Slit Lamp And Extra Lecture 4 Theory Flashcards
What filters are there
Cobalt blue light- used with nafl fluoroscein and it excites it illuminating it a green colour, good to identify abnormalities within the corneal epithelium. Blue filter is also good at evaluating fit of gas permeable lenses.
Yellow filter- used to screen out excessive blue light used as well with nafl to make the green even more vibrant helping to detect subtle disruptions
Green filter- for viewing vascularisation of the cornea, vessels appear almost black under this light
Neutral density- if larger slit heights or widths are used then this decreases the brightness, useful when using volk to decrease light= to avoid blinding the px
Red free- enhances contrast between blood vessels and surrounding ocular structures
Diffuser- overall view of anterior eye and adnexa. Useful for photography. Allows you to see cornea under an even illumination
What is slit lamp biomicroscopy used for
Screening eye, fitting of contact lenses, managing posterior and anterior eye disorders, examines posterior and anterior segments of the eye, detects diagnoses and manages progression of ocular diseases.
What do the observation and illumination system have in common
And overall what does the slit lamp consist of
They have a common pivot point
Slit lamp combines a illumination system with a focusable beam and an observation system which is a high resolution microscope to look into.
How to focus the slit lamp
We need a focussed eyepiece. So push them apart and rotate each of them anti clockwise and then look through each one monocularly and place a focusing rod in the centre of the pivot point and rotate each one monocularly till the beam of light hitting the focusing rod becomes clear.
What is the pivot point
How does light shine onto the focusing rod
Where the observation and illumination system pivots
Flat part of focusing rod should be facing the examiner, turn on illumination system and the slit beam should go from the illumination system straight onto the rod.
Describe the eyepieces
2 eyepieces with varying magnification. These can be removed. They come in either 10x or 16x magnification.
What if there is no rod
And what is parallax
Then you can focus it using the parallax method.
Parallax is when objects are moving at a constant speed but appear to be moving a greater amount if they are closer to the observer than at a distance.
How to focus it using the parallax method
Rotate light from the illumination system left or right whilst using a flat background eg the bridge of someones nose, or a flat box on pxs head.
Eyepiece should be focused at the centre of rotation
To find this centre of rotation push the slit lamp back and fwds whilst rotating it left and right till achieve parallax movement= constant speed.
If you go too far in= with
Too far out=against
Where does illumination usually come from
And how can we achieve a sharp edge using what-
Illumination usually comes from above and reflects off a mirror into the eye. This creates an image for the observation system. Using a condensing lens creates an aerial image between the slit lamp and the examiner.
We can achieve a sharp edge by using a physical aperture and an optical system
What can we do to the slit lamp slit
The slit beam can be varied in height width angle and intensity by using the rheostat voltage dial
When you widen beam make sure to reduce illum of rheostat to avoid blinding the px
Describe the observation system
What does it have to change mag
Describe eyepieces and what can we do to them
Turret to modify the magnification. (6.3x, 10x, 16x, 25x, 40x)
Flipper for 1x/1.6x mag
Has various mag systems (biomicroscope has parallel eyepieces)
Eyepieces can be interchanged to increase mag to 10x or 16x
Reticle can be added to assess ocular structure, size and shape= Measurement device which needs to be calibrated
Describe the illumination system
It has a lever to change the slit height and this varies on diff instruments, some may be a dial
Lamp slit height and filters
Use it to monitor progression of pathology
Slit height can measure tear meniscus height
Endothelial polymegathism
What can practitioners do with these 2 systems
Practitioners can manipulate these 2 systems to achieve 6 main methods of slit lamp examination
BIO advantages
What can you see with BIO
Increased detail of fundus compared to direct
Stereoscopic view so can see disc cupping, raised lesions, retinal tears, sub retinal neovascular membrane, any feature w height or depth
Wide fov
Rx doesnt affect magnification
Media opacities dont affect mag so sharper image as image is formed anterior to the eye
Greater wds but this varies with power changing
BIO disadvantages
Px often needs dilating (mydriatic= tropicamide) or sympathomimetic (phenylephrine) which can cause blurred vision or photosensitivity. Note pre and post IOP measurement in case of acute glaucoma
V bright light so discomfort- no viewing over 40 seconds
Less portable
Requires additional lenses
Difficult to master
Expensive
Horizontal and vertical Diplopia- adjust headset for head mounted BIO