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Enferm Infecc Microbiol Clin ; 18(4): 162-4, 2000 Apr.
Artigo em Espanhol | MEDLINE | ID: mdl-10932392

RESUMO

BACKGROUND: Amphotericin B is the medication of choice in systemic or invasive fungal infections, but its use often is limited by nephrotoxicity. Lipid formulations of amphotericin B have reduced this risk, but it is not known if these medications also prevent the deterioration of kidney function in patients with previous kidney failure or at risk of kidney failure, such as newborns and patients treated with cyclosporine A. METHOD: A retrospective analysis was made of epidemiological, clinical and analytic data collected from the clinical histories of patients with previous renal failure or at high risk of nephrotoxicity who were treated with liposomal amphotericin B at our hospital between January 1991 and January 1997. RESULTS: An analysis was made of 23 patients (15 men and 8 women, mean age 38 years) who met established criteria. All had severe immunosuppression. Twelve patients had been treated previously with conventional amphotericin B, but treatment was interrupted for kidney failure. The other 11 patients in the group received cyclosporine A (9 cases) or were at risk of nephrotoxicity because of their underlying disease or situation (2 cases). No deterioration of kidney function due to liposomal amphotericin B was observed in any patient. In 5 of the 12 patients who had deterioration of kidney function as a result of previous use of conventional amphotericin B and lived more than one week after changing treatment, it was observed that kidney function recovered and baseline creatinine levels were reached. CONCLUSIONS: Our findings suggest that liposomal amphotericin B can be used safely in immunocompromised patients with fungal infection who have failure or high risk of kidney failure.


Assuntos
Anfotericina B/uso terapêutico , Antifúngicos/uso terapêutico , Antiprotozoários/uso terapêutico , Rim/efeitos dos fármacos , Adulto , Anfotericina B/efeitos adversos , Antifúngicos/efeitos adversos , Antiprotozoários/efeitos adversos , Feminino , Humanos , Lipossomos , Masculino , Estudos Retrospectivos
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