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The pharmacokinetics of ketoconazole in severely immunocompromised patients

Forty patients severely immunocompromised because of the nature of their underlying disease (marrow aplasia, acute leukaemia or solid tumour) and/or the treatment they were receiving, received ketoconazole 400 mg daily. All patients also received gut decontamination with non-absorbable antibiotics,...

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Published in:Journal of antimicrobial chemotherapy 1982-12, Vol.10 (6), p.489-496
Main Authors: Hann, I. M., Prentice, H. G., Keaney, M., Corringham, R., Blacklock, H. A., Fox, J., Gascoigne, E., Van Custem, J.
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container_end_page 496
container_issue 6
container_start_page 489
container_title Journal of antimicrobial chemotherapy
container_volume 10
creator Hann, I. M.
Prentice, H. G.
Keaney, M.
Corringham, R.
Blacklock, H. A.
Fox, J.
Gascoigne, E.
Van Custem, J.
description Forty patients severely immunocompromised because of the nature of their underlying disease (marrow aplasia, acute leukaemia or solid tumour) and/or the treatment they were receiving, received ketoconazole 400 mg daily. All patients also received gut decontamination with non-absorbable antibiotics, skin antisepsis, sterile food and oral co-trimoxazole. Mean (±S.D.) peak serum ketoconazole levels of 5·14±1·4 mg/l occurred 3 h after drug intake. In patients not receiving an allogeneic bone marrow transplant (BMT), the mean serum level at 2 h post-dose remained in the range of 3 to 5 mg/l during prolonged therapy. In contrast, serum ketoconazole levels in allogeneic BMT patients declined during continued treatment. In addition, the incidence of fungal infections was significantly higher in allogeneic-BMT patients than in the other group (P
doi_str_mv 10.1093/jac/10.6.489
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source Oxford University Press Archive
subjects Adult
Antifungal Agents - metabolism
Bone Marrow Transplantation
Female
Humans
Imidazoles - metabolism
Immune Tolerance
Ketoconazole
Kinetics
Leukemia - immunology
Leukemia - metabolism
Male
Piperazines - metabolism
title The pharmacokinetics of ketoconazole in severely immunocompromised patients
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