RT Journal Article
SR Electronic
T1 Cytomegalovirus retinitis after the initiation of highly active antiretroviral therapy: a 2 year prospective study
JF British Journal of Ophthalmology
JO Br J Ophthalmol
FD BMJ Publishing Group Ltd.
SP 652
OP 655
DO 10.1136/bjo.83.6.652
VO 83
IS 6
A1 Suzanne M Mitchell
A1 William L Membrey
A1 Michael S Youle
A1 Adanna Obi
A1 Simon Worrell
A1 Brian G Gazzard
YR 1999
UL http://bjo.bmj.com/content/83/6/652.abstract
AB BACKGROUND/AIMS There have been several recent reports suggesting that the natural history of cytomegalovirus retinitis (CMVR) has been significantly modified with the development of highly active antiretroviral therapy (HAART). This 2 year prospective cohort study assesses the effect of HAART on the incidence and progression of CMV retinitis in patients with CD4 cell counts below 50 cells ×106/l. METHODS 63 patients, with CD4 cell counts below 50 cells ×106/l, who were recruited to a 2 year prospective cohort study at the commencement of combination antiretroviral therapy including the use of the proteinase inhibitor, indinavir, were reported. The response to HAART was assessed in terms of a rise in the CD4 cell count and fall in HIV viral load. An experienced ophthalmologist performed dilated funduscopy at the time of recruitment and thereafter at 2 weekly intervals and retinal photography was performed at monthly intervals in patients with CMVR. The activity and progression of CMV retinitis was assessed on the basis of the characteristic clinical and photographic findings. RESULTS 34 patients achieved at least 50 CD4 cells ×106/l at 3 months after initiation of therapy. New diagnoses of CMVR were seen only in the non-responder group (p=0.085). Overall, the relative risk of a new retinitis event in this group was 3.52 (95% CI 1.16, 10.68) at 3 months compared with those patients who were responsive to HAART. 12 of the 63 patients had previous CMVR. Disease progression was associated with non-response to therapy (p=0.182 exact). In patients with CMVR the median time to first progression was 18 days (95% CI 8, 91) in non-responders and 121 days (95% CI 0.59, 3.65) in responders. By the end of the 2 year follow up period all surviving patients had >50 CD4 cells ×106/l. No CMV events were seen after 8 months of therapy in either group of patients. CONCLUSIONS These findings suggest that significant clinical immunorestoration to CMV occurs in response to HAART in patients with CMVR after a lag time of 3–8 months. Initially, a rise in CD4 count is predictive of CMVR response but after the lag period all survivors appear to have developed a clinical immunorestoration to CMV. If HAART is commenced in at risk patients before the development of CMVR the incidence of new disease falls significantly.