High costs, with dosing especially problematic for children younger than six
High costs, with dosing especially problematic for children younger than six years, largely a result of the low priority that is given globally to the development of paediatric formulations and regimens [26]. 3TC monotherapy and other sub-optimal interim measures, although being used in some resource-limited settings, are not evidence based, whereas continued PI therapy, even when it does not achieve virological success, could nevertheless PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/25636517 render immunological and clinical benefit in children [27], but at the potential cost of resistance accumulation.BX795 site competing interests The authors declare that they have no competing interests. Received: 30 May 2011 Accepted: 15 November 2011 Published: 15 November 2011 References 1. Chadwick EG, Capparelli EV, Yogev R, Pinto JA, Robbins B, PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/27488460 Rodman JH, Chen J, Palumbo P, Serchuck L, Smith E, Hughes M, P1030 team: Pharmacokinetics, safety and efficacy of lopinavir/ritonavir in infants less than 6 months of age: 24 week results. AIDS 2008, 22(2):249-255. 2. Ren Y, Nuttall JJ, Egbers C, Eley BS, Meyers TM, Smith PJ, Maartens G, McIlleron HM: Effect of rifampicin on lopinavir pharmacokinetics in HIVinfected children with tuberculosis. J Acquir Immune Defic Syndr 2008, 47(5):566-569. 3. van Zyl GU, van der Merwe L, Claassen M, Cotton MF, Rabie H, Prozesky HW, Preiser W: Protease Inhibitor Resistance in South African Children With Virologic Failure. Pediatr Infect Dis J 2009, 28(12):1125-1127. 4. van Zyl GU, Claassen M, Engelbrecht S, Laten JD, Cotton MF, Theron GB, Preiser W: Zidovudine with nevirapine for the prevention of HIV motherto-child transmission reduces nevirapine resistance in mothers from the Western Cape, South Africa. J Med Virol 2008, 80(6):942-946. 5. Jaspan HB, Berrisford AE, Boulle AM: Two-year outcomes of children on non-nucleoside reverse transcriptase inhibitor and protease inhibitor regimens in a South African pediatric antiretroviral program. Pediatr Infect Dis J 2008, 27(11):993-998. 6. Palumbo P, Lindsey JC, Hughes MD, Cotton MF, Bobat R, Meyers T, Bwakura-Dangarembizi M, Chi BH, Musoke P, Kamthunzi P, Schimana W, Purdue L, Eshleman SH, Abrams EJ, Millar L, Petzold E, Mofenson LM, JeanPhilippe P, Violari A: Antiretroviral treatment for children with peripartum nevirapine exposure. N Engl J Med 2010, 363(16):1510-1520. 7. Palumbo P, Violari A, Lindsey J, Hughes M, Jean-Philippe P, Mofenson L, Bwakura-Dangarembizi M, Kamthunzi P, Eshleman S, Purdue L: NVP-vs LPV/rbased ART among HIV+ Infants in Resource-limited Settings: The IMPAACT P1060 Trial 18th Conference on Retroviruses and Oppurtunistic Infections Boston, MA, USA; 2011. 8. Coovadia A, Abrams EJ, Stehlau R, Meyers T, Martens L, Sherman G, Hunt G, Hu CC, Tsai WY, Morris L, Kuhn L: Reuse of nevirapine in exposed HIVinfected children after protease inhibitor-based viral suppression: a randomized controlled trial. JAMA 304(10):1082-1090. 9. Frange P, Briand N, Avettand-Fenoel V, Veber F, Moshous D, Mahlaoui N, Rouzioux C, Blanche S, Chaix ML: Lopinavir/Ritonavir-based Antiretroviral Therapy in Human Immunodeficiency Virus Type 1-infected Naive Children: Rare Protease Inhibitor Resistance Mutations But High Lamivudine/Emtricitabine Resistance at the Time of Virologic Failure. Pediatr Infect Dis J 2011, 30(8):684-688. 10. Soares EA, Santos AF, Gonzalez LM, Lalonde MS, Tebit DM, Tanuri A, Arts EJ, Soares MA: Mutation T74S in HIV-1 subtype B and C proteases resensitizes them to ritonavir and indinavir and confers fitness advantage. J Anti.
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