Cause and Management of Patients With Failed Endonasal Dacryocystorhinostomy

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Abstract

INTRODUCTION

Endonasal dacryocystorhinostomy (DCR) is used to treat lacrimal drainage system obstructions using a nasal approach with an electrical burr [1]. The overall success rate of endonasal DCR is reported to range from 80% to 95% [2].

Endoscopic DCR has many advantages over external DCR; it ensures no external scar formation on the skin of the eyelid, direct visualization of the nasal anatomy, and preservation of the medial canthal tendon for the lacrimal pump function. Endoscopic DCR is currently a well-established treatment method in patients with nasolacrimal duct obstruction. However, endoscopic DCR only has a short history of widespread use. Consequently, management protocols for failed endonasal DCR have yet to be established for surgeons performing endoscopic DCR. Some surgeons could try to solve the failed endonasal DCR in its degree. As such, there are only a few reports on the management of failed endonasal DCR, and these can be divided into two groups: endoscopic revisional surgery group [3,4], and functional epiphora group [5,6]. To date, there are a few reports about the overall management of failed endonasal DCR. Therefore, in the present study, we have evaluated the cause of failed endonasal DCR and investigated methods for the overall management of failed endonasal DCR. Our study would be helpful for surgeons planning the management of failed endonasal DCR.

MATERIALS AND METHODS

RESULTS

Of the total 61 patients, 46 were female (75%) and the overall mean age was 54 years. Twenty eight patients were operated upon the right side and 33 on the left side. The mean interval between the primary and revision surgeries was 15.3 months. The average follow-up period after revision surgery was 12.2 months. The average follow-up period was 11.2±5.2 months in endoscopic revision surgery group and 16.4±5.9 months in lacrimal silicone tube intubation group. The overall mean preoperative and postoperative TMH values were 3.38±0.61 mm and 1.15±0.44 mm, respectively. In the group of patients whose revision surgery was successful (i.e., the success group), the preoperative and postoperative TMH values were 3.44±0.57 mm and 1.00±0.23 mm, respectively; the postsurgical TMH change in this group was significant (P<0.001). In the group of patients whose revision surgery failed (i.e., the failure group), the preoperative and postoperative TMH values were 2.86±0.49 mm and 2.29±0.88 mm, respectively; the postsurgical TMH change in this group was not significant (P=0.103) (Table 1).

Table 1.

Patient demographics and characteristics

Cause of failed endonasal DCR was divided into two groups–one is anatomical failure, while the other is functional failure. Anatomical failure was divided into two categories based on nasal endoscopic findings. The most common cause of anatomical failure was membranous obstruction in the nasal ostium (31 patients; 51%); the other causes included membranous obstruction of the nasal ostium with canalicular obstruction (12 patients; 20%), granuloma formation in the nasal ostium (4 patients; 7%), and synechiae formation in the nasal ostium (1 patient; 2%). These patients did not show the nasal opening under nasal endoscopy. Four patients (7%) showed canalicular obstruction with good-opened nasal ostium under nasal endoscopy. And 9 patients (15%) showed functional failure (Table 2).

Table 2.

Causes of failed endonasal dacryocystorhinostomy

The success rate of revision surgery was 89% (54 patients). The success rate of the endoscopic revision surgery was 90% (43/48 patients), while that of lacrimal silicone tube intubation was 85% (11/13 patients). The success rate according to the cause of failed endonasal DCR were as follows: membranous obstruction in the nasal ostium (27/31 patients; 87%), membranous obstruction of the nasal ostium with canalicular obstruction (11/12 patients; 92%), granuloma formation in the nasal ostium (4/4 patients; 100%), synechiae formation in the nasal ostium (1/1 patient; 100%), functional epiphora (8/9 patients; 89%), and canalicular obstruction with good-opened nasal ostium (3/4 patients; 75%) (Table 3).

Table 3.

Success rates of revision surgery after failed endonasal dacryocystorhinostomy

DISCUSSION

In this study, we achieved an overall success rate of 89% in revision surgery by one surgeon. Previously reported success rates of endoscopic revision surgery ranged from 60% to 94% [7-15]. However, the criteria for success differed among the studies, and not all of the studies considered both anatomical and functional criteria for the success of surgery.

The cause of failed endonasal DCR is multifactorial, with the most common cause being granuloma in the nasal ostium due to excess scar tissue formation during the wound healing process. In addition, adhesion of the nasal ostium with the middle turbinate or the nasal septum, and common canalicular obstruction are known to cause failure of endonasal DCR [4]. In our study, membranous obstruction of the nasal ostium (51%) were most common cause of failure of endonasal DCR, followed by membranous obstruction of the nasal ostium with canalicular obstruction (20%), functional epiphora (15%), granuloma formation in the nasal ostium (7%), canalicular obstruction with good-opened nasal ostium (7%), and synechiae formation in the nasal ostium (2%).

The healing process is known to play an important role in the failure of endonasal DCR. Jordan et al. [16] reported that suppression of reepithelialization during the healing process can induce an inflammatory response as well as an excessive proliferation of capillaries that eventually form a pyogenic granuloma. This becomes a vicious cycle because of the inhibition of reepithelialization by the pyogenic granuloma. In the present study, we analyzed patients with granuloma formation around the nasal ostium (13 patients; 21%) before reoperation; of the 13 patients, 11 patients underwent reoperation because of membranous obstruction of the nasal ostium, and 1 patient each underwent reoperation because of granuloma formation in the nasal ostium and membranous obstruction of the nasal ostium with common canalicular obstruction. These results suggest that granuloma formation around the nasal ostium after primary endonasal DCR might be associated with the failure of primary endonasal DCR.

In our study, we analyzed the causes for reoperation of 43 patients according to the area of obstruction before the primary surgery; in patients with nasolacrimal duct obstruction, membranous obstruction of the nasal ostium accounted for 76% (19/25 patients), granulation formation in the nasal ostium for 12% (3/25 patients), and canalicular obstruction for 12% (3/25 patients) of the cases. In patients who presented with common canalicular obstruction in primary surgery, the causes for reoperation are as follows: membranous obstruction of the nasal ostium accounted for 80% (8/10 patients) and common canalicular obstruction for 20% (2/10 patients). In patients who showed canalicular obstruction before the primary surgery, the causes for reoperation included canalicular obstruction (63%; 5/8 patients), membranous obstruction of the nasal ostium in (25%; 2/8 patients), and common canalicular obstruction (13%; 1/8 patients). The cause of failure of endonasal DCR seems to be associated with the area of obstruction before the primary surgery. However, we could not statistically analyze this correlation because of the small number of patients for whom the area of obstruction was known before the primary endonasal DCR. Further evaluation is required to determine the exact relationship between the cause of failure and the area of obstruction before primary endonasal DCR.

We prescribed the postoperative application of 0.02% MMC eye drops to all of the patients after the endoscopic revision surgery. MMC has been widely used in ophthalmic surgery for the prevention of granuloma formation. Several controlled studies have investigated the efficacy of MMC in the enhancement of the success of primary or revisional endonasal DCR [17-19]. The use of MMC could inhibit scarring and the formation of granulation tissue around the nasal ostium. In our hospital, the patients who underwent primary endonasal DCR were prescribed 0.02% MMC eye drops to inhibit granuloma formation around the ostium.

Endoscopic revision surgery aids the direct visualization of the site of any type of obstruction and helps ensure the appropriate size and position of the nasal ostium. Surgeons commonly perform endoscopic revision surgery to remove membranes and scar tissues by two methods. The first method is the same as the primary endoscopic DCR technique [5], and the second method involves the use of diode lasers, similar to the technique applied in the present study [20]. A few studies [21,22] have shown that DCR using diode laser is effective and has the shortest surgical time, with success rates similar to those of external or endonasal DCR. Surgery using diode laser is a simple, rapid, and bloodless method for revision surgery to remove the cause of obstruction of the nasal ostium. A diode laser is a semiconductor that converts electrical energy into light energy that is mainly absorbed by the soft tissues. The use of diode lasers avoids damage caused by beam escape to the adjacent structures such as the canaliculus, which makes it safer compared to the other lasers; it also has the ability to cut tissue and perform coagulation and hemostasis [23].

The key to successful endoscopic revision surgery is creating an appropriate-sized and accurately positioned nasal ostium and a healthy lacrimal sac mucosa. An appropriate-sized and optimally located nasal ostium ensures complete exposure of the lacrimal sac and intraoperative visual assessment of the common canalicular patency. Healthy lacrimal sac mucosa can encourage the normal healing processes of the nasal ostium and help tear flow to the ostium. This was confirmed by manometric measurements in a lacrimal sac pressure study [24], which concluded that the lacrimal pump remains functional after DCR; however, the suction power might decrease in the fibrotic lacrimal sac, leading to epiphora.

In the patients with functional epiphora, we inserted a lacrimal silicone tube and achieved a success rate of 89% (8/9 patients) in the revision surgery. Although the exact cause of functional epiphora is unclear, several studies have investigated its potential causes. For instance, in one study [25], magnetic resonance imaging dacryocystography was used to evaluate the signal intensity at the site of the nasal ostium after instillation of artificial tears into the conjunctival sac before and after blinking; the results revealed that patients with functional epiphora showed reduced post-blinking signal intensities. This result implies a defect in the lacrimal pump function. Another study [26] reported increased fluorescein transit time from the conjunctival sac to the nasal ostium in patients with functional epiphora. Currently, there are no known methods to enhance the lacrimal pump function; however, lacrimal silicone tube intubation is known to encourage lacrimal pump function. The exact mechanism by which lacrimal silicone tube intubation relieves epiphora is unclear. Kim et al. [5] proposed the theory the following theory to explain the effect of the silicone tube on the lacrimal pump: first, the silicone tube controls the punctual position and enhances lacrimal pump function; second, the small canaliculi might act as capillary tubes, and the capillarity tends to be strong in patients who exhibit the narrow capillary phenomenon.

In our study, the mean follow-up period was 12.2 month; since the standard deviation was 8 months, the follow-up period varied greatly among the patients. This variation could be explained by two factors. First, the minimum follow-up period varies according to the revision surgery method. The follow-up period for endoscopic revision surgery is at least 4 months, while that for lacrimal silicone tube intubation is at least 7 months. In our study, average follow-up period was 11.2±5.2 months in endoscopic revision surgery and 16.4±5.9 months in lacrimal silicone tube intubation. It was not a short period if we checked follow-up period in each operation. The second factor was that, in the present study, patients who were satisfied with the surgery did not visit the hospital for follow-up despite having appointments for the same. Moreover, patients with symptoms of epiphora could easily visit the hospital without the need for an appointment because of good accessibility to the hospital.

All of the patients who underwent endoscopic revision surgery in the present study were inserted with silicone tubes. Many surgeons agree that the use of silicone tubing in primary DCR has both pros and cons. Among recently published studies, most have reported no advantage of the use of silicone tubing in primary DCR [27,28], while some have reported negative effects of the use of silicone tubing on the surgical outcome of primary DCR [29]. However, there have been no reports on the role of silicone tubing in endoscopic revision surgery. We assumed that the possibility of obstruction of the nasal ostium by granuloma caused by lacrimal sac fibrosis was higher in endoscopic revision surgery compared to primary DCR, especially in patients who showed obstruction of the nasal ostium by granuloma after the primary DCR. Therefore, we believed that silicone tubing would help maintain the osteotomy site during the healing process. Moreover, even if granulation tissue was found to have formed during the follow-up period because of the silicone tubing, we could have removed the tissue easily in an outpatient clinic while still maintaining the osteotomy site. Further study about the effect of silicone tubing in endoscopic revision surgery is required.

The limitations of our study include its retrospective design and the fact that we did not evaluate other factors affecting lacrimal tear flow, such as lid laxity and conjunctivochalasis. In case patients with failed endonasal surgery present with these factors, and they are corrected, the success rate of revision surgery might increase further. Further studies investigating the factors that affect lacrimal tear flow are required.

In conclusion, membranous obstruction is the most common cause of failed endonasal DCR. The overall success rate of the revision surgeries in our study was 89%. Additionally, our results indicate that lacrimal silicone tube intubation is an effective treatment procedure for patients with functional epiphora. In patients with failed endonasal DCR, it is important to identify the cause of surgical failure, because surgeons should decide the method for revision surgery on the basis of this cause. An appropriate revision surgery might increase the final success rate of endonasal DCR.

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