dc.description.abstract |
Objective—
To describe patterns of suboptimal immune recovery (SO-IR) and associated HIV-
related-illnesses during the first 5 years following first-line antiretroviral therapy (ART) initiation
across seven ART sites in East Africa.
Design—
Retrospective analysis of data from seven ART clinical sites (three Uganda, two Kenya
and two Tanzania).
Methods—
SO-IR was described by proportions of ART-treated adults with CD4
+
cell counts less
than 200, less than 350 and less than 500 cells/μl. Kaplan–Meier survival analysis techniques were
used to assess predictors of SO-IR, and incident rates of HIV-related illnesses at CD4
+
cell counts
less than 200, 200–350, 351–499, and >500 cells/μl, respectively.
Results—
Overall 80 843 adults initiated non-nucleoside reverse transcriptase inhibitor-based
first-line ART; 65% were women and median CD4
+
cell count was 126 [interquartile range (IQR),
52–202] cells/μl. Cumulative probability of SO-IR <200 cells/μl, <350 cells/μl and <500 cells/μl, after 5 years, was 11, 38 and 63%, respectively. Incidence of HIV-related illnesses was higher
among those with CD4
+
cell counts less than 200 and 200–350 cells/μl, than those who achieved
CD4 counts above these thresholds. The most common events, at CD4 <200 cells/μl, were
pulmonary tuberculosis [incident rate 15.98 (15.47–16.51)/100 person-years at risk (PYAR), oral
candidiasis [incident rate 12.5 (12.03–12.94)] and herpes zoster [incident rate 6.30 (5.99–6.64)]
events/100 PYAR. With attainment of a CD4
+
cell count level 200–350 cells/μl, there was a
substantial reduction in events/100 PYAR – by 91% to 1.45 (1.29–1.63) for TB, by 94% to 0.75
(0.64–0.89) for oral candidiasis, by 84% to 0.99 (0.86–1.14) for Herpes Zoster, and by 78% to
1.22 (1.07–1.39) for chronic diarrhea. The incidence of all events decreased further with CD4
counts above these thresholds.
Conclusion—
Around 40% of adults initiated on ART have suboptimal immune recovery with
CD4 counts <350 cells/ml after five years. Such patients will require closer monitoring for both
HIV-related and non-HIV-related clinical events. |
en_US |