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Pushed monocanalicular intubation: a preliminary report
1Department of Ophthalmology, Hôtel-Dieu de Paris, University of Paris VI Medical School, Paris, France. brunofayet@club-internet.fr <brunofayet@club-internet.fr>
Insights
This study introduces a simplified "pushed" monocanalicular stent technique for congenital nasolacrimal duct obstruction. Nasal endoscopy confirmed the pushed method
Area of Science:
- Ophthalmology
- Pediatric Surgery
Background:
- Congenital nasolacrimal duct obstruction (CNLDO) is a common condition in infants.
- Current intubation techniques for CNLDO can be complex and may require a nasal retrieval step.
Purpose of the Study:
- To evaluate the behavior and efficacy of a novel
- pushed
- monocanalicular stent in treating CNLDO using nasal endoscopy.
Main Methods:
- Four children with CNLDO underwent monocanalicular intubation with a "pushed" stent.
- Nasal endoscopy was employed to assess stent position, mucosal integrity, and behavior during guide removal.
- The procedure involved probing and guide insertion within the silicone stent, followed by punctal removal of the guide.
Main Results:
- The pushed intubation method was successful in four cases of simple dacryostenosis without complications.
- Endoscopic evaluation revealed no submucosal tunneling, significant mucosal damage, or stent bunching during guide removal.
- Tearing resolved within one week post-stent removal in all treated cases.
Conclusions:
- The "pushed" monocanalicular intubation technique simplifies the procedure for CNLDO.
- Further studies are needed to define the specific indications for this simplified intubation method.
Objective:
To study the behavior of a "pushed" monocanalicular stent by means of nasal endoscopy.
Patients And Methods:
Four children (six affected sides) with congenital nasolacrimal duct obstruction were treated with monocanalicular intubation with an anchoring plug. The children's mean age at the time of the operation was 33 months (range, 30-37 months). The procedure began with probing in order to verify (a) dacryostenosis (simple or extensive nasolacrimal duct impatency) and (b) the metal-to-metal contact in the lower nasal meatus. The stent was similar to a Monoka(TM), but the guide (a malleable stainless steel probe) is located inside the silicone stent rather than projecting from it. The silicone's total length is 40 mm and the external diameter 0.96 mm. Simultaneously, the guide acts to catheterize the nasolacrimal duct by pushing the silicone through the upper and lower parts of the outflow system. The guide is removed via a punctal approach. This mode of intubation dispenses with the nasal recovery step. Nasal endoscopy was used to monitor (a) the position of the stent in the lower nasal meatus (free or submucosal), (b) mucosal damage and bleeding, and (c) the behavior of the silicone tube during removal of the guide.
Results:
Because of the complexity of nasolacrimal ducts, two of the six sides were treated with the classical Monoka intubation method of pulling the silicone tubing out from the nasal exit of the duct (the pull technique). The pushed intubation method was used for the four simple nasolacrimal stenoses, with no problems whatsoever. In all four cases, endoscopic examination showed (a) no submucosal tunneling (false passage), (b) no noteworthy mucosal damage, and (c) no retraction (bunch-up) of the silicone tube during the metal guide removal. No particular complications were reported during the procedure or the intubation period, which lasted an average of 3 weeks. The stents were removed in the consulting room. Tearing ceased during the 1(st) week in two cases, during the intubation period. Tearing persisted throughout the intubation period in the other two cases, but ceased during the week following stent removal. The follow-up lasted 2 months.
Conclusions:
The pushed procedure simplifies monocanalicular nasal intubation. Its indications remain to be determined.
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