Characteristics, mortality and outcomes at transition for adolescents with perinatal HIV infection in Asia.



Adam W. Bartlett; Khan Huu Truong; Wipaporn Natalie Songtaweesin; Kulkanya Chokephaibulkit; Rawiwan Hansudewechakul; Penh Sun Ly; Pagakrong Lumbiganon; Tavitiya Sudjaritruk; Lam Van Nguyen; Viet Chau Do; Nagalingeswaran Kumarasamy; Nik Khairulddin Nik Yusoff; Nia Kurniati; Moy Siew Fong; Dewi Kumara Wati; Revathy Nallusamy; Annette H. Sohn; Matthew G. Law; Thahira Jamal Mohamed.

AIDS. 2018 Jul 31;32(12):1689-1697.

Abstract

OBJECTIVES:

 

The aim of this study was to describe characteristics of perinatally HIV-infected adolescents (PHIVAs), factors associated with mortality, and outcomes at transition.

DESIGN:

 

Ongoing observational database collating clinical data on HIV-infected children and adolescents in Asia.

METHODS:

 

Data from 2001 to 2016 relating to adolescents (10-19 years) with perinatal HIV infection were analysed to describe characteristics at adolescent entry and transition and combination antiretroviral therapy (cART) regimens across adolescence. A competing risk regression analysis was used to determine characteristics at adolescent entry associated with mortalityOutcomes at transition were compared on the basis of age at cART initiation.

RESULTS:

 

Of 3448 PHIVA, 644 had reached transition. Median age at HIV diagnosis was 5.5 years, cART initiation 7.2 years and transition17.9 years. At adolescent entry, 35.0% had CD4 cell count less than 500 cells/μl and 51.1% had experienced a WHO stage III/IV clinical event. At transition, 38.9% had CD4 cell count less than 500 copies/ml, and 53.4% had experienced a WHO stage III/IV clinical event. Mortality rate was 0.71 per 100 person-years, with HIV RNA ≥1000 copies/ml, CD4 cell count less than 500 cells/μl, height-for-age or weight-for-age z-score less than -2, history of a WHO stage III/IV clinical event or hospitalization and at least second cART associated with mortality. For transitioning PHIVA, those who commenced cART age less than 5 years had better virologic and immunologic outcomes, though were more likely to be on at least second cART.

CONCLUSION:

 

Delayed HIV diagnosis and cART initiation resulted in considerable morbidity and poor immune status by adolescent entry. Durable first-line cART regimens to optimize disease control are key to minimizing mortality. Early cART initiation provides the best virologic and immunologic outcomes at transition.

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