2017
DOI: 10.1016/j.jpeds.2016.12.034
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Mortality in Children with Human Immunodeficiency Virus Initiating Treatment: A Six-Cohort Study in Latin America

Abstract: Objectives To assess the risks of and factors associated with mortality, loss to followup, and changing regimens after perinatally HIV-infected children initiate combination antiretroviral therapy (cART) in Latin America and the Caribbean. Study design This 1997–2013 retrospective cohort study included 1174 ART-naïve perinatally-infected children who started cART age<18 years (median 4.7 years; interquartile range [IQR] 1.7–8.8) at one of six cohorts from Argentina, Brazil, Haiti, and Honduras, within the Ca… Show more

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Cited by 8 publications
(9 citation statements)
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“…Second-line ART was defined as the regimen after a switch of ≥2 ARVs in the initial regimen, the addition of ≥2 ARVs to the initial regimen, or a substitution of a single drug that was different from the initial drug class. 14…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Second-line ART was defined as the regimen after a switch of ≥2 ARVs in the initial regimen, the addition of ≥2 ARVs to the initial regimen, or a substitution of a single drug that was different from the initial drug class. 14…”
Section: Methodsmentioning
confidence: 99%
“…8,9 Moreover, the need for second-line and third-line treatment options is projected to increase as countries incorporate WHO recommendations for viral load monitoring that will result in increased identification of virologic failure. 10 Although a number of studies on switching regimens after starting first-line ART in pediatric populations have been conducted globally, 3,[10][11][12][13][14] little is known about outcomes among children and adolescents after initiating a second-line ART regimen. One recent global analysis investigated CD4 rebound, loss to follow-up, and mortality among children after starting second-line ART.…”
Section: Introductionmentioning
confidence: 99%
“…Additional outcomes of interest included cumulative incidence of LTFU at 12 months and 5 years of postpartum [14], time to LTFU and virological suppression at 12 months postpartum. Virological suppression was determined by whether the closest VL to 12 months postpartum (AE6 months) was <200 copies/mL.…”
Section: Outcomes and Follow-upmentioning
confidence: 99%
“…Observational data from clinical care cohorts can fill evidence gaps by providing detailed information on critical outcomes, including age and CD4 at ART start, retention and loss to follow-up, and mortality. 3 , 20 22 Such data are particularly valuable for addressing clinical questions that are unlikely to be evaluated in randomized controlled trials and for assessing the real-world impact of implementing new guidelines or interventions.…”
Section: What Are Observational Data?mentioning
confidence: 99%