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超声乳化吸除联合iStent注射与超声乳化吸除联合Hydrus微支架的疗效比较。

Comparison of Efficacy of Combined Phacoemulsification and iStent Inject versus Combined Phacoemulsification and Hydrus Microstent.

作者信息

Chee Wai Kitt, Yip Vivien Cherng Hui, Tecson Ivan O'Neill, Chua Chun Hau, Ang Bryan Chin Hou, Kee Ae Ra, Hu Jeremy Youwei, Kan Tsia-Chuen John, Yip Leonard Wei Leon

机构信息

Department of Ophthalmology, National Healthcare Group Eye Institute, Tan Tock Seng Hospital, Singapore, Singapore.

Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.

出版信息

Clin Ophthalmol. 2023 Apr 14;17:1151-1159. doi: 10.2147/OPTH.S403386. eCollection 2023.

Abstract

AIM

This study aims to compare the efficacy and safety of combined phacoemulsification with iStent inject (Phaco-iStent) and Hydrus microstent (Phaco-Hydrus).

METHODS

This was a retrospective comparative study of patients who underwent Phaco-iStent from April 2019 to August 2020 and Phaco-Hydrus from August 2019 to December 2020 at a tertiary eye centre in Singapore. Sixty-nine Phaco-iStent eyes and 49 Phaco-Hydrus eyes were included in this study. Complete surgical success was defined as freedom from second glaucoma surgery, Intraocular pressure (IOP) of 18 mmHg or less, and discontinuation of all antiglaucoma medications.

RESULTS

At 12 months, both Phaco-iStent and Phaco-Hydrus groups had comparable surgical success rate (68.1% vs 51%, =0.061), reduction in antiglaucoma medication use (-1.3 ± 0.1 vs -1.4 ± 0.10, =0.880) and intraocular pressure reduction (-1.1 ± 0.5 mmHg vs -1.6 ± 0.9 mmHg, =0.323). Overall intraoperative and postoperative complications rate were similar in both groups, though hyphema was more commonly seen in early postoperative period in the Phaco-Hydrus compared to the Phaco-iStent group (8% vs 0%, =0.028), with majority of cases resolving without any need for surgical intervention. Device obstruction was also more common in the Phaco-Hydrus group compared to the Phaco-iStent group (14% vs 4.3%, =0.04).

CONCLUSION

Phaco-iStent and Phaco-Hydrus have similar surgical efficacy and safety profiles at 12 months.

摘要

目的

本研究旨在比较超声乳化联合iStent注射(超声乳化-iStent)与Hydrus微支架(超声乳化-Hydrus)的疗效和安全性。

方法

这是一项回顾性比较研究,研究对象为2019年4月至2020年8月在新加坡一家三级眼科中心接受超声乳化-iStent治疗以及2019年8月至2020年12月接受超声乳化-Hydrus治疗的患者。本研究纳入了69只接受超声乳化-iStent治疗的眼睛和49只接受超声乳化-Hydrus治疗的眼睛。完全手术成功定义为无需进行二次青光眼手术、眼压在18 mmHg或以下,并且停用所有抗青光眼药物。

结果

在12个月时,超声乳化-iStent组和超声乳化-Hydrus组的手术成功率相当(68.1%对51%,P = 0.061),抗青光眼药物使用减少情况相当(-1.3±0.1对-1.4±0.10,P = 0.880),眼压降低情况相当(-1.1±0.5 mmHg对-1.6±0.9 mmHg,P = 0.323)。两组的总体术中和术后并发症发生率相似,不过与超声乳化-iStent组相比,超声乳化-Hydrus组在术后早期更常见前房积血(8%对0%,P = 0.028),大多数病例无需手术干预即可自行消退。与超声乳化-iStent组相比,Hydrus微支架组的装置阻塞也更常见(14%对4.3%,P = 0.04)。

结论

超声乳化-iStent和超声乳化-Hydrus在12个月时具有相似的手术疗效和安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e01c/10112347/fc5ae1ea5411/OPTH-17-1151-g0001.jpg

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