Indexed in / abstracted by
Stimati cititori, va reamintim ca autorii primi ai articolelor stiintifice pot acumula 80 de credite EMC in urma publicarii. Daca un articol are mai multi autori, cele 80 de credite [...]
Starting with 2016, The Romanian National Society of Infectious Diseases offers Society’s Prize – for the authors who published the best scientific articles [...]
Tema plagiatului este tot mai mult discutata in ultima vreme. Aparitia unor programe performante de cautare si identificare a similitudinilor intre texte [...]
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
Objectives. The primary objective of the study was to determine whether first-line once-daily Emtricitabine/ Tenofovir disoproxil fumarate/Efavirenz (Atripla®) is associated with a lower rate of virologic failure compared with alternative first-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 first-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, defined as having a viral load over 400 copies/ml after 12 weeks of therapy or failure to ever reach this threshold.
Results. No significant 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, first-line Atripla® regimen is lower compared to alternative regimens in our HIV-infected youth population. Adherence and psychosocial factors are important determinants of first-line regimen success and require particular consideration before offering Atripla®.
Keywords: HIV, adolescents, teens, adherence, virologic failure, treatment failure, antiretroviral therapy, HAART