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Comparative effectiveness of antiretroviral drug classes for the treatment of HIV infection in patients with high viral loads: a multicentre retrospective cohort study.
Adams, J L; Murray, M; Patel, N; Sawkin, M T; Boardman, R C; Pham, C; Kaur, H; Patel, D; Yager, J L; Pontiggia, L; Baxter, J.
Afiliação
  • Adams JL; Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, PA, USA.
  • Murray M; Division of Infectious Diseases, Cooper University Hospital, Camden, NJ, USA.
  • Patel N; Chicago College of Pharmacy, Midwestern University, Downers Grove, IL, USA.
  • Sawkin MT; Northwestern Memorial Hospital, Chicago, IL, USA.
  • Boardman RC; Skaggs School of Pharmacy & Pharmaceutical Sciences, University of California San Diego, San Diego, CA, USA.
  • Pham C; Albany Stratton VA Medical Center, Albany, NY, USA.
  • Kaur H; KC CARE Health Center, Kansas City, MO, USA.
  • Patel D; Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, PA, USA.
  • Yager JL; Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, PA, USA.
  • Pontiggia L; Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, PA, USA.
  • Baxter J; Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, PA, USA.
HIV Med ; 22(1): 28-36, 2021 01.
Article em En | MEDLINE | ID: mdl-32964664
ABSTRACT

OBJECTIVES:

We aimed to compare the effectiveness of antiretroviral therapy (ART) classes for achieving HIV RNA suppression to < 50 HIV-1 RNA copies/mL within 6 months of initiation with high viral loads (VLs). Secondary objectives were to compare viral suppression (VS) at 12 weeks and 12 months, partial HIV RNA suppression to < 200 copies/mL, time to VS, time to rebound, and change in CD4 cell count.

METHODS:

This was a multicentre, retrospective, observational study. Adult patients were included if they initiated ART between January 2005 and December 2016 with a VL ≥ 100 000 copies/mL.

RESULTS:

There were 220 patients included in the study. The median VL was 252 919 [interquartile range (IQR) 149 472-500 000] copies/mL. Nonnucleoside reverse transcriptase inhibitor (NNRTI) recipients were more likely to achieve VS by 6 months compared to those initiating ART containing protease inhibitors (PIs) [75.4% vs. 44.1%, respectively; odds ratio (OR) 3.34; 95% confidence interval (CI) 1.62-6.90] or integrase strand transfer inhibitors (INSTIs) (75.4% vs. 55.8%, respectively; OR 2.40; 95% CI 1.03-5.58). VS at 12 weeks was more frequent with INSTI-containing regimens than with PIs (28.9% vs. 9.0%, respectively; OR 4.10; 95% CI 1.69-9.92). VS at 12 months did not significantly differ between treatment regimens. Median time to complete VS for INSTI, PI and NNRTI recipients was 22.3 (95% CI 13.4-33), 30.1 (95% CI 25-36) and 19.9 (95% CI 16-22.3) weeks, respectively. There were no significant differences in time to viral rebound or change in CD4 cell counts.

CONCLUSIONS:

Patients with high VLs initiated on NNRTIs were more likely to achieve VS by 6 months on ART compared to INSTI and PI recipients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Inibidores da Transcriptase Reversa / Inibidores de Integrase de HIV / Carga Viral Tipo de estudo: Etiology_studies / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: HIV Med Assunto da revista: SINDROME DA IMUNODEFICIENCIA ADQUIRIDA (AIDS) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Inibidores da Transcriptase Reversa / Inibidores de Integrase de HIV / Carga Viral Tipo de estudo: Etiology_studies / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: HIV Med Assunto da revista: SINDROME DA IMUNODEFICIENCIA ADQUIRIDA (AIDS) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos