Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/201
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dc.contributor.authorKoller, Manuel
dc.contributor.authorPatel, Kunjal
dc.contributor.authorChi, Benjamin H.
dc.contributor.authorWool-Kaloustian, Kara
dc.contributor.authorDicko, Fatoumata
dc.contributor.authorChokephaibulkit, Kulkanya
dc.contributor.authorChimbetete, Cleophas
dc.contributor.authorAvila, Dorita
dc.contributor.authorHazra, Rohan
dc.contributor.authorAyaya, Samual
dc.contributor.authorLeroy, Valeriane
dc.contributor.authorTrong, Huu Khanh
dc.contributor.authorEgger, Matthias
dc.contributor.authorDavies, Mary-Ann
dc.date.accessioned2017-10-11T14:58:01Z
dc.date.available2017-10-11T14:58:01Z
dc.date.issued2015-01
dc.identifier.otherdoi:10.1097/QAI.0000000000000380.
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351302/
dc.identifier.urihttp://ir.mu.ac.ke:8080/xmlui/handle/123456789/201
dc.description.abstractBackground: The CD4 cell count or percent (CD4%) at the start of combination antiretroviral therapy (cART) are important prognostic factors in children starting therapy and an important indicator of program performance. We describe trends and determinants of CD4 measures at cART initiation in children from low-, middle- and high-income countries. Methods: We included children aged <16 years from clinics participating in a collaborative study spanning sub-Saharan Africa, Asia, Latin America and the United States of America (USA). Missing CD4 values at cART start were estimated through multiple imputation. Severe immunodeficiency was defined according to World Health Organization criteria. Analyses used generalized additive mixed models adjusted for age, country and calendar year. Results: 34,706 children from nine low-income, six lower middle-income, four upper middle-income countries and one high-income country (United States of America, USA) were included; 20,624 children (59%) had severe immunodeficiency. In low-income countries the estimated prevalence of children starting cART with severe immunodeficiency declined from 76% in 2004 to 63% in 2010. Corresponding figures for lower middle-income countries were from 77% to 66% and for upper middle-income countries from 75% to 58%. In the USA, the percentage decreased from 42% to 19% during the period 1996 to 2006. In low- and middle-income countries infants and children aged 12-15 years had the highest prevalence of severe immunodeficiency at cART initiation. Conclusions: Despite progress in most low- and middle-income countries, many children continue to start cART with severe immunodeficiency. Early diagnosis and treatment of HIV-infected children to prevent morbidity and mortality associated with immunodeficiency must remain a global public health priority.en_US
dc.description.sponsorshipFunding sources: The African regions of the International epidemiologic Databases to Evaluate AIDS (IeDEA) are supported by the National Cancer Institute (NCI), the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) and the National Institute of Allergy And Infectious Diseases (NIAID) as part of the International epidemiologic Databases to Evaluate AIDS (IeDEA) (Grants 5U01AI069919-04, 5U01-AI069924-05, 1U01 AI069927, U01AI069911-01). The TREAT Asia HIV Observational Database, TREAT Asia Studies to Evaluate Resistance, and the Australian HIV Observational Database are initiatives of TREAT Asia, a program of amfAR, The Foundation for AIDS Research, with support from the Dutch Ministry of Foreign Affairs through a partnership with Stichting Aids Fonds, and NIAID, NICHD and NCI, as part of IeDEA (U01AI069907). Queen Elizabeth Hospital and the Integrated Treatment Centre received additional support from the Hong Kong Council for AIDS Trust Fund. The Kirby Institute is funded by the Australian Government Department of Health and Ageing, and is affiliated with the Faculty of Medicine, University of New South Wales. The NICHD Site Development Initiative (NISDI) was funded by the NIH and NICHD (contracts N01-HD-3-3345 and N01-HD-8-0001). The Pediatric HIV/AIDS Cohort Study (PHACS) was supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development with co-funding from the National Institute on Drug Abuse, the National Institute of Allergy and Infectious Diseases, the Office of AIDS Research, the National Institute of Mental Health, the National Institute of Neurological Disorders and Stroke, the National Institute on Deafness and Other Communication Disorders, the National Heart Lung and Blood Institute, the National Institute of Dental and Craniofacial Research, and the National Institute on Alcohol Abuse and Alcoholism, through cooperative agreements with the Harvard University School of Public Health (HD052102, 3 U01 HD052102-05S1, 3 U01 HD052102-06S3) and the Tulane University School of Medicine (HD052104, 3U01HD052104-06S1). Support for the International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT) 219C study is provided by the NIAID (U01 AI068632) and NICHD (contract N01-3-3345 and HHSN267200800001C). This work was also supported by the Statistical and Data Analysis Center at Harvard School of Public Health, under the NIAID cooperative agreement #5 U01 AI41110 with the Pediatric AIDS Clinical Trials Group (PACTG) and #1 U01 AI068616 with the IMPAACT Group.en_US
dc.language.isoenen_US
dc.publisherPubMed Central (PMC)en_US
dc.relation.ispartofseries;PMC4351302
dc.subjectImmunodeficiency in childrenen_US
dc.subjectAntiretroviral therapyen_US
dc.subjectLowen_US
dc.subjectMiddleen_US
dc.subjectLow, middle and high-income countriesen_US
dc.titleImmunodeficiency in children starting antiretroviral therapy in low-, middle- and high-income countriesen_US
dc.typeArticleen_US
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