1998
DOI: 10.1097/00006454-199802000-00013
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Liposomal amphotericin B treatment for neonatal fungal infections

Abstract: To our knowledge this is the largest study of the treatment of neonates with liposomal amphotericin B, and the results confirm its effectiveness and safety. However, randomized clinical trials are required to establish the most effective administration protocol for AmBisome, i.e. the starting dosage, the maximum effective dosage and the cumulative dosage, and to verify whether the preparation should be associated with another antifungal agent.

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Cited by 130 publications
(74 citation statements)
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“…Because renal tubular cells are high in cholesterol, nephrotoxicity is an undesirable side effect of amphoB therapy. 24 Two strategies have been demonstrated to ameliorate renal toxicity, ie, incorporation into a liposomal amphotericin system [25][26][27][28][29][30] and salt loading before amphoB administration. [14][15][16][17][18][19][20][21]24,31 Although some clinical trials have demonstrated decreased amphoB-induced nephrotoxicity with the use of liposomal amphoB, other controlled clinical trials have failed to demonstrate improved outcomes or decreased mortality rates, compared with conventional amphoB.…”
Section: Discussionmentioning
confidence: 99%
“…Because renal tubular cells are high in cholesterol, nephrotoxicity is an undesirable side effect of amphoB therapy. 24 Two strategies have been demonstrated to ameliorate renal toxicity, ie, incorporation into a liposomal amphotericin system [25][26][27][28][29][30] and salt loading before amphoB administration. [14][15][16][17][18][19][20][21]24,31 Although some clinical trials have demonstrated decreased amphoB-induced nephrotoxicity with the use of liposomal amphoB, other controlled clinical trials have failed to demonstrate improved outcomes or decreased mortality rates, compared with conventional amphoB.…”
Section: Discussionmentioning
confidence: 99%
“…Los ensayos prospectivos se han hecho en base a L-amB donde la tasa de respuesta a tratamiento es comparable con anfo B-d (84 y 89%, respectivamente) 34 . Con el uso de L-amB no se describen efectos adversos significativos, salvo hipokalemia leve que se recupera pronto con el aporte de potasio [35][36][37] . Un grupo de expertos de la Sociedad Europea de Microbiología Clínica e Infectología (ESCMID) se refiere al uso de L-amB, en dosis de 2,5 a 7 mg/kg/día en RN con un adecuado perfil de seguridad 38 .…”
Section: Tratamientounclassified
“…26 Information on the use of lipid formulations of amphotericin B is derived from case reports. Scarcella et al 27 used liposomal amphotericin B in 40 preterm and four full-term infants, finding a 72% efficacy. No side effects were observed.…”
Section: Treatmentmentioning
confidence: 99%
“…The standard dosage of lipid formulations ranges from 3 to 5 mg/kg/day. 18,19,[26][27][28][29][30] The Infectious Diseases Society of America (2004) recommends that lipid formulations be considered as secondline drugs. They would be recommended in the following situations: 19 unsuccessful treatment with traditional amphotericin B; patients with history of renal insufficiency; children with significant rise in creatinine levels during treatment (above 1.5 mg/dl).…”
Section: Treatmentmentioning
confidence: 99%