NearVision CK should not be used in patients
with the following characteristics:
• Peripheral pachymetry reading < 560 µm (measured
at the 6 mm optical zone)
• Strabismus surgery or are likely to develop strabismus
following the Conductive Keratoplasty procedure
• Anterior segment pathology, including a cataract, in the
eye to be treated
• Any corneal abnormality, such as recurrent corneal erosion
or severe basement membrane disease, in the eye to be treated
• Ophthalmoscopic signs of progressive or unstable hyperopia
in the eye to be treated
• Distorted or unclear central keratometry corneal mires
in the eye to be treated
• Blindness in the fellow eye(one eyed patient)
• Previous intraocular or corneal surgery, including any
refractive or therapeutic surgery, in the eye to be treated
• History of herpes zoster or herpes simplex keratitis
• History of steroid-responsive rise in intraocular pressure,
glaucoma, or have a preoperative IOP >21 mm Hg
• Risks for angle-closure or have a potentially occludable
angle
• Diabetes, diagnosed autoimmune disease, connective tissue
disease or clinically significant atopic syndrome
• Current treatment with chronic systemic corticosteroid
or other immunosuppressive therapy that may affect wound healing,
and any immunocompromised patients
• Using ophthalmic medications, other than artificial tears,
for treatment of any ocular disease
• Using systemic medications with significant ocular side
effects
• History of keloid fomation
• History or current case of intractable keratoconjunctivitis
sicca
• Pregnant, lactating or plan to become pregnant
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