ARVO celebrates 75 years of research, vision
May 3rd 2003Special keynote speech to be delivered by Dr. Folkman of Harvard MedicalSchoolThe Association for Research in Vision and Ophthalmology (ARVO) turns75 years this year. To commemorate this major milestone, several specialevents are planned during the annual meeting from May 4 to 8 in Fort Lauderdale,FL.The anniversary celebration will officially open with a keynote symposiumon Sunday, May 4 at 5 p.m. during which Judah Folkman, MD, director of surgicalresearch, and the Andrus professor of pediatric surgery and professor ofcell biology, Children's Hospital, Harvard Medical School, Boston, willdeliver the keynote address. The 75th Anniversary Celebration Social willfollow from 7 to 9 p.m.
Single-use microkeratome results similar to reusable blade
May 1st 2003S?o Paulo-A comparative study has demonstrated that the M2 130 Single-Use microkeratome (Moria, Antony, France) performs identically to its reusable counterpart, the conventional M2 110. In addition, the Single-Use microkeratome is significantly easier to use and allows greater visibility, according to Renato A. Neves, MD, director of Eye Care Oftalmologia LASER Vision Centers here.
Exposures of porous orbital implants can be avoided
May 1st 2003In the past decade, porous orbital implants have become the implant of choice for many surgeons managing the anophthalmic socket after enucleation or evisceration. By permitting fibrovascular ingrowth, these porous implants are better able to resist infection, migration, and extrusion when compared with acrylic or silicone implants.
Craniocervical arterial dissection a diagnostic challenge
May 1st 2003A craniocervical arterial dissection usually results from a tear in the intimal arterial layer. This tear allows the formation of a false lumen containing a clot, which can lead to thromboembolic complications (stroke). If the dissection is subintimal, stenosis of the artery is the likely end result. If it is subadventitial, the result is a "pseudo-aneurysm" (Figure 1).
Ocular allergy control possible with once-daily dosing
May 1st 2003Niagara Falls, Ontario-Switching to once-daily instillation of nedocromil sodium 2% ophthalmic solution (Alocril, Allergan) is an effective alternative for maintaining control of ocular symptoms of seasonal allergic conjunctivitis after acute relief is obtained with twice-daily administration, according to an environmental study conducted by Michael Alexander, MD.
Ocular agent provides prolonged pruritus prophylaxis
May 1st 2003Boston-The mast-cell stabilizer pemirolast potassium 0.1% (Alamast, Santen) is a safe, comfortable, and effective agent for preventing and relieving ocular itching of seasonal allergic conjunctivitis throughout the allergy season, according to a pooled analysis of data from phase III trials.
Corticosteroid shown to be safe for long-term SAC control
May 1st 2003Tampa, FL-Loteprednol etabonate ophthalmic suspension 0.2% (Alrex, Bausch & Lomb Pharmaceuticals and Pharmos Corp.), the first corticosteroid specifically designed for signs and symptoms of seasonal allergic conjunctivitis (SAC), is safe for long-term use, according to a recent multicenter study.
Early allergy season springs into action
May 1st 2003This year's fierce winter is now about to bring a big dose of misery to the 60 million Americans who suffer from seasonal allergies. Experts predict a fast-peaking, intense spring allergy season. Moisture accumulated from heavy snow and excessive rain has nurtured mold, and will fuel tree-pollen production-all of which will trigger an early and severe allergy season.
New guidelines focus on medical management of glaucoma
May 1st 2003Maui, HI-Evidence-based guidelines for the medical management of glaucoma developed by a panel of glaucoma specialists aim to enhance clinical decision-making for the general ophthalmologist, said Anne L. Coleman, MD, PhD, at the annual Royal Hawaiian Eye meeting here.
Hyperhomocysteinemia may be risk factor for exfoliation syndrome
May 1st 2003S?o Paulo, Brazil-Hyperhomocysteinemia appears to be associated with exfoliation syndrome and might be a modifiable risk factor for that disorder, said Roberto M. Vessani, MD, who was a glaucoma fellow with Glaucoma Associates of New York and is currently glaucoma preceptor, glaucoma service, department of ophthalmology, University of S?o Paulo, Brazil.
ASCRS survey LASIK continues to be predominant
May 1st 2003San Francisco-LASIK continues to be the predominant refractive procedure for treating patients with refractive errors ranging from +3 to -9 to -10 D, according to Richard J. Duffey, MD, who presented the results of the 2002 ASCRS survey of U.S. trends in refractive sur-gery.
TTT trial to test potential treatment for wet AMD
May 1st 2003Mountain View, CA-IRIDEX Corp. has completed enrollment in a clinical trial for its TTT4CNV, to determine whether trans-pupillary thermotherapy (TTT) laser treatment can reduce the risk of vision loss for patients with occult wet age-related macular degeneration (AMD).
ISTA to try again after FDA panel rejects Vitrase
May 1st 2003Irvine, CA-ISTA Pharmaceuticals is regrouping after an FDA advisory committee said the company's tests of ovine hyal-uronidase (Vitrase) failed to demonstrate sufficient statistical evidence to support its efficacy in treating vitreous hemorrhage.
Allergan begins launch of cyclosporine
May 1st 2003Irvine, CA-In early April, cyclosporine ophthalmic emulsion 0.05% (Restasis, Allergan) became commercially available for the treatment of eye inflammation associated with keratoconjunctivitis sicca. The introduction of the product marks the first therapeutic option for people with dry eye by not only providing temporary relief of dry eye, but also treating the associated ocular inflammation, according to the company.
Anti-VEGF treatment shows promise in preliminary trials
April 15th 2003Boston-Multiple intravitreal injections of rhuFab V2 (Genentech Inc., San Francisco) are well-tolerated and appear to have favorable biologic activity for the treatment of exudative age-related macular degeneration (AMD), said Jeffrey S. Heier, MD, of Ophthalmic Consultants of Boston and the Center for Eye Research, principal investigator for that trial.