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Clin Drug Investig ; 26(4): 195-202, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17163251

RESUMO

BACKGROUND: Hyperhomocysteinaemia is an independent cardiovascular risk factor in patients with renal disease. The current study aimed to determine the effect of intravenous N-acetylcysteine on plasma homocysteine levels when administered during haemodialysis in patients with end-stage renal failure. PATIENTS AND METHODS: Sixty patients with end-stage renal failure were randomised to receive a 4-hour intravenous infusion of N-acetylcysteine or placebo during a 4-hour haemodialysis session. Plasma homocysteine levels were measured before and after haemodialysis. Haemodynamic parameters, including pulse pressure, were also measured. RESULTS: After haemodialysis in the placebo treatment group, plasma homocysteine was reduced by 23.7% from the pre-dialysis level, whereas patients treated with N-acetylcysteine exhibited an 88.3% decrease (p < 0.001). Reduction of plasma homocysteine concentration was significantly correlated with a reduction of pulse pressure (p = 0.001). A 10% decrease in plasma homocysteine concentration was associated with a 1.45mm Hg decrease in pulse pressure. CONCLUSIONS: Intravenous administration of N-acetylcysteine during haemodialysis normalises plasma homocysteine concentration, and this is associated with improved pulse pressure in patients with end-stage renal failure. Intravenous administration of N-acetylcysteine during haemodialysis may be a promising approach to help reduce cardiovascular risk in this vulnerable group of patients.


Assuntos
Acetilcisteína/uso terapêutico , Homocisteína/sangue , Falência Renal Crônica/terapia , Diálise Renal/métodos , Acetilcisteína/administração & dosagem , Acetilcisteína/efeitos adversos , Adulto , Idoso , Pressão Sanguínea/efeitos dos fármacos , Proteínas Sanguíneas/análise , Nefropatias Diabéticas/diagnóstico , Esquema de Medicação , Feminino , Frequência Cardíaca/efeitos dos fármacos , Hematócrito , Humanos , Hipertensão/diagnóstico , Infusões Intravenosas , Cálculos Renais/diagnóstico , Falência Renal Crônica/sangue , Masculino , Pessoa de Meia-Idade , Resultado do Tratamento , Urticária/induzido quimicamente
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