Abstract

Abstract. In previous studies in humans, mannito (20%, 250 ml) has been shown to reduce the in cidence of acute renal failure (ARF) after transplan tation from 54% to 19%. In rats, atrial natriuretic peptide appears to prevent ischemia-induced ARF We therefore decided to evaluate the effects of α-human atrial natriuretic peptide (α-h-ANP) both alone and combined with mannitol during transplantation in humans. First, we demonstrated thai systemic α-h-ANP infusion during kidney transplantation was safe in dosages up to 0. 08 μg/kg pei minute. In these patients the calculated metabolic clearance rate of α-h-ANP was relatively low ranging from 0. 68 to 1. 801/min. In a second study of 11 renal graft recipients, no mannitol was used and α-h-ANP (0. 05 μg/kg per minute) was infused into the donor kidney artery during transplantation for 46 ± 2min, followed by IV administration for 71 ± 2 min. Our aim was to reduce the incidence of ARF. Nevertheless, ARF occurred immediately after surgery in four of the patients (36%) in this group and, as a result, mannitol was reintroduced. A third group of nine renal graft recipients received α-h-ANP (total dose 400 μg) as five IV injections within 90 min after transplantation. ARF occurred in four of these patients (44%). We conclude that α-h-ANP, administered according to the aforementioned protocols in such small groups of patients, does not seem to be of value in the prevention of ARF after transplantation.

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