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Objective: To examine possible differences in success rates of primary dacryocystorhinostomy (DCR) with and without silicone intubation, and to find out whether the use of silicone tubes is beneficial.
Design: A literature search was conducted in the PubMed, EMBASE, and Cochrane Controlled Trials Register to identify potentially relevant controlled trials.
Methods: Language was restricted to English. The surgical techniques were categorized into external DCR (EX-DCR), endonasal laser-assisted DCR (LA-DCR), and nonlaser endoscopic endonasal DCR techniques (EN-DCR). The main outcome measure was success rates after DCR-with and DCR-without silicone intubation. The statistical analysis was carried out using a RevMan 5.0 software.
Results: Of 188 retrieved trials from the electronic database, 9 trials (5 randomized controlled trials and 4 cohort studies) involving 514 cases met our inclusion criteria. There was no statistically significant heterogeneity between the studies. The pooled risk ratio was 0.99, with a 95% confidence interval (0.91-1.08). There was no significant difference in the success rates between the DCR with and without silicone intubation (p = 0.81). Sensitivity analysis and subgroups analyses suggested that the result was comparatively reliable.
Conclusions: Based on this meta-analysis that included 5 randomized controlled trials and 4 cohort studies, no benefit was found for silicone tube intubation in primary DCR. Further well-organized, prospective, randomized studies involving larger patient numbers are required.
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http://dx.doi.org/10.1016/j.jcjo.2011.09.008 | DOI Listing |
BMC Ophthalmol
September 2025
Department of Ophthalmology, Tongji Hospital, School of Medicine, Tongji University, No.389 Xincun Road, Putuo District, Shanghai, 200065, China.
Purpose: To evaluate the clinical efficacy and safety of a novel shape-memory Bi-hook device in facilitating antegrade stent implantation for canalicular laceration repair.
Methods: In this retrospective comparative study, 76 patients (76 eyes) with canalicular laceration were enrolled: 39 patients (39 eyes) underwent Bi-hook-assisted stent implantation (Bi-hook group) and 37 patients received conventional Ritleng stent intubation (control group). The Bi-hook device was fabricated using a thermally shaped 0.
Klin Monbl Augenheilkd
September 2025
Klinik für Augenheilkunde, Medizinische Hochschule Hannover, Deutschland.
Purpose: To describe the risk management at a university eye hospital after two outbreaks of nosocomial endophthalmitis cases after pars plana vitrectomy.
Methods: In two series of postoperative endophthalmitis cases after in-house vitrectomy, the basic workflows in direct patient care were evaluated with regard to patient safety. Hygienic microbiological environmental examinations were performed on relevant materials and surfaces.
Medicine (Baltimore)
August 2025
Department of Ophthalmology, Keçiören Dünyagöz Hospital, Ankara, Türkiye.
This study evaluates the application and clinical efficacy of sutured Ritleng silicone tube intubation in children with congenital nasolacrimal duct obstruction (CNDO). A retrospective review was conducted on 561 eyes of 463 patients who underwent Ritleng tube intubation due to nasolacrimal duct obstruction. Patients were divided into 2 groups as those who had previously undergone probing (Group 1) and those who underwent Ritleng primarily (Group 2).
View Article and Find Full Text PDFOphthalmic Plast Reconstr Surg
August 2025
Department of Ophthalmology, Ankara Training and Research Hospital, Ankara, Türkiye.
Purpose: Canalicular lacerations require timely and effective surgical repair to prevent epiphora and maintain lacrimal function. While various intubation techniques exist, there is no clear consensus on the optimal method. This study compares monocanalicular, bicanalicular, and annular intubation techniques in terms of success rates and complications.
View Article and Find Full Text PDFCureus
June 2025
Department of Anaesthesiology, Singapore General Hospital, Singapore, SGP.
Tracheal stenosis is a rare condition that poses significant challenges in airway management. We report a case of failed emergency awake fiberoptic intubation necessitating difficult front-of-neck access in a patient with respiratory failure, tracheal stenosis, and an in situ tracheal stent. The patient presented to the emergency department with acute respiratory distress and was urgently transferred to the operating theatre for emergent intubation.
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