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1.
Pediatrics ; 121(3): e513-21, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18310171

RESUMEN

OBJECTIVE: An unstructured treatment interruption in children with perinatally acquired HIV infection is an issue with unresolved significance. The objective of this study was to investigate the actual prevalence and clinical outcomes of a treatment interruption in children and adolescents with perinatally acquired HIV-1 infection. METHODS: Clinical data were analyzed for 72 children and adolescents who had HIV-1 infection and stopped their medications at 4 academic centers in the United States between January 2000 and September 2004. RESULTS: Among 405 patients with perinatal HIV-1 infection, 72 (17.8%) experienced a treatment interruption during the observation period. The mean age of patients at the time of the treatment interruption was 12.8 years, and the mean length of the treatment interruption was 14 months. Medication fatigue was the most common reason for a treatment interruption. The CD4+ T-cell percentage nadir before the treatment interruption did not predict CD4+ T-cell percentage declines during the treatment interruption; however, the CD4+ T-cell percentage gain from nadir to the time of the treatment interruption predicted CD4+ T-cell percentage declines during the treatment interruption. During the median follow-up of 19 months (range: 6-48 months), 48 (67%) patients resumed antiretroviral medications. As expected, there was a continuous CD4+ T-cell percentage decrease and plasma HIV-1 RNA increase during the observation period. Overall, 7 (10%) patients were admitted to the hospital; 2 (3%) patients experienced an AIDS-defining illness. CONCLUSIONS: An unstructured treatment interruption seems to be a major issue for youth with perinatally acquired HIV-1 infection. Patients who experienced the greatest rise in CD4+ T-cell percentage on treatment had the largest CD4+ T-cell percentage decline after the treatment interruption. Close monitoring is required when a treatment interruption occurs in children and adolescents with HIV infection.


Asunto(s)
Terapia Antirretroviral Altamente Activa/métodos , Infecciones por VIH/congénito , Infecciones por VIH/tratamiento farmacológico , Negativa del Paciente al Tratamiento/estadística & datos numéricos , Adolescente , Antígenos CD4/análisis , Recuento de Linfocito CD4 , Niño , Preescolar , Relación Dosis-Respuesta a Droga , Esquema de Medicación , Femenino , Estudios de Seguimiento , Infecciones por VIH/epidemiología , Humanos , Estudios Longitudinales , Masculino , Probabilidad , Sistema de Registros , Estudios Retrospectivos , Medición de Riesgo , Índice de Severidad de la Enfermedad , Estadísticas no Paramétricas , Factores de Tiempo , Resultado del Tratamiento , Carga Viral
2.
Sex Transm Dis ; 34(2): 65-8, 2007 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-16794560

RESUMEN

BACKGROUND: We sought to evaluate the tolerability and feasibility of establishing an HIV postexposure prophylaxis (PEP) program at our hospital using the guidelines for children and adolescents after sexual assault. METHODS: This study was a prospective, nonrandomized observational study conducted from March 1999 until September 2002. Subjects (age <19 years) who presented to a pediatric emergency room within 72 hours of a sexual assault were eligible for enrollment. A 28-day PEP regimen of zidovudine and lamivudine was given. RESULTS: In all, 70 adolescents were evaluated and 33 (31 females and 2 males) were enrolled. The mean age of enrolled subjects was 15 years, 61% were Hispanic, 30% black, and 79% presented to the emergency room within 24 hours of assault. Vaginal exposure was the most common site of penetration (64% [21 of 33]), but 18% (6 of 33) reported anal penetration. Only 9 subjects (27%) took >or=90% of all the medications. All subjects who returned for follow up tested HIV-negative. Adverse events occurred in 48% (16 of 33) of subjects; the most common events were abdominal pain, nausea, or vomiting. CONCLUSION: Poor adherence to medications and visits is a significant problem in PEP programs for sexually assaulted children and adolescents.


Asunto(s)
Fármacos Anti-VIH/administración & dosificación , Infecciones por VIH/prevención & control , VIH/crecimiento & desarrollo , Lamivudine/administración & dosificación , Delitos Sexuales , Zidovudina/administración & dosificación , Adolescente , Adulto , Fármacos Anti-VIH/efectos adversos , Niño , Combinación de Medicamentos , Femenino , Humanos , Lamivudine/efectos adversos , Masculino , Persona de Mediana Edad , Ciudad de Nueva York , Cooperación del Paciente , Estudios Prospectivos , Análisis de Regresión , Zidovudina/efectos adversos
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