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1.
HIV Med ; 14(4): 226-32, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23094820

ABSTRACT

OBJECTIVES: Virological failure on first-line nonnucleoside reverse transcriptase inhibitor (NNRTI)-based treatment regimens has become a problem in HIV-infected children on long-term antiretroviral therapy (ART). Protease inhibitor (PI)-based regimens are therefore often given to children failing NNRTI-based regimens. The aim of the study was to assess the 48-week effectiveness, safety and predictive factors for viral suppression of PI-based regimens in HIV-infected Thai children who had failed NNRTI-based regimens. METHODS: This study assessed 41 HIV-infected children who had failed first-line NNRTI-based regimens and were switched to PI-based regimens for at least 48 weeks. We assessed their CD4 cell counts, plasma HIV RNA levels, weight-for-age and height-for-age z-scores, and adverse events. RESULTS: The children's median age was 9.5 years (range 1.5-15.8 years). At baseline, their median CD4 cell count was 276 cells/µL [interquartile range (IQR) 160-749 cells/µL], and their median plasma HIV RNA level was 4.5 log10 HIV-1 RNA copies/mL (IQR 3.9-4.8 log10 copies/mL). After 48 weeks of PI-based therapy, their CD4 cell counts increased to a median of 572 cells/µL (IQR 343-845 cells/µL) and in 73.2% plasma HIV RNA levels decreased to < 50 copies/mL. Their median weight-for-age and height-for-age z-scores were stable over the period of the study. Diarrhoea occurred in 29.3% of patients. Triglyceride levels were significantly higher at weeks 24 and 48 in comparison to baseline measurements. CONCLUSIONS: PI-based regimens are safe and effective for HIV-infected Thai children who have failed first-line NNRTI-based regimens. However, long-term follow-up is warranted in order to ascertain the feasibility and sustainability of these new regimens.


Subject(s)
Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , HIV-1 , Protease Inhibitors/therapeutic use , Adolescent , Analysis of Variance , Anti-HIV Agents/adverse effects , Antiretroviral Therapy, Highly Active , Child , Child, Preschool , Female , HIV Infections/virology , Humans , Infant , Male , Protease Inhibitors/adverse effects , RNA, Viral/analysis , Retrospective Studies , Reverse Transcriptase Inhibitors/therapeutic use , Thailand , Treatment Failure
2.
Int J STD AIDS ; 23(5): 335-9, 2012 May.
Article in English | MEDLINE | ID: mdl-22648887

ABSTRACT

This study identified causes of first hospitalization among perinatally acquired HIV-infected children at Chiang Mai University Hospital between 1989 and 2009. Data were stratified into three seven-year time periods: pre-Pneumocystis jiroveci pneumonia (PJP) prophylaxis, pre-antiretroviral therapy (ART) and ART period. Over the 21-year study period, 1121 children were hospitalized. The mean age at admission was 2.7 years and had become older over time. Of the 1121 hospitalization causes, 50.6% were AIDS-defining illnesses (ADIs), 48.1% were non-AIDS-defining illnesses (NADIs) and 1.3% were related to immune reconstitution syndrome. Types of ADIs changed over time: PJP and recurrent Salmonella septicaemia decreased, while mycobacterial infection and systemic fungal infection increased. For NADIs, bacterial infections, viral infections and gastrointestinal problems decreased, but haematological problems increased in the third period. Decline in the number of hospitalizations and mortality rate, increase in the mean age of hospitalized children, change in the distribution of specific illnesses and appearance of immune reconstitution syndrome were observed in the ART period.


Subject(s)
AIDS-Related Opportunistic Infections/complications , AIDS-Related Opportunistic Infections/diagnosis , HIV Infections/complications , HIV Infections/diagnosis , Hospitalization/statistics & numerical data , AIDS-Related Opportunistic Infections/mortality , Age Factors , Bacterial Infections/epidemiology , Bacterial Infections/mortality , Child , Child, Preschool , Female , HIV Infections/mortality , Humans , Infant , Male , Mycoses/epidemiology , Mycoses/mortality , Parasitic Diseases/epidemiology , Parasitic Diseases/mortality , Survival Analysis , Thailand/epidemiology , Virus Diseases/epidemiology , Virus Diseases/mortality
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