Background
In 2021, Nigeria introduced the 10mg paediatric dolutegravir (DTG) formulation for children living with HIV (CLHIV) aiming to improve virological outcomes, and immediately commenced transitioning children < 10 years old on first-line non-DTG-based regimen to DTG. We assessed the association between the transition to DTG-based ART and virological suppression among CLHIV.
Methods
We conducted a retrospective cohort study using routinely collected data from 121 PEPFAR-supported health facilities in Akwa Ibom and Cross River States. We included all ART-experienced CLHIV who were transitioned to DTG between July and December 2021, had a baseline viral load (VL) assessment before the transition and VL ≥ 6 months after transitioning. We defined VL as a three-level outcome (i.e., ≤ 50 copies/ml – undetectable, 51–999 copies/ml – low-level viremia and ≥ 1,000 copies/ml – unsuppressed). We assessed the association between the transition to DTG and VL using ordinal logistic regression with generalized estimating equations. We also conducted additional sensitivity analyses on a complete case dataset and assessed the impact of the transition on various definitions of virological suppression including undetectable (< 50 copies/ml) vs. detectable (≥ 50 copies/ml).
Results
Out of 1,951 CLHIV included in this analysis, 1,250 (64.1%) were between the ages of five and nine, 993 (50.9%) were male. Among these, 1,786 (91.5%) had undetectable VL levels, up from 1,611 (82.6%) at baseline, while 123 (6.3%) had low-level viraemia, down from 271 (13.9%) initially. The transition to DTG-based ART was associated with virological suppression (adjusted odds ratio [aOR]: 1.70, 95%CI: 1.20, 2.41) and undetectable VL (aOR: 2.56, 95%CI: 2.06, 3.19). Findings were consistent in sensitivity analyses.
Conclusions
CLHIV achieved favourable virological changes when transitioned to DTG-based ART, including undetectable viral load rates. Findings suggest DTG can improve overall program outcomes and reduce the risk for low-level viremia in CLHIV, emphasizing its role in achieving HIV epidemic control among CLHIV.