Hoc. Guembel et al., Complications after implantation of intraocular devices in patients with cytomegalovirus retinitis, GR ARCH CL, 237(10), 1999, pp. 824-829
Citations number
26
Categorie Soggetti
Optalmology
Journal title
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
Purpose: The authors report their surgical experience after sustained-relea
se ganciclovir treatment, as well as replacing empty ganciclovir implants i
n patients with acquired immune deficiency syndrome (AIDS) and cytomegalovi
rus (CMV) retinitis. Methods: Between November 1995 and August 1998, 79 eye
s of 49 patients received 99 intravitreal ganciclovir implants. Patients we
re examined monthly after implant surgery. Follow-up periods ranged from 6
to 128 weeks. Results: At the first 3-week postoperative visit, 73 eyes (97
.2%) of 46 patients exhibited stable conditions. In 6 eyes (3.8%) of 3 pati
ents, further progression was noted due to resistance to ganciclovir. The m
ost common early complication (within 6 weeks after implantation) was cysto
id macular edema, observed in 7 eyes receiving implants. Retinal detachment
was the most common late complication (over 6 weeks after implantation) in
11 eyes. In almost all eyes with CMV retinitis and retinal detachment, inv
olvement of more than 25% of the retina was observed. Additional severe com
plications included extrusion of the first pellet in 2 eyes and cataract as
a late complication in 5 eyes. A total of 28 eyes (35.4%) of 16 patients r
eceiving a second implant did not experience significant three-line loss by
the end of the follow-up period. Conclusion: In the treatment of CMV retin
itis, sustained-release ganciclovir implantation seems to be an alternative
to intravenous ganciclovir. Early implantation and additional replacement
of the device has the potential to decrease the risk of developing retinal
detachment. We would recommend additional systemic antiviral CMV therapy to
avoid infection of the fellow eye and CMV disease.