Kaufman L M, Guay-Bhatia L A
Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago 60612-7243, USA.
Ophthalmology. 1998 Feb;105(2):336-41. doi: 10.1016/s0161-6420(98)93445-5.
Nasolacrimal duct intubation with Silastic tubes often is used for the treatment of congenital nasolacrimal duct obstruction. The more established intubation technique uses tubing designed for bicanalicular intubation. A commercial product now is available for monocanalicular intubation (Monoka tube, FCI, Issy-Les-Moulineaux Cedex, France), made possible by a punctal anchor attached to the proximal end of the tubing. The authors evaluated the complications and results of their experience with Silastic tube monocanalicular intubation for treatment of congenital nasolacrimal duct obstruction.
The study design was a retrospectively reviewed clinical trial with the results compared to a historic cohort treated with an alternative medical device.
Thirty-nine pediatric patients with 48 obstructed congenital nasolacrimal ducts were available for treatment and postoperative follow-up. The historic cohort included 25 cases of congenital nasolacrimal duct obstruction.
The participants were treated with monocanalicular Silastic tube intubation. The historic cohort was treated with bicanalicular Silastic tube intubation. The tubes were left in place for 4 to 6 months before planned removal.
Dye disappearance tests were performed before and after surgery after removal of the tube. Intraoperative and postoperative complications were noted.
Significant complications of the monocanalicular tubing included 1 case of bilateral preseptal cellulitis, 1 case of migration of the punctal anchor into the canaliculus that required surgical correction, 2 cases of a corneal abrasion, 1 case of a corneal ulcer, and 21 cases of premature removal of the tube. Of the 21 cases with premature tube removal, 13 (62%) of the eyes showed an improvement in the symptoms and results of dye disappearance test. Of the 27 cases that completed the full course of tube placement, all the tubes were removed successfully in an office setting, and 25 (93%) showed an improvement in the symptoms and results of dye disappearance test. Significant complications of the authors' bicanalicular intubation include stretching of the punctum, tube dislodgement, and tube removal requiring general anesthesia to the patient. Of the authors' 25 cases treated with bicanalicular intubation, 17 (68%) showed an improvement in the symptoms and results of dye disappearance test.
The recently introduced Silastic monocanalicular tubing offers an alternative to bicanalicular tubing for treatment with intubation of congenital nasolacrimal duct obstruction. Complications due to intubation persist with the monocanalicular tube. However, some of the complications the authors encountered may be avoided by a recent change in the design of the tubing and by familiarity with recommended techniques. The overall success rate of 79% with the Monoka tube is lower than that for published reports of bicanalicular intubation.
硅胶管鼻泪管插管术常用于治疗先天性鼻泪管阻塞。更成熟的插管技术使用的是设计用于双泪小管插管的管材。现在有一种商业产品可用于单泪小管插管(Monoka管,FCI,法国伊西莱穆利诺 Cedex),这得益于附在管材近端的泪点锚定器。作者评估了硅胶管单泪小管插管治疗先天性鼻泪管阻塞的并发症及效果。
本研究设计为一项回顾性临床研究,将结果与使用另一种医疗设备治疗的历史队列进行比较。
39例患有48条阻塞性先天性鼻泪管的儿科患者可接受治疗及术后随访。历史队列包括25例先天性鼻泪管阻塞病例。
参与者接受单泪小管硅胶管插管治疗。历史队列接受双泪小管硅胶管插管治疗。在计划拔除前,将管子留置4至6个月。
在拔除管子后手术前后进行染料消失试验。记录术中及术后并发症。
单泪小管管材的显著并发症包括1例双侧睑前蜂窝织炎、1例泪点锚定器移入泪小管需要手术矫正、2例角膜擦伤、1例角膜溃疡以及21例管子过早拔除。在21例管子过早拔除的病例中,13只眼(62%)症状改善且染料消失试验结果改善。在完成整个置管疗程的27例中,所有管子均在门诊成功拔除,25例(93%)症状改善且染料消失试验结果改善。作者双泪小管插管的显著并发症包括泪点拉伸、管子移位以及需要对患者进行全身麻醉才能拔除管子。在作者治疗的25例双泪小管插管病例中,17例(68%)症状改善且染料消失试验结果改善。
最近推出的硅胶单泪小管管材为先天性鼻泪管阻塞插管治疗提供了双泪小管管材之外的另一种选择。单泪小管管插管仍存在并发症。然而,作者遇到的一些并发症可通过管材设计的近期改进以及熟悉推荐技术来避免。Monoka管79%的总体成功率低于已发表的双泪小管插管报告中的成功率。