CA2186379C - Epithelium removal - Google Patents
Epithelium removal Download PDFInfo
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- CA2186379C CA2186379C CA002186379A CA2186379A CA2186379C CA 2186379 C CA2186379 C CA 2186379C CA 002186379 A CA002186379 A CA 002186379A CA 2186379 A CA2186379 A CA 2186379A CA 2186379 C CA2186379 C CA 2186379C
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- 210000000981 epithelium Anatomy 0.000 title claims abstract description 71
- 238000002679 ablation Methods 0.000 claims abstract description 22
- 210000004087 cornea Anatomy 0.000 claims abstract description 18
- 102000008186 Collagen Human genes 0.000 claims description 28
- 108010035532 Collagen Proteins 0.000 claims description 28
- 229920001436 collagen Polymers 0.000 claims description 28
- 230000005855 radiation Effects 0.000 claims description 9
- 238000000608 laser ablation Methods 0.000 claims description 4
- 238000001514 detection method Methods 0.000 claims description 2
- 210000003560 epithelium corneal Anatomy 0.000 claims description 2
- 230000001678 irradiating effect Effects 0.000 claims description 2
- 230000005670 electromagnetic radiation Effects 0.000 claims 1
- 238000007493 shaping process Methods 0.000 claims 1
- 210000001519 tissue Anatomy 0.000 description 16
- 238000000034 method Methods 0.000 description 7
- 210000004027 cell Anatomy 0.000 description 4
- 210000003850 cellular structure Anatomy 0.000 description 3
- 208000001491 myopia Diseases 0.000 description 3
- 230000004379 myopia Effects 0.000 description 3
- 238000007790 scraping Methods 0.000 description 3
- 210000005081 epithelial layer Anatomy 0.000 description 2
- 201000006318 hyperopia Diseases 0.000 description 2
- 230000004305 hyperopia Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 210000003786 sclera Anatomy 0.000 description 2
- 208000005156 Dehydration Diseases 0.000 description 1
- 206010020675 Hypermetropia Diseases 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- 201000009310 astigmatism Diseases 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
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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
- 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
- A61F9/007—Methods or devices for eye surgery
- A61F9/008—Methods or devices for eye surgery using laser
- A61F9/00802—Methods or devices for eye surgery using laser for photoablation
- A61F9/00817—Beam shaping with masks
- A61F9/00819—Beam shaping with masks with photoablatable masks
-
- 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
- A61F9/007—Methods or devices for eye surgery
- A61F9/008—Methods or devices for eye surgery using laser
- A61F9/00802—Methods or devices for eye surgery using laser for photoablation
- A61F9/00804—Refractive treatments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B2017/00017—Electrical control of surgical instruments
- A61B2017/00022—Sensing or detecting at the treatment site
- A61B2017/00057—Light
- A61B2017/00061—Light spectrum
-
- 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
- A61F9/007—Methods or devices for eye surgery
- A61F9/008—Methods or devices for eye surgery using laser
- A61F2009/00861—Methods or devices for eye surgery using laser adapted for treatment at a particular location
- A61F2009/00872—Cornea
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- Health & Medical Sciences (AREA)
- Ophthalmology & Optometry (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Optics & Photonics (AREA)
- Surgery (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Physics & Mathematics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Laser Surgery Devices (AREA)
- Radiation-Therapy Devices (AREA)
Abstract
This invention is an accurate, non- mechanical removal of the epithelium (16) from essentially only the area of the cornea to be treated. In particular, an epithelium ablative laser device irradi- ates the selected region of the epithelium with ablative laser energy (21), a spectro- scopic system nonitors (90) the ablation and spectroscopically determines whether epithelium is being ablated, and a control system (50) terminates the epithelium re- moval upon spectroscopic determination of a substantial absence of epithelium ab- lation.
Description
EPITHELIUM REMOVAL
Field of invention This invention relates to treatment of the eye and, more particularly, to a system and method for controlled removal of the epithelium of the cornea.
Backaround of Invention Photorefractive keratectomy is a procedure in which excimer lasers are used to correct optical errors of the eye, such as myopia, near-sightedness, hyperopia, far-sightedness and astigmatism. One typical procedure is to remove corneal tissue using a laser configured at 193 nanometers, although other wavelengths may also be used.
Each pulse of the laser removes a small amount of corneal tissue and, by controlling the number of pulses and exposure pattern of the laser, the cornea can be reshaped as desired.
For example, to correct near-sightedness, more tissue is removed from the center than at the edge, so that there is an overall flattening of the cornea.
An initial step in the procedure is to remove from the cornea the surface layer of cells known as the epithelium.
The Epithelium, typically about fifty microns thick, covers and protects the underlying tissue, principally collagen, that makes up the bulk of the cornea. In the past, the epithelium has been removed by scraping with a mechanical device, such as the edge of a blade or other surgical instrument. This has a number of disadvantages.
For example, the use of any mechanical instrument presents some risk of infection, and mechanical removal is also inherently irregular and highly dependent on the skill WO 95126162 2186379 PCT/[7s95l037940 -z- -of the person accomplishing the procedure. Scraping may injure the underlying cornea, e.g., by causing nicks or scratches which--may in turnaffect the smoothness of the later removal of the underlying collagen, and small "is-lands" of epithelium may remain after it is thought that all the epithelium has been removed or, in the course of-scraping away the epithelium, some of the underlying collagen may be removed also, Moreover, to_assure that the entire area to be._treated has been exposed, it is usually necessary to remove the epithelium from an area that is larger than that to be-treated. This is--undesirable since, among other things, a larger area requires longer to heal and results inan increasedrisk ofinfection. For example, if the area of.the collagen 16 to be treated is 5 millimeters in diameter, using mechanical ablation techniques it is usually necessary to remove the overlying epithelium 14 from a 6 or even a 7 millimeter zone. This result is that the overall exposed area is between about one and a half and two times the size of the treatment sone.
Further, if the epithelium is mechanically removed,-the laser used to ablate the underlying collagen cannot be positioned until after the epithelium removal has been completed, and this undesirably increases potential dehydra-tion and the.overall length.af the surgical procedure.
Su[~narv of Invention The present invention provides for accurate, non-mechanical removal of the epithelium from essentially only the area of the cornea to be treated. -In particular, an epithelium-ablative laser device irradiates the selected region of the epithelium with ablative laser energy, a spectroscopic system monitors the ablation and spectroscopically determines whether epithelium is being ablated, and a control system terminates the epithelium removal upon spectroscopic determination of a substantial absence of epithelium ablation.
In preferred embodiments in which the same laser device is then used to reshape the exposed cornea after the covering epithelium has been removed, the spectroscopic system detects characteristic fluorescence from corneal epithelium being ablated, the laser delivers energy in pulses, and the spectroscopic system examines for presence of epithelium fluorescence between pulses.
In accordance with this invention, there is provided a system for controlled removal of epithelium from a selected region of a cornea, said system comprising: an epithelium-ablative laser device for irradiating a selected region of the epithelium with ablative radiation such irradiation resulting in fluorescence of the cornea, a spectroscopic system arranged to spectroscopically monitor the fluorescence in selected regions of the cornea during ablation for spectroscopically determining ablation of epithelium, and a control system responsive to the spectroscopic system for terminating application of ablative radiation from said laser device to said region upon spectroscopic detection of substantial absence of the ablation of epithelium.
Description of Drawings Figure 1 is a schematic illustrating a system according to the present invention.
Figure 2 is a schematic illustrating a modified system also embodying the invention.
-3a-Detailed Description of Preferred Embodiments Figures 1 and 2 show a portion of a human eye, generally designated 10. As is well known, the cornea 12, surrounded by the sclera 14, includes an outer epithelial layer 16 (the epithelium) overlying the tissue 18 (largely collagen) that forms the bulk of the corneal structure. The epithelium 16 is typically about 50 microns thick, but the thickness varies from person to person. For example, the epithelium of a contact lens wearer is often only about 60%
as thick as that of a typical person who does not wear contact lenses.
Figures 1 and 2 also show an excimer laser 20, e.g., an Omnimed II manufactured and sold by Summit Technology, Inc. of Waltham, Massachusetts. Laser 20 emits a beam 21 of pulsed laser energy at a wavelength of about 193 nanometers, and is conventionally used to reshape the collagen 18 forming the corneal lens by selective ablation of the collagen tissue after the protective epithelium layer 16 has been mechanically removed. A variable aperture diaphragm 22 is provided in the beam path to control, and as necessary to vary, the diameter of the laser beam 21. As conventionally used, the aperture is set so that the diameter of the beam incident on the-cornea is equal to that of the area to be treated. when different corneal thicknesses are to be removed from different areas; a smaller aperture may be employed and only a small amount of the overall treatment area ablated at any particular time. In either event, each pulse of the excimer laser ablates a small amount of corneal collagen tissue. - - -It has been found that the laser ablation of the corneal collagen tissue causes emitted fluorescence_- See Tuft et al., "Qiialification of the Fluoresceiice Spectra Pro-duced by ArF Laser Ablation of the Coraea and Sclera,"
Tnvestiaative Opthalmolow and Visual Science, Vol. 31 No. 4 (Supp.) 1990, 477. Typically, the fluorescence caused by each ablating laser pulse follows, and exists for a period of time considerably shorter-than the width of, the.laser pulse i.tself. Tuft et al. found that the fluorescence -resuYting from a pulsed ArF laser had a duration on-the order A.f 1-3 nanoseconds, about an order of magnitude less than the laser pulse width.
It has been found that the laser beam from an excimer laser may also be used to ablate or remove the epithelial layer overlying the collagen structure of the cornea, but this has been proved difficult for a number of reasons. The thickness of the epithelium is difficult to measure accurately and, as has already been noted that the thickness of the epithelium varies from person to person.
Additionally, the cellular structures of theepithelium and .95I 03 7 9 4 =
2186379 IPEA/US i,1 ocr. w underlying collagen are sufficiently different that the two ablate at different rates. Accordingly, although the laser will ablate the epithelium as well as the collagen tissue, it is not practical simply to use the laser to start ablation at the outer surface of the epithelium 16, and then to work down into the underlying collagen tissue 18.
Rather, it is important to know when the covering epithelium has been completely removed, and only then to begin removal of the underlying collagen. If the point at which collagen tissue commences is not precisely known, it is difficult, if not effectively impossible, to have control collagen removal as is necessary for accurate corneal reshaping.
it also has been found that, because of their different cellular structures, the collagen and overlying epithelium have significantly different spectroscopic characteristics, and that these spectroscopic differences may be used to provide an accurate measure of epithelium removal.
For example, the fluorescence caused by excimer laser ablation of the epithelium 16 differs from produced by ablation of the underlying collagen 18. The fluorescence from the collagen tissue is a mixture of wavelengths, peaking at about 300 nanometers, in the ultraviolet range.
Ablation of the epith.elium also produces a range of fluorescence, but the peak is in the barely visible blue range, e.g., is in the range of about 400 nanometers. Both wavelengths can be detected using a conventional diode array detector such as that employed by Tuft; and the type of cells being ablated by the laser (e.g., epithelial cells or collagen cells) can be determined by monitoring the presence or absence of a fluorescence peak at the corresponding wavelength, e.g., barely visible blue (about 400 nanometer) or ultraviolet (about 300 nanometer). Since fluorescence from the abraded epithelium is visible to the human eye and r1PAcNG'ED SHEET
Field of invention This invention relates to treatment of the eye and, more particularly, to a system and method for controlled removal of the epithelium of the cornea.
Backaround of Invention Photorefractive keratectomy is a procedure in which excimer lasers are used to correct optical errors of the eye, such as myopia, near-sightedness, hyperopia, far-sightedness and astigmatism. One typical procedure is to remove corneal tissue using a laser configured at 193 nanometers, although other wavelengths may also be used.
Each pulse of the laser removes a small amount of corneal tissue and, by controlling the number of pulses and exposure pattern of the laser, the cornea can be reshaped as desired.
For example, to correct near-sightedness, more tissue is removed from the center than at the edge, so that there is an overall flattening of the cornea.
An initial step in the procedure is to remove from the cornea the surface layer of cells known as the epithelium.
The Epithelium, typically about fifty microns thick, covers and protects the underlying tissue, principally collagen, that makes up the bulk of the cornea. In the past, the epithelium has been removed by scraping with a mechanical device, such as the edge of a blade or other surgical instrument. This has a number of disadvantages.
For example, the use of any mechanical instrument presents some risk of infection, and mechanical removal is also inherently irregular and highly dependent on the skill WO 95126162 2186379 PCT/[7s95l037940 -z- -of the person accomplishing the procedure. Scraping may injure the underlying cornea, e.g., by causing nicks or scratches which--may in turnaffect the smoothness of the later removal of the underlying collagen, and small "is-lands" of epithelium may remain after it is thought that all the epithelium has been removed or, in the course of-scraping away the epithelium, some of the underlying collagen may be removed also, Moreover, to_assure that the entire area to be._treated has been exposed, it is usually necessary to remove the epithelium from an area that is larger than that to be-treated. This is--undesirable since, among other things, a larger area requires longer to heal and results inan increasedrisk ofinfection. For example, if the area of.the collagen 16 to be treated is 5 millimeters in diameter, using mechanical ablation techniques it is usually necessary to remove the overlying epithelium 14 from a 6 or even a 7 millimeter zone. This result is that the overall exposed area is between about one and a half and two times the size of the treatment sone.
Further, if the epithelium is mechanically removed,-the laser used to ablate the underlying collagen cannot be positioned until after the epithelium removal has been completed, and this undesirably increases potential dehydra-tion and the.overall length.af the surgical procedure.
Su[~narv of Invention The present invention provides for accurate, non-mechanical removal of the epithelium from essentially only the area of the cornea to be treated. -In particular, an epithelium-ablative laser device irradiates the selected region of the epithelium with ablative laser energy, a spectroscopic system monitors the ablation and spectroscopically determines whether epithelium is being ablated, and a control system terminates the epithelium removal upon spectroscopic determination of a substantial absence of epithelium ablation.
In preferred embodiments in which the same laser device is then used to reshape the exposed cornea after the covering epithelium has been removed, the spectroscopic system detects characteristic fluorescence from corneal epithelium being ablated, the laser delivers energy in pulses, and the spectroscopic system examines for presence of epithelium fluorescence between pulses.
In accordance with this invention, there is provided a system for controlled removal of epithelium from a selected region of a cornea, said system comprising: an epithelium-ablative laser device for irradiating a selected region of the epithelium with ablative radiation such irradiation resulting in fluorescence of the cornea, a spectroscopic system arranged to spectroscopically monitor the fluorescence in selected regions of the cornea during ablation for spectroscopically determining ablation of epithelium, and a control system responsive to the spectroscopic system for terminating application of ablative radiation from said laser device to said region upon spectroscopic detection of substantial absence of the ablation of epithelium.
Description of Drawings Figure 1 is a schematic illustrating a system according to the present invention.
Figure 2 is a schematic illustrating a modified system also embodying the invention.
-3a-Detailed Description of Preferred Embodiments Figures 1 and 2 show a portion of a human eye, generally designated 10. As is well known, the cornea 12, surrounded by the sclera 14, includes an outer epithelial layer 16 (the epithelium) overlying the tissue 18 (largely collagen) that forms the bulk of the corneal structure. The epithelium 16 is typically about 50 microns thick, but the thickness varies from person to person. For example, the epithelium of a contact lens wearer is often only about 60%
as thick as that of a typical person who does not wear contact lenses.
Figures 1 and 2 also show an excimer laser 20, e.g., an Omnimed II manufactured and sold by Summit Technology, Inc. of Waltham, Massachusetts. Laser 20 emits a beam 21 of pulsed laser energy at a wavelength of about 193 nanometers, and is conventionally used to reshape the collagen 18 forming the corneal lens by selective ablation of the collagen tissue after the protective epithelium layer 16 has been mechanically removed. A variable aperture diaphragm 22 is provided in the beam path to control, and as necessary to vary, the diameter of the laser beam 21. As conventionally used, the aperture is set so that the diameter of the beam incident on the-cornea is equal to that of the area to be treated. when different corneal thicknesses are to be removed from different areas; a smaller aperture may be employed and only a small amount of the overall treatment area ablated at any particular time. In either event, each pulse of the excimer laser ablates a small amount of corneal collagen tissue. - - -It has been found that the laser ablation of the corneal collagen tissue causes emitted fluorescence_- See Tuft et al., "Qiialification of the Fluoresceiice Spectra Pro-duced by ArF Laser Ablation of the Coraea and Sclera,"
Tnvestiaative Opthalmolow and Visual Science, Vol. 31 No. 4 (Supp.) 1990, 477. Typically, the fluorescence caused by each ablating laser pulse follows, and exists for a period of time considerably shorter-than the width of, the.laser pulse i.tself. Tuft et al. found that the fluorescence -resuYting from a pulsed ArF laser had a duration on-the order A.f 1-3 nanoseconds, about an order of magnitude less than the laser pulse width.
It has been found that the laser beam from an excimer laser may also be used to ablate or remove the epithelial layer overlying the collagen structure of the cornea, but this has been proved difficult for a number of reasons. The thickness of the epithelium is difficult to measure accurately and, as has already been noted that the thickness of the epithelium varies from person to person.
Additionally, the cellular structures of theepithelium and .95I 03 7 9 4 =
2186379 IPEA/US i,1 ocr. w underlying collagen are sufficiently different that the two ablate at different rates. Accordingly, although the laser will ablate the epithelium as well as the collagen tissue, it is not practical simply to use the laser to start ablation at the outer surface of the epithelium 16, and then to work down into the underlying collagen tissue 18.
Rather, it is important to know when the covering epithelium has been completely removed, and only then to begin removal of the underlying collagen. If the point at which collagen tissue commences is not precisely known, it is difficult, if not effectively impossible, to have control collagen removal as is necessary for accurate corneal reshaping.
it also has been found that, because of their different cellular structures, the collagen and overlying epithelium have significantly different spectroscopic characteristics, and that these spectroscopic differences may be used to provide an accurate measure of epithelium removal.
For example, the fluorescence caused by excimer laser ablation of the epithelium 16 differs from produced by ablation of the underlying collagen 18. The fluorescence from the collagen tissue is a mixture of wavelengths, peaking at about 300 nanometers, in the ultraviolet range.
Ablation of the epith.elium also produces a range of fluorescence, but the peak is in the barely visible blue range, e.g., is in the range of about 400 nanometers. Both wavelengths can be detected using a conventional diode array detector such as that employed by Tuft; and the type of cells being ablated by the laser (e.g., epithelial cells or collagen cells) can be determined by monitoring the presence or absence of a fluorescence peak at the corresponding wavelength, e.g., barely visible blue (about 400 nanometer) or ultraviolet (about 300 nanometer). Since fluorescence from the abraded epithelium is visible to the human eye and r1PAcNG'ED SHEET
vanishes when epithelium removal has been completed, it is also possible to monitor epithelial ablation visually.
Thus, according to one aspect of the present invention, a photodiode (designated 40 in Figure 1) sensitive to the characteristic peak of.either collagen or epithelium ablative fluorescence is used to determine which of the two types of cells is being ablated. Preferably, the photodiode 40 is sensitive to epithelium-caused fluorescence (e.g., to fluorescence in the about 400 nanometer wavelength range, and the presence or absence of such a fluorescence peak is used as a control signal. Fluorescence having such a peak will be present so long as the laser is removing epithelium.
Once the epithelium has been removed, that peak drops significantly. Control system 50, connected to both laser 20 and photodiode 40, is responsive to the photodiode 40 and either causes-the lasing action of the laser to stop (as in the illustrated embodiment) or automatically causes the control system to commence the corneal-reshaping.
Preferable, the same laser source and beam are used for both epithelium removal and subsequent reshaping of the underlying corneal tissue. As will be evident, this substantially avoids the previously significant difficulty of iasuring that the laser is properly registered relative to the exposed area. It will also be noted that the width of the beam used for epithelium removal is same as the maximum laser beam diameter to be used for subsequent corneal reshaping, i.e., the laser is used first to remove the epithelium from the entire area to be treated, and then to provide the collagen ablation required for reshaping. If a smaller diameter laser beam is used for reshaping, e.g., because different thicknesses are to be removed from different sub-areas of the entire treatment area, it will be seen that the epithelium bordering the complete treatment area acts as a protective mask.
Thus, according to one aspect of the present invention, a photodiode (designated 40 in Figure 1) sensitive to the characteristic peak of.either collagen or epithelium ablative fluorescence is used to determine which of the two types of cells is being ablated. Preferably, the photodiode 40 is sensitive to epithelium-caused fluorescence (e.g., to fluorescence in the about 400 nanometer wavelength range, and the presence or absence of such a fluorescence peak is used as a control signal. Fluorescence having such a peak will be present so long as the laser is removing epithelium.
Once the epithelium has been removed, that peak drops significantly. Control system 50, connected to both laser 20 and photodiode 40, is responsive to the photodiode 40 and either causes-the lasing action of the laser to stop (as in the illustrated embodiment) or automatically causes the control system to commence the corneal-reshaping.
Preferable, the same laser source and beam are used for both epithelium removal and subsequent reshaping of the underlying corneal tissue. As will be evident, this substantially avoids the previously significant difficulty of iasuring that the laser is properly registered relative to the exposed area. It will also be noted that the width of the beam used for epithelium removal is same as the maximum laser beam diameter to be used for subsequent corneal reshaping, i.e., the laser is used first to remove the epithelium from the entire area to be treated, and then to provide the collagen ablation required for reshaping. If a smaller diameter laser beam is used for reshaping, e.g., because different thicknesses are to be removed from different sub-areas of the entire treatment area, it will be seen that the epithelium bordering the complete treatment area acts as a protective mask.
in the embodiment of Figure 1, it will be seen that the laser beam 21 is substantially perpendicular to the entire portion of the eye being treated.- The diameter of the treated portion, e.g., about 5 mm, is sufficiently small that the laser beam is substantially normal to all portions -- -of the eye being treated. If a larger, e.g., 8-9 mm diameter, area is to be treated, the curvature of the eye may become significant. In such circumstances, although the radiation from the laser 18 is emitted as parallel rays, they will impinge on the eye at different angles and may cause ablation of epithelium at different rates in different areas. Accorrlingly, it may be to provide additional means to insure ablation of epithelium throughout the selected regionis substantially the same.
Figure 2 shows a lens 70 placed between the laser and eye. Although the laser beam 21 is emitted from laser 18 as parallel rays, the opticalcharacteristics of the lens 70 are such that, after passing through the lens, the laser beam rays are slightly convergent so that, throughout the treatment area, each ray is incident on the eye at a substantially normal angle.
Alternatively, an ablative-mask of varying thickness may T3e provided between the laser source and the eye surface.- The various portions of the mask block the laser beam until the particular mask portion has been ablated, and thus make it possible to vary the period of time during which the laser is incident on different areas of the epithelium and thus assure equal thickness of epithelium ablation over the entire treatment area.
Whatever the circumstances, the system determines when all the epithelium has been removed, and the transition into the underlying collagen has begun, by sensing a spectroscopic difference between the epithelial and collagenic tissue.
WO 95/26162 PCT/[JS95/03790 Ot1?er Embodiments In other embodiments, other spectral characteristics of the epithelium may be employed to provide a control signal indicative of the fact that the epithelium overlying the treatment area, but little-or none of the underlying tissue, has been removed. For example, either reflective or transmissive spectroscopy may be employed. Figure 2 illustrates a --light source 80 incident on the treatment -area, and a sensor 90 (rather than a photodiode as in Figure 1) that is responsive to the reflected li.ght from the source. Since, as is well.known, the characteristics of the reflected light depend onthe cellular structure of-the sur-face on which light from the source is incident (and from which it is reflected), sensor 90 provides a control-signal indicating that the reflected light is from a collagen tissue,surface (or, alternatively, is not from epithelium tissue), and that substantially all of the epithelium has been removed.
Regardless of the particularspectroscopic methodology employed,thetransition between epithelium and collagen removal is indicated with considerably more accuracy than heretofore possible, and the.size and thickness of any residual "islands" of epithelial material are substantially reduced.
These and other embodiments will be within the scope of the following claims.
Figure 2 shows a lens 70 placed between the laser and eye. Although the laser beam 21 is emitted from laser 18 as parallel rays, the opticalcharacteristics of the lens 70 are such that, after passing through the lens, the laser beam rays are slightly convergent so that, throughout the treatment area, each ray is incident on the eye at a substantially normal angle.
Alternatively, an ablative-mask of varying thickness may T3e provided between the laser source and the eye surface.- The various portions of the mask block the laser beam until the particular mask portion has been ablated, and thus make it possible to vary the period of time during which the laser is incident on different areas of the epithelium and thus assure equal thickness of epithelium ablation over the entire treatment area.
Whatever the circumstances, the system determines when all the epithelium has been removed, and the transition into the underlying collagen has begun, by sensing a spectroscopic difference between the epithelial and collagenic tissue.
WO 95/26162 PCT/[JS95/03790 Ot1?er Embodiments In other embodiments, other spectral characteristics of the epithelium may be employed to provide a control signal indicative of the fact that the epithelium overlying the treatment area, but little-or none of the underlying tissue, has been removed. For example, either reflective or transmissive spectroscopy may be employed. Figure 2 illustrates a --light source 80 incident on the treatment -area, and a sensor 90 (rather than a photodiode as in Figure 1) that is responsive to the reflected li.ght from the source. Since, as is well.known, the characteristics of the reflected light depend onthe cellular structure of-the sur-face on which light from the source is incident (and from which it is reflected), sensor 90 provides a control-signal indicating that the reflected light is from a collagen tissue,surface (or, alternatively, is not from epithelium tissue), and that substantially all of the epithelium has been removed.
Regardless of the particularspectroscopic methodology employed,thetransition between epithelium and collagen removal is indicated with considerably more accuracy than heretofore possible, and the.size and thickness of any residual "islands" of epithelial material are substantially reduced.
These and other embodiments will be within the scope of the following claims.
Claims (13)
1. A system for controlled removal of epithelium from a selected region of a cornea, said system comprising:
an epithelium-ablative laser device for irradiating a selected region of the epithelium with ablative radiation such irradiation resulting in fluorescence of the cornea, a spectroscopic system arranged to spectroscopically monitor the fluorescence in selected regions of the cornea during ablation for spectroscopically determining ablation of epithelium, and a control system responsive to the spectroscopic system for terminating application of ablative radiation from said laser device to said region upon spectroscopic detection of substantial absence of the ablation of epithelium.
an epithelium-ablative laser device for irradiating a selected region of the epithelium with ablative radiation such irradiation resulting in fluorescence of the cornea, a spectroscopic system arranged to spectroscopically monitor the fluorescence in selected regions of the cornea during ablation for spectroscopically determining ablation of epithelium, and a control system responsive to the spectroscopic system for terminating application of ablative radiation from said laser device to said region upon spectroscopic detection of substantial absence of the ablation of epithelium.
2. The system of claim 1 wherein said spectroscopic system includes a detector for detecting fluorescence from said location during incidence of laser ablation energy on epithelium.
3. The system of claim 2 wherein said spectroscopic system includes a detector arranged to detect a characteristic blue fluorescence from corneal epithelium being ablated.
4. The system of claim 3 wherein said device produces the ablative radiation, and the ablative radiation substantially comprises electromagnetic radiation of about 193 nm wavelength.
9a
9a
5. The system of claim 1 wherein said ablative laser device comprises a device for ablating collagen for reshaping the cornea upon completion of the removal of the epithelium.
6. The system of claim 5 wherein the laser device includes a controlled aperture for shaping, over the duration of exposure, a radiation pattern ablating the collagen for effecting a preselected refractive correction.
7. The system of claim 1 wherein said laser device is an excimer laser.
8. The system of claim 1 in which said epithelium-ablative laser is arranged to deliver at least most of its energy in pulses and said spectroscopic system is arranged to examine for the presence of epithelium between pulses.
9. The system of claim 1 wherein said device is arranged to emit radiation as parallel rays, and including means to cause rays distributed over the range of curvature in the selected region to have substantially the same ablation of epithelium thickness.
10. The system of claim 9 wherein said means is adapted to cause the rays to have substantially a normal angle of incidence over the selected region of epithelium.
11. The system of claim 10 in which said means comprises a lens system.
12. The system of claim 9 including means for varying the energy deposited over said selected area to assure equal thickness of epithelium ablation over said area.
13. The system of claim 12 including an erodible mask shaped to produce equal ablation over all points of said selected area.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/218,720 | 1994-03-28 | ||
US08/218,720 US5505724A (en) | 1994-03-28 | 1994-03-28 | Epithelium removal |
PCT/US1995/003794 WO1995026162A1 (en) | 1994-03-28 | 1995-03-27 | Epithelium removal |
Publications (2)
Publication Number | Publication Date |
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CA2186379A1 CA2186379A1 (en) | 1995-10-05 |
CA2186379C true CA2186379C (en) | 2007-06-26 |
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Application Number | Title | Priority Date | Filing Date |
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CA002186379A Expired - Lifetime CA2186379C (en) | 1994-03-28 | 1995-03-27 | Epithelium removal |
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1995
- 1995-03-27 CA CA002186379A patent/CA2186379C/en not_active Expired - Lifetime
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