Quality Assurance Program for Clinical Measurement of Antiretrovirals: AIDS Clinical Trials Group Proficiency Testing Program for Pediatric and Adult Pharmacology Laboratories

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Published in:Antimicrobial Agents and Chemotherapy Vol. 48; no. 3; pp. 824 - 831
Main Authors: HOLLAND, Diane T, DIFRANCESCO, Robin, STONE, Judith, HAMZEH, Fayez, CONNOR, James D, MORSE, Gene D
Format: Journal Article
Language:English
Published: Washington, DC American Society for Microbiology 01-03-2004
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Abstract Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to AAC .asm.org, visit: AAC       
AbstractList Clinical trials designed to compare antiretroviral regimens, investigate therapeutic drug monitoring, or measure pharmacometrics often include protease inhibitors (PIs), nonnucleoside reverse transcriptase inhibitors (NNRTIs), and nucleoside reverse transcriptase inhibitors, requiring the measurement of these antiretrovirals in plasma. Within the adult and pediatric AIDS Clinical Trials Group (ACTG), a network of Pharmacology Support Laboratories (PSLs) is a component of the group laboratory infrastructure and conducts these types of pharmacologic assays. The adult ACTG has developed a comprehensive quality assurance program for the conduct of clinical pharmacology protocols, one component of which is the antiretroviral proficiency testing (PT) program that has been implemented between the adult and pediatric pharmacology laboratories of the ACTG. PT testing samples were prepared and distributed in July 2001, February 2002, and July 2002. High, medium, and low concentrations of PIs (indinavir, saquinavir, amprenavir, lopinavir, ritonavir, and nelfinavir) and NNRTIs (nevirapine and efavirenz) were added to drug-free EDTA plasma and distributed, on dry ice, to eight ACTG PSLs. One testing laboratory used liquid chromatography-tandem mass spectrometry, and seven used high-performance liquid chromatography-UV analysis. A result was considered acceptable if it was within 20% deviation of the assigned concentration. For all concentrations of PIs evaluated, 96% of samples tested (430 of 448 measurements) met the acceptance criteria. For both NNRTIs, 100% of samples tested (140 of 140 measurements) met the acceptance criteria. In conclusion, the PT program results presented demonstrate excellent interlaboratory agreement for all antiretrovirals tested and provide support for the merger of plasma concentration data among laboratories for large clinical trials.
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Author Fayez Hamzeh
James D. Connor
Gene D. Morse
Judith Stone
Diane T. Holland
Robin DiFrancesco
AuthorAffiliation Adult and Pediatric AIDS Clinical Trials Group Pharmacology Laboratory Committees, Pediatric AIDS Clinical Trials Group, Division of AIDS, National Institute of Allergy and Infections Diseases, National Institutes of Health, Bethesda, Maryland
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  surname: DIFRANCESCO
  fullname: DIFRANCESCO, Robin
  organization: Adult and Pediatric AIDS Clinical Trials Group Pharmacology Laboratory, Committees, Pediatric AIDS Clinical Trials Group, Division of AIDS, National Institute of Allergy and Infections Diseases, National Institutes of Health, Bethesda, Maryland, United States
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  givenname: Judith
  surname: STONE
  fullname: STONE, Judith
  organization: Adult and Pediatric AIDS Clinical Trials Group Pharmacology Laboratory, Committees, Pediatric AIDS Clinical Trials Group, Division of AIDS, National Institute of Allergy and Infections Diseases, National Institutes of Health, Bethesda, Maryland, United States
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  givenname: Fayez
  surname: HAMZEH
  fullname: HAMZEH, Fayez
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  givenname: James D
  surname: CONNOR
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  givenname: Gene D
  surname: MORSE
  fullname: MORSE, Gene D
  organization: Adult and Pediatric AIDS Clinical Trials Group Pharmacology Laboratory, Committees, Pediatric AIDS Clinical Trials Group, Division of AIDS, National Institute of Allergy and Infections Diseases, National Institutes of Health, Bethesda, Maryland, United States
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Issue 3
Keywords Human
Immunopathology
Pediatrics
Antiretroviral agent
Infant
AIDS
Pharmacology
Round robin test
Immune deficiency
Infection
Therapeutic drug monitoring
Quality assurance
Viral disease
Reverse transcriptase inhibitor
Adult
Antiviral
Clinical trial
Child
Protease inhibitor
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Corresponding author. Mailing address: AACTG Pharmacology Support Laboratory, School of Pharmacy and Pharmaceutical Sciences, University at Buffalo, The State University of New York, Room 317, Hochstetter Hall, Buffalo, NY 14260. Phone: (716) 645-3635, ext. 252. Fax: (716) 645-2001. E-mail: emorse@acsu.buffalo.edu.
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Clinical trials designed to compare antiretroviral regimens, investigate therapeutic drug monitoring, or measure pharmacometrics often include protease...
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SubjectTerms Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome - drug therapy
Adult
Anti-HIV Agents
Anti-HIV Agents - blood
Anti-HIV Agents - therapeutic use
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antiviral Agents
Biological and medical sciences
Child
Chromatography, High Pressure Liquid
Humans
Laboratories
Laboratories - standards
Medical sciences
Pharmacology. Drug treatments
Quality Assurance, Health Care
Reproducibility of Results
Spectrophotometry, Ultraviolet
Title Quality Assurance Program for Clinical Measurement of Antiretrovirals: AIDS Clinical Trials Group Proficiency Testing Program for Pediatric and Adult Pharmacology Laboratories
URI http://aac.asm.org/content/48/3/824.abstract
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