Purpose: This study was conducted to evaluate the ocular hypotensive effica
cy, safety, and side effects of latanoprost 0.005% administered as adjuncti
ve therapy in patients with Sturge-Weber syndrome (SWS) and glaucoma.
Methods: Commercially available latanoprost 0.005% was added as a single dr
op once daily to other antiglaucoma medications. Intraocular pressure (IOP)
was measured at 1, 3, and 6 months of treatment. A successful response was
defined as a reduction of at least 20% in IOP at the final follow-up evalu
ation without additional medical or surgical therapy and no adverse events
related to latanoprost.
Results: 18 eyes of 18 patients with SWS and glaucoma were enrolled from 9
clinical centers. Mean baseline IOP was 28.4 +/- 7.1 mmHg (range, 17-42 mmH
g). Using Kaplan-Meier analysis, a successful response to latanoprost was o
bserved in 3 of 18 (16.7%) patients at the 6-month interval. Seven (38.9%)
patients required surgery; three (16.7%) patients required additional medic
al therapy, seven (38.9%) patients had no change in therapy. One (5.6%) pat
ient discontinued latanoprost treatment because of intolerable conjunctival
hyperemia. Two successfully treated patients had significantly greater epi
scleral vessel engorgement after initiation of latanoprost therapy.
Conclusion: Patients with SWS and glaucoma respond poorly to adjunctive lat
anoprost therapy and often require additional medical or surgical intervent
ion. Increased episcleral vascular engorgement might result in greater oper
ative risks should filtration surgery become necessary in these patients.