glanatec has been researched along with Edema* in 3 studies
3 other study(ies) available for glanatec and Edema
Article | Year |
---|---|
Use of ripasudil for rapid resolution of acute hydrops in keratoconus.
Topics: Acute Disease; Corneal Edema; Edema; Humans; Isoquinolines; Keratoconus; Sulfonamides | 2022 |
Honeycomb epithelial oedema due to ripasudil: clinical, optical coherence tomography and histopathological correlation.
A male in his 50s, who had undergone Descemet's stripping automated endothelial keratoplasty (DSAEK) for corneal oedema following irido-corneal-endothelial syndrome and glaucoma drainage device surgery for secondary glaucoma presented with gradual decreased vision. The patient was on ripasudil 0.4% for the past 4 months prior to the presentation. Honeycomb epithelial oedema was seen with vesicles and intraepithelial microcyst formation which were also noted on anterior segment optical coherence tomography (OCT) and histopathology, that co-related with the slit-lamp findings. The patient underwent repeat DSAEK and had a good outcome. While the clinical features and OCT findings have been reported earlier, the histopathological features have not been reported. Topics: Corneal Diseases; Descemet Stripping Endothelial Keratoplasty; Edema; Endothelium, Corneal; Humans; Isoquinolines; Male; Middle Aged; Sulfonamides; Tomography, Optical Coherence | 2022 |
Long-term Side Effects Including Blepharitis Leading to Discontinuation of Ripasudil.
Blepharitis was the most common side effect leading to discontinuation of ripasudil therapy. Prior allergic reactions to other topical glaucoma were found to be a risk factor for ripasudil-induced blepharitis.. To report the incidence proportion of blepharitis and its relating factors due to long-term use of 0.4% riapasudil, a Rho-kinase inhibitor, in glaucoma patients of a clinical setting.. One hundred three eyes of 103 consecutive glaucoma patients who started ripasudil treatment between December 2014 and February 2017 at our institute, and who had a follow-up period of over 6 months were enrolled in this study. Incidence proportion, time required for recovery and risk factors associated with blepharitis and other side effects that led to discontinuation of ripasudil treatment were considered.. The most frequently observed side effect was blepharitis (25.2%). The 12- and 24-month discontinuation rate due to blepharitis was 21.1%±8.2% and 34.6%±11.8% (average±SE), respectively (Kaplan-Meier analysis). Most patients recovered from blepharitis symptoms within 4 weeks, but 5 patients required over 8 weeks for recovery. Past history of allergic reactions to other topical glaucoma medication was significantly correlated with the manifestation of blepharitis (Cox proportional hazard model, P<0.007) while age, sex, intraocular pressure reduction rate, number of administered eye drops, history of systemic allergic diseases were not.. Blepharitis was the most common reason for discontinuation of ripasudil treatment. Although most cases were resolved spontaneously, prolonged blepharitis was observed in a few patients. A past history of allergic reaction to other glaucoma medication indicates a higher possibility of blepharitis with ripasudil use and warrants careful administration. Topics: Adult; Aged; Aged, 80 and over; Antihypertensive Agents; Blepharitis; Edema; Erythema; Female; Glaucoma, Open-Angle; Humans; Intraocular Pressure; Isoquinolines; Male; Middle Aged; Ophthalmic Solutions; Ophthalmoscopy; rho-Associated Kinases; Sulfonamides | 2019 |