Senthilkumar Vijayalakshmi A, Akbar Umme Salma, Rajendrababu Sharmila
Department of Glaucoma, Aravind Eye Hospital and Postgraduate Institute of Ophthalmology, Madurai, Tamil Nadu, India.
Indian J Ophthalmol. 2025 Mar 1;73(Suppl 2):S267-S271. doi: 10.4103/IJO.IJO_958_24. Epub 2024 Sep 19.
To report the incidence, etiology, and risk factors for tube explantation in patients undergoing patch-free glaucoma drainage device (GDD).
Of the total 1303 patients who underwent patch-free GDD (703 non-valved GDD and 600 valved GDD) for refractory glaucoma during January 2020-October 2023, we identified five cases of postoperative complications following GDD that required tube or shunt removal.
Median (IQR) age of our study cohorts was 54.5 (8-66) years. The incidence of tube exposure and tube explantation was 0.003% and 0.004%, respectively. The median time interval for tube or plate explantation from the time of GDD surgery was 11.5 (2-16) months. The diagnoses of refractory glaucoma for which GDD was performed were secondary glaucoma following multiple vitreoretinal (VR) surgery (60%), primary open-angle glaucoma (20%), and aphakic glaucoma (20%). Of these, two patients (40%) presented with recurrent tube exposures, two patients (40%) with tube exposure and early endophthalmitis, and one patient (20%) with persistent hypotony. Four patients (80%) had undergone non-valved Aurolab aqueous drainage implant and one underwent (20%) Ahmed glaucoma implant. Three patients (60%) had diabetes mellitus with a history of multiple VR surgical intervention. GDD explantation was done in three patients (60%), and the remaining two patients (40%) required only tube amputation. One patient presented with orbital cellulitis, and there was no culture growth seen in any of our study cohorts.
Tube and plate exposures pose a significant risk for potential infections and warrant prompt explantation of GDD to avoid endophthalmitis. Previous history of multiple VR surgeries, diabetes mellitus, and non-valved implants were the common risk associations noted for tube exposures in our retrospective study.
报告接受无补片青光眼引流装置(GDD)植入术患者的引流管取出率、病因及危险因素。
在2020年1月至2023年10月期间接受无补片GDD植入术治疗难治性青光眼的1303例患者(703例无瓣膜GDD和600例有瓣膜GDD)中,我们确定了5例GDD术后需要取出引流管或分流装置的并发症病例。
我们研究队列的中位(四分位间距)年龄为54.5(8 - 66)岁。引流管暴露和引流管取出率分别为0.003%和0.004%。从GDD手术到引流管或引流板取出的中位时间间隔为11.5(2 - 16)个月。接受GDD植入术治疗的难治性青光眼诊断类型为多次玻璃体视网膜(VR)手术后的继发性青光眼(60%)、原发性开角型青光眼(20%)和无晶状体性青光眼(20%)。其中,2例患者(40%)出现反复引流管暴露,2例患者(40%)出现引流管暴露并早期眼内炎,1例患者(20%)出现持续性低眼压。4例患者(80%)接受了无瓣膜的Aurolab房水引流植入物,1例患者(20%)接受了Ahmed青光眼植入物。3例患者(60%)患有糖尿病且有多次VR手术干预史。3例患者(60%)进行了GDD取出,其余2例患者(40%)仅需要进行引流管截断。1例患者出现眼眶蜂窝织炎,我们的研究队列中均未培养出细菌。
引流管和引流板暴露对潜在感染构成重大风险,需要及时取出GDD以避免眼内炎。在我们的回顾性研究中,多次VR手术史、糖尿病和无瓣膜植入物是引流管暴露常见的风险关联因素。