Slit lamp is the most important equipment in the present day.
Modern slit lamp with its additional device provides qualitative and quantitative measurements and photographic records.
3. INTRODUCTION
In 1911, GULLSTRAND is credited with the invention of slit
lamp.
Slit lamp is the most important equipment in the present day.
Modern slit lamp with its additional device provides qualitative
and quantitative measurements and photographic records.
Qualitative measurements - magnified view of every part of
the eye from cornea to retina.
Quantitative measurement - IOP, endothelial cells counts,
pupil size, corneal thickness, anterior chamber depth.
5. PRINCIPLE
A slit beam of very bright light produced by lamp.
This beam is focused on to the eye which is then viewed
under magnification with a microscope.
8. OBSERVATION SYSTEM (MICROSCOPE)
It is a compound microscope.
It consists of two optical elements i.e. an objective and an eyepiece.
It provides to the observer an enlarged view of a near object.
An objective lens consists of two plano-convex lens, with their
convexities put together, providing a composite power of +22 Dioptre.
An eyepiece lens is of + 10 D.
In slit lamp, uses a pair of prism is placed between the objective and
eyepiece, to re-invert the image.
Prism is used to overcome the problem of inverted image, produced by
compound microscope.
11. ILLUMINATION SYSTEM
Illumination system is provide a bright and fine focused adjustable slit of
light at the eye.
LIGHT SOURCE
CONDENSER
LENS SYSTEM
SLIT &
DIAPHRAGM
FILTERS
PROJECTION
LENS MIRRORS
& PRISMS
14. LIGHT SOURCE
Nitra lamp, arc lamp, mercury vapour lamp and halogen lamp.
It provides an illumination of 2X 10 to 4 X 10 LUX.
CONDENSER LENS SYSTEM
Two plano-convex lenses, their convexities put together.
SLIT AND DIAPHRAGMS
Height & width of slit can be varied by knobs.
It provides, examination of fundus and angle of anterior chamber.
15. FILTERS
Cobalt blue and red free filters.
PROJECTION LENS
It forms an image of the slit.
It keeps lesser the aberration,
better the image quality.
MIRRORS/ PRISMS
Normally arranged vertical axis with either mirror/ prism, reflecting the
light along horizontal axis.
16. MECHANICAL SYSTEM
1. JOYSTICK ARRANGEMENT
2. UP AND DOWN MOVEMENT ARRANGEMENT
3. PATIENT SUPPORT ARRANGEMENT
4. FIXATION TARGET
5. MECHANICAL COUPLING
18. JOYSTICK ARRANGEMENT
Movement of the microscope and illumination system towards or away
from the eye and from side to side is usually achieved.
UP AND DOWN MOVEMENT ARRANGEMENT
It moves the whole illumination and viewing system up and down
relative to chin rest.
PATIENT SUPPORT ARRANGEMENT
A vertically movable chin rest and adjust the height of the table.
19. FIXATION TARGET
A movable fixation target greatly facilitates the examination under some
conditions.
MECHANICAL COUPLING
It not only provides a support but also a coupling of microscope and
illumination system along a common axis of rotation.
20. BEGINNING OF SLIT LAMP EXAMINATION
Examination
should be in semi
dark room
Start with the
diffuse
illumination
Start with the
Low
magnification
Low to medium
to high
Do not use any
medication
21. TECHNIQUE OF BIOMICROSCOPY
The patient should be positioned
comfortably in front of the slit lamp with
his/her chin resting on the chin rest and
forehead against to head rest.
PATIENT
ADJUSTME
NT
The microscope and illumination system should be
aligned with the patients eye to be examined.
The height can be varied using knobs as per patients
height.
Fixation target should be placed at the required
position.
INSTRUMENT
ADJUSTMENT
22. METHODS OF ILLUMINATION
Diffuse illumination
Direct illumination
Indirect illumination
Retro illumination
Sclerotic scatter
Oscillating illumination
23. DIFFUSE ILLMINATION
45 degree angle between light and
microscope
Fully open slit
Diffusing filter
Variable magnification (low to
medium to high)
Variable illumination (medium to
high)
Overall view of - lids and lashes,
conjunctiva, cornea, sclera, iris, pupil
24. DIRECT ILLUMINATION
Vary angle of illumination
Low to high magnification
Vary width and height of light
source
Variable illumination
27. Conical Beam:
Small, bright, circular light
source.
Use with high magnification.
Used for observation of flare
and cells in the anterior
chamber.
28. INDIRECT ILLUMINATION
Observation and illumination systems
are not focused at the same point.
Vary angle of illumination
Slit beam is offset
Vary beam width
Low to high magnification
Valuable for observing: Iris pathology,
Epithelial vesicles, Epithelial erosions,
Iris sphincter.
29. RETRO ILLUMINATION
Vary angle of illumination
Moderately wide beam
Slit beam is offset
Medium to high magnification
The cornea is illuminated by light
reflected from the iris, crystalline lens or
fundus.
Valuable for observing: Epithelial
oedema, Microcysts, Vacuoles,
Dystrophies, lens opacities, Contact lens
deposits.
30. SPECULAR REFLECTION
The angle of incident light is equal
to the angle of reflected light.
Valuable for observing: Endothelial
cells, Tear film debris, Tear film lipid
layer.
31. SCLEROTIC SCATTER
Illumination of the cornea by
total internal reflection of a wide
angle light source.
The light beam is directed at the
limbal region while observing
the cornea.
Valuable for observing: Localized
epithelial oedema, Corneal scars,
Foreign bodies in the cornea.
32. TANGENTIAL ILLUMINATION METHOD
Large angle of 70 - 80属 between
illumination and observation
system.
Valuable for observing: Iris
freckles, Tumours, General
integrity of the cornea and iris.
33. CLINICAL USES
Anterior segment evaluation.
Tear evaluation.
Measures corneal thickness.
Evaluate intra ocular pressure.
Examine angle of anterior chamber.
Removal of foreign particle.
Contact lens fitting.
Evaluation of post fitting contact lens.
Epilation of lashes.