Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?

Background: Amphotericin B is efficacious for the treatment of systemic candidiasis, however it has potentially serious toxic effects. Administration as lipid emulsions has been advocated to decrease its toxicity. Aim: To compare the safety and tolerance of amphotericin B administered as lipid emuls...

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Autores principales: Hernández P,Glenn, Altermatt C,Fernando, Bernucci P,Francisca, Acuña C,Darwin, Apablaza E,Felipe, Valenzuela P,Felipe, Lefio C,Alvaro, Pérez C,Carlos, Bugedo T,Guillermo, Castillo F,Luis
Lenguaje:Spanish / Castilian
Publicado: Sociedad Médica de Santiago 2000
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872000001000004
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spelling oai:scielo:S0034-988720000010000042001-01-29Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?Hernández P,GlennAltermatt C,FernandoBernucci P,FranciscaAcuña C,DarwinApablaza E,FelipeValenzuela P,FelipeLefio C,AlvaroPérez C,CarlosBugedo T,GuillermoCastillo F,Luis Adverse effects Amphotericin B Antibiotics, antifungal Drug toxicity Background: Amphotericin B is efficacious for the treatment of systemic candidiasis, however it has potentially serious toxic effects. Administration as lipid emulsions has been advocated to decrease its toxicity. Aim: To compare the safety and tolerance of amphotericin B administered as lipid emulsion or dissolved in dextrose in water. Patients and methods: Forty five patients with confirmed or highly suspected systemic candidiasis were studied. Between January 1996 and June 1997 amphotericin B was administered in dextrose in water to 17 patients (group 1). Between July 1997 and December 1998, the drug was delivered in lipid emulsions (Intralipid, group 2). Clinical and laboratory parameters (serum creatinine, urea nitrogen and potassium), were assessed daily. Results: Both treatment groups were clinically comparable and had the same survival. Accumulative amphotericin B dose administered was 343.2 ± 197 and 414.6 ± 518 mg respectively. Hypokalemia was more frequent in group 2 (52 and 25 % respectively, p < 0.05). There were no differences in the outcome of renal function or other adverse reactions. Conclusions: Administration of amphotericin B as lipid emulsions did not reduce its toxicity in critical patients (Rev Méd Chile 2000; 128: 1101-07)info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.128 n.10 20002000-10-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872000001000004es10.4067/S0034-98872000001000004
institution Scielo Chile
collection Scielo Chile
language Spanish / Castilian
topic Adverse effects
Amphotericin B
Antibiotics, antifungal
Drug toxicity
spellingShingle Adverse effects
Amphotericin B
Antibiotics, antifungal
Drug toxicity
Hernández P,Glenn
Altermatt C,Fernando
Bernucci P,Francisca
Acuña C,Darwin
Apablaza E,Felipe
Valenzuela P,Felipe
Lefio C,Alvaro
Pérez C,Carlos
Bugedo T,Guillermo
Castillo F,Luis
Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?
description Background: Amphotericin B is efficacious for the treatment of systemic candidiasis, however it has potentially serious toxic effects. Administration as lipid emulsions has been advocated to decrease its toxicity. Aim: To compare the safety and tolerance of amphotericin B administered as lipid emulsion or dissolved in dextrose in water. Patients and methods: Forty five patients with confirmed or highly suspected systemic candidiasis were studied. Between January 1996 and June 1997 amphotericin B was administered in dextrose in water to 17 patients (group 1). Between July 1997 and December 1998, the drug was delivered in lipid emulsions (Intralipid, group 2). Clinical and laboratory parameters (serum creatinine, urea nitrogen and potassium), were assessed daily. Results: Both treatment groups were clinically comparable and had the same survival. Accumulative amphotericin B dose administered was 343.2 ± 197 and 414.6 ± 518 mg respectively. Hypokalemia was more frequent in group 2 (52 and 25 % respectively, p < 0.05). There were no differences in the outcome of renal function or other adverse reactions. Conclusions: Administration of amphotericin B as lipid emulsions did not reduce its toxicity in critical patients (Rev Méd Chile 2000; 128: 1101-07)
author Hernández P,Glenn
Altermatt C,Fernando
Bernucci P,Francisca
Acuña C,Darwin
Apablaza E,Felipe
Valenzuela P,Felipe
Lefio C,Alvaro
Pérez C,Carlos
Bugedo T,Guillermo
Castillo F,Luis
author_facet Hernández P,Glenn
Altermatt C,Fernando
Bernucci P,Francisca
Acuña C,Darwin
Apablaza E,Felipe
Valenzuela P,Felipe
Lefio C,Alvaro
Pérez C,Carlos
Bugedo T,Guillermo
Castillo F,Luis
author_sort Hernández P,Glenn
title Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?
title_short Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?
title_full Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?
title_fullStr Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?
title_full_unstemmed Uso de anfotericina B en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?
title_sort uso de anfotericina b en mezcla lipídica: ¿previene la toxicidad de la droga en pacientes críticos?
publisher Sociedad Médica de Santiago
publishDate 2000
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872000001000004
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