Group-based trajectory modeling to determine long-term HIV viral load trends among children with HIV in Kenya

Author:

Neary Jillian1ORCID,Njuguna Irene23,Wagner Anjuli D.2,Richardson Barbra A.245,Chebet Daisy6,Langat Agnes6,Ngugi Evelyn6,Benki-Nugent Sarah2,Moraa Hellen6,Hawes Stephen E.1,Overbaugh Julie5,Slyker Jennifer A.12,Lehman Dara A.25,Wamalwa Dalton6,John-Stewart Grace1278

Affiliation:

1. Department of Epidemiology, University of Washington, Seattle, WA

2. Department of Global Health, University of Washington, Seattle, WA

3. Kenyatta National Hospital, Nairobi, Kenya

4. Department of Biostatistics, University of Washington, Seattle, WA

5. Fred Hutchinson Cancer Center, Seattle, WA, USA

6. Department of Pediatrics and Child Health, University of Nairobi, Nairobi, Kenya

7. Department of Medicine, University of Washington, Seattle, WA

8. Department of Pediatrics, University of Washington, Seattle, WA

Abstract

Background: Identifying determinants of longitudinal HIV viral load (VL) trajectories using group-based trajectory modeling (GBTM) can inform clinical strategies and mechanisms of non-adherence among children. Methods: Children under 12 months of age who were newly diagnosed with HIV were enrolled in the Optimizing Pediatric HIV Therapy (OPH; NCT00428116) from 2007-2010. Children initiated antiretroviral therapy (ART) at enrollment, and VL was assessed every 3 months for 24 months post-ART and 6-monthly thereafter up to 8 years of age. VL trajectory groups were defined using GBTM. Fisher’s exact and Kruskal-Wallis tests were used to determine correlates of each trajectory group compared to the sustained-low VL group. Results: Five VL trajectory groups were identified among 89 children with 522 VL visits from 6-24 months: sustained-low VL (63% of children), sustained-very-high (16%), sustained-high (9%), low-to-high (7%), and high-with-periods-of-low (6%). Children in the sustained-high group were more frequently on a first-line protease inhibitor (PI)-based regimen (63% vs 38%; p=0.03) and had younger caregivers (median: 22 vs 28 years; p=0.02). Among 54 children with 560 VL visits followed from 48-96 months, 5 trajectory groups were identified: sustained-low (74%), mid-range (4%), periods-of-low (7%), high-to-low (7%), and sustained-high (7%). Those in the high-to-low group had younger caregivers (21 vs 29 years; p=0.01). Conclusions: GBTM identified unique VL patterns among children with unsuppressed VL. Caregiver and regimen-related characteristics were associated with patterns of non-suppression. Younger caregivers may benefit from tailored counseling to help them support child ART adherence. Palatable regimens are necessary for viral suppression among children with HIV.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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