Figures & data
Figure 1. Temporal evolution first-line regimens and immunologic criteria for treatment initiation based on Brazilian ART guidelines, 2008–2017.
![Figure 1. Temporal evolution first-line regimens and immunologic criteria for treatment initiation based on Brazilian ART guidelines, 2008–2017.](/cms/asset/42b6cef3-815c-4bb9-a8f5-de21f5168fea/caic_a_2190954_f0001_ob.jpg)
Figure 2. The proposed operational model depicting the relationship between exposure, outcome, and covariates.
![Figure 2. The proposed operational model depicting the relationship between exposure, outcome, and covariates.](/cms/asset/6d31e1b1-b17c-4e13-9afb-4469930afa43/caic_a_2190954_f0002_ob.jpg)
Figure 3. Flowchart of the study population, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.
![Figure 3. Flowchart of the study population, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.](/cms/asset/bf360326-e693-4ee3-90d0-ddb46aea39cc/caic_a_2190954_f0003_ob.jpg)
Figure 4. Percentage of individuals initiating first-line antiretroviral therapy (ART) by type of ART regimen (NNRTI-based regimens [at least 2 NRTIs plus 1 NNRTI], PI-based regimens [at least 2 NRTIs plus 1 PI], INSTI-based regimens [at least 2 NRTIs plus 1 INSTI], and single-tablet regimen [STR, Tenofovir 300 mg, Lamivudine 300 mg plus Efavirenz 600 mg as a single pill]) and year, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.
![Figure 4. Percentage of individuals initiating first-line antiretroviral therapy (ART) by type of ART regimen (NNRTI-based regimens [at least 2 NRTIs plus 1 NNRTI], PI-based regimens [at least 2 NRTIs plus 1 PI], INSTI-based regimens [at least 2 NRTIs plus 1 INSTI], and single-tablet regimen [STR, Tenofovir 300 mg, Lamivudine 300 mg plus Efavirenz 600 mg as a single pill]) and year, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.](/cms/asset/dd905572-46ea-4ebd-bc4d-208d91c0f7ee/caic_a_2190954_f0004_ob.jpg)
Table 1. Socio-demographic and clinical characteristics at first-line antiretroviral therapy (ART) initiation, overall, and by first-line ART regimen, INI Clinical Cohort, 2008-2018, Rio de Janeiro, Brazil.
Figure 5. Viral load availability: percentage of individuals with viral load measurements at 6- (left) and 12-months (right) of initiating ART by year of ART initiation, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.
![Figure 5. Viral load availability: percentage of individuals with viral load measurements at 6- (left) and 12-months (right) of initiating ART by year of ART initiation, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.](/cms/asset/c7c0680f-7440-46d6-991e-72e6e6a9ec88/caic_a_2190954_f0005_ob.jpg)
Figure 6. Viral suppression: percentage of individuals with viral suppresion at 6- (left) and 12-months (right) of initiating ART by year of ART initiation, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.
![Figure 6. Viral suppression: percentage of individuals with viral suppresion at 6- (left) and 12-months (right) of initiating ART by year of ART initiation, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.](/cms/asset/15fe62fe-f65d-4ea1-8d6d-49b6290e09a5/caic_a_2190954_f0006_ob.jpg)
Figure 7. Immune response: CD4 cell counts (median and interquartile range) at ART initiation and at 6- and 12-months after initiating ART by ART regimen, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.
![Figure 7. Immune response: CD4 cell counts (median and interquartile range) at ART initiation and at 6- and 12-months after initiating ART by ART regimen, INI Clinical Cohort, Rio de Janeiro, Brazil, 2008–2018.](/cms/asset/fd93db11-22c5-412b-b412-1925c92475db/caic_a_2190954_f0007_oc.jpg)
Table 2. Unadjusted and adjusted odds ratio (95% credibility interval) for factors associated with viral suppression at six months, INI Clinical Cohort, 2008-2018, Rio de Janeiro, Brazil.
Table 3. Unadjusted and adjusted odds ratio (95% credibility interval) for factors associated with viral suppression at 12 months, INI Clinical Cohort, 2008-2018, Rio de Janeiro, Brazil.
Supplemental Material
Download MS Word (158 KB)Data availability statement
The final dataset used for the current study is available from the corresponding author on reasonable request.