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Comparative Study
. 2012 Nov;16(8):2257-66.
doi: 10.1007/s10461-011-0072-2.

HIV-infected individuals with co-occurring bipolar disorder evidence poor antiretroviral and psychiatric medication adherence

Collaborators, Affiliations
Comparative Study

HIV-infected individuals with co-occurring bipolar disorder evidence poor antiretroviral and psychiatric medication adherence

David J Moore et al. AIDS Behav. 2012 Nov.

Abstract

The contribution of bipolar disorder (BD), a prevalent serious mental illness characterized by impulsivity and mood instability, to antiretroviral (ART) and psychiatric medication adherence among HIV-infected (HIV+) individuals is unknown. We examined medication adherence among 44 HIV+/BD+ persons as compared to 33 demographically- and medically-comparable HIV+/BD- persons. Classification of adherent (≥ 90%) or non-adherent (<90%) based on proportion of correctly taken doses over 30 days was determined using electronic medication monitoring devices. HIV+/BD+ persons were significantly less likely to be ART adherent (47.7%) as compared to HIV+/BD- (90.9%) persons. Within the HIV+/BD+ group, mean psychiatric medication adherence was significantly worse than ART medication adherence, although there was a significant correlation between ART and psychiatric adherence levels. Importantly, 30-day ART adherence was associated with plasma virologic response among HIV+/BD+ individuals. Given the high overlap of HIV and BD, and the observed medication adherence difficulties for these persons, specialized adherence improvement interventions are needed.

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Figures

Figure 1
Figure 1
HIV+/BD+ participants evidence worse 30-day MEMS antiretroviral adherence rates as compared to HIV+/BD− participants. Note: Thick bar represents Median; error bars include 95% of the distribution; significance determined via Wilcoxon Rank Sum Test.
Figure 2
Figure 2
30-day MEMS psychotropic adherence rates for HIV+/BD+ participants are lower, but not significantly worse as compared to HIV+/BD− participants. Note: Thick bar represents Median; error bars include 95% of the distribution; significance determined via Wilcoxon Rank Sum Test.

References

    1. Gifford AL, Bormann JE, Shively MJ, Wright BC, Richman DD, Bozzette SA. Predictors of self-reported adherence and plasma HIV concentrations in patients on multidrug antiretroviral regimens. J Acquir Immune Defic Syndr. 2000 Apr 15;23(5):386–395. - PubMed
    1. Descamps D, Flandre P, Calvez V, et al. Mechanisms of virologic failure in previously untreated HIV-infected patients from a trial of induction-maintenance therapy. Trilege (Agence Nationale de Recherches sur le SIDA 072) Study Team) JAMA. 2000 Jan 12;283(2):205–211. - PubMed
    1. Montaner JS, Reiss P, Cooper D, et al. A randomized, double-blind trial comparing combinations of nevirapine, didanosine, and zidovudine for HIV-infected patients: the INCAS Trial. Italy, The Netherlands, Canada and Australia Study. JAMA. 1998 Mar 25;279(2):930–937. - PubMed
    1. Race E, Dam E, Obry V, Paulous S, Clavel F. Analysis of HIV cross-resistance to protease inhibitors using a rapid single-cycle recombinant virus assay for patients failing on combination therapies. AIDS. 1999 Oct 22;13(15):2061–2068. - PubMed
    1. Harrigan PR, Wynhoven B, Brumme ZL, et al. HIV-1 drug resistance: degree of underestimation by a cross-sectional versus a longitudinal testing approach. J Infect Dis. 2005 Apr 15;191(8):1325–1330. - PubMed

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