The Efficacy and Safety of Probing as a Treatment Procedure for Congenital Nasolacrimal Duct Obstruction
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Original Investigation
P: 191-194
September 2013

The Efficacy and Safety of Probing as a Treatment Procedure for Congenital Nasolacrimal Duct Obstruction

İstanbul Med J 2013;14(3):191-194
1. Bağcılar Eğitim ve Araştırma Hastanesi, Göz Kliniği, İstanbul, Türkiye
2. Okmeydanı Eğitim ve Araştırma Hastanesi, Göz Kliniği, İstanbul, Türkiye
No information available.
No information available
Received Date: 03.07.2012
Accepted Date: 27.08.2012
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ABSTRACT

Objective:

To evaluate the efficacy and safety of Probing as a treatment procedure for congenital nasolacrimal duct obstruction.

Methods:

In this study, 55 eyes of 45 patients who underwent probing for congenital nasolacrimal duct obstruction were retrospectively reviewed. The patients were divided into three groups based on the timing of the procedure as Group 1 (11-17 months), Group 2 (18-24 months) and Group 3 (25-36 months). Postoperative follow up, safety and efficacy were evaluated.

Results:

The mean age of 25 female and 20 male patients was 19.3 months (11-36 month). Mean follow up was 11,8 months (6-18 months). The success was 88.4% (23 of 26 eyes) in Group 1, 70.5% (12 eyes of 17 eyes) in Group 2, and 41.7% (5 of 12 eyes) in Group 3. No complications were noted during follow-up.

Conclusion:

Probing procedure appears to be an effective and safety procedure for congenital nasolacrimal duct obstruciton in the early age group.

Keywords: Congenital nasolacrimal duct obstruction, probing, age

References

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