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Success of endoscopic dacryocystorhinostomy with or without stents: systematic review and meta-analysis

机译:内窥镜泪囊化的成功与或没有支架:系统评价和荟萃分析

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Purpose: To evaluate the effect of stents on the success of endoscopic dacryocystorhinostomy (DCR-EN) for treating primary acquired nasolacrimal duct obstruction (NLDO). Method: A systematic review of randomized clinical trials of DCR-EN for NLDO comparing outcomes of surgeries performed with and without the use of bicanalicular stents and the complications associated with each procedure. Two authors independently searched six databases (Scopus, PubMed, EMBASE, Google Scholar, Cochrane Central Register of Controlled Trials, and Web of Science) up to May 2019. Statistical analysis and meta-analysis were performed using RevMan 5.3 software provided by the Cochrane Collaboration. Results: Twelve studies involving 997 surgeries were included in this systematic review. The meta-analysis using a fixed-effects model showed a 94% success rate with stents versus 90.6% without stent. Although stent use favors greater success of DCR-EN, the confidence interval (CI) was wide and very close to nullity line (1.01), decreasing the strength of the recommendation for stent (odds ratio: 1.62, 95% CI: 1.01-2.59, I-2 = 0%). Meta-analysis of the adverse effects was not possible. A descriptive analysis was performed of the general complications related to the stents. Conclusions: There is evidence that the use of bicanalicular stents slightly improves the success rate of DCR-EN, but the quality of evidence is low. Future prospective, randomized trials enrolling larger sample sizes may provide stronger evidence to determine whether the stent use influences the success of primary acquired DCR-EN.
机译:目的:评估支架对治疗原发性肺癌管道阻塞(NLDO)的内窥镜泪囊化术(DCR-ZH)的成功。方法:对NLDO的DCR-ZH随机临床试验进行系统审查,用于比较使用和不使用与每个程序相关的手术的手术的结果和与每个程序相关的并发症。 2019年5月,两位作者独立搜索了六个数据库(Scopus,Pubmed,Embase,Google Scholar,Cochrane中央登记和科学网站),使用Cochrane协作提供的Revman 5.3软件进行统计分析和元分析。结果:在这次系统审查中涉及997个手术的12项研究。使用固定效果模型的META分析显示出94%的成功率,支架与90.6%没有支架。虽然支架使用的最有利于DCR-ZH的成功,但置信区间(CI)宽,非常接近无效线(1.01),降低支架推荐的强度(差距:1.62,95%CI:1.01-2.59 ,I-2 = 0%)。荟萃分析不可能。对与支架相关的一般并发症进行了描述性分析。结论:有证据表明,使用双囊支架略微提高了DCR-ZH的成功率,但证据质量低。未来的预期,注册更大的样本尺寸的随机试验可以提供更强的证据来确定支架使用是否会影响初级获得的DCR-ZH的成功。

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