Hepatitis B prevalence and influence on HIV treatment outcome and mortality in the Chilean AIDS Cohort
Author
dc.contributor.author
Otto Knapp, Ralf
Author
dc.contributor.author
Cortés Moncada, Claudia
es_CL
Author
dc.contributor.author
Saavedra, Felipe
es_CL
Author
dc.contributor.author
Wolff Reyes, Marcelo
es_CL
Author
dc.contributor.author
Weitzel, Thomas
es_CL
Admission date
dc.date.accessioned
2014-01-14T18:46:27Z
Available date
dc.date.available
2014-01-14T18:46:27Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
International Journal of Infectious Diseases 17 (2013) e919–e924
en_US
Identifier
dc.identifier.other
DOI: 10.1016/j.ijid.2013.05.009
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/129150
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
Objectives: To analyze the prevalence of hepatitis B virus (HBV) co-infection and its influence on
mortality and treatment outcome within a large AIDS cohort in Chile.
Methods: Clinical and epidemiological data from the Chilean AIDS Cohort were retrospectively analyzed.
Adult patients tested for hepatitis B surface antigen (HBsAg) during the time period of October 2001 to
October 2007 were included.
Results: Of 5115 cohort patients, 1907 met the inclusion criteria. The prevalence of HBV co-infection was
8.4%. Overall mortality rates were 2.15 and 1.77 per 100 person-years for HBsAg-positive and HBsAg-
negative HIV patients, respectively, with a mortality rate ratio of 1.22 (95% confidence interval 0.58–
2.54). Kaplan–Meier survival and Cox regression analysis did not show significant differences between
the groups. Virological and immunological responses to antiretroviral therapy (ART) were not influenced
by HBsAg status, but in co-infected patients, initial ART was more frequently changed.
Conclusions: The prevalence of hepatitis B co-infection was 8.4%, indicating a markedly elevated
hepatitis B risk compared to the general population in Chile. Neither treatment outcome nor overall
mortality was influenced by hepatitis B co-infection. Still, patients with hepatitis B co-infection had less
stable ART regimens, which might be related to a higher risk of hepatotoxic drug effects.