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泪道内镜下治疗鼻泪管阻塞或狭窄的临床疗效及预后因素分析。

Clinical outcomes and prognostic factors in patients with nasolacrimal duct obstruction or stenosis using dacryoendoscopy.

机构信息

Department of Orbital and Oculoplastic Surgery, Tianjin Eye Hospital, Tianjin, China.

Tianjin Key Lab of Ophthalmology and Visual Science, Tianjin, China.

出版信息

BMJ Open Ophthalmol. 2024 Oct 31;9(1):e001743. doi: 10.1136/bmjophth-2024-001743.

Abstract

OBJECTIVE

To evaluate the effectiveness of dacryoendoscopic-assisted laser dacryoplasty with silicone intubation (DLDI) for the management of nasolacrimal duct obstruction (NLDO) or stenosis, and to identify the factors associated with DLDI failure.

METHODS AND ANALYSIS

This study was designed as a prospective, single-centre cohort study. Patients with NLDO or stenosis who underwent DLDI from December 2019 to December 2021 at Tianjin Eye Hospital were considered for enrolment. The Kaplan-Meier estimator was used to assess the anatomical and functional success rate of DLDI within 2 years follow-up after removal of the silicone stent. Cox proportional hazards regression models were used to identify risk factors for treatment failure.

RESULTS

170, 174 and 178 eyes were included in Groups A (proximal NLDO), B (distal NLDO) and C (nasolacrimal duct stenosis), respectively. The overall anatomical success rate was 84.8% for the entire cohort at the 2-year follow-up. The cumulative anatomical or functional success rate for Groups B and C was significantly higher than that for Group A. In the multivariable model, a higher risk of failed DLDI surgery was associated with a history of chronic dacryocystitis (HR=3.07; p<0.001) and a longer duration of epiphora than 1 year (HR=2.67; p<0.001). Of the 522 eyes, 37 patients (7.1%) had surgery-related complications.

CONCLUSIONS

DLDI is an effective minimally invasive technique for treatment in patients with distal NLDO or stenosis. Factors associated with a higher risk of reoperation include a longer duration of epiphora and a history of chronic dacryocystitis.

TRIAL REGISTRATION NUMBER

NCT05999058.

摘要

目的

评估经鼻内窥镜辅助激光泪道成形术联合硅胶管植入(DLDI)治疗鼻泪管阻塞(NLDO)或狭窄的有效性,并确定与 DLDI 失败相关的因素。

方法与分析

本研究设计为前瞻性、单中心队列研究。纳入 2019 年 12 月至 2021 年 12 月在天津市眼科医院接受 DLDI 治疗的 NLDO 或狭窄患者。采用 Kaplan-Meier 估计器评估 2 年内取出硅胶支架后 DLDI 的解剖和功能成功率。采用 Cox 比例风险回归模型确定治疗失败的危险因素。

结果

A 组(近段 NLDO)、B 组(远段 NLDO)和 C 组(鼻泪管狭窄)分别纳入 170、174 和 178 只眼。整个队列在 2 年随访时的总体解剖成功率为 84.8%。B 组和 C 组的累积解剖或功能成功率明显高于 A 组。多变量模型显示,慢性泪囊炎病史(HR=3.07;p<0.001)和流泪时间超过 1 年(HR=2.67;p<0.001)与 DLDI 手术失败的风险增加相关。在 522 只眼中,37 名患者(7.1%)发生与手术相关的并发症。

结论

DLDI 是治疗远端 NLDO 或狭窄患者的一种有效微创技术。与再次手术风险增加相关的因素包括流泪时间较长和慢性泪囊炎病史。

试验注册号

NCT05999058。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc7/11529774/2a36251f4598/bmjophth-9-1-g001.jpg

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