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In general, AlphaCor artificial cornea
is suitable for those patients who would benefit from a human donor
corneal graft but are either at high risk of graft failure or are
unable to receive a graft due to an inability to tolerate the post
operative medications associated with donor graft procedures in some
high-risk cases.
The appropriate selection of patients for AlphaCor is crucial for
its success.
In adults, AlphaCor can be used to replace scarred, vascularized,
oedemetus or painful corneal tissue when a conventional donor
corneal graft is expected to be unsuccessful or unavailable.
AlphaCor performs best in a relatively normal ocular environment.
This includes good eyelid health and tear film production and an
absence of any inflammation. Ideally the patient has a functioning
retina and the intraocular pressure is normal or controlled. Surgery
may be easier if there has been a minimum of 12 months since the
most recent donor transplant.
There are a number of factors that would preclude a patient from
receiving an AlphaCor. These include:
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Age under 18 years (the device is not approved for use in
children). |
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Inability to administer medications at home. |
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Smoking – smoke has the ability to cause discoloration of
the device. |
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HSV – Pending further trials, a history of ocular Herpes
Simplex Virus (HSV) infection is currently considered an
exclusion factor for AlphaCor surgery. |
Surgeons can find out more about the
indications for AlphaCor through the instructions for use available
in the surgeon section. |
AlphaCor
Indications & Use
Design Features
Surgical Procedure
Availability
AlphaCor FAQ
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