Your browser doesn't support javascript.
loading
Dolutegravir: Virologic response and tolerability of initial antiretroviral regimens for adults living with HIV.
Correa, Analú; Monteiro, Polyana; Calixto, Fernanda; Batista, Joanna d'Arc Lyra; de Alencar Ximenes, Ricardo Arraes; Montarroyos, Ulisses Ramos.
Afiliação
  • Correa A; Medical Sciences College, University of Pernambuco, Recife, Pernambuco, Brazil.
  • Monteiro P; Medical Sciences College, University of Pernambuco, Recife, Pernambuco, Brazil.
  • Calixto F; Teaching Hospital Oswaldo Cruz, University of Pernambuco, Recife, Pernambuco, Brazil.
  • Batista JDL; Medical Sciences College, Federal University of Fronteira Sul, Chapecó, Santa Catarina, Brazil.
  • de Alencar Ximenes RA; Medical Sciences College, University of Pernambuco, Recife, Pernambuco, Brazil.
  • Montarroyos UR; Post-Graduation Program in Tropical Medicine, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
PLoS One ; 15(8): e0238052, 2020.
Article em En | MEDLINE | ID: mdl-32866163
The integrase inhibitor dolutegravir was included in initial antiretroviral therapy in Brazil in January 2017. Studies have demonstrated that the efficacy and safety of antiretrovirals have improved with the introduction of new classes of antiretrovirals, such as integrase inhibitors. This study aimed to estimate the frequency of individuals with a virologic response by week 24 of antiretroviral treatment and to describe the adverse events of the regimen containing dolutegravir. This was a cohort of people living with HIV followed up at a referral hospital. Patients were included who had initiated their first treatment between January and August 2017. Data were obtained from medical records, the Drug Logistics Management System and from the Laboratory Tests Control System. Two hundred and twenty-two patients were included for the tolerability analysis and one hundred and thirty-seven for the virologic response analysis. The mean age was 34 years, the median time between diagnosis and initiating treatment was 1.9 months and the median time on antiretroviral therapy was 13.2 months. The frequency of adverse events was 10% (95% CI: 7% to 15.2%), of these, amongst the most frequent events, 91% presented gastrointestinal effects, and 47.8% neuropsychiatric. By week 24 the estimated incidence of virologic response was 89.1% (95% CI: 83% to 93.5%), with an increase during the first 6 months in the number of T-CD4 lymphocytes of 50.7 cells/mm 3 (95% CI: 42 to 59.3). Initial antiretroviral regimens containing dolutegravir were well tolerated and effective in viral suppression during the first 24 weeks after initiating treatment. The occurrence of adverse events was low, either mild or moderate.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Segurança / Infecções por HIV / Fármacos Anti-HIV / Compostos Heterocíclicos com 3 Anéis Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Segurança / Infecções por HIV / Fármacos Anti-HIV / Compostos Heterocíclicos com 3 Anéis Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos