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Disposition of didanosine in HIV-seropositive patients with normal renal function or chronic renal failure: influence of hemodialysis and continuous ambulatory peritoneal dialysis.
Knupp, C A; Hak, L J; Coakley, D F; Falk, R J; Wagner, B E; Raasch, R H; van der Horst, C M; Kaul, S; Barbhaiya, R H; Dukes, G E.
Afiliação
  • Knupp CA; Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Company, Princeton, NJ 08543, USA.
Clin Pharmacol Ther ; 60(5): 535-42, 1996 Nov.
Article em En | MEDLINE | ID: mdl-8941026
ABSTRACT

OBJECTIVE:

To evaluate the pharmacokinetics of didanosine in patients with normal kidney function or chronic kidney failure.

METHODS:

Three groups of patients with human immunodeficiency virus (HIV) infection were studied group I, six men with normal kidney function (creatinine clearance > 90 ml/min/1.73 m2); group II, six men with chronic renal failure maintained on continuous ambulatory peritoneal dialysis (CAPD); and group III, four men and two women with chronic renal failure receiving hemodialysis three times a week. A 300 mg dose of didanosine was administered orally and intravenously according to a two-period randomized crossover design. Patients in group III were studied between hemodialysis sessions during the crossover periods. In addition, patients in group III were studied in a third period after administration of a 300 mg oral dose of didanosine 4 hours before hemodialysis.

RESULTS:

After intravenous administration in group I, the mean (+/-SD) total clearance (CLT) was 13.0 +/- 1.6 ml/min/kg and the elimination half-life (t 1/2) was 1.56 +/- 0.43 hour. In groups II and III, the CLT decreased significantly to 3.4 +/- 1.2 and 3.2 +/- 1.2 ml/min/kg, respectively, whereas the t1/2 increased to 3.60 +/- 0.82 hours and 3.11 +/- 0.88 hours, respectively. The absolute bioavailability of didanosine in groups I, II, and III was 42% +/- 12%, 52% +/- 6%, and 38% +/- 11%, respectively, and did not differ significantly. CAPD had little effect on the removal of didanosine, whereas approximately 30% of the drug present in the body at the start of dialysis was eliminated by an average 3-hour dialysis session.

CONCLUSION:

The clearance of didanosine is impaired in patients with chronic renal failure. To compensate, the dose and schedule of administration should be adjusted. It is recommended that one-fourth of the total daily dose of didanosine be administered once a day in this patient population.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Soropositividade para HIV / Didanosina / Fármacos Anti-HIV / Rim / Falência Renal Crônica Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Soropositividade para HIV / Didanosina / Fármacos Anti-HIV / Rim / Falência Renal Crônica Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Estados Unidos