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Factors associated to modification of first-line antiretroviral therapy due to adverse events in people living with HIV/AIDS
Azevedo, Larissa Negromonte; Ximenes, Ricardo Arraes de Alencar; Monteiro, Polyana; Montarroyos, Ulisses Ramos; Miranda-Filho, Demócrito de Barros.
  • Azevedo, Larissa Negromonte; Universidade de Pernambuco. Programa de Pós-graduação em Ciências da Saúde. Recife. BR
  • Ximenes, Ricardo Arraes de Alencar; Universidade de Pernambuco. Programa de Pós-graduação em Ciências da Saúde. Recife. BR
  • Monteiro, Polyana; Universidade de Pernambuco. Faculdade de Ciências Médicas. Serviço de Doenças Infecciosas. Recife. BR
  • Montarroyos, Ulisses Ramos; Universidade de Pernambuco. Programa de Pós-graduação em Ciências da Saúde. Recife. BR
  • Miranda-Filho, Demócrito de Barros; Universidade de Pernambuco. Programa de Pós-graduação em Ciências da Saúde. Recife. BR
Braz. j. infect. dis ; 24(1): 65-72, Feb. 2020. tab, graf
Article in English | LILACS | ID: biblio-1089327
ABSTRACT
ABSTRACT Antiretroviral therapy (ART) has modified the outcome of patients with HIV infection, providing virological control and reducing mortality. However, there are several reasons as to why patients may discontinue their antiretroviral therapy, with adverse events being one of the main reasons reported in the literature. This is a case-control nested in a cohort of people living with HIV/AIDS, conducted to identify the incidence of ART modification due to adverse events and the associated factors, in two referral services in Recife, Brazil, between 2011 and 2014. Of the modifications occurred in the first year of ART, 25.7% were driven by adverse events. The median time elapsed between initiating ART and the first modification due to adverse events was 70.5 days (95% CI 26-161 days). The main adverse events were dermatological, neuropsychiatric and gastrointestinal. Dermatological events were the earliest to appear after initiating ART. Efavirenz was the most prescribed and most modified drug during the study period. The group of participants who used zidovudine, lamivudine, and efavirenz had a 2-fold greater chance (adjusted OR 2.16 95% CI 1.28-3.65) of switching ART due to adverse events when compared to the group that used tenofovir with lamivudine and efavirenz.
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Full text: Available Index: LILACS (Americas) Main subject: Acquired Immunodeficiency Syndrome / Anti-HIV Agents Type of study: Etiology study / Prognostic study / Risk factors Limits: Adolescent / Adult / Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: Braz. j. infect. dis Journal subject: Communicable Diseases Year: 2020 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de Pernambuco/BR

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Full text: Available Index: LILACS (Americas) Main subject: Acquired Immunodeficiency Syndrome / Anti-HIV Agents Type of study: Etiology study / Prognostic study / Risk factors Limits: Adolescent / Adult / Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: Braz. j. infect. dis Journal subject: Communicable Diseases Year: 2020 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de Pernambuco/BR