Cycloplegic Retinoscopy in Infancy
April 22, 2017 | Author: Strauss de Lange | Category: N/A
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Retinoscopy in infancy: cycloplegic versus non-cycloplegic C-18551 O/D
Yeotikar et al.2 evaluated the difference in refractive error in non-strabismic children between the ages of seven years and 16 years, using static retinoscopy
Fabrizio Bonci, Dip. Optom (ITA), MCOptom Luigi Lupelli, Dip. Optom (ITA), FAILAC, FIACLE, FBCLA The assessment of refractive status in very young children is often not conducted in the same manner as for adult patients. In particular, the child’s age, their cooperation and dynamic refractive status will be key factors which influence the accuracy of refraction. For this reason, it is often necessary to choose procedures which inhibit or minimise accommodative activity. This can be achieved by fogging with positive lenses or rousing the tonic (resting) accommodation (dry refraction), or with pharmacological agents (wet refraction). This review article compares the two approaches, focusing on the retinoscopy techniques.
under two conditions – first by fogging the contralateral eye with a positive lens and second with cycloplegia using cyclopentolate 1%. The study found that the average difference in refractive error between these two conditions was only 0.29DS more hypermetropic with cyclopentolate, highlighting the accurate results that can be obtained when there is adequate accommodative control
during
Furthermore,
static
Chan
retinoscopy.
and
Edward3
suggested a calculation which can be
Dry retinoscopy
to download a number of videoclips,
Static retinoscopy
especially
The patient views a distance target (four-
animations. Practitioners should also
six metres) so that accommodation is
consider not using a phoropter or trial
presumed to be static and in a relaxed
frame when conducting retinoscopy
condition. The fixating eye (contralateral
on a very young child, as this can be
to the one being examined) should be
intimidating for the child. It is preferable
adequately “fogged” with a positive lens
to use single trial lenses or a lens rack.
(resulting in an “against” movement seen
Speed during retinoscopy is essential
on the retinoscopy swipe).1 For children,
when performing this technique in
maintaining fixation at this distance
young
can be difficult and new computerised
maintain fixation only for very short
test charts generally provide dynamic
periods of time. In cases of fluctuation of
Mohindra retinoscopy
and more interesting targets to view
accommodation, the practitioner should
The Mohindra technique, also known
than a standard spotlight (Figure 1)
follow the “with” movement, ignoring the
as near retinoscopy or near monocular
to help with this. It is also possible
occasional “against” movements seen.
retinoscopy, carries the main advantage
cartoons,
children,
with
especially
different
as
they
used to match the dry retinoscopy result to that which would be obtained using cyclopentolate 1%, in children between 3.5 to five years of age. The astigmatic component is kept the same whilst the spherical component found in both meridians is multiplied by 1.45 and a value of 0.39D is added. However, this depends on an accurate static retinoscopy result having been obtained.
of being child-friendly and requiring less co-operation from the child.4 In this case, the stimulus is the dimmed light source of the retinoscope in a darkened room. The darkness of the room will facilitate the child to keep their attention on the retinoscope’s
light.
The
retinoscope
is held at a distance of 50cm (errors in distance are not clinically relevant), with hand-held trial lenses used to find
Figure 1 Examples of exciting targets presented by computerized test charts during retinoscopy. Different face expressions allow to the practitioner to talk to the child to maintain attention on the target (Courtesy of Thomson Software Solutions, UK).
49
the neutral point. The accommodation activity during the examination is small and the same in both eyes. It is important during the examination to keep the light of the retinoscope on the child’s pupil
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(to see the retinal reflex) for only a short
which can be uncomfortable, or even
period of time so as not to stimulate
distressing, for the child. This is notably
accommodation;
the
so because the acidic pH of the cycloplegic
optometrist’s attention should be focused
agent leads to stinging on instillation.
on the pupil, watching for maximum
Some practitioners advocate the use of a
dilation (indicating no accommodation).
5
local anaesthetic prior to instillation of
The procedure should be carried out
the cycloplegic agent; proxymetacaine
subsequently
with one eye occluded, preferably by the parent, while the other eye is evaluated. However, Wesson et al. confirmed that 6
there is no substantial difference in the result if binocular fixation is allowed (Figure 2); indeed this can be useful if the infant is resistant and becomes agitated
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with occlusion. Several people advocate neutralisation
of
the
two
principal
meridians of the eye separately, using loose spherical trial lenses. However, Saunders and Westall confirmed that 7
the accuracy of the technique can be improved using a combination of spherical and cylindrical lenses instead. Once the retinoscopy result is obtained, the refractive error was originally calculated by adding -1.25DS to the gross finding.
8,9
Saunders and Westall7 have reported that the accuracy can be improved if -0.75DS is added instead, for children aged between 0-2 years, and -1.00DS added for those children over two years of age. They also affirmed that the result achieved by the Mohindra procedure in children between six months and four years of age is similar to wet retinoscopy (using cyclopentolate 1% – see later), with a difference of only 0.50DS. Others have reported similar results,
10
and
certainly no differences greater than 1.00DS,
whilst similar results were
11
also obtained for children with Down’s syndrome
12
and
even
in
adults.
13
The Mohindra technique is useful for practitioners in Europe who are not permitted to used cycloplegic agents,
14
0.5% is the drug of choice as it stings less
Figure 2 Mohindra retinoscopy. Hand-held trial lenses are placed in front of both eyes whilst the child fixates the retinoscope light. The procedure should be run in darkened room (the high level of room light in this image was for photographic purposes only). accuracy of results will naturally depend on
the
practitioner’s
experience.16
Control of accommodation in children of pre-school age is more commonly achieved by pharmacological means, cycloplegic
agents
such
as
cyclopentolate and tropicamide; atropine can only be used by therapeutically qualified practitioners. All of these drugs are muscarinic receptor blockers, thus they work by blocking the muscarinic receptors in the ciliary body, which in A
turn
prevents
mydriatic
achieved
effect
by
accommodation. is
concurrently
inhibiting
muscarinic
stimulation of the iris sphincter muscle. An ideal cycloplegic would have no ocular and systemic adverse effects. Also, it should produce a rapid onset of cycloplegia, blocking accommodation completely
for
of
before
time,
an
accommodative studies
have
adequate
period
swiftly
restoring
ability.17
Several
reported
both
ocular
and systemic side effects (especially using atropine) in those children who have in
had
addition
a
cycloplegic to
this is not always recommended due to the risks associated with an anaesthetised cornea. To facilitate the application of
cycloplegics,
cyclopentolate
has
been instilled in spray form onto the eyelashes and the closed upper lid.19 Practitioners should also be conscious of their instillation technique, since different degrees of cycloplegia between
Cycloplegic agents
using
than other topical anaesthetics. However,
expected
refraction, mydriasis
the eyes can occur, especially if the child does not keep their eyes open wide enough and/or if there is significant postinstillation tearing (which is very likely). As such, practitioners can opt to instil the higher concentration of cycloplegic agent and/or instil further drops if regular review (eg, periodic measurement of the amplitude of accommodation) reveals differing levels of cycloplegia. Differences in the main cycloplegic agents are summarised in Table 1. The optometrist should select an appropriate agent considering factors such as the patient’s age and whether they have dark, or light coloured, irides. Adequate cycloplegic effect could be achieved with tropicamide in a teenage patient suspected of having latent hypermetropia, for
example,
whereas
cyclopentolate
is likely to be required for an infant suspected of having an accommodative esotropia. Those with light coloured irides may exhibit an increased response to
drugs
as
compared
with
darkly
pigmented irides, and therefore a lower
and cycloplegia, as detailed later.18
concentration/dose ought to be selected.
repeated use of cycloplegic agents.
Drug selection and instillation
be avoided in children with Down’s
One must remember, however, that the
Cycloplegia is an invasive technique
syndrome or those affected by cerebral
whilst there are benefits for conducting frequent follow-up assessments without 15
Overdose of cycloplegic agent has to
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palsy, trisomy 13 and 18, and other
Mydriasis
central nervous system (CNS) disorders.
Cycloplegia
Agent
Concentration Max effect
Recovery time
Max effect
Recovery time
Atropine
0.5-3.0%
1-2 hours
7-12 days
60-180 min
6-12 days
Cyclopentolate
0.5-2.0%
30-60 min.
1 days
25-75 min
6-12 hours
caused by LSD drugs.20,21 These reactions
Tropicamide
0.5-1.0%
20-40 min
6 hours
20-35 min
4-6 hours
generally occur within 20-30 minutes
Homatropine
2.0-5.0%
40-60 min.
1-3 days
30-60 min
1-3 days
Scopolamine
0.25%
20-30 min
3-7 days
30-60 min
3-7 days
these people, especially children, which causes
stimulation
of
the
medulla
and the cerebral centres, leading to hallucinogenic effects similar to those
after
administration.22
Tropicamide
1% should be considered in these children as opposed to cyclopentolate. Cyclopentolate Cyclopentolate
0.5%
or
1.0%
51
Table 1 Cycloplegic and mydriatic effects amongst the main cycloplegic drugs used in optometric practice
is
commonly used by practitioners as
(cycloplegia) at the 1% concentration.
the refractive examination. This drug is an
the cycloplegic agent of choice for
Although tropicamide is mostly used for
antagonist of the muscarinic acetylcholine
paediatric examinations. The cycloplegia
mydriasis, to examine the optical media
receptors, thus it dampens mediation of
achieved is not too deep, as compared
and the ocular fundus, several studies
the parasympathetic nervous system. As
with atropine, but it is quicker in
have suggested that this drug can be used
a result, systemic absorption of atropine
onset, often achieved after 30 minutes
for a cycloplegic effect.
In particular,
can lead to difficulties with swallowing
from its administration. Recovery of
it is a cycloplegic agent that can at least
food (opposed effects of the vagus nerve),
accommodation is typically between six-
detect latent hypermetropia, for example
inhibition of the salivary glands leading
12 hours after instillation whilst mydriasis
in school children, teenagers and those
to a dry mouth, and reduction of sweating.
resolves by 24 hours after instillation.
in their early 20s, with otherwise normal
Atropine can also increase firing of the
Although full cycloplegia is achieved
refractive status and/or with moderate
sino-atrial node (SA) and conduction
with atropine, the cycloplegic refractive
hypermetropia,
through the atrio-ventricular node (AV)
results obtained with cyclopentolate
during the post-natal period.
36
35
as well as for children 37
In adult
of the heart, leading to tachycardia. It
23
are comparable in “normals”,
high
patients undergoing refractive surgery, a
also
hypermetropic
and
also
study showed no significant difference
which can make breathing difficult.
in
between
Other side effects that have been reported
cyclopentolate
include dizziness, nausea and sensation
those
children24,25
children
with
strabismus.
26,27
cycloplegic
secretions,
tropicamide
months, it is advised that two drops of
1%.38 In the same patients, however,
of
cyclopentolate 0.5% are used as opposed
the study showed that cyclopentolate
reactions of the eyelids and conjunctiva.
to 1%. This is becasue drug absorption
was more effective than tropicamide
Atropine is able to pass through the
through the conjunctival epithelium and
in reducing accommodative amplitude
blood-cerebral-barrier and alter the state
skin is more rapid in infants compared
in adult myopes (near-point testing).
of consciousness of the child. Therefore,
to adults,
29,30
due to immature metabolic
and
bronchial
For children under the age of three
28
1%
refraction
decreases
being
unbalanced
and
allergic
in order to minimise the systemic Atropine sulphate
absorption of atropine, the practitioner
This is a natural alkaloid extracted
can gently press the punctum of both eyes
from the deadly nightshade (Atropa
and keep the patient’s head tilted back.
belladonna) plant. Its administration
A
is justified in children of pre-verbal
cycloplegic
psychosis and visual disturbances.
age or when other cycloplegic agents
2%
fail to produce a satisfactory level of
between the ages of four and 10 years by
Tropicamide
cycloplegia. Atropine is administrated
retinoscopy and automated refraction.
This is an anti-muscarinic drug with
three times a day during the three days
As expected, the study reported that
short-lasting
pupil
before the eye examination. Associated
homatropine produced a significantly
accommodation
mydriasis decreases in two weeks after
lesser cycloplegic effect than atropine,
enzyme systems in neonates and young children, which may prolong the effects of the drug.31,32 The main side effects of cyclopentolate include incoherent speech, hallucinations and disorientation, 33,34
(mydriasis)
effect and
on
on
the
recent
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and
study39 efficacy atropine
compared of 1%
the
homatropine in
children
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with residual accommodation being
anterior chamber (especially with
should remember that autorefractometry
greater
cyclopentolate)
and
vs.
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(1.80±0.40D
3.10±0.50D
with
with
atropine
videorefractometry,
although
useful as a guide and screening tool,
homatropine;
p
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