- Oral presentation
- Open Access
Outcome of Treatment of Tuberculosis in HIV Infected Persons in the Era of Highly Active Antiretroviral Therapy (HAART) as Seen in the Second City Tuberculosis Hospital in Saint Petersburg, Russia
© The Author(s) 2005
- Published: 8 December 2005
- Human Immunodeficiency Virus
- Tuberculosis Treatment Outcome
- Human Immunodeficiency Virus Medication
- Opportunistic Illness
Tuberculosis (TB) is the leading cause of morbidity and mortality among persons with HIV/AIDS in highly affected regions including Russia. Despite the fact that Russia has the infrastructure for the treatment of TB unlike developing countries, authorities are not yet paying attention to provide antiretroviral treatment for these category of people who are mostly IDU users, former prisoners and jobless. As such the benefit of highly active antiretroviral therapy (HAART) in the treatment of patients co-infected with tuberculosis (TB) and human immunodeficiency virus (HIV) has never been explored in this country.
To assess the risks and benefits of administering highly active antiretroviral therapy (HAART) during the treatment of tuberculosis (TB) in HIV-infected patients.
53 HIV-infected persons diagnosed with active TB were recruited in the special HIV and TB unit of the second city tuberculosis hospital in Saint- Petersburg, Russia into an observational, prospective study aimed to evaluate tuberculosis treatment outcomes between Dec.2003 and March 2005. Only 15 patients (28.3%) with a median CD4 cell count of 235 cells/mm3 were on ART (AZT+3TC+EFV), while the rest 38 (71.7%) with a median CD4 cell count of 267 cells/mm3 received antituberculosis medications only. Clinical and immunologic responses were assessed within the two groups by comparing incidence of new AIDS-associated opportunistic illnesses (OIs), adverse events and CD4 cells dynamics.
Among antiretroviral patients, CD4 cell count increased to 297 cells/mm3 versus a decrease to 212 cell/mm3 in patients on anti-tuberculosis treatment alone (p = 0.10). The risk for HIV progression to new OIs was lower among antiretroviral group (3.5 versus 24.5%; relative risk (RR) = 0.14. Adverse events (AE) occurred in 3 (20%) of the15 patients on antiretroviral, all with a CD4 cell count of < 100 cells/mm3 and one patient interrupted HIV medication. The majority of AE occurred within the first 2 months, with anemia, increased cough, rash and gastrointestinal upset occurring most commonly.