The consensus of current international guidelines for the treatment of HIV infection is that data on therapeutic drug monitoring (TDM) of non-nucleoside reverse transcriptase inhibitors and protease inhibitors provide a framework for the implementation of TDM in certain defined scenarios in clinical practice. However, the utility of TDM is considered to be on an individual basis until more data are obtained from large clinical trials showing the benefit of TDM. In April 2004, a panel of experts met in Rome, Italy. This followed an inaugural meeting in Perugia, Italy, in October 2000, which resulted in the article published in AIDS 2002, 16(Suppl 1):S5-S37. The objectives of this second meeting were to review the questions surrounding TDM of antiretroviral drugs and discuss the clinical utility, current concerns and future prospects of drug concentration monitoring in the care of HIV-1-infected individuals. This report, which has been updated to include material published or presented at international conferences up to the end of September 2004, reviews pharmacokinetic and pharmacodynamic data and reports the issues discussed by the panel, offering advice to clinical care providers who may be currently, or are considering incorporating TDM into the routine care of their patients. In addition, the panel formulated a series of position statements that are relevant to the interpretation of current data and can aid the design of future clinical trials. © 2005 International Medical Press.

Boffito, M., Acosta, E., Burger, D., Fletcher, C., Flexner, C., Garaffo, R., et al. (2005). Current status and future prospects of therapeutic drug monitoring and applied clinical pharmacology in antiretroviral therapy. ANTIVIRAL THERAPY, 10(3), 375-392.

Current status and future prospects of therapeutic drug monitoring and applied clinical pharmacology in antiretroviral therapy

GATTI, ANTONIO;PERNO, CARLO FEDERICO;
2005-01-01

Abstract

The consensus of current international guidelines for the treatment of HIV infection is that data on therapeutic drug monitoring (TDM) of non-nucleoside reverse transcriptase inhibitors and protease inhibitors provide a framework for the implementation of TDM in certain defined scenarios in clinical practice. However, the utility of TDM is considered to be on an individual basis until more data are obtained from large clinical trials showing the benefit of TDM. In April 2004, a panel of experts met in Rome, Italy. This followed an inaugural meeting in Perugia, Italy, in October 2000, which resulted in the article published in AIDS 2002, 16(Suppl 1):S5-S37. The objectives of this second meeting were to review the questions surrounding TDM of antiretroviral drugs and discuss the clinical utility, current concerns and future prospects of drug concentration monitoring in the care of HIV-1-infected individuals. This report, which has been updated to include material published or presented at international conferences up to the end of September 2004, reviews pharmacokinetic and pharmacodynamic data and reports the issues discussed by the panel, offering advice to clinical care providers who may be currently, or are considering incorporating TDM into the routine care of their patients. In addition, the panel formulated a series of position statements that are relevant to the interpretation of current data and can aid the design of future clinical trials. © 2005 International Medical Press.
2005
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/41 - ANESTESIOLOGIA
English
abacavir; amprenavir; amprenavir phosphate; antiretrovirus agent; atazanavir; cyclosporin; drug metabolizing enzyme; efavirenz; enfuvirtide; immunosuppressive agent; indinavir; lamivudine; lopinavir; nelfinavir; nevirapine; proteinase inhibitor; ritonavir; RNA directed DNA polymerase inhibitor; saquinavir; zidovudine; anti human immunodeficiency virus agent; area under the curve; calculation; childhood disease; clinical pharmacology; clinical trial; diarrhea; dose liver function relation; drug blood level; drug distribution; drug efficacy; drug elimination; drug exposure; drug half life; drug metabolism; drug monitoring; drug potentiation; drug protein binding; drug resistance; drug response; drug safety; drug tolerability; ethnic difference; food drug interaction; good laboratory practice; hepatitis B; human; Human immunodeficiency virus infection; hyperbilirubinemia; hyperlipidemia; IC 50; inhibitory quotient; lipodystrophy; liver dysfunction; liver toxicity; mixed infection; neurotoxicity; organ transplantation; patient compliance; pharmacogenetics; pharmacological parameters; pregnancy; priority journal; review; sex difference; virology; virus inhibition; child; conference paper; consensus development; ethnic group; female; liver failure; male; protein binding; transplantation; Anti-HIV Agents; Child; Drug Monitoring; Ethnic Groups; Female; HIV Infections; Humans; Liver Failure; Male; Patient Compliance; Pregnancy; Protein Binding; Sex Factors; Transplantation
PMID: 15918329
Boffito, M., Acosta, E., Burger, D., Fletcher, C., Flexner, C., Garaffo, R., et al. (2005). Current status and future prospects of therapeutic drug monitoring and applied clinical pharmacology in antiretroviral therapy. ANTIVIRAL THERAPY, 10(3), 375-392.
Boffito, M; Acosta, E; Burger, D; Fletcher, C; Flexner, C; Garaffo, R; Gatti, A; Kurowski, M; Perno, Cf; Peytavin, G; Regazzi, M; Back, D
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/28999
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