Dubay Sareta K, Dwarika Dorian, Bhola Ronnie, Kumar Balakrishna Vineeth
Trinidad Eye Hospital (Caribbean Vitreous and Retina Surgery Ltd), Trinidad.
Med Hypothesis Discov Innov Ophthalmol. 2022 Apr 30;11(1):44-51. doi: 10.51329/mehdiophthal1445. eCollection 2022 Spring.
Pars plana vitrectomy with implantation of an Ahmed glaucoma valve in the vitreous cavity has been reported with a success rate in the management of refractory and neovascular glaucoma. This study aimed to present the outcomes of pars plana Ahmed glaucoma valve (PPAV) surgical implantation in cases with refractory glaucoma.
In this single-center, retrospective, comparative study, 87 consecutive patients diagnosed with refractory glaucoma who underwent PPAV surgical implantation between October 2015 and October 2019 were evaluated. A successful postoperative outcome was defined as intraocular pressure (IOP) ≤ 21 mmHg upon examination and a reduction in the number of anti-glaucoma agents used at the latest follow-up.
Finally, 81 eyes of 78 patients with refractory glaucoma were included; 54 (66.66%) of the eyes had neovascular glaucoma. The mean follow-up was 20.65 ± 12.17 months (range: 2-52 months). The mean preoperative IOP was 40.01 ± 1.19 mmHg and reduced significantly to 16.73 ± 0.82 mmHg at the latest follow-up ( < 0.001); a successful IOP outcome was achieved in 88.89% of eyes. The mean number of anti-glaucoma agents decreased significantly from 2.86 ± 0.09 preoperatively to 1.46 ± 0.11 at the latest follow-up (P < 0.001); while 61 (75.31%) of eyes had a reduction in the number of IOP lowering eye drops, and 14 (17.28%) had no need for IOP lowering eye drops.
PPAV surgery is a successful procedure for IOP reduction in patients with refractory glaucoma. Our study demonstrated either reduction or elimination of IOP lowering eye drops postoperatively. Large scale studies with a comparison group, a longer follow-up, and having various subtypes of glaucoma are required as future research to confirm these outcomes.
有报道称,在玻璃体腔植入艾哈迈德青光眼引流阀的玻璃体切除术在难治性和新生血管性青光眼的治疗中具有一定成功率。本研究旨在介绍难治性青光眼患者行玻璃体腔艾哈迈德青光眼引流阀(PPAV)手术植入的结果。
在这项单中心、回顾性、对照研究中,对2015年10月至2019年10月期间连续87例行PPAV手术植入的难治性青光眼患者进行了评估。术后成功的结果定义为检查时眼压(IOP)≤21 mmHg,且在最近一次随访时使用的抗青光眼药物数量减少。
最终,纳入了78例难治性青光眼患者的81只眼;其中54只眼(66.66%)患有新生血管性青光眼。平均随访时间为20.65±12.17个月(范围:2 - 52个月)。术前平均眼压为40.01±1.19 mmHg,在最近一次随访时显著降至16.73±0.82 mmHg(P<0.001);88.89%的眼眼压控制成功。抗青光眼药物的平均数量从术前的2.86±0.09显著降至最近一次随访时的1.46±0.11(P<0.001);61只眼(75.31%)降低眼压滴眼液的使用量减少,14只眼(17.28%)不再需要使用降低眼压的滴眼液。
PPAV手术是降低难治性青光眼患者眼压的一种成功手术。我们的研究表明术后降低眼压滴眼液的使用量减少或不再使用。未来研究需要进行有对照组、更长随访时间以及纳入各种青光眼亚型的大规模研究来证实这些结果。