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Title: Efficacy and Safety of Adjunctive Triamcinolone in Nasal Endoscopic Dacryocystorhinostomy
Authors: Teyyeb Azeem Janjua, Abu ul Ala Nafees, Bushra Akbar, Rabbiya Mirza, Shagufta Parveen, Mohammed Shahid Tarrar
Journal: Pakistan Armed Forces Medical Journal (PAFMJ)
Publisher: Army Medical College, Rawalpindi.
Country: Pakistan
Year: 2023
Volume: 73
Issue: Supplementary 2
Language: English
DOI: 10.51253/pafmj.v73iSUPPL-2.7501
Keywords: EfficacySafetyTriamcinolone acetonideEndoscopic dacryocystorhinostomy
Objective: To assess safety and long-term efficacy of use of triamcinolone acetonide (TA) soaked absorbable gel foam dressing in Endoscopic Dacryocystorhinostomy in our population.
Study Design: Quasi experimental study
Place and Duration of Study: Armed Forces Institute of Ophthalmology, Rawalpindi Pakistan, from Jan 2016 to Jan 2019.
Methodology: Endoscopic Dacryocystorhinostomy was performed on 103 eyes of 98 patients for unilateral or bilateral primary acquired nasolacrimal duct obstruction or previously failed Endoscopic Dacryocystorhinostomy without triamcinolone acetonide. Endoscopic Dacryocystorhinostomy was done using a standardized technique employing a 30° nasal endoscope (Karl Storz, Germany). In addition, a gel foam (15x10x5mm) soaked with 1ml of 40mg triamcinolone acetonide was threaded along the silicone tube metallic guide and advanced to ostium at the end of procedure. Anatomical success (patent lacrimal passage on irrigation), functional success (resolution of epiphora) and complications at 6 and 12 months of follow up, were the outcome measures documented and analyzed.
Results: Out of 103 cases, there were 41(39.8%) male and 62(60.2%) female patients. Mean age was 47.10±12.80 years (age range 18–72 years). Anatomical success rate of 90(87.4%) and 89(56.4%) was observed at 6 and 12 months, whereas functional success rate of 88(85.4%) was observed at both 6 and 12 months follow up respectively. No major complications were observed in our study.
Conclusion: Endoscopic Dacryocystorhinostomy with triamcinolone acetonide is a safe and effective procedure for epiphora secondary to previous failed Endoscopic Dacryocystorhinostomy or primary acquired nasolacrimal duct obstruction.
To assess the safety and long-term efficacy of using triamcinolone acetonide (TA) soaked absorbable gel foam dressing in Endoscopic Dacryocystorhinostomy (ENDO-DCR) in the Pakistani population.
A quasi-experimental study was conducted on 103 eyes of 98 patients diagnosed with unilateral or bilateral primary acquired nasolacrimal duct obstruction or previously failed ENDO-DCR. The procedure involved ENDO-DCR using a standardized technique with a 30° nasal endoscope. A gel foam soaked with triamcinolone acetonide was placed at the ostium. Anatomical success (patent lacrimal passage on irrigation) and functional success (resolution of epiphora) were assessed at 6 and 12 months. Data was analyzed using SPSS ver 23.0.
graph TD;
A["Patient Recruitment 103 eyes, 98 patients"] --> B["Perform ENDO-DCR with TA-soaked gel foam"];
B --> C["Follow-up Assessment"6 & 12 months""];
C --> D["Document Anatomical & Functional Success"];
C --> E["Record Complications"];
D --> F["Data Analysis"];
E --> F;
F --> G["Conclusion"];
The study suggests that ENDO-DCR with triamcinolone acetonide is a safe and effective procedure, potentially improving success rates compared to procedures without adjuvants. The anti-inflammatory properties of steroids are believed to reduce granulation tissue formation and scarring. The study also considered the possibility of the gel foam acting as a mechanical barrier, but evidence from other studies suggests this is less likely to be the primary benefit.
Anatomical success rates were 87.4% at 6 months and 86.4% at 12 months. Functional success rates were 85.4% at both 6 and 12 months. No major complications were observed. Minor complications included one case of secondary hemorrhage and one case of infection in the gel foam.
Endoscopic Dacryocystorhinostomy with triamcinolone acetonide is a safe and effective procedure for symptomatic epiphora secondary to previous failed ENDO-DCR or primary acquired nasolacrimal duct obstruction.
- The study included 103 eyes of 98 patients.
- Anatomical success rate at 6 months was 87.4%.
- Functional success rate at 12 months was 85.4%.
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