WO1990011716A1 - Optical spacing device - Google Patents
Optical spacing device Download PDFInfo
- Publication number
- WO1990011716A1 WO1990011716A1 PCT/GB1990/000465 GB9000465W WO9011716A1 WO 1990011716 A1 WO1990011716 A1 WO 1990011716A1 GB 9000465 W GB9000465 W GB 9000465W WO 9011716 A1 WO9011716 A1 WO 9011716A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- screen
- lens
- spacing device
- retina
- optical spacing
- Prior art date
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 28
- 210000001525 retina Anatomy 0.000 claims description 38
- 238000005259 measurement Methods 0.000 claims description 18
- 125000006850 spacer group Chemical group 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 11
- 230000002207 retinal effect Effects 0.000 claims description 11
- 208000014733 refractive error Diseases 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 4
- 238000005286 illumination Methods 0.000 claims description 3
- 238000007689 inspection Methods 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 2
- 238000003384 imaging method Methods 0.000 claims description 2
- 238000009540 indirect ophthalmoscopy Methods 0.000 abstract description 2
- 230000003902 lesion Effects 0.000 description 19
- 238000010586 diagram Methods 0.000 description 4
- 230000002093 peripheral effect Effects 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- 206010028980 Neoplasm Diseases 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 208000001491 myopia Diseases 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 206010020675 Hypermetropia Diseases 0.000 description 2
- 206010025421 Macule Diseases 0.000 description 2
- 206010062942 Optic Nerve Hypoplasia Diseases 0.000 description 2
- 206010038848 Retinal detachment Diseases 0.000 description 2
- 208000004350 Strabismus Diseases 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000003745 diagnosis Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 208000026611 isolated optic nerve hypoplasia Diseases 0.000 description 2
- 230000004807 localization Effects 0.000 description 2
- 238000002577 ophthalmoscopy Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 230000000284 resting effect Effects 0.000 description 2
- 230000004256 retinal image Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000002604 ultrasonography Methods 0.000 description 2
- 201000009487 Amblyopia Diseases 0.000 description 1
- 206010002945 Aphakia Diseases 0.000 description 1
- 201000005072 Chorioretinal scar Diseases 0.000 description 1
- 230000003667 anti-reflective effect Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 208000035250 cutaneous malignant susceptibility to 1 melanoma Diseases 0.000 description 1
- 201000000255 cycloplegia Diseases 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 230000007849 functional defect Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- BWHLPLXXIDYSNW-UHFFFAOYSA-N ketorolac tromethamine Chemical group OCC(N)(CO)CO.OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 BWHLPLXXIDYSNW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 201000001441 melanoma Diseases 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 210000001747 pupil Anatomy 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B3/00—Apparatus for testing the eyes; Instruments for examining the eyes
- A61B3/10—Objective types, i.e. instruments for examining the eyes independent of the patients' perceptions or reactions
- A61B3/14—Arrangements specially adapted for eye photography
- A61B3/15—Arrangements specially adapted for eye photography with means for aligning, spacing or blocking spurious reflection ; with means for relaxing
- A61B3/154—Arrangements specially adapted for eye photography with means for aligning, spacing or blocking spurious reflection ; with means for relaxing for spacing
Definitions
- the present invention relates to a device for use with the indirect ophthalmoscope which is an instrument used to allow visualisation of the retina .
- the device allows accurate localisation of the image of the retina in three-dimensions so that measurements relative to anatomical features of the retina can be carried out.
- One aspect of the present invention provides an optical spacing device for use with an indirect opthalmoscope which allows accurate localisation of the image of the retina.
- the spacing device comprises a body adapted to be coupled to a convex lens of focal length suitable to allow inspection of the retina and a transparent screen spaced from the lens by the body at the focal length of the lens such that the image produced by the lens is focused in plane of the screen.
- the optical spacing means includes means to vary the distance of the screen from the lens to allow for condensing lenses of different focal length to be used.
- optical spacer body The primary purpose of the optical spacer body is to allow accurate positioning of the lens and the screen.
- An additional spacer may also be provided in front of the lens to locate the optical spacer and lens at the correct distance from the eye.
- the spacer can be positioned using the patients orbital rim as a reference point to compensate for axial refractive error.
- a coaxial illumination source may be combined with the optical spacing device.
- the light source may be arranged to shine directly through the convex lens by using a beam splitter prism interposed in the optical pathway.
- the convex lens has a focal length suitable to allow convenient inspection of the retina by the ophthalmologist, so that the lens power has a rating of usually 15 - 30 Dioptres but higher power lenses may be used with a slit lamp microscope.
- the screen is formed of a transparent material, such as a plastics material or glass.
- the screen is preferably curved to take account of the curvature of the retina.
- the screen may be tinted or treated with an anti-reflective material to reduce spurious reflections. If the screen is tinted green, blood vessels appear dark and are thus easier to distinguish.
- the screen will.be disc-shaped and may be provided with calibration markings such as a grid of orthogonal lines or concentric circles to facilitate direct measurement of retinal features.
- the screen may also include a fixation target which is brought to a focus on the retina of the patient's unaccommodated eye.
- a fixation target which is brought to a focus on the retina of the patient's unaccommodated eye.
- the patient is asked to look at a point in a darkened room (which he cannot see) in order to keep the eye still. This generally proves very difficult for the patient to do for any length of time.
- any target on the screen will automatically be brought into focus by the convex lens on the retina of the eye, it is most effective to provide a fixation target on the screen itself. This may be in the form of a simple cross. If the lens with spacer and screen is rotated such that the patient's line of sight is varied, this allows the ophthalmologist to inspect different parts of the retina.
- a further aspect of the invention provides a method of obtaining a record of information from the retina of an eye, which comprises the steps of, placing a convex lens and an imaging screen in front of the eye; focusing an image of the retina in the plane of the screen; and
- an additional spacer may be coupled in front of the lens and spacer using the orbital rim as a reference point. This is only necessary for refractive errors greater than 3 Dioptres.
- Figure 1 is a schematic view of an ophthalmologist using the device according to an embodiment of the invention to examine the eye of a patient
- Figure 2 is an enlarged exploded view of the device coupled to the lens, as shown in Fig. 1
- Figure 3 is an optical ray diagram illustrating the principles of the indirect ophthalmoscope
- Figures 4a, b and c are an optical ray diagram depicting ' the effect of focusing using a lens with normal, long and short-sighted eyes;
- Figure 5 shows an optional fixation attachment;
- Figure 6 shows two different screens for use with the optical spacing device.
- Figure 7 shows a composite retinal map made up of thirteen individual retinal images.
- the holder is spaced by hollow opaque cylinder 3 from a circular screen holder 4 to minimise stray light.
- the lens holder 2, cylinder 3 and screen holder 4 constitute the optical spacing device.
- Transparent screen 5 is curved to take account of the retina curvature, and is formed of a plastics material upon which a fixation target
- Figure 3 is an optical ray diagram showing the retinal plane R s and lens P s of the eye having anterior focus F a .
- Convex lens 1 of the device is arranged so that its first principal focal plane Fi coincides with focus F a of the eye.
- F2 the second principal focal plane
- the optics of the convex lens are such that when placed before an emmetropic (i.e. a normal sighted eye when resting and focused at infinity) the emerging parallel rays originating from the retina are brought to a focus at the second principal focal plane F2 as shown in Fig. 4a. Because the rays emerging from the eye are parallel, the size of the image formed is independent of the distance of the lens from the eye. However, rays emerging from an ametropic (i.e. long (hypertropic) or short sighted (myopic)), because they are not parallel, form an image the size of which and whose distance from the lens depends on the distance the lens is held from the eye as-shown by planes marked M (myopic) and H (hypertropic) in Figs.
- M myopic
- H hypertropic
- Figure 5 shows a fixation light 8 mounted on the end of a ' telescopic arm 9 depending from a slideable mounting 10 arranged to slide around a ring 11.
- the ring is intended to fit around screen holder 4.
- Use of the fixation light which extends beyond the ambit of the screen allows the more peripheral parts of the retina to be inspected.
- Figure 7 shows a typical result of a mapping of the inner and outer regions of the retina out to 200° by building up a series of overlapping disc maps of the entire retinal region acquired by use of the different fixation targets shown in Figure 6 (a)(b) and light source of Figure 4.
- Figure 6b shows a screen 5 having a series of concentric circular graduations 12 inscribed thereon at constant radial spacing. These graduations are helpful in taking absolute measurements of the retina.
- the tube may be replaced by spaced legs of a fixed length and the screen graduations do not have to be constant.
- the device may include micrometer adjustments to move cross-wires on the screen to facilitate measurement.
- the patient is positioned and the condensing lens, with spacer and screen attached, introduced in front of his eye. ' The patient immediately becomes aware of the central fixation target and as his attention is directed to it, it becomes aligned with his fovea quickly centring his posterior pole in the doctor's field of view. Having examined the posterior pole his attention is directed to the second fixation target located at the upper extreme of the screen. As his eye rotates upwards to take up fixation a new 60° field is brought into view still including the fovea but with, in addition, an extra 30° of superior fundus not previously visualised. The condensing lens is now rotated slowly clockwise about its principal axis while the patient maintains fixation.
- the doctor's field of view also progresses in a clockwise manner until he has systematically examined a 120° field.
- an optional illuminated fixation target attached to the rim of the lens Figure 4
- the entire fundus may be examined in a similarly controlled way.
- Example 2 (use as a visuscope)
- the central fixation target may be used to assess the point and steadiness of fixation e.g. in a child with amblyopia (a squint or lazy eye) or indeed in any condition where acular function (e.g. detached retina) may be felt to be impaired.
- acular function e.g. detached retina
- Diagnosis or exclusion of optic nerve hypoplasia may have important clinical implications for a patient, particularly in children.
- the present device can provide accurate measurements as follows:
- Adequate pupil dilatation and cycloplegia are achieved with an approriate drop.
- the child is positioned for indirect ophthalmoscopy and the condensing lens with appropriate spacer and screen (b) ( Figure 5) attached are introduced.
- the +14 D lens may be used to obtain higher magnification of the posterior pole.
- his attention is directed to the central fixation target. This automatically aligns the optic disc graticule 15° from his fixation point. By then rotating the condensing lens about its principal axis the graticule is readily superimposed upon the disc which may be directly measured with an accuracy of +0.05mm.
- Ultrasonography is unsuitable for measuring non-elevated lesions or lesions with inadequate acoustic impedance.
- Serial photography may be employed to assess changes in a lesion but this may be fraught with technical problems for the photographer and inconvenience for both patient and doctor. Even then, accurate absolute measurements may not be possible without sophisticated photographic techniques.
- the technique for measuring fundus lesions directly with the device and graticule screen is as follows: The size of the lesion is first estimated by conventional ophthalmoscopy. A condensing lens is then selected which will provide the maximum magnification of the lesion while keeping its boundaries within the field of view. The lens is fitted with the appropriate spacer mounted with screen (b) ( Figure 6) . Any significant refractive error is taken into account if necessary as described above. The eye is correctly positioned by adjusting the fixation of the fellow eye with the adjustable fixation target mounted to the condensing lens so that the graticule scale is adequately superimposed upon the lesion to be studied. Accurate measurements may then be made in any meridian as long as the limited of the lesion can be visualised.
- the production of drawings of the retina showing its important features accurately located and inter-related is important, particularly for surgeons concerned with operations to cure detached retinas.
- the device of the present invention may be used as follows. Screen (a) of Figure 6 is first selected and the disc and macula are outlined over the etched markings using a water soluble marking pen. The screen is then mounted on the spacer which is then attached to the +20 or +30 D condensing lens. The patient is asked to fixate the foveal target. The accuracy with which he does this will provide important information as to his foveal function. The lens is then rotated about its principal axis until the inscribed disc is superimposed over that of the patient.
- Example 6 Self assessment of central visual field
- Targets introduced at the principal focal plane of the condensing lens are brought sharply into focus on the retina by the unaccommodated eye.
- the +20 D lens has a diameter of 50mm and produces an image on the screen of the central 60° of the posterior pole. This corresponds almost exactly, therefore, to the angle subtended by the standard Bjerrum screen.
- the screen may be arranged as an oculokinetic chart combining a central stimulus and a series of peripheral fixation targets as described by Damato B.E. Oculokinetic Perimetry - A simple test for use in the community. Br. J. Oththalmol. 1985. Vol 69, 927 - 931.
- the patient is positioned and the condensing lens with its attachments introduced as previously described.
- An appropriate fixation target is selected which brings the area of retina of interest to the doctor into the field of view. While the patient maintains fixation a suitable target is introduced to overlie the area of interest (eg. a chorioretinal scar) .
- the functional boundaries of the lesion may then be delineated in exactly the way that one would plot a functional deficiency in the visual field with the conventional tangent screen.
- the important advantage being, however, that one may immediately correlate the functional defect with the morphological appearance of the retina. Careful application of the device as a research tool may improve the understanding of many disease processes which disturb the function of the retina.
- the device can be used in the vetinary field to inspect animal retinas as well as those of humans.
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medical Informatics (AREA)
- Animal Behavior & Ethology (AREA)
- Ophthalmology & Optometry (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Surgery (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Eye Examination Apparatus (AREA)
- Optical Head (AREA)
- Led Device Packages (AREA)
- Optical Communication System (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB898907156A GB8907156D0 (en) | 1989-03-30 | 1989-03-30 | Optical spacing device |
GB8907156.7 | 1989-03-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1990011716A1 true WO1990011716A1 (en) | 1990-10-18 |
Family
ID=10654170
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB1990/000465 WO1990011716A1 (en) | 1989-03-30 | 1990-03-29 | Optical spacing device |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0465519A1 (en) |
JP (1) | JPH04506465A (en) |
AU (1) | AU643682B2 (en) |
CA (1) | CA2049331A1 (en) |
GB (1) | GB8907156D0 (en) |
WO (1) | WO1990011716A1 (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1884137A (en) * | 1929-11-25 | 1932-10-25 | Newman Ephraim Arthur | Optical instrument |
US1891041A (en) * | 1929-12-14 | 1932-12-13 | Reuel W Bennett | Iridometer |
FR1442458A (en) * | 1965-04-30 | 1966-06-17 | Eyepiece, in particular for ophthalmometer | |
US3787112A (en) * | 1972-08-03 | 1974-01-22 | J Lyons | Apparatus and method for the self-examination of certain conditions of the eye |
US3903870A (en) * | 1974-02-04 | 1975-09-09 | Applied Optics Corp | Method and apparatus for ocular self-examination |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4728183A (en) * | 1986-10-01 | 1988-03-01 | Ocular Instruments, Inc. | Ophthalmic lens for observing the fundus of the eye |
-
1989
- 1989-03-30 GB GB898907156A patent/GB8907156D0/en active Pending
-
1990
- 1990-03-29 JP JP2505180A patent/JPH04506465A/en active Pending
- 1990-03-29 EP EP19900905215 patent/EP0465519A1/en not_active Ceased
- 1990-03-29 WO PCT/GB1990/000465 patent/WO1990011716A1/en not_active Application Discontinuation
- 1990-03-29 CA CA 2049331 patent/CA2049331A1/en not_active Abandoned
- 1990-03-29 AU AU53406/90A patent/AU643682B2/en not_active Ceased
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1884137A (en) * | 1929-11-25 | 1932-10-25 | Newman Ephraim Arthur | Optical instrument |
US1891041A (en) * | 1929-12-14 | 1932-12-13 | Reuel W Bennett | Iridometer |
FR1442458A (en) * | 1965-04-30 | 1966-06-17 | Eyepiece, in particular for ophthalmometer | |
US3787112A (en) * | 1972-08-03 | 1974-01-22 | J Lyons | Apparatus and method for the self-examination of certain conditions of the eye |
US3903870A (en) * | 1974-02-04 | 1975-09-09 | Applied Optics Corp | Method and apparatus for ocular self-examination |
Also Published As
Publication number | Publication date |
---|---|
CA2049331A1 (en) | 1990-10-01 |
AU643682B2 (en) | 1993-11-25 |
EP0465519A1 (en) | 1992-01-15 |
AU5340690A (en) | 1990-11-05 |
JPH04506465A (en) | 1992-11-12 |
GB8907156D0 (en) | 1989-05-10 |
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