NZ755995B2 - Intraocular pseudophakic contact lenses and related systems and methods - Google Patents
Intraocular pseudophakic contact lenses and related systems and methods Download PDFInfo
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- NZ755995B2 NZ755995B2 NZ755995A NZ75599515A NZ755995B2 NZ 755995 B2 NZ755995 B2 NZ 755995B2 NZ 755995 A NZ755995 A NZ 755995A NZ 75599515 A NZ75599515 A NZ 75599515A NZ 755995 B2 NZ755995 B2 NZ 755995B2
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- lens
- intraocular
- optical lens
- optical
- pseudophakic contact
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2/1602—Corrective lenses for use in addition to the natural lenses of the eyes or for pseudo-phakic eyes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2/1613—Intraocular lenses having special lens configurations, e.g. multipart lenses; having particular optical properties, e.g. pseudo-accommodative lenses, lenses having aberration corrections, diffractive lenses, lenses for variably absorbing electromagnetic radiation, lenses having variable focus
- A61F2/1648—Multipart lenses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2/1694—Capsular bag spreaders therefor
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2002/1681—Intraocular lenses having supporting structure for lens, e.g. haptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2002/1681—Intraocular lenses having supporting structure for lens, e.g. haptics
- A61F2002/16902—Separable from intraocular lens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2220/0008—Fixation appliances for connecting prostheses to the body
- A61F2220/0016—Fixation appliances for connecting prostheses to the body with sharp anchoring protrusions, e.g. barbs, pins, spikes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F9/00—Methods or devices for treatment of the eyes; Devices for putting-in contact lenses; Devices to correct squinting; Apparatus to guide the blind; Protective devices for the eyes, carried on the body or in the hand
- A61F9/0008—Introducing ophthalmic products into the ocular cavity or retaining products therein
- A61F9/0017—Introducing ophthalmic products into the ocular cavity or retaining products therein implantable in, or in contact with, the eye, e.g. ocular inserts
Abstract
apparatus comprising: an intraocular pseudophakic contact lens 100 comprising: a first optical lens 102 configured to at least partially correct a residual refractive error in an eye, the residual refractive error comprising a refractive error that exists in the eye after implantation of an artificial intraocular lens in the eye; multiple anchors 106a, 106b configured to be inserted through an anterior surface of the artificial intraocular lens into lens material forming a second optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and multiple projections 104a, 104b comprising extensions of the first optical lens such that the first optical lens and the projections comprise a common material, the anchors partially embedded in or configured to pass through the extensions of the first optical lens, the projections substantially or completely coplanar with the first optical lens; wherein the artificial intraocular lens lacks predefined openings that receive the anchors; wherein the anchors are configured to pierce the lens material forming the second optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and wherein the anchors comprise substantially straight pins extending axially along an optical axis of the intraocular pseudophakic contact lens away from the first optical lens. ificial intraocular lens in the eye; multiple anchors 106a, 106b configured to be inserted through an anterior surface of the artificial intraocular lens into lens material forming a second optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and multiple projections 104a, 104b comprising extensions of the first optical lens such that the first optical lens and the projections comprise a common material, the anchors partially embedded in or configured to pass through the extensions of the first optical lens, the projections substantially or completely coplanar with the first optical lens; wherein the artificial intraocular lens lacks predefined openings that receive the anchors; wherein the anchors are configured to pierce the lens material forming the second optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and wherein the anchors comprise substantially straight pins extending axially along an optical axis of the intraocular pseudophakic contact lens away from the first optical lens.
Description
INTRAOCULAR PSEUDOPHAKIC CONTACT LENSES AND RELATED
SYSTEMS AND METHODS
TECHNICAL FIELD
[0001] This application is a divisional of New Zealand patent application no. 729994,
the entire disclosure of which is incorporated herein by reference.
[0002] This disclosure relates generally to implantable optical devices. More
specifically, this disclosure relates to intraocular pseudophakic contact lenses and related
systems and methods.
BACKGROUND
[0003] In a normal human eye, light enters through the cornea and passes through the
pupil, and the natural crystalline lens focuses the light onto the retina of the eye. However,
due to cataracts or other problems, the natural crystalline lens of an eye may need to be
replaced with an artificial intraocular lens (IOL). The term “pseudophakia” is used to
describe an eye in which the natural crystalline lens has been replaced with an intraocular
lens.
[0004] Before an intraocular lens is placed into a patient’s eye, a doctor or other
personnel typically selects an intraocular lens that is designed to provide desired refractive
correction for the patient’s eye. For example, an intraocular lens could have an optical lens
designed to correct myopia (near-sightedness), hyperopia (far-sightedness), astigmatism, or
other refractive errors that occur naturally in the patient’s eye. However, it is often the case
that the intraocular lens selected for a patient’s eye does not fully correct (and may even
cause) some form of refractive error in the patient’s eye. This refractive error is referred to as
“residual” refractive error.
[0005] There are various conventional options for correcting residual refractive error,
all of which have their disadvantages. For example, one intraocular lens in a patient’s eye
could be replaced with a different intraocular lens, but this typically has a high risk of
surgical complications. Ablation surgery (such as LASIK) on the cornea of a patient’s eye
could be done to correct residual refractive error, but this can have a high level of unwanted
side effects, particularly for older patients. An additional intraocular lens (often referred to as
a “piggyback” IOL) could be inserted in front of an existing intraocular lens, but this is
typically an invasive procedure with less predictability associated with the final refractive
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outcome. In addition, intracorneal lenses (ICLs) can be inserted into the cornea of a patient’s
eye, but this is often more invasive and has a high degree of rejection. In general, the above
procedures are typically not predictable and have a higher degree of surgical risk. Also, the
devices used in the above procedures are difficult to remove and “reverse” any residual
refractive error, resulting in a higher risk of leaving the patient with induced visual
aberration.
SUMMARY
[0006] This disclosure relates to intraocular pseudophakic contact lenses and related
systems and methods.
[0007] In a first embodiment, an apparatus includes an intraocular pseudophakic
contact lens, which includes a first optical lens and multiple anchors. The first optical lens is
configured to at least partially correct a residual refractive error in an eye. The anchors are
configured to be inserted through an anterior surface of an intraocular lens into lens material
forming a second optical lens of the intraocular lens in order to secure the intraocular
pseudophakic contact lens to the intraocular lens.
[0008] More specifically, in this embodiment, the invention provides an apparatus
comprising: an intraocular pseudophakic contact lens comprising: a first optical lens
configured to at least partially correct a residual refractive error in an eye, the residual
refractive error comprising a refractive error that exists in the eye after implantation of an
artificial intraocular lens in the eye; multiple anchors configured to be inserted through an
anterior surface of the artificial intraocular lens into lens material forming a second optical
lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact
lens to the artificial intraocular lens; and multiple projections comprising extensions of the
first optical lens such that the first optical lens and the projections comprise a common
material, the anchors partially embedded in or configured to pass through the extensions of
the first optical lens, the projections substantially or completely coplanar with the first optical
lens; wherein the artificial intraocular lens lacks predefined openings that receive the
anchors; wherein the anchors are configured to pierce the lens material forming the second
optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic
contact lens to the artificial intraocular lens; and wherein the anchors comprise substantially
straight pins extending axially along an optical axis of the intraocular pseudophakic contact
lens away from the first optical lens.
[0009] In a second embodiment, a system includes an intraocular pseudophakic
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contact lens and an intraocular lens. The intraocular pseudophakic contact lens includes a first
optical lens configured to at least partially correct a residual refractive error in an eye and
multiple anchors. The intraocular lens includes a second optical lens, where the second
optical lens is formed of lens material. The anchors are configured to be inserted through an
anterior surface of the intraocular lens into the lens material in order to secure the intraocular
pseudophakic contact lens to the intraocular lens.
[0010] More specifically, in this embodiment, the invention provides a system
comprising: an intraocular pseudophakic contact lens comprising: a first optical lens
comprising an anterior optical surface and a posterior optical surface, the first optical lens
configured to at least partially correct a residual refractive error in an eye; and multiple
projections radially extending from the first optical lens; and multiple anchors axially
extending from the projections, the anchors partially embedded in the projections or
configured to pass through the projections; and an artificial intraocular lens comprising a
second optical lens, the second optical lens comprising an anterior optical surface and a
posterior optical surface and formed of lens material, wherein the residual refractive error
comprises a refractive error that exists in the eye after implantation of the artificial intraocular
lens in the eye; wherein the artificial intraocular lens is not specifically designed to be
coupled to or receive the intraocular pseudophakic contact lens; wherein the anchors are
configured to be inserted through the anterior optical surface of the second optical lens into
the lens material in order to secure the intraocular pseudophakic contact lens to the artificial
intraocular lens; wherein the artificial intraocular lens lacks predefined openings that receive
the anchors; wherein the anchors comprise barbed or ribbed pins configured to pierce the lens
material forming the second optical lens of the artificial intraocular lens in order to secure the
intraocular pseudophakic contact lens to the artificial intraocular lens; wherein the first
optical lens has an uneven weight distribution around a central axis of the first optical lens in
order to cause the first optical lens to obtain a specified orientation with respect to the
artificial intraocular lens; and wherein the first optical lens is configured such that, when the
anchors secure the intraocular pseudophakic contact lens to the artificial intraocular lens: an
outer portion of the posterior optical surface of the first optical lens contacts the lens material
of the second optical lens; and a remaining portion of the posterior optical surface of the first
optical lens remains spaced apart from the anterior optical surface of the second optical lens.
[0011] In a further embodiment, the invention provides a system comprising an
intraocular pseudophakic contact lens comprising: a first optical lens configured to at least
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partially correct a residual refractive error in an eye; multiple anchors; and multiple
projections comprising extensions of the first optical lens such that the first optical lens and
the projections comprise a common material, the anchors partially embedded in or configured
to pass through the extensions of the first optical lens, the projections substantially or
completely coplanar with the first optical lens; and an artificial intraocular lens comprising a
second optical lens, the second optical lens formed of lens material; wherein the anchors are
configured to be inserted through an anterior surface of the artificial intraocular lens into the
lens material in order to secure the intraocular pseudophakic contact lens to the artificial
intraocular lens; wherein the artificial intraocular lens lacks predefined openings that receive
the anchors; wherein the anchors are configured to pierce the lens material forming the
second optical lens of the artificial intraocular lens in order to secure the intraocular
pseudophakic contact lens to the artificial intraocular lens; and wherein the anchors comprise
substantially straight pins extending axially along an optical axis of the intraocular
pseudophakic contact lens away from the first optical lens.
[0012] In a further embodiment, an apparatus includes an intraocular pseudophakic
contact lens, which includes a first optical lens configured to at least partially correct a
residual refractive error in an eye. The intraocular pseudophakic contact lens also includes at
least one drug-eluting device located on the first optical lens and configured to deliver at least
one medication. The intraocular pseudophakic contact lens is configured to be associated
with an intraocular lens in the eye, where the residual refractive error is at least partially
caused by the intraocular lens.
[0013] In a further embodiment, the invention provides a method comprising:
coupling an intraocular pseudophakic contact lens to an artificial intraocular lens; wherein the
intraocular pseudophakic contact lens comprises: a first optical lens comprising an anterior
optical surface and a posterior optical surface, the first optical lens configured to at least
partially correct a residual refractive error in an eye; multiple projections radially extending
from the first optical lens; and multiple anchors axially extending from the projections, the
anchors partially embedded in the projections or configured to pass through the projections;
wherein the artificial intraocular lens comprises a second optical lens, the second optical lens
comprising an anterior optical surface and a posterior optical surface and formed of lens
material, wherein the residual refractive error comprises a refractive error that exists in the
eye after implantation of the artificial intraocular lens in the eye, wherein the artificial
intraocular lens is not specifically designed to be coupled to or receive the intraocular
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pseudophakic contact lens; wherein coupling the intraocular pseudophakic contact lens to the
artificial intraocular lens comprises inserting the multiple anchors through the anterior optical
surface of the second optical lens into the lens material forming the second optical lens of the
artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the
artificial intraocular lens; wherein the artificial intraocular lens lacks predefined openings that
receive the anchors; wherein the anchors comprise barbed or ribbed pins configured to pierce
the lens material forming the second optical lens of the artificial intraocular lens in order to
secure the intraocular pseudophakic contact lens to the artificial intraocular lens; wherein the
first optical lens has an uneven weight distribution around a central axis of the first optical
lens in order to cause the first optical lens to obtain a specified orientation with respect to the
artificial intraocular lens; and wherein the first optical lens is configured such that, when the
anchors secure the intraocular pseudophakic contact lens to the artificial intraocular lens: an
outer portion of the posterior optical surface of the first optical lens contacts the lens material
of the second optical lens; and a remaining portion of the posterior optical surface of the first
optical lens remains spaced apart from the anterior optical surface of the second optical lens
[0014] In a further embodiment, the invention provides a method comprising:
coupling an intraocular pseudophakic contact lens to an artificial intraocular lens; wherein the
intraocular pseudophakic contact lens comprises: a first optical lens configured to at least
partially correct a residual refractive error in an eye; multiple anchors; and multiple
projections comprising extensions of the first optical lens such that the first optical lens and
the projections comprise a common material, the anchors partially embedded in or configured
to pass through the extensions of the first optical lens; wherein coupling the intraocular
pseudophakic contact lens to the artificial intraocular lens comprises inserting the multiple
anchors through an anterior surface of the artificial intraocular lens into lens material forming
a second optical lens of the artificial intraocular lens in order to secure the intraocular
pseudophakic contact lens to the artificial intraocular lens; wherein the artificial intraocular
lens lacks predefined openings that receive the anchors; wherein the anchors are configured
to pierce the lens material forming the second optical lens of the artificial intraocular lens in
order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and
wherein the anchors comprise substantially straight pins extending axially along an optical
axis of the intraocular pseudophakic contact lens away from the first optical lens.
[0015] Other technical features may be readily apparent to one skilled in the art from
the following figures, descriptions, and claims.
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BRIEF DESCRIPTION OF THE DRAWINGS
[0016] For a more complete understanding of this disclosure and its features,
reference is now made to the following description, taken in conjunction with the
accompanying drawings, in which:
[0017] FIGURES 1 through 3 illustrate a first example intraocular pseudophakic
contact lens (IOPCL) according to this disclosure;
[0018] FIGURES 4 through 7 illustrate a second example intraocular pseudophakic
contact lens according to this disclosure;
[0019] FIGURE 8 illustrates a third example intraocular pseudophakic contact lens
according to this disclosure;
[0020] FIGURE 9 illustrates a fourth example intraocular pseudophakic contact lens
according to this disclosure;
[0021] FIGURES 10 through 12 illustrate an example intraocular lens (IOL) attached
to an example intraocular pseudophakic contact lens according to this disclosure;
[0022] FIGURES 13 and 14 illustrate an example intraocular lens and an example
intraocular pseudophakic contact lens in a patient’s eye according to this disclosure;
[0023] FIGURE 15 illustrates an example anchor for attaching an intraocular
pseudophakic contact lens to an intraocular lens according to this disclosure;
[0024] FIGURES 16 through 24 illustrate example additional features that could be
used with an intraocular pseudophakic contact lens according to this disclosure; and
[0025] FIGURE 25 illustrates an example method for using an intraocular
pseudophakic contact lens with an intraocular lens according to this disclosure.
DETAILED DESCRIPTION
[0026] FIGURES 1 through 25, discussed below, and the various embodiments used
to describe the principles of the present invention in this patent document are by way of
illustration only and should not be construed in any way to limit the scope of the invention.
Those skilled in the art will understand that the principles of the invention may be
implemented in any type of suitably arranged device or system.
[0027] This disclosure provides various intraocular pseudophakic contact lenses
(IOPCLs) that can be used in conjunction with intraocular lenses (IOLs). An intraocular
pseudophakic contact lens generally represents a contact lens-type device that can be
implanted within a patient’s eye and placed on the anterior surface of an intraocular lens in
the patient’s eye. The intraocular pseudophakic contact lens substantially corrects residual
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refractive error present after implantation of the intraocular lens, such as after a lensectomy
(cataract) procedure.
[0028] Unlike conventional approaches, an intraocular pseudophakic contact lens can
be implanted with less surgical risk. Moreover, an intraocular pseudophakic contact lens
allows a patient to see immediately after implantation of the intraocular pseudophakic contact
lens. Further, an intraocular pseudophakic contact lens can be easily replaced if a different
lens is needed to correct residual refractive error or even removed if necessary. In addition,
with techniques such as intraoperative wavefront aberrometry now available, refractive
outcome can be measured during the actual procedure in which an intraocular pseudophakic
contact lens is being implanted, which helps to identify immediately that a desired refractive
target is obtained.
[0029] FIGURES 1 through 3 illustrate a first example intraocular pseudophakic
contact lens (IOPCL) 100 according to this disclosure. In particular, FIGURE 1 illustrates an
oblique view of the intraocular pseudophakic contact lens 100, FIGURE 2 illustrates a top
view of the intraocular pseudophakic contact lens 100, and FIGURE 3 illustrates a cut-away
view of the intraocular pseudophakic contact lens 100 along line A-A in FIGURE 2.
[0030] As shown in FIGURES 1 through 3, the intraocular pseudophakic contact lens
100 includes an optical lens 102. The optical lens 102 denotes the portion of the intraocular
pseudophakic contact lens 100 that alters light passing through the intraocular pseudophakic
contact lens 100. The light that passes through the optical lens 102 then travels through an
associated intraocular lens before reaching the retina of a patient’s eye.
[0031] The optical lens 102 can be formed from any suitable material(s), such as
silicone or acrylic. The optical lens 102 can also be formed in any suitable manner, such as
by using a mold or lathe cut manufacturing process. Different lenses 102 can be designed and
manufactured to provide a wide range of diopters, and each optical lens 102 can be designed
to correct any suitable refractive error(s). Example types of refractive errors that can be
corrected include myopia, hyperopia, and astigmatism.
[0032] The optical lens 102 in this example has a convex top surface and a concave
bottom surface. However, the optical lens 102 can have any other suitable shape, which could
depend (at least in part) on the type of refractive error(s) being corrected. As particular
examples, the optical lens 102 could be convex, concave, spherical, aspherical, toric, mono-
focal, or multi-focal. The specific lens platform used as the optical lens 102 in the intraocular
pseudophakic contact lens 100 can be selected to provide the desired refractive correction in a
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patient’s eye. The optical lens 102 could also include various other features as needed or
desired, such as when the optical lens 102 is weighted (like at its bottom) so that the optical
lens 102 orients itself on an intraocular lens in a desired orientation (like for toric platforms)
or when the optical lens 102 is tinted, is photochromic, or includes an ultraviolet (UV)
absorber.
[0033] Multiple projections 104a-104b extend from multiple sides of the optical lens
102. The projections 104a-104b are used to retain multiple anchors 106a-106b that extend
below the intraocular pseudophakic contact lens 100. Each projection 104a-104b could be
formed from any suitable material(s) and in any suitable manner. For example, the
projections 104a-104b could represent portions of the material(s) forming the optical lens 102
and therefore represent extensions of the optical lens 102 itself. However, this need not be the
case. For instance, the optical lens 102 could be placed within a retaining ring that is integral
with or attached to the projections 104a-104b, or the projections 104a-104b could be secured
to the optical lens 102 itself using adhesive or other suitable connecting mechanism. Note
that while two projections 104a-104b are shown here, the intraocular pseudophakic contact
lens 100 could include any number of projections, including a single projection.
[0034] The anchors 106a-106b are used to secure the intraocular pseudophakic
contact lens 100 to an intraocular lens. For example, after the intraocular pseudophakic
contact lens 100 is inserted into a patient’s eye, a surgeon or other personnel could push the
projections 104a-104b or other portion(s) of the intraocular pseudophakic contact lens 100
down onto an intraocular lens. This drives the anchors 106a-106b through the anterior (front)
surface of the intraocular lens and helps to secure the intraocular pseudophakic contact lens
100 to the intraocular lens. Each anchor 106a-106b represents any suitable structure for
securing an intraocular pseudophakic contact lens to an intraocular lens. In this example, the
anchors 106a-106b represent barbed or ribbed pins, although other types of anchors could
also be used, such as screw picks. Each anchor 106a-106b could be formed from any suitable
material(s) and in any suitable manner. Note that while two anchors 106a-106b are shown
here, the intraocular pseudophakic contact lens 100 could include any number of anchors,
including a single anchor.
[0035] In the intraocular pseudophakic contact lens 100 of FIGURES 1 through 3, the
anchors 106a-106b can be permanently embedded in the projections 104a-104b of the
intraocular pseudophakic contact lens 100. However, this need not be the case.
[0036] FIGURES 4 through 7 illustrate a second example intraocular pseudophakic
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contact lens 400 according to this disclosure. In particular, FIGURE 4 illustrates an oblique
view of the intraocular pseudophakic contact lens 400, and FIGURE 5 illustrates a top view
of the intraocular pseudophakic contact lens 400. Also, FIGURE 6 illustrates a cut-away view
of the intraocular pseudophakic contact lens 400 along line B-B in FIGURE 5, and FIGURE
7 illustrates a bottom view of the intraocular pseudophakic contact lens 400.
[0037] As shown in FIGURES 4 through 7, the intraocular pseudophakic contact lens
400 has various components that are the same as or similar to those forming the intraocular
pseudophakic contact lens 100. For example, the intraocular pseudophakic contact lens 400
includes an optical lens 402 and multiple projections 404a-404b. Also, the intraocular
pseudophakic contact lens 400 is secured to an intraocular lens using multiple anchors 406a-
406b. However, the intraocular pseudophakic contact lens 400 here includes holes 408a-408b
formed through the projections 404a-404b, and the anchors 406a-406b are inserted through
the holes 408a-408b.
[0038] The optical lens 402 can be formed from any suitable material(s), such as
silicone or acrylic. The optical lens 402 can also be formed in any suitable manner, such as
by using a mold or lathe cut manufacturing process. Different lenses 402 can be designed and
manufactured to provide a wide range of diopters, and each optical lens 402 can be designed
to correct any suitable refractive error(s). While the optical lens 402 in this example has a
convex top surface and a concave bottom surface, the optical lens 402 can have any other
suitable shape, which could depend (at least in part) on the type of refractive error(s) being
corrected. As particular examples, the optical lens 402 could be convex, concave, spherical,
aspherical, toric, mono-focal, or multi-focal. The specific lens platform used as the optical
lens 402 in the intraocular pseudophakic contact lens 400 can be selected to provide the
desired refractive correction in a patient’s eye. The optical lens 402 could also include
various other features as needed or desired, such as when the optical lens 402 is weighted
(like at its bottom) so that the optical lens 402 orients itself on an intraocular lens in a desired
orientation (like for toric platforms) or when the optical lens 402 is tinted, is photochromic,
or includes an ultraviolet (UV) absorber.
[0039] Each projection 404a-404b could be formed from any suitable material(s) and
in any suitable manner. For example, the projections 404a-404b could represent portions of
the material(s) forming the optical lens 402 and therefore represent extensions of the optical
lens 402 itself. However, this need not be the case. For instance, the optical lens 402 could be
placed within a retaining ring that is integral with or attached to the projections 404a-404b, or
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the projections 404a-404b could be secured to the optical lens 402 itself using adhesive or
other suitable connecting mechanism.
[0040] Each anchor 406a-406b represents any suitable structure for securing an
intraocular pseudophakic contact lens to an intraocular lens. In this example, the anchors
406a-406b represent barbed or ribbed pins, although other types of anchors could also be
used, such as screw picks. Each anchor 406a-406b could be formed from any suitable
material(s) and in any suitable manner.
[0041] Each hole 408a-408b could have any suitable size, shape, and dimensions.
Also, each hole 408a-408b could be formed in any suitable manner. For example, in some
embodiments, a hole 408a-408b could be formed through an associated projection 404a-404b
after the projection 404a-404b is formed, such as by using a mechanical or laser drill. In other
embodiments, each projection 404a-404b could be formed already including the associated
hole 408a-408b.
[0042] Note that while two projections 404a-404b, two anchors 406a-406b, and two
holes 408a-408b are shown here, the intraocular pseudophakic contact lens 400 could include
any number of projections, anchors, and holes. Also, while each projection 404a-404b is
shown as including a single cylindrical hole 408a-408b, each projection 404a-404b could
include one or more holes of any suitable shape(s).
[0043] After the intraocular pseudophakic contact lens 400 is inserted into a patient’s
eye, a surgeon or other personnel could place the intraocular pseudophakic contact lens 400
onto an intraocular lens. Before, during, or after insertion of the intraocular pseudophakic
contact lens 400, the surgeon or other personnel could insert the anchors 406a-406b through
the holes 408a-408b of the intraocular pseudophakic contact lens 400. The surgeon or other
personnel can push the anchors 406a-406b or other portion(s) of the intraocular pseudophakic
contact lens 400 down onto the intraocular lens, which drives the anchors 406a-406b through
the anterior surface of the intraocular lens and helps to secure the intraocular pseudophakic
contact lens 400 to the intraocular lens.
[0044] FIGURE 8 illustrates a third example intraocular pseudophakic contact lens
800 according to this disclosure. This embodiment of the intraocular pseudophakic contact
lens 800 is similar in structure to the intraocular pseudophakic contact lens 400. The
intraocular pseudophakic contact lens 800 includes an optical lens 802, projections 804a-
804b, and holes 808a-808b configured to receive anchors. All of the discussion above
regarding the optical lens 402, projections 404a-404b, and holes 408a-408b apply to the
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corresponding components in FIGURE 8.
[0045] In this example, the holes 808a-808b are angled to a larger degree compared to
the holes 408a-408b described above. The larger angle of the holes 808a-808b could be
needed or desired in certain circumstances. For instance, the larger angle of the holes 808a-
808b could be used to attach the intraocular pseudophakic contact lens 800 near the edge of
an intraocular lens, where the anterior surface of the intraocular lens may be angled more.
[0046] While various prior approaches have secured an “add-on” lens to an
intraocular lens, these prior approaches require a specific add-on lens to be designed for use
with a specific intraocular lens and the specific intraocular lens to be designed for use with
the specific add-on lens. That is, the add-on lens can only be used with a specific type of
intraocular lens, where that intraocular lens is designed specifically for use with that add-on
lens. As particular examples, an add-on lens may include haptics or other structures that are
designed to mate with corresponding structures of specific intraocular lenses, or an
intraocular lens may have a recess designed to receive a specific type of add-on lens. This can
be problematic for a number of reasons. For instance, many patients already have existing
intraocular lenses, and it may be impractical or even dangerous to try to remove those
existing intraocular lenses in order to implant new intraocular lenses that are designed for use
with add-on lenses.
[0047] The embodiments of the intraocular pseudophakic contact lenses 100, 400,
800 shown in FIGURES 1 through 8 can help to alleviate these problems since the anchors of
the intraocular pseudophakic contact lenses are driven into the actual lens material forming
an intraocular lens. In other words, the intraocular pseudophakic contact lens 100, 400, 800
need not be designed to work specifically with particular structures of any specific intraocular
lens. Rather, the intraocular pseudophakic contact lens 100, 400, 800 can simply be sized so
that, when the intraocular pseudophakic contact lens 100, 400, 800 is placed on an intraocular
lens, its anchors can be driven into the lens material of the intraocular lens. This allows the
intraocular pseudophakic contact lenses 100, 400, 800 to be used with a wide variety of
intraocular lenses, including different types of intraocular lenses and including existing
intraocular lenses already implanted into patients. There is no need to remove an existing
intraocular lens from a patient in order to install a new intraocular lens and an intraocular
pseudophakic contact lens.
[0048] Moreover, the anchors of an intraocular pseudophakic contact lens 100, 400,
800 could be easily removed from the lens material of an intraocular lens in order to remove
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the intraocular pseudophakic contact lens 100, 400, 800 from the intraocular lens. Among
other things, this allows one intraocular pseudophakic contact lens to be removed and
replaced with a different intraocular pseudophakic contact lens if a different refractive
correction is needed or desired.
[0049] FIGURE 9 illustrates a fourth example intraocular pseudophakic contact lens
900 according to this disclosure. As shown in FIGURE 9, the intraocular pseudophakic
contact lens 900 includes an optical lens 902, which could be the same as or similar to the
optical lenses described above. The intraocular pseudophakic contact lens 900 also includes
projections 904a-904b, which could be the same as or similar to the projections described
above.
[0050] Unlike the intraocular pseudophakic contact lenses described above, the
projections 904a-904b here are coupled to haptic loops 906a-906b. The haptic loops 906a-
906b are used to secure the intraocular pseudophakic contact lens 900 to portions 908a-908b
of the capsular bag in a patient’s eye. The haptic loops 906a-906b could be formed from any
suitable material(s) and in any suitable manner. For example, the haptic loops 906a-906b
could be formed from polyimide. Also, the haptic loops 906a-906b could have any suitable
size, shape, and dimensions. As particular examples, the haptic loops 906a-906b could be
about 2mm to about 4mm in length. Also, if desired, the haptic loops 906a-906b could have
an angled down posture (such as an angle of about 3º), which can help to provide easier
anchoring to the anterior capsule wall.
[0051] Note that while two projections and two haptic loops are shown here, the
intraocular pseudophakic contact lens 900 could include any number of projections and
haptic loops. Also, while not shown, a combination of haptic loops and anchors could be used
in the intraocular pseudophakic contact lens 900. For instance, the projections 904a-904b
could be coupled to the haptic loops 906a-906b, and anchors could be inserted into or
embedded within the projections 904a-904b. As another example, one set of projections
could be coupled to the haptic loops 906a-906b, and anchors could be inserted into or
embedded within another set of projections.
[0052] Also note that while anchors and haptic loops are described above to couple an
intraocular pseudophakic contact lens to an intraocular lens, any other suitable mechanisms
could be used to attach an intraocular pseudophakic contact lens to an intraocular lens. For
example, an intraocular pseudophakic contact lens could include an optical lens (with or
without projections), and the intraocular pseudophakic contact lens could be held in place on
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an intraocular lens via surface tension with the anterior surface of the intraocular lens.
[0053] The various intraocular pseudophakic contact lenses described above could
have any suitable size, shape, and dimensions. For example, the intraocular pseudophakic
contact lenses could be made available in a range of diameters from about 4mm to about
6mm. Also, the intraocular pseudophakic contact lenses could be made available with varying
base curvatures for their optical lenses. Of course, an intraocular pseudophakic contact lens
could also be custom designed for a particular patient’s eye, such as when one or more
specific curvatures are needed to correct for residual refractive error in the particular patient’s
eye.
[0054] The intraocular pseudophakic contact lenses disclosed here can be implanted
non-invasively in patients’ eyes and easily positioned on intraocular lenses. The implantation
is non-invasive because an intraocular pseudophakic contact lens is being installed on the
anterior surface of an intraocular lens, which is typically easily accessible by a surgeon or
other personnel during an implantation procedure. The implantation is also non-invasive
because some of the intraocular pseudophakic contact lenses can be attached to intraocular
lenses without requiring attachment of the intraocular pseudophakic contact lenses to
anatomical structures within the patients’ eyes, such as to the suculus of a patient’s eye.
[0055] The non-invasive implantation and easy positioning of an intraocular
pseudophakic contact lens provides a safe and effective refractive surgical procedure to
correct unwanted residual refractive error, such as after a lensectomy procedure. As a
refractive modality, the intraocular pseudophakic contact lenses contribute to a surgeon’s
ability to alter the current refractive error of a pseudophakic patient in an effort to adjust the
patient’s vision to achieve a finely-tuned desired refraction. Specific examples of this
functionality include allowing adjustments to a patient’s eye in order to achieve unilateral or
bilateral emmetropia, to induce unilateral myopia to allow for intermediate and near visual
function, to introduce multi-focality, and to treat unwanted residual astigmatism.
[0056] Although FIGURES 1 through 9 illustrate examples of intraocular
pseudophakic contact lens, various changes may be made to FIGURES 1 through 9. For
example, any combination of features shown in FIGURES 1 through 9 could be used in a
single intraocular pseudophakic contact lens, whether or not that specific combination of
features is shown in the figures or described above. Also, each intraocular pseudophakic
contact lens could include any suitable number of each component shown in the figure(s). In
addition, while anchors and haptic loops are shown as being used on projections from optical
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lenses, anchors and haptic loops could instead be used directly with the optical lenses (such
as when the optical lenses are larger than needed in order to correct residual refractive errors).
[0057] FIGURES 10 through 12 illustrate an example intraocular lens (IOL) 1000
attached to an example intraocular pseudophakic contact lens 100 according to this
disclosure. In particular, FIGURE 10 illustrates an oblique view of the system, FIGURE 11
illustrates a top view of the system, and FIGURE 12 illustrates a cut-away view of the system
along line C-C in FIGURE 11.
[0058] As shown in FIGURES 10 and 11, the intraocular lens 1000 includes an
optical lens 1002 and multiple haptics 1004a-1004b. The optical lens 1002 receives light
entering the eye (including light that passes through the intraocular pseudophakic contact lens
100) and focuses the light onto the retina of a patient’s eye. The haptics 1004a-1004b help to
hold the optical lens 1002 in a desired position within a patient’s eye. For example, the entire
intraocular lens 1000 could be placed within the capsular bag of a patient’s eye, and the
haptics 1004a-1004b could contact the inner walls of the capsular bag to hold the optical lens
1002 in the desired position.
[0059] As shown in FIGURES 10 through 12, the intraocular pseudophakic contact
lens 100 has been placed on the intraocular lens 1000, and the anchors 106a-106b of the
intraocular pseudophakic contact lens 100 have been driven through the anterior surface of
the intraocular lens 1000 into lens material 1006 of the optical lens 1002. As noted above,
this secures the intraocular pseudophakic contact lens 100 to the intraocular lens 1000.
Moreover, this can be done without requiring the intraocular lens 1000 to be designed
specifically for use with the intraocular pseudophakic contact lens 100 and without requiring
the intraocular pseudophakic contact lens 100 to be designed specifically for use with the
intraocular lens 1000.
[0060] This can be advantageous in various circumstances, such as when the
intraocular lens 1000 has already been implanted into a patient’s eye and cannot be removed
without excessive surgical risks or cannot be removed at all (such as due to long-standing
pseudophakia). Also, if the selected intraocular pseudophakic contact lens 100 does not
remedy residual refractive error or if the intraocular pseudophakic contact lens 100 actually
creates additional refractive error, the anchors 106a-106b can be extracted from the lens
material 1006 in order to remove the intraocular pseudophakic contact lens 100 from the
intraocular lens 1000. A different intraocular pseudophakic contact lens could then be placed
on the intraocular lens 1000 in the same or similar manner.
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[0061] Note that in FIGURE 12, outer portions of the intraocular pseudophakic
contact lens 100 are actually driven into the lens material 1006. However, this is not required.
Moreover, in FIGURE 12, only the outer portions of the intraocular pseudophakic contact
lens 100 are contacting the lens material 1006, and the remaining lower surface of the optical
lens 102 in the intraocular pseudophakic contact lens 100 is spaced apart from the lens
material 1006. However, it is possible for more (or substantially all) of the lower surface of
the optical lens 102 in the intraocular pseudophakic contact lens 100 to contact the lens
material 1006.
[0062] Although FIGURES 10 through 12 illustrate one example of an intraocular
lens attached to one example of an intraocular pseudophakic contact lens, various changes
may be made to FIGURES 10 through 12. For example, the intraocular lens 1000 could be
attached to any other intraocular pseudophakic contact lens, such as the contact lens 400 or
800 described above. Also, there are a number of intraocular lenses available, and the
intraocular lens 1000 represents one specific type of intraocular lens. Intraocular
pseudophakic contact lenses could be coupled to any other suitable intraocular lenses.
[0063] FIGURES 13 and 14 illustrate an example intraocular lens 1000 and an
example intraocular pseudophakic contact lens 100 in a patient’s eye 1300 according to this
disclosure. As shown in FIGURES 13 and 14, the eye 1300 includes a cornea 1302, a sclera
1304, and an iris 1306. The cornea 1302 represents the clear front portion of the eye 1300
through which light passes to enter into the eye 1300. The sclera 1304 is the tough outer
white portion of the eye. The iris 1306 controls the size of the eye’s pupil to thereby control
the amount of light from the cornea 1302 that enters into the interior of the eye 1300.
[0064] The eye 1300 also includes a capsular bag 1308, which typically holds the
natural crystalline lens of the eye 1300. However, in this example, the natural crystalline lens
has been removed and replaced with the intraocular lens 1000. The haptics 1004a-1004b of
the intraocular lens 1000 help to hold the intraocular lens 1000 within the capsular bag 1308
so that the optical lens 1002 of the intraocular lens 1000 is in a desired position within the
eye.
[0065] An intraocular pseudophakic contact lens 100 has also been placed on the
intraocular lens 1000 within the capsular bag 1308. The intraocular pseudophakic contact
lens 100 is placed on the anterior surface of the intraocular lens 1000, meaning the front
surface of the intraocular lens 1000 with respect to the eye 1300. Light enters through the
cornea 1302 and passes through the pupil before entering the intraocular pseudophakic
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contact lens 100, which modifies the light. The modified light then passes through the optical
lens 1002 of the intraocular lens 1000 and is again modified. The twice-modified light then
travels through the remainder of the eye 1300 to reach the retina at the back of the eye 1300.
[0066] By properly selecting the optical lens 102 of the intraocular pseudophakic
contact lens 100, the intraocular pseudophakic contact lens 100 can ideally correct any
residual refractive error that remains after implantation of the intraocular lens 1000. If
necessary, the intraocular pseudophakic contact lens 100 can also be removed and replaced
with a different intraocular pseudophakic contact lens if the intraocular pseudophakic contact
lens 100 does not properly correct the residual refractive error or if the intraocular
pseudophakic contact lens 100 actually causes additional refractive errors.
[0067] Although FIGURES 13 and 14 illustrate one example of an intraocular lens
and one example of an intraocular pseudophakic contact lens in a patient’s eye, various
changes may be made to FIGURES 13 and 14. For example, the intraocular lens 1000 could
be attached to any other intraocular pseudophakic contact lens, such as the contact lens 400 or
800 described above. Also, there are a number of intraocular lenses available, and an
intraocular pseudophakic contact lens could be coupled to any other suitable intraocular lens
in the eye 1300. In addition, some intraocular lenses need not reside within the capsular bag
of an eye, in which case the intraocular pseudophakic contact lens would also not reside
within the capsular bag of the eye.
[0068] FIGURE 15 illustrates an example anchor 1500 for attaching an intraocular
pseudophakic contact lens to an intraocular lens according to this disclosure. The anchor
1500 could, for example, be used in conjunction with any of the intraocular pseudophakic
contact lenses described above.
[0069] As shown in FIGURE 15, the anchor 1500 includes a head 1502 and a shaft
1504. The head 1502 represents the top of the anchor 1500 and is larger than the shaft 1504,
although this need not be the case depending on how the anchor 1500 is used (such as when
the head 1502 is embedded in a projection). The shaft 1504 extends downward from the head
1502 to a sharp tip 1506. The tip 1506 is designed to be inserted into lens material of an
intraocular lens. The shaft 1504 also includes a barbed or ribbed section 1508, which is
designed to be inserted into the lens material of the intraocular lens and resist (but not
necessarily prevent) removal of the shaft 1504 from the lens material of the intraocular lens.
This helps to secure an intraocular pseudophakic contact lens to the lens material of the
intraocular lens while still allowing removal of the intraocular pseudophakic contact lens
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from a patient’s eye if needed or desired.
[0070] Although FIGURE 15 illustrates one example of an anchor 1500 for attaching
an intraocular pseudophakic contact lens to an intraocular lens, various changes may be made
to FIGURE 15. For example, an anchor could be used without any larger head or without any
barbed or ribbed section. Also, any other suitable anchor(s) could be used to attach an
intraocular pseudophakic contact lens to an intraocular lens.
[0071] FIGURES 16 through 24 illustrate example additional features that could be
used with an intraocular pseudophakic contact lens according to this disclosure. None, one, or
any suitable combination of these features could be used with an intraocular pseudophakic
contact lens, including any of the intraocular pseudophakic contact lenses described above.
[0072] FIGURE 16 illustrates a top view of an intraocular pseudophakic contact lens
1600 that includes an optical lens 1602 and projections 1604a-1604b, which may be the same
as or similar to the corresponding components described above. While not shown, the
intraocular pseudophakic contact lens 1600 also includes multiple holes configured to receive
multiple anchors.
[0073] In addition, the intraocular pseudophakic contact lens 1600 includes alignment
markings 1606a-1606b. The alignment markings 1606a-1606b generally identify the desired
or optimal positioning of the anchors once inserted through the holes. For example, the
optical lens 1602 and the projections 1604a-1604b could be substantially transparent, so
anchors inserted into the projections 1604a-1604b and exiting underneath the intraocular
pseudophakic contact lens 1600 could be visible from over the intraocular pseudophakic
contact lens 1600. The alignment markings 1606a-1606b can be used by a surgeon or other
personnel to help ensure that the anchors are being inserted straight into the underlying lens
material of an intraocular lens, rather than being inserted crooked into the underlying lens
material of the intraocular lens or even missing the lens material altogether. In addition, these
markers 1606a-1606b can be used to identify the refractive correction (cylinder) in a toric
application to allow the surgeon or other personnel to orientate the optical lens 1602 at a
desired axis.
[0074] FIGURE 17 illustrates a top view of an intraocular pseudophakic contact lens
1700 that includes an optical lens 1702 and projections 1704a-1704b, which may be the same
as or similar to the corresponding components described above. While the projections 1704a-
1704b are shown as having holes configured to receive multiple anchors, this may not be
required, such as when tops of the anchors are embedded in the projections 1704a-1704b.
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[0075] The intraocular pseudophakic contact lens 1700 also includes a drug-eluting
matrix 1706 formed on at least part of the optical lens 1702. The drug-eluting matrix 1706 in
this example represents small areas where at least one medication has been deposited on the
optical lens 1702, possibly within a gel or other mechanism that controls the release of the
medication. Once implanted, the drug-eluting matrix 1706 releases the medication into a
patient’s eye.
[0076] Any suitable medication could be deposited on the optical lens 1702, such as
(but not limited to) medication for treating glaucoma or uveitis. The deposition could have
any suitable pattern and can be done in any suitable manner. For example, the medication
could be deposited in an annular pattern, such as a ring about 0.5mm thick, with an aperture
or “donut hole” in the center of the pattern. Other depositions could be used, such as a “slit
design” in the optical center of the optical lens 1702 allowing for enhanced vision with
optical advantages (like increased depth of focus, cylinder reduction, or treatment of
unwanted aberration).
[0077] FIGURE 18 illustrates a top view of an intraocular pseudophakic contact lens
1800 that includes an optical lens 1802 and projections 1804a-1804b, which may be the same
as or similar to the corresponding components described above. While the projections 1804a-
1804b are shown as having holes configured to receive multiple anchors, this may not be
required, such as when tops of the anchors are embedded in the projections 1804a-1804b.
[0078] The intraocular pseudophakic contact lens 1800 also includes a drug-eluting
film 1806 formed on at least part of the optical lens 1802. The film 1806 in this example
represents a continuous area where drug-eluting material that can deliver at least one
medication has been deposited on the optical lens 1802. Any suitable medication could be
deposited on the optical lens 1802, and the deposition could have any suitable pattern and can
be done in any suitable manner. In this example, the medication is deposited in an annular
pattern, such as a ring about 0.5mm in thickness. Other depositions could be used, such as a
“slit design” in the optical center of the optical lens 1802 allowing for enhanced vision with
optical advantages. As a particular example, the film 1806 could represent a drug-eluting
hydrogel.
[0079] FIGURE 19 illustrates an oblique view of an intraocular pseudophakic contact
lens 1900 that includes an optical lens 1902 and projections 1904a-1904b, which may be the
same as or similar to the corresponding components described above. While the projections
1904a-1904b are shown as having holes configured to receive multiple anchors, this may not
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be required, such as when tops of the anchors are embedded in the projections 1904a-1904b.
[0080] The intraocular pseudophakic contact lens 1900 also includes a drug-eluting
ring 1906 formed along at least part of the edge of the optical lens 1902. The ring 1906 elutes
at least one medication into a patient’s eye once implanted. The ring 1906 may or may not be
continuous around the entire optical lens 1902. In some embodiments, one or more rings
1906 could be used, where each ring is about 3mm in length by about 0.5mm in width. In
particular embodiments, the ring 1906 could represent a polyimide or other reservoir formed
along the edge of the optical lens 1902.
[0081] Note that FIGURES 17 through 19 have illustrated specific examples of drug-
eluting structures for an intraocular pseudophakic contact lens. However, any other suitable
type or types of drug-eluting structure(s) could be used at one or more locations of an
intraocular pseudophakic contact lens.
[0082] FIGURE 20 illustrates a cut-away view of an intraocular pseudophakic contact
lens 2000 that includes an optical lens 2002, which may be the same as or similar to the
corresponding components described above. Also, the intraocular pseudophakic contact lens
2000 includes multiple projections 2004a-2004b. In the examples described above,
projections have extended away from an associated optical lens at opposing angles, which
could allow for a natural opposing force that helps to ensure the forward permanent
placement of anchors into the anterior surface of an intraocular lens. However, this may not
be required, and the projections 2004a-2004b of the intraocular pseudophakic contact lens
2000 in FIGURE 20 are generally linear with respect to one another. Holes 2006a-2006b
through the projections 2004a-2004b could be formed straight up and down as shown in
FIGURE 20 or angled (such as in FIGURE 19), which helps to direct the anchors inward
toward a central axis of the optical lens 2002.
[0083] FIGURES 21A through 24 illustrate examples of various optical lenses that
could be included in an intraocular pseudophakic contact lens. However, any other suitable
optical lenses could be used in an intraocular pseudophakic contact lens. In FIGURES 21A
and 21B, optical lenses 2100 and 2150 of varying thicknesses are shown. The optical lens
2100 has a larger central thickness and is generally spherical on both top and on bottom. The
optical lens 2150 has a smaller central thickness and is somewhat flattened on top.
[0084] FIGURES 22A and 22B illustrate examples of optical lens 2200 and 2250 that
include enlarged portions 2202 and 2252, respectively. The enlarged portions 2202 and 2252
have greater weights than other corresponding portions of the optical lenses 2200 and 2250,
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which causes the optical lenses 2200 and 2250 to move into the orientations shown in
FIGURES 22A and 22B due to the larger weights of the enlarged portions 2202 and 2252. In
other words, the optical lenses 2200 and 2250 have uneven weight distributions around
central axes of the optical lenses 2200 and 2250. This can be useful, for example, when the
optical lenses 2200 and 2250 are aspherical and need to have a particular orientation to
correct a specific refractive error (such as astigmatism) in a patient’s eye. The enlarged
portions 2202 and 2252 could denote any enlarged portion of an optical lens, such as an
enlarged edge of the optical lens in one quadrant of the optical lens.
[0085] In FIGURE 22A, the enlarged portion 2202 has top and bottom surfaces
generally even with top and bottom surfaces at an edge of the optical lens 2200. FIGURE
22B shows a transparent image with the optic edge emphasized. Each of the enlarged
portions 2202 and 2252 represents a weighted edge that allows the intraocular pseudophakic
contact lens 2200 and 2250 to align a cylinder correction at a required axis, giving way to
better stability and avoiding unwanted rotation.
[0086] FIGURE 23 illustrates an example optical lens 2300 in which the lens 2300
represents a toric lens. A toric lens refers to a lens having different optical powers and focal
lengths in different perpendicular orientations. This can be seen in FIGURE 23, where a top
surface 2302 of the optical lens 2300 is curved in one direction (perpendicular to the figure)
and a bottom surface 2304 of the optical lens 2300 is curved in a perpendicular direction
(left-to-right in the figure).
[0087] FIGURE 24 illustrates an example non-spherical optical lens 2400 supporting
multi-focality. In FIGURE 24, the optical lens 2400 includes a central region 2402 and one or
more annular regions 2404-2406 that surround the spherical region 2402. Different regions
2402-2406 can be designed to provide different refractive powers. For example, some of the
regions 2402-2406 could be designed for near vision, while others of the regions 2402-2406
could be designed for far vision.
[0088] In general, a wide variety of optical lenses can be used in intraocular
pseudophakic contact lenses in order to provide desired refractive corrections for patients
with residual refractive errors. One or more intraocular pseudophakic contact lenses for a
specific patient could be selected or designed based on the type(s) of refractive correction
needed in the patient’s eye(s).
[0089] Although FIGURES 16 through 24 illustrate examples of additional features
that could be used with an intraocular pseudophakic contact lens, various changes may be
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made to FIGURES 16 through 24. For example, each intraocular pseudophakic contact lens
or optical lens could include any number of each feature shown for that intraocular
pseudophakic contact lens or optical lens. Also, other or additional features could be used
with the intraocular pseudophakic contact lenses described above.
[0090] FIGURE 25 illustrates an example method 2500 for using an intraocular
pseudophakic contact lens with an intraocular lens according to this disclosure. As shown in
FIGURE 25, residual refractive error in a patient’s eye having an intraocular lens is identified
at step 2502. This could include, for example, personnel testing the patient’s vision and
identifying any refractive error that remains after implantation of the intraocular lens 1000.
The testing could be done in any suitable manner, such as by using intraoperative wavefront
aberrometry. One goal of the testing can be to identify what refractive errors exist in the
patient’s eye after implantation of the intraocular lens in the patient’s eye. This testing could
be performed at any suitable time, such as after a lensectomy procedure.
[0091] An intraocular pseudophakic contact lens is selected to (ideally) correct the
identified residual refractive error at step 2504. This could include, for example, personnel
selecting an intraocular pseudophakic contact lens from a kit, where the selected intraocular
pseudophakic contact lens has an optical lens that substantially neutralizes the identified
residual refractive error. This could also include the personnel selecting an optical lens from a
kit and inserting the optical lens into an intraocular pseudophakic contact lens, where the
selected optical lens substantially cancels the identified residual refractive error. This could
further include the personnel obtaining an intraocular pseudophakic contact lens having a
custom-designed optical lens or obtaining a custom-designed optical lens for insertion into an
intraocular pseudophakic contact lens, where the custom-designed optical lens substantially
cancels the identified residual refractive error. In general, any mechanism can be used to
obtain a suitable intraocular pseudophakic contact lens.
[0092] The selected intraocular pseudophakic contact lens is inserted into the
patient’s eye at step 2506. This could include, for example, a surgeon or other personnel
forming a small incision in the patient’s eye and inserting the intraocular pseudophakic
contact lens into the eye through the incision. The intraocular pseudophakic contact lens can
be rolled, folded, or otherwise reduced in cross-sectional size in order to insert the intraocular
pseudophakic contact lens through a smaller incision.
[0093] One or more anchors are used to secure the intraocular pseudophakic contact
lens to an intraocular lens in the patient’s eye at step 2508. This could include, for example,
21
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the surgeon or other personnel placing the intraocular pseudophakic contact lens at a desired
position (and possibly in a desired orientation) on the intraocular lens. This could also include
the surgeon or other personnel pushing down onto the intraocular pseudophakic contact lens
or the anchors of the intraocular pseudophakic contact lens to push the anchors into the lens
material of the intraocular lens in the patient’s eye. This could further include placing haptic
loops of the intraocular pseudophakic contact lens around portions of the capsular bag in the
patient’s eye.
[0094] A vision test for the patient occurs at step 2510. The vision test could be done
in any suitable manner, such as by using intraoperative wavefront aberrometry. This vision
test could also be performed at any suitable time, such as during the surgical procedure in
which the intraocular pseudophakic contact lens is being implanted or after the surgical
procedure has been completed. A determination is made whether the tested vision is
satisfactory at step 2512. This could include, for example, personnel determining whether the
patient’s eye is still experiencing any residual refractive error and, if so, to what extent.
[0095] A determination is made whether to change the intraocular pseudophakic
contact lens at step 2514. This could include, for example, the personnel and the patient
determining whether the remaining residual refractive error (if any) is inconvenient or
otherwise problematic for the patient. If so, different steps could be taken to try and fix the
problem. For instance, the currently-implanted intraocular pseudophakic contact lens could
be repositioned to adjust for cylinder axis correction. If that fails, another intraocular
pseudophakic contact lens is selected at step 2516. This could include, for example, personnel
selecting another intraocular pseudophakic contact lens that (ideally) provides a better
refractive correction for the patient’s eye compared to the currently-inserted intraocular
pseudophakic contact lens. The currently-inserted intraocular pseudophakic contact lens is
removed from the patient’s eye at step 2518. This could include, for example, the surgeon or
other personnel removing the anchors of the currently-inserted intraocular pseudophakic
contact lens from the lens material of the intraocular lens and removing the currently-inserted
intraocular pseudophakic contact lens from the patient’s eye. The process then returns to step
2506, where the newly-selected intraocular pseudophakic contact lens can be inserted into the
patient’s eye and the vision test can be repeated.
[0096] Although FIGURE 25 illustrates one example of a method 2500 for using an
intraocular pseudophakic contact lens with an intraocular lens, various changes may be made
to FIGURE 25. For example, while shown as a series of steps, various steps in FIGURE 25
22
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could overlap, occur in parallel, occur in a different order, or occur any number of times.
[0097] It may be advantageous to set forth definitions of certain words and phrases
used throughout this patent document. The terms “include” and “comprise,” as well as
derivatives thereof, mean inclusion without limitation. The term “or” is inclusive, meaning
and/or. The phrase “associated with,” as well as derivatives thereof, may mean to include, be
included within, interconnect with, contain, be contained within, connect to or with, couple to
or with, be communicable with, cooperate with, interleave, juxtapose, be proximate to, be
bound to or with, have, have a property of, have a relationship to or with, or the like. The
phrase “at least one of,” when used with a list of items, means that different combinations of
one or more of the listed items may be used, and only one item in the list may be needed. For
example, “at least one of: A, B, and C” includes any of the following combinations: A, B, C,
A and B, A and C, B and C, and A and B and C.
[0098] The description in this patent document should not be read as implying that
any particular element, step, or function is an essential or critical element that must be
included in the claim scope.
[0099] While this disclosure has described certain embodiments and generally
associated methods, alterations and permutations of these embodiments and methods will be
apparent to those skilled in the art. Accordingly, the above description of example
embodiments does not define or constrain this disclosure. Other changes, substitutions, and
alterations are also possible without departing from the spirit and scope of this disclosure, as
defined by the following claims.
23
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Claims (19)
1. An apparatus comprising: an intraocular pseudophakic contact lens comprising: a first optical lens configured to at least partially correct a residual refractive error in an eye, the residual refractive error comprising a refractive error that exists in the eye after implantation of an artificial intraocular lens in the eye; multiple anchors configured to be inserted through an anterior surface of the artificial intraocular lens into lens material forming a second optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and multiple projections comprising extensions of the first optical lens such that the first optical lens and the projections comprise a common material, the anchors partially embedded in or configured to pass through the extensions of the first optical lens, the projections substantially or completely coplanar with the first optical lens; wherein the artificial intraocular lens lacks predefined openings that receive the anchors; wherein the anchors are configured to pierce the lens material forming the second optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and wherein the anchors comprise substantially straight pins extending axially along an optical axis of the intraocular pseudophakic contact lens away from the first optical lens.
2. The apparatus of claim 1, wherein the anchors are configured to couple the intraocular pseudophakic contact lens to different types of artificial intraocular lenses, including artificial intraocular lenses not specifically designed to be coupled to or receive the intraocular pseudophakic contact lens.
3. The apparatus of claim 1 or claim 2, further comprising at least one drug-eluting device located on the first optical lens and configured to deliver at least one medication.
4. The apparatus of any preceding claim, wherein the extensions of the first optical lens 24 100265995 forming the projections extend away from the optical axis of the intraocular pseudophakic contact lens at opposing angles.
5. The apparatus of any preceding claim, wherein each anchor comprises a head that is embedded in one of the projections.
6. The apparatus of any preceding claim, wherein each of the projections comprises one or more holes and the anchors are configured to be inserted into and pass through the holes.
7. The apparatus of any preceding claim, wherein the pins comprise barbed or ribbed pins.
8. The apparatus of any preceding claim, wherein the first optical lens has an uneven weight distribution around a central axis of the first optical lens in order to cause the first optical lens to obtain a specified orientation with respect to the artificial intraocular lens.
9. The apparatus of any preceding claim, wherein the first optical lens is mono-focal or spherical.
10. The apparatus of any one of claims 1 to 8, wherein the first optical lens is multi-focal or non-spherical.
11. The apparatus of any preceding claim, wherein the first optical lens is configured such that, when the anchors secure the intraocular pseudophakic contact lens to the artificial intraocular lens: an outer portion of a surface of the first optical lens contacts the lens material of the second optical lens; and a remaining portion of the surface of the first optical lens remains spaced apart from the lens material of the second optical lens.
12. A system comprising: an intraocular pseudophakic contact lens comprising: a first optical lens configured to at least partially correct a residual refractive error in an eye; multiple anchors; and 25 100265995 multiple projections comprising extensions of the first optical lens such that the first optical lens and the projections comprise a common material, the anchors partially embedded in or configured to pass through the extensions of the first optical lens, the projections substantially or completely coplanar with the first optical lens; and an artificial intraocular lens comprising a second optical lens, the second optical lens formed of lens material; wherein the anchors are configured to be inserted through an anterior surface of the artificial intraocular lens into the lens material in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; wherein the artificial intraocular lens lacks predefined openings that receive the anchors; wherein the anchors are configured to pierce the lens material forming the second optical lens of the artificial intraocular lens in order to secure the intraocular pseudophakic contact lens to the artificial intraocular lens; and wherein the anchors comprise substantially straight pins extending axially along an optical axis of the intraocular pseudophakic contact lens away from the first optical lens.
13. The system of claim 12, wherein the artificial intraocular lens is not specifically designed to be coupled to or receive the intraocular pseudophakic contact lens.
14. The system of claim 12 or claim 13, further comprising at least one drug-eluting device located on the first optical lens and configured to deliver at least one medication.
15. The system of any one of claims 12 to 14, wherein the anchors extend inward from the projections at opposing angles toward the optical axis of the intraocular pseudophakic contact lens and away from the first optical lens.
16. The system of any one of claims 12 to 15, wherein each of the projections comprises one or more holes and the anchors are configured to be inserted into and pass through the holes.
17. The system of claim 16, wherein the first optical lens comprises alignment markings configured to identify optimal positions for insertion of the anchors into the lens material, the 26 100265995 alignment markings and the anchors both visible during insertion of the anchors into the lens material.
18. The system of any one of claims 12 to 17, wherein the first optical lens has an uneven weight distribution around a central axis of the first optical lens in order to cause the first optical lens to obtain a specified orientation with respect to the artificial intraocular lens.
19. The system of any one of claims 12 to 18, wherein the first optical lens is configured such that, when the anchors secure the intraocular pseudophakic contact lens to the artificial intraocular lens: an outer portion of a surface of the first optical lens contacts the lens material of the second optical lens; and a remaining portion of the surface of the first optical lens remains spaced apart from the lens material of the second optical lens. 27
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ767870A NZ767870A (en) | 2014-09-22 | 2015-09-22 | Intraocular pseudophakic contact lenses and related systems and methods |
NZ767865A NZ767865A (en) | 2014-09-22 | 2015-09-22 | Intraocular pseudophakic contact lenses and related systems and methods |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201462053771P | 2014-09-22 | 2014-09-22 | |
US62/053,771 | 2014-09-22 | ||
US14/860,629 | 2015-09-21 | ||
US14/860,629 US10159562B2 (en) | 2014-09-22 | 2015-09-21 | Intraocular pseudophakic contact lenses and related systems and methods |
NZ729994A NZ729994A (en) | 2014-09-22 | 2015-09-22 | Intraocular pseudophakic contact lenses and related systems and methods |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ755995A NZ755995A (en) | 2021-04-30 |
NZ755995B2 true NZ755995B2 (en) | 2021-08-03 |
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