SCLERAL BUCKLE FOR ALLEVIATION OF RETINAL DETACHMENT AND REFRACTIVE ERROR
20220241109 · 2022-08-04
Inventors
Cpc classification
A61F2/147
HUMAN NECESSITIES
International classification
A61F2/14
HUMAN NECESSITIES
Abstract
A rhegmatogenous retinal detachment (RRD) occurs when a tear in the retina leads to fluid accumulation with a separation of the neurosensory retina from the underlying retinal pigment epithelial (RPE); this is the most common type of retinal detachment and can lead to blindness. The present invention features an eye shape modification (ESM) system (a scleral buckle) for the prevention and repair of retinal detachment as well for the adjustment of refractive error and the prevention of induced refractive error caused by scleral buckles. The present invention creates a scleral buckle with protuberances on the interior surface of the buckle. These protuberances produce corrugation/indentations in the eye which allows for both axial and circumferential relaxation. Additionally, the present invention creates on scleral buckle that remove excess bulky material from the scleral buckle band, producing a scleral buckle that is easier and safer to surgically implant onto the eye.
Claims
1. A scleral buckle (100) comprising: a) a scleral buckle first end (101) and an opposite scleral buckle second end (102); b) a scleral buckle exterior surface (110); and c) a scleral buckle interior surface (111) having a plurality of protuberances disposed thereon; wherein the scleral buckle is adapted to be wrapped around the eye by the scleral buckle first end (101) and the scleral buckle second end (102) being brought and held together such that the plurality of protuberances on the interior surface (111) makes contact with a surface of the eye.
2. The scleral buckle (100) of claim 1, wherein the plurality of protuberances are raised and extend from the scleral buckle first end (101) to the scleral buckle second end (102).
3. The scleral buckle (100) of claim 2, wherein the raised protuberances (160) are uniform or irregular.
4. The scleral buckle (100) of claim 1 having an aspect ratio of at least 2:1.
5. The scleral buckle (100) of claim 1, wherein the plurality of protuberances are ridges (161) extending from the scleral buckle first end (101) to the scleral buckle second end (102).
6. The scleral buckle (100) of claim 1, wherein the plurality of protuberances are ridges (163) extending from a scleral buckle third end (103) to a scleral buckle fourth end (104).
7. The scleral buckle (100) of claim 1, wherein a connector region (120) is disposed perpendicularly on the scleral buckle (100) at or near the scleral buckle first end (101) and the scleral buckle second end (102) to close the scleral buckle (100).
8. The scleral buckle (100) of claim 7, wherein the connector region (120) comprises a domed top (122) attached to an extension zone (121).
9. The scleral buckle (100) of claim 1, further comprising a groove (130) disposed along the scleral buckle exterior surface (110).
10. The scleral buckle (100) of claim 9, further comprising a silicone band that is placed inside the groove (130) to close the scleral buckle (100).
11. The scleral buckle (100) of claim 1, wherein the scleral buckle (100) is effective for alleviating myopia or alleviating hyperopia.
12. (canceled)
13. The scleral buckle (100) of claim 1, wherein the scleral buckle (100) is effective for alleviating and preventing retinal detachment, or for adjustment of refractive error.
14. (canceled)
15. A method of scleral buckling an eye, comprising providing the scleral buckle (100) of claim 1, inserting the scleral buckle (100) underneath rectus muscles of the eye such that the interior surface (111) of the scleral buckle is in contact with the sclera, connecting the scleral buckle first end (101) and scleral buckle second end (102), and suturing the scleral buckle with sutures.
16. A scleral buckle (200) comprising: a) a scleral buckle first end (101) and an opposite scleral buckle second end (102); b) a scleral buckle third end (103) and an opposite scleral buckle fourth end (104); c) a scleral buckle exterior surface (110) and an opposite scleral buckle interior surface (111); d) a plurality of linkage sections (220) running perpendicular between the scleral buckle third end (103) and the scleral buckle forth end (104); e) a series of indentation ridges (230) running parallel between the scleral buckle third end (103) and the scleral buckle forth end (104), wherein each indentation ridge is in between the linkage sections (220); f) a plurality of open sections (210) between the indentation ridges (230) and the linkage sections (220); wherein the scleral buckle is adapted to be wrapped around the eye by the scleral buckle first end (101) and the scleral buckle second end (102) being brought and held together.
17. The scleral buckle (200) of claim 16 having an aspect ratio of at least 2:1.
18. The scleral buckle (200) of claim 16 having a connector region (120) disposed on the scleral buckle at or near the scleral buckle first end (101) and the scleral buckle second end (102).
19. The scleral buckle (200) of claim 18, wherein the connector region (120) comprises a domed top (122) attached to an extension zone (121).
20. The scleral buckle (200) of claim 16, wherein the scleral buckle (200) is effective for alleviating myopia or for alleviating hyperopia.
21. (canceled)
22. The scleral buckle (200) of claim 16, wherein the scleral buckle (200) is effective for alleviating and preventing retinal detachment or for adjustment of refractive error.
23. (canceled)
24. A method of scleral buckling an eye, comprising providing the scleral buckle (200) of claim 16, inserting the scleral buckle (200) underneath rectus muscles of the eye, connecting the scleral buckle first end (101) and scleral buckle second end (102) and suturing the scleral buckle (200) to the sclera with sutures placed around the indentation ridges and/or the entire scleral buckle.
Description
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S)
[0026] The present invention is not limited to the configurations shown in the figures. The features and advantages of the present invention will become apparent from a consideration of the following detailed description presented in connection with the accompanying drawings in which:
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DETAILED DESCRIPTION OF THE INVENTION
[0041] Following is a list of elements corresponding to a particular element referred to herein: [0042] 100,200 Scleral buckle [0043] 101 Scleral buckle first end [0044] 102 Scleral buckle second end [0045] 103 Scleral buckle third end [0046] 104 Scleral buckle fourth end [0047] 110 Scleral buckle exterior surface [0048] 111 Scleral buckle interior surface [0049] 120 Connector Region [0050] 121 Extension Zone [0051] 122 Domed Top [0052] 130 Groove [0053] 140 Tapered Region [0054] 150 Suture Flange [0055] 160 Raised protuberances [0056] 161 Circumferential ridges [0057] 162 Axial ridges [0058] 210 Open Section [0059] 220 Linkage Section [0060] 230 Indentation Ridges
[0061] Referring now to
[0062] In some embodiments, the present invention may features a scleral buckle (100) comprising a scleral buckle first end (101) and an opposite scleral buckle second end (102), a scleral buckle third end (103) and an opposite scleral buckle fourth end (104), a scleral buckle exterior surface (110) and an opposite scleral buckle interior surface (111) (
[0063] In some embodiments, the scleral buckle (100, 200) comprises a connector region (120) disposed perpendicularly at or near the scleral buckle first end (101) and at or near the scleral buckle second end (102). In some embodiments, the connector region (120) comprises a domed top (122) attached to an extension zone (121) (
[0064] In other embodiments, the scleral buckle (100) comprises a groove (130) disposed along the scleral buckle exterior surface (110) (
[0065] In other embodiments, the present invention may feature a scleral buckle (200) (
[0066] In some embodiments, the scleral buckle (200) comprises a connector region (120) disposed perpendicularly on the scleral buckle at or near the scleral buckle first end (101) and at or near the scleral buckle second end (102), a connector region (120) comprising a domed top (122) attached to an extension zone (121) (
[0067] Without wishing to limit the invention, the scleral buckle (200) allows for a lower profile and easier installation onto the eye. In some embodiments, the scleral buckle (200) may have a series of indentation ridges attached at regular intervals to allow for a thinner, more open design (
[0068] In some embodiments, the scleral buckle first end (101) and scleral buckle second end (102) are shorter than the scleral buckle third end (103) and scleral buckle fourth end (104). As used herein “aspect ratio” may refer to the ratio of the scleral buckle's (100, 200) longer side to its shorter side (the ratio of length to width of the scleral buckle). In some embodiments, the aspect ratio of the scleral buckle (100, 200) is at least 2:1. In some embodiments, the aspect ratio of the scleral buckle (100, 200) is at least 3:1. In some embodiments, the aspect ratio of the scleral buckle (100, 200) is at least 4:1. In some embodiments, the aspect ratio of the scleral buckle (100, 200) is at least 5:1. In some embodiments, the aspect ratio of the scleral buckle (100, 200) is about 2:1. In some embodiments, the aspect ratio of the scleral buckle (100, 200) is about 3:1. In some embodiments, the aspect ratio of the scleral buckle (100, 200) is about 4:1.
[0069] In some embodiments, the present invention scleral buckle designs (100, 200) take into consideration a number of variables, including but not limited to equatorial ocular diameter, chord length of band cross section, width of ridges on ocular surface, height of ridges, spacing of ridges, outer surface anterior-posterior contour, and inner anterior-posterior contour. In some embodiments, these variables help the scleral buckle (100, 200) to accommodate for the natural variations in eye circumference that exist between individuals.
[0070] As used herein “equatorial ocular diameter” or “ocular diameter” may refer to horizontal diameter (from side to side, or top to bottom, or oblique position) of the eye. In some embodiments, the equatorial ocular diameter of an eye may range from 20 mm to 34 mm. As used herein “chord length of band cross section” may refer to the linear length between two anterior-posterior points on a scleral buckle. In some embodiments, the chord length of band cross section may range from 1 mm to 2 cm. As used herein “outer surface anterior-posterior contour” may refer to the anterior-posterior contour of the outer (non-ocular) surface of a scleral buckle. In some embodiments, the outer surface anterior-posterior contour may be convex or flat which may prevent friction on Tenon's capsule or conjunctiva. As used herein “inner anterior-posterior contour (in contact with ocular surface)” may refer to anterior-posterior contour of the inner surface of a scleral buckle. In some embodiments, the inner anterior-posterior contour may be concave, convex, or flat. As used herein “axial length” may refer to the linear distance from the front of the cornea to either the retinal surface of the eye or the posterior surface of the sclera.
[0071] In some embodiments, emmetropia occurs where the focusing power of the eye is correct for the length of the eye. In some embodiments, emmetropic eyes have normal axial lengths. In other embodiments emmetropic eyes may have an axial length of about 23.5 mm. In some embodiment emmetropic eyes may have normal axial lengths and an increase in ocular equatorial diameter. In some embodiments, the scleral buckle (100, 200) is effective for reducing the equatorial ocular diameter without increasing the axial length. In other embodiments, the scleral buckle (100, 200) is effective for reducing the equatorial ocular diameter without inducing the axial length elongation.
[0072] In some embodiments, myopia or near sightedness is a disease in which images are focused on a point inside the eye rather than being focused on the retina. In some embodiments, myopia or near sightedness, occurs when the focusing power of the eye is too strong for the length of the eye. In some embodiments, myopes focus an image in front of the retina and require a concave lens (negative diopter lens) to increase the focal length and focus light on the retina. In some embodiments, the scleral buckle (100, 200), is effective for alleviating myopia. In some embodiments, myopia is caused by an increase in equatorial diameter and axial length. In some embodiments, myopia is caused by a global expansion of the eye, with an increase in the length, width, and height of the eye. In other embodiments, myopia is cause by an increase in axial length. In some embodiments, the myopic eyes have an axial length greater than 23.5 mm. In some embodiments, myopia is caused by axial elongation with no increase in height or width of the eye. In some embodiments, the scleral buckle (100, 200), is effective in reducing the ocular diameter and reducing the axial length. In some embodiments, the scleral buckle (100, 200), is effective for primarily reducing the axial length as well as to reduce the ocular diameter.
[0073] Without wishing to be bound to a particular theory or mechanism, it is believed that the present invention is the first scleral buckle that is capable of shortening the axial length of an eye, thereby alleviating myopia. The present invention therefore offers an alternative to more traditional forms of surgical treatments for myopia, such as laser-assisted in situ keratomileusis (LASIK) or photo refractive keratectomy (PRK), particularly in patients with severe myopia (greater than 6 diopters), who are at increased risk for RRD due to the shape and thickness of their eyes. In those patient subpopulations, this invention not only provides a method of alleviating myopia but also of preventing or alleviating RRD.
[0074] In some embodiments, hyperopia, or farsightedness, is a disease in which light is focused on a point behind the eye rather than on the retina. In some embodiments, hyperopia, or farsightedness occurs when the focusing power of the eye is too weak for the length of the eye. In some embodiments, hyperopes focus an image behind the retina and require a convex lens (positive diopter lens) to decrease the focal length and focus light on the retina. In some embodiments, the scleral buckle (100, 200) is effective at alleviating hyperopia. In further embodiments, hyperopia is causes by a decrease in axial length. In some embodiments, the have an axial length less than 23.5 mm. In some embodiments, hyperopic eyes may have enlarged equatorial ocular diameters. In other embodiments, hyperopic eye may require reduction of equatorial ocular diameter for the treatment or prevention of retinal detachment. In some embodiments, the scleral buckle (100, 200), is effective for reducing equatorial ocular diameter or the treatment or prevention of retinal detachment.
[0075] In some embodiments, the choice of scleral buckle (100, 200) design depends on the combination of axial length of equatorial diameter of the eye. This allows for the present scleral buckle designs to be utilized with a wide variety of eye shapes and sizes.
[0076] In some embodiments, the scleral buckle (100, 200) effective for alleviating and preventing retinal detachment. In some embodiments, the scleral buckle (100, 200) is effective for the adjustment of refractive error. In further embodiments, the scleral buckle (100, 200) effective for preventing the refractive error that may be caused by a scleral buckle.
[0077] In some embodiments, the connector region (120) is self-locking and can be used to attach the scleral buckle first end (101) to the scleral buckle second end (102) to achieve a fix ocular diameter (
[0078] In some embodiments, the scleral buckle interior surface (111) comprises a plurality of protuberances. In some embodiments, the scleral buckle interior surface (111) comprises a plurality of raised protuberances (160) extending from the scleral buckle first end (101) to the scleral buckle second end (102) and from the scleral buckle third end (103) to the scleral buckle fourth end (104). In some embodiment the plurality of raised protuberances (160) are uniform (
[0079] In some embodiments, the raised protuberances (160) are separated by a spacing of 500 μm. In some embodiments, the raised protuberances (160) are separated by a spacing of 10 mm. In some embodiments, the raised protuberances (160) are separated by a spacing of 100 mm. In some embodiments, the raised protuberances (160) are separated by a spacing of 500 mm. In some embodiments, the raised protuberances (160) are separated by a spacing of 1 cm. In some embodiments, the spacing separating the raised protuberances (160) is between 500 μm to 1 cm. In some embodiments, the raised protuberances (160) may be spaced apart from one another in a uniform manner. For example, the raised protuberances (160) may be spaced linearly along the scleral buckle third end (103) and/or the scleral buckle fourth end (104). For example, the plurality of raised protuberances may all be spaced linearly along the scleral buckle third end (103) and/or scleral buckle fourth end (104) 5 mm apart from one another. In some embodiments, the raised protuberances (160) may be spaced apart from one another in a varying or irregular manner. For example, the linear spacing along the scleral buckle third end (103) and/or scleral buckle fourth end (104) of a first raised protuberance (160) and a second raised protuberance (160) may be 0.5 mm, while the spacing between a third raised protuberance (160) and a fourth raised protuberance (160) may be 2 mm.
[0080] In some embodiments, the raised protuberances (160) are 500 μm in width. In some embodiments, the raised protuberances (160) are 10 mm in width. In some embodiments, the raised protuberances (160) are 100 mm in width. In some embodiments, the raised protuberances (160) are 500 mm in width. In some embodiments, the raised protuberances (160) are 1 cm in width. In some embodiments, the raised protuberances (160) are 2 cm in width. In some embodiments, the width of the raised protuberances (160) is about 500 μm to about 2 cm in width.
[0081] In some embodiments, the plurality of raised protuberances (160) is 500 μm in height. In some embodiments, the raised protuberances (160) are 10 mm in height. In some embodiments, the raised protuberances (160) are 100 mm in height. In some embodiments, the raised protuberances (160) are 500 mm in height. In some embodiments, the raised protuberances (160) are 1.0 cm in height. In some embodiments, the height of the raised protuberances (160) is between 500 μm to 1.0 cm. In some embodiments, the plurality of raised protuberances (160) may be of uniform height. In some embodiments, the raised protuberances (160) may be of varying or irregular height. For example, a portion of the raised protuberances (160) may be 0.5 mm in height, while another portion of the raised protuberances (160) may be 1.0 mm in height, and so on.
[0082] In some embodiments, the plurality of raised protuberances (160) may be of uniform shape (
[0083] In some embodiments, the scleral buckle design (100, 200) may have 1 raised protuberance (160). In some embodiments, the scleral buckle design (100, 200) may have 10 raised protuberances (160). In some embodiments, the scleral buckle design (100, 200) may have raised protuberances (160). In some embodiments, the scleral buckle design (100, 200) may have raised protuberances (160). In some embodiments, the scleral buckle design (100, 200) may have raised protuberances (160). In some embodiments, the scleral buckle design (100, 200) may have raised protuberances (160). In some embodiments, the scleral buckle design (100, 200) may have about 1-200 raised protuberances (160).
[0084] In some embodiments, the scleral buckle interior surface (111) comprises a plurality of protuberances. In one embodiment, the plurality of protuberances comprises parallel ridges (161) extending circumferentially from the scleral buckle first end (101) to the scleral buckle second end (102) (
[0085] In some embodiments, the circumferential ridges (161) are separated by a spacing of 500 μm. In some embodiments, the circumferential ridges (161) are separated by a spacing of 10 mm. In some embodiments, the circumferential ridges (161) are separated by a spacing of 100 mm. In some embodiments, the circumferential ridges (161) are separated by a spacing of 500 mm. In some embodiments, the circumferential ridges (161) are separated by a spacing of 1 cm. In some embodiments, the spacing separating the circumferential ridges (161) is about 500 μm to about 1 cm. In some embodiments, the circumferential ridges (161) may be spaced apart from one another in a uniform manner (
[0086] In some embodiments, the circumferential ridges (161) are 500 μm in width. In some embodiments, the circumferential ridges (161) are 10 mm in width. In some embodiments, the circumferential ridges (161) are 100 mm in width. In some embodiments, the circumferential ridges (161) are 500 mm in width. In some embodiments, the circumferential ridges (161) are 1.0 cm in width. In some embodiments, the circumferential ridges (161) are 2.0 cm in width. In some embodiments, the width of the circumferential ridges (161) is about 500 μm to about 2.0 cm in width.
[0087] In some embodiments, the circumferential ridges (161) are 500 μm in height. In other embodiments, the circumferential ridges (161) are 10 mm in height. In some embodiments, the circumferential ridges (161) are 100 mm in height. In some embodiments, the circumferential ridges (161) are 500 mm in height. In some embodiments, the circumferential ridges (161) are 1 cm in height. In some embodiments, the height of the circumferential ridges (161) is about 500 μm to about 1 cm. In some embodiments, the circumferential ridges (161) may be uniform in height. Alternatively, the circumferential ridges (161) may vary in height. For example, a portion of the circumferential ridges (161) may be 500 μm in height, while another portion of the circumferential ridges (161) may be 1 mm in height, and so on.
[0088] In some embodiments, the circumferential ridges (161) may be of uniform shape. For example, the circumferential ridges (161) may all have a semicircular cross section. In some embodiments, the circumferential ridges (161) may be of varying or irregular shape. For example, the circumferential ridges (161) may have a complex and irregular shape.
[0089] In some embodiments, the scleral buckle design (100, 200) may have 1 circumferential ridge (161). In other embodiments, the scleral buckle design (100, 200) may have 10 circumferential ridges (161). In some embodiments, the scleral buckle design (100, 200) may have 50 circumferential ridges (161) or 100 circumferential ridges (161). In some other embodiments, the scleral buckle design (100, 200) may have 150 circumferential ridges (161) or 200 circumferential ridges (161). In some embodiments, the scleral buckle design (100, 200) may have about 1-200 circumferential ridges (161).
[0090] In other embodiments, as shown in
[0091] In some embodiments, the axial ridges (162) are separated by a spacing of 500 μm. In some embodiments, the axial ridges (162) are separated by a spacing of 10 mm. In some embodiments, the axial ridges (162) are separated by a spacing of 100 mm. In some embodiments, the axial ridges (162) are separated by a spacing of 500 mm. In some embodiments, the axial ridges (162) are separated by a spacing of 1 cm. In some embodiments, the spacing separating the axial ridges (162) is about 500 μm to 1 cm. In some embodiments, the axial ridges (162) may be spaced apart from one another in a uniform manner (
[0092] In some embodiments, the axial ridges (162) are 500 μm in width. In some embodiments, the axial ridges (162) are 10 mm in width. In some embodiments, the axial ridges (162) are 100 mm in width. In some embodiments, the axial ridges (162) are 500 mm in width. In some embodiments, the axial ridges (162) are 1.0 cm in width. In some embodiments, the axial ridges (162) are 2.0 cm in width. In some embodiments, the width of the axial ridges (162) is about 500 μm and 2.0 cm in width.
[0093] In some embodiments, the axial ridges (162) are 500 μm in height. In some embodiments, the axial ridges (162) are 10 mm in height. In some embodiments, axial ridges (162) are 100 mm in height. In some embodiments, the axial ridges (162) are 500 mm in height. In some embodiments, the axial ridges (162) are 1 cm in height. In some embodiments, the height of the axial ridges (162) is between 500 μm to 1 cm. In some embodiments, the axial ridges (162) may be uniform in height. In some embodiments, the axial ridges (162) may be irregular in height. For example, a portion of the axial ridges (162) may be 500 μm in height, while another portion of axial ridges (162) may be 1 mm in height, and so on.
[0094] In some embodiments, the axial ridges (162) may be of uniform shape. For example, the axial ridges (162) may all have a semicircular cross section. In some embodiments, the axial ridges (162) may be of varying or irregular shape. For example, the axial ridges (162) may have a complex and irregular shape.
[0095] In some embodiments, the scleral buckle design (100, 200) may have 1 axial ridge (162). In some embodiments, the scleral buckle design (100, 200) may have 10 axial ridges (162). In some embodiments, the scleral buckle design (100, 200) may have 50 axial ridges (162). In some embodiments, the scleral buckle design (100, 200) may have 100 axial ridges (162). In some embodiments, the scleral buckle design (100, 200) may have 150 axial ridges (162). In some embodiments, the scleral buckle design (100, 200) may have 200 axial ridges (162). In some embodiments, the scleral buckle design (100, 200) may have about 1-200 axial ridges (162).
[0096] In some embodiments, the scleral buckle (200) comprises a series of indentation ridges (230). In some embodiments, the indentation ridges (230) are separated by a spacing of 500 μm. In some embodiments, the indentation ridges (230) are separated by a spacing of 10 mm. In some embodiments, the indentation ridges (230) are separated by a spacing of 100 mm. In some embodiments, the indentation ridges (230) are separated by a spacing of 500 mm. In some embodiments, the indentation ridges (230) are separated by a spacing of 1 cm. In some embodiments, the spacing separating the indentation ridges (230) is about 500 μm to about 1 cm. In some embodiments, the indentation ridges (230) may be spaced apart from one another in a uniform manner (
[0097] In some embodiments, the indentation ridges (230) are 500 μm in width. In some embodiments, the indentation ridges (230) are 10 mm in width. In some embodiments, the indentation ridges (230) are 100 mm in width. In some embodiments, the indentation ridges (230) are 500 mm in width. In some embodiments, the indentation ridges (230) are 1.0 cm in width. In some embodiments, the indentation ridges (230) are 2.0 cm in width. In some embodiments, the width of the indentation ridges (230) is about 500 μm to about 2.0 cm in width.
[0098] In some embodiments, the indentation ridges (230) are 500 μm in height. In other embodiments, the indentation ridges (230) are 10 mm in height. In some embodiments, the indentation ridges (230) are 100 mm in height. In some embodiments, the indentation ridges (230) are 500 mm in height. In some embodiments, the indentation ridges (230) are 1 cm in height. In some embodiments, the height of the indentation ridges (230) is about 500 μm to about 1 cm. In some embodiments, the indentation ridges (230) may be uniform in height. Alternatively, the indentation ridges (230) may vary in height. For example, a portion of the indentation ridges (230) may be 500 μm in height, while another portion of the indentation ridges (230) may be 1 mm in height, and so on.
[0099] In some embodiments, the indentation ridges (230) may be of uniform shape. For example, the indentation ridges (230) may all have a circular cross section (
[0100] In some embodiments, the scleral buckle design (100, 200) may have 1 indentation ridge (230). In other embodiments, the scleral buckle design (100, 200) may have 10 indentation ridges (230). In some embodiments, the scleral buckle design (100, 200) may have 50 indentation ridges (230) or 100 indentation ridges (230). In some other embodiments, the scleral buckle design (100, 200) may have 150 indentation ridges (230) or 200 indentation ridges (230). In some embodiments, the scleral buckle design (100, 200) may have about 1-200 indentation ridges (230).
[0101] In some embodiment the scleral buckle (100) comprises a groove (130) that is 0.5 mm wide. In some embodiment the groove (130) is 1.0 mm wide. In some embodiment the groove (130) is 1.5 mm wide. In some embodiment the groove (130) is 2.0 mm wide. In some embodiment the groove (130) is 2.5 mm wide. In some embodiment the groove (130) is 3.0 mm wide. In some embodiment the groove (130) is 3.5 mm wide. In some embodiment the groove (130) is 4.0 mm wide. In some embodiment the groove (130) is 4.5 mm wide. In some embodiment the groove (130) is 5.0 mm wide. In some embodiment the groove (130) is between 0.5 mm and 5.0 mm wide.
[0102] Without wishing to limit the present invention to any theory or mechanism, the shape of the eye will conform to the shape of the surface of the scleral buckle interior surface (111). For example, the eye may be indented in by the raised protuberances (160), or the circumferential ridges (161) or the axial ridges (162). The indentation of the eye will allow for changes in the axial length and/or ocular diameters and/or the circumferential length as well as allows for the prevention or retinal detachment. In some embodiment the scleral buckle exterior surface (110) can also be adjusted for the variation in eye shapes. In some embodiment, the scleral buckle exterior surface (110) can be flat, or convex, or concave.
[0103] In some embodiments, the scleral buckle (100, 200) may be made from biocompatible material including, by not limited to, silicone rubber, nylon, polypropylene, or other biocompatible polymers or elastomers.
[0104] In further embodiments, the present invention may feature a method of scleral buckling the eye. In some embodiments, the method comprises of inserting the scleral buckle (100, 200) underneath the rectus muscles of the eye, connecting the scleral buckle first end (101) and the scleral buckle second end (101) and suturing the scleral buckle to the sclera with sutures.
[0105] In some embodiments, the scleral buckle (100, 200) may be attached the sclera of the patient's eye by a suture flange (131). In some embodiments, the scleral buckle can be attached to the sclera with sutures placed around the entire scleral buckle (
[0106] As used herein, the term “about” refers to plus or minus 10% of the referenced number.
[0107] Various modifications of the invention, in addition to those described herein, will be apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. Each reference cited in the present application is incorporated herein by reference in its entirety.
[0108] Although there has been shown and described the preferred embodiment of the present invention, it will be readily apparent to those skilled in the art that modifications may be made thereto which do not exceed the scope of the appended claims. Therefore, the scope of the invention is only to be limited by the following claims. The reference numbers recited in the below claims are solely for ease of examination of this patent application, and are exemplary, and are not intended in any way to limit the scope of the claims to the particular features having the corresponding reference numbers in the drawings. In some embodiments, the figures presented in this patent application are drawn to scale, including the angles, ratios of dimensions, etc. In some embodiments, the figures are representative only and the claims are not limited by the dimensions of the figures. In some embodiments, descriptions of the inventions described herein using the phrase “comprising” includes embodiments that could be described as “consisting essentially of” or “consisting of”, and as such the written description requirement for claiming one or more embodiments of the present invention using the phrase “consisting essentially of” or “consisting of” is met.