TY - JOUR
T1 - Intravitreal dexamethasone implant as an adjunct weapon for severe and refractory uveitis in Behçet's disease
AU - Fabiani, Claudia
AU - Emmi, Giacomo
AU - Lopalco, Giuseppe
AU - Vannozzi, Lorenzo
AU - Bacherini, Daniela
AU - Guerriero, Silvana
AU - Franceschini, Rossella
AU - Frediani, Bruno
AU - Iannone, Florenzo
AU - Tosi, Gian Marco
AU - Rigante, Donato
AU - Cantarini, Luca
PY - 2017
Y1 - 2017
N2 - Objective: To investigate both efficacy and safety of dexamethasone (DEX) implant in the treatment of refractory Behçet’s disease (BD)-related panuveitis or posterior uveitis.
Method: A total of 5 eyes from 5 patients with active refractory BD-uveitis were enrolled in the study. A single intravitreal injection of DEX implant was applied to each eye. Best corrected visual acuity (BCVA), central macular thickness (CMT) assessed with optical coherence tomography, occurrence of vasculitis assessed by fluorescein angiography, vitreous haze score (Nussenblatt scale), intraocular pressure (IOP), and lens status (LOCS III, Lens Opacities Classification System III) were recorded at baseline and subsequently at each follow-up visit at 1 month, 3 months, and 6 months post-treatment.
Results: At baseline, all eyes showed marked macular edema and 4 out of 5 had concomitant active retinal vasculitis. The mean BCVA was increased from baseline at each control visit with a mean improvement at 6-month follow-up of 0.26±0.18 lines. Mean CMT decreased from baseline at each control visit with a mean improvement at 6-month follow-up of 198.80±80.08 µm. At the end of treatment none of the eyes showed signs of macular edema, and the mean CMT was 276.80±24.94 µm. Retinal vasculitis resolved in all affected eyes. One eye experienced an IOP spike (<20 mmHg) during treatment, that resolved spontaneously; one eye developed a clinically significant lens opacity at the 6-month follow-up.
Conclusions: The application of DEX implant in refractory BD uveitis and inflammatory macular edema was safe and effective as an additional treatment combined with systemic immunomodulatory drugs.
AB - Objective: To investigate both efficacy and safety of dexamethasone (DEX) implant in the treatment of refractory Behçet’s disease (BD)-related panuveitis or posterior uveitis.
Method: A total of 5 eyes from 5 patients with active refractory BD-uveitis were enrolled in the study. A single intravitreal injection of DEX implant was applied to each eye. Best corrected visual acuity (BCVA), central macular thickness (CMT) assessed with optical coherence tomography, occurrence of vasculitis assessed by fluorescein angiography, vitreous haze score (Nussenblatt scale), intraocular pressure (IOP), and lens status (LOCS III, Lens Opacities Classification System III) were recorded at baseline and subsequently at each follow-up visit at 1 month, 3 months, and 6 months post-treatment.
Results: At baseline, all eyes showed marked macular edema and 4 out of 5 had concomitant active retinal vasculitis. The mean BCVA was increased from baseline at each control visit with a mean improvement at 6-month follow-up of 0.26±0.18 lines. Mean CMT decreased from baseline at each control visit with a mean improvement at 6-month follow-up of 198.80±80.08 µm. At the end of treatment none of the eyes showed signs of macular edema, and the mean CMT was 276.80±24.94 µm. Retinal vasculitis resolved in all affected eyes. One eye experienced an IOP spike (<20 mmHg) during treatment, that resolved spontaneously; one eye developed a clinically significant lens opacity at the 6-month follow-up.
Conclusions: The application of DEX implant in refractory BD uveitis and inflammatory macular edema was safe and effective as an additional treatment combined with systemic immunomodulatory drugs.
KW - Behçet's disease
KW - Behçet's disease
UR - http://hdl.handle.net/10807/104841
M3 - Article
SN - 1565-1088
VL - 2017
SP - 415
EP - 419
JO - Israel Medical Association Journal
JF - Israel Medical Association Journal
ER -