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A
watery eye can be the product of excess tear production (hyper-lacrimation),
disturbed ocular surface tear flow (lid malposition) or disturbed
outflow (epiphora). Occasionally all three mechanisms can be involved.
Epiphora is due to some form of compromised drainage which
may be caused by: a) punctal Plimosis, b) canalicular stenosis and
obstruction or c) naso-lacrimal duct blockage. Obstruction of the
naso-lacrimal duct may be congenital, in which case it is most usually
due to delayed canalization of the valve of Hasner, or it may be
acquired.
In
adults the commonest cause of epiphora is primary acquired nasolacrimal
duct obstruction (NLDO) which is associated with inflammation of
the nasolacrimal duct.
Epiphora
in the presence of a patent lacrimal system to syringing and in
the absence of excess tear production or lid malposition is defined
as functional NLDO.
Management
of less common causes of epiphora such as congenital facial abnormalities
and secondary acquired obstructions am not discussed in this article.
EPIPHORA
IN CHILDREN
Symptomatic
NLDO occurs in approximately 5-6% of infants. A sticky, watery eye
with positive regurgitation on pressure over the lacrimal sac confirms
the diagnosis. Other diagnostic measures such as probing or dacryoscytography
(DCG) may be combined with treatment under general anaesthesia.
As
there is a high spontaneous rate of remission (60-90%) in the first
year of life, probing should be delayed until 10-12 months of age.1,
2 Parents can be instructed to undertake lacrimal sac massage during
the intervening period. Earlier probing is only justified if their
is severe recurrent infection.
Probing
of the naso-lacrimal duct is the first line of treatments However
probe failure increases with age and is known to double every 6
months.1 For this reason and in cases of persistent epiphora, a
second probing two to four months later is advocated. In failed
cases with persistent epiphora and recurrent infection, it may be
necessary to perform a dacryocystorhinostomy (DCR). Alternatively
bicanalicular silicone incubation with Crawford, Juneman or Ritleng
tubes can be carried out with a claimed success rate of 88-95%.4,5
EPIPHORA
IN ADULTS
Causes
of disturbed ocular surface tear flow such as lid malposition (euryblepharon,
punctal ectropion, punctal phimosis) or ocular surface irritation
(dry eye, blepharitis) should be excluded first.
Identification
of the site of the obstruction causing epiphora is most important,
This information has been shown to dramatically increase the chance
of successful tmatrnent.6
INVESTIGATIONS
Identification
of the site of blockage requires one or more of the following tests:
Dye
tests
Two
or three drops of sodium fluorescein are instilled into the lateral
fornix. Dye may drain completely (dye disappearance) and be collected
by a swab at the inferior meatus (Jones I), when the drainage system
is patent. No more tests are necessary at this stage. With compromised
drainage, dye usually overflows medially onto the cheek. In the
presence of lid malpositions it overflows medially, centrally or
laterally, according to the lid position.
The
ocular surface is examined simultaneously. Conjunctival and corneal
staining should be noted to rule out ocular surface disease. On
the whole dye tests are objective and not reliable.
Syringing
and probing
The
lower puncti are gently dilated under topical anaesthesia. Next,
one or two mls of local anaesthesia are injected using a lacrimal
canula. If there is regurgitation, the largest lacrimal probe which
can be inserted without damaging the annulus is used. If it enters
the sac without my resistance, the site of blockage is most probably
NLD. If a site of resistance is noted, the probe is grasped with
forceps at the punctum and withdrawn. The exposed end is measured
to identify accurately the site of the blockage. A smaller sized
probe is then inserted. Resistance at the same site reveals a complete
canalicular obstruction. In the case of stenosis the smaller probe
can be passed through and into the sac. Syringing of the NLD then
follows. The same examination is repeated for the upper puncti.
An experienced examiner can gather enough information at this stage
to plan treatment.
Macro
dacryocystography (MDCG) and scintigraphy
These
further investigations may be used to confirm the diagnosis. MDCG
is particularly useful to reveal details of lacrimal sac anatomy
and the site of nasolacrimal duct obstruction.8 MDCG with a delayed
erect film 5 minutes after injection of contrast medium can detect
functional NLDO by showing delayed clearance of the lacrimal sac.9
Scintigraphy is mainly used to confirm a diagnosis of functional
blockage when there is delayed or no out- flow of radioactive media
in the presence of a normal DCG.
Canalicular
Endoscopy
More
recent investigative tools are available such as the microcanalicular
endoscope, which can demonstrate the site and type of blockage.
However, experienced lacrimal surgeons can usually gather sufficient
information by simply probing the canaliculi.
TREATMENT
Nasolacrimal
duct blockage
External
DCR is still the most popular choice for NLDO and dacryocystitis
and has a success rate of 80-95%. If there is canalicular damage
or a narrow upper nasal cavity it may be necessary to insert a silicone
tube. Day-case external DCR under local anaesthesia is gaining popularity.
Endonasal
DCR is acknowledged to have a lower success rate.10,11 Power tool
and laser assisted DCR's can be performed as day case procedures
and can be less time consuming.12
Balloon
dilatation dacryoplasty his also been shown to be effective in partial
nasolacrimal duct obstruction with a claimed success rate of 60%.12
Canalicular
obstruction
a)
Canalicular blockage
More complex surgical procedures are necessary if intubation is
not successful. The micro-surgical repair of canaliculi has been
proposed with a canaliculo-DCR being reserved for distal canalicular
blockage. Retrograde intubation of the canaliculi combined with
DCR is used for proximal canalicular obstruction and punctal agenesis,
with a success rate of 60-70%.13 During a standard DCR the inner
opening of the common canaliculus is identified and probed towards
the blocked canaliculi. On reaching the site of the blockage a pseudo
punctum is fashioned. A silicone tube is then inserted through the
same route.
b)
Canalicular stenosis
Silicone tube insertion during DCR is necessary. Alternatively canaliculoplasty
by closed technique bicanalicular silicone tube insertion can be
performed. A success rate of up to 70% has been reported. 15,16
Early anecdotal reports indicate that endocanalicular Erbium laser,
used prior to intubation, has an arguably (but as yet unproven)
better outcome.
In
cases of failure of the above procedures, a by-pass operation is
the only remaining option. Conjunctivo-DCR with a Lester-Jones tube
can be performed as a closed technique in the presence of a previous
osteotomy
Functional
blockage
Functional
blockage due to preductal or ductal narrowing, identified by delayed
MDCG or scintigraphy can be treated by DCR and a silicone stent.
Many cases of functional blockage have also been successfully treated
using lid shortening and punctal snip procedures.16 It seems that
in such cases other underlying causes have been responsible such
as punctal phimosis. Functional blockage due to pump failure (facial
nerve palsy) might require by-pass lacrimal surgery. Treatment remains
controversial.
SUMMARY
- Ocular
surface irritation and lid mal-positions should be addressed initially.
After identification of the site of blockage an appropriate plan
of action should be adopted.
- Probing
of the canaliculi in experienced hands is an effective diagnostic
tool.
- Partial
canalicular blockage can be treated by either DCR and silicone
tube insertion or by closed technique canaliculoplasty involving
bicanalicular insertion of a stent into the naso-lacrimal duct.
- Extensive
canalicular blockage requires more complex surgery. Canaliculo-DCR
for distal obstruction and DCR with retrograde intubation for
proximal obstruction.
- Lacrimal
by-pass surgery with a Lester-Jones tube is the last resort when
other techniques have failed to achieve recanalisation of the
drainage system.
Bijan
Beigi, Norwich Hospital.
References:
1
Paul TO, Shepherd R. Congenital Nasolacrimal Duct Obstruction. J
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R, MacEwen CJ Young JD. The Natural History of Epiphora in Childhood.
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GE, Rose GE, Frimpon-Ansah, Ezra E. Factors Affecting the Success
of Nasolacrimal Duct Probing for Congenital Nasolacrimal Duct Obstruction.
AmJ Ophthalmol 1999 May; 127 (5):616-7.
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RK, Misson GP, Donaldson L Willshaw HE. The Role of Nasolacrimil
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Focus
Published by the Royal
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