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Using Mechanistic Models to Simulate Comparative Effectiveness Trials of Therapy and to Estimate Long-term Outcomes in HIV Care

Dados Bibliográficos

ID9099412
AutoresMark S Roberts (0000-0002-8277-0425, University of Pittsburgh, autor correspondente), Kimberly A Nucifora, R Scott Braithwaite (0000-0001-7067-3655)
Ano2010
Volume48
Fascículo6
PáginasS90-S95
Data de publicação2010-06-01
Peer ReviewedSim
Open AccessNão
TipoARTICLE
PeriódicoMedical Care (JOURNAL)
Identificadores do periódicoISSN: 0025-7079 • E-ISSN: 1537-1948
EditoraOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/mlr.0b013e3181e2b744
PMID20473184
OpenAlexW2054987174
IdiomaEN
Citações recebidas2
Referências citadas28

BACKGROUND: In HIV care, it is difficult to decide when to initiate therapy, which drugs to use for initial treatment, and which drugs to use if drug resistance develops. With hundreds of possible drug regimens available and variable patterns of drug resistance, randomized controlled trials cannot answer all HIV treatment decisions. Mechanistic models of HIV infection can be used to conduct virtual therapeutic trials with the goal of predicting outcomes, some of which are long-term and may not fall within the time frame of a typical therapeutic trial. METHODS: We used a previously developed and validated model of HIV infection to replicate 2 arms of an HIV initial treatment trial (ACTG A5142) and predict long-term outcomes. The model incorporated data about biologic processes involved in the development of drug resistance. RESULTS: The model reproduced the proportion that developed AIDS (0.04 and 0.05 for the efavirenz arm and lopinavir arms, respectively, vs. 0.04 and 0.06 for the trial), the development of virologic failure (0.27 and 0.33 for the Efavirenz arm and lopinavir arms, respectively, vs. 0.24 and 0.37 for the trial), and drug resistance. The hazard ratio for the time to treatment failure, a combination of resistance and other causes (0.96 for the model vs. 0.75 for the trial; 95% confidence interval, 0.57-0.98), and changes in CD4 cell count, were less accurate. The model estimated longer-term life expectancy, quality-adjusted life expectancy, and HIV-related deaths. CONCLUSIONS: Mechanistic models of HIV infections have the potential to be useful in comparative effectiveness research

Antiretroviral therapy · Biology · Clinical trial · Confidence interval · Drug resistance · Efavirenz · HIV drug resistance · Human immunodeficiency virus (HIV) · Intensive care medicine · Life expectancy · Lopinavir · Population · Viral load · HIV Research and Treatment · HIV/AIDS drug development and treatment · HIV/AIDS Research and Interventions · Immunology · Internal Medicine · Medicine

  • Comparative Effectiveness Research Methods

    Kathleen N Lohr•Medical Care•2010

  • A Simulation-based Approach for Improving Utilization of Thrombolysis in Acute Brain Infarction

    Maarten M H Lahr, Durk-Jouke van der Zee et al.•Medical Care•2013

  • Prognosis of HIV-1-infected patients starting highly active antiretroviral therapy

    Open Access•Matthias Egger, Margaret May et al.•The Lancet•2002

Obras citantes distintas2
Citações por ano0,13
Intervalo de citações2010 - 2013 (4)
Velocidade de citaçãohistorical
Altamente citadoNão
Tipos de citaçãoNeutras: 2
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