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. 2006 Jul;90(7):852–855. doi: 10.1136/bjo.2005.086546

Table 2 Laboratory confirmation of CMV infection and visual outcome of patients after specific antiviral therapy.

Patient Initial flare (ph/ms) Diagnostic testing and results (CMV) Systemic therapy Topical treatment (at last follow up) No of relapses (time after Rx) Final IOP (mm Hg) Final flare (ph/ms) Final VA Follow up (months)
1 39 LAP+ iv GCV Rmx 2 (after 6 and 12 months) 18* 14 20/30 24
PCR+ ×2 ValGCV Drz
2 28 LAP+ iv FCN Rmx 0 14 11 20/25 16
PCR+ ValGCV Acl
3 18 LAP+ ValGCV Fmt 1 (after 5 months) 20 9 20/20 9
PCR+ ×2 timolol
4 16 LAP+ iv GCV Rmx 0 15 10 20/20 10
PCR+ ValGCV timolol
5 ND PCR+ ×2 ValGCV Prednisolone 1 (1 month) 20† 42 20/25 24
timolol

Acl, apraclonidine; Drz, dorzolamide; FCN, foscarnet; Fmt, fluorometholone; GCV, ganciclovir; IOP, intraocular pressure; LAP, local antibody production; ND, not done; Rmx, rimexolone; Rx, treatment; VA, visual acuity; valGCV, valganciclovir.

*Required trabeculectomy †Required glaucoma drainage device.