TY - JOUR
T1 - RATE AND DETERMINANTS OF VIROLOGIC FAILURE IN HIV-INFECTED YOUTH RECEIVING FIRST-LINE EMTRICITABINE/ TENOFOVIR DISOPROXIL FUMARATE/ EFAVIRENZ (ATRIPLA®) COMPARED TO OTHER ANTIRETROVIRAL DRUG REGIMENS
AU - Van Ramshorst, Ryan
AU - Gingaras, Cosmina
AU - Kozinetz, Claudia A.
AU - Collins, Elizabeth Montgomery
AU - Hansen, Ingrid
AU - Schwarzwald, Heidi
N1 - Funding Information:
We would like to acknowledge the patients who have participated in this study. Funding for CG was provided by the Baylor Pediatric AIDS Initiative NIH training grant from the Fogarty International Center of the NIH (D43 TW001036). Funding for HS, CAK, and EGM was provided by Baylor College of Medicine and IH was supported by Harris County Hospital District. The funding institutions were not involved in the design or conduct of the study, in the collection, management, analysis, and interpretation of the data, or in the preparation, review, or approval of the manuscript.
Publisher Copyright:
© 2014, Amaltea Medical Publishing House. All rights reserved.
PY - 2014
Y1 - 2014
N2 - Objectives. The primary objective of the study was to determine whether fi rst-line once-daily Emtricitabine/ Tenofovir disoproxil fumarate/Efavirenz (Atripla®) is associated with a lower rate of virologic failure compared with alternative fi rst-line regimens in HIV-infected youth. The secondary objective was to identify predictors of virologic failure in the overall study sample and in the Atripla® group. Methods. Fifty two HIV-infected youth followed at an urban HIV clinic, ages 17-25, not pregnant, with no history of prevention of mother-to-child transmission of HIV, starting their fi rst-line antiretroviral regimen, and with at least 12 weeks of follow-up on their regimen were eligible to be included in a retrospective review of medical charts. The main outcome was virologic failure, defi ned as having a viral load over 400 copies/ml after 12 weeks of therapy or failure to ever reach this threshold. Results. No signifi cant difference in the rate of virologic failure was found between the two treatment groups. Overall, 52% of patients failed their first-line regimen. The only significant independent predictor of virologic failure was history of AIDS. Tobacco use was associated with failure in the Atripla® group. No significant difference was noted in time to failure after the start of either Atripla® or an alternative regimen. Development of resistance mutations and adherence levels did not significantly differ between the two regimen groups. However, adherence levels were significantly lower in those who failed their regimen compared to those who did not. Conclusions. Our data do not support the hypothesis that rate of virologic failure in a simple, once-daily, fi rst-line Atripla® regimen is lower compared to alternative regimens in our HIV-infected youth population. Adherence and psychosocial factors are important determinants of fi rst-line regimen success and require particular consideration before offering Atripla® .
AB - Objectives. The primary objective of the study was to determine whether fi rst-line once-daily Emtricitabine/ Tenofovir disoproxil fumarate/Efavirenz (Atripla®) is associated with a lower rate of virologic failure compared with alternative fi rst-line regimens in HIV-infected youth. The secondary objective was to identify predictors of virologic failure in the overall study sample and in the Atripla® group. Methods. Fifty two HIV-infected youth followed at an urban HIV clinic, ages 17-25, not pregnant, with no history of prevention of mother-to-child transmission of HIV, starting their fi rst-line antiretroviral regimen, and with at least 12 weeks of follow-up on their regimen were eligible to be included in a retrospective review of medical charts. The main outcome was virologic failure, defi ned as having a viral load over 400 copies/ml after 12 weeks of therapy or failure to ever reach this threshold. Results. No signifi cant difference in the rate of virologic failure was found between the two treatment groups. Overall, 52% of patients failed their first-line regimen. The only significant independent predictor of virologic failure was history of AIDS. Tobacco use was associated with failure in the Atripla® group. No significant difference was noted in time to failure after the start of either Atripla® or an alternative regimen. Development of resistance mutations and adherence levels did not significantly differ between the two regimen groups. However, adherence levels were significantly lower in those who failed their regimen compared to those who did not. Conclusions. Our data do not support the hypothesis that rate of virologic failure in a simple, once-daily, fi rst-line Atripla® regimen is lower compared to alternative regimens in our HIV-infected youth population. Adherence and psychosocial factors are important determinants of fi rst-line regimen success and require particular consideration before offering Atripla® .
KW - adherence
KW - adolescents
KW - antiretroviral therapy
KW - HAART
KW - HIV
KW - teens
KW - treatment failure
KW - virologic failure
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M3 - Article
AN - SCOPUS:85142828830
SN - 1454-3389
VL - 17
SP - 189
EP - 196
JO - Romanian Journal of Infectious Diseases
JF - Romanian Journal of Infectious Diseases
IS - 4
ER -