BACKGROUND The purpose of this study was to compare the efficacy of self-retaining stent (SRS) bicanalicular intubation with bicanalicular silicone (Crawford) intubation in patients with canalicular and punctal obstruction. METHODS In this prospective, randomized clinical trial, 38 patients with canalicular or punctal obstruction (25 partial, 13 complete) and epiphora were randomized into two...

Dermoid tumors in the medial canthal area are rare, but when present they commonly adhere to the lacrimal canaliculi. Three patients presented with a mass in the medial canthal area. The authors performed excisional biopsies, and the masses were diagnosed as dermoid tumors. In two patients, canalicular lacerations were found after mass excision, which suggested that the masses had been firmly a...

PURPOSE To compare the clinical effects of the single wide-diameter bicanalicular silicone tube and the double bicanalicular silicone tube in endonasal dacryocystorhinostomy (DCR) with canalicular trephinization for canalicular obstruction. METHODS We retrospectively reviewed the records of 121 patients with monocanalicular or common canalicular obstruction who had undergone endonasal DCR wit...

purpose: to evaluate the success rate of bicanalicular silicone tube intubation in children with congenital nasolacrimal duct obstruction (cnldo). methods: hospital records of 71 cases of bicanalicular silicone intubation in 62 children with cnldo were reviewed. success was defined as resolution of symptoms and signs such as epiphora and discharge 6 months after removal of the silicone tube. re...

purpose: to compare the success rate of external dacryocystorhinostomy (dcr) with and without bicanalicular silicone intubation for the management of primary acquired nasolacrimal duct obstruction. methods: in this study, 51 eyes from 50 patients who were diagnosed with primary acquired nasolacrimal duct obstruction underwent external dcr. patients with history of trauma and/ or surgery in the ...

Objective: To compare the results and complications of monocanalicular and bicanalicular Ritleng intubation under endoscopic guidance in patients with congenital nasolacrimal duct obstruction. Methods: This prospective study was performed on 24 patients with congenital NLD obstruction in the age between (2-5 years), divided into 2 groups. Group (A) underwent monocanalicular intubation, while gr...

Aim. To compare the surgical outcomes of surgery with and without bicanalicular silicon tube intubation for the treatment of patients who have primary uncomplicated nasolacrimal duct obstruction. Methods. This retrospective study is comprised of 113 patients with uncomplicated primary nasolacrimal duct obstruction. There were 2 groups in the study: Group 1 (n = 58) patients underwent transcanal...

PURPOSE To compare the success rate of monocanalicular versus bicanalicular silicone intubation of the nasolacrimal duct for congenital nasolacrimal duct obstruction (CNLDO). METHODS In a prospective randomized clinical trial, 70 eyes of 57 children with CNLDO underwent either monocanalicular silicone intubation (MCI) (n = 35 eyes) or bicanalicular silicone intubation (BCI) (n = 35 eyes). All...

PURPOSE To assess the effectiveness of bicanalicular silicone intubation (SI) in acquired partial nasolacrimal duct (NLD) obstruction. DESIGN Retrospective nonrandomized case series METHODS 72 tear ducts from 53 patients with severe epiphora due to acquired partial NLD obstruction underwent bicanalicular SI. Mean age at intubation was 55.9 years. The silicone tubes were removed after, on av...

PURPOSE To compare success and extrusion rates of the monocanalicular and bicanalicular Crawford intubation systems (JEDMED Instrument Company, St. Louis, MO). METHODS A retrospective review of all children who were diagnosed as having congenital nasolacrimal duct obstruction and treated with lacrimal intubation from 2005 to 2014 was performed. The total number of eyes included was 168 (75 an...