Kaushik Sushmita, Kataria Pankaj, Raj Srishti, Pandav Surinder Singh, Ram Jagat
Advanced Eye Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Br J Ophthalmol. 2017 Dec;101(12):1623-1627. doi: 10.1136/bjophthalmol-2017-310276. Epub 2017 May 6.
To evaluate the safety and efficacy of a low-cost glaucoma drainage device (GDD), Aurolab aqueous drainage implant (AADI), similar in design to the Baerveldt glaucoma implant (BGI), in refractory childhood glaucoma.
This prospective interventional study was conducted in a tertiary care postgraduate teaching institute. Children aged <16 years with uncontrolled intraocular pressure (IOP) refractory to medical treatment and considered at high risk of failure following trabeculectomy were recruited. Eligible children were implanted with the AADI. Those completing minimum 6-month follow-up were included. Main outcome measures were IOP reduction from preoperative values and postoperative complications.
34 eyes of 31 patients were analysed. Average follow-up was 18.3±6.9 months. Mean IOP reduced from 27.4±7.5 mm Hg on maximum medication to 14.6±10.74 mm Hg, 13.8±7.5 mm Hg, 12.8±5.6 mm Hg and 14.7±5.8 mm Hg at 1 week, 6 months, 1 year (32 eyes of 29 children) and 2 years (25 eyes of 22 children) postoperatively, respectively (p<0.001). The cumulative probability of success was 91.18% at 6 months and 81.7% at 18-24 months. Mean number of topical medications decreased from 3.1±0.6 to 1.8±1.3 at 6 months and 1.6±1.1 at 24 months (p<0.001). Preoperatively, 25 patients required systemic acetazolamide, decreasing to three patients at 2 years. There was no tube erosion or infection. One eye developed retinal detachment.
The AADI appears to be a viable low-cost GDD with effectiveness and safety profile comparable with published reports of the BGI and Ahmed glaucoma valve implant in children.
为评估一种低成本青光眼引流装置(GDD)——Aurolab房水引流植入物(AADI)的安全性和有效性,该装置在设计上与Baerveldt青光眼植入物(BGI)相似,用于治疗难治性儿童青光眼。
这项前瞻性干预研究在一家三级医疗研究生教学机构进行。招募年龄小于16岁、眼压控制不佳且药物治疗无效、小梁切除术后失败风险高的儿童。符合条件的儿童植入AADI。纳入至少随访6个月的儿童。主要观察指标为眼压较术前值的降低情况及术后并发症。
分析了31例患者的34只眼。平均随访时间为18.3±6.9个月。平均眼压从最大药物治疗时的27.4±7.5 mmHg分别降至术后1周时的14.6±10.74 mmHg、6个月时的13.8±7.5 mmHg、1年时(29例儿童的32只眼)的12.8±5.6 mmHg和2年时(22例儿童的25只眼)的14.7±5.8 mmHg(p<0.001)。6个月时成功的累积概率为91.18%,18 - 24个月时为81.7%。局部用药的平均数量从3.1±0.6降至6个月时的1.8±1.3和24个月时的1.6±1.1(p<0.001)。术前,25例患者需要全身使用乙酰唑胺,2年时降至3例。未发生引流管侵蚀或感染。1只眼发生视网膜脱离。
AADI似乎是一种可行的低成本GDD,其有效性和安全性与已发表的关于BGI和Ahmed青光眼阀植入物用于儿童的报告相当。