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dc.contributor.authorRotsaert, Anke
dc.contributor.authorOgara, Collin
dc.contributor.authorMwanga-Amumpaire, Juliet
dc.contributor.authorKekitiinwa, Adeodata R.
dc.contributor.authorMusiime, Victor
dc.contributor.authorNajjingo, Elizabeth
dc.contributor.authorKisitu, Grace P.
dc.contributor.authorNazzinda, Rashidah
dc.contributor.authorNambi, Esther
dc.contributor.authorLee, Janice
dc.contributor.authorDiallo, Mariama
dc.contributor.authorKyomuhendo, Flavia
dc.contributor.authorWaweru, Moses
dc.contributor.authorAndrieux-Meyer, Isabelle
dc.contributor.authorNöstlinger, Christiana
dc.date.accessioned2023-03-31T09:09:24Z
dc.date.available2023-03-31T09:09:24Z
dc.date.issued2023
dc.identifier.citationRotsaert, A., Ogara, C., Mwanga-Amumpaire, J., Kekitiinwa, A. R., Musiime, V., Najjingo, E., ... & Nöstlinger, C. (2023). Acceptability of a new 4-in-1 Abacavir/Lamivudine/Lopinavir/Ritonavir paediatric fixed-dose combination: the caregiver–child dyads’ perspective. , 10, 20499361231159993.en_US
dc.identifier.urihttp://ir.must.ac.ug/xmlui/handle/123456789/2837
dc.description.abstractBackground: Worldwide, 1.7 million children younger than 15 years were living with HIV in 2021. Only 52% of them had access to antiretrovirals (ARVs). Lack of age-appropriate ARV formulations (i.e. easy to swallow for young infants, acceptable taste) remains the main obstacle to the access to ARVs. Therefore, a strawberry-flavoured Abacavir/Lamivudine/ Lopinavir/Ritonavir (30/15/40/10 mg) fixed-dose combination of granules in a capsule (4-in-1) for children living with HIV weighing 3–25 kg was developed. Objective: We assessed caregivers’ perceived acceptability of the 4-in-1 compared with previous paediatric ARV formulations and factors influencing acceptability. Methods: This exploratory qualitative case study embedded in a phase I/II, open-label, randomized cross-over pharmacokinetic, safety and acceptability study (LOLIPOP) was conducted in three sites in Uganda (May 2019–October 2020). Thirty-six children weighingbetween 3 and 19.9 kg participated in the main study. We purposively sampled caregiver– child dyads according to weight bands, and conducted 20 semi-structured interviews with caregivers and 5 with healthcare providers. We triangulated these results with a quantitative acceptability questionnaire. We analysed interviews inductively using NVivo12 adopting a thematic analysis approach and acceptability questionnaires descriptively to assess concordance between them. Results: All caregivers found the 4-in-1 formulation highly acceptable and easier to use than previous formulations (i.e. pellets/tables/syrup). Appealing taste, ease of administration, easy storage and children’s acceptance contributed to acceptability despite structural challenges of food shortage and HIV stigma. Visible improvements in children’s health and comprehensive and tailored healthcare provider support to overcome initial difficulties such as vomiting increased caregivers’ acceptance. Concordant results from questionnaire- and interview-data confirmed high acceptability. Conclusion: Caregivers of children in all weight bands in this sample found the 4-in-1 granules highly acceptable compared with the pellets/tablets combination. Healthcare providers’ support to caregivers allowed for individual tailoring of drug administration despite challenges such as food shortage. This enabled short-term adherence. These findings informed further practical recommendations.en_US
dc.language.isoen_USen_US
dc.publisherTherapeutic Advances in Infectious Diseaseen_US
dc.subjectAcceptabilityen_US
dc.subjectAntiretroviral therapyen_US
dc.subjectFixed-dose combinationen_US
dc.subjectHIVen_US
dc.subjectPaediatric ARVen_US
dc.titleAcceptability of a new 4-in-1 Abacavir/ Lamivudine/Lopinavir/Ritonavir paediatric fixed-dose combination: the caregiver–child dyads’ perspectiveen_US
dc.typeArticleen_US


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