Itraconazole solution: Higher serum drug concentrations and better clinical response rates than the capsule formulation in acquired immunodeficiency syndrome patients with candidosis

被引:91
作者
Cartledge, JD [1 ]
Midgely, J [1 ]
Gazzard, BG [1 ]
机构
[1] CHELSEA & WESTMINSTER HOSP,ST STEPHENS CTR,LONDON SW10 9NH,ENGLAND
关键词
itraconazole solution; AIDS; candidosis;
D O I
10.1136/jcp.50.6.477
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aims-To compare the serum concentrations of itraconazole and hydroxyitraconazole after treatment with intraconazole cyclodextrin solution and itraconazole capsules in human immunodeficiency virus (HIV) positive patients with oral candidosis. Methods-The pharmacokinetics of itraconazole and its active metabolite hydroxy-itraconazole were assessed on days 1 and 7 of therapy in aquired immunodeficiency syndrome (AIDS) patients with oral candidosis taking either itraconazole solution or capsules and the serum concentrations (measured by high performance liquid chromatography) correlated with the clinical response to therapy. In addition, the in vitro susceptibility of Candida spp isolates taken from patients at the start of the therapy was assessed. Results-Nine of 16 patients treated with itraconazole capsules and eight of 15 treated with the solution responded to treatment. Three of the non-responders in each treatment group were infected with isolates resistant to itraconazole in vitro. Although with both preparations there was considerable inter-patient variability in the maximum recorded serum concentrations of itraconazole, they were significantly lower on day 1 and day 7 in those receiving capsules compared with those taking the solution. Patients unresponsive to therapy, but infected with susceptible isolates, had significantly lower concentrations of itraconazole and hydroxyitraconazole levels on days 1 and 7 than patients responding to treatment. However, patients infected with itraconazole resistant isolates (tested in vitro) failed to respond to treatment despite achieving similar serum concentrations of itraconazole and hydroxy-itraconazole to the responsive patients. For patients with in vitro susceptible isolates a serum itraconazole concentration of < 1000 ng/ml on day 7 was predictive of therapeutic failure (specificity 71%, sensitivity 100%). Conclusions-Itraconazole cyclodextrin solution achieves higher serum itraconazole and hydroxy-itraconazole concentrations than the capsule formulation in AIDS patients, and this is associated with improved efficacy.
引用
收藏
页码:477 / 480
页数:4
相关论文
共 7 条
  • [1] Itraconazole cyclodextrin solution: The role of in vitro susceptibility testing in predicting successful treatment of HIV-related fluconazole-resistant and fluconazole-susceptible oral candidosis
    Cartledge, JD
    Midgley, J
    Gazzard, BG
    [J]. AIDS, 1997, 11 (02) : 163 - 168
  • [2] ITRACONAZOLE CYCLODEXTRIN SOLUTION - EFFECTIVE TREATMENT FOR HIV-RELATED CANDIDOSIS UNRESPONSIVE TO OTHER AZOLE THERAPY
    CARTLEDGE, JD
    MIDGLEY, J
    YOULE, M
    GAZZARD, BG
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 33 (05) : 1071 - 1073
  • [3] PHARMACOKINETICS OF ITRACONAZOLE FOLLOWING ORAL-ADMINISTRATION TO NORMAL VOLUNTEERS
    HARDIN, TC
    GRAYBILL, JR
    FETCHICK, R
    WOESTENBORGHS, R
    RINALDI, MG
    KUHN, JG
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (09) : 1310 - 1313
  • [4] GASTROPATHY AND KETOCONAZOLE MALABSORPTION IN THE ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS)
    LAKEBAKAAR, G
    TOM, W
    LAKEBAKAAR, D
    GUPTA, N
    BEIDAS, S
    ELSAKR, M
    STRAUS, E
    [J]. ANNALS OF INTERNAL MEDICINE, 1988, 109 (06) : 471 - 473
  • [5] ANTIFUNGAL SUSCEPTIBILITY TESTING OF CANDIDA SPP BY RELATIVE GROWTH MEASUREMENT AT SINGLE CONCENTRATIONS OF ANTIFUNGAL AGENTS
    ODDS, FC
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (08) : 1727 - 1737
  • [6] STEIN A, 1987, BR J CLIN PHARM, V27, P105
  • [7] COMPARISON OF HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC AND MICROBIOLOGICAL METHODS FOR DETERMINATION OF ITRACONAZOLE
    WARNOCK, DW
    TURNER, A
    BURKE, J
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1988, 21 (01) : 93 - 100