M. Labetoulle et al., INCIDENCE AND EVOLUTION OF VIRAL RETINITIS IN HIV-INFECTED PATIENTS TREATED WITH HIV-PROTEASE INHIBITORS, Journal francais d'ophtalmologie, 21(8), 1998, pp. 567-576
Background Since the beginning of the use of HN-Protease Inhibitors (P
I) to treat HIV-infected patients, a decrease of the incidence of extr
aocular opportunistic infections has been observed. We studied the inc
idence of CMV-retinitis in patients treated with a highly active antir
etroviral therapy (HAART) containing PI over a mean follow-up of 12 mo
nths. Methods Ninety-three HIV-infected patients treated with HAART co
ntaining PI were included. The mean initial CD4+ cell-count was 54/mu
l (median: 22/mu l), and the mean plasma HN-load was 5.46 log10 RNA-co
pies /ml. Fundus examination was performed each month in case of a pre
viously treated and controlled CMV-retinitis or if initial CD4 cells w
ere below 50/mu l. In other patients, fundus examination was performed
every 3 months. The mean follow-up was 362 days. Results Among the 7
patients with a previously treated and controlled CMV-retinitis, one e
xperienced a progression during the study (after 163 days of PI). Amon
g the 59 patients with CD4 cells below 50/mu l and without previous CM
V-retinitis before the beginning of PI, 5 experienced a CMV-retinitis
(mean delay after the onset of HAART: 141 days), including 2 with rela
pse. When retinitis occurred CD4 cells were below 32/mu l except in on
e case (147/mu l). Conclusions Compared to previously published report
s, this study, showed an increase of the time to progression of previo
usly treated and controlled CMV-retinitis in patients treated with PI.
Considering deeply immunocompromised patients (less than 50 CD4-cells
/mu l), the risk of suffering from CMV-retinitis tvas 8.5 % after 12 m
onths of PI treatment Longer follow-up remains necessary to confirm th
ese results.