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HIV viral load suppression in adults and children receiving antiretroviral therapy-results from the IeDEA collaboration

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2017
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Jiamsakul, Awachana
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HIV viral load suppression in adults and children receiving antiretroviral therapy-results from the IeDEA collaboration
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Author
  • Jiamsakul, Awachana;
  • Kariminia, Azar;
  • Althoff, Keri N.;
  • Cesar, Carina;
  • Cortés Moncada, Claudia;
  • Davies, Mary Ann;
  • Do, Viet Chau;
  • Eley, Brian;
  • Gill, John;
  • Kumarasamy, Nagalingeswaran;
  • Machado, Daisy Maria;
  • Moore, Richard;
  • Prozesky, Hans;
  • Zaniewski, Elizabeth;
  • Law, Matthew;
Abstract
Background: Having 90% of patients on antiretroviral therapy (ART) and achieving an undetectable viral load (VL) is 1 of the 90: 90: 90 by 2020 targets. In this global analysis, we investigated the proportions of adult and paediatric patients with VL suppression in the first 3 years after ART initiation. Methods: Patients from the IeDEA cohorts who initiated ART between 2010 and 2014 were included. Proportions with VL suppression (<1000 copies/ mL) were estimated using (1) strict intention to treat (ITT)-loss to follow-up (LTFU) and dead patients counted as having detectable VL; and (2) modified ITT-LTFU and dead patients were excluded. Logistic regression was used to identify predictors of viral suppression at 1 year after ART initiation using modified ITT. Results: A total of 35,561 adults from 38 sites/16 countries and 2601 children from 18 sites/6 countries were included. When comparing strict with modified ITT methods, the proportion achieving VL suppression at 3 years from ART initiation changed from 45.1% to 90.2% in adults, and 60.6% to 80.4% in children. In adults, older age, higher CD4 count preART, and homosexual/bisexual HIV exposure were associated with VL suppression. In children, older age and higher CD4 percentage pre-ART showed significant associations with VL suppression. Conclusions: Large increases in the proportion of VL suppression in adults were observed when we excluded those who were LTFU or had died. The increases were less pronounced in children. Greater emphasis should be made to minimize LTFU and maximize patient retention in HIV-infected patients of all age groups.
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U.S. National Institutes of Health's National Institute of Allergy and Infectious Diseases Eunice Kennedy Shriver National Institute of Child Health and Human Development National Cancer Institute U01AI035004 U01AI035039 U01AI035040 U01AI035041 U01AI035042 U01AI037613 U01AI037984 U01AI038855 U01AI038858 U01AI042590 U01AI068634 U01AI068636 U01AI069432 U01AI069434 Centers for Disease Control and Prevention, USA CDC-200-2006-18797 CDC-200-2015-63931 Agency for Healthcare Research and Quality, USA 90047713 Health Resources and Services Administration, USA 90051652 Canadian Institutes of Health Research, Canada CBR-86906 CBR-94036 HCP-97105 TGF-96118 Ontario Ministry of Health and Long Term Care Government of Alberta, Canada Intramural Research Program of the National Cancer Institute Australian Government Department of Health and Ageing NCI P30AI027757 P30AI027763 P30AI027767 P30AI036219 P30AI050410 P30AI094189 P30AI110527 P30MH62246 R01AA016893 R01CA165937 R01DA004334 R01DA011602 R01DA012568 R24AI067039 U01AA013566 U01AA020790 U01AI1031834 U01AI034989 U01AI034993 U01AI034994 M01RR000052 National Cancer Inst NCI U54MD007587 UL1RR024131 UL1TR000004 UL1TR000083 UL1TR000454 UM1AI035043 Z01CP010214 Z01CP010176 U01AI069907 U01AI069923 U01AI069924 U01AI069918 F31DA037788 G12MD007583 K01A1093197 K23EY013707 K24DA000432 K24AI065298 KL2TR000421 N02CP055504 National Cancer InstNCI U01AI103390 U01AI103397 U01AI103401 U01AI103408 U01DA036935 U01HD032632 U10EY008057 U10EY008052 U10EY008067 U24AA020794
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Artículo de publicación ISI
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URI: https://repositorio.uchile.cl/handle/2250/148532
ISSN: 1077-9450
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Jaids-Journal of Acquired Immune Deficiency Syndromes Vol. 76 (3): 319-329
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