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Perceptions of rapid antiretroviral therapy initiation among participants of the Netherlands cohort study on acute HIV Infection
van Paassen, P., Dijkstra, M., Peay, H., Rokx, C., Verbon, A., Reiss, P., Prins, J., Henderson, G. E., Rennie, S., Nieuwkerk, P., & de Bree, G. (2024). Perceptions of rapid antiretroviral therapy initiation among participants of the Netherlands cohort study on acute HIV Infection. AIDS Research and Human Retroviruses, 40(5), 286-292. https://doi.org/10.1089/AID.2022.0169
Starting antiretroviral therapy (ART) same-day, or as soon as possible after HIV diagnosis is advised in guidelines worldwide. Especially during acute HIV infection (AHI), rapid ART start may be more urgent because of a higher risk of transmission or symptoms of acute retroviral syndrome. During this phase, rapid ART start may have additional benefits for viral reservoir size and host immunity. We explored perceptions of rapid ART start among participants of The Netherlands Cohort Study on Acute HIV infection (NOVA study), who started ART rapidly after diagnosis of AHI. We conducted 20 in-depth qualitative interviews with NOVA study participants between October and December 2018. Data were analyzed thematically, using inductive and iterative coding techniques. Roughly half of the participants stated they felt well-informed about the importance of (rapid) ART. Starting ART rapidly was perceived positively by almost all participants, mostly because of the expected benefits on their health, and to prevent HIV transmission. Rapid ART start was seen as a way to cope with the diagnosis. However, a more negative perception was that rapid ART start confronted participants with their diagnosis, when they were still adjusting to a new situation. Our results show that among people diagnosed during AHI, rapid ART is well-accepted. These results should be encouraging to HIV care providers who encounter people with AHI in their clinical practice and to researchers who carry out cure-related studies, in which early ART is often included. The Clinical Trial Registration number is NCT05728996.