The aim of this study was to compare nifedipine and carvedilol in the treatment of de novo arterial hypertension after orthotopic liver transplantation (OLT). The study included 50 patients who developed arterial hypertension after OLT. Twenty-five patients received nifedipine (group A), and 25 received carvedilol (group B). Patients were defined as intolerant to nifedipine or carvedilol if severe adverse effects developed. These patients stopped the first drug and were switched to the other one. Patients were defined as full responders to monotherapy if there was normalization of blood pressure, and they were defined as partial responders by the need to add a second antihypertensive drug, ramipril. The 2 groups of patients were similar for baseline conditions. At the end of the study, patients intolerant to monotherapy were 48% of group A and 12.5% of group B (P Ͻ 0.01). Full responders were 20% of group A and 33.33% of group B (P Ͻ 0.01). Partial responders were 22% of group A and 54.1% of group B (P Ͻ 0.01). The addition of ramipril normalized blood pressure in 19% of partial responders to monotherapy (75% in partial responders to nifedipine and 30% in partial responders to carvedilol, P Ͻ 0.01). In responders to either monotherapy or combined therapy, there was a significant improvement of renal function. In responders to carvedilol, but not in responders to nifedipine, the daily dose of tacrolimus at 1 year should be reduced to 50% compared to the baseline dose to maintain the blood trough level in the therapeutic range. Liver Transpl 14: [1020][1021][1022][1023][1024][1025][1026][1027][1028] 2008. © 2008 AASLD.
Received September 30, 2007; accepted January 9, 2008.Liver transplantation is the standard care for end-stage liver disease and for fulminant hepatic failure. During recent years, advances in both medical management and surgical techniques have led to an increase in graft and patient survival following orthotopic liver transplantation (OLT). Nowadays, patient survival after OLT is about 85% at 5 years 1 and 70% at 10 years.
2Early mortality (within 1 year after OLT) has been reduced. The major causes of early mortality are infections, surgical complications, allograft failure due to primary allograft dysfunction, and allograft rejection.Late complications are increased because of the enhancement of survival after OLT. Major late complications are cardiovascular events, metabolic complications, renal dysfunction, disease recurrence, and malignancy. Arterial hypertension is one of the major late complications after liver transplantation and is an important risk factor for cardiovascular events. De novo arterial hypertension is defined as the development of arterial blood pressure Ͼ 140/90 mm Hg in patients that were normotensive before OLT.3 De novo arterial hypertension has a prevalence exceeding 50% after liver trans-