Sophie Desmonde1, François T Eboua, Karen Malateste, Fatoumata Dicko, Didier K Ekouévi, Sylvie Ngbeché, Fla Koueta, Haby Signate Sy, Lorna Renner, Siriatou A Koumakpai, Valeriane Leroy. 1. aInstitut de Santé Publique, d'Epidémiologie et de Développement, Université Bordeaux bInserm, Centre Inserm U897-Epidémiologie-Biostatistique, Bordeaux, France cCHU de Yopougon, Abidjan, Côte d'Ivoire dHopital Gabriel Toure, Bamako, Mali eIeDEA Regional Center, PACCI, CHU de Treichville fCentre pédiatrique de Prise en charge, de Recherche et de Formation (CePReF), Abidjan, Côte d'Ivoire gHôpital pédiatrique, CHU Charles de Gaulle, Ouagadougou, Burkina Faso hHôpital d'enfants Albert-Royer, Dakar, Sénégal iKorle Bu Hospital, Accra, Ghana jService pédiatrie CHU National, Cotonou, Benin. *See composition in Acknowledgements.
Abstract
BACKGROUND: We described reasons for switching to second-line antiretroviral treatment (ART) and time to switch in HIV-infected children failing first-line ART in West Africa. METHODS: We included all children aged 15 years or less, starting ART (at least three drugs) in the paediatric IeDEA clinical centres in five West-African countries. We estimated the incidence of switch (at least one a drug class change) within 24 months of ART and associated factors were identified in a multinomial logistic regression. Among children with clinical-immunological failure, we estimated the 24-month probability of switching to a second-line and associated factors, using competing risks. Children who switched to second-line ART following the withdrawal of nelfinavir in 2007 were excluded. RESULTS: Overall, 2820 children initiated ART at a median age of 5 years; 144 (5%) were on nelfinavir. At 24-month post-ART initiation, 188 (7%) had switched to second-line. The most frequent reasons were drug stock outs (20%), toxicity (18%), treatment failure (16%) and poor adherence (8%). Over the 24-month follow-up period, 322 (12%) children failed first-line ART after a median time of 7 months. Of these children, 21 (7%) switched to second-line after a median time of 21 weeks in failure. This was associated with older age [subdistribution hazard ratio (sHR) 1.21, 95% confidence interval (95% CI) 1.10-1.33] and longer time on ART (sHR 1.16, 95% CI 1.07-1.25). CONCLUSION: Switches for clinical failure were rare and switches after an immunological failure were insufficient. These gaps reveal that it is crucial to advocate for both sustainable access to first-line and alternative regimens to provide adequate roll-out of paediatric ART programmes.
BACKGROUND: We described reasons for switching to second-line antiretroviral treatment (ART) and time to switch in HIV-infectedchildren failing first-line ART in West Africa. METHODS: We included all children aged 15 years or less, starting ART (at least three drugs) in the paediatric IeDEA clinical centres in five West-African countries. We estimated the incidence of switch (at least one a drug class change) within 24 months of ART and associated factors were identified in a multinomial logistic regression. Among children with clinical-immunological failure, we estimated the 24-month probability of switching to a second-line and associated factors, using competing risks. Children who switched to second-line ART following the withdrawal of nelfinavir in 2007 were excluded. RESULTS: Overall, 2820 children initiated ART at a median age of 5 years; 144 (5%) were on nelfinavir. At 24-month post-ART initiation, 188 (7%) had switched to second-line. The most frequent reasons were drug stock outs (20%), toxicity (18%), treatment failure (16%) and poor adherence (8%). Over the 24-month follow-up period, 322 (12%) children failed first-line ART after a median time of 7 months. Of these children, 21 (7%) switched to second-line after a median time of 21 weeks in failure. This was associated with older age [subdistribution hazard ratio (sHR) 1.21, 95% confidence interval (95% CI) 1.10-1.33] and longer time on ART (sHR 1.16, 95% CI 1.07-1.25). CONCLUSION: Switches for clinical failure were rare and switches after an immunological failure were insufficient. These gaps reveal that it is crucial to advocate for both sustainable access to first-line and alternative regimens to provide adequate roll-out of paediatric ART programmes.
Authors: Avy Violari; Jane C Lindsey; Michael D Hughes; Hilda A Mujuru; Linda Barlow-Mosha; Portia Kamthunzi; Benjamin H Chi; Mark F Cotton; Harry Moultrie; Sandhya Khadse; Werner Schimana; Raziya Bobat; Lynette Purdue; Susan H Eshleman; Elaine J Abrams; Linda Millar; Elizabeth Petzold; Lynne M Mofenson; Patrick Jean-Philippe; Paul Palumbo Journal: N Engl J Med Date: 2012-06-21 Impact factor: 91.245
Authors: Mary-Ann Davies; Harry Moultrie; Brian Eley; Helena Rabie; Gilles Van Cutsem; Janet Giddy; Robin Wood; Karl Technau; Olivia Keiser; Matthias Egger; Andrew Boulle Journal: J Acquir Immune Defic Syndr Date: 2011-03-01 Impact factor: 3.731
Authors: Andrea L Ciaranello; Yuchiao Chang; Andrea V Margulis; Adam Bernstein; Ingrid V Bassett; Elena Losina; Rochelle P Walensky Journal: Clin Infect Dis Date: 2009-12-15 Impact factor: 9.079
Authors: Avy Violari; Mark F Cotton; Diana M Gibb; Abdel G Babiker; Jan Steyn; Shabir A Madhi; Patrick Jean-Philippe; James A McIntyre Journal: N Engl J Med Date: 2008-11-20 Impact factor: 91.245
Authors: Kara Wools-Kaloustian; Irene Marete; Samuel Ayaya; Annette H Sohn; Lam Van Nguyen; Shanshan Li; Valériane Leroy; Beverly S Musick; Jamie E Newman; Andrew Edmonds; Mary-Ann Davies; François T Eboua; Marie-Thérèse Obama; Marcel Yotebieng; Shobna Sawry; Lynne M Mofenson; Constantin T Yiannoutsos Journal: J Acquir Immune Defic Syndr Date: 2018-06-01 Impact factor: 3.731
Authors: Kayla Somerville; Cathy A Jenkins; James G Carlucci; Anna K Person; Daisy M Machado; Marco T Luque; Jorge A Pinto; Vanessa Rouzier; Ruth K Friedman; Catherine C McGowan; Bryan E Shepherd; Peter F Rebeiro Journal: J Acquir Immune Defic Syndr Date: 2021-07-01 Impact factor: 3.771
Authors: George Awungafac; Elvis T Amin; Akemfua Fualefac; Noah F Takah; Lucy A Agyingi; Julius Nwobegahay; Pascale Ondoa; Patrick A Njukeng Journal: PLoS One Date: 2018-06-11 Impact factor: 3.240