Articles
A new MIGS in a new space
An investigator for the CyPass Micro-Stent offers advice on training, the learning curve and patient selection.
By Steven R. Sarkisian, Jr., MD
A new-venture integration plan
Quash hasty impulses; launching any product, service or surgery requires a complete, detailed blueprint to succeed.
By Robert Calandra, Contributing
Anterior segment imaging
AS-OCT vs. UBM vs. endoscope; case-based approaches
By Benjamin Bert, MD, FACS
Corneal hysteresis is gaining respect
The measurement may be a step forward in predicting glaucoma progression.
By Kenneth Chang, MS
IN SO MANY WORDS
Zeiss’ Ludwin Monz
Instrument Insider
By Robert Stoneback, associate editor
Quick Hits
By Robert Stoneback, associate editor
Resuscitating refractive surgery
With an ever-growing number of procedures, the need for education is essential.
By Nicole A. Lemanski, MD, Aaron
Rx Perspective
By Robert Stoneback, associate editor
Spotlight
By Robert Stoneback, associate editor
Technology reigns in oculoplastics, too
Some, like CT scans and MRIs, these surgeons have adopted. But then there is the Medpor Titan 3D orbital ...
By Charles Kim, MD, and
This cancer doesn’t want to be found
Primary vitreoretinal lymphoma presents as chronic uveitis; it remains a challenge to identify.
By Edmund Tsui, MD
Viewpoint
Too many qualifiers
A Safe, Effective Balance
Prescribing both generic and branded drugs, physicians weigh efficacy, adherence, and cost
Multifactorial Choices in Glaucoma
Considering drugs, pricing, and packaging in an area where long-term adherence is vitally important
Optimal Instruments for DMEK
Challenges encountered by early adopters prompted the creation of surgeon-friendly instruments to help improve outcomes
By By Thomas
The Future of Branded vs. Generic
Forecasting trends and innovations that will affect prescribing
The Role of Cost in the Branded vs. Generic Equation
Choices are often driven by financial considerations — for both patients and physicians
What Makes an Ophthalmic Generic Bioequivalent?
A researcher discusses how the FDA establishes the bioequivalence of generic ophthalmic drugs