Skip to main content
. Author manuscript; available in PMC: 2014 Jun 20.
Published in final edited form as: Arch Ophthalmol. 2012 Jan;130(1):113–115. doi: 10.1001/archophthalmol.2011.380

Table 2.

Clinical details of patients undergoing ganciclovir-resistance evaluation using ocular fluid

Pt/Age/Sex Associated medical conditions Months of valganciclovir or ganciclovir prior to CMV reactivation Presence of point mutations in CMV UL97 or UL54 genes associated with ganciclovir- resistance? CMV retinitis treatment prior to ganciclovir- resistance testing Change in therapy?
1/73/M Natural killer cell leukemia > 12 Yes (9/2008) – UL97: C592G*; UL54: T503I*; No (1/2008) Valganciclovir Yes, intravitreal foscarnet
2/67/F Lung transplant, mycophenolate mofetil, prednisone, tacrolimus > 12 Yes – UL97: M460I*; UL54: A987G*
UL54 mutations identified but not associated with ganciclovir-resistance: S655L, N685S, A885T, N898D
Valganciclovir Yes, intravitreal and intravenous foscarnet
3/32/M HIV 1 No Valganciclovir, intravitreal foscarnet No
4/41/M HIV 2, poorly compliant with valganciclovir No** Valganciclovir, intravitreal foscarnet No, ganciclovir implant both eyes due to poor medication compliance
5/10 mo/M Acute lymphocytic leukemia 2 No Intravenous foscarnet/ganciclovir, Intravitreal foscarnet No
6/72/F Diabetes mellitus 6 No Valganciclovir, intravitreal foscarnet No

CMV reactivation was confirmed with positive CMV PCR with both qualitative and quantitive real-time PCR (data not shown). HSV, VZV, and toxoplasmosis DNA of ocular fluids were negative for all patients. Aqueous humor specimens were obtained in patients 1–5 and a vitreous specimen was obtained in patient 6.

*

UL97 or UL54 point mutations associated with ganciclovir-resistance

**

No UL97 mutations conferring resistance, UL54 base changes identified but none know to confer phenotypic resistance