#viralsuppression
From @ofidjournal.bsky.social 🦠

Most adults with #HIV1 who achieve #ViralSuppression on oral DTG/3TC successfully switch to injectable CAB/RPV, highlighting the value of offering flexible, patient-preferred transition options after initial treatment-induced suppression. #IDSky
Early Switch to Long-Acting CAB/RPV After DTG/3TC Sustains HIV-1 Control
Treatment-naive adults with HIV-1 who suppress on DTG/3TC can successfully transition to LA CAB/RPV.
www.infectiousdiseaseadvisor.com
August 21, 2026 at 11:14 PM
From @ofidjournal.bsky.social 🦠
A phase 3b trial shows DTG/3TC offers noninferior #ViralSuppression when compared with BIC/FTC/TAF in adults initiating #AntiretroviralTherapy, highlighting the utility of simplified 2-drug regimens for initial #HIV1 treatment across a broad patient population. #IDSky
Dolutegravir Plus Lamivudine Matches 3-Drug ART in Treatment-Naive HIV-1
DTG/3TC achieves noninferior virologic suppression when compared with BIC/FTC/TAF in adults initiating first-line ART for HIV-1.
www.infectiousdiseaseadvisor.com
August 21, 2026 at 6:19 PM
Tenofovir alafenamide fumarate achieves #ViralSuppression rates comparable to tenofovir disoproxil fumarate in patients with chronic #HepatitisB virus infection, with an improved safety profile, highlighting its potential to optimize clinical outcomes while minimizing organ toxicity. #IDSky
TAF vs TDF for Chronic HBV: Comparable Efficacy With Improved Safety Profile
TAF demonstrates similar efficacy to TDF for chronic HBV but offers an improved safety profile.
www.infectiousdiseaseadvisor.com
July 28, 2026 at 7:48 PM
JMIR Formative Res: A Remote Intervention Based on mHealth and Community Health Workers for Antiretroviral Therapy Adherence in People With HIV: Pilot Randomized Controlled Trial #HIV #ARTadherence #mHealth #CommunityHealthWorkers #ViralSuppression
A Remote Intervention Based on mHealth and Community Health Workers for Antiretroviral Therapy Adherence in People With HIV: Pilot Randomized Controlled Trial
Background: Despite the availability of antiretroviral therapy (ART), only 66% of people with HIV in the United States achieve viral suppression, largely due to suboptimal ART adherence. Barriers such as limited access to care and forgetfulness impact adherence rates, which must be maintained at ≥95% to prevent viral load rebound. Combination interventions leveraging community health worker (CHW) support and mobile health (mHealth) technologies have the potential to overcome previously identified barriers and provide cost-effective support for improving adherence and viral suppression outcomes in people with HIV. Objective: This pilot study aimed to evaluate the #feasibility, acceptability, and preliminary efficacy of remote delivery of the Community Health Worker and mHealth to Improve Viral Suppression (CHAMPS) intervention, combining the WiseApp, CHW support, and the CleverCap smart pill bottle. A secondary aim was to gather participants’ feedback on the #usability of the app and pill bottle as well as to better understand their experiences with remote study procedures. Methods: This mixed methods pilot study involved 40 participants with HIV, who were randomly assigned to a control group (n=20, 50%) or the CHAMPS intervention (n=20, 50%) over 3 months. The intervention group participated in up to 12 sessions with CHWs and used the WiseApp, paired with a CleverCap smart pill bottle, to support ART adherence. Remote baseline and follow-up visits were conducted via Zoom and included surveys measuring adherence, self-efficacy, and #usability (measured by Health Information Technology #usability Evaluation Scale [Health-ITUES] and Poststudy System #usability Questionnaire [PSSUQ]). Semistructured interviews explored participants’ experiences with the intervention. Thematic analysis was used to identify key facilitators and barriers based on the Mobile Health Technology Acceptance Model. Results: Remote delivery of the CHAMPS intervention was feasible, with high #usability ratings for both the WiseApp and CleverCap (overall scores on Health-ITUES: mean 4.35, SD 0.58 and PSSUQ: mean 2.04, SD 1.03). In the intervention group, there were nonsignificant improvements in self-reported adherence scores (P=.29) and in self-efficacy scores (P=.07). The adjusted odds ratio for achieving undetectable viral load in the intervention group compared to the control group was 3.01 (95% CI –1.59 to 4.12), indicating a medium effect size in favor of the intervention. Overall study retention was 75% (30/40), with higher retention in the control group. Participants valued the flexibility of remote study procedures, particularly Zoom-based study visits and mailed blood sample kits. Qualitative feedback highlighted the intervention’s acceptability and ability to overcome logistical barriers. Conclusions: The remote CHAMPS pilot study demonstrated the #feasibility and acceptability of combining mHealth tools with CHW support to promote medication adherence among people with HIV. While further optimization is needed to enhance its impact, this intervention shows potential for improving health outcomes in diverse underserved populations. Trial Registration: ClinicalTrials.gov NCT05938413; https://clinicaltrials.gov/study/NCT05938413
dlvr.it
April 2, 2025 at 8:32 PM