KIAWAH ISLAND, S.C. – At the Kiawah Eye meeting, Reay H. Brown, MD, discusses the role of the Alcon CyPass micro-stent in the context of the current minimally invasive glaucoma surgery landscape.
Author: Healio ophthalmology
Acucela’s oral DR formulation shows potential to reduce retinal thickness
Oral emixustat hydrochloride reduced central subfield retinal thickness more than placebo in patients with proliferative diabetic retinopathy, with and without macular edema, Acucela announced in a press release.
The randomized, placebo-controlled, phase 2 trial enrolled 24 subjects to receive placebo or the study drug, titrated up to 40 mg per day. Patients in the study group experienced a mean reduction in central subfield thickness of 48.1 µm (P = .0764), as well as a mean reduction in total macular volume (P = .0263), compared with placebo.
“We are thrilled to (Read more...)
Telling it like it is about cataract surgery with no restrictions
Robert H. Osher
The ninth annual Cataract Surgery: Telling It Like It Is meeting will provide top-quality, uncensored, cutting-edge education to ophthalmologists unrestricted by current CME guidelines.
The meeting will be held Feb. 6-10, 2019, at Disney’s Yacht and Beach Club Resort in Lake Buena Vista, Florida.
Uncensored education
The meeting will feature more than 40 faculty members, comprised of some of the most talented ophthalmologists from around the world. These teachers will provide attendees with instructional materials at introductory, intermediate and advanced levels to ensure
VIDEO: Visual outcomes of an EDOF toric IOL targeted for emmetropia or nanovision
KIAWAH ISLAND, S.C. – At the Kiawah Eye meeting here, Kerry D. Solomon, MD, compares visual outcomes, patient satisfaction and visual disturbances in patients undergoing routine cataract surgery and implantation of an extended depth of focus toric IOL when both eyes are targeted for emmetropia and the non-dominant eye is targeted for nanovision.
Early VA gain predictive of visual response after dexamethasone treatment
Early visual acuity gain of 10 or more letters was predictive of a sustained response at 24 months after intravitreal dexamethasone treatment of macular edema in patients with retinal vein occlusion, according to a study.The 24-month, retrospective, mu…
VIDEO: Automated capsulotomy: Pearls for surgical success
KIAWAH ISLAND, S.C. – At the Kiawah Eye meeting, OSN Cornea/External Disease Section Editor Elizabeth Yeu, MD, presents on the intraoperative use of the Zepto automated capsulotomy system (Mynosys Cellular Devices) in the OR at the time of cataract surgery.
Kala plans advancement of dry eye treatment
Kala Pharmaceuticals plans to submit a new drug application to the FDA this year for a formulation of a short-term treatment for dry eye disease, according to a company press release.
KPI-121 0.25% is being investigated as a 2-week course of therapy intended for the temporary relief of the signs and symptoms of dry eye. The formulation uses “Kala’s mucus-penetrating particle (MPP) technology to enhance penetration of loteprednol etabonate (LE) into target tissue of the eye,” the release said.
Data from one phase 2 trial and two phase 3 efficacy (Read more...)
FDA lifts warning letter against STAAR Surgical
The FDA has issued a close-out letter to STAAR Surgical, lifting a 2014 warning regarding the manufacture of Visian Implantable Collamer Lens devices, the company announced in a press release.
The FDA action is a result of “a comprehensive remediation program” that addresses the issues raised by the FDA and includes “assessment, remediation and upgrade of all aspects of STAAR’s quality systems to assure compliance with Quality System Regulations (QSR),” Caren Mason, president and CEO of STAAR, said.
The initial warning letter, issued May 21, 2014, listed multiple
VIDEO: More efficient, safer and effective cataract and glaucoma surgery
KIAWAH ISLAND, S.C. — At the Kiawah Eye meeting here, OSN Glaucoma Section Editor Thomas W. Samuelson, MD, gives tips on increasing safety in cataract and glaucoma surgery.
ACP: Trump’s new insurance rule weakens patient protections
On Tuesday, President Donald J. Trump issued a new health insurance rule that would roll back essential patient protections established by the Affordable Care Act, including important health benefit coverage requirements, according to a press release i…
Quantel launches LacryDiag dry eye diagnosis device
At the World Ophthalmology Congress in Barcelona, Spain, Quantel Medical launched the LacryDiag ocular surface analyzer for the diagnosis of dry eye.
Approved by the FDA and CE marked, the device analyzes the three tear film layers with four non-contact exams, according to a company press release.
“Dry eye is a real public health problem, but the symptoms are often misunderstood. As a multifactorial pathology that results from damage to the tear film, this pathology is often underdiagnosed and underestimated,” Jean-Marc Gendre, CEO of Quantel Medical, said in the release. (Read more...)
Iridex’s Cyclo G6 glaucoma laser approved in South Korea
South Korea’s Ministry of Food and Drug Safety has approved the Cyclo G6 glaucoma laser system, Iridex announced in a press release.
The Cyclo G6 is available in more than 50 countries to treat patients with a range of glaucoma disease, the release said. It uses Iridex’s MicroPulse technology.
“International expansion in the Asia-Pacific region remains a top priority for us, and we believe that Korea represents an attractive market for our G6 technology,” President and CEO of Iridex William M. Moore said in the release.
AMA opposes CVS-Aetna merger
Barbara L. McAneny
AMA has determined that the proposed merger of CVS Health and Aetna should be blocked due to its likely negative consequences for patients and health insurance markets, according to a press release.
“After very careful consideration over the past months, the AMA has come to the conclusion that this merger would likely substantially lessen competition in many health care markets, to the detriment of patients,” Barbara L. McAneny, MD, president of AMA, said during testimony to California Department of Insurance.
During the analysis of the merger, the (Read more...)
Choroidal melanoma treatment shows promising early results in phase 1b/2 trial
Light-activated AU-011 for the treatment of primary choroidal melanoma was well tolerated with no severe adverse events, while showing promising early efficacy results, in a phase 1b/2 trial, Aura Biosciences announced in a press release.The open-label…
First Argentinian patient receives EyeMax Mono lens for AMD
The first EyeMax Mono lens implant procedure for age-related macular degeneration was performed in Argentina, LEH Pharma announced in a press release.
Hugo Nano, MD, of Buenos Aires, implanted the lens in both eyes of the patient. The device is delivered during cataract surgery and helps to improve vision in patients with wet or dry AMD, the release said.
“It is wonderful to have brought the EyeMax Mono lens into Argentina for the first time. The operation was a success, and this patient will be the first of many to (Read more...)
VIDEO: Simplifying the management of the loose lens
KIAWAH ISLAND, S.C. — At the Kiawah Eye meeting here, Michael D. Patterson, DO, discusses managing complicated cases.
First patient enrolled in phase 3 epi-on cross-linking trial
Avedro has enrolled the first patient in a pivotal phase 3 trial of its epi-on corneal collagen cross-linking procedure for progressive keratoconus, the company announced in a press release.
The multicenter, randomized, controlled study will evaluate the safety and efficacy of the procedure in 275 patients at 20 U.S. sites.
“Since the 2016 FDA approval of Avedro’s epi-off cross-linking treatment, thousands of patients with progressive keratoconus, a potentially debilitating disease, have benefited from this procedure,” Rajesh K. Rajpal, MD, chief medical officer for Avedro,
ICD-11 updates resistance codes, adds gaming as addictive disorder
WHO previewed a new International Classification of Diseases, ICD-11, which includes updates to codes related to antimicrobial resistance, adds gaming as an addictive disorder and categorizes gender incongruence as a matter of sexual health, not a ment…
FDA approves iDESIGN Refractive Studio for LASIK
Johnson & Johnson Vision’s iDESIGN Refractive Studio LASIK platform has been approved by the FDA, according to a press release.
The iDESIGN, which uses topography-integrated, wavefront-guided technology, allows physicians to take precise measurements of both the inside and outside of the eye to personalize the LASIK procedure to each patient, the release said.
It has been approved for myopia, hyperopia and mixed astigmatism, and is the only LASIK platform for monovision LASIK in presbyopic myopia.
“The new iDESIGN Refractive Studio provides surgeons with the ability to deliver
enVista toric MX60T IOL gets premarket approval
The FDA has issued premarket approval to Bausch + Lomb for its enVista toric MX60T hydrophobic acrylic IOL for astigmatism correction, according to a press release.
Featuring a one-piece aberration-free aspheric optic with a fenestrated, step-vaulted modified C-loop haptic design, the lens demonstrated 5° or less of absolute rotation in 100% of subjects in a prospective study, the release said.
“Building on the proven features and benefits of the enVista family of IOLs, MX60T represents another innovation in the continued expansion of this lens platform,” Chuck Hess, vice