TY - JOUR
T1 - Disparities in dolutegravir utilisation in children, adolescents and young adults (0-24 years) living with HIV. An analysis of the IeDEA Pediatric West African cohort
AU - IeDEA Pediatric West African cohort
AU - Desmonde, Sophie
AU - Dame, Joycelyn
AU - Malateste, Karen
AU - David, Agatha
AU - Amorissani-Folquet, Madeleine
AU - N'gbeche, Sylvie
AU - Sylla, Mariam
AU - Takassi, Elom
AU - Eboua, François Tanoh
AU - Kouakou, Kouadio
AU - Bagnan Tossa, Lehila
AU - Yonaba, Caroline
AU - Leroy, Valeriane
AU - Yonaba, Caroline
AU - Bagnan, Lehila
AU - Dame, Jocelyn
AU - N'Gbeche, Sylvie Marie
AU - Folquet, Madeleine Amorissani
AU - Eboua, François Tanoh
AU - Traore, Fatoumata Dicko
AU - Ezchechi, Oliver
AU - David, Agatha
AU - Audu, Rosemary
AU - Takassi, Elom
AU - Jaquet, Antoine
AU - Ekouevi, Didier Koumavi
AU - Dabis, François
AU - Bernard, Charlotte
AU - Couturier, Caroline
AU - Malateste, Karen
AU - Marcy, Olivier
AU - Plaisy, Marie Kerbie
AU - Rabourdin, Elodie
AU - Tiendrebeogo, Thierry
AU - Dahourou, Désiré
AU - Desmonde, Sophie
AU - Hedible, Gildas Boris
AU - Jesson, Julie
AU - Leroy, Valeriane
AU - Sodinyessi, Emile
AU - Moh, Raoul
AU - Azani, Jean Claude
AU - Diarra, Kadidja
AU - Koffi, Jean Jacques
AU - Bengali, Maika
AU - Cissé, Abdoulaye
AU - Gnepa, Guy
AU - Komena, Eric
AU - Lenaud, Séverin
AU - Boni, Simon
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.
PY - 2025/1/14
Y1 - 2025/1/14
N2 - Introduction We describe the 24-month incidence of Dolutegravir (DTG)-containing antiretroviral treatment (ART) initiation since its introduction in 2019 in West Africa. Methods We included all patients aged 0-24 years on ART from nine clinics in Côte d'Ivoire (n=4), Ghana, Nigeria, Mali, Benin, and Burkina Faso. Baseline varied by clinic and was defined as date of first DTG prescription; patients were followed up until database closure/death/loss to follow-up (LTFU, no visit ≥7 months), whichever came first. We computed the cumulative incidence function for DTG initiation; associated factors were explored in a shared frailty model, accounting for clinic heterogeneity. Results Since 2019, 3350 patients were included; 47.2% were female; 78.9% had been on ART ≥12 months. Median baseline age was 12.5 years (IQR 8.4-15.8). Median follow-up was 14 months (IQR 7-22). The overall cumulative incidence of DTG initiation reached 22.7% (95% CI 21.3 to 24.2) and 56.4% (95% CI 54.4 to 58.4) at 12 and 24 months, respectively. In univariate analyses, those aged <5 years and female were overall less likely to switch. Adjusted on ART line and available viral load (VL) at baseline, females aged >10 years were less likely to initiate DTG compared with males of the same age (adjusted HR among 10-14 years: 0.62, 95% CI 0.54 to 0.72; among ≥15 years: 0.43, 95% CI 0.36 to 0.50), as were those with detectable VL (>50 copies/mL) compared with those in viral suppression (aHR 0.86, 95% CI 0.77 to 0.97) and those on PIs compared with those on non-nucleoside reverse-transcriptase inhibitors (aHR after 12 months of roll-out: 0.75, 95% CI 0.65 to 0.86). Conclusion Paediatric DTG uptake was incomplete and unequitable in west African settings: DTG use was least likely in children <5 years, females ≥10 years and those with detectable VL. Maintained monitoring and support of treatment practices is required to better ensure universal and equal uptake.
AB - Introduction We describe the 24-month incidence of Dolutegravir (DTG)-containing antiretroviral treatment (ART) initiation since its introduction in 2019 in West Africa. Methods We included all patients aged 0-24 years on ART from nine clinics in Côte d'Ivoire (n=4), Ghana, Nigeria, Mali, Benin, and Burkina Faso. Baseline varied by clinic and was defined as date of first DTG prescription; patients were followed up until database closure/death/loss to follow-up (LTFU, no visit ≥7 months), whichever came first. We computed the cumulative incidence function for DTG initiation; associated factors were explored in a shared frailty model, accounting for clinic heterogeneity. Results Since 2019, 3350 patients were included; 47.2% were female; 78.9% had been on ART ≥12 months. Median baseline age was 12.5 years (IQR 8.4-15.8). Median follow-up was 14 months (IQR 7-22). The overall cumulative incidence of DTG initiation reached 22.7% (95% CI 21.3 to 24.2) and 56.4% (95% CI 54.4 to 58.4) at 12 and 24 months, respectively. In univariate analyses, those aged <5 years and female were overall less likely to switch. Adjusted on ART line and available viral load (VL) at baseline, females aged >10 years were less likely to initiate DTG compared with males of the same age (adjusted HR among 10-14 years: 0.62, 95% CI 0.54 to 0.72; among ≥15 years: 0.43, 95% CI 0.36 to 0.50), as were those with detectable VL (>50 copies/mL) compared with those in viral suppression (aHR 0.86, 95% CI 0.77 to 0.97) and those on PIs compared with those on non-nucleoside reverse-transcriptase inhibitors (aHR after 12 months of roll-out: 0.75, 95% CI 0.65 to 0.86). Conclusion Paediatric DTG uptake was incomplete and unequitable in west African settings: DTG use was least likely in children <5 years, females ≥10 years and those with detectable VL. Maintained monitoring and support of treatment practices is required to better ensure universal and equal uptake.
KW - Cohort study
KW - HIV
KW - Paediatrics
KW - Public Health
UR - https://www.scopus.com/pages/publications/85215424317
U2 - 10.1136/bmjgh-2024-016512
DO - 10.1136/bmjgh-2024-016512
M3 - Article
AN - SCOPUS:85215424317
SN - 2059-7908
VL - 10
JO - BMJ Global Health
JF - BMJ Global Health
IS - 1
M1 - e016512
ER -