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On p 379 Schöffski et al present their results of a randomised
phase II study comparing the feasibility of treatment with, and safety
and toxicity of, amphotericin B 0.75 mg/kg/day in either glucose 5%
or intralipid 20%, for the empirical treatment of neutropenic cancer
patients with refractory fever of unknown origin or pneumonia. The
trial did not confirm previous observations of improved renal toxicity
and better tolerance with amphotericin B in intralipid emulsions, but
showed potential respiratory complications from self made lipid
emulsions. The drug combination has high toxicity and unknown efficacy
and should not be given to patients.