Week 13 - Paediatric patients Flashcards

1
Q

When should children be managed soley by an Optometrist in community:

A
  1. Normal VA
  2. Normal Fundus examination
  3. Normal binocular status

• Fully accommodative esotropia
• Anisometropia with Normal VA (under age 8)
• Anisometropia, strabismus and amblyopia following discharge from HES
• Anisometropia with amblyopia in children over age 8
• Cosmetically acceptable strabismus with amblyopia over age 8
• Minor eye conditions within your area of competence and confidence

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2
Q

When might children be managed solely in HES

A

• Amblyopia and are under age 8
• Strabismic and need surgery or botox I
• Congenital ocular anomalies
- Ocular disease requiring treatment/monitoring beyond the scope of optometric practice - e.g. vernal keratoconjunctivitis, rare congenitial conditions
- Which require surgery e.g. congenital cataract
- Which require amblyopia therapy e.g. optic disc hypoplasia, congenital cataract, albinism
• If they have additional support needs - may attend HES / a specialist service (e.g. in Glasgow in one of the Child Development Centres, or GCU additional needs clinic)

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3
Q

When they may be co-managed with an orthoptist in the hospital and an optometrist in practice.

A

• In some areas all children being seen at HES are co-managed with community optometrists
• If VA at visual screening is borderline. 0.1 to 0.2 LogMar
• If patient is receiving amblyopia treatment and there is not optometric capacity available at the hospital

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4
Q

Responsibilities when co-managing with an orthoptist

A
  • Cycloplegic refraction - with the appropriate cycloplegic agent
  • Ocular examination - using an appropriate technique
  • Other tests you deem appropriate
    • If patient is discharged from HES they ARE NOT under the care of HES anymore and duty of care lies with you
  • You need a full GOS test and are your clinical responsibility
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5
Q

Responsibilities when testing children under GOS: Supplementary eye exam

A

• 2.0 Cycloplegic Refraction
- For when you have carried out a GOS exam and deem a cycloplegic refraction to be clinically appropriate
• 2.1 Paediatric Review within 12 months
- Used for children who require follow up following a primary exam
~ Amblyopia
~ Binocular Vision Anomaly
~ Reduced Stereopsis
- Including appropriate follow up tests

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6
Q

Responsibilities when testing children under GOS: Enhanced supplementary eye exam

A

• 4.1 - Paediatric Review (with dilation/cycloplegia that does not follow a primary eye examination)
- This code is to be used to review a child within 12 months of a primary eye examination, as judged clinically necessary, and dilation/ cycloplegia is required.
• 4.6 - Enhanced supplementary Sight test for patient under age 16 referred from the hospital eye service
- Referred for a cycloplegic refraction and internal and external examination

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7
Q

Full paed assessment:

A

• Relevant History and symptoms
• Vision
• Binocular status
• Pupil Reflexes
• Ocular Motility
• Refraction
• VA
• Ocular examination
• Visual Fields
• Other tests you feel are appropriate

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8
Q

Differences needed for a paediatric H and S

A

• How are they managing at school at home? Any tasks they struggle with? e.g. smartboard at school, reading at home?
• Ask about birth history
• History of strabismus/amblyopia/refractive error
• Medical History
- Down’s syndrome, Marfan’s syndrome
- Did they reach developmental milestones at correct age e.g. crawling, smiling, walking and talking
• Family ocular/medical history
• Allergies?

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9
Q

Measuring Vision:

A

• Age 1 - 3years Cardiff Cards
• 2 - 4 years Kay’s Picture test Crowded LogMar
• 3-4 - 8-10years Keeler Crowded LogMar letter test or Sonksen Crowded LogMar test
• Thomson test chart has crowded LogMar chart and a crowded Kays picture chart - make up your own identification chart and laminate it!

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10
Q

Kays Pictures

A

Normative values for children under 4 years of age are:
• Uniocular acuities of 0.100 LogMAR (6/7.5 Snellen) or better with an intraocular difference of no more than 0.050 LogMAR (two pictures).

Normative values for children aged 4+ years are:
• Uniocular acuities of 0.050 LogMAR ( 6/6-2 Snellen) or better, with an intraocular difference of no more than 0.025 LogMAR (one picture).

• If either eye is 0.200 or less then referral should be considered
• An intraocular difference of 0.100 may be indicative of mild amblyopia,
• An intracular difference of 0.200 should warrant referral

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11
Q

Tests for children Binocular vision status:

A

• Appropriate test very much dependent on patient age and cooperation Ideally
- Cover test with and without Rx - try using your hand instead of the occluder for young children
- Ocular motility - may have to ask mum to hold their head and you shine a light peripherally and check if corneal reflexes are symmetrical
- Stereopsis - chose an appropriate test and know what normal and abnormal values are for that test - beware of TNO

• Other tests which may be useful if cooperation is poor or attention is limited
- Check corneal reflexes - 1mm deviation of corneal reflex = 10^ deviation
- Objection to occlusion
- 20 A base out test

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12
Q

Management of Common Binocular Vision Disorders

A

• If under age 8 and you detect a strabismus which is not fully accommodative and has not been seen at ophthalmology before refer
• If patient over age 8 or has been discharged from HES you may manage in the community
• Refer if amblyopia suspected and within visual plasticity period
- e.g. a decrease of 0.2 LogMar compared to age matched normal, or an interocular difference of 0.2
- e.g. over age 4-5 refer if VA worse than 0.2 LogMar either eye
• Nystagmus which has not previously been investigated refer to ophthalmology to ensure no pathological cause

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13
Q

Refraction on child:

A

• Cycloplegic or non-cycloplegic refraction
• Mohindra’s technique

• Cycloplegia required
- First visit to your practice
- All children under age 8
- Under age 8 with significant refractive error
- Suspicion of latent hyperopia at any age
- Reduced VA
- All children with evidence of strabismus - even if VA appears normal

• Cycloplegia may not be required
- Children age 6-8 who have had a cycloplegic refraction in the past and are cooperative i.e. can answer questions during subjective refraction well
- Older children
- Myopia over age 8

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14
Q

Prior to cycloplegic refraction

A

• Give patient information leaflet to parents
• Discuss effects of the drops and how long the effects will last and potential side effects
• Obtain parental consent (often this is now written consent) prior to administering the drops

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15
Q

Drug used for refraction of paed + contraindications

A

• Cycloplegia
- Cyclopentalate 0.5% for under age 1
- Cyclopentalate 1% for age 1-8
- 0.5% can be used in older children age 12/13…. If light irises
- If poor VA, patient has very dark irides and insufficent cycloplegia with 1% then refer to HES for atropine refraction
- No published evidence that 2x1% cyclopentalate leads to more effective cycloplegia than 1%

• Contraindications
- Children with Down’s syndrome - high proportion of heart defects
- Children with congenital heart problems

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16
Q

Helpful tips on cycloplegic refraction in children:

A

• Bracket!!!!!
• Speed is of the essence
• Don’t worry about distance fixation too much - they should have little residual accommodation if cycloplegia has worked well
• Make sure you are on axis
• Make it into a game - have mum holding a toy near your head to keep their fixation
• Be as accurate as possible - but sometimes you have to prescribe your best estimate based on bracketing

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17
Q

When to prescribe for paed:

A

• VA reduced
• Significant Refractive error
• Strabismus and significant refractive error present
• Amblyopia and significant refractive error

• If you find significant refractive error and you need to refer for strabismus and or amblyopia prescribe full plus Rx prior to referral to improve the visual outcome

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18
Q

Normal levels of hyperopia in infants?

A
  • 3 months = +2.16 ÷ 1.30 D (mean + sd)
  • 1 year = +1.46 ‡ 1.01D (mean + sd)
    • Be very cautious about prescribing spectacles below age 1 as emmetropisation is taking place
  • Balance up the need for a clear image to aid normal visual development with the possibility of disrupting emmetropisation
  • The kinds of prescriptions which should be prescribed for are:
    : highly hyperopic infants e.g. +8.00 to +10.00,
    : infants with infantile esotropia and a hyperopic Rx
    : highly myopic infants -5.00 plus (under correct by 2D as emmetropisation can occu myopes)
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19
Q

What is Significant Refractive error based on age?

A

• Age 2-5
- Prescribe for hyperopia ≥ +3.50DS if assymptomatic
- Prescribe for myopia >-2.00D (reduce by 0.50-1.00D until school age)
- Prescribe for astigmatism ≥ 1.50DC

• Age 5 plus
- Hyperopia > +1.50DS
- Myopia > -0.50DS prescribe full correction if improves VA
- Prescribe for astigmatism ≥ 0.75DC

• Anisometropia
- ≥1.00D if aged 1-8 and anisometropia is presistent after 4-6 months

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20
Q

Ocular examination:

A

• Use the best techniques available.
• Ideally slit lamp assessment of anterior chamber on older children - especially if you suspect a problem, kids can stand or kneel!
• Ophthalmoscopy assessment of anterior segment in younger children… if possible
• Posterior segment
- Headmounted binocular indirect with a 20 or 30D Volk lens gives the best stereoscopic view on young children
- Can also use direct opthalmoscope with 20D lens
- Direct ophthalmoscopy, if no 20 or 30D and too small for conventional slit lamp bio
- Slit lamp bio for older kids

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21
Q

Ocular exam: 20D vs 30D

A
  • 20D smaller field and more magnified image than 30D
  • 20D great for children with better concentration but still not able to sit at a slit lamp
  • 30D great for babies and children with poor concentration
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22
Q

Visual Fields

A

• Strategy dependent on patient age
• Saccadic Vector Optokinetic Perimetry - ideal for children but not widely available
• Face outline for you babies toddlers, ideally monocular but may need to be binocular
• Confrontation for children age 4-8/10 - ask how many fingers seen each quadrant, monocular
• Standard automated perimetry for children age 8-10+ e.g Humphrey C40

23
Q

Other tests to consider:

A

• Colour Vision
• Fundus Photography
• ост
• Pentacam
• Tonometry?

24
Q

Some other considerations

A

• Review for paediatric patients may need to be more frequent if monitoring
VA due to the visual plasticity period
• All children under 16 need to have their glasses fitted by a qualified optometrist or dispensing optician - during your pre-reg you will need you supervisor to supervise these fits
• Make sure your advice to the parents properly explains what they need to do and THE IMPORTANCE OF COMPLIANCE

25
Q

Most common childhood anterior eye conditions

A

• Allergic eye conditions
• Conjunctivitis
• Chalazion/Hordeolum
• Cataract

26
Q

Allergy treatment

A

• Need to be extremely careful with your treatment regime
• Prescribe only within licensing laws
• Systemic antihistamines -
- loratidine/claritin licensed from age 2
- piriton/chlorphenamine licensed from age - Sodium cromoglicate - no minimum age for generic (POM), but for opticrom (P)!

27
Q

Most common type of infection in babies

A
  • Chlamydia trachomatis incubation 5-14 days
  • Neisseria gonorrhoeae incubation 2-5 days
    • Management - Urgent referral to ophthalmologist due to risk of sight threatening sequelae and need for systemic treatment
28
Q

Gonorrhoea: Onset, presentation, gram stain, treatment

A

Onset: Hyperacute (1-3 days)
Presentation: Severe purulent discharge keratitis, can progress quick to cornea presentation
Gram stain: Gram -ve,
Treatment: Ceftriaxone 50mg/kg x 1 week, saline irrigation

29
Q

Chlamydia: Onset, presentation, gram stain, treatment

A

Onset: Subacute (4-28 days)
presentation: Mucopurulent discharge papillae, +/- preseptal cellulitis
Gram stain: Chlamydia inclusion bodies, immunofluorescence
Treatment: Etythomycin 25mg/kg x 2weeks

30
Q

Two most common conjunctival infections in children:

A
  • Bacterial conjunctivitis (often gram positive organisms)
  • Adenoviral conjunctivitis
31
Q

Hordeolum and chalazion:

A

• Hordeolum: Infection of glands, redness and tender
- Internal : Meibomian glands
- External : Stye; Gland of Zeis or Moll

• Chalazion: Sterile chronic inflammation that results from blocked meibomian gland, hard and non-tender
- May develop from internal hordeolum

32
Q

Management of Chalazion/hordeolum:

A

• Management Chalazion
- refer if not resolving, recurrent or if inducing astigmatism
- most often self resolve, treat any associated blepharitis and advise hot compresses
• Management Hordeolum
- Normally hot compresses and lid hygiene
- May prescribe topical antibiotics if copious micropurulent discharge - be careful of patient age!

33
Q

Describe congenital cataract:

A

• 1 in 3000 live births
• Congenital cataracts normally spotted at new-born screening, however cataract can also develop through childhood
• High risk of amblyopia with significant cataracts which develop before age 6-7, especially if unilateral

34
Q

Cataract Symptoms and signs

A

Symptoms
- Undiagnosed cataract may present with
• Strabismus
• Nystagmus
• Clumsy behaviours

Signs
- Cataract visible on retinoscopy
- Childhood cataracts vary in appearance and have a different appearance to age related cataracts

35
Q

Cataract management:

A

• urgent referral if not previously diagnosed in an infant
• If discharged from HES refractive correction
- IOL then need multifocal lenses (but only in eyes with lOL if unilateral)
- If cataract in situ then full refractive correction and assess accommodative function

36
Q

What important signs seen in a childs eye would indicate a problem?

A

• White reflex: think retinoblastoma/cataract
• Squint: ? underlying eye disease or nerve palsy
• Large eyes or foggy corneas: think glaucoma
• Unhappy child with watery eyes: think glaucoma
• Swollen eye with reduced movement: cellulitis
• Purulent conjunctivitis in an infant: gonorrhoea/chlamydia

37
Q

Most common childhood posterior eye conditions

A

• Optic Disc Hypoplasia
• Ocular Albinism
• Foveal hypoplasia
• Retinopathy of Prematurity
• Autosomal dominant optic atrophy

38
Q

5 most common causes of childhood blindness in USA

A
  1. Cortical Visual Impairment
  2. Retinopathy of Prematurity
  3. Optic Nerve Hypoplasia
  4. Albinism
  5. Optic Atrophy
39
Q

Childhood posterior eye conditions

A

• Tilted and torsional optic discs
• Optic disc hypoplasia
• Optic disc coloboma
• Optic disc drusen
• Autosomal dominant Optic Atrophy
• Papilloedema
• Retinoblastoma
• Retinal Dystrophies
• Albinism

40
Q

Describe optic disc hypoplasia

A

• Diminished number of nerve fibres in the optic nerve
• Relatively rare
• Unilateral or bilateral

• Linked to teratogenic agents
- Agents which the mother is exposed to during pregnancy which can cause birth defects
- Quinine, PCP (Phenylcyclidine), LSD, Cocaine, Heroin, Alcohol, Dilantin, Maternal diabetes

• Numerous systemic associations
- Septo-optic displasia
- Developmental midline brain defects
- Pituitary and hypothalamic defects

• Ocular associations
- Aniridia, VF loss, foveal hypoplasia, microphthalmos and AMBLYOPIA

41
Q

optic disc hypoplasia: Symptoms and Signs

A

• Symptoms
- If severe can present with roving eye movements nystagmus in infancy
- If unilateral, or less severe may present with strabismus or decreased VA at visual screening
- Mild cases may be asymptomatic

• Signs
- VA from normal to LP
- An RAPD if unilateral and severe and sluggish pupil responses bilaterally if both discs severely hypoplastic
- Smaller than normal disc - measure using slit lamp if possible
- A foveal to disc centre which is three or more times the disc diameter highly suggestive of hypoplasia

42
Q

Optic disc coloboma:

A

• Congenital, non progressive, unilateral or bilateral
• In more pronounced cases may affect ability to meet visual field driving standard

43
Q

Optic disc drusen

A

• Often first noted in childhood
• In younger children are often buried and may present as pseudopapilloedema
• In early teens drusen often become more visible as pearly raised areas on the disc
• Can cause visual field loss which may be progressive, but is rarely sight threatening

44
Q

Optic disc drusen: Management

A
  • Assess automated visual fields for progression where possible
  • OCT to assess/monitor RNFL and to assess drusen
  • Refer if struggle to tell if optic disc drusen or papilloedema… may wish to discuss with opthalmology urgency of referral based on individual patient circumstances
45
Q

Papilloedema: Symptoms/Signs

A
  • Headache, worse in the morning
  • Nausea and projectile vomiting
  • Diplopia due to 6th nerve palsy
  • Pulsatile tinitus
  • Swollen optic nerve
  • Visual obscuration lasting up to 30 seconds
  • Reduced Vision
  • Absence of spontaneous venous pulsation
46
Q

Papilloedema differentisls

A

• Differential diagnosis
- Tilted discs
- Disc drusen
- Peripapillary myelinated nerve fibres
- Crowded discs in hyperopic patients

47
Q

Papilloedema: diagnostic techniques

A
  • Papilloedema
  • A normal neurological examination aside from 6th cranial nerve palsy
  • Normal CSF composition associated with an elevated opening pressure (>250 mm CS in adults and > 280 mm CSF in children)
  • Neuroimaging (MRI typically, or CT if MRI is contraindicated) showing normal brain parenchyma and no evidence of mass or structural lesion, hydrocephalus, or meningeal enhancement
  • In the absence of papilloedema, a definitive diagnosis requires a 6th nerve palsy
  • In the absence of papilledema and a 5th nerve palsy, a suggestive diagnosis requires 3 of 4 neuroimaging findings
  • A diagnosis is deemed “probable” if all other criteria are met but no lumbar puncture is performed to determine opening pressure
48
Q

Papiloedema: optometrist management

A
  • Emergency referral to ophthalmology
49
Q

Autosomal dominant optic atrophy

A

• Hereditary disorder - most common heriditary optic neuropathy
• Presentation in 1st and Second decade of life with progressive vision loss
• Most patients maintain VA above 6/60
• Colour vision disorders
• VA loss is symmetrical, insidious, slow and gradual
• Typically temporal wedge shaped atrophy but can be diffuse atrophy of the NRR

50
Q

Retinoblastoma; Describe; Signs; Symptoms

A

• Rare childhood condition, however it is the most common ocular childhood cancer. 1 in 18,000 live births
• Can be unilateral (60%) or bilateral

• Symptoms
- White pupil
- Strabismus
- Associated painful red eye with secondary glaucoma

• Signs
- Dome shaped white elevation (s)
- White elevation of the retina which project into the vitreous
- Subretinal mass(es) causing an overlying retinal detachment

• Management: Urgent referral to ophthalmology

51
Q

Retinal dystrophies

A

• Stargardt macular dystrophy
• Best vitelliform macular dystrophy
• Retinitis pigmentosa
• Usher syndrome
• Leber congenital amaurosis
• Bardet-Biedl syndrome

Management: Referral to ophthalmology

52
Q

Types of albinism:

A

OA - ocular albinism
OCA - oculocutaneous albinism

53
Q

Albinism: Signs

A
  • Foveal hypoplasia - lack of an observable foveal pit, or underdeveloped foveal pit
  • Poor VA
  • Translucent pinkish blue irides
  • Nystagmus - typically pendular and horizontal
  • Lack of fundus pigmentation with visbility of choroidal vessels
  • Abnormal VEP’s as fewer uncrossed fibres at chiasm
  • High RX
  • Strabismus
54
Q

Albinism: Management

A

Management
- Photochormatic lenses for everyday use
- Sunglasses for summer
- Advise use of hats with brim, especially in summer
- Low vision aids
- Referral to ophthalmology if previously undiagnosed