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Tytuł pozycji:

Patterns of efavirenz use as first-line antiretroviral therapy in the United States: 1999-2015.

Tytuł:
Patterns of efavirenz use as first-line antiretroviral therapy in the United States: 1999-2015.
Autorzy:
Bengtson AM; Department of Epidemiology, Brown University, Providence, RI, USA.
Pence BW; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Eaton EF; Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL, USA.
Edwards JK; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Eron JJ; Division of Infectious Diseases, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Mathews WC; Department of Medicine, University of California at San Diego, San Diego, CA, USA.
Mollan K; Center for AIDS Research, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Moore RD; School of Medicine and Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA.
O'Cleirigh C; Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.; The Fenway Institute, Boston, MA, USA.
Geng E; School of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Mugavero MJ; Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL, USA.
Źródło:
Antiviral therapy [Antivir Ther] 2018; Vol. 23 (4), pp. 363-372.
Typ publikacji:
Historical Article; Journal Article; Research Support, N.I.H., Extramural
Język:
English
Imprint Name(s):
Publication: [London] : SAGE Publications
Original Publication: London : International Medical Press
MeSH Terms:
Practice Patterns, Physicians'*
Anti-HIV Agents/*therapeutic use
Benzoxazines/*therapeutic use
HIV Infections/*drug therapy
HIV Infections/*epidemiology
Adult ; Alkynes ; Antiretroviral Therapy, Highly Active ; CD4 Lymphocyte Count ; Cyclopropanes ; Female ; HIV Infections/history ; HIV Infections/virology ; History, 20th Century ; History, 21st Century ; Humans ; Male ; Middle Aged ; United States/epidemiology ; Viral Load
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Grant Information:
L30 MH110572 United States MH NIMH NIH HHS; P30 AI094189 United States AI NIAID NIH HHS; U01 DA036935 United States DA NIDA NIH HHS; R24 AI067039 United States AI NIAID NIH HHS; K99 MH112413 United States MH NIMH NIH HHS; K01 AI125087 United States AI NIAID NIH HHS; P30 AI060354 United States AI NIAID NIH HHS; P30 AI036219 United States AI NIAID NIH HHS; P30 AI050410 United States AI NIAID NIH HHS; R01 MH100970 United States MH NIMH NIH HHS; P30 AI027767 United States AI NIAID NIH HHS; P30 AI027763 United States AI NIAID NIH HHS; U01 AI069918 United States AI NIAID NIH HHS; P30 AI036214 United States AI NIAID NIH HHS; P30 AI027757 United States AI NIAID NIH HHS
Substance Nomenclature:
0 (Alkynes)
0 (Anti-HIV Agents)
0 (Benzoxazines)
0 (Cyclopropanes)
JE6H2O27P8 (efavirenz)
Entry Date(s):
Date Created: 20180210 Date Completed: 20190926 Latest Revision: 20240331
Update Code:
20240331
PubMed Central ID:
PMC6085156
DOI:
10.3851/IMP3223
PMID:
29424697
Czasopismo naukowe
Background: Efavirenz has been a mainstay of antiretroviral therapy (ART) for over 15 years in the US. Its association with neuropsychiatric side effects may influence clinical prescribing and management.
Methods: We included HIV-infected adults enrolled in care at seven sites across the US, who initiated combination ART between 1999 and 2015. We examined the proportion initiating and continuing on efavirenz, overall and by mental health status. Log binomial and Cox models were used to estimate associations between mental health, clinical and sociodemographic characteristics and initiating or switching from efavirenz as first-line ART.
Results: Of the 8,230 participants included, 3,710 (45%) initiated efavirenz. In multivariable analyses, prior mono- or dual-ART, ART initiation after 2006, being female, intravenous drug use, antidepressant prescription, previous mental health diagnosis and baseline CD4 + T-cell count >350 cells/mm 3 were inversely associated with initiating efavirenz. Participants initiating efavirenz had a faster time to a regimen switch, compared with those initiating an efavirenz-free regimen (P-value <0.01). Among efavirenz initiators, starting efavirenz in more recent time periods and a previous mental health diagnosis were associated with faster time to switching from efavirenz. Despite this, 40-50% of participants with a previous mental health diagnosis initiated and continued on efavirenz for much of the follow-up period.
Conclusions: Multiple clinical factors, including mental health diagnoses, appeared to influence efavirenz use. While mental health diagnosis status and more recent treatment starts were associated with shorter duration of efavirenz therapy, a previous mental health diagnosis did not preclude efavirenz initiation or continuation in many participants.

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