Dr. Hoover et al., OCCURRENCE OF CYTOMEGALOVIRUS RETINITIS AFTER HUMAN-IMMUNODEFICIENCY-VIRUS IMMUNOSUPPRESSION, Archives of ophthalmology, 114(7), 1996, pp. 821-827
Objective: To estimate the incidence and prevalence of cytomegalovirus
retinitis (CMV-R) in late-stage human immunodeficiency virus type 1 d
isease. Design: Cohort study. Setting: The Multicenter AIDS Cohort Stu
dy, an ongoing 10-year study of human immunodeficiency virus type 1-in
fected homosexual men with semiannual visits and CD4(+) cell testing.
Study Participants: Three hundred sixty-seven human immunodeficiency v
irus type 1-infected men from the Multicenter AIDS Cohort Study who we
re receiving zidovudine and Pneumocystis carinii prophylaxis and who h
ad CD4(+) cell counts fall below 0.10x10(9)/L (100/mu L). Main Outcome
Measures: Kaplan-Meier-type estimates for various longitudinal quanti
fications of incidence and prevalence of CMV-R were obtained. Results:
Among these 367 individuals, cytomegalovirus disease developed in 103
, of whom 73 (71%) had ocular complications. At 4 years after the firs
t CD4 cell count (<0.10x10(9)/L), the probability for these subjects t
o have (1) remained living without CMV-R was 11%, (2) died without exp
eriencing CMV-R was 66%, (3) experienced CMV-R and be living was 6%, a
nd (4) experienced CMV-R and died was 18%. During these 4 years; there
was a 25% chance for the development of CMV-R and, on average, 0.211
person-years of CMV-R morbidity. Among those subjects in whom CMV-R de
veloped, about 19% did have CMV-R before a CD4(+) cell count of less t
han 0.05x10(9)/L (<50/mu L) was observed, and 81% had CMV-R after the
CD4(+) cell count reached this threshold. Conclusion: These estimates
may be relevant to current clinical practice and help in allocating re
sources and planning for treatment and prophylaxis against cytomegalov
irus disease.