U.S. patent application number 13/786357 was filed with the patent office on 2013-10-24 for ocular implant system.
The applicant listed for this patent is Glaukos Corporation. Invention is credited to Hosheng Tu.
Application Number | 20130281910 13/786357 |
Document ID | / |
Family ID | 23079551 |
Filed Date | 2013-10-24 |
United States Patent
Application |
20130281910 |
Kind Code |
A1 |
Tu; Hosheng |
October 24, 2013 |
OCULAR IMPLANT SYSTEM
Abstract
The invention relates generally to medical devices and methods
for reducing the intraocular pressure in an animal eye and, more
particularly, to stent type devices for permitting aqueous outflow
from the eye's anterior chamber and associated methods thereof for
the treatment of glaucoma. Some aspects provide a self-trephining
glaucoma stent and methods thereof which advantageously allow for a
"one-step" procedure in which the incision and placement of the
stent are accomplished by a single device and operation. This
desirably allows for a faster, safer, and less expensive surgical
procedure.
Inventors: |
Tu; Hosheng; (Newport Coast,
CA) |
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Applicant: |
Name |
City |
State |
Country |
Type |
Glaukos Corporation |
Laguna Hills |
CA |
US |
|
|
Family ID: |
23079551 |
Appl. No.: |
13/786357 |
Filed: |
March 5, 2013 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13301648 |
Nov 21, 2011 |
8529493 |
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13786357 |
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12366508 |
Feb 5, 2009 |
8062244 |
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13301648 |
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11598542 |
Nov 13, 2006 |
7563241 |
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12366508 |
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10118578 |
Apr 8, 2002 |
7135009 |
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11598542 |
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60281973 |
Apr 7, 2001 |
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Current U.S.
Class: |
604/9 |
Current CPC
Class: |
A61M 27/00 20130101;
A61F 9/00781 20130101 |
Class at
Publication: |
604/9 |
International
Class: |
A61M 27/00 20060101
A61M027/00 |
Claims
1. An ocular implant system for implanting an ocular device into
the eye, comprising: a fluid drainage device configured to be
deployed in the eye so as to locate a first end of the fluid
drainage device in communication with the suprachoroidal space, the
fluid drainage device having an internal lumen wherein a first end
of the lumen of the drainage device communicates with the
suprachoroidal space and a second end of the lumen of the drainage
device opens into the anterior chamber when implanted in a deployed
location in the eye such that the internal lumen provides a fluid
passageway from the anterior chamber towards the suprachoroidal
space, so as to provide aqueous pressure regulation by draining
aqueous humor from the anterior chamber towards the suprachoroidal
space via the internal lumen, said fluid drainage device configured
to be inserted into the eye through a self-sealing incision in the
cornea and wherein the fluid drainage device has a second end
configured to be located inside the anterior chamber such that the
second end is outside of the ciliary body and posterior of an inner
surface of the cornea when in the deployed location; and a delivery
instrument comprising an elongated member that removably couples to
the fluid drainage device, wherein the delivery instrument is
configured to introduce the fluid drainage device into the anterior
chamber through the corneal incision, advance the fluid drainage
device through the anterior chamber, detach at least a portion of
the ciliary body from the sclera to form an internal space between
the ciliary body and the sclera, advance the implant through the
internal space, and detach the fluid drainage device from the
elongated member and into the deployed location.
2. The device of claim 1, wherein the device is formed of a
biocompatible elastomeric material.
3. The device of claim 1, wherein at least a portion of the device
has a curvature that matches the curvature of the eye.
4. An ocular device as in claim 1, wherein the entire device is
cylindrical.
5. An ocular device as in claim 1, wherein the fluid drainage
device is a tube.
6. The system of claim 1, wherein, when the device is in
communication with the suprachoroidal space, at least a portion of
the device is in contact with the choroid.
7. The system of claim 1, wherein the device has a length
sufficient to extend from the anterior chamber to the choroid when
implanted.
8. The system of claim 1, wherein the device has a length
sufficient to extend from the anterior chamber to a uveal scleral
outflow pathway when implanted.
9. The system of claim 1, wherein the delivery instrument comprises
a cannula.
10. The system of claim 9, wherein the cannula is configured to
detach the at least a portion of the ciliary body from the sclera
to form the internal space between the ciliary body and the
sclera.
11. An ocular implant system for implanting an ocular device into
the eye, comprising: a fluid drainage device configured to be
deployed in the eye so as to locate a first end of the fluid
drainage device in communication with the suprachoroidal space, the
fluid drainage device having an internal lumen wherein a first end
of the lumen of the drainage device communicates with the
suprachoroidal space and a second end of the lumen of the drainage
device opens into the anterior chamber when implanted in a deployed
location in the eye such that the internal lumen provides a fluid
passageway from the anterior chamber towards the suprachoroidal
space, so as to provide aqueous pressure regulation by draining
aqueous humor from the anterior chamber towards the suprachoroidal
space via the internal lumen, wherein the fluid drainage device has
a second end configured to be located inside the anterior chamber
such that the second end is outside of the ciliary body and
posterior of an inner surface of the cornea when the device is in
the deployed location, wherein the device is configured to be
implanted into the eye through an incision in the cornea; and a
delivery instrument comprising an elongated member that removably
couples to the fluid drainage device, wherein the delivery
instrument is configured to introduce the fluid drainage device
into the anterior chamber through the corneal incision, advance the
fluid drainage device through the anterior chamber, detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera, advance the implant
through the internal space, and detach the fluid drainage device
from the elongated member and into the deployed location.
12. The device of claim 11, wherein the device is formed of a
biocompatible elastomeric material.
13. An ocular device as in claim 11, wherein the entire device is
cylindrical.
14. An ocular device as in claim 11, wherein the fluid drainage
device is a tube.
15. The system of claim 11, wherein, when the device is in
communication with the suprachoroidal space, at least a portion of
the device is in contact with the choroid.
16. The system of claim 11, wherein the device has a length
sufficient to extend from the anterior chamber to the choroid when
implanted.
17. The system of claim 11, wherein the device has a length
sufficient to extend from the anterior chamber to a uveal scleral
outflow pathway when implanted.
18. The system of claim 11, wherein the delivery instrument further
comprises a cannula.
19. The system of claim 18, wherein the cannula is configured to
detach the at least a portion of the ciliary body from the sclera
to form the internal space between the ciliary body and the
sclera.
20. An ocular implant system for implanting an ocular device into
the eye, comprising: a fluid drainage device configured to be
deployed in the eye so as to locate a first end of the fluid
drainage device in communication with the suprachoroidal space, the
fluid drainage device having an internal lumen wherein a first end
of the lumen of the drainage device communicates with the
suprachoroidal space and a second end of the lumen of the drainage
device opens into the anterior chamber when implanted in a deployed
location in the eye such that the internal lumen provides a fluid
passageway from the anterior chamber towards the suprachoroidal
space, so as to provide aqueous pressure regulation by draining
aqueous humor from the anterior chamber towards the suprachoroidal
space via the internal lumen, wherein the fluid drainage device has
a second end configured to be located inside the anterior chamber
such that the second end is outside of the ciliary body and
posterior of an inner surface of the cornea, wherein the device is
configured to be implanted into the eye through an incision in the
cornea; and a delivery instrument comprising an elongated member
that removably couples to the fluid drainage device, wherein the
delivery instrument is configured to introduce the fluid drainage
device into the anterior chamber through the corneal incision,
advance the fluid drainage device through the anterior chamber,
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera,
advance the implant through the internal space, and detach the
fluid drainage device from the elongated member and into the
deployed location.
21. The device of claim 20, wherein the device is formed of a
biocompatible elastomeric material.
22. The device of claim 20, wherein sutures are not required to
hold the device in the eye.
23. The device of claim 20, wherein the device is manufactured of a
material that is sufficiently soft as to not erode choroid material
when inserted into the eye.
24. An ocular device as in claim 20, wherein the entire device is
cylindrical.
25. An ocular device as in claim 20, wherein the fluid drainage
device is a tube.
26. The system of claim 20, wherein, when the device is in
communication with the suprachoroidal space, at least a portion of
the device is in contact with the choroid.
27. The system of claim 20, wherein the device has a length
sufficient to extend from the anterior chamber to the choroid when
implanted.
28. The system of claim 20, wherein the device has a length
sufficient to extend from the anterior chamber to a uveal scleral
outflow pathway when implanted.
29. The system of claim 20, wherein the delivery instrument
comprises a cannula.
30. The system of claim 29, wherein the cannula is configured to
detach the at least a portion of the ciliary body from the sclera
to form the internal space between the ciliary body and the
sclera.
31. An ocular implant system for implanting an ocular device into
the eye, comprising: a fluid drainage device configured to be
implanted in a deployed location in the eye via an incision in the
cornea so that a first end of the fluid drainage device is
positioned in the anterior chamber of the eye and a second end of
the fluid drainage device is positioned in communication with the
suprachoroidal space of the eye, the fluid drainage device having
an internal lumen wherein a first opening at a first end of the
internal lumen of the drainage device opens into the anterior
chamber and a second opening at a second end of the internal lumen
of the drainage device communicates with the suprachoroidal space
when in the deployed location such that the internal lumen provides
a direct fluid passageway from the anterior chamber towards the
suprachoroidal space for aqueous pressure regulation when implanted
in the deployed location in the eye and wherein the first end of
the fluid drainage device is configured to be located inside the
anterior chamber such that the first end is outside of the ciliary
body and posterior of an inner surface of the cornea; and a
delivery instrument comprising an elongated member that removably
couples to the fluid drainage device, wherein the delivery
instrument is configured to introduce the fluid drainage device
into the anterior chamber through the corneal incision, advance the
fluid drainage device through the anterior chamber, detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera, advance the implant
through the internal space, and detach the fluid drainage device
from the elongated member and into the deployed location.
32. An ocular device as in claim 31, wherein sutures are not
required to hold the device in the eye.
33. An ocular device as in claim 31, wherein the fluid drainage
device is cylindrical.
34. An ocular device as in claim 31, wherein the fluid drainage
device is positioned entirely within the interior of the eye
radially inward of an outer globular boundary defined by an outer
surface of the sclera when in the deployed location.
35. An ocular device as in claim 31, wherein the entire device is
cylindrical.
36. An ocular device as in claim 31, wherein the fluid drainage
device is a tube.
37. The system of claim 31, wherein, when the device is in
communication with the suprachoroidal space, at least a portion of
the device is in contact with the choroid.
38. The system of claim 31, wherein the device has a length
sufficient to extend from the anterior chamber to the choroid when
implanted.
39. The system of claim 31, wherein the device has a length
sufficient to extend from the anterior chamber to a uveal scleral
outflow pathway when implanted.
40. The system of claim 31, wherein the delivery instrument
comprises a cannula.
41. The system of claim 40, wherein the cannula is configured to
detach the at least a portion of the ciliary body from the sclera
to form the internal space between the ciliary body and the
sclera.
42. An ocular implant system, comprising: an ocular implant
comprising an elongated body having a proximal end region, a distal
end region, and an internal lumen communicating with an inlet port
in the proximal end region and an outlet port in the distal end
region, the ocular implant configured to be introduced into the
anterior chamber of the eye via an incision in the cornea and
positioned in a deployed location wherein the inlet port is in the
anterior chamber of the eye and the outlet port is in communication
with the suprachoroidal space and at least a portion of implant is
in contact with an inner surface of sclera of the eye so that the
internal lumen provides a fluid passageway from the anterior
chamber towards the suprachoroidal space; and a delivery instrument
comprising an elongated member that removably couples to the ocular
implant, wherein the delivery instrument is configured to introduce
the ocular implant into the anterior chamber through the corneal
incision, advance the ocular implant through the anterior chamber,
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera,
advance the implant through the internal space, and detach the
ocular implant from the elongated member and into the deployed
location.
43. A system as in claim 42, wherein the ocular implant is a
tube.
44. A system as in claim 42, wherein the ocular implant is
cylindrical.
45. A system as in claim 42, wherein the elongated member of the
delivery instrument is a cannula.
46. A system as in claim 42, wherein the delivery instrument is
configured to introduce the ocular implant into the anterior
chamber through a self-sealing corneal incision.
47. A system as in claim 42, wherein the elongated member of the
delivery instrument is sized to deliver the implant across the
anterior chamber to a delivery site positioned 180 degrees from the
incision.
48. The system of claim 42, wherein, when the device is in
communication with the suprachoroidal space, at least a portion of
the device is in contact with the choroid.
49. The system of claim 42, wherein the device has a length
sufficient to extend from the anterior chamber to the choroid when
implanted.
50. The system of claim 42, wherein the device has a length
sufficient to extend from the anterior chamber to a uveal scleral
outflow pathway when implanted.
51. The system of claim 42, wherein the delivery instrument
comprises a cannula.
52. The system of claim 51, wherein the cannula is configured to
detach the at least a portion of the ciliary body from the sclera
to form the internal space between the ciliary body and the
sclera.
53. A system for implanting a device into the eye, comprising: a
device configured to be implanted in the eye such that a first end
of the device is in communication with the choroid, the device
having a lumen wherein a first end of the lumen of the device
communicates with the choroid and a second end of the lumen of the
device opens into the anterior chamber when implanted in the eye
such that the lumen provides a flow pathway from the anterior
chamber towards the choroid, so as to provide intraocular pressure
balancing by providing aqueous humor outflow from the anterior
chamber towards the choroid through the lumen, said device
configured to be inserted into the eye through a self-sealing
incision in the cornea and wherein the device has a second end
configured to reside in the anterior chamber when in an
implantation location; and a delivery apparatus comprising an
elongate tip that is removably attached to the device, wherein the
delivery apparatus is configured to introduce the device into the
anterior chamber through the corneal incision, advance the device
through the anterior chamber, advance the implant through an
opening formed in eye tissue, and release the device from the
elongate tip and into the implantation location.
54. The system of claim 53, wherein the device is formed of a
biocompatible elastomer.
55. The system of claim 53, wherein the device is elastomeric.
56. The system of claim 53, wherein at least a portion of the
device has an outer dimension sized such that the device can be
placed within a diameter of Schlemm's canal.
57. The system of claim 53, wherein the device has an external
diameter sized such that the device can be inserted through a
corneal incision of less than about 1 mm.
58. The system of claim 53, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
59. The system of claim 53, wherein at least a portion of the
device has a curvature.
60. The system of claim 59, wherein the curvature matches the
curvature of at least a portion of the eye.
61. The system of claim 53, wherein the device is at least
partially cylindrical.
62. The system of claim 53, wherein the device is a tube.
63. The system of claim 53, wherein, when the device is in
communication with the choroid, at least a portion of the device is
in contact with the choroid.
64. The system of claim 53, wherein the first end of the device is
configured to be located so as to be in communication with a uveal
scleral outflow route.
65. The system of claim 64, wherein the lumen provides a flow
pathway from the anterior chamber towards the uveal scleral outflow
route.
66. The system of claim 53, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation.
67. The system of claim 53, wherein the device is configured to be
positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
68. The system of claim 53, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera into which the device may be placed.
69. The system of claim 53, wherein the delivery apparatus further
comprises at least one member selected from the group consisting
of: a cutting device, a guidewire, a cannula, a blade, a trephine,
a punch, and an ocular tissue drill.
70. The system of claim 69, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
71. The system of claim 69, wherein the member is configured to
form the opening in eye tissue.
72. The system of claim 53, wherein the first end of the device is
configured to be located so as to be in communication with a uveal
scleral outflow route, wherein the second end of the device resides
entirely within the confines of the sclera and the cornea upon
implantation, and wherein the delivery apparatus is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
73. The system of claim 53, wherein the first end of the device is
configured to be located so as to be in communication with the
uveal scleral outflow route, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula configured to detach at least a
portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
74. The system of claim 53, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
75. The system of claim 53, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
76. A system for implanting a device into the eye, comprising: a
device for establishing an outflow pathway configured to be
implanted in the eye so as to locate a first end of the device in
communication with the choroid, the device having a lumen wherein a
first end of the lumen of the device communicates with the choroid
and a second end of the lumen of the device opens into the anterior
chamber when implanted in an implantation location in the eye such
that the lumen provides a flow pathway from the anterior chamber
towards the choroid, so as to provide intraocular pressure
balancing by providing aqueous humor outflow from the anterior
chamber towards the choroid through the lumen, wherein the device
has a second end configured to reside in the anterior chamber,
wherein the device is configured to be implanted into the eye
through an incision in the cornea; and a delivery apparatus
comprising an elongate tip that is removably attached to the
device, wherein the delivery apparatus is configured to advance the
device through the corneal incision and into the anterior chamber,
advance the device through the anterior chamber, advance the device
through an opening formed in eye tissue, and release the device
from the elongate tip and into the implantation location.
77. The system of claim 76, wherein the device is formed of a
biocompatible elastomer.
78. The system of claim 76, wherein the device is elastomeric.
79. The system of claim 76, wherein at least a portion of the
device has an outer dimension sized such that the device can be
placed within a diameter of Schlemm's canal.
80. The system of claim 76, wherein the device has an external
diameter sized such that the device can be inserted through a
corneal incision of less than about 1 mm.
81. The system of claim 76, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
82. The system of claim 76, wherein the device is at least
partially cylindrical.
83. The system of claim 76, wherein the device is a tube.
84. The system of claim 76, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation.
85. The system of claim 76, wherein, when the device is in
communication with the choroid, at least a portion of the device is
in contact with the choroid.
86. The system of claim 76, wherein the first end is located so as
to be in communication with a uveal scleral outflow route.
87. The system of claim 86, wherein the lumen provides a flow
pathway from the anterior chamber towards the uveal scleral outflow
route.
88. The system of claim 76, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
89. The system of claim 76, wherein the delivery apparatus further
comprises at least one member selected from the group consisting
of: a cutting device, a guidewire, a cannula, a blade, a trephine,
a punch, and an ocular tissue drill.
90. The system of claim 89, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
91. The system of claim 89, wherein the member is configured to
form the opening in eye tissue.
92. The system of claim 76, wherein the first end of the device is
located so as to be in communication with the uveal scleral outflow
route, wherein the second end of the device resides entirely within
the confines of the sclera and the cornea upon implantation, and
wherein the delivery apparatus is configured to detach at least a
portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
93. The system of claim 76, wherein the first end of the device is
configured to be located so as to be in communication with the
uveal scleral outflow route, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula configured to detach at least a
portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
94. The system of claim 76, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
95. The system of claim 76, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
96. A system for implanting a device into the eye, comprising: a
device for establishing an outflow pathway configured to be
implanted in the eye so as to locate a first end of the device in
communication with the choroid, the device having a lumen wherein a
first end of the lumen of the device communicates with the choroid
and a second end of the lumen of the device opens into the anterior
chamber when implanted in an implantation location in the eye such
that the lumen provides a flow pathway from the anterior chamber
towards the choroid, so as to provide intraocular pressure
balancing by providing aqueous humor outflow from the anterior
chamber towards the choroid via the lumen, wherein the device has a
second end configured to reside in the anterior chamber, wherein
the device is configured to be implanted into the eye through an
incision in the cornea; and a delivery apparatus comprising an
elongate tip that is removably attached to the device, wherein the
delivery apparatus is configured to advance the device through the
corneal incision and into the anterior chamber, advance the device
through the anterior chamber, advance the device through an opening
formed in eye tissue, and release the device from the elongate tip
and into the implantation location.
97. The system of claim 96, wherein the device is formed of a
biocompatible elastomer.
98. The system of claim 96, wherein the device is elastomeric.
99. The system of claim 96, wherein at least a portion of the
device has an outer dimension sized such that the device can be
placed within a diameter of Schlemm's canal.
100. The system of claim 95, wherein the device has an external
diameter sized such that the device can be inserted through a
corneal incision of less than about 1 mm.
101. The system of claim 96, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
102. The system of claim 96, wherein the structure of the device
secures the device in the eye.
103. The system of claim 96, wherein the device is manufactured of
a biocompatible material.
104. The system of claim 96, wherein the device is at least
partially cylindrical.
105. The system of claim 96, wherein the device is a tube.
106. The system of claim 96, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation.
107. The system of claim 96, wherein, when the device is in
communication with the choroid, at least a portion of the device is
in contact with the choroid.
108. The system of claim 96, wherein the first end is located so as
to be in communication with a uveal scleral outflow route.
109. The system of claim 108, wherein the lumen provides a flow
pathway from the anterior chamber towards the uveal scleral outflow
route.
110. The system of claim 96, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
111. The system of claim 96, wherein the delivery apparatus further
comprises at least one member selected from the group consisting
of: a cutting device, a guidewire, a cannula, a blade, a trephine,
a punch, and an ocular tissue drill.
112. The system of claim 111, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
113. The system of claim 111, wherein the member is configured to
form the opening in eye tissue.
114. The system of claim 96, wherein the first end of the device is
located so as to be in communication with a uveal scleral outflow
route, wherein the second end of the device resides entirely within
the confines of the sclera and the cornea upon implantation, and
wherein the delivery apparatus is configured to detach at least a
portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
115. The system of claim 96, wherein the first end of the device is
configured to be located so as to be in communication with the
uveal scleral outflow route, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula configured to detach at least a
portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
116. The system of claim 96, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
117. The system of claim 96, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
118. A system for implanting a device into the eye, comprising: a
device for establishing an outflow pathway configured to be
implanted in an implantation location in the eye via an incision in
the cornea so that a first end of the device is positioned in the
anterior chamber of the eye and a second end of the device is
positioned in communication with the choroid, the device having a
lumen wherein a first opening at a first end of the lumen of the
device opens into the anterior chamber and a second opening at a
second end of the lumen of the device communicates with the choroid
when in the implantation location such that the lumen provides a
direct flow pathway from the anterior chamber towards the choroid
for intraocular pressure balancing when implanted in the
implantation location in the eye, wherein the first end of the
device is configured to reside in the anterior chamber; and a
delivery-apparatus comprising an elongate tip that is removably
attached to the device, wherein the delivery apparatus is
configured to advance the device through the corneal incision and
into the anterior chamber, advance the device through the anterior
chamber, advance the device through an opening formed in eye
tissue, and release the device from the elongate tip and into the
implantation location.
119. The system of claim 118, wherein the structure of the device
secures the device in the eye.
120. The system of claim 118, wherein the device is
cylindrical.
121. The system of claim 118, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
122. The system of claim 118, wherein the device is positioned
entirely within the interior of the eye radially inward of an outer
globular boundary defined by an outer surface of the sclera when in
the implantation location.
123. The system of claim 118, wherein the entire device is
cylindrical.
124. The system of claim 118, wherein the device is a tube.
125. The system of claim 118, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation.
126. The system of claim 118, wherein, when the device is in
communication with the choroid, at least a portion of the device is
in contact with the choroid.
127. The system of claim 118, wherein the first end is located so
as to be in communication with the uveal scleral outflow route.
128. The system of claim 127, wherein the lumen provides a flow
pathway from the anterior chamber towards the uveal scleral outflow
route.
129. The system of claim 118, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
130. The system of claim 118, wherein the delivery apparatus
further comprises at least one member selected from the group
consisting of: a cutting device, a guidewire, a cannula, a blade, a
trephine, a punch, and an ocular tissue drill.
131. The system of claim 130, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
132. The system of claim 130, wherein the member is configured to
form the opening in eye tissue.
133. The system of claim 118, wherein the first end of the device
is located so as to be in communication with the uveal scleral
outflow route, wherein the second end of the device resides
entirely within the confines of the sclera and the cornea upon
implantation, and wherein the delivery apparatus is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
134. The system of claim 118, wherein the first end of the device
is configured to be located so as to be in communication with the
uveal scleral outflow route, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula configured to detach at least a
portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
135. The system of claim 118, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
136. The system of claim 118, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
137. A system, comprising: an implant comprising an elongated
device having a second end region, a first end region, and an lumen
communicating with an inlet port in the second end region and an
outlet port in the first end region, the implant configured to be
advanced into the anterior chamber of the eye via an incision in
the cornea and positioned in an implantation location wherein the
inlet port is in the anterior chamber of the eye and the outlet
port is in communication with the choroid and at least a portion of
the implant is in contact with an inner surface of sclera of the
eye so that the lumen provides a flow pathway from the anterior
chamber towards the choroid; and a delivery apparatus comprising an
elongate tip that is removably attached to the implant, wherein the
delivery apparatus is configured to advance the implant through the
corneal incision and into the anterior chamber, advance the implant
through the anterior chamber, advance the device through an opening
formed in eye tissue, and release the implant from the elongate tip
and into the implantation-location.
138. A system as in claim 137, wherein the implant is a tube.
139. A system as in claim 137, wherein the implant is
cylindrical.
140. A system as in claim 137, wherein the delivery apparatus
comprises a cannula.
141. A system as in claim 137, wherein the delivery apparatus is
configured to introduce the implant into the anterior chamber
through a self-sealing corneal incision.
142. A system as in claim 137, wherein the elongate tip of the
delivery apparatus is configured to deliver the implant across the
anterior chamber to a delivery site positioned 180 degrees from the
incision.
143. The system of claim 137, wherein, when the device is in
communication with the choroid, at least a portion of the device is
in contact with the choroid.
144. The system of claim 137, wherein the first end is located so
as to be in communication with a uveal scleral outflow route.
145. The system of claim 144, wherein the lumen provides a flow
pathway from the anterior chamber towards the uveal scleral outflow
route.
146. The system of claim 137, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
147. The system of claim 137, wherein the delivery apparatus
further comprises at least one member selected from the group
consisting of: a cutting device, guidewire, cannula, blade,
trephine, punch, hot tip, and ocular tissue drill.
148. The system of claim 147, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
149. The system of claim 147, wherein the member is configured to
form the opening in eye tissue.
150. The system of claim 137, wherein the first end of the device
is located so as to be in communication with a uveal scleral
outflow route, wherein the delivery apparatus is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
151. The system of claim 137, wherein the first end of the device
is located so as to be in communication with a uveal scleral
outflow route, wherein the delivery apparatus further comprises a
blade or cannula configured to detach at least a portion of the
ciliary body from the sclera to form an internal space between the
ciliary body and the sclera into which the device may be
placed.
152. A system for implanting a device into the eye, comprising: a
device configured to be implanted in the eye such that a first end
of the device is in communication with a uveal scleral outflow
route, the device having a lumen wherein a first end of the lumen
of the device communicates with the uveal scleral outflow route and
a second end of the lumen of the device opens into the anterior
chamber when implanted in an implantation location in the eye such
that the lumen provides a flow pathway from the anterior chamber
towards the uveal scleral outflow route, so as to provide
intraocular pressure balancing by providing aqueous humor outflow
from the anterior chamber towards the uveal scleral outflow route
through the lumen, said device configured to be inserted into the
eye through a self-sealing incision in the cornea and wherein the
device has a second end configured to reside in the anterior
chamber; and a delivery apparatus comprising an elongate tip that
is removably attached to the device, wherein the delivery apparatus
is configured to introduce the device into the anterior chamber
through the corneal incision, advance the device through the
anterior chamber, advance the implant through an opening formed in
eye tissue, and release the device from the elongate tip and into
the implantation location.
153. The system of claim 152, wherein the device is formed of a
biocompatible elastomer.
154. The system of claim 152, wherein the device is
elastomeric.
155. The system of claim 152, wherein at least a portion of the
device has an outer dimension such that the device can be placed
within a diameter of Schlemm's canal.
156. The system of claim 152, wherein the device has an external
diameter sized such that the device can be inserted through a
corneal incision of less than about 1 mm.
157. The system of claim 152, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
158. The system of claim 152, wherein at least a portion of the
device has a curvature.
159. The system of claim 158, wherein the curvature matches the
curvature of at least a portion of the eye.
160. The system of claim 152, wherein the device is at least
partially cylindrical.
161. The system of claim 152, wherein the device is a tube.
162. The system of claim 152, wherein, when the device is in
communication with the uveal scleral outflow route, at least a
portion of the device is in contact with the choroid.
163. The system of claim 152, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation.
164. The system of claim 152, wherein the device is configured to
be positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
165. The system of claim 152, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera into which the device may be placed.
166. The system of claim 152, wherein the delivery apparatus
comprises at least one member selected from the group consisting
of: a cutting device, a guidewire, a cannula, a blade, a trephine,
a punch, and an ocular tissue drill.
167. The system of claim 166, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
168. The system of claim 166, wherein the member is configured to
form the opening in eye tissue.
169. The system of claim 152, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
170. The system of claim 152, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
171. A system for implanting a device into the eye, comprising: a
device for establishing an outflow pathway configured to be
implanted in the eye so as to locate a first end of the device in
communication with a uveal scleral outflow route, the device having
a lumen wherein a first end of the lumen of the device communicates
with the uveal scleral outflow route and a second end of the lumen
of the device opens into the anterior chamber when implanted in an
implantation location in the eye such that the lumen provides a
flow pathway from the anterior chamber towards the uveal scleral
outflow route, so as to provide aqueous pressure balancing by
providing aqueous outflow from the anterior chamber towards the
uveal scleral outflow route via the lumen, wherein the device has a
second end configured to reside in the anterior chamber, wherein
the device is configured to be implanted into the eye through an
incision in the cornea; and a delivery apparatus comprising an
elongate tip that is removably attached to the device, wherein the
delivery apparatus is configured to advance the device through the
corneal incision and into the anterior chamber, advance the device
through the anterior chamber, advance the device through an opening
formed in eye tissue, and release the device from the elongate tip
and into the implantation location.
172. The system of claim 171, wherein the device is formed of a
biocompatible elastomer.
173. The system of claim 171, wherein the device is
elastomeric.
174. The system of claim 171, wherein at least a portion of the
device has an outer dimension such that the device can be placed
within a diameter of Schlemm's canal.
175. The system of claim 171, wherein the device has an external
diameter sized such that the device can be inserted through a
corneal incision of less than about 1 mm.
176. The system of claim 171, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
177. An ocular system as in claim 171, wherein the device is at
least partially cylindrical.
178. An ocular system as in claim 171, wherein the device is a
tube.
179. The system of claim 171, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation.
180. The system of claim 171, wherein, when the device is in
communication with the uveal scleral outflow route, at least a
portion of the device is in contact with the choroid.
181. The system of claim 171, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
182. The system of claim 171, wherein the delivery apparatus
further comprises at least one member selected from the group
consisting of: a cutting device, a guidewire, a cannula, a blade, a
trephine, a punch, and an ocular tissue drill.
183. The system of claim 182, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
184. The system of claim 182, wherein the member is configured to
form the opening in eye tissue.
185. The system of claim 171, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
186. The system of claim 171, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
187. A system for implanting a device into the eye, comprising: a
device for establishing an outflow pathway configured to be
implanted in the eye so as to locate a first end of the device in
communication with a uveal scleral outflow route, the device having
a lumen wherein a first end of the lumen of the device communicates
with the uveal scleral outflow route and a second end of the lumen
of the device opens into the anterior chamber when implanted in an
implantation location in the eye such that the lumen provides a
flow pathway from the anterior chamber towards the uveal scleral
outflow route, so as to provide intraocular pressure balancing by
providing aqueous humor outflow from the anterior chamber towards
the uveal scleral outflow route via the lumen, wherein the device
has a second end configured to reside in the anterior chamber,
wherein the device is configured to be implanted into the eye
through an incision in the cornea; and a delivery apparatus
comprising an elongate tip that is removably attached to the
device, wherein the delivery apparatus is configured to advance the
device through the corneal incision and into the anterior chamber,
advance the device through the anterior chamber, advance the device
through an opening formed in eye tissue, and release the device
from the elongate tip and into the implantation location.
188. The system of claim 187, wherein the device is formed of a
biocompatible elastomer.
189. The system of claim 187, wherein the device is
elastomeric.
190. The system of claim 187, wherein at least a portion of the
device has an outer dimension sized such that the device can be
placed within a diameter of Schlemm's canal.
191. The system of claim 187, wherein the device has an external
diameter sized such that the device can be inserted through a
corneal incision of less than about 1 mm.
192. The system of claim 187, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
193. The system of claim 187, wherein the structure of the device
secures the device in the eye.
194. The system of claim 187, wherein the device is manufactured of
a biocompatible material.
195. The system of claim 187, wherein the device is at least
partially cylindrical.
196. The system of claim 187, wherein the device is a tube.
197. The system of claim 187, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation
198. The system of claim 187, wherein, when the device is in
communication with the uveal scleral outflow route, at least a
portion of the device is in contact with the choroid.
199. The system of claim 187, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
200. The system of claim 187, wherein the delivery apparatus
further comprises at least one member selected from the group
consisting of: a cutting device, a guidewire, a cannula, a blade, a
trephine, a punch, and an ocular tissue drill.
201. The system of claim 200, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
202. The system of claim 200, wherein the member is configured to
form the opening in eye tissue.
203. The system of claim 187, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
204. The system of claim 187, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
205. A system for implanting a device into the eye, comprising: a
device for establishing an outflow pathway configured to be
implanted in a location in the eye via an incision in the cornea so
that a first end of the device is positioned in the anterior
chamber of the eye and a second end of the device is positioned in
communication with a uveal scleral outflow route, the device having
a lumen wherein a first opening at a first end of the lumen of the
device opens into the anterior chamber and a second opening at a
second end of the lumen of the device communicates with the uveal
scleral outflow route when in the implanted location such that the
lumen provides a direct flow pathway from the anterior chamber
towards the uveal scleral outflow route for intraocular pressure
balancing when implanted in the implantation location in the eye
and wherein the first end of the device is configured to reside in
the anterior chamber; and a delivery apparatus comprising an
elongate tip that is removably attached to the device, wherein the
delivery apparatus is configured to advance the device through the
corneal incision and into the anterior chamber, advance the device
through the anterior chamber, advance the device through an opening
formed in eye tissue, and release the device from the elongate tip
and into the implantation location.
206. The system of claim 205, wherein the structure of the device
secures the device in the eye.
207. The system of claim 205, wherein the device is
cylindrical.
208. The system of claim 205, wherein the device is
elastomeric.
209. The system of claim 205, wherein at least a portion of the
device has an outer dimension such that the device can be placed
within a diameter of Schlemm's canal.
210. The system of claim 205, wherein the device has an external
diameter sized such that the device can be inserted through a
corneal incision of less than about 1 mm.
211. The system of claim 205, wherein the device has a length that
extends from the anterior chamber to the choroid when
implanted.
212. The system of claim 205, wherein the device is positioned
entirely within the interior of the eye radially inward of an outer
globular boundary defined by an outer surface of the sclera when in
the implanted location.
213. The system of claim 205, wherein the entire device is
cylindrical.
214. The system of claim 205, wherein the device is a tube.
215. The system of claim 205, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation.
216. The system of claim 205, wherein, when the device is in
communication with the uveal scleral outflow route, at least a
portion of the device is in contact with the choroid.
217. The system of claim 205, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
218. The system of claim 205, wherein the delivery apparatus
further comprises at least one member selected from the group
consisting of: a cutting device, a guidewire, a cannula, a blade, a
trephine, a punch, and an ocular tissue drill.
219. The system of claim 218, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
220. The system of claim 218, wherein the member is configured to
form the opening in eye tissue.
221. The system of claim 205, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus is configured
to detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
222. The system of claim 205, wherein the second end of the device
resides entirely within the confines of the sclera and the cornea
upon implantation, and wherein the delivery apparatus further
comprises a blade or cannula that is configured to detach at least
a portion of the ciliary body from the sclera to form an internal
space between the ciliary body and the sclera into which the device
may be placed.
223. A system, comprising: an implant comprising an elongated
device having a second end region, a first end region, and an lumen
communicating with an inlet port in the second end region and an
outlet port in the first end region, the implant configured to be
advanced into the anterior chamber of the eye via an incision in
the cornea and positioned in a location wherein the inlet port is
in the anterior chamber of the eye and the outlet port is in
communication with a uveal scleral outflow route and at least a
portion of implant is in contact with an inner surface of sclera of
the eye so that the lumen provides a flow pathway from the anterior
chamber towards the uveal scleral outflow route; and a delivery
apparatus comprising an elongate tip that is removably attached to
the implant, wherein the delivery apparatus is configured to
advance the implant through the corneal incision and into the
anterior chamber, advance the implant through the anterior chamber,
advance the implant through an opening formed in eye tissue, and
release the implant from the elongate tip and into the
implantation-location.
224. A system as in claim 223, wherein the implant is a tube.
225. A system as in claim 223, wherein the implant is
cylindrical.
226. A system as in claim 223, wherein the delivery apparatus
comprises a cannula.
227. A system as in claim 223, wherein the delivery apparatus is
configured to introduce the implant into the anterior chamber
through a self-sealing corneal incision.
228. A system as in claim 223, wherein the elongate tip of the
delivery apparatus is configured to deliver the implant across the
anterior chamber to a delivery site positioned 180 degrees from the
incision.
229. The system of claim 223, wherein, when the device is in
communication with the uveal scleral outflow route, at least a
portion of the device is in contact with the choroid.
230. The system of claim 223, wherein the delivery apparatus is
configured to detach at least a portion of the ciliary body from
the sclera to form an internal space between the ciliary body and
the sclera.
231. The system of claim 223, wherein the delivery apparatus
further comprises at least one member selected from the group
consisting of: a cutting device, a guidewire, a cannula, a blade, a
trephine, a punch, and an ocular tissue drill.
232. The system of claim 231, wherein the member is configured to
detach at least a portion of the ciliary body from the sclera to
form an internal space between the ciliary body and the sclera into
which the device may be placed.
233. The system of claim 231, wherein the member is configured to
form the opening in eye tissue.
234. The system of claim 76, wherein the device is configured to be
positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
235. The system of claim 96, wherein the device is configured to be
positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
236. The system of claim 118, wherein the device is configured to
be positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
237. The system of claim 137, wherein the device is configured to
be positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
238. The system of claim 171, wherein the device is configured to
be positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
239. The system of claim 187, wherein the device is configured to
be positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
240. The system of claim 205, wherein the device is configured to
be positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
241. The system of claim 223, wherein the device is configured to
be positioned in the anterior chamber such that the second end is
outside of the ciliary body and posterior of an inner surface of
the cornea.
Description
RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 13/301,648, filed Nov. 21, 2011, entitled
OCULAR IMPLANT SYSTEMS, which is a continuation of U.S. patent
application Ser. No. 12/366,508, filed Feb. 5, 2009, entitled
SELF-TREPHINING IMPLANT AND METHODS THEREOF FOR TREATMENT OF OCULAR
DISORDERS, now U.S. Pat. No. 8,062,244, which is a divisional of
U.S. patent application Ser. No. 11/598,542, filed Nov. 13, 2006,
entitled IMPLANT AND METHODS THEREOF FOR TREATMENT OF OCULAR
DISORDERS, now U.S. Pat. No. 7,563,241, which is a continuation of
U.S. patent application Ser. No. 10/118,578, filed Apr. 8, 2002,
entitled GLAUCOMA STENT AND METHODS THEREOF FOR GLAUCOMA TREATMENT,
now U.S. Pat. No. 7,135,009, which claims the benefit of U.S.
Provisional Application No. 60/281,973, filed Apr. 7, 2001,
entitled GLAUCOMA SHUNT AND METHODS THEREOF FOR GLAUCOMA TREATMENT,
the entire contents of each of which are hereby incorporated by
reference herein.
BACKGROUND OF THE INVENTION
[0002] 1. Field of the Invention
[0003] The invention relates generally to medical devices and
methods for reducing the intraocular pressure in an animal eye and,
more particularly, to shunt type devices for permitting aqueous
outflow from the eye's anterior chamber and associated methods
thereof for the treatment of glaucoma.
[0004] 2. Description of the Related Art
[0005] The human eye is a specialized sensory organ capable of
light reception and able to receive visual images. The trabecular
meshwork serves as a drainage channel and is located in anterior
chamber angle formed between the iris and the cornea. The
trabecular meshwork maintains a balanced pressure in the anterior
chamber of the eye by draining aqueous humor from the anterior
chamber.
[0006] About two percent of people in the United States have
glaucoma. Glaucoma is a group of eye diseases encompassing a broad
spectrum of clinical presentations, etiologies, and treatment
modalities. Glaucoma causes pathological changes in the optic
nerve, visible on the optic disk, and it causes corresponding
visual field loss, resulting in blindness if untreated. Lowering
intraocular pressure is the major treatment goal in all
glaucomas.
[0007] In glaucomas associated with an elevation in eye pressure
(intraocular hypertension), the source of resistance to outflow is
mainly in the trabecular meshwork. The tissue of the trabecular
meshwork allows the aqueous humor ("aqueous") to enter Schlemm's
canal, which then empties into aqueous collector channels in the
posterior wall of Schlemm's canal and then into aqueous veins,
which form the episcleral venous system. Aqueous humor is a
transparent liquid that fills the region between the cornea, at the
front of the eye, and the lens. The aqueous humor is continuously
secreted by the ciliary body around the lens, so there is a
constant flow of aqueous humor from the ciliary body to the eye's
front chamber. The eye's pressure is determined by a balance
between the production of aqueous and its exit through the
trabecular meshwork (major route) or uveal scleral outflow (minor
route). The trabecular meshwork is located between the outer rim of
the iris and the back of the cornea, in the anterior chamber angle.
The portion of the trabecular meshwork adjacent to Schlemm's canal
(the juxtacanilicular meshwork) causes most of the resistance to
aqueous outflow.
[0008] Glaucoma is grossly classified into two categories:
closed-angle glaucoma, also known as angle closure glaucoma, and
open-angle glaucoma. Closed-angle glaucoma is caused by closure of
the anterior chamber angle by contact between the iris and the
inner surface of the trabecular meshwork. Closure of this
anatomical angle prevents normal drainage of aqueous humor from the
anterior chamber of the eye.
[0009] Open-angle glaucoma is any glaucoma in which the angle of
the anterior chamber remains open, but the exit of aqueous through
the trabecular meshwork is diminished. The exact cause for
diminished filtration is unknown for most cases of open-angle
glaucoma. Primary open-angle glaucoma is the most common of the
glaucomas, and it is often asymptomatic in the early to moderately
advanced stage. Patients may suffer substantial, irreversible
vision loss prior to diagnosis and treatment. However, there are
secondary open-angle glaucomas which may include edema or swelling
of the trabecular spaces (e.g., from corticosteroid use), abnormal
pigment dispersion, or diseases such as hyperthyroidism that
produce vascular congestion.
[0010] Current therapies for glaucoma are directed at decreasing
intraocular pressure. Medical therapy includes topical ophthalmic
drops or oral medications that reduce the production or increase
the outflow of aqueous. However, these drug therapies for glaucoma
are sometimes associated with significant side effects, such as
headache, blurred vision, allergic reactions, death from
cardiopulmonary complications, and potential interactions with
other drugs. When drug therapy fails, surgical therapy is used.
Surgical therapy for open-angle glaucoma consists of laser
trabeculoplasty, trabeculectomy, and implantation of aqueous shunts
after failure of trabeculectomy or if trabeculectomy is unlikely to
succeed. Trabeculectomy is a major surgery that is widely used and
is augmented with topically applied anticancer drugs, such as
5-flurouracil or mitomycin-C to decrease scarring and increase the
likelihood of surgical success.
[0011] Approximately 100,000 trabeculectomies are performed on
Medicare-age patients per year in the United States. This number
would likely increase if the morbidity associated with
trabeculectomy could be decreased. The current morbidity associated
with trabeculectomy consists of failure (10-15%); infection (a
lifelong risk of 2-5%); choroidal hemorrhage, a severe internal
hemorrhage from low intraocular pressure, resulting in visual loss
(1%); cataract formation; and hypotony maculopathy (potentially
reversible visual loss from low intraocular pressure).
[0012] For these reasons, surgeons have tried for decades to
develop a workable surgery for the trabecular meshwork.
[0013] The surgical techniques that have been tried and practiced
are goniotomy/trabeculotomy and other mechanical disruptions of the
trabecular meshwork, such as trabeculopuncture, goniophotoablation,
laser trabecular ablation, and goniocurretage. These are all major
operations and are briefly described below.
[0014] Goniotomy/Trabeculotomy:
[0015] Goniotomy and trabeculotomy are simple and directed
techniques of microsurgical dissection with mechanical disruption
of the trabecular meshwork. These initially had early favorable
responses in the treatment of open-angle glaucoma. However,
long-term review of surgical results showed only limited success in
adults. In retrospect, these procedures probably failed due to
cellular repair and fibrosis mechanisms and a process of "filling
in." Filling in is a detrimental effect of collapsing and closing
in of the created opening in the trabecular meshwork. Once the
created openings close, the pressure builds back up and the surgery
fails.
[0016] Trabeculopuncture:
[0017] Q-switched Neodynium (Nd) YAG lasers also have been
investigated as an optically invasive technique for creating
full-thickness holes in trabecular meshwork. However, the
relatively small hole created by this trabeculopuncture technique
exhibits a filling-in effect and fails.
[0018] Goniophotoablation/Laser Trabecular Ablation:
[0019] Goniophotoablation is disclosed by Berlin in U.S. Pat. No.
4,846,172 and involves the use of an excimer laser to treat
glaucoma by ablating the trabecular meshwork. This was demonstrated
not to succeed by clinical trial. Hill et al. used an Erbium:YAG
laser to create full-thickness holes through trabecular meshwork
(Hill et al., Lasers in Surgery and Medicine 11:341-346, 1991).
This technique was investigated in a primate model and a limited
human clinical trial at the University of California, Irvine.
Although morbidity was zero in both trials, success rates did not
warrant further human trials. Failure was again from filling in of
surgically created defects in the trabecular meshwork by repair
mechanisms. Neither of these is a viable surgical technique for the
treatment of glaucoma.
[0020] Goniocurretage:
[0021] This is an ab interno (from the inside), mechanically
disruptive technique that uses an instrument similar to a
cyclodialysis spatula with a microcurrette at the tip. Initial
results were similar to trabeculotomy: it failed due to repair
mechanisms and a process of filling in.
[0022] Although trabeculectomy is the most commonly performed
filtering surgery, viscocanulostomy (VC) and non penetrating
trabeculectomy (NPT) are two new variations of filtering surgery.
These are ab externo (from the outside), major ocular procedures in
which Schlemm's canal is surgically exposed by making a large and
very deep scleral flap. In the VC procedure, Schlemm's canal is
cannulated and viscoelastic substance injected (which dilates
Schlemm's canal and the aqueous collector channels). In the NPT
procedure, the inner wall of Schlemm's canal is stripped off after
surgically exposing the canal.
[0023] Trabeculectomy, VC, and NPT involve the formation of an
opening or hole under the conjunctiva and scleral flap into the
anterior chamber, such that aqueous humor is drained onto the
surface of the eye or into the tissues located within the lateral
wall of the eye. These surgical operations are major procedures
with significant ocular morbidity. When trabeculectomy, VC, and NPT
are thought to have a low chance for success, a number of
implantable drainage devices have been used to ensure that the
desired filtration and outflow of aqueous humor through the
surgical opening will continue. The risk of placing a glaucoma
drainage device also includes hemorrhage, infection, and diplopia
(double vision).
[0024] Examples of implantable shunts and surgical methods for
maintaining an opening for the release of aqueous humor from the
anterior chamber of the eye to the sclera or space beneath the
conjunctiva have been disclosed in, for example, U.S. Pat. No.
6,059,772 to Hsia et al., and U.S. Pat. No. 6,050,970 to
Baerveldt.
[0025] All of the above surgeries and variations thereof have
numerous disadvantages and moderate success rates. They involve
substantial trauma to the eye and require great surgical skill in
creating a hole through the full thickness of the sclera into the
subconjunctival space. The procedures are generally performed in an
operating room and have a prolonged recovery time for vision.
[0026] The complications of existing filtration surgery have
prompted ophthalmic surgeons to find other approaches to lowering
intraocular pressure.
[0027] The trabecular meshwork and juxtacanilicular tissue together
provide the majority of resistance to the outflow of aqueous and,
as such, are logical targets for surgical removal in the treatment
of open-angle glaucoma. In addition, minimal amounts of tissue are
altered and existing physiologic outflow pathways are utilized.
[0028] As reported in Arch. Ophthalm. (2000) 118:412, glaucoma
remains a leading cause of blindness, and filtration surgery
remains an effective, important option in controlling the disease.
However, modifying existing filtering surgery techniques in any
profound way to increase their effectiveness appears to have
reached a dead end. The article further states that the time has
come to search for new surgical approaches that may provide better
and safer care for patients with glaucoma.
[0029] Therefore, there is a great clinical need for a method of
treating glaucoma that is faster, safer, and less expensive than
currently available modalities.
SUMMARY OF THE INVENTION
[0030] The trabecular meshwork and juxtacanilicular tissue together
provide the majority of resistance to the outflow of aqueous and,
as such, are logical targets for surgical approach in the treatment
of glaucoma. Various embodiments of glaucoma shunts are disclosed
herein for aqueous to exit through the trabecular meshwork (major
route) or uveal scleral outflow (minor route) or other route
effective to reduce intraocular pressure (IOP).
[0031] Glaucoma surgical morbidity would greatly decrease if one
were to bypass the focal resistance to outflow of aqueous only at
the point of resistance, and to utilize remaining, healthy aqueous
outflow mechanisms. This is in part because episcleral aqueous
humor exerts a backpressure that prevents intraocular pressure from
going too low, and one could thereby avoid hypotony. Thus, such a
surgery would virtually eliminate the risk of hypotony-related
maculopathy and choroidal hemorrhage. Furthermore, visual recovery
would be very rapid, and the risk of infection would be very small,
reflecting a reduction in incidence from 2-5% to about 0.05%.
[0032] Copending U.S. application Ser. No. 09/549,350, filed Apr.
14, 2000, entitled APPARATUS AND METHOD FOR TREATING GLAUCOMA, and
copending U.S. application Ser. No. 09/704,276, filed Nov. 1, 2000,
entitled GLAUCOMA TREATMENT DEVICE, disclose devices and methods of
placing a trabecular shunt ab interna, i.e., from inside the
anterior chamber through the trabecular meshwork, into Schlemm's
canal. The entire contents of each of these copending patent
applications are hereby incorporated by reference herein. The
invention encompasses both ab interno and ab externo glaucoma
shunts or stents and methods thereof.
[0033] Techniques performed in accordance with aspects herein may
be referred to generally as "trabecular bypass surgery." Advantages
of this type of surgery include lowering intraocular pressure in a
manner which is simple, effective, disease site-specific, and can
potentially be performed on an outpatient basis.
[0034] Generally, trabecular bypass surgery (TBS) creates an
opening, a slit, or a hole through trabecular meshwork with minor
microsurgery. TBS has the advantage of a much lower risk of
choroidal hemorrhage and infection than prior techniques, and it
uses existing physiologic outflow mechanisms. In some aspects, this
surgery can potentially be performed under topical or local
anesthesia on an outpatient basis with rapid visual recovery. To
prevent "filling in" of the hole, a biocompatible elongated device
is placed within the hole and serves as a stent. U.S. patent
application Ser. No. 09/549,350, filed Apr. 14, 2000, the entire
contents of which are hereby incorporated by reference herein,
discloses trabecular bypass surgery.
[0035] As described in U.S. patent application. Ser. No.
09/549,350, filed Apr. 14, 2000, and U.S. application Ser. No.
09/704,276, filed Nov. 1, 2000, the entire contents each one of
which are hereby incorporated by reference herein, a trabecular
shunt or stent for transporting aqueous humor is provided. The
trabecular stent includes a hollow, elongate tubular element,
having an inlet section and an outlet section. The outlet section
may optionally include two segments or elements, adapted to be
positioned and stabilized inside Schlemm's canal. In one
embodiment, the device appears as a "T" shaped device.
[0036] In one aspect of the invention, a delivery apparatus (or
"applicator") is used for placing a trabecular stent through a
trabecular meshwork of an eye. Certain embodiments of such a
delivery apparatus are disclosed in copending U.S. application Ser.
No. 10/101,548, filed Mar. 18, 2002, entitled APPLICATOR AND
METHODS FOR PLACING A TRABECULAR SHUNT FOR GLAUCOMA TREATMENT, and
U.S. Provisional Application No. 60/276,609, filed Mar. 16, 2001,
entitled APPLICATOR AND METHODS FOR PLACING A TRABECULAR SHUNT FOR
GLAUCOMA TREATMENT, the entire contents of each one of which are
hereby incorporated by reference herein.
[0037] The stent has an inlet section and an outlet section. The
delivery apparatus includes a handpiece, an elongate tip, a holder
and an actuator. The handpiece has a distal end and a proximal end.
The elongate tip is connected to the distal end of the handpiece.
The elongate tip has a distal portion and is configured to be
placed through a corneal incision and into an anterior chamber of
the eye. The holder is attached to the distal portion of the
elongate tip. The holder is configured to hold and release the
inlet section of the trabecular stent. The actuator is on the
handpiece and actuates the holder to release the inlet section of
the trabecular stent from the holder. When the trabecular stent is
deployed from the delivery apparatus into the eye, the outlet
section is positioned in substantially opposite directions inside
Schlemm's canal. In one embodiment, a deployment mechanism within
the delivery apparatus includes a push-pull type plunger.
[0038] Some aspects of the invention relate to devices for reducing
intraocular pressure by providing outflow of aqueous from an
anterior chamber of an eye. The device generally comprises an
elongated tubular member and cutting means. The tubular member is
adapted for extending through a trabecular meshwork of the eye. The
tubular member generally comprises a lumen having an inlet port and
an outlet port for providing a flow pathway. The cutting means is
mechanically connected to the tubular member for creating an
incision in the trabecular meshwork for receiving at least a
portion of the tubular member.
[0039] In one aspect, a self-trephining glaucoma stent is provided
for reducing and/or balancing intraocular pressure in an eye. The
stent generally comprises a snorkel and a curved blade. The snorkel
generally comprises an upper seat for stabilizing said stent within
the eye, a shank and a lumen. The shank is mechanically connected
to the seat and is adapted for extending through a trabecular
meshwork of the eye. The lumen extends through the snorkel and has
at least one inlet flow port and at least one outlet flow port. The
blade is mechanically connected to the snorkel. The blade generally
comprises a cutting tip proximate a distal-most point of the blade
for making an incision in the trabecular meshwork for receiving the
shank.
[0040] Some aspects of the invention relate to methods of
implanting a trabecular stent device in an eye. In one aspect, the
device has a snorkel mechanically connected to a blade. The blade
is advanced blade through a trabecular meshwork of the eye to cut
the trabecular meshwork and form an incision therein. At least a
portion of the snorkel is inserted in the incision to implant the
device in the eye.
[0041] Some aspects provide a self-trephining glaucoma stent and
methods thereof which advantageously allow for a "one-step"
procedure in which the incision and placement of the stent are
accomplished by a single device and operation. This desirably
allows for a faster, safer, and less expensive surgical procedure.
In any of the embodiments, fiducial markings, indicia, or the like
and/or positioning of the stent device in a preloaded applicator
may be used for proper orientation and alignment of the device
during implantation.
[0042] Among the advantages of trabecular bypass surgery is its
simplicity. The microsurgery may potentially be performed on an
outpatient basis with rapid visual recovery and greatly decreased
morbidity. There is a lower risk of infection and choroidal
hemorrhage, and there is a faster recovery, than with previous
techniques.
[0043] For purposes of summarizing the invention, certain aspects,
advantages and novel features of the invention have been described
herein above. Of course, it is to be understood that not
necessarily all such advantages may be achieved in accordance with
any particular embodiment of the invention. Thus, the invention may
be embodied or carried out in a manner that achieves or optimizes
one advantage or group of advantages as taught or suggested herein
without necessarily achieving other advantages as may be taught or
suggested herein.
[0044] All of these embodiments are intended to be within the scope
of the invention herein disclosed. These and other embodiments of
the invention will become readily apparent to those skilled in the
art from the following detailed description of the preferred
embodiments having reference to the attached figures, the invention
not being limited to any particular preferred embodiment(s)
disclosed.
BRIEF DESCRIPTION OF THE DRAWINGS
[0045] Having thus summarized the general nature of the invention
and some of its features and advantages, certain preferred
embodiments and modifications thereof will become apparent to those
skilled in the art from the detailed description herein having
reference to the figures that follow, of which:
[0046] FIG. 1 is a coronal cross-sectional view of an eye;
[0047] FIG. 2 is an enlarged cross-sectional view of an anterior
chamber angle of the eye of FIG. 1;
[0048] FIG. 3 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0049] FIG. 4 is a side elevation view of the stent of FIG. 3;
[0050] FIG. 5 is a top plan view of the stent of FIG. 3;
[0051] FIG. 6 is a bottom plan view of the stent of FIG. 3;
[0052] FIG. 7 is a front end view of the stent of FIG. 3 (along
line 7-7 of FIG. 4);
[0053] FIG. 8 is a rear end view of the stent of FIG. 3 (along line
8-8 of FIG. 4);
[0054] FIG. 9 is an enlarged top plan view of a cutting tip of the
stent of FIG. 3;
[0055] FIG. 10 is a top plan view of one exemplary embodiment of a
snorkel top seating surface;
[0056] FIG. 11 is a top plan view of another exemplary embodiment
of a snorkel top seating surface;
[0057] FIG. 12 is a top plan view of yet another exemplary
embodiment of a snorkel top seating surface;
[0058] FIG. 13 is a top plan view of still another exemplary
embodiment of a snorkel top seating surface;
[0059] FIG. 14 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with another embodiment of the invention;
[0060] FIG. 15 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with a further embodiment of the invention;
[0061] FIG. 16 is a side elevation view of a glaucoma stent having
features and advantages in accordance with one embodiment of the
invention;
[0062] FIG. 17 is a top plan view of the stent of FIG. 16;
[0063] FIG. 18 is a bottom plan view of the stent of FIG. 16;
[0064] FIG. 19 is a front end view along line 19-19 of FIG. 16;
[0065] FIG. 20 is a rear end view along line 20-20 of FIG. 16;
[0066] FIG. 21 is a side elevation view of a glaucoma stent having
features and advantages in accordance with one embodiment of the
invention;
[0067] FIG. 22 is a top plan view of the stent of FIG. 21;
[0068] FIG. 23 is a bottom plan view of the stent of FIG. 21;
[0069] FIG. 24 is a front end view along line 24-24 of FIG. 21;
[0070] FIG. 25 is a rear end view along line 25-25 of FIG. 21;
[0071] FIG. 26 is a front elevation view of a glaucoma stent having
features and advantages in accordance with one embodiment of the
invention;
[0072] FIG. 27 is a side elevation view along line 27-27 of FIG.
26;
[0073] FIG. 28 is a rear end view along line 28-28 of FIG. 26;
[0074] FIG. 29 is a simplified partial view of an eye illustrating
the temporal implantation of a glaucoma stent using a delivery
apparatus having features and advantages in accordance with one
embodiment of the invention;
[0075] FIG. 30 is an oblique elevational view of an articulating
arm stent delivery/retrieval apparatus having features and
advantages in accordance with one embodiment of the invention;
[0076] FIG. 31 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent using a delivery apparatus
crossing through the eye anterior chamber;
[0077] FIG. 32 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0078] FIG. 33 is a detailed enlarged view of the barbed pin of
FIG. 32;
[0079] FIG. 34 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0080] FIG. 35 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0081] FIG. 36 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0082] FIG. 37 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0083] FIG. 38 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0084] FIG. 39 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0085] FIG. 40 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0086] FIG. 41 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0087] FIG. 42 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with one embodiment of the invention;
[0088] FIG. 43 is a simplified partial view of an eye illustrating
the implantation of a valved tube stent device having features and
advantages in accordance with one embodiment of the invention;
[0089] FIG. 44 is a simplified partial view of an eye illustrating
the implantation of an osmotic membrane device having features and
advantages in accordance with one embodiment of the invention;
[0090] FIG. 45 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent using ab externo procedure
having features and advantages in accordance with one embodiment of
the invention;
[0091] FIG. 46 is a simplified partial view of an eye illustrating
the implantation of a glaucoma stent having features and advantages
in accordance with a modified embodiment of the invention; and
[0092] FIG. 47 is a simplified partial view of an eye illustrating
the implantation of a drug release implant having features and
advantages in accordance with one embodiment of the invention.
[0093] FIG. 48 is an oblique elevational view of a trabecular shunt
applicator with a retractable blade mechanism.
[0094] FIGS. 49A and 49B are schematic cross sections of a
trabecular punch device.
[0095] FIGS. 50A and 50B are elevational views of a control arm and
trabeculotomy device for the trabecular shunt applicator.
[0096] FIGS. 51A through 51C are schematic oblique elevational
views of various trabecular meshwork punching and drilling
devices.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0097] The preferred embodiments of the invention described herein
relate particularly to surgical and therapeutic treatment of
glaucoma through reduction of intraocular pressure. While the
description sets forth various embodiment specific details, it will
be appreciated that the description is illustrative only and should
not be construed in any way as limiting the invention. Furthermore,
various applications of the invention, and modifications thereto,
which may occur to those who are skilled in the art, are also
encompassed by the general concepts described herein.
[0098] FIG. 1 is a cross-sectional view of an eye 10, while FIG. 2
is a close-up view showing the relative anatomical locations of a
trabecular meshwork 21, an anterior chamber 20, and a Schlemm's
canal 22. A sclera 11 is a thick collagenous tissue which covers
the entire eye 10 except a portion which is covered by a cornea
12.
[0099] Referring to FIGS. 1 and 2, the cornea 12 is a thin
transparent tissue that focuses and transmits light into the eye
and through a pupil 14, which is a circular hole in the center of
an iris 13 (colored portion of the eye). The cornea 12 merges into
the sclera 11 at a juncture referred to as a limbus 15. A ciliary
body 16 extends along the interior of the sclera 11 and is
coextensive with a choroid 17. The choroid 17 is a vascular layer
of the eye 10, located between the sclera 11 and a retina 18. An
optic nerve 19 transmits visual information to the brain and is the
anatomic structure that is progressively destroyed by glaucoma.
[0100] Still referring to FIGS. 1 and 2, the anterior chamber 20 of
the eye 10, which is bound anteriorly by the cornea 12 and
posteriorly by the iris 13 and a lens 26, is filled with aqueous
humor (hereinafter referred to as "aqueous"). Aqueous is produced
primarily by the ciliary body 16, then moves anteriorly through the
pupil 14 and reaches an anterior chamber angle 25, formed between
the iris 13 and the cornea 12.
[0101] As best illustrated by the drawing of FIG. 2, in a normal
eye, aqueous is removed from the anterior chamber 20 through the
trabecular meshwork 21. Aqueous passes through the trabecular
meshwork 21 into Schlemm's canal 22 and thereafter through a
plurality of aqueous veins 23, which merge with blood-carrying
veins, and into systemic venous circulation. Intraocular pressure
is maintained by an intricate balance between secretion and outflow
of aqueous in the manner described above. Glaucoma is, in most
cases, characterized by an excessive buildup of aqueous in the
anterior chamber 20 which leads to an increase in intraocular
pressure. Fluids are relatively incompressible, and thus
intraocular pressure is distributed relatively uniformly throughout
the eye 10.
[0102] As shown in FIG. 2, the trabecular meshwork 21 is adjacent a
small portion of the sclera 11. Exterior to the sclera 11 is a
conjunctiva 24. Traditional procedures that create a hole or
opening for implanting a device through the tissues of the
conjunctiva 24 and sclera 11 involve extensive surgery, as compared
to surgery for implanting a device, as described herein, which
ultimately resides entirely within the confines of the sclera 11
and cornea 12.
Self-Trephining Glaucoma Stent
[0103] FIG. 3 generally illustrates the use of one embodiment of a
trabecular stenting device 30 for establishing an outflow pathway,
passing through the trabecular meshwork 21, which is discussed in
greater detail below. FIGS. 4-9 are different views of the stent
30. Advantageously, and as discussed in further detail later
herein, the self-trephining-stent allows a one-step procedure to
make an incision in the trabecular mesh 21 and place the stent or
implant 30 at the desired or predetermined position within the eye
10. Desirably, this facilitates the overall surgical procedure.
[0104] In the illustrated embodiment of FIGS. 3-9, the shunt or
stent 30 generally comprises a snorkel 32 and a main body portion
or blade 34. The snorkel 32 and blade 34 are mechanically connected
to or in mechanical communication with one another. The stent 30
and/or the body portion 34 have a generally longitudinal axis
36.
[0105] In the illustrated embodiment of FIGS. 3-9, the stent 30
comprises an integral unit. In modified embodiments, the stent 30
may comprise an assembly of individual pieces or components. For
example, the stent 30 may comprise an assembly of the snorkel 32
and blade 34.
[0106] In the illustrated embodiment of FIGS. 3-9, the snorkel 32
is in the form of a generally elongate tubular member and generally
comprises an upper seat, head or cap portion 38, a shank portion 40
and a lumen or passage 42 extending therethrough. The seat 38 is
mechanically connected to or in mechanical communication with the
shank 40 which is also mechanically connected to or in mechanical
communication with the blade 34. The snorkel 32 and/or the lumen 42
have a generally longitudinal axis 43.
[0107] In the illustrated embodiment of FIGS. 3-9, the seat 38 is
generally circular in shape and has an upper surface 44 and a lower
surface 46 which, as shown in FIG. 3, abuts or rests against the
trabecular meshwork 21 to stabilize the glaucoma stent 30 within
the eye 10. In modified embodiments, the seat 38 may efficaciously
be shaped in other suitable manners, as required or desired, giving
due consideration to the goals of stabilizing the glaucoma stent 30
within the eye 10 and/or of achieving one or more of the benefits
and advantages as taught or suggested herein. For example, the seat
38 may be shaped in other polygonal or non-polygonal shapes and/or
comprise one or more ridges which extend radially outwards, among
other suitable retention devices.
[0108] In the illustrated embodiment of FIGS. 3-9, and as best seen
in the top view of FIG. 5, the seat top surface 44 comprises
fiducial marks or indicia 48. These marks or indicia 48 facilitate
and ensure proper orientation and alignment of the stent 30 when
implanted in the eye 10. The marks or indicia 48 may comprise
visual differentiation means such as color contrast or be in the
form of ribs, grooves, or the like. Alternatively, or in addition,
the marks 48 may provide tactile sensory feedback to the surgeon.
Also, the seat 38 and/or the seat top surface 44 may be configured
in predetermined shapes aligned with the blade 34 and/or
longitudinal axis 36 to provide for proper orientation of the stent
device 30 within the eye 10. For example, the seat top surface 44
may be oval or ellipsoidal (FIG. 10), rectangular (FIG. 11),
hexagonal (FIG. 12), among other suitable shapes (e.g. FIG.
13).
[0109] In the illustrated embodiment of FIGS. 3-9, and as indicated
above, the seat bottom surface 46 abuts or rests against the
trabecular meshwork 21 to stabilize and retain the glaucoma stent
30 within the eye 10. For stabilization purposes, the seat bottom
surface 46 may comprise a studded surface, a ribbed surface, a
surface with pillars, a textured surface, or the like.
[0110] In the illustrated embodiment of FIGS. 3-9, the snorkel
shank 40 is generally cylindrical in shape. With the stent 30
implanted, as shown in FIG. 3, the shank 40 is generally positioned
in an incision or cavity 50 formed in the trabecular meshwork 21 by
the self-trephining stent 30. Advantageously, and as discussed
further below, this single step of forming the cavity 50 by the
stent 30 itself and placing the stent 30 in the desired position
facilitates and expedites the overall surgical procedure. In
modified embodiments, the snorkel shank 40 may efficaciously be
shaped in other suitable manners, as required or desired. For
example, the shank 40 may be in the shape of other polygonal or
non-polygonal shapes, such as, oval, elliposoidal, and the
like.
[0111] In the illustrated embodiment of FIGS. 3-9, and as best seen
in FIG. 3, the shank 40 has an outer surface 52 in contact with the
trabecular meshwork 21 surrounding the cavity 50. For stabilization
purposes, the shank outer surface 52 may comprise a studded
surface, a ribbed surface, a surface with pillars, a textured
surface, or the like.
[0112] In the illustrated embodiment of FIGS. 3-9, the snorkel
lumen 42 has an inlet port, opening or orifice 54 at the seat top
surface 44 and an outlet port, opening or orifice 56 at the
junction of the shank 40 and blade 34. The lumen 42 is generally
cylindrical in shape, that is, it has a generally circular
cross-section, and its ports 54, 56 are generally circular in
shape. In modified embodiments, the lumen 42 and ports 54, 56 may
be efficaciously shaped in other manners, as required or desired,
giving due consideration to the goals of providing sufficient
aqueous outflow and/or of achieving one or more of the benefits and
advantages as taught or suggested herein. For example, the lumen 42
and/or one or both ports 54, 56 may be shaped in the form of ovals,
ellipsoids, and the like, or the lumen 42 may have a tapered or
stepped configuration.
[0113] Referring in particular to FIG. 3, aqueous from the anterior
chamber 20 flows into the lumen 42 through the inlet port 54 (as
generally indicated by arrow 58) and out of the outlet port 56 and
into Schlemm's canal 22 (as generally indicated by arrows 60) to
lower and/or balance the intraocular pressure (IOP). In another
embodiment, as discussed in further detail below, one or more of
the outlet ports may be configured to face in the general direction
of the stent longitudinal axis 36. In modified embodiments, the
snorkel 32 may comprise more than one lumen, as needed or desired,
to facilitate multiple aqueous outflow transportation into
Schlemm's canal 22.
[0114] In the illustrated embodiment of FIGS. 3-9, the blade
longitudinal axis 36 and the snorkel longitudinal axis 43 are
generally perpendicular to one another. Stated differently, the
projections of the axes 36, 43 on a common plane which is not
perpendicular to either of the axes 36, 43 intersect at 90.degree..
The blade longitudinal axis 36 and the snorkel longitudinal axis 43
may intersect one another or may be offset from one another.
[0115] In the illustrated embodiment of FIGS. 3-9, the main body
portion or blade 34 is a generally curved elongated sheet- or
plate-like structure with an upper curved surface 62 and a lower
curved surface 64 which defines a trough or open face channel 66.
The perimeter of the blade 34 is generally defined by a curved
proximal edge 68 proximate to the snorkel 32, a curved distal edge
70 spaced from the proximal edge 68 by a pair of generally straight
lateral edges 72, 74 with the first lateral edge 72 extending
beyond the second lateral edge 74 and intersecting with the distal
edge 70 at a distal-most point 76 of the blade 34 proximate a blade
cutting tip 78.
[0116] In the illustrated embodiment of FIGS. 3-9, and as shown in
the enlarged view of FIG. 9, the cutting tip 78 comprises a first
cutting edge 80 on the distal edge 70 and a second cutting edge 82
on the lateral edge 72. The cutting edges 80, 82 preferably extend
from the distal-most point 76 of the blade 34 and comprise at least
a respective portion of the distal edge 70 and lateral edge 72. The
respective cutting edges 80, 82 are formed at the sharp edges of
respective beveled or tapered surfaces 84, 86. In one embodiment,
the remainder of the distal edge 70 and lateral edge 72 are dull or
rounded. In one embodiment, the tip 78 proximate to the distal-most
end 76 is curved slightly inwards, as indicated generally by the
arrow 88 in FIG. 5 and arrow 88 (pointed perpendicular and into the
plane of the paper) in FIG. 9, relative to the adjacent curvature
of the blade 34.
[0117] In modified embodiments, suitable cutting edges may be
provided on selected portions of one or more selected blade edges
68, 70, 72, 74 with efficacy, as needed or desired, giving due
consideration to the goals of providing suitable cutting means on
the stent 30 for effectively cutting through the trabecular
meshwork 21 (FIG. 3) and/or of achieving one or more of the
benefits and advantages as taught or suggested herein.
[0118] Referring in particular to FIG. 9, in one embodiment, the
ratio between the lengths of the cutting edges 80, 82 is about 2:1.
In another embodiment, the ratio between the lengths of the cutting
edges 80, 82 is about 1:1. In yet another embodiment, the ratio
between the lengths of the cutting edges 80, 82 is about 1:2. In
modified embodiments, the lengths of the cutting edges 80, 82 may
be efficaciously selected in other manners, as required or desired,
giving due consideration to the goals of providing suitable cutting
means on the stent 30 for effectively cutting through the
trabecular meshwork 21 (FIG. 3) and/or of achieving one or more of
the benefits and advantages as taught or suggested herein.
[0119] Still referring in particular to FIG. 9, in one embodiment,
the ratio between the lengths of the cutting edges 80, 82 is in the
range from about 2:1 to about 1:2. In another embodiment, the ratio
between the lengths of the cutting edges 80, 82 is in the range
from about 5:1 to about 1:5. In yet another embodiment, the ratio
between the lengths of the cutting edges 80, 82 is in the range
from about 10:1 to about 1:10. In modified embodiments, the lengths
of the cutting edges 80, 82 may be efficaciously selected in other
manners, as required or desired, giving due consideration to the
goals of providing suitable cutting means on the stent 30 for
effectively cutting through the trabecular meshwork 21 (FIG. 3)
and/or of achieving one or more of the benefits and advantages as
taught or suggested herein.
[0120] As shown in the top view of FIG. 9, the cutting edge 80
(and/or the distal end 70) and the cutting edge 82 (and/or the
lateral edge 72) intersect at an angle .theta.. Stated differently,
.theta. is the angle between the projections of the cutting edge 80
(and/or the distal end 70) and the cutting edge 82 (and/or the
lateral edge 72) on a common plane which is not perpendicular to
either of these edges.
[0121] Referring to in particular to FIG. 9, in one embodiment, the
angle .theta. is about 50.degree.. In another embodiment, the angle
.theta. is in the range from about 40.degree. to about 60.degree..
In yet another embodiment, the angle .theta. is in the range from
about 30.degree. to about 70.degree.. In modified embodiments, the
angle .theta. may be efficaciously selected in other manners, as
required or desired, giving due consideration to the goals of
providing suitable cutting means on the stent 30 for effectively
cutting through the trabecular meshwork 21 (FIG. 3) and/or of
achieving one or more of the benefits and advantages as taught or
suggested herein.
[0122] The stent 30 of the embodiments disclosed herein can be
dimensioned in a wide variety of manners. Referring in particular
to FIG. 3, the depth of Schlemm's canal 22 is typically about less
than 400 microns (.mu.m). Accordingly, the stent blade 34 is
dimensioned so that the height of the blade 34 (referred to as
H.sub.41 in FIG. 4) is typically less than about 400 .mu.m. The
snorkel shank 40 is dimensioned so that it has a length (referred
to as L.sub.41 in FIG. 4) typically in the range from about 100
.mu.m to about 300 .mu.m which is roughly the typical range of the
thickness of the trabecular meshwork 21.
[0123] Of course, as the skilled artisan will appreciate, that with
the stent 30 implanted, the blade 34 may rest at any suitable
position within Schlemm's canal 22. For example, the blade 34 may
be adjacent to a front wall 90 of Schlemm's canal 22 (as shown in
FIG. 3), or adjacent to a back wall 92 of Schlemm's canal 22, or at
some intermediate location therebetween, as needed or desired.
Also, the snorkel shank 40 may extend into Schlemm's canal 22. The
length of the snorkel shank 40 and/or the dimensions of the blade
34 may be efficaciously adjusted to achieve the desired implant
positioning.
[0124] The trabecular stenting device 30 (FIGS. 3-9) of the
exemplary embodiment may be manufactured or fabricated by a wide
variety of techniques. These include, without limitation, by
molding, thermo-forming, or other micro-machining techniques, among
other suitable techniques.
[0125] The trabecular stenting device 30 preferably comprises a
biocompatible material such that inflammation arising due to
irritation between the outer surface of the device 30 and the
surrounding tissue is minimized. Biocompatible materials which may
be used for the device 30 preferably include, but are not limited
to, titanium, titanium alloys, medical grade silicone, e.g.,
Silastic.TM., available from Dow Corning Corporation of Midland,
Mich.; and polyurethane, e.g., Pellethane.TM., also available from
Dow Corning Corporation.
[0126] In other embodiments, the stent device 30 may comprise other
types of biocompatible material, such as, by way of example,
polyvinyl alcohol, polyvinyl pyrolidone, collagen, heparinized
collagen, polytetrafluoroethylene, expanded
polytetrafluoroethylene, fluorinated polymer, fluorinated
elastomer, flexible fused silica, polyolefin, polyester,
polysilicon, and/or a mixture of the aforementioned biocompatible
materials, and the like. In still other embodiments, composite
biocompatible material may be used, wherein a surface material may
be used in addition to one or more of the aforementioned materials.
For example, such a surface material may include
polytetrafluoroethylene (PTFE) (such as Teflon.TM.), polyimide,
hydrogel, heparin, therapeutic drugs (such as beta-adrenergic
antagonists and other anti-glaucoma drugs, or antibiotics), and the
like.
[0127] In an exemplary embodiment of the trabecular meshwork
surgery, the patient is placed in the supine position, prepped,
draped and anesthetized as necessary. In one embodiment, a small
(less than about 1 mm) incision, which may be self-sealing is made
through the cornea 12. The corneal incision can be made in a number
of ways, for example, by using a micro-knife, among other
tools.
[0128] An applicator or delivery apparatus is used to advance the
glaucoma stent 30 through the corneal incision and to the
trabecular meshwork 21. Some embodiments of such a delivery
apparatus are disclosed in copending U.S. application Ser. No.
10/101,548, filed Mar. 18, 2002, entitled APPLICATOR AND METHODS
FOR PLACING A TRABECULAR SHUNT FOR GLAUCOMA TREATMENT, and U.S.
Provisional Application No. 60/276,609, filed Mar. 16, 2001,
entitled APPLICATOR AND METHODS FOR PLACING A TRABECULAR SHUNT FOR
GLAUCOMA TREATMENT, the entire contents of each one of which are
hereby incorporated by reference herein. Some embodiments of a
delivery apparatus are also discussed in further detail later
herein. Gonioscopic, microscopic, or endoscopic guidance may be
used during the trabecular meshwork surgery.
[0129] With the device 30 held by the delivery apparatus, the blade
34 of the self-trephining glaucoma stent device 30 is used to cut
and/or displace the material of the trabecular meshwork 21. The
snorkel shank 40 may also facilitate in removal of this material
during implantation. The delivery apparatus is withdrawn once the
device 30 has been implanted in the eye 10. As shown in FIG. 3,
once proper implantation has been accomplished the snorkel seat 38
rests on a top surface 94 of the trabecular meshwork 21, the
snorkel shank 40 extends through the cavity 50 (created by the
device 30) in the trabecular meshwork 21, and the blade extends
inside Schlemm's canal 22.
[0130] Advantageously, the embodiments of the self-trephining stent
device of the invention allow for a "one-step" procedure to make an
incision in the trabecular meshwork and to subsequently implant the
stent in the proper orientation and alignment within the eye to
allow outflow of aqueous from the anterior chamber through the
stent and into Schlemm's canal to lower and/or balance the
intraocular pressure (IOP). Desirably, this provides for a faster,
safer, and less expensive surgical procedure.
[0131] Many complications can arise in trabecular meshwork
surgeries, wherein a knife is first used to create an incision in
the trabecular meshwork, followed by removal of the knife and
subsequent installation of the stent. For instance, the knife may
cause some bleeding which clouds up the surgical site. This may
require more effort and time to clean the surgical site prior to
placement of the stent. Moreover, this may cause the intraocular
pressure (IOP) to rise. Thus, undesirably, such a multiple step
procedure may demand crisis management which slows down the
surgery, makes it less safe, and more expensive.
[0132] FIG. 14 is a simplified partial view of an eye 10
illustrating the implantation of a self-trephining glaucoma stent
device 30a having features and advantages in accordance with one
embodiment. The stent 30a is generally similar to the stent 30 of
FIGS. 3-9 except that its snorkel 32a comprises a longer shank 40a
which extends into Schlemm's canal 22 and a lumen 42a which
bifurcates into two output channels 45a.
[0133] In the illustrated embodiment of FIG. 14, the shank 40a
terminates at the blade 34. Aqueous flows from the anterior chamber
20 into the lumen 42a through an inlet port 54a (as generally
indicated by arrow 58a). Aqueous then flows through the output
channels 45a and out of respective outlet ports 56a and into
Schlemm's canal 22 (as generally indicated by arrows 60a). The
outlet channels 45a extend radially outwards in generally opposed
directions and the outlet ports 56a are configured to face in the
general direction of the stent longitudinal axis 36 so that they
open into Schlemm's canal 22 and are in proper orientation to allow
aqueous outflow into Schlemm's canal 22 for lowering and/or
balancing the intraocular pressure (TOP). As indicated above,
fiducial marks or indicia and/or predetermined shapes of the
snorkel seat 38 allow for proper orientation of the blade 34 and
also the output channels 45a and respective ports 56a within
Schlemm's canal.
[0134] In the illustrated embodiment of FIG. 14, two outflow
channels 45a are provided. In another embodiment, only one outflow
channel 45a is provided. In yet another embodiment, more than two
outflow channels 45a are provided. In modified embodiments, the
lumen 42a may extend all the way through to the blade 34 and
provide an outlet port as discussed above with reference to the
embodiment of FIGS. 3-9.
[0135] FIG. 15 is a simplified partial view of an eye 10
illustrating the implantation of a self-trephining glaucoma stent
device 30b having features and advantages in accordance with one
embodiment. The stent 30b is generally similar to the stent 30 of
FIGS. 3-9 except that its snorkel 32b comprises a longer shank 40b
which extends into Schlemm's canal 22 and a lumen 42b which
bifurcates into two output channels 45b.
[0136] In the illustrated embodiment of FIG. 15, the shank 40b
extends through the blade 34. Aqueous flows from the anterior
chamber 20 into the lumen 42b through an inlet port 54b (as
generally indicated by arrow 58b). Aqueous then flows through the
output channels 45b and out of respective outlet ports 56b and into
Schlemm's canal 22 (as generally indicated by arrows 60b). The
outlet channels 45b extend radially outwards in generally opposed
directions and the outlet ports 56b are configured to face in the
general direction of the stent longitudinal axis 36 so that they
open into Schlemm's canal 22 and are in proper orientation to allow
aqueous outflow into Schlemm's canal 22 for lowering and/or
balancing the intraocular pressure (IOP). As indicated above,
fiducial marks or indicia and/or predetermined shapes of the
snorkel seat 38 allow for proper orientation of the blade 34 and
also the output channels 45b and respective ports 56b within
Schlemm's canal.
[0137] In the illustrated embodiment of FIG. 15, two outflow
channels 45b are provided. In another embodiment, only one outflow
channel 45b is provided. In yet another embodiment, more than two
outflow channels 45b are provided. In modified embodiments, the
lumen 42b may extend all the way through to the blade 34 and
provide an outlet port as discussed above with reference to the
embodiment of FIGS. 3-9.
[0138] FIGS. 16-20 show different views of a self-trephining
glaucoma stent device 30c having features and advantages in
accordance with one embodiment. The stent 30c is generally similar
to the stent 30 of FIGS. 3-9 except that it has a modified blade
configuration. The stent 30c comprises a blade 34c which is a
generally curved elongated sheet- or plate-like structure with an
upper curved surface 62c and a lower curved surface 64c which
defines a trough or open face channel 66c. The perimeter of the
blade 34c is generally defined by a curved proximal edge 68c
proximate to the snorkel 32, a curved distal edge 70c spaced from
the proximal edge 68c by a pair of generally straight lateral edges
72c, 74c which are generally parallel to one another and have about
the same length.
[0139] In the illustrated embodiment of FIGS. 16-20, the blade 34c
comprises a cutting tip 78c. The cutting tip 78c preferably
includes cutting edges formed on selected portions of the distal
edge 70c and adjacent portions of the lateral edges 72c, 74c for
cutting through the trabecular meshwork for placement of the
snorkel 32. The cutting edges are sharp edges of beveled or tapered
surfaces as discussed above in reference to FIG. 9. The embodiment
of FIGS. 16-20 may be efficaciously modified to incorporate the
snorkel configuration of the embodiments of FIGS. 14 and 15.
[0140] FIGS. 21-25 show different views of a self-trephining
glaucoma stent device 30d having features and advantages in
accordance with one embodiment. The stent 30d is generally similar
to the stent 30 of FIGS. 3-9 except that it has a modified blade
configuration. The stent 30d comprises a blade 34d which is a
generally curved elongated sheet- or plate-like structure with an
upper curved surface 62d and a lower curved surface 64d which
defines a trough or open face channel 66d. The perimeter of the
blade 34d is generally defined by a curved proximal edge 68d
proximate to the snorkel 32, a pair of inwardly converging curved
distal edges 70d', 70d'' spaced from the proximal edge 68d by a
pair of generally straight respective lateral edges 72d, 74d which
are generally parallel to one another and have about the same
length. The distal edges 70d', 70d'' intersect at a distal-most
point 76d of the blade 34d proximate a blade cutting tip 78d.
[0141] In the illustrated embodiment of FIGS. 21-25, the cutting
tip 78d preferably includes cutting edges formed on the distal
edges 70d', 70d'' and extending from the distal-most point 76d of
the blade 34d. In one embodiment, the cutting edges extend along
only a portion of respective distal edges 70d', 70d''. In another
embodiment, the cutting edges extend along substantially the entire
length of respective distal edges 70d', 70d''. In yet another
embodiment, at least portions of the lateral edges 72d, 74d
proximate to respective distal edges 70d', 70d'' have cutting
edges. In a further embodiment, the tip 78d proximate to the
distal-most end 76d is curved slightly inwards, as indicated
generally by the arrow 88d in FIG. 21 and arrow 88d (pointed
perpendicular and into the plane of the paper) in FIG. 22, relative
to the adjacent curvature of the blade 34d.
[0142] In the embodiment of FIGS. 21-25, the cutting edges are
sharp edges of beveled or tapered surfaces as discussed above in
reference to FIG. 9. The embodiment of FIGS. 21-25 may be
efficaciously modified to incorporate the snorkel configuration of
the embodiments of FIGS. 14 and 15.
[0143] FIGS. 26-28 show different views of a self-trephining
glaucoma stent device 30e having features and advantages in
accordance with one embodiment. The stent device 30e generally
comprises a snorkel 32e mechanically connected to or in mechanical
communication with a blade or cutting tip 34e. The snorkel 32e has
a seat, head or cap portion 38e mechanically connected to or in
mechanical communication with a shank 40e, as discussed above. The
shank 40e has a distal end or base 47e. The snorkel 32e further has
a lumen 42e which bifurcates into a pair of outlet channels 45e, as
discussed above in connection with FIGS. 14 and 15. Other lumen and
inlet and outlet port configurations as taught or suggested herein
may also be efficaciously used, as needed or desired.
[0144] In the illustrated embodiment of FIGS. 26-28, the blade 34e
extends downwardly and outwardly from the shank distal end 47e. The
blade 34e is angled relative to a generally longitudinal axis 43e
of the snorkel 32e, as best seen in FIGS. 27 and 28. The blade 34e
has a distal-most point 76e. The blade or cutting tip 34e has a
pair of side edges 70e', 70e'', including cutting edges,
terminating at the distal-most point 76e, as best seen in FIG. 26.
In one embodiment, the cutting edges are sharp edges of beveled or
tapered surfaces as discussed above in reference to FIG. 9.
[0145] Referring to FIGS. 26-28, in one embodiment, the blade 34e
includes cutting edges formed on the edges 70e', 70e'' and
extending from the distal-most point 76e of the blade 34d. In one
embodiment, the cutting edges extend along only a portion of
respective distal edges 70e', 70e''. In another embodiment, the
cutting edges extend along substantially the entire length of
respective distal edges 70e', 70e''. In yet another embodiment, the
blade or cutting tip 34e comprises a bent tip of needle, for
example, a 30 gauge needle.
[0146] In general, any of the blade configurations disclosed herein
may be used in conjunction with any of the snorkel configurations
disclosed herein or incorporated by reference herein to provide a
self-trephining glaucoma stent device for making an incision in the
trabecular meshwork for receiving the corresponding snorkel to
provide a pathway for aqueous outflow from the eye anterior chamber
to Schlemm's canal, thereby effectively lowering and/or balancing
the intraocular pressure (IOP). The self-trephining ability of the
device, advantageously, allows for a "one-step" procedure in which
the incision and placement of the snorkel are accomplished by a
single device and operation. In any of the embodiments, fiducial
markings or indicia, and/or preselected configuration of the
snorkel seat, and/or positioning of the stent device in a preloaded
applicator may be used for proper orientation and alignment of the
device during implantation.
Delivery Apparatus
[0147] In many cases, a surgeon works from a temporal incision when
performing cataract or goniometry surgery. FIG. 29 illustrates a
temporal implant procedure, wherein a delivery apparatus or
"applicator" 100 having a curved tip 102 is used to deliver a stent
30 to a temporal side 27 of the eye 10. An incision 28 is made in
the cornea 10, as discussed above. The apparatus 100 is then used
to introduce the stent 30 through the incision 28 and implant it
within the eye 10.
[0148] Still referring in particular to FIG. 29, in one embodiment,
a similarly curved instrument would be used to make the incision
through the trabecular meshwork 21. In other embodiments, a
self-trephining stent device 30 may be used to make this incision
through the trabecular meshwork 21, as discussed above. The
temporal implantation procedure illustrated in FIG. 29 may be
employed with the any of the various stent embodiments taught or
suggested herein.
[0149] FIG. 30 illustrates one embodiment of an apparatus
comprising an articulating stent applicator or retrieval device
100a. In this embodiment, a proximal arm 106 is attached to a
distal arm 108 at a joint 112. This joint 112 is movable such that
an angle formed between the proximal arm 106 and the distal arm 108
can change. One or more claws 114 can extend from the distal arm
108, in the case of a stent retrieval device. Similarly, this
articulation mechanism may be used for the trabecular stent
applicator, and thus the articulating applicator or retrieval
device 100a may be either an applicator for the trabecular stent, a
retrieval device, or both, in various embodiments. The embodiment
of FIG. 30 may be employed with the any of the various stent
embodiments taught or suggested herein.
[0150] FIG. 31 shows another illustrative method for placing any of
the various stent embodiments taught or suggested herein at the
implant site within the eye 10. A delivery apparatus 100b generally
comprises a syringe portion 116 and a cannula portion 118. The
distal section of the cannula 118 has at least one irrigating hole
120 and a distal space 122 for holding the stent device 30. The
proximal end 124 of the lumen of the distal space 122 is sealed
from the remaining lumen of the cannula portion 118. The delivery
apparatus of FIG. 30 may be employed with the any of the various
stent embodiments taught or suggested herein.
[0151] In one aspect of the invention, a delivery apparatus (or
"applicator") is used for placing a trabecular stent through a
trabecular meshwork of an eye. Certain embodiments of such a
delivery apparatus are disclosed in copending U.S. application Ser.
No. 10/101,548, filed Mar. 18, 2002, entitled APPLICATOR AND
METHODS FOR PLACING A TRABECULAR SHUNT FOR GLAUCOMA TREATMENT, and
U.S. Provisional Application No. 60/276,609, filed Mar. 16, 2001,
entitled APPLICATOR AND METHODS FOR PLACING A TRABECULAR SHUNT FOR
GLAUCOMA TREATMENT, the entire contents of each one of which are
hereby incorporated by reference herein.
[0152] FIG. 48 illustrates one embodiment of the trabecular shunt
applicator 502, holding the trabecular shunt 510 in place.
Additionally, a trabecular meshwork blade 528 extends from the
distal end of the applicator 502. In this embodiment, the blade 528
may be extended by spring action from the distal end of the
applicator 502 when the operator pushes a button 530 or similarly
actuates extension of the blade 528. The blade 528 can be retracted
within the applicator 502 by means of a slide button 538, which the
operator can move proximally to retract the blade 528.
Alternatively, a plunger 532 may move the blade 528 forward and
backward within the applicator 502. Also shown is the outer tube
534 of the applicator 502, as well as holes 536 in the applicator
502. These holes 536 may be used for aspiration or irrigation of
the anterior chamber of the eye during the performance of
trabecular meshwork surgery.
[0153] FIG. 49A shows one embodiment of a trabecular meshwork
trephine, or punch 542. An inner tube 506 resides within an outer
tube 504. The inner tube 506 is in communication with an inner
plunger 546. The proximal end 550 of the inner plunger 546 is acted
upon by a hammer 552 that is attached to a spring 548. The spring
548 may be recoiled or loaded, storing potential energy, and the
hammer 552 is then held in place by an actuator 554 or other
similar member in communication with the actuator 554. When the
actuator 554 is acted upon by an operator, the spring 548 releases
its potential energy, causing the hammer 552 to move forward,
contacting the proximal end 550 of the inner plunger 546. This in
turn causes the punch 544 to move forward, contacting the
trabecular meshwork.
[0154] FIG. 49B view is a close-up, cross-sectional view of the
punch 544. Again seen as the outer tube 504, the inner tube 506,
and the punch 544 of the device. This trephine or punch may
comprise a circular blade 556 or other similar configuration known
to those skilled in the art for making a cut or punch hole in the
trabecular meshwork of an eye.
[0155] FIGS. 50A and 50B illustrate embodiments of a control arm
598 which is attached to a mechanism for performing trabeculotomy.
In FIG. 50A, a blade 570 extends from an end of the control arm
598. In some embodiments, the long axis of the control arm 598 runs
parallel or semiparallel to the long axis of the applicator 502.
The blade 570 may be used to make a trabeculotomy in preparation
for placing the trabecular shunt 510 through the trabecular
meshwork and into Schlemm's canal.
[0156] FIG. 50B shows a "hot tip" 571 at the end of the control arm
598. This hot tip 571 may be a cautery, laser, or other energy
transfer device for making a hole in the trabecular meshwork in
preparation for placing the shunt 510 through the trabecular
meshwork and into Schlemm's canal.
[0157] FIGS. 51A through 51C illustrate various embodiments of
devices, such as trephines, that can punch holes in the trabecular
meshwork. In FIG. 51A, a trabecular meshwork punch 560 is
illustrated. This punch 560 can make holes 561 in the trabecular
meshwork 595. These holes 561 can be of various configurations,
depending on the shape of the distal blade of the trabecular
meshwork punch 560.
[0158] In FIG. 51B, a blade 566 extends from the end of a
trabecular meshwork cutter 565. This blade 566 can make various
punch holes 567 in the trabecular meshwork 595, as illustrated.
[0159] FIG. 51C illustrates a trabecular meshwork drill 568. The
drill 568 has a distal drill bit 569, which can make a drill hole
561 in the trabecular meshwork 595.
[0160] The stent has an inlet section and an outlet section. The
delivery apparatus includes a handpiece, an elongate tip, a holder
and an actuator. The handpiece has a distal end and a proximal end.
The elongate tip is connected to the distal end of the handpiece.
The elongate tip has a distal portion and is configured to be
placed through a corneal incision and into an anterior chamber of
the eye. The holder is attached to the distal portion of the
elongate tip. The holder is configured to hold and release the
inlet section of the trabecular stent. The actuator is on the
handpiece and actuates the holder to release the inlet section of
the trabecular stent from the holder. When the trabecular stent is
deployed from the delivery apparatus into the eye, the outlet
section is positioned in substantially opposite directions inside
Schlemm's canal. In one embodiment, a deployment mechanism within
the delivery apparatus includes a push-pull type plunger.
[0161] In some embodiments, the holder comprises a clamp. In some
embodiments, the apparatus further comprises a spring within the
handpiece that is configured to be loaded when the stent is being
held by the holder, the spring being at least partially unloaded
upon actuating the actuator, allowing for release of the stent from
the holder.
[0162] In various embodiments, the clamp comprises a plurality of
claws configured to exert a clamping force onto the inlet section
of the stent. The holder may also comprise a plurality of
flanges.
[0163] In some embodiments, the distal portion of the elongate tip
is made of a flexible material. This can be a flexible wire. The
distal portion can have a deflection range, preferably of about 45
degrees from the long axis of the handpiece.
[0164] The delivery apparatus can further comprise an irrigation
port in the elongate tip.
[0165] Some aspects include a method of placing a trabecular stent
through a trabecular meshwork of an eye, the stent having an inlet
section and an outlet section, including advancing a delivery
apparatus holding the trabecular stent through an anterior chamber
of the eye and into the trabecular meshwork, placing part of the
stent through the trabecular meshwork and into a Schlemm's canal of
the eye; and releasing the stent from the delivery apparatus.
[0166] In various embodiments, the method includes using a delivery
apparatus that comprises a handpiece having a distal end and a
proximal end; an elongate tip connected to the distal end of the
handpiece, the elongate tip having a distal portion and being
configured to be placed through a corneal incision and into an
anterior chamber of the eye; a holder attached to the distal
portion of the elongate tip, the holder configured to hold and
release the inlet section of the trabecular stent; and an actuator
on the handpiece that actuates the holder to release the inlet
section of the trabecular stent from the holder.
[0167] In one aspect, the trabecular stent is removably attached to
a delivery apparatus (also known as "applicator"). When the
trabecular stent is deployed from the delivery apparatus into the
eye, the outlet section is positioned in substantially opposite
directions inside Schlemm's canal. In one embodiment, a deployment
mechanism within the delivery apparatus includes a push-pull type
plunger. In some embodiments, the delivery applicator may be a
guidewire, an expandable basket, an inflatable balloon, or the
like.
Other Embodiments
Screw/Barb Anchored Stent
[0168] FIGS. 32 and 33 illustrate a glaucoma stent device 30f
having features and advantages in accordance with one embodiment.
This embodiment of the trabecular stent 30f includes a barbed or
threaded screw-like extension or pin 126 with barbs 128 for
anchoring. The barbed pin 126 extends from a distal or base portion
130 of the stent 30f.
[0169] In use, the stent 30f (FIG. 32) is advanced through the
trabecular meshwork 21 and across Schlemm's canal 22. The barbed
(or threaded) extension 126 penetrates into the back wall 92 of
Schlemm's canal 22 up to the shoulder or base 130 that then rests
on the back wall 92 of the canal 22. The combination of a shoulder
130 and a barbed pin 126 of a particular length limits the
penetration depth of the barbed pin 126 to a predetermined or
preselected distance. In one embodiment, the length of the pin 126
is about 0.5 mm or less. Advantageously, this barbed configuration
provides a secure anchoring of the stent 30f. As discussed above,
correct orientation of the stent 30f is ensured by appropriate
fiducial marks, indicia or the like and by positioning of the stent
in a preloaded applicator.
[0170] Referring to FIG. 32, the aqueous flows from the anterior
chamber 20, through the lumen 42f, then out through two side-ports
56f to be directed in both directions along Schlemm's canal 22.
Alternatively, flow could be directed in only one direction through
a single side-port 56f. In other embodiments, more than two outlet
ports 56f, for example, six to eight ports (like a pin wheel
configuration), may be efficaciously used, as needed or
desired.
[0171] Still referring to FIG. 32, in one embodiment, the stent 30f
is inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30f may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Deeply Threaded Stent:
[0172] FIG. 34 illustrates a glaucoma stent device 30g having
features and advantages in accordance with one embodiment. The
stent 30g has a head or seat 38g and a shank or main body portion
40g with a base or distal end 132. This embodiment of the
trabecular stent 30g includes a deep thread 134 (with threads 136)
on the main body 40g of the stent 30g below the head 38g. The
threads may or may not extend all the way to the base 132.
[0173] In use, the stent 30g (FIG. 34) is advanced through the
meshwork 21 through a rotating motion, as with a conventional
screw. Advantageously, the deep threads 136 provide retention and
stabilization of the stent 30g in the trabecular meshwork 21.
[0174] Referring to FIG. 34, the aqueous flows from the anterior
chamber 20, through the lumen 42g, then out through two side-ports
56g to be directed in both directions along Schlemm's canal 22.
Alternatively, flow could be directed in only one direction through
a single side-port 56g. In other embodiments, more than two outlet
ports 56g may be efficaciously used, as needed or desired.
[0175] One suitable applicator or delivery apparatus for this stent
30g (FIG. 34) includes a preset rotation, for example, via a wound
torsion spring or the like. The rotation is initiated by a release
trigger on the applicator. A final twist of the applicator by the
surgeon and observation of suitable fiducial marks, indicia or the
like ensure proper alignment of the side ports 56g with Schlemm's
canal 22.
[0176] Referring to FIG. 34, in one embodiment, the stent 30g is
inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30g may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Rivet Style Stent:
[0177] FIG. 35 illustrates a glaucoma stent device 30h having
features and advantages in accordance with one embodiment. The
stent has a base or distal end 138. This embodiment of the
trabecular stent 30h has a pair of flexible ribs 140. In the unused
state, the ribs are initially generally straight (that is, extend
in the general direction of arrow 142).
[0178] Referring to FIG. 35, upon insertion of the stent 30h
through the trabecular meshwork 21, the ends 144 of respective ribs
140 of the stent 30h come to rest on the back wall 92 of Schlemm's
canal 22. Further advancement of the stent 30h causes the ribs 140
to deform to the bent shape as shown in the drawing of FIG. 35. The
ribs 140 are designed to first buckle near the base 138 of the
stent 30h. Then the buckling point moves up the ribs 140 as the
shank part 40h of the stent 30h is further advanced through the
trabecular meshwork 21.
[0179] The lumen 42h (FIG. 35) in the stent 30h is a simple
straight hole. The aqueous flows from the anterior chamber 20,
through the lumen 42h, then out around the ribs 140 to the
collector channels further along Schlemm's canal 22 in either
direction.
[0180] Referring to FIG. 35, in one embodiment, the stent 30h is
inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30h may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Grommet Style Stent:
[0181] FIG. 36 illustrates a glaucoma stent device 30i having
features and advantages in accordance with one embodiment. This
embodiment of the trabecular stent 30i includes a head or seat 38i,
a tapered base portion 146 and an intermediate narrower waist
portion or shank 40i.
[0182] In use, the stent 30i (FIG. 36) is advanced through the
trabecular meshwork 21 and the base 146 is pushed into Schlemm's
canal 22. The stent 30i is pushed slightly further, if necessary,
until the meshwork 21 stretched by the tapered base 146 relaxes
back and then contracts to engage the smaller diameter portion
waist 40i of the stent 30i. Advantageously, the combination of the
larger diameter head or seat 38i and base 146 of the stent 30i
constrains undesirable stent movement. As discussed above, correct
orientation of the stent 30i is ensured by appropriate fiducial
marks, indicia or the like and by positioning of the stent in a
preloaded applicator.
[0183] Referring to FIG. 36, the aqueous flows from the anterior
chamber 20, through the lumen 42i, then out through two side-ports
56i to be directed in both directions along Schlemm's canal 22.
Alternatively, flow could be directed in only one direction through
a single side-port 56i. In other embodiments, more than two outlet
ports 56i may be efficaciously used, as needed or desired.
[0184] Still referring to FIG. 36, in one embodiment, the stent 30i
is inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30i may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Biointeractive Stent:
[0185] FIG. 37 illustrates a glaucoma stent device 30j having
features and advantages in accordance with one embodiment. This
embodiment of the trabecular stent 30j utilizes a region of
biointeractive material 148 that provides a site for the trabecular
meshwork 21 to firmly grip the stent 30j by ingrowth of the tissue
into the biointeractive material 148. As shown in FIG. 37,
preferably the biointeractive layer 148 is applied to those
surfaces of the stent 30j which would abut against or come in
contact with the trabecular meshwork 21.
[0186] In one embodiment, the biointeractive layer 148 (FIG. 37)
may be a region of enhanced porosity with a growth promoting
chemical. In one embodiment, a type of bio-glue 150 that dissolves
over time is used to hold the stent secure during the time between
insertion and sufficient ingrowth for stabilization. As discussed
above, correct orientation of the stent 30j is ensured by
appropriate fiducial marks, indicia or the like and by positioning
of the stent in a preloaded applicator.
[0187] Referring to FIG. 37, the aqueous flows from the anterior
chamber 20, through the lumen 42j, then out through two side-ports
56j to be directed in both directions along Schlemm's canal 22.
Alternatively, flow could be directed in only one direction through
a single side-port 56j. In other embodiments, more than two outlet
ports 56j may be efficaciously used, as needed or desired.
[0188] Still referring to FIG. 37, in one embodiment, the stent 30j
is inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30j may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Glued or Welded Stent:
[0189] FIG. 38 illustrates a glaucoma stent device 30k having
features and advantages in accordance with one embodiment. This
embodiment of the trabecular stent 30k is secured in place by using
a permanent (non-dissolving) bio-glue 152 or a "welding" process
(e.g. heat) to form a weld 152. The stent 30k has a head or seat
38k and a lower surface 46k.
[0190] The stent 30k is advanced through the trabecular meshwork 21
until the head or seat 38k comes to rest on the trabecular meshwork
21, that is, the head lower surface 46k abuts against the
trabecular meshwork 21, and the glue or weld 152 is applied or
formed therebetween, as shown in FIG. 38. As discussed above,
correct orientation of the stent 30k is ensured by appropriate
fiducial marks, indicia or the like and by positioning of the stent
in a preloaded applicator.
[0191] Referring to FIG. 38, the aqueous flows from the anterior
chamber 20, through the lumen 42k, then out through two side-ports
56k to be directed in both directions along Schlemm's canal 22.
Alternatively, flow could be directed in only one direction through
a single side-port 56k. In other embodiments, more than two outlet
ports 56k may be efficaciously used, as needed or desired.
[0192] Still referring to FIG. 38, in one embodiment, the stent 30k
is inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30k may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Hydrophilic Latching Stent:
[0193] FIG. 39 illustrates a glaucoma stent device 30m having
features and advantages in accordance with one embodiment. This
embodiment of the trabecular stent 30m is fabricated from a
hydrophilic material that expands with absorption of water.
Desirably, this would enable the device 30m to be inserted through
a smaller incision in the trabecular meshwork 21. The subsequent
expansion (illustrated by the smaller arrows 154) of the stent 30m
would advantageously enable it to latch in place in the trabecular
meshwork 21. As discussed above, correct orientation of the stent
30m is ensured by appropriate fiducial marks, indicia or the like
and by positioning of the stent in a preloaded applicator.
[0194] Referring to FIG. 39, the aqueous flows from the anterior
chamber 20, through the lumen 42m, then out through two side-ports
56m to be directed in both directions along Schlemm's canal 22.
Alternatively, flow could be directed in only one direction through
a single side-port 56m. In other embodiments, more than two outlet
ports 56m may be efficaciously used, as needed or desired.
[0195] Still referring to FIG. 39, in one embodiment, the stent 30m
is inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30m may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Photodynamic Stent:
[0196] FIG. 40 illustrates a glaucoma stent device 30n having
features and advantages in accordance with one embodiment. This
embodiment of the trabecular stent 30n is fabricated from a
photodynamic material that expands on exposure to light.
[0197] It is commonly known that there is a diurnal variation in
the aqueous humor production by the eye--it is higher during the
day than it is at night. The lumen 42n of the stent 30n responds to
light entering the cornea during the day by expanding and allowing
higher flow of aqueous through the lumen 42n and into Schlemm's
canal 22. This expansion is generally indicated by the smaller
arrows 156 (FIG. 40) which show the lumen 42n (and ports) expanding
or opening in response to light stimulus. (The light or radiation
energy E is generally given by E=hv, where h is Planck's constant
and v is the frequency.) At night, in darkness, the lumen diameter
decreases and reduces the flow allowed through the lumen 42n. In
one embodiment, an excitation wavelength that is different from
that commonly encountered is provided on an as-needed basis to
provide higher flow of aqueous to Schlemm's canal 22.
[0198] This photodynamic implementation is shown in FIG. 40 for the
self-latching style of stent 30n, but can be efficaciously used
with any of the other stent embodiments, as needed or desired. As
discussed above, correct orientation of the stent 30n is ensured by
appropriate fiducial marks, indicia or the like and by positioning
of the stent in a preloaded applicator.
[0199] Referring to FIG. 40, the aqueous flows from the anterior
chamber 20, through the lumen 42n, then out through two side-ports
56n to be directed in both directions along Schlemm's canal 22.
Alternatively, flow could be directed in only one direction through
a single side-port 56n. In other embodiments, more than two outlet
ports 56n may be efficaciously used, as needed or desired.
[0200] Still referring to FIG. 40, in one embodiment, the stent 30n
is inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30n may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Collector Channel Alignment Stent:
[0201] FIG. 41 illustrates a glaucoma stent device 30p having
features and advantages in accordance with one embodiment. This
figure depicts an embodiment of a stent 30p that directs aqueous
from the anterior chamber 20 directly into a collector channel 29
which empties into aqueous veins. The stent 30p has a base or
distal end 160.
[0202] In the illustrated embodiment of FIG. 41, a removable
alignment pin 158 is utilized to align the stent lumen 42p with the
collector channel 29. In use, the pin 158 extends through the stent
lumen 42p and protrudes through the base 160 and extends into the
collector channel 29 to center and/or align the stent 30p over the
collector channel 29. The stent 30p is then pressed firmly against
the back wall 92 of Schlemm's canal 22. A permanent bio-glue 162 is
used between the stent base and the back wall 92 of Schlemm's canal
22 to seat and securely hold the stent 30p in place. Once
positioned, the pin 158 is withdrawn from the lumen 42p to allow
the aqueous to flow directly from the anterior chamber 20 into the
collector duct 29. The collector ducts are nominally 20 to 100
micrometers (.mu.m) in diameter and are visualized with a suitable
microscopy method (such as ultrasound biomicroscopy (UBM)) or laser
imaging to provide guidance for placement of the stent 30p.
[0203] Referring to FIG. 41, in one embodiment, the stent 30p is
inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30p may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Barbed Stent (Anterior Chamber to Collector Channel):
[0204] FIG. 42 illustrates a glaucoma stent device 30q having
features and advantages in accordance with one embodiment. This
figure depicts an embodiment of a stent 30q that directs aqueous
from the anterior chamber 20 directly into a collector channel 29
which empties into aqueous veins. The stent 30q has a base or
distal end 166 and the channel 29 has wall(s) 164.
[0205] In the illustrated embodiment of FIG. 42, a barbed,
small-diameter extension or pin 168 on the stent base 166 is guided
into the collector channel 29 and anchors on the wall(s) 164 of the
channel 29. The pin 168 has barbs 170 which advantageously provide
anchoring of the stent 30q. The collector ducts 29 are nominally 20
to 100 micrometers (.mu.m) in diameter and are visualized with a
suitable microscopy method (such as ultrasound biomicroscopy (UBM))
or laser imaging to provide guidance for placement of the
stent.
[0206] Referring to FIG. 42, in one embodiment, the stent 30q is
inserted through a previously made incision in the trabecular
meshwork 21. In other embodiments, the stent 30q may be combined
with any of the blade configurations taught or suggested herein to
provide self-trephining capability. In these cases, the incision
through the trabecular meshwork 21 is made by the self-trephining
stent device which has a blade at its base or proximate to the
base.
Valved Tube Stent (Anterior Chamber to Choroid):
[0207] FIG. 43 illustrates a valved tube stent device 30r having
features and advantages in accordance with one embodiment. This is
an embodiment of a stent 30r that provides a channel for flow
between the anterior chamber 20 and the highly vascular choroid 17.
Clinically, the choroid 17 can be at pressures lower than those
desired for the eye 10. Therefore, this stent 30r includes a valve
with an opening pressure equal to the desired pressure difference
between the choroid 17 and the anterior chamber 10 or a
constriction that provide the desired pressure drop.
Osmotic Membrane (Anterior Chamber to Choroid):
[0208] FIG. 44 illustrates an osmotic membrane device 30s having
features and advantages in accordance with one embodiment. This
embodiment provides a channel for flow between the anterior chamber
20 and the highly vascular choroid 17. The osmotic membrane 30s is
used to replace a portion of the endothelial layer of the choroid
17. Since the choroid 17 is highly vascular with blood vessels, the
concentration of water on the choroid side is lower than in the
anterior chamber 20 of the eye 10. Therefore, the osmotic gradient
drives water from the anterior chamber 20 into the choroid 17.
[0209] Clinically, the choroid 17 (FIG. 44) can be at pressures
lower than those desired for the eye 10. Therefore, desirably, both
osmotic pressure and the physical pressure gradient are in favor of
flow into the choroid 17. Flow control is provided by proper sizing
of the area of the membrane,--the larger the membrane area is the
larger the flow rate will be. This advantageously enables tailoring
to tune the flow to the desired physiological rates.
Ab Externo Insertion of Stent Via Small Puncture:
[0210] FIG. 45 illustrates the implantation of a stent 30t using an
ab externo procedure having features and advantages in accordance
with one embodiment. In the ab externo procedure of FIG. 45, the
stent 30t is inserted into Schlemm's canal 21 with the aid of an
applicator or delivery apparatus 100c that creates a small puncture
into the eye 10 from outside.
[0211] Referring to FIG. 45, the stent 30t is housed in the
applicator 100c, and pushed out of the applicator 100c once the
applicator tip is in position within the trabecular meshwork 21.
Since the tissue surrounding the trabecular meshwork 21 is
optically opaque, an imaging technique, such as ultrasound
biomicroscopy (UBM) or a laser imaging technique, is utilized. The
imaging provides guidance for the insertion of the applicator tip
and the deployment of the stent 30t. This technique can be used
with a large variety of stent embodiments with slight modifications
since the trabecular meshwork 21 is punctured from the scleral side
rather than the anterior chamber side in the ab externo
insertion.
[0212] FIG. 46 a glaucoma stent device 30u having features and
advantages in accordance with a modified embodiment. This
grommet-style stent 30u for ab externo insertion is a modification
of the embodiment of FIG. 36. In the embodiment of FIG. 46, the
upper part or head 38u is tapered while the lower part or base 172
is flat, as opposed to the embodiment of FIG. 36. The stent 30u is
inserted from the outside of the eye 10 through a puncture in the
sclera. Many of the other embodiments of stents taught or suggested
herein can be modified for similar implantation.
[0213] This ultra-microscopic device 30u (FIG. 46) can be used with
(1) a targeting Lasik-type laser, or with (2) contact on eyes or
with (3) combined ultrasound microscope or (4) other device
insertor handpiece.
Targeted Drug Delivery to the Trabecular Meshwork:
[0214] FIG. 47 illustrates a targeted drug delivery implant 30v
having features and advantages in accordance with one embodiment.
This drawing is a depiction of a targeted drug delivery concept.
The slow release implant 30v is implanted within the trabecular
meshwork 21.
[0215] A drug that is designed to target the trabecular meshwork 21
to increase its porosity, or improve the active transport across
the endothelial layer of Schlemm's canal 22 can be stored in this
small implant 30v (FIG. 47). Advantageously, slow release of the
drug promotes the desired physiology at minimal dosage levels since
the drug is released into the very structure that it is designed to
modify.
[0216] While the components and techniques of the invention have
been described with a certain degree of particularity, it is
manifest that many changes may be made in the specific designs,
constructions and methodology herein above described without
departing from the spirit and scope of this disclosure. It should
be understood that the invention is not limited to the embodiments
set forth herein for purposes of exemplification, but is to be
defined only by a fair reading of the appended claims, including
the full range of equivalency to which each element thereof is
entitled.
* * * * *