Directly observed therapy for chronic hepatitis C: A randomized clinical trial in the prison setting |
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Authors: | Pablo Saiz de la Hoya,Joaquí n Portilla,André s Marco,Julio Garcí a-Guerrero,Inmaculada Faraco,José Antó n,José de Juan,Edelmira Pozo |
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Affiliation: | 1. Servicios Médicos Centro Penitenciario Fontcalent, Alicante 1, Spain;2. Unidad de Enfermedades Infecciosas y Servicio de Medicina Interna, Hospital General Universitario de Alicante, Universidad Miguel Hernández, Elche, Spain;3. Servicios Médicos Centro Penitenciario Barcelona Hombres, Spain;4. Servicios Médicos Centro Penitenciario, Castellón 1, Spain;5. Servicios Médicos Centro Penitenciario, Sevilla 1, Spain;6. Servicios Médicos Centro Penitenciario Albolote, Granada, Spain;g Servicios Médicos Centro Penitenciario Córdoba, Spain;h Servicios Médicos Centro Penitenciario Villabona, Asturias, Spain |
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Abstract: | BackgroundThe diagnosis and treatment of chronic hepatitis C are major concerns in prisons.ObjectivesThe aim of this randomized clinical trial was to determine the extent to which directly observed therapy (DOT) improved the efficacy of the standard treatment for chronic hepatitis C in the prison setting.Patients and methodsA randomized clinical trial was carried out to evaluate the efficacy of a DOT compared with a self-administered therapy in prison inmates who underwent standard treatment for chronic hepatitis C (based on pegylated interferon alpha-2a and ribavirin).ResultsA total of 252 inmates were randomized, of which 244 were analyzed: 109 in the DOT group and 135 in the non-DOT group. The mean age was 35.88 years (SD 6.54), 94.3% were men, 72.1% reported intravenous drug use, 21.3% were HIV co-infected, and 55.3% had genotype 1 or 4. The patients received the study treatment for a median time of 33.9 weeks in the overall sample. Sustained virological response was achieved in 60.6% (95% CI, 51.17–69.22) of the DOT group and in 65.9% (95% CI, 57.59–73.38) of the standard therapy group (risk ratio = 0.92; 95% CI, 0.76–1.12). The mean proportion of patients continuing the treatment was 83% (SD = 31). Adverse events were reported in 93.4% of the patients, and serious adverse events were reported in 8.2%, with no significant differences between groups.ConclusionsSustained virological response was remarkably high, although there were no differences between groups, probably due to high treatment adherence. |
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Keywords: | Chronic hepatitis C Directly observed therapy HCV Pegylated interferon Ribavirin |
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