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Efficacy of probing as treatment of epiphora in adults with blocked nasolacrimal ducts
  1. Ana Guinot-Saera,
  2. Peter Koay
  1. Department of Ophthalmology, Darlington Memorial Hospital, Darlington, County Durham DL3 6HX
  1. Dr A Guinot-Saera, C/Alvaro de Bazan, 22, 17, 46010-Valencia, Spain.


AIMS To determine the efficacy of probing in the initial treatment of epiphora and the symptom free period in adults with blocked nasolacrimal ducts.

METHODS The results of probing in 85 eyes with epiphora due to nasolacrimal duct obstruction were studied retrospectively after a mean follow up of 7.4 months (SD 11.6) by a questionnaire and interview survey of patients.

RESULTS 35% of the eyes had an outcome of no watering after probing, 17% mild watering, 35% moderate watering, and 11% severe watering. The patients’ satisfaction (watering subjectively improved) after undergoing this procedure was 82%, which is higher than previously reported. The mean symptom free period in eyes with no watering was 11.25 months, in eyes with mild watering 8.20 months, in eyes with moderate watering 5.35 months, and in eyes with severe watering 0.95 months. There was a significant difference (p=0.001) in the symptom free period between the no watering and severe watering groups.

CONCLUSIONS Probing in adults with confirmed nasolacrimal duct obstruction can be recommended as an initial treatment procedure because of its relatively good efficacy and high patient satisfaction without compromising subsequent surgical treatment if unsuccessful.

  • epiphora
  • nasolacrimal ducts
  • probing

Statistics from

Idiopathic or primary acquired nasolacrimal duct obstruction (NLDO)1 is a syndrome of unknown aetiology and accounts for the majority of NLDO found in adults. It is postulated that inflammation of unknown cause results in possible occlusive fibrosis2 of the nasolacrimal system (NLS) causing obstruction and subsequent epiphora3 4 or “watering eye”. Studies in children below the age of 4 months show that probing is an effective treatment. However, the risk of failure from probing increases with age, doubling every 6 months.5To our knowledge, only one published study has investigated the efficacy of probing as a method for treating epiphora in adults.6 The authors of that study reported a 52% success rate measured by subjective improvement in watering after probing. Probing in adults is quick, safe, easily performed with local anaesthesia,7 cost effective, and potentially an outpatient procedure. Probing as an initial procedure for adult epiphora has been carried out in this institution for the past 7 years providing the opportunity for the analysis of its efficacy by a survey of the probed patients.


In this retrospective study, adult patients aged 18 or older, of either sex who had probing for epiphora from January 1992 to November 1996 were selected. All probing were carried out by ophthalmologists at the consultant level. Patients were excluded if they had epiphora present from birth (congenital abnormality of NLS),5 8watering secondary to a herpetic canaliculitis, dacryocystitis, and lacrimal sac mucocele. 9 10 Patients with previous trauma,9 surgical intervention, intranasal disease, neoplasm of the lacrimal sac,10 11 corneal ulcer or foreign body, and any overproduction of tears (that is, any condition that causes reflex stimulation of the ophthalmic division of the trigeminal area) were excluded. Patients with abnormal punctal apposition, ectropion, and those with minimal symptoms (watering outdoors, only in cold wind that may occur in individuals with normal lacrimal excretory system) were also excluded. 9-14

Of the 108 eyes identified in the study period, eight eyes did not meet the study criteria and were excluded. Of these eyes, five had dacryocystitis and two had unsatisfactory probing on the operating table (characterised by difficulty in passing the probe and subsequent inability to irrigate saline through the NLS to the nose) and one patient had died (see Table 2). From the 100 eyes which met the criteria, 15 eyes with an unknown outcome belonging to 11 patients (four patients with bilateral and seven patients with unilateral NLDO) were also excluded. This study is based on the remaining 85 eyes (41 right NLS and 44 left NLS) from 65 patients; 45 patients had unilateral and 20 patients had bilateral NLDO.

Table 2

Outcome following the probing procedure

All patients had symptomatic epiphora and blockage of the lacrimal system confirmed on syringing.15 The mean age of the patients was 64.1 (SD 15.5, range 19–89) years. There were 38 females and 27 males. Table 1 summaries the demographic data.

Table 1

Demographic data

Probing was carried out with a Foster’s probe usually size 0.8 and through the upper canaliculus. We used the anaesthetic amethocaine drops to the conjunctival sac and lignocaine 2% and adrenaline infiltration around the medial canthus, the lower lid and deep up to the periosteum. The probe was advanced to the point of obstruction and pushed through with a gentle pressure.16 Patency following the probing was confirmed by syringing. Patients were treated with topical chloramphenicol, four times daily, following the procedure17 for a period of 7–10 days.

The results obtained by questionnaire and by interview following the probing procedure were recorded. Patients’ post probing epiphora was graded into four groups: no watering, mild watering (watering outdoors only), moderate watering, and severe watering. These groups were considered as excellent, good, medium, and failure, respectively. If the epiphora was present, patients were asked if this was tolerable or not. Special attention was paid to the length of time free of symptoms (symptom free period). Probing was arbitrarily judged to be a success if there was no watering or mild watering for at least 6 months following the procedure. Patient satisfaction with the procedure was also determined. Statistical comparison of discrete variables between the outcome groups was made with the unpaired Student’s ttest.


Ninety eight per cent of the NLDs were patent in the operating theatre following the probing procedure. This includes the 85 eyes that met the criteria. The mean follow up time of probed patients was 7.4 (SD 11.6) months. There were no significant age and sex ratio differences between patients of the different outcome groups (that is, no watering, mild, moderate, and severe watering). Thirty eyes (35%) had an outcome of no watering and 15 (17%) were mild watering (waters only out of doors, in cold weather, or wind). The clinical success rate of the procedure was of 52% in terms of either completely relieving or resulting in only mild watering. Thirty eyes (35%) had an outcome of moderate watering and only 10 of the eyes (11%) still suffering of severe watering after the procedure (Fig 1).

Figure 1

The number of eyes in each category of epiphora after probing.

Of the 15 patients with mild watering after probing, all of them (100%) describe their symptoms as tolerable. In patients with moderate and severe watering, 80% and 1% describe their symptoms as tolerable, respectively (Table 2). Eighty two per cent of the patients felt that their symptoms of watering had improved after probing, reflecting patient satisfaction with the procedure. Figure 2 and Table 3 show the mean symptom free period in the eyes after probing for each of the groups. There was significant difference (p=0.001, unpairedt test) in the symptom free period between the no watering and severe watering groups. No statistical significance (p>0.01) was found between the others groups.

Figure 2

Length of time from probing to reported symptoms.

Table 3

Symptom free period after probing procedure in months (SD) for each group

Out of the 85 probing procedures carried out, there were two postoperative complications consisting of one nasal obstruction and one dacryocystitis. The complication rate for probing in this study was 2%. Nine of the 85 eyes (10.5%) subsequently required a dacryocystorhinostomy (DCR), eight of these eyes were in the outcome group of severe watering, and one was in the moderate watering outcome group.


Epiphora due to obstruction of the nasolacrimal system is a common ophthalmic problem1 causing discomfort, visual disturbances, and skin problems such as excoriation.9Probing is a simple operative procedure easily performed in adults under local anaesthesia with minimal postoperative morbidity.18 19 In contrast, other treatments for adult epiphora due to NLDO are more invasive and are associated with a greater risk of complications. Such procedures include DCR9 20 21 22 Jones’s procedure,23 Palmaz balloon expandable metallic stents,24 and canaliculodacryo intubation.25 These procedures are complex, time consuming, requiring more resources, and often involve general anaesthesia with its attendant risks. The success rates (that is, not watering and mild watering) for DCR with comparable criteria to this study range from 83% to 87.4%.26-29 However, complications of DCR includes intraoperative problems such as haemorrhage, trauma, loss of nasal mucosa, CSF leak, and postoperative problems such as haemorrhage, infections, acute dacryocystitis, tube complications (granuloma formation), and scar complications (webbing).

In conclusion, probing for NLDO in adults with symptomatic watering has an 82% success in relieving symptoms. These results are more favourable than the earlier report.6 It is a simple, quick, cost effective, day case procedure and does not compromise the patient for further nasolacrimal surgery. A single probing procedure is effective in producing symptomatic improvement, when limited to use in patients with complete obstruction of the nasolacrimal duct and when watering was the only symptom. Our investigation confirms that probing, as an initial procedure, is an adequate and minimally invasive treatment for adult epiphora and can be an alternative to DCR, especially in elderly patients.


We wish to acknowledge assistance of Mr M S Dang, Mr L Singh, and Mr J D Haslam in the survey of their patients.

I want to specially than Dr K Narayanan and Dr J Ritter for their help.


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