BRIEFLY
- EPIKERATOME DEVICE RECEIVES CE MARK
APPROVAL. CIBA Vision"s Centurion SES EpiEdge epikeratome
has received CE Mark approval for sub-epithelial separation during
Epi-LASIK, a new refractive surgical procedure developed by LASIK
pioneer Ioannis Pallikaris, MD, PhD of Greece. The EpiEdge epikeratome
is compatible with the Centurion SES System, which is available with
two separate handpieces and blades: one for use in traditional LASIK
procedures and one for Epi-LASIK procedures. The EpiEdge epikeratome
is not a blade per se; it is a blunt "separator" that produces
an epithelial sheet via a disposable, oscillating PMMA block, with
no cutting. It eliminates the need for alcohol used in some refractive
laser procedures, thus offering a less toxic environment with faster
healing and less pain for patients. For more information, go to www.cibavision.com.
- NEW TONOMETER INTRODUCED.
Ziemer Ophthalmic Systems AG will introduce its Pascal Dynamic Contour
Tonometer for measuring intraocular pressure (IOP) at the annual meeting
of the American Academy of Ophthalmology (November 15 to 18, 2003).
The Pascal, which was developed by Swiss Microtechnology AG, a member
of Ziemer"s Ophthalmic Systems group, is said to eliminate the influence
of corneal thickness and rigidity on IOP estimates that occur with
conventional applanation tonometers. Its "SensorTip" is
a built-in pressure sensor that matches corneal curvature and measures
IOP directly. The Pascal is slitlamp mounted and operates in a similar
fashion as the Goldmann tonometer, but it records the dynamics of
IOP and thus allows the operator to gather information on the entire
range of short-term pressure fluctuations to which eyes are subjected.
For more information, go to www.smtag.ch
or www.ziemer-ophthalmics.com.
- VISUDYNE APPROVED IN JAPAN FOR TREATING
WET AMD. Health authorities in Japan have approved Visudyne
(verteporfin) for the treatment of the wet form of age-related macular
degeneration (AMD). Visudyne, the product of QLT, Inc. and Novartis
Ophthalmics, the eye health unit of Novartis AG, was approved by Japanese
authorities for the orphan indication of AMD with all types of subfoveal
choroidal neovascularization (it was designated as an orphan drug
in Japan in 1997). Approval of Visudyne was based on the results of
a 12-month clinical study in that country; approximately two out of
every three patients participating either maintained or improved their
vision as a result of Visudyne therapy. QLT, Inc. says it will now
focus on securing reimbursement for Japanese AMD patients who previously
had no treatment options.
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