Purpose: To report our results of 4 patients about the efficacy and safety of intravitreal dexamethasone implant for type 1 idiopathic macular telangiectasia (IMT).

Methods: Four patients' charts with type 1 IMT treated with intravitreal dexamethasone implant were retrospectively reviewed. All patients underwent full ophthalmic examination including best corrected visual acuity (BCVA), spectral domain optical coherence tomography, and fluorescein angiography. BCVA, central macular thickness (CMT), and macular volume (MV) were evaluated.

Results: The median BCVA was logMAR 0.55 (range 0.2-1.3) at baseline, improved to logMAR 0.45 (range 0.2-1) at 2 months after the first injection, and deteriorated to logMAR 0.7 (range 0.2-1) at final visit. The median CMT was 393 μm (range 283-410 μm) and MV was 2.70 mm(3) (range 1.96-2.87 mm(3)) at baseline. Two months after the first injection median CMT decreased to 327 μm (range 269-356 μm) and MV decreased to 2.45 mm(3) (range 1.93-2.57 mm(3)). At final visit median CMT slightly increased to 342 μm (range 258-444 μm) and MV slightly increased to 2.56 mm(3) (range 1.93-2.89 mm(3)). None of the changes were statistically significant.

Conclusion: Considering the effects of dexamethasone on macular edema intravitreal dexamethasone implant can be used in selected cases. Randomized clinical trials with larger sample size are needed for further evaluation.

Download full-text PDF

Source
http://dx.doi.org/10.1089/jop.2015.0146DOI Listing

Publication Analysis

Top Keywords

dexamethasone implant
16
intravitreal dexamethasone
12
median cmt
12
range
9
type idiopathic
8
idiopathic macular
8
macular telangiectasia
8
range 02-1
8
months injection
8
final visit
8

Similar Publications

: The PreserFlo™ MicroShunt (PFMS) is a bleb-forming device considered to be less invasive than traditional glaucoma surgery such as trabeculectomy. This study evaluates the 1-year success rates as well as safety profile of PFMS in patients having high intraocular pressure (IOP) and/or glaucoma refractory to drop therapy with a history of prior intravitreal dexamethasone therapy. : A total of 16 eyes after PFMS implantation due to elevated IOP after intravitreal dexamethasone implant (DEX-I) administration were included in this retrospective cohort study.

View Article and Find Full Text PDF

: In this study, we evaluated the incidence of cystoid macular edema (CME) after pars plana vitrectomy (PPV) for different retinal pathologies and assessed the role of optical coherence tomography (OCT) biomarkers in guiding treatment decisions in post-surgical CME patients who were refractory to medical therapy over a follow-up period of 12 months. : Medical records of consecutive pseudophakic patients, who underwent PPV for different retinal pathologies, were retrospectively evaluated in this single-center, uncontrolled study. The incidence of post-PPV CME was assessed.

View Article and Find Full Text PDF

A 3-year-old spayed male mixed-breed Labrador presented to the Emergency and Critical Care Unit with lethargy, loss of appetite, vomiting, a recent history of presyncopal episodes, and severe exercise intolerance. On admission, the patient had bradycardia, low blood pressure, and mild abdominal pain. Serum biochemistry information revealed severe hyperkalemia, hyponatremia, hypoglycemia, and mildly increased liver and kidney parameters.

View Article and Find Full Text PDF

Background: Immune checkpoint inhibitors (ICIs) are effective antineoplastic agents but can cause adverse effects in many organ systems. Cardiovascular toxicities include arrhythmias, myocarditis, heart failure, takotsubo syndrome, pericarditis, coronary artery disease, and vasculitis.

Case Summary: A 66-year-old woman with Stage 3C2 endometrial carcinoma presented for her second cycle of pembrolizumab, carboplatin, and paclitaxel.

View Article and Find Full Text PDF

Background: Ozurdex® (Allergan®, AbbVie Company, North Chicago, Illinois, EUA), is composed of 0.7 mg of dexamethasone, fused in a solid biodegradable PLGA polymer, whose degradation occurs naturally in the vitreous cavity, usually in six months after its application.

Methods: In this study, we included patients aged ≥ 18 years with one or two eyes who had an indication for Ozurdex implants.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!