Guide
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Page 1
Slit Lamp Imaging Guide
BX 900 ® PHOTO SLIT LAMP
Preamble On August 3rd, 1911, Alvar Gullstrand introduced the first rudimentary model of the slit lamp illuminator. An occasion of tremendous significance to ophthalmology had just taken place. Gullstrand described a device with the potential to advance the understanding of the eye and its problems as profoundly as did the direct ophthalmoscope 50 years earlier. By 1916, Henker had developed a practical combination of Gullstrand's illuminator and Czapski's corneal microscope, marking the first major advance in methods of examining the external eye in more than a century. In 1936 Comberg established the co-pivotal and iso-centric relationship between the microscope and slit illuminator and, in 1938, Goldmann’s collaboration with Haag-Streit produced the first par-focal instrument which also featured the single control lever design in use to this day. Goldmann also influenced the shift to Köhler illumination, greatly improving the efficiency of the slit lamp illuminator, the very heart of this marvelous device. These significant milestones, with contributions from a host of other individuals, have coalesced into the highly sophisticated instruments that are placed at our disposal today. In light of such capabilities in instrumentation, it follows that our results in slit lamp examination and slit lamp photography will rest on the level of sophistication we apply to the practice of these challenging and stimulating art forms. Csaba L. Mártonyi, COPRA, CRA Emeritus Associate Professor University of Michigan, Ann Arbor
BX User Guide This guide is intended to assist all those who seek to capture images of the eye using the slit lamp to improve the quality of their photography by using simple to follow illumination diagrams and high quality image examples. We hope this book provides inspiration and motivation to anyone who is involved the art of documenting the unique properties and pathologies of the eye and through Haag-Streit we offer a number of instruments to help you. The Haag-Streit BX900 slit lamp marries the latest imaging technology with the proven versatility, optical brilliance and build quality of the Haag-Streit tradition. The BX900 is the leading slit lamp-imaging device that is designed to assist the Ophthalmic Photographer with his demanding job. Furthermore it will also provide a valuable asset for all Eye Cap Specialists who demand the highest clinical and educational standards. Haag-Streit greatly appreciates and thanks all those who have contributed to this publication with special thanks to Cees van Beek of Leyenburg Hospital, Den Haag who provided many of the images. Steve Thomson Haag-Streit AG
CONTENTS BX900® PHOTO SLIT LAMP
4
TECHNICAL DATA
6
PHYSICAL AND OPTICAL CONDITIONS
7
TYPES OF ILLUMINATION
7
STANDARD SETTING
8
ILLUMINATION AND EXPOSURE SETTINGS
8
PICTOGRAMS
8
OVERVIEW
9
LIDS
10
CONJUNCTIVA
10
CORNEA
11
ANTERIOR CHAMBER, CHAMBER ANGLE
14
IRIS, IRIS-ANGIOGRAPHY
15
LENS
16
VITREOUS
17
FUNDUS
18
4
BX 900® PHOTO SLIT LAMP
1. Cable guide 3 1
2
2. Flash housing
4 5
3. Flash intensity changer for background illumination
6
4. Objective tube
7
5. Camera body
8 9
6. Eye-piece with double cross hair reticle 7. Mirror housing
11
8. Background illumination 9. Mirror and Diffusion filter
10
10. Cold light source 11. Shutter release bar 12. Photo control unit
12
The Haag-Streit Photo-Slit Lamp BX 900® is based on the Slit Lamp BQ 900®. It is therefore possible to use the same instrument both for ocular examination and documentation. A photo-slit lamp is a combination of a biomicroscope, and illumination system and the photo attachment. The Photo-Slit Lamp BX 900® and the Slit Lamp BQ 900® share the same microscope. The illumination system of the photo-slit lamp has in addition a flash unit and a background illumination. Two different light sources are available: the flash illumination and the modelling light. On the following page the different components will be explained.
5
1. The cable guide contains the high voltage cable for the flash light. 2. The flash housing contains the flash tube. Firing the BX900 trigger will simultaneously deliver a flash through the illumination system and, via a glass fibre cable, the fill background illumination while synchronising with the camera shutter.
7. The background illumination is swivel-mounted on a horizontal level and is illuminated through two glass fibre cables. The flash fill light comes from the flash housing and the modelling light comes from the cold light source. The modelling light is used to show where any reflection of the fill flash will fall. 8. The cold light source is mounted under the table and it provides the background modelling illumination.
3. The background illumination changer has seven settings: = 100 % = 10 %
= 50 % = 5%
= 0%
= 25 % = blue filter
These selections are only for the fill flash of the background illumination. The modelling light is controlled by the cold light source. 4. The camera body is mounted on the top of the biomicroscope allowing full visibility of the patient’s eyes from either side of the microscope. Not all cameras available on the market can be used. Haag-Streit has selected a number of models and has made the necessary adaptations. The correct function of the photo-slit lamp is guaranteed only by the use of cameras that are recommended by Haag-Streit. A list of current camera models is available at: www.haag-streit.com. Note that the camera has to be in the «MANUAL» operating mode and the shutter speed should be set to 1/90 sec. The recommended ISO rating for general use is 200 and colour temperature of the flash is 6000k but users have the option to apply other setting as required. 5. The 12.5x eyepiece with double cross hair reticule is inserted into the right ocular of the microscope. This must be correctly focused for the user’s eye to ensure sharp images are captured. Note that this setting is not the user’s refractive error. 6. The principal component of the Haag-Streit Photo-Slit Lamp BX 900® is the mirror housing with its built-in diaphragms. It mounts between the magnification changer and the binocular tube. When capturing an image all light is directed, via a mirror, to the camera. This allows the maximum utilisation of the available light: 100% for the examination and 100% for the image. The built-in diaphragm setting with five apertures is applied automatically on image capture. For the aperture intervals: Step 1 = largest aperture, Step 5 = smallest aperture. The small knobs on each side of the mirror housing can be used during examination to quickly activate the diaphragms to the pre-set position. This allows a preview prior to capture so that the image subject and depth of field may be checked.
9. With the diffusion filter the slit beam can be covered allowing overview pictures with diffuse illumination. 10. The shutter release bar is conveniently positioned in front of the joystick on the cross-slide. It can be used either right or left-handed. 11. The photo control unit is mounted under the left hand side of the table and has the main switch for the power supply. On the front side there are two switches and four error light indicators. With the main power switch it is possible to turn off the entire electrical system of the slit lamp. The camera may be turned off separately. The power switch on the front side is only for the photo control unit. With the flash-intensity switch in the high position, the flash light increases by one aperture step. Optical and acoustic warning signals will be activated in the case of an error when the shutter release bar is pressed. Once the cause of the problem has been removed, press the shutter release bar and the optical warning signal will be cancelled and the camera will be ready for use.
6
TECHNICAL DATA BIOMICROSCOPE Magnification Changer Ocular Magnification Range of Adjusting Oculars Reticle Inter-pupillary Distance
6.3 x 10 x 16 x 25 x 40 x 12.5 x +8 to -8 dioptres right ocular 52–78 mm
SLIT LAMP ILLUMINATOR Slit Height Slit Width Spotlight Horizontal Arc Vertical Arc Filters Slit Beam Diffuser Light Source Illumination Device Light Source Background Illumination
1– 8 mm 0–8 mm 0.2, 1, 2, 3, 5, 8 mm diameter +/- 90° 5°, 10°, 15°, 20° blue, green (red free), N. D. 10% yes 6V 4.5A Tungsten Halogen
PHOTO ATTACHMENT Image Delivery Objective Tube Focal Length Light Source Flash Light
Quick Return Mirror 100 % light for examination or photography 170 mm normal 200 Ws, high 400 Ws
DEPTH OF FIELD
IMAGE AND MAGNIFICATION DATA
dependent on magnification and aperture
Setting at magnification changer
Magnification
Extent of depth of focus (+/- in mm) with aperture
Chip dimensions Size of field in mm Magnification in plane of the chip
24x36 mm Mono
15x22.5 mm Mono
Magnification in plane of the chip
24x36 mm Stereo
1
2
3
4
5
6.3 x
1.3
1.8
2.6
3.6
5.2
6.3 x
0.63x
38x57
23.8x35.7
0.63x
38x28.5
10 x
0.5
0.7
1
1.4
2
10 x
1x
24x36
15x22.5
1x
24x18
16 x
0.2
0.3
0.4
0.5
0.8
16 x
1.6x
15x22.5
9.4x14.1
1.6x
15x11
25 x
0.1
0.1
0.15
0.2
0.3
25 x
2.5x
9.5x14
6x9
2.5x
3.5x7
40 x
0.05
0.05
0.05
0.1
0.15
40 x
4x
6x9
3.88x5.6
4x
6x4.5
Values will be increased by 35% in transparent media of the eyes
Circles: visible field of the eye-piece
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PHYSICAL AND OPTICAL CONDITIONS The binocular examination of the eyes with the slit lamp takes place in a three-dimensional space with great depth of field. Normal slit lamp imaging is a two-dimensional documentation with a very small depth of field. The difference between stereo viewing and monocular imaging can sometimes prove troublesome. However, viewing monocularly can help. Note only the image through the right eyepiece is recorded.
The BX900 has a clear screen with a cross hair reticule. The accommodative abilities of the photographer’s own eye are normally not noticeable during an examination: It is important that the photographer must establish the correct eye-piece setting (see page 5) to neutralise any accommodation. Only by viewing a sharp image of the reticule overlying a focused image of the eye will sharply focused images be captured.
The photographer’s view through the eyepieces is not the same as the recorded image. Through the eyepieces a circular image is visible whereas the image captured is rectangular (see page 6). The Haag-Streit BX900 has no measurements for the lightintensity and no automatic exposure system. It is therefore useful to take notes in the early stages of using the BX. Downloading images into EyeCap or a suitable image viewer will enable instant evaluation and will enable adjustments to be made that optimise the image. The practical examples will help, but they are only starting-points.
It should also be considered that the examiner’s attention is focused on the details that are of interest and by selective viewing the brain suppresses certain artefacts. The camera however does not!
TYPES OF ILLUMINATION The correct illumination will allow optimal recording of ocular pathology. DIFFUSE ILLUMINATION The slit lamp beam should be completely opened and covered by the diffusing filter. The background illumination can be used in conjunction with the slit illumination for more uniform lighting. The diffuse illumination is normally used for overview pictures with low magnification (10x and 16x). DIRECT FOCAL ILLUMINATION Direct focal illumination refers to projecting the light on the subject at the plane of focus. Unlike diffused light concentrated light penetrates transparent structures. With a centred slit beam there is always direct focal illumination. INDIRECT ILLUMINATION With indirect illumination the light does not fall directly on the pathology. The slit beam is decentred and projected just adjacent to the subject area and it is illuminated by scattered internally reflected light.
RETROILLUMINATION Retroillumination is an indirect illumination too. Light reflected from the fundus or iris illuminates the pathology from behind. If the slit beam is decentred and higher magnification is used, unwanted reflections can be minimised. PHOTOGRAPHY WITH THREE-MIRROR CONTACT LENS OR 90-DIOPTER LENS With these instruments there are more optical interfaces (air / glass and glass / cornea). All interfaces cause reflexes and therefore it is better to take images without the background illumination. Furthermore any scratches or damage to the lens will increase the number of image artefacts. If the space between the diagnostic contact lens and the slit illuminator is very small, the background illumination can be locked in the centre position.
8
STANDARD SETTING The BX900 has many different adjustments and its correct use can give optimal illumination and exposure. It is advantageous to always start with a standard setting and to make adjustments after each image captured. An example for a standard setting is the diffuse illumination: 1. Main switch on, photo control unit POWER ON and camera body on. 2. After waiting a few seconds, set the flash intensity on HIGH. 3. 100% Background illumination 45°Angle between microscope and background illumination Slit beam vertical
Slit beam fully open (slit width and height) Slit beam centred (screw tightened) 100% slit illumination (without filter) Slit beam covered with the diffusion filter Angle between microscope and illumination device 30°–45° Magnification 10x Aperture 4 with a sensor rating ISO 200 4. Define the image field, close the left eye (note the difference between eye-piece and photo tube picture) 5. Focus control (eye-piece setting correct?) 6. Capture Image.
ILLUMINATION AND EXPOSURE SETTINGS The following table shows the different settings of illumination and exposure adjustments. This table is also used for practical examples and will give a starting point.
ISO: 200 Flash Intensity: high / normal Background: 100%, 50%, 25%, 10%, 0%, blue filter Angle: 0° – 90° Slit Beam: 0 (= closed) to 8 mm (= full open) Filter: blue, red free (green), grey (10% N. D.), diffused Angle: 0° – 90° Magnification: 10x 16x 25x 40x Aperture: 1–5 1–5 1–5 1–5
PICTOGRAMS Background Illumination:
Moderate Slit Beam:
Slit Beam with Diffused Filter:
Wide Slit Beam:
Slit Beam Centered:
Slit Beam Decentered:
Narrow Slit Beam:
Microscope:
9
OVERVIEW DIFFUSE ILLUMINATION WITH SLIT ILLUMINATION AND BACKGROUND ILLUMINATION
The diffuse illumination with slit beam and background illumination gives a shadowfree illumination with natural colours and two light reflexes. This is most useful for low magnification overview images.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 100% 30°–45° fully open diffused 30° 10x 16x 4 4
25x 3
40x 2
200 high 100% 30°–45° closed – – 10x 16x 4 3
25x 3
40x 2
DIFFUSE ILLUMINATION WITH BACKGROUND ILLUMINATION ONLY
The diffuse illumination with only the background illumination increases the contrast. The structures of the iris are more visible and there is only one light reflex.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
10
LIDS DIFFUSE ILLUMINATION
Diffuse illumination provides evenly balanced lighting.
CONJUNCTIVA
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 low 50% 30°–45° fully open diffused 30° 10x 16x 4 4
25x 3
40x 2
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 low 50% 30°–45° fully open diffused 30° 10x 16x 5 5
25x 4
40x 3
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 25% 30°–45° 0.1 mm – 45° 10x 16x 3 2
25x 2
40x 1
DIFFUSE ILLUMINATION
Diffuse illumination provides evenly balanced lighting. Exposure control is more varied due to increased reflectivity.
NARROW SLIT
A centred, narrow slit beam projected at a 45° angle demonstrates surface topography and trans-illumination of the lesion. The background illumination gives the position of the slit beam.
11
INDIRECT ILLUMINATION
A moderately wide and decentred slit beam is projected just adjacent to the border of the lesion. The light penetrates conjunctiva and illuminates the clear fluid below. In the presence of blood or scar tissue, the light is absorbed.
CORNEA
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 10% 30°–45° 2–4 mm – decentred 10x 16x 2 2
25x 1
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 100% 30°–45° fully open diffused 30° 10x 16x 4 4
25x 3
40x 2
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0%–25% 45° open 10% 60°–80° 10x 16x – 4
25x 3
40x 2
DIFFUSE ILLUMINATION
This illumination technique can only be used in the presence of dense corneal pathologies because diffuse light does not penetrate very well through the cornea. Dilating the pupil can enhance pathology by creating a darker background.
WIDE SLIT BEAM – TANGENTIAL ILLUMINATION
This technique can provide more information as the oblique illumination is reflected and refracted by the cornea and any pathology. Experiment with the illumination angle slit beam width for optimum results.
12
MODERATE SLIT BEAM WITH SEPARATION OF ILLUMINATED EPITHELIUM AND ENDOTHELIUM
The moderate beam produces two different layers of illumination, one on the epithelium and one on the endothelium. Note the corneal changes are closer to the posterior reflection and therefore they lie deep in the cornea.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0%–25% 30° 2–3 mm – 45° 10x 16x – 3
25x 3
40x 2
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0–10% 45° 0.1 mm – 45°–60° 10x 16x – 1
25x 1
40x –
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0% – 1–2 mm – decentred 10x 16x – 2
25x 1
40x 1
NARROW SLIT BEAM – OPTICAL SECTIONING
A narrow focal slit beam is projected at a 45° to 60° angle. It cuts an optical section through the cornea like a knife. With this technique it is possible to locate the layer of the pathological changes. These examples demonstrate endothelial and surface pathology.
DIRECT RETROILLUMINATION FROM THE IRIS
A moderate slit beam is decentred and angled to project onto the iris directly behind the pathology. The light reflects and backlights the cornea. If there is some cataract present the lens can also be used to reflect light directly onto the area of interest.
13
INDIRECT RETROILLUMINATION FROM THE IRIS
The moderate slit beam is now decentred even more and angled to project onto the iris adjacent to the area behind the area of interest. The background is dark and the edges of non-pigmented lesions are well defined by the diffuse light reflecting from the iris.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0–10% – 1–2 mm – decentred 10x 16x – 2
25x 1
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0% – 2 mm – decentred 10x 16x – 2
25x 1
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high blue filter 30° fully open blue filter 60°–80° 10x 16x 3 3
25x 2
40x 1
SCLEROTIC SCATTER
The wide decentred slit beam is projected onto the limbus. The light striking the limbus is internally reflected through the corneal tissue like a fibre optic. Corneal changes or abnormalities can be visualised by reflecting the scattered light. Careful post capture cropping can enhance images.
TOPICAL ADMINISTRATION OF SODIUM FLUORESCEIN
Sodium fluorescein is applied gently to the bulbar conjunctiva. The patient should blink once or twice for the dye to be dispersed over the eye. If the epithelium of the conjunctiva or the cornea is damaged, the fluorescein stains the underlying tissue. The remaining dye fluoresces a yellow green colour when excited by the blue light. Healthy epithelium does not stain. Rose Bengal is a dye that can be used to demonstrate abnormal epithelial cells. The dye is applied like sodium fluorescein and is usually imaged using direct white light.
14
ANTERIOR CHAMBER, CHAMBER ANGLE AQUEOUS FLARE – TYNDALL’S PHENOMENON
Cells, pigment or proteins in the aqueous humour reflect the light like a faint fog. To visualise this the slit illuminator is adjusted to the smallest circular beam and is projected through the anterior chamber from a 42° to 90° angle. The strongest reflection is possible at 90°.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0%–25% 30° 0.1–1 mm – 50° 10x 16x – 1
25x 1
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0% – 2 mm – 10° 10x 16x – 5
25x 5
40x 4
CHAMBER ANGLE – GONIOPHOTOGRAPHY
The desired mirror of the gonioscopy lens is positioned opposite to the area of pathology. A wide slit beam is projected in the desired mirror from a near coaxial position to the biomicroscope. Light reflections can be eliminated by tilting the lens.
15
IRIS, IRIS-ANGIOGRAPHY WIDE SLIT BEAM - TANGENTIAL ILLUMINATION
The wide slit beam is projected at an oblique angle of 80° – 90° onto the iris. This illumination creates strong shadows and the surface texture is enhanced. If the headrest doesn’t allow a wide oblique angle it is sometimes necessary to turn the patient’s head a little away from the light.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0%–10% 45° open – 80° 10x 16x 5 5
25x 4
40x 4
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0%–10% 45° Ø 1–2 mm – coaxial 10x 16x – 2
25x 1
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
800 high blue filter 45° open blue filter 45°–60° 10x 16x – 1
25x –
40x –
IRIS TRANSILLUMINATION
The slit illuminator is positioned coaxially to the biomicroscope and adjusted to provide a small circular beam of light. This beam is projected through the pupil which should be at mid dilation. The light reflects from the fundus and backlights the iris. Normally the iris pigment absorbs the light, but pigmentation defects let the red fundus light pass through..
IRIS ANGOIGRAPHY
The illumination technique of the iris angiography is like the tangential illumination with the background illumination opposite the slit beam. Both slit illuminator and background illumination have a blue excitation filter. The yellow barrier filter is positioned between the magnification changer and the mirror housing. The barrier filter only works on the image from the right eyepiece which is directed to the camera. Control of the focus of the image during the angiography is possible through the left eyepiece.
16
LENS NARROW SLIT BEAM – OPTICAL SECTIONING
A narrow focal slit beam is projected at a 45° angle to the lens as an optical section is made. Because of the problematic depth of field it is not possible to photograph the entire lens section in focus. It is therefore necessary to focus on the anterior or the posterior lens surface.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 25% 45° 0.1 mm – 45° 10x 16x – 1
25x 1
40x –
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 10% 45° 2–4 mm – 45° 10x 16x – 2
25x 2
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 10% 45–60° 2–6 mm – 45°–60° 10x 16x – 2
25x 2
40x 1
MODERATE SLIT BEAM – DIRECT ILLUMINATION
A moderate slit beam is projected at a 45° angle to the lens pathology and is directly illuminated. Dilation of the pupil is required for effective imaging.
MODERATE SLIT BEAM – TANGENTIAL ILLUMINATION
A moderate to wide slit beam is projected at an angle greater then 45 degrees to provide oblique tangential illumination that can enhance detail by providing shadows. Pupil dilation will aid this illumination technique.
17
RETROILLUMINATION FROM THE FUNDUS – RED-REFLEX PHOTOGRAPHY
The slit illuminator is positioned in an almost coaxial position with the biomicroscope. A wide slit beam is decentered and adjusted to a half circle by using the slit width and height controls. The decentred slit beam is projected near the pupil margin through a dilated pupil. Careful composition can minimise the direct reflection.
VITREOUS
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0% – 2 mm – decentred 10x 16x – 2
25x 1
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0%–10% 45° 0.1–1.0 mm – 45° 10x 16x – 1
25x 1
40x –
NARROW SLIT BEAM
Without diagnostic lenses it is only possible to examine and to document the anterior part of the vitreous. Anterior Vitreous pathology can be seen with a narrow slit beam. Only when the dioptric power of the eye is reduced is it possible to focus more posteriorly.
18
FUNDUS CENTRAL RETINA PHOTOGRAPHS WITH THE THREE-MIRROR CONTACT LENS
The posterior pole can be documented with the centre of the three-mirror contact lens. The slit lamp illuminator is in an almost coaxial position. If the slit beam is too wide disturbing light reflections may occur.
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0% – 2 mm 10% 5°–10° 10x 16x – 2
25x 1
40x 1
ISO: Flash Intensity: Background: Angle: Slit Beam: Filter: Angle: Magnification: Aperture:
200 high 0% – 2 mm 10% 5°–10° 10x 16x – 2
25x 1
40x –
CENTRAL RETINA PHOTOGRAPHS WITH A 90-DIOPTER LENS
Diagnostic contact lenses are sometimes contraindicated after intra-ocular surgery. In such cases the use of the 90- dioptre lens is necessary. The handling of this lens is more difficult because there is no physical contact with the eye. A moderate slit beam in the almost coaxial position gives the best results.
Recommended Reading Clinical Slit Lamp Biomicroscopy and Photo Slit Lamp Biomicrography Martonyi, Bahn & Meyer Time One Ink, Ltd. Sedona, AZ This book is currently in revision. An expanded Third Edition is expected late 2005. Copies of the Third Edition and other books of interest to the Ophthalmic Photographer can be found at; http://www.twinchimney.com
Photos by: Cees van Beek Leyenburg Hospital, Den Haag, Netherlands Tarek Shaarawy University Hospiral of Geneva, Switzerland Steve Thomson Haag-Streit, Bern, Switzerland