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Universal antiretroviral therapy for HIV-infected children: a review of the benefits and risks to consider during implementation

Universal antiretroviral therapy for HIV-infected children: a review of the benefits and risks to consider during implementation

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dc.contributor.author Barlow-Mosha, Linda
dc.contributor.author Musiime, Victor
dc.contributor.author Davies, Mary-Ann
dc.contributor.author Prendergast, Andrew J.
dc.contributor.author Musoke, Philippa
dc.contributor.author Siberry, George
dc.contributor.author Penazzato, Martina
dc.date.accessioned 2021-01-01T21:58:18Z
dc.date.available 2021-01-01T21:58:18Z
dc.date.issued 2017
dc.identifier.uri http://combine.alvar.ug/handle/1/48256
dc.description.abstract Background: The 2016 World Health Organization (WHO) consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection, recommended to start all HIV-infected children on antiretroviral therapy (ART). Here, we explore the possible benefits and risks of implementing universal ART for all HIV-infected children and adolescents and outline some of the key considerations that led to the 2016 revision of WHO guidelines. Methods: We conducted a review of the published data from 2000 to 2016, to ascertain the clinical and programmatic benefits, as well as the risks of implementing universal ART for all children. Results and discussion: Universal ART for all children has the potential to increase treatment coverage, which in 2015 was only 51% globally, as well as providing several biological benefits, by preventing: premature death/loss to follow-up, progressive destruction of the immune system, poor growth and pubertal delay, poor neuro-cognitive outcomes and future burden to the health care system with complications of untreated HIV-infection. However, the strategy could be associated with risks, notably development of HIV drug resistance, antiretroviral drug toxicities and increased costs to an already stretched health system. Conclusion: Overall, our findings suggest that the benefits could outweigh the risks and support universal ART for all HIV-infected children, but recognize that national programmes will need to put measures in place to minimize the risks if they choose to implement the strategy.
dc.description.sponsorship World Health Organization, Geneva, SwitzerlandWorld Health Organization
dc.description.sponsorship NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASESUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Allergy & Infectious Diseases (NIAID) [U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924, U01AI069924] Funding Source: NIH RePORTER
dc.language English
dc.publisher JOHN WILEY & SONS LTD
dc.relation.ispartof Journal of the International AIDS Society
dc.subject Universal Antiretroviral Therapy
dc.subject Children
dc.subject Adolescents
dc.subject Resource Limited Settings
dc.subject Review
dc.subject Sub Saharan Africa
dc.subject Who Guidelines
dc.title Universal antiretroviral therapy for HIV-infected children: a review of the benefits and risks to consider during implementation
dc.type Review
dc.identifier.isi 000404152300001
dc.identifier.doi 10.7448/IAS.20.1.21552
dc.identifier.pmid 28691434
dc.publisher.city CHICHESTER
dc.publisher.address THE ATRIUM, SOUTHERN GATE, CHICHESTER PO19 8SQ, W SUSSEX, ENGLAND
dc.identifier.eissn 1758-2652
dc.identifier.volume 20
dc.subject.wc Immunology
dc.subject.wc Infectious Diseases
dc.subject.sc Immunology
dc.subject.sc Infectious Diseases
dc.description.oa DOAJ Gold
dc.description.oa Green Published
dc.description.pages 7
dc.subject.kwp Human-Immunodeficiency-Virus
dc.subject.kwp Chronic Lung-Disease
dc.subject.kwp Drug-Resistance
dc.subject.kwp Viral Load
dc.subject.kwp Immune-Responses
dc.subject.kwp African Children
dc.subject.kwp Adolescents
dc.subject.kwp Growth
dc.subject.kwp Lipodystrophy
dc.subject.kwp Mortality
dc.identifier.articleno 21552
dc.description.affiliation Makerere Univ John Hopkins Univ MUJHU Res Collabo, Clin Dept, Kampala, Uganda
dc.description.affiliation Makerere Univ, Coll Hlth, Dept Paediat & Child Hlth, Kampala, Uganda
dc.description.affiliation Joint Clin Res Ctr, Res Dept, Kampala, Uganda
dc.description.affiliation Univ Cape Town, Sch Publ Hlth & Family Med, Cape Town, South Africa
dc.description.affiliation Queen Mary Univ London, Blizard Inst, London, England
dc.description.affiliation Zvitambo Inst Maternal & Child Hlth Res, Res Dept, Harare, Zimbabwe
dc.description.affiliation Johns Hopkins Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD USA
dc.description.affiliation NIH, Maternal & Pediat Infect Dis Branch, Bldg 10, Bethesda, MD 20892 USA
dc.description.affiliation World Hlth Org, HIV Dept, Geneva, Switzerland
dc.description.email vmusiime@chs.mak.ac.ug
dc.description.corr Musiime, V (corresponding author), Makerere Univ, Coll Hlth Sci, POB 7072, Kampala, Uganda.
dc.description.orcid Prendergast, Andrew/0000-0001-7904-7992
dc.description.orcid Barlow-Mosha, Linda/0000-0003-3241-2141


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