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| Abstract ID | 13-129 |
| Title | Early experience with a new type of Lester Jones Tube |
| Oral, Poster or Video? | Either: Poster preferred |
| temp | 563 |
| Review result | [518] |
| Purpose |
Extrusion is the most common reason for failure after Jones tube placement. The StopLoss Jones tube (SLJT) is a new innovation in Jones tubes that incorporates a flexible silicone internal flange to resist extrusion. We present our early experience of using this new tube. |
| Methods |
Case note review of a single surgeon consecutive series of patients having SLJT placement from Nov 2011- present. |
| Results |
21 SLJTs were placed in 17 eyes of 13 patients, 9 female, 4 male; age range 23-83 years, mean 60. Follow-up ranged from 0.5-15 months. Indications for initial SLJT placement were: previous LJT complications 9 (53%), failed canalicular-DCR surgery 6 (35%), primary placement for inoperable canalicular occlusion 2 (12%). 86% tubes (18/21) had a 4.0mm flange, 3 tubes had a 3.5mm flange (14%); the most common tube length was 11 mm, range 10-15mm. There were no intra-operative complications. The extrusion rate was 0%. 4 tubes were replaced: 1 was too long, 2 others had conjunctival overgrowth (at 2/12 and 12/12), 1 tube migrated medially at 3/12. 1 tube (3.5mm flange) migrated medially at 12/12 but the track remained patent and the patient was reluctant for replacement. Patient satisfaction with the tube was: 90% fully satisfied, 5% was moderately satisfied, 5% not satisfied. The overall final surgical success rate (defined as: patent tube, no significant watering) at last follow-up was 95%. |
| Conclusion |
In this short follow-up initial study the StopLoss Jones tube appears to be effective in preventing extrusion and has a high rate of success and patient satisfaction. |