Category: Peer-reviewed

Reply

We appreciate the interest of Carifi and associates in our recent article. They have raised some excellent points regarding the limitations of our study, some of which we acknowledged in the article. Since our study was retrospective and included patie…

Reply

We appreciate the interest shown in our article. We agree that the Wilcoxon signed-rank test would be more appropriate. We have run the data using this test and have found that the results are statistically significantly consistent with the results usi…

Reply

We appreciate the interest of Galvis and associates in our study. We additionally applaud them for doing a surveillance of the local bacterial pathogens encountered in their geographic area. The authors point out the results of the ESCRS endophthalmiti…

Reply

We had proposed the short-term external buckling with pneumatic retinopexy as a novel and effective treatment for rhegmatogenous retinal detachment (RRD) with inferior retinal breaks, with a comparable success rate to other treatment methods.

Voriconazole for Fungal Keratitis

In their recently published trial, Sharma et al found topical voriconazole to be more effective than intrastromal voriconazole when added to topical natamycin in patients with recalcitrant fungal keratitis. This trial shares a similar protocol with se…

Who’s on first?

“There are basically two kinds of people in this world. Those who accomplish something and those that claim to. The first group is less crowded.”—Mark Twain Eratosthenes, an ancient Greek mathematician, calculated the earth’s circumference in a…

Retinal Ganglion Cell Analysis in Leber’s Hereditary Optic Neuropathy

Leber’s hereditary optic neuropathy (LHON) is a rare, maternally inherited disorder that results in bilateral loss of central vision. Characteristic visual field defects in LHON consist of either central or cecocentral scotomas, with about 70% of the patients being young adult men. More than 90% of these patients carry 1 of 3 mitochondrial DNA (mtDNA) mutations, located at nucleotide positions 3460, 11778, or 14484, respectively, although >20 mtDNA point mutations have been reported in LHON patients worldwide. Retinal ganglion cells decrease by apoptosis, and finally the retinal nerve fiber thins in LHON. Recently, gene therapy has been considered likely to hold the most promise for the treatment of mitochondrial diseases, especially the hereditary optic neuropathies in which targeted therapy to the retinal ganglion cells is feasible. Although treatment options for these disorders are still in their infancy, prompt and exact diagnosis of LHON is important to help select the appropriate strategy.

This Issue At A Glance

Can ionizing radiation be used as an adjunctive treatment for neovascular age-related macular degeneration (AMD)? In the INTREPID study of low-voltage, external-beam, stereotactic radiotherapy (SRT), Jackson et al (p. 1893) found that SRT can signific…

Fluoroquinolones in Corneal Ulcers

We read with interest the article by Sharma et al on moxifloxacin 0.5% in treatment of corneal ulcers. Authors indicated that corneal scrapings were examined using the Gram stain and potassium hydroxide wet mount, and that any case showing fungal elem…