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BioDOptix Amniotic Membrane PROKERA Amniotic Membrane “Amniotic membrane placement may be indicated
in the treatment of ocular surface disease when
Tissue stabilization is Tissue stabilization is
accomplished by a dehydration medical management fails, is not tolerated, or
accomplished by a
technique cryopreservation technique is contraindicated”
Self-retaining biologic corneal The goal of amniotic membrane therapy is
bandage ocular surface reconstruction
Amniotic membrane is fastened to Moderately-severe and severe dry eye syndrome
a thermoplastic symblepharon
Corneal edema
ring
Band keratopathy
Allograft device is designed to
maintain space in the orbital Chronic conjunctivitis
cavity and to prevent closure or Anterior basement membrane dystrophy
conjunctival adhesions
1
2/16/2016
Membrane placement
generally can be
maintained with a soft
bandage contact lens
• 72-year-old man 5 years after complicated cataract surgery in the right eye Allograft typically
• Epithelial disruption in a linear-shaped band at 8:00 revealed with fluorescein incorporates into the
• Patient suffers from chronic foreign body sensation and hyperlacrimation tissues of the ocular
• Patient has been to three different ophthalmologists in the past 5 years surface in 4-7 days
• Significant improvement in symptoms after 2 days of amniotic membrane therapy
PROKERA SLIM
amniotic membrane
insert device is placed
under the eyelids
between the eyeball
and the eyelid
Amniotic membrane
graft is fastened to an
ophthalmic conformer
(i.e., thermoplastic
• Neurotrophic keratopathy is a degenerative disease of the corneal epithelium resulting symblepharon ring)
from impaired corneal innervation
• A reduction in corneal sensitivity is the hallmark of the disease and is responsible for
producing epithelial keratopathy, ulceration and perforation