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Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice.

Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice. Research Abstract Details 

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  • Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice. Abstract Text:

    r m m cleijsenR M M Cleijsen,m e van de endeM E van de Ende,f p kroonF P Kroon,f verduyn lunelF Verduyn Lunel,p p koopmansP P Koopmans,l grasL Gras,f de wolfF de Wolf,d m burgerD M Burger,r m m cleijsenR M M Cleijsen,m e van de endeM E van de Ende,f p kroonF P Kroon,f verduyn lunelF Verduyn Lunel,p p koopmansP P Koopmans,l grasL Gras,f de wolfF de Wolf,d m burgerD M Burger,

    BACKGROUND: Therapeutic drug monitoring (TDM) is being applied for a number of antiretroviral agents. Little is known about the use of TDM for atazanavir. METHODS: This is a retrospective cohort analysis on the use of TDM of atazanavir at three clinical sites in The Netherlands. Patients were divided into three groups: (i) all patients with evaluable data of plasma atazanavir concentrations and its relationship with hyperbilirubinaemia; (ii) patients who started atazanavir without documented evidence of protease inhibitor (PI) mutations; (iii) patients who started atazanavir with documented evidence of PI mutations. The genotypic inhibitory quotient (GIQ) was calculated by dividing the mean atazanavir plasma trough concentration by the number of PI mutations. RESULTS: A total of 108 patients were included; 70 (65.8%) were using atazanavir/ritonavir (300/100 mg once daily). No significant relationship was observed between atazanavir plasma trough concentration and antiviral response in patients starting atazanavir without PI mutations (group 2; n = 82). In contrast, a significant relationship was observed between atazanavir GIQ and treatment response in patients starting atazanavir while having PI mutations (group 3; n = 26). The cut-off value for GIQ most predictive of virological failure was 0.23 mg/L/mutation: patients (n = 8) with a GIQ equal to or below this value had 50% virological failure whereas patients (n = 18) with a GIQ above 0.23 mg/L/mutation had only 11% virological failure (chi(2): P = 0.030). Atazanavir plasma trough concentrations were significantly related with the occurrence of increased total bilirubin concentrations. CONCLUSIONS: TDM of atazanavir might be beneficial for patients with documented PI resistance or patients with hyperbilirubinaemia.

    Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice. Publishing Authors By Initials

    rm cleijsenRM Cleijsen,me van de endeME van de Ende,fp kroonFP Kroon,fv lunelFV Lunel,pp koopmansPP Koopmans,l grasL Gras,f de wolfF de Wolf,dm burgerDM Burger,rm cleijsenRM Cleijsen,me van de endeME van de Ende,fp kroonFP Kroon,fv lunelFV Lunel,pp koopmansPP Koopmans,l grasL Gras,f de wolfF de Wolf,dm burgerDM Burger,

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    PUBMED ID PMID:

    MEDLINE DATE:

    Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: The Journal of antimicrobial chemotherapy

    VOLUME: 60

    Page Numbers: 897-900

    Journal Abbreviation: J. Antimicrob. Chemother.

    ISSN: 0305-7453

    DAY: 17

    MONTH: 08

    YEAR: 2007

    Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7513617

    Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice. Keywords Mesh Terms:

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    Grant and Affiliation Information for Therapeutic drug monitoring of the HIV protease inhibitor atazanavir in clinical practice.

    AFFILIATION: Department of Clinical Pharmacy, Radboud University Medical Centre Nijmegen, The Netherlands.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: J Antimicrob Chemother

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