Slit lamp – biomicroscopy of eye

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SLIT LAMP – BIO MICROSCOPY OF EYE By- Dr. Paresh Vijay Nichlani Moderators- Dr. K Srikanth Dr N Swathi

Transcript of Slit lamp – biomicroscopy of eye

Page 1: Slit lamp – biomicroscopy of eye

SLIT LAMP – BIO MICROSCOPY OF EYE

By- Dr. Paresh Vijay NichlaniModerators- Dr. K Srikanth

Dr N Swathi

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NEED OF SLIT LAMP ???

Magnified View Stereoscopic view Quantitative measurement

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EVOLUTION OF SLIT LAMP Purkinje (1823)- One hand held lamp and one hand held lens De Wecker (1863)- mono-ocular microscope Albert & Greenough (1891)- Binocular microscope Czapski (1897)- binocular corneal microscope Gullstrand (1911)- Illumination system with a slit Henker (1916) – Combined the two Hans Goldmann (1933) – Both the lamp and slit beam with

horizontal and vertical adjustment were placed on single stage, Haag-Streit model

Littmann (1950) - incorporated rotatory magnification changer- galilean teliscopee – zeiss slit lamp

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PARTS OF MODERN SLIT LAMP Observation system (Microscope) Illumination system Mechanical system

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BRUSHUP • Ray of light passing from optical center will not be refracted.• Rays coming from infinity ( zero vergence ) will converge to focal point• Rays originating from focus will come parallel after refracting

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OBSERVATION SYSTEM – MICROSCOPE Based on principle of Keplerian

telescope

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OBSERVATION SYSTEM 1. Objective lens – two Plano convex

lens, convexities put together -+22.00 D

2. Eye piece - +10.00 D, Tubes converged at an angle of 10-15 degrees- stereopsis

3. Prisms- rectify problem of inverted image

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GALILEAN MAGNIFICATION CHANGER

Based on principle of Galilean Telescope

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MAGNIFICATION SYSTEM

Haag Streit magnification system- Grenough typeGalilean Magnification changer

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PRINCIPLE OF ILLUMINATION SYSTEM Kohler illumination principle

Converts light source to a beam of homogenous brightness with minimal glare

Advantage is that a very sharp and bright light is obtained

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ILLUMINATION SYSTEM1. Light source – nerst lamp > arc lamp >

Mercury vapour lamp > halogen Lamp> LED lampsIllumination – 2*105 to 4*105 lux

2. Condenser lens – coupled Plano convex lens

3. Slit and other diaphragm – horizontal and vertical diaphragm

4. Filters – cobalt blue filter, red free filter

5. Projection lens - diameter of lens is smaller

- Better quality image- Increases depth of focus

of slit – better optical section.6. Reflecting mirror/ prism – illumination axis

do not obstruct field of vision

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TYPES – LOCATION OF ILLUMINATION SYSTEM

Zeiss Haag-streit

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MECHANICAL SUPPORT SYSTEM

Joystick

Patient support arrangement

Fixation target

Mechanical coupling

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TYPES OF ILLUMINATION Depending upon the structures and

there different optical property we use different types of illumination.

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1. DIFFUSE ILLUMINATIONSettings

- Slit fully opened (annular diaphragm)- Inserted diffuser- Microscope positioned at 0°-Angle of slit illumination system approx. 30° - 50°-Magnification – 5-12x

Uses- general surveys of anterior eye segments- general observation of the surfacesof crystalline lens and cornea- assessment of the lachrymal reflex-assessment of soft contact lenses-It can be used with filters

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Pterygium

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2. DIRECT FOCAL ILLUMINATION• Slit beam is regulated until it coincides with exact focus of the microscope• Settings – Narrow slit at oblique angle (30), slit 2-3mm , 5-45x • 3d layered view

- cornea lens and ant. Phase of vitreous disperse light and gets visible against dark back ground.

• This type of illumination can be used with 3 types of different beam

1. Optical Section2. parallelepiped3. conical beam

effect

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OPTICAL SECTION A narrow slit is focused obliquely 2-

3mm, 30-45, – knife like histological sections of cornea, lens & ant. phase of vitreous

Optical section of cornea – 1.Tear layer- ant. Most bright zone2. Epithelium- dark line3. Bowman’s membrane – bright line 4. Stroma- Wider granular grey zone 5. Descemet’s membrane – bright zone

Uses – 1. corneal curvature 2. Corneal thickness 3. Location of corneal pathology

4. Van Her-rick method of ac depth

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OPTICAL SECTION OF LENS Optical section of lens

1. Ant capsule 2. sub capsular clear zone – c1 3. Bright narrow zone of discontinuity 4.second clear cortical

zone – c2

5.Light scratting zone of deep cortex – c3 6.Clear zone of deep cortex. 7. Nucleus

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Parallelopiped – 2-3mm wide focal slit – used for pathologies on epithelial and stroma

Conical beam- small circular beam – examining aqueous for cells and flares – at 45-60 degrees, at high mag.

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3 INDIRECT ILLUMINATION Slit beam is focused beside the area

to be observed- The axes of illuminating and viewing path do not intersect at the point of image focus.

Angle-60, variable, slit max height

Uses –1. Corneal infiltrates2. Corneal microcytes3. Corneal vacuoles4. Epithelial cells

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4RETRO ILLUMINATION • Light is reflected off from

iris or fundus• system and observation axis

are set to 0°. • it is essential that the pupil is• dilated as otherwise the

resulting relatively small field of view through a normal size pupil makes observation

• almost impossible.

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• Direct- Observer is in direct pathway of light reflected from structure. Pathology- against illuminating background.

• Indirect – observer right angled to observing structure. Not in line with light , Pathology – against dark non illuminated background.

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GRAVES – PATHOLOGY- OPTICAL PROPERTIES

Obstructive- opaque to light- dark against bright background eg- pigments

Respersive- scatter light but do not obstruct – brightly against dark background epithelial edema, precipitates.

Refrectile- distort view as refrective index is different from surrounding. Eg – vacuole.

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5. SPECULAR REFLECTION Reflection accurse – beam of

light incident on optical surface- zone of discontinuity

Observer in path of reflected light – dazzling reflex - specular reflex – dark areas in reflex

Technique – Pt to look 30 degree temporally , light beam focused from opp. side, focused under high magnification, 3-4 mm from limbus- slit is rotated more temporally to about 60 degree (i=r)

Uses – endothelial cell count

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6. SCLEROTIC SCATTER

Uses- outline finest corneal pathology

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COBALT BLUE FILTER This throws a blue

light, Principle – fluorescence

– these substance absorbs light of a colour and then emit a light of other colour in this case it absorbs blue and emits yellowish green.

Uses – corneal ulcer, scidel test etc, tear BUT etc.

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RED FREE FILTER This filter emits green

light – This causes obscure red colour

Blood vessels and haemorrhages appear black

Areas of episclera with lymphocyte appears yellow

Fleischer ring

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ACCESSORY DEVICES Gonioscopy Fundus examination using lens Pachymetry Applenation tonometry Slit lamp photography Slit lamp video graphy Slit lamp – argon, diode and yag laser Others

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WHAT DO WE KNOW?? WHAT WE HAVE LEARNT??

Evolution of slit lamp Parts of slit lamp Optics of slit lamp Uses Types of illumination Accessory devices

The future- dime illumination coupled with electronic light amplification system

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