cases, 22.2%), infection (6 casos, 22.2%), lymphoma (4 cases, 14.8%), Kaposi sarcoma (2 cases, 7.4%), constrictive pericarditis (2 cases, 7.4%) and Chagas disease reactivation in the central nervous system (1 case, 7.1%). Finally, the conclusions are: 1) heart transplantation is still the only way to modify the natural course of chagasic myocardiopathy, 2) early diagnosis coupled to the rapid introduction of benzonidazol leads to a pattern recognition of normal myocardial histology without sequelae and 3) the doses of immunosuppressants used should be lower than those used in other etiologies.