泪道梗阻及翻修手术中硅胶插管对泪道系统通畅功能影响的评价

Rashmi A Joshi, Sarita Maharia, A. Kochar
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引用次数: 0

摘要

目的:本研究的目的是报告作者在小管阻塞和翻修手术中使用硅胶插管治疗泪系统通畅的功能结果的经验。材料和方法:-本研究于2015年1月至2017年3月在萨达尔帕特尔医学院进行。本研究共纳入32例。本研究共招募了12例小管阻滞患者和20例DCR技术失败的患者。2例患者两次DCR失败,18例患者一次DCR失败。12例失败的DCR是内窥镜DCR, 6例是外部泪囊鼻腔造口术(E-DCR)。所有病例均由同一位外科医生使用相同的插管技术进行手术。结果:在我们的研究中,我们发现硅胶插管是治疗小管阻滞和DCR失败的有效方法。硅胶管柔软,相对惰性,灵活,对脆弱的小管和鼻黏膜的伤害最小。它通过维持导管的开口来维持导管的通畅。主要观察指标为上睑下垂的消退和随访中解剖和功能的成功。结论:在各种研究中,硅胶插管的成功率从69%到100%不等。本研究中94.5%的成功率与先前报道的结果完全相当,并发症最少。管阻塞。尽管手术一丝不苟,但还是经常遇到失败。泪囊鼻腔吻合术(DCR)后的溢泪对患者和外科医生来说都是一个令人痛苦的情况。据报道,外部DCR的失败率为5%-10%,4-6或更少,而内腔DCR的失败率为35%-40%,7-9。DCR失败最常见的原因是常见的小管梗阻和鼻造口部位梗阻,原因是截骨面积减小2、肉芽组织形成3、吻合口纤维化以及识别和吻合有缺陷。硅胶插管已被证明是成功的管理失败的DCR和小管阻滞。硅胶插管是一个简单的程序;评估了该程序的有效性。一个基本的手术原则是在尽可能少的并发症的情况下获得最成功的结果。在现代外科时代,以具有成本效益的方式获得成功的结果也很重要。本研究的目的是评估硅胶插管作为小管阻滞的初始手术和失败的DCR作为改良手术的成功率。摘要被纳入本研究。其中包括12例首次手术的小管阻滞患者和20例各种DCR技术失败的患者。2例患者两次DCR失败,18例患者一次DCR失败。这些失败的DCR中有12例是内窥镜DCR, 6例是外部泪囊鼻腔造口术(DCR)。该手术的纳入标准是既往手术后有外显和总小管阻滞的患者。排除标准为无点状点、怀疑恶性肿瘤、放疗、创伤后眼睑及骨畸形、鼻泪管阻塞(未手术)患者。
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Evaluation of Functional Outcome of Silicone Intubation on Patency of Lacrimal System in Canalicular Obstruction and Revision Surgeries
Purpose:- The purpose of the present study is to report authors’ experience of functional outcome of Silicone intubation on patency of lacrimal system in canalicular obstruction and revision surgeries. Materials and Methods:- This study was conducted at Sardar Patel Medical College from January 2015 to March 2017. A total of 32 cases were enrolled in this study. Twelve patients of canalicular block and 20 patients of various failed DCR techniques were recruited for the study. Two patients had failed DCR twice, and 18 patients had failed DCR once. Twelve of these previous failed DCR were endoscopic DCR, and 6 were external dacryocystorhinostomy (E-DCR). All cases were operated by a single surgeon using the same technique of intubation. Results:- In our study we found that Silicone intubation is an effective method for treating canalicular block and failed DCR. Silicone tube is soft, relatively inert, and flexible, causing minimal injury to the delicate canaliculi and nasal mucosa. It maintained duct patency by maintaining an opening. The main outcome measures were the resolution of epiphora and the anatomical and functional successes by patency on follow up. Conclusion:- The success rates reported for silicone intubation range from 69% to 100% in various studies. The 94.5% success rate noted in the present study is entirely comparable to these previously reported results, with minimal complication. duct obstruction. Despite meticulous surgery, failures are often met with. Epiphora after Dacryocystorhinostomy (DCR) is a distressing situation for both patient and the surgeon. Failure rate for external DCR has been reported to be 5%–10% 4-6 or less and 35%–40% 7-9 for endonasal DCR. The most common causes of DCR failure are common canalicular obstruction and obstruction at the rhinostomy site due to reduction in osteotomy size 2 , granulation tissue formation 3 , fibrosis in anastomosis and defective identification and anastomosis. Silicone intubation has been shown to be successful in the management of failed DCR and canalicular block. Silicone intubation is a simple procedure; the effectiveness of this procedure was assessed. A basic surgical principle is to reach the most successful results with the least possible complication. In the modern surgical era, achieving successful results in a cost effective fashion is also important. The aim of this study to evaluate the success rate of silicone intubation in canalicular block as primary surgery and in failed DCR as revised surgery. Abstract were enrolled in this study. These included 12 patients of canalicular block, that were operated for the first time and 20 patients of various failed DCR techniques. Two patients had failed DCR twice, and 18 patients had failed DCR once. 12 of these previous failed DCR were endoscopic DCR, and 6 were external dacryocystorhinostomy (DCR). The inclusion criteria for the procedures were patients having epiphora after previous surgery and common canalicular block. Exclusion criteria was patients having absent puncta, suspicion of malignancy, radiation therapy, posttraumatic lids and bony deformity, nasolacrimal duct block (not operated previously).
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