Unit 3 Ocular Examination Flashcards

1
Q

why/when do we test colour vision

A

 Careers – Police, Armed Forces, Pilots, Electrical engineers
 Educational – Chemistry, Geography, History
 Safety – Traffic Light, Electrical Wiring, Electronic PCBs
 Acquired CVDs

  • Around 8% of the male population have a red-green CVD i.e. 1 in 12
  • Around 4% of the female population have a red-green CVD i.e. 1 in 200
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2
Q

what is the genetic of a red green CVD

A

 The gene which causes inherited red/green defects is only found on the X chromosome
 Red/green CVDS = X-linked recessive
o Males XY= one altered copy is sufficient to cause CVD
o Females XX = mutation must occur on both copies of the gene
o This is why males are affected by X-linked recessive disorders much more frequently
o There is no male-male transmission (mother must be at least a carrier)
o 8% male’s vs 1 in 200 women
o Colour blind father & mother not a carrier = no colour-blind sons & 100% daughters’ carriers
o Normal father & carrier mother = 50% colour blind son & 50% daughter carrier
o Colour blind father & carrier mother = 50% colour blind son & 50% daughter carrier/50% daughter colour blind
o Normal father & mother colour blind = 100% sons colour blind & 50% daughters’ carriers

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3
Q

tritan congenital defects

A

 Blue/yellow defects (tritan) CVD has an autosomal dominant inheritance
o One mutated copy of the gene is sufficient to cause CVD
o Encoded on chromosome 7
o Are not sex linked – affect men & women equally
RARE

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4
Q

 Monochromacy

A

monochromats = typically totally colour blind, single functioning cone
o Rod monochromat (rare 1 in 30,000) – truly colour blind, no functioning cones VA ~6/60
* Reduced VA
* Photophobia
* Nystagmus
o Cone monochromat (rare 1 in 100,000) – only 1 functioning cone, VA ~6/9

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5
Q

Anomalous trichromacy

A

anomalous trichromats = have all 3 cone pigments, however one cone pigment is anomalous having a shifted peak sensitivity

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6
Q

Trichromacy / trichromats

A

normal CV

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7
Q

Protan CVD - red = long = 700nm

A

o Protanopia – L wavelength cone missing
o Protanomaly – L wavelength cone is anomalous/reduced sensitivity

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8
Q

Deutan CVD - Green = medium = 540nm

A

o Deuteranopia – M wavelength cone missing
o Deuteranomaly – M wavelength cone is anomalous/reduced sensitivity

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9
Q

 Tritan – blue = short = 490nm

A

o Tritanopia = S wavelength cone missing
o Tritanomaly = S wavelength cone is anomalous/reduced sensitivity

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10
Q

how should acquired CVD be tested

A

 City should be used as it is sensitive to blue-yellow defects
 Monocular testing – may be unilateral or bilateral/asymmetrical
 Secondary to pathology both ocular and systemic disease
 Associated with loss of VA and VF

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11
Q

types of CVD acquired

A
  • Type 1 (similar to protan) – Red/Green – found in macular
    dystrophy/hydroxychloroquine retinal toxicity (rheumatoid arthritis)
  • Type 2 (similar to deutran) – Red/Green – found in retrobulbar optic neuritis
    (common with ON defect)
  • Type 3 (similar to tritan) – Blue found in many central and peripheral retinal
    lesions and lesions of the visual pathway – POAGlaucoma, AMD, DR, cataract
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12
Q

how should ishihara be used

A

 A Confusion test used to screen for protan and deutan (R-G) CVDs
o No blue/yellow plates
 38 or 24 plate version, does not grade severity – pass or fail basis
 38 – three fails = pass
 24 – two fails = pass
 Should be used @ 30- 75cm (at WD)
 Plates should be illuminated by daylight/artificial daylight, illuminant C or D65 luminance in the range 250-600 lux
 4 seconds per plate
 Px must have a VA of at least 6/24
 Colour normal will make immediate decisions, CVD takes time to use brightness cues

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13
Q

classification plates

A

o Used to differentiate protan from deutan and employ a vanishing design set on a neutral background
o 2 digits one made up in reddish dots – lies on protan isochromatic confusion line, one in purple which lies on deutan isochromatic confusion line

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14
Q

City CV test

A

 Three editions – edition 3 in practice
 This is useful for acquired CVD and to grade the severity of a congenital defect
 Confusion test – used for classification
 Subjects select the peripheral colour that looks closest to the central spot
o 3 peripheral colours are isochromatic confusions with central spot, the fourth colour is the next colour in the D15 sequence
 4 screening plates
 6 detection plates
 Classification based on number of errors
o Includes 4 screening plates, but screening efficiency not known and probably not good – of px sees 10/10 or 9/10 different colour spots then it is normal
o 6 classification/grading plates – only 4 plates are equivalent to the 2nd edition

 Advantages = available in book form, not available online so px can’t practice
 Disadvantages = px can give mixed response (go for the majority), protan classification poor due to brightness cues, different pages have different classification efficacies.
 Use @50cm

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15
Q

Farnsworth D15

A

 15 loose caps, on fixed cap/reference cap in the box
 Colour confusion test (based on isochromatic confusion lines)
 Caps have approx. equal hue differences, colours lie on isochromatic confusion lines
 Not a screening test
 Pass and fail criteria varies;
o 1 minor error (transposition of adjacent caps permitted
o 1 major error (isochromatic confusion) permitted
o 2 major errors (isochromatic confusion) permitted

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16
Q

Farnsworth 100 hue

A

 Colour matching / hue discrimination test
 Developed for vocational use
 CVD classified from position of errors, does not reliably identify mild CVDs
 TES is calculated, perfect observer error score = 0

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17
Q

HRR cvd TEST

A

 Out of print now
 Pseudoisochromatic plates, similar to ishihara
 Uses shapes, can be useful in children

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18
Q

CAD CVD TEST

A

 Computer-based test
 New approach to CV assessment, by isolating the use of colour signals in the eye
 Detects acquired & congenital; protan/deutan/tritan – provides automatic classification
 100% sensitivity & specificity – picks up on very low levels of colour deficient
 Provides automatic outcome report based on CAA / FAA reports

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19
Q

Anomaloscope

A

 Based on a colour match
 Two different light sources must be matched to the same colour

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20
Q

Vocational standards CVD

A

Police Scotland
o Monochromats rejected
o Mild anomalous trichromats acceptable and treated as normal
o Severe anomalous trichromats and dichromats also acceptable and are to be instructed in coping strategies
o Applicants who show lowered discrimination for blue colours are to be referred to an ophthalmologist for further assessment. This must include a measure of their dark adaptation performance.

Army/RAF/Navy
o Ishihara normal

Fire services
o Minimum standard – pass Farnsworth D15
o Monochromats & dichromats = not accepted
o Anomalous trichromats = occupational testing

Electrical engineers
o No more than two incorrect plates with ishihara
o Holmes-Wright or Giles-archer lantern test
o CAM lantern

Pilots
o Ishihara – 24 plate, must pass first 16 plates
o Ishihara fail
▪ Anomaloscope – Nagel or equivalent
▪ Colour assessment and diagnosis i.e. CAD test: pass if threshold is < 6 SU deutans / <12 SU for protan

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21
Q

City CVD procedure edition 1 and 2

A

Procedure
* Testing distance: 35cm 2nd edition
* Viewing time: 6 seconds per page
* Complete score sheet for section 1 (out of 6) and section 2 (out of 4)
* Fail if more than 2 mistakes

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22
Q

mode of action anaesthetic

A

Blocks the initiation and propagation of action potentials by preventing
the voltage dependent increase in Na+ via blocking Na+ channels on the nerve cell
membrane. Cationic portion of the Topical Anaesthetic binds causing a physical occlusion
and preventing an axon depolarisation.

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23
Q

uses of anaesthetic

A
  • Anaesthesia prior to contact tonometry
    Þ Goldmann’s or Perkins
  • Anaesthesia prior to foreign body removal
    Þ In either cornea or sub-tarsus
  • Anaesthesia prior to punctual plug insertion or removal
  • Anaesthesia prior to eye impressions
    Þ Scleral Contact Lenses
    Þ Ocular Prosthetics
  • Anaesthesia prior to diagnostic procedures
    Þ Gonioscopy
    Þ Schirmer test
    Þ Pachymetry
  • Irrigation of the eye
    Þ Foreign body removal
    Þ Burns
    Þ Chemical Injuries
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24
Q

Contraindications for Anaesthetics

A
  • Known hypersensitivity
  • Premature babies (don’t have the enzymes to metabolise amides especially)
  • Global penetrating injuries
  • Pregnancy & Breastfeeding
  • Where wound healing would be compromised
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25
perkins calibration
Calibration 1. Take off battery pack 2. Place instrument on its back, with black disc under head of the instrument 3. Place 2g or 5g weight on the probe 4. The probe should lift at 2 and 5. 5. If it does not, compensate by removing/adding the difference. As long as the difference is equal between the 2 and 5g weight, then the instrument can be used.
26
goldmann calibration
1. Place metal rod into the side of the probe 2. The probe should rock at 2g and 6g (first line and second line) 3. Make sure biprism probe is horizontal 4. Slit-lamp should be cobalt blue and wratten 32
27
errors of contact tonometry
* Calibration * Incorrect alignment * lids touching the probe * Quantity/quality of tears, * high astigmatism (distorted mires) * Repeated measurements: reduce IOP – 2-4mmhHg
28
why is only one reading required for applanation tonometry
Goldman/Perkins takes ocular pulse into account, so the reading is an average = only 1 required
29
errors of perkins - high cyls what would be done
 If astigmatism exceeds 3DC: needs to be compensated for as cornea is elliptical  Causes misreading if this is not compensated for  In this instance, the axis of the prism must be set to 43 degrees to the flattest meridian to ensure an area of 7.354mm2 is applanated  This is achieved by aligning the minus cyl axis with the red mark on the cone holder (Goldman) / align with A (Perkins)
30
advise after anaesthetic
 Drops take 60 secs to work  May last for up to 25 mins  Do not rub eyes for at least 30 mins  Avoid getting dust/grit in eyes  Do not reinsert CLs until at least 30 mins post drops instillation  If experience any unusual symptoms (pain/blurred vision), contact practice or seek medical advice  Give leaflet
31
principle of NCT
 Produces applanation using controlled air puff that impinges cornea  Interval of time required for air pulse to produce applanation is proportional to IOP  Requires at least 3 readings to take an average so ocular pulse is accounted for
32
IOPs Factors affecting accuracy
Diurnal variation of up to 5mmHg; lowest in morning, increases throughout day  The fluctuation of IOP with the heart rate, being equal to the difference between systolic and diastolic IOP is the ocular pulse amplitude (OPA)  Stress / apprehension / eye squeezing (increase)  Exercise (increase by up to 50%)  Unstable tear film  Accommodation can decrease IOP by 2-3mmHg
33
SIGN Referral guidelines IOPS
 IOP > 25mmHg – irrespective of CCT  IOP between 21-25– when CCT is <555 (thin) & px 65 or under  IOP < 26 & CCT > or equal to 555 (thick) – MONITOR
34
NICE guidelines
IOP >24mmHg, asymmetry of 5mmHg
35
Risks of anaesthetic
Px may have adverse reaction (RARE) Ocular - Delayed healing & tear flow - Lowering IOP - Increase permeability & compromise integrity of cornea - Desquamation/corneal melt risk if repeated drops instilled (VA suddenly reduces but recovers with artificial tears) Systemic - Light headedness - Tinnitus - Occasional fainting Px may have allergic response (in form of blepharoconjunctivitis)
36
which group of anaesthetics does lidocaine belong to
amide
37
what are included in esters
proxymetacaine oxybuprocaine tetracaine
38
normal VF
 Superior 60 degrees  Inferior 70 degrees  Nasally 60 degrees  Temporally 100 degrees  Blind spot = 15 degrees temporally
39
differnece between supra and full threshold VFs
Supra-Threshold: Tests at a threshold assumed achievable based on px age. * Full-Threshold: Measures the patients threshold, by increasing the brightness until the patient reports that they have seen the stimulus
40
why confrontation with a red target
It may be beneficial to perform the confrontation test with a red target. In chiasmal lesions due to pituitary tumours, colour desaturation occurs across the vertical midline
41
Cecocentral scotomas
Cecocentral scotomas can be caused by damage to the optic nerve or certain areas of the brain, and can be a symptom of a number of conditions, including: Glaucoma Optic neuritis Stroke Tumors
42
adjustments for VFs when VA <6/18
larger target for confrontation, chart 2 for amsler, diamond for Humphrey.
43
pituitary tumour causes which VF defect
bitemporal hemianopia
44
different types of VF test types eg sita fast
 24-2 o 24 degrees from fixation (in 3 directions, 30 degrees nasally) o 58 locations over central 25 degrees, extends 30 degrees nasally, pts are 3 degrees apart o 2 = at each side of horizontal, no points on horizontal midline o Slightly quicker than 30-2 (reduces test time by 25%)  30-2 o 30 degrees from fixation (in 4 directions) o 76 locations over central 30 degrees, pts are 6 degrees apart o Glaucoma, cataract, neurological  10-2 o 10 degrees from fixation o 69 points, 2 degrees apart o Useful for macular investigation  C40 o Central 40 points
45
visual field plot information givne - what does it mean
Reliable: <20% Fixation losses, <20% False Postives and False Negatives Sensitivity Plot – visual threshold level for each tested point measured in Decibel (db) (higher number= more sensitive to dimmer light) Greyscale – visual representation of reduced sensitivity (light colour= high sensitivity and vice versa) 4. & 5. Compares normative data with a person of similar age 6. & 7. looks at focal losses after taking into account general loss due to cataracts etc 8. Anayses symmetry of 5 predefined areas in Superior and Inferior VFs 9. VFI – reflects the Ganglion Cell Loss as a %, 100%= NORMAL 10. Self explanatory
46
what is MD and PSD in VFs
 MD (mean deviation) = mean difference in decibels between the normal expected hill of vision and the patients hill of vision o If deviation out with norm a p value will be given  PSD (Pattern standard deviation) = takes into account generalised loss i.e., overall depression This indicates a deviation in the shape of the hill of vision. It has a positive sign. A low value indicates a normal shape of the hill of vision, whereas a higher value indicates an irregular hill of visio
47
kinetic vs static VFs
 Static o Measures the sensivity of retinal points o Stimulus is stationary, luminance changes o 3D hill of vision  Kinetic o Measures the extent of the VF by plotting isopters o Stimulus moves from a non-seeing to seeing area o 2D measurement of hill of vision o Only done with a Goldmann visual field
48
false negative meaning VFs
* False Negative: Patient doesn’t respond to a brighter stimulus, even though they had already responded to a duller one in the same spot.
49
what does -2 mean in VFs, like in 24-2
“-2” presents the points 2-3 degrees away from the midline, so that the practitioner can more easily discern if the defect respects the horizontal midline.
50
(Right/Left) (Superior/Inferior) Homonymous quadrantanopia types
o Pie in the sky - Meyer’s loop, temporal lobe o Pie on the floor - Baum’s loop, parietal lobe Cause: * Vascular, such as a stroke
51
Binasal Defect causes
Causes: * Compression of temporal nerve fibres * Vigabatrin for Epilepsy * Atheroma of the Internal Carotid Artery
52
What does the G chart on OCT tell us?
G chart represents normative data comparison for Ganglion Cell Complex (GCC). This comprises of the inner most retinal layers (ILM, RNFL, GCL, IPL, INL). The GCC is clinically proven to be the only layers of the retina affected by GLAUCOMA. The S/I shows the comparison between superior and inferior GCC. This plot shows up altitudinal defects and early glaucomatous changes
53
what percentage of dry needs to be used when flashes or floaters
College guidelines state MUST use 1% solution when investigating new onset flashes and floaters.
54
generally how long does anaesthetic last and how long does it take
produces anaesthesia within 1 minute last 15-30mins
55
what is an amide
lidocaine
56
contradindication of tetracaine
not for children if px on sulphonamides (antibacterial type of drug) then cannot use
57
which is the only anaesthetic that could be used for pregnant and lactating
lidocaine and NaFl, have been used for many yrs without apparent ill effects
57
proxymetacaine use cautiously in who
known allergy cardiac disease hyperthyroidism (because of increased risk of sensitivity)
58
ocular side effects of anaesthetic drops
transient stinging (all) transient burning (all) punctate keratitis (all) conjunctival hyperaemia (proxy,tetra) pupillary dilation or cycloplegic effects rarely (proxy) proxy/tetra: severe, immediate type, hyperallergic corneal reactions occur rarely (acute, intense diffuse epithelial keratitis, a grey ground glass appearance, sloughing of large areas of necrotic epithelium) Oxy, lido: hypersensitivity may occur rarely, (allergic conjunctivitis, peri orbital oedema)
59
general side effects of anaethetic
proxy, oxy ,lido - none reported tetra - systemic toxicity mainly involves CNS, systemic effects unlikely with topical application (topical here mean skin)
60
storage of anaesthetics
somewhere dark oxy, tetra, lido - store in <25 degrees Proxy - once opened 2-8 degrees ( in fridge) if kept in room temp then store <25 degrees for up to 1 month
61
before using anaesthetics ask about what
pregnancy and lactating contact lenses (cannot wear for minimum 30mins after) GH and meds (proxy hyperthyroid, cardiac - use cautiously) (tetra - cannot be used if on sulphonamides)
62
which anaesthetic has the least antibacterial action
proxy - good for taking swabs
63
what are the 2 ways to dilate the pupil
1. sphincter pupillae relaxation (tropicamide, cyclopentolate), antimuscarinic sphincter muscle has the biggest effect on pupil size 2. dilator pupillae contraction (phenylephrine 2.5/10%) sympathomimetic
64
topical anaesthetics mode of action
Mode of Action - Blocks the initiation and propagation of action potentials by preventing the voltage dependent increase in Na+ by blocking Na+ channels on the nerve cell membrane. Cationic portion of the Topical Anaesthetic binds causing a physical occlusion and preventing an axon depolarisation
65
typical guidance for percentage of cyclo
child 3 months to 11 yrs - 1% 12-17 yrs - 0.5%
66
atropine poisioning systemic effects
blind as a bat - accommodation paralysis dry as a bone - inhibition of sweat and salivary glands red as a beetroot - dilation of BVs mad as a hatter - CNS effects
67
advise after dilation drops (tropicamide)
Advice: * Cannot Drive 4-6 hours after dilation * Sx of AACG and action required * Dilation leaflet o Practical risk in driving and operating heavy machinery post dilation. o Advise sunglasses due to glare. o concern of inducing an ACG attack (1/5000) but often the risks of not dilating outweigh risks of dilating (VH and IOP). ACG is most likely to occur during the recovery phase of dilation whereby the mid dilated pupil in close apposition to anterior surface of the lens can impeded aqueous outflow
68
systemic effects after cyclo
dry mouth dry skin flushing increased body temp increased heart rate HAs CNS effects - drowsy, hallucinations, drowsiness (young kids and elderly more likely to get side effects)
69
phenylephrine contraindications
GH: aneuryms, thyrotoxicois, caridovascular diseases MEDS: MAOIs, (anti depressants), beta blockers PX age: 10% should not be used in kids or elderly Children & over 65 as increased risk of systemic toxicity * Neonates Cautions: asthma,
70
side effects of phenylephrine
Ocular Side Effects of Phenylephrine * Transient pain (but not as stingy as tropicamide) * Lacrimation * Keratitis * Pigmented aqueous floaters * Rebound miosis * Rebound conjunctival congestion * Conjunctival hypoxia Systemic Side Effects of Phenylephrine * Systemic hypertension * Occipital headache * Subarachnoid haemorrhage * Ventricular arrythmia * Tachycardia * Reflex bradycardia * Blanching of skin