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ORIGINAL ARTICLE
Year : 2009  |  Volume : 16  |  Issue : 2  |  Page : 85-87 Table of Contents     

Prevalence of punctal stenosis among ophthalmology patients


King Abdulaziz University Hospital, Jeddah, Saudi Arabia

Date of Web Publication17-Jul-2009

Correspondence Address:
Amal Bukhari
P.O. Box 118846, Jeddah, 21312
Saudi Arabia
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0974-9233.53867

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   Abstract 

Purpose: To estimate the prevalence of punctal stenosis among patients visiting the general ophthalmology clinic for routine checkup.
Design: Prospective, observational case series.
Materials and Methods: A total of 682 patients were evaluated for evidence of punctal stenosis from May to November 2008. Any associated findings from clinical examination were recorded.
Results: As many as 54.3% (370/682) of the candidates had punctal stenosis. The prevalence is associated significantly with increasing age (p=.001), and no gender predilection was found. It was due to chronic blepharitis in 97% (359/370), entropion in 1.4% (5/370) and unknown causes in 1.6% (6/370) of the patients. As many as 58.1% (215/370) did not have subjective or objective evidence of epiphora, and all of them had a tear film breakup time of less than 10 seconds and positive corneal fluorescein staining.
Conclusion: Punctal stenosis is a common finding among patients presenting for routine eye checkup. It increases with advancing age, and the most common predisposing factor is chronic blepharitis. A significant number of patients can be asymptomatic as they have concurrent dry eye disease. Surgical intervention is not recommended unless the patient is symptomatic after treating any associated blepharitis and dry eye disease.

Keywords: Blepharitis, Dry Eye, Epiphora, Prevalence, Punctal Stenosis


How to cite this article:
Bukhari A. Prevalence of punctal stenosis among ophthalmology patients. Middle East Afr J Ophthalmol 2009;16:85-7

How to cite this URL:
Bukhari A. Prevalence of punctal stenosis among ophthalmology patients. Middle East Afr J Ophthalmol [serial online] 2009 [cited 2019 Jun 27];16:85-7. Available from: http://www.meajo.org/text.asp?2009/16/2/85/53867


   Introduction Top


Punctal stenosis can be congenital or acquired. The acquired type can result from a variety of causes, including lid trauma, malpositions, infections, tumors, blepharitis, toxic effects of some topical or systemic medications, autoimmune diseases like  Stevens-Johnson syndrome More Details and graft-versus-host reactions and from fibrosis secondary to punctal plug insertion. [1],[2],[3],[4],[5],[6],[7] Aging was also found to be a predisposing factor for acquired punctal stenosis. [8]

The aim of this study was to estimate the prevalence of punctal stenosis among patients visiting the ophthalmology clinic for regular checkup and to determine the predisposing factors.


   Materials and Methods Top


All patients that visited the general ophthalmology clinic from May to November 2008 were asked about any history of tearing, use of anti-glaucoma medications, systemic chemotherapy, facial radiotherapy, lacrimal surgeries and trauma. All underwent slit-lamp examination to evaluate the punctal size. Punctal stenosis was diagnosed using the criteria used by Kashkouli et al.,[9],[10] viz., a punctum that is visible but smaller than 0.3 mm and required a punctal finder followed by a standard punctal dilator to insert a #00 Bowman probe. Tear meniscus height was then measured using a slit-lamp biomicroscope. A level of more than 2 mm was considered high. Tear film breakup time (BUT) was also measured by touching the infero-temporal bulbar conjunctiva with a fluorescein sodium strip wetted with a preservative-free isotonic saline. Patients were asked to blink, and the precorneal tear film was examined under blue light illumination using a slit-lamp biomicroscope. The mean value of three measurements was recorded. The BUT was considered low when it was less than 10 seconds. The corneal surface was then examined for fluorescein staining and its presence or absence recorded. The cases were labeled asymptomatic if they did not complain of epiphora and their tear meniscus height was less than 2 mm. The patients were labeled as having dry eye if they had a BUT less than 10 seconds and positive corneal staining with fluorescein. A general ocular examination was then performed looking for associated diseases such as blepharitis, entropion, trichiasis, mass of the lacrimal drainage system and corneal or conjunctival scars.

The entire data was then analyzed using SPSS MS Window Release 11 (SPSS, Chicago, Illinois, USA). Using a Chi-square test, a 'p' value of less than 0.05 was considered significant


   Results Top


Both eyes of the 682 candidates, with a mean age of 34.1 (range, 10-73 years), were evaluated for signs of punctal stenosis. Among them, 62.3% were females. As many as 370/682 (54.3%) patients had punctal stenosis. [Table 1] shows the prevalence of punctal stenosis in relation to location, and [Table 2] shows the prevalence in relation to age. As many as 51% (131/257) of the males and 56.2% (239/425) of the females were affected (p=0.18).

Blepharitis was found in 359/370 (97%) of the cases (p=0.001). As many as 345/370 (93.2%) patients had dry eye disease (p=0.001), and 89.3% (308/345) of those dry eye patients had a form of chronic blepharitis (p=0.031).

As many as 155/370 (41.9%) patients gave history of tearing. All of them had a high tear meniscus height, 96.8% (150/155) of them had chronic blepharitis (p=0.042) and 20% (31/155) had dry eye disease (p=0.87). As many as 215/370 (58.1%) patients did not complain of tearing, and all had a normal tear meniscus height; while 88.8% (191/215) of the patients had chronic blepharitis (p=0.0281), and 97.2% (209/215) had dry eye (p=0.001).

An associated entropion was found in 5/370 (1.4%) patients, and 6/370 (1.6%) patients had no apparent cause for punctal stenosis. None of the patients had trichiasis, masses of the lacrimal drainage system, corneal or conjunctival scars. None of the patients were using anti-glaucoma medications, and none were on systemic chemotherapy No history of facial radiotherapy or lacrimal surgery or trauma was elicited.


   Discussion Top


The prevalence of punctal stenosis was 54.3% among all the patients visiting the general eye clinic for routine checkup, which is considered a valid prevalence rate over the period of this study. It was found significantly correlated with increasing age, an observation that has also been noted by Kristan et al.[8] and Kashkouli et al.[9] This association is possibly due to aging changes and tissue atrophy, which can make the punctum a dense fibrous structure and less resilient. It can also make the surrounding orbicularis fibers atonic with a resultant punctal stenosis. [8]

In this study, gender was not found to have any statistically significant association with punctal stenosis, although Kashkouli et al.[9] and Offutt et al.[14] noted a female predominance among their patients (70% and 71%, respectively). They suggested that postmenopausal hormonal changes might account for this sex predilection.

Chronic blepharitis was the most common predisposing factor, affecting 97% of our patients. This observation is similar to that reported by Kashkouli et al.,[9] who found that 45% of their patients had blepharitis. The authors suggested that chronic blepharitis might predispose to punctal stenosis, as as associated chronic inflammation would result in inflammatory membrane formation, conjunctival epithelial overgrowth and keratinization around the walls of the punctum. Edelstein et al.[11] also correlated the recurrence of punctal stenosis after wedge punctoplasty to coexisting chronic blepharitis that causes causes punctal cicatrization.

As many as 58.1% of the cases lacked subjective or objective evidence of epiphora. Of all the cases, 88.8% had chronic blepharitis and 97.2% had dry eye disease. We believe that this group of patients did not have epiphora because of the increased tear evaporation from the associated dry eye disease which was caused by blepharitis. This observation made us suggest that having punctal stenosis might be an adaptation mechanism to compensate for the increased tear evaporation from the associated dry eye disease.

To conclude, punctal stenosis was a very common finding among our patients that were seen in the general eye clinic for routine checkup, a finding that would be expected to be higher if it was estimated among patients visiting the oculoplastic clinic. Punctal stenosis appeared to increase with advancing age, and the majority of patients had associated blepharitis. There were a significant number of asymptomatic patients and most of them had dry eye disease. We do not recommend surgical intervention for punctal stenosis in symptomatic patients until associated blepharitis or dry eye disease is well controlled.

 
   References Top

1.Tabbara K, Bobb A. lacrimal system complications in trachoma. Ophthalmology 1980;87:298-301.  Back to cited text no. 1    
2.Esmaeli B, Valero V, Ahmadi M, Booser D. canalicular stenosis secondary to docetaxel (Taxotere), a newly recognized side effect. Ophthalmology 2001;108:994-5.  Back to cited text no. 2    
3.McNab A. Lacrimal canalicular obstruction associated with topical ocular medication. Aust NZ Ophthalmolol 1998;26:219-23.  Back to cited text no. 3    
4.O'Donnell F. Medial ectropion: Association with lower lacrimal obstruction and combined management. Opthalmo Surg 1986;17:573-6.  Back to cited text no. 4    
5.Jager G, Bijsterveld O. Canalicular stenosis in the course of primary herpes simplex infection. Br J Ophthalmol 1997;81:332.  Back to cited text no. 5    
6.Kamoi M, Ogawa Y, Dogru M, Uchino M, Kawashima M, Goto I, et al . Spontaneous lacrimal punctal occlusion associated with chronic graf-versus-host disease. Current eye Research 2007;32:837-42.  Back to cited text no. 6    
7.Boldin I, Klein A, Haller-Schober EM, Horwath-Winter J. Am J Ophthalmol 2008;146:968-72.  Back to cited text no. 7    
8.Kristan R, Branch L. Treatment of lacrimal punctal stenosis with a one-snip canaliculotomy and temporary punctal plug. Arch Ophthalmol 1988;106:878-9.  Back to cited text no. 8    
9.Kashkouli M, Beigi B, Murthy R, Astbury N. Acquired external punctal stenosis: Etiology and associated findings. AJO 2003;136:1079-84.  Back to cited text no. 9    
10.Kashkouli M, Nilforushan N, Nojomi N, Rezaee R. External lacrimal punctum grading: Reliability and interobserver variation. Eur J Ophthalmol 2008;18:507-11.  Back to cited text no. 10    
11.Edelstein J, Reiss G. the wedge punctoplasty for treatment of punctal stenosis. Opthalm Surg 1992;23:818-21.  Back to cited text no. 11    
12.Carter K, Nelson C, Martonyi C. Size variation of the lacrimal punctum in adults. Ophthalmol Plast Reconstr Surg 1988;4:231-3.  Back to cited text no. 12    
13.Yoon K, Jeong S, Park Y. Study of lacrimal punctual size in normal adults. J Korean Ophthalmol Soc 1997;38:1961-20.  Back to cited text no. 13    
14.Offut W, Cowen D. Stenotic punctal: Microsurgical punctoplasty. Ophthalmol Plast Reconstr Surg 1993;9:201-5.  Back to cited text no. 14    



 
 
    Tables

  [Table 1], [Table 2]


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