Research outlined for surgical technique
for implantable telescope for severe Age-related
Macular Degeneration
Newswise — Recent studies
have explored the use of an implantable
prosthetic device -- an implantable miniature
telescope -- for end-stage age-related macular
degeneration. While the device has not yet been
approved by the Food and Drug Administration,
physicians have described a recommended surgical
technique to ensure proper product placement
while minimizing damage to the eye. Their
technique is published in the August issue of
the Archives of Ophthalmology.
AMD is the leading cause of
irreversible visual impairment and blindness
among persons aged 60 and older. With the
elderly population steadily growing, the burden
related to this loss of visual function will
increase. “At the very end stages of this
disease, vision is very poor and quality of life
is compromised,” said Lead Author Kathryn Colby,
M.D., Ph.D., director of the Joint Clinical
Research Center at the Massachusetts Eye and Ear
Infirmary. “An implantable miniature telescope
can improve the vision and quality of life for
patients, but surgeons must be very careful in
implanting it.”
The implantable
telescope has completed two years of
follow-up in a pivotal multicenter trial. In
this phase 2/3 clinical trial, 206 patients
received the telescope prosthesis implant.
One-year outcomes showed that 67 percent of
eyes with the implant achieved a three line
or greater improvement in best-corrected
distance visual acuity, as indicated by
reading an eye chart, compared with 13
percent of the fellow eyes in control
patients. Meaningful improvements in quality
of life measurements were also shown.
Surgical implantation of
this device is challenging, the authors wrote.
It is critical that surgeons not view this
first-of-a-kind device as simply a larger
intraocular lens, like that used to replace the
lens in cataract surgeries. The paper describes
the recommended surgical technique, based upon
the results of the clinical trial and will be a
useful resource for ophthalmic surgeons when the
device is approved for use.
The authors of the paper
include Dr. Colby, David Chang, M.D., University
of California, San Francisco; Doyle Stulting,
M.D., Ph.D., Emory Vision Center, Emory
University, Atlanta, Georgia; and Stephen S.
Lane, M.D., Associated Eye Care, Stillwater,
Minn. This device is being developed by
VisionCare Ophthalmic Technologies, Inc.
About the Massachusetts Eye
and Ear Infirmary,
http://www.meei.harvard.edu:
The Massachusetts Eye and Ear Infirmary, an
independent specialty hospital, is an
international center for treatment and research
and a teaching hospital of Harvard Medical
School.