Literature DB >> 27128199

Acceptability of lopinavir/r pellets (minitabs), tablets and syrups in HIV-infected children.

Adeodata Kekitiinwa1, Victor Musiime2,3, Margaret J Thomason4, Grace Mirembe2, Marc Lallemant5, Sarah Nakalanzi1, David Baptiste4, A Sarah Walker4, Diana M Gibb4, Ali Judd4.   

Abstract

BACKGROUND: Lopinavir/ritonavir 'pellets' were recently tentatively approved for licensing. We describe their acceptability for infants and children up to 48 weeks.
METHODS: CHAPAS-2 was a randomized, two-period crossover trial comparing syrup and pellets in HIV-infected infants (n=19, group A, aged 3-<12 months) and children (n=26, group B, 1-<4 years) and tablets and pellets in older children (n=32, group C, 4-<13 years) from two clinics ('JCRC', 'PIDC') in Uganda. At week 8, all groups chose which formulation to continue. Acceptability data were collected at weeks 0, 4, 8, 12 and 48.
RESULTS: For groups A and B overall, the proportion preferring pellets increased between week 0 and week 12 and decreased at week 48 (group A 37%, 72%, 44%; group B 12%, 64% and 36%, respectively), although there were marked differences between clinics. For group C, pellets were progressively less preferred to tablets over time: 41%, 19% and 13% at weeks 0, 12 and 48, respectively. During follow-up unpleasant taste was similarly reported among young children taking pellets and syrups (37%/43% group A; 29%/26% group B), whereas among older children, pellets tasted worse than tablets (40%/2%). No participants reported problems with storage/transportation for pellets (0%/0%) unlike syrups (23%/13%).
CONCLUSIONS: For children <4 years, pellets were more acceptable at week 12 but not week 48. Clinic differences could reflect bias among health-care workers for different formulations. Pellets taste similar to syrup, are easier to store and transport than syrup and represent an alternative formulation for young children unable to swallow tablets; improvements in taste and support for health-care workers may help sustain acceptability.

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Year:  2016        PMID: 27128199      PMCID: PMC6029664          DOI: 10.3851/IMP3054

Source DB:  PubMed          Journal:  Antivir Ther        ISSN: 1359-6535


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