Article Type : Research Article
Authors : Yazicioglu T and Simsek S
Keywords : Dacryocystorhinostomy; Silicone tube intubation; Complications
Obstruction of the
nasolacrimal duct can be treated by dacryocystorhinostomy (DCR) operation,
which was first described by Toti in 1904, took its current form in 1921 with
the modification of this technique by proposing an end-to-end anastomosis
between the lacrimal sac and the nasal mucosa [1,2]. In order to increase the
success rate of DCR operation, silicone tube insertion is recommended, which
was first introduced by Quickert and Dryden in 1970 [3]. The use of silicone
tubes in DCR operations, prevents the common canaliculus or osteotomy site
obstructions and thus improve surgical results [3-6]. Although silicone tube
intubation is a safe and effective procedure for canalicular or nasolacrimal
duct disorders and generally tolerated in the lacrimal drainage system, it may
cause various complications such as chronic infection, punctual or canalicular
erosion, and conjunctival irritation [7-11].
In this study, we aimed to investigate silicone
tube related complications and its relationship with their removal time.
We reviewed the medical records of 141 patients
complaining about epiphora and discharge for a long period of time. The study
was prepared according to the Helsinki Declaration Criteria, and written
informed consent forms were obtained. Eyelid and lacrimal system examinations
were performed in all patients with epiphora. Examination of the puncta,
determination of the obstruction with lacrimal irrigation and probing and
supported by dacryocystography (DSG) with contrast were done. Full endoscopic
examination of the nasal cavity for any nasal pathology were also evaluated.
All the patients had common canalicular obstruction. Patients with symptoms of
dry eye causes by previous trauma, canalicular obstruction, suspicion of
malignancy, traumatic dacryostenosis were not included in this study. We
performed external DCR by Dupuy-Dutemps and Bourguet technique, and use
silicone stents routinely in all cases. We used two different sized tubes that
we currently have. One of them is straight stainless steel probes with silicone
tubing 35 cm length, 0.30 mm inside diameter, 0.64 mm outside diameter, the
other one is angled stainless steel probes with solid silicone tubing - 40 cm
length x 0.80 mm diameter. All operations were done by the same surgeon (TY)
under general anaesthesia. After lacrimal sac was exposed and dissected from
the lacrimal fossa, a 1 cm sized bone window was created on the lacrimal bone
and ‘H’ shaped anterior and posterior flaps of the nasal mucosa and lacrimal
sac were performed. After the posterior flaps of nasal mucosa and lacrimal sac
was sutured we inserted bicanalicular silicone tube and we knot the ends
together and directed into the nose. Then the anterior flaps were sutured, and
skin incision was closed with 6/0 vicryl sutures. Patients were checked on
postoperative first day, first week, first month, and then every 3 months until
one year. Unless there was a stent-related complication, it was not taken
before 6 months.
There were 117(82%) women and 24(18%) men, and the mean age was 51.6 ±
8.3 years (range 38 to 64 years). 137 eyes of 141 patients were relieved of
epiphora, with a success rate of 97.2%. Lacrimal irrigation test showed good
passage without any resistance. Postoperative silicone tube related
complications were observed in 42 (29%) of 141 patients. 13 (9.2%) of them had
rhinitis and complaining about bad smell from the nose, 8 (5.6%) had developed polyploid
tissue on the osteotomy side, seen by endoscopic examination. Tube related punctal
slitting was observed in 4 (2.8%) cases, especially in the tubes with thin
silicone structure.
3 (2.1%) had falling tube spontaneously before 3 months, 3(2.1%) had tube prolapse causing conjunctival irritation, 3 (2.1%) had stenosis in the canaliculus, 3 (2.1%) had peripunctal granulation tissue, 4 (2.8%) had secretion inside the tube. 2 (1.4%) had Punctal synechiae. 3 (2.1%) had canalicular stenosis continued to suffer from tearing (Table 1).
Table 1: Silicone tube related complications.
|
Eyes (n:%) |
Rhinitis |
13(9.2%) |
Polypoid tissue |
8(5.6%) |
Punctal slitting |
4(2.8%) |
Tube loss |
3(2.1%) |
Tube prolapsus |
3(2.1%) |
Canalicular stenosis |
3(2.1%) |
Peripunctal granulation
tissue |
3(2.1%) |
Punctal synechia |
2(1.4%) |
Dirty tube |
4(2.8%) |
Table 2: Complications related to removal time.
Complications |
Intubation
period 0-3 months |
Eyes (n) 3-6 months |
6 months- 1 year |
Canalicular stenosis |
- |
- |
3 |
Punctal slitting |
- |
- |
4 |
Tube dislocation |
2 |
1 |
- |
Peripunctal granulation tissue |
- |
- |
3 |
Secretion inside the tube |
- |
- |
4 |
Intranasal synechia |
- |
- |
8 |
Rhinitis |
- |
- |
13 |
Insertion of a tube into the nasolacrimal drainage system in DCR surgery
can prevent postoperative blockages, by providing an open pathway in the
healing process [12]. The most suitable, ideal synthetic material in living
tissues should be chemically inert and should not initiate inflammation or
foreign body reaction [13]. Tissue response to silicone implant was tested in
mice and found that it is not only well tolerated but also has the tissue
response same as the normal healing response in a sterile wound [13]. In DCR
operations, although the osteotomy site is made large enough, it can be narrow
up to 2 mm due to tissue growth and scarring. Also, the problems such as damage
the nasal mucosa or sac flaps, suturing errors, and excessive bleeding during
surgery reduce the success rate [14]. The success rate in cases with DCR with
silicone tube intubation was reported as 92-94% [9]. In order to obtain a
successful result, the inserted tube must be stayed in the patient’s lacrimal
canal until the damaged mucosa is re-epithelized, but postoperative
complications and stent failure are common conditions [15]. Complications of
the silicone tube can be listed as punctual erosion, punctual slitting,
granuloma formation, nasal migration, tube prolapse, inter-punctual symblepharon, corneal erosions, recurrent nose
bleeding, and chronic nasal irritation. The rate of postoperative complications
are seen in the first 3 months. Tube prolapse is the most common complication
and this may be due to the loose knotting of the silicone tube, and the most
common late complication is secretion inside the tube [11].
The surface of the silicone tubes creates granulomatous inflammation at
the rhinostomy site, making the operation unsuccessful [16]. On the other hand,
the use of silicone does not increase the risk of soft tissue infection. There
is no definite consensus on the average length of stay of silicone tube
intubation. Although the reported time for tube removal has been reported to be
from 1 week to several years, recent studies have indicated that the ideal time
is between 2-6 months. The widely suggested theory is that the incidence of inflammatory
reaction due to delayed removal of the tube may be high [15-18]. It is suggested
that removing the tube before any inflammatory reaction begins may reduce the
potential for late failure [13]. In one of the study, the complication rate was
reported as high as 41% in the first 3 months after surgery [11].
Although it is a
common opinion that long-term intubation is required to ensure repithelization
and prevent recurrence in severe cases, it has been stated that this increases
the risk of complications and may cause granulation tissue in the punctum
[19-20]. This granulated tissue formation can also be occur along the entire
lachrymal system, which can be caused by infection and/or mechanical stress.
Punctual slitting might be another punctual-related complication after
prolonged intubation. Leaving the tubes tight during surgery may cause punctual
erosion and slitting. In addition, the patient should be told not to pull the
tube and not to rub his eye sharply. Infection is the most serious complication
associated with prolonged intubation. The tube should not be removed before the
infection is controlled with irrigation and antibiotic treatment, as it may
cause more mucosal damage with recurrent occlusion. In our study, we used
silicone tube in all DCR operations and left in place for an average of 6
months. In the first three months we generally observed loss of the silicone
tube. In the late period we observed peripunctal granulation tissue, intranasal
synechia, inter-punctual symblepharon, canalicular stenosis. Peripunctal
granulation tissue is simply removed from the site of the punctum. Minimal
damage to the puncta was observed in our patients with low education level and
very uncomfortable with the tube inside the nose. We think that this might have
been due to the thin design of the silicone tube. Pulling the tube through the
nose caused a tear in the canaliculus. In cases where the tube was too
prolapsed to be pushed back, we removed them early.
Placement of silicone stents prevents rhinostomy stenosis and helps
stabilize epithelization between two mucosal surfaces with surgical continuity.
To achieve successful results proper intubation and endoscopic observation are
necessary.
I’m grateful to all with whom I have had work together.
The author has no relevant affiliations or financial involvement with a
financial interest in or financial with the subject matter or materials
discussed in the manuscript.
There is no conflict of interest
This paper was no financial support.