M. Ruhnke et al., SINGLE-DOSE PHARMACOKINETICS OF FLUCONAZOLE IN PATIENTS WITH LIVER-CIRRHOSIS, Journal of antimicrobial chemotherapy, 35(5), 1995, pp. 641-647
The pharmacokinetics of a single 100 mg iv dose of fluconazole were st
udied in parallel groups of ten normal subjects and nine patients with
liver cirrhosis, a condition with a high risk of life-threatening fun
gal infection. The following mean pharmacokinetic parameters were foun
d for the patient group: terminal elimination constant 0.0101/h (norma
l 0.0214/h); mean residence time 134 h (normal 46.7 h); area under the
curve 200 h.mg/L (normal 69.4 h.mg/L); plasma clearance 0.96 L/h.kg (
normal 2.16 L/h.kg). All these differences were statistically signific
ant (P < 0.05). The majority of the patients were being concomitantly
treated with duretics (frusemide and spironolactone). It is suggested
that the known slight interaction between such drugs and fluconazole w
as intensified by the disease state. These results emphasize the need
for caution in the treatment with fluconazole of patients with severe
liver disease. Nevertheless, in view of the wide range of values found
in the patients, and low toxicity of fluconazole, a dosage reduction
in cirrhosis does not seem to be justified in the present state of kno
wledge.