Skip to main content
. 1998 Aug 8;317(7155):379–384. doi: 10.1136/bmj.317.7155.379

Table 5.

Prospective trials comparing toxicity of amphotericin B in glucose or intralipid

Authors Underlying disease (No of patients) Infection treated Preparation and administration of amphotericin B in intralipid
Chavanet et al12 HIV positive (22) Oral candidiasis 1.0 mg/kg/day amphotericin B (mixed directly with intralipid 20%) as 1 hour intravenous infusion for 4 days*
Moreau et al13 Tumour (32) Fever of unknown origin 0.7-1.0 mg/kg/day amphotericin B (dissolved in glucose then mixed with intralipid 20%) as a 4 hour intravenous infusion for 11/18 days*
Caillot et al14 Haematological disorders (42) Fever or documented mycosis 1.0-1.1 mg/kg/day amphotericin B (mixed directly with intralipid 20%) as a 2 hour intravenous infusion for 8/12 days*
Thakur8 Kala-azar (22) Visceral leishmaniasis 0.05-1.0 mg/kg/day amphotericin B (dissolved in water then mixed with intralipid 10%) as a 2-4 hour intravenous infusion until dose of 20 mg/kg reached*
Schoffski et al Tumour (51) Fever of unknown origin or pneumonia 0.75 mg/kg/day amphotericin B (Moreau type preparation) as a 1-4 hour intravenous infusion for 15/13 days**
*

Significant reduction of amphotericin B related side effects such as renal toxicity, fever, or chills.  

**

Significant increase in pulmonary toxicity without evidence of renal protection or improved subjective tolerance.