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在中低收入国家,白内障手术后玻璃体内注射曲安奈德-莫西沙星的疗效和安全性 - 一年期审计。

Efficacy and safety of intravitreal injection of triamcinolone-moxifloxacin after cataract surgery in a low to middle income country - a one-year audit.

机构信息

Department of Ophthalmology, Aga Khan University Hospital, Karachi, Pakistan.

出版信息

J Pak Med Assoc. 2023 Jan;73(1):92-97. doi: 10.47391/JPMA.5207.

Abstract

OBJECTIVE

To evaluate the safety and efficacy of intravitreal injection of triamcinolone and moxifloxacin regime administered immediately following cataract surgery.

METHODS

The retrospective study was conducted from January to June 2021 at a tertiary care referral centre in Karachi and comprised record of all patients who underwent dropless cataract surgery from April 2018 to June 2019. Data included slit lamp examination, dilated fundal exam, uncorrected visual acuity, best corrected visual acuity, and intraocular pressure. Cataract assessment and anterior chamber reaction were graded according to the World Health Organisation cataract grouping system. Efficacy of the regime was defined as the ability to prevent postoperative endophthalmitis. Stratification analysis was done to note if gender has any role in terms of effectiveness. Data was analysed using Microsoft Excel version 16.0 and IBM SPSS version 27.

RESULTS

Of 240 eyes of 161 patients analysed, 114(47.5%) were of men who had a mean age of 57.89±14.32 years, and 126(52.5%) were of females with a mean age of 58.02±10.85 years. Overall, 2(1.75%) male subjects and 1(0.8%) female subject developed breakthrough inflammation within one week of the procedure. They were treated with anti-inflammatory drops and in 1(33%) of the cases antibiotic drop for 1 week. At day 90, no patient had residual inflammation or new onset inflammation. Also, 15(6.25%) patients developed raised intraocular pressure from day 7 to day 30. Most cases 10(66.7%) resolved within 1 week of using intraocular pressure-lowering drops. No patient developed endophthalmitis postoperatively.

CONCLUSIONS

Dropless cataract regime was found to be an effective and safe alternative that was easy to administer.

摘要

目的

评估白内障手术后立即给予曲安奈德和莫西沙星玻璃体腔内注射的安全性和疗效。

方法

本回顾性研究于 2021 年 1 月至 6 月在卡拉奇的一家三级转诊中心进行,纳入了 2018 年 4 月至 2019 年 6 月期间接受无滴剂白内障手术的所有患者的记录。数据包括裂隙灯检查、散瞳眼底检查、未矫正视力、最佳矫正视力和眼压。白内障评估和前房反应根据世界卫生组织白内障分组系统进行分级。该方案的疗效定义为预防术后眼内炎的能力。进行分层分析以注意性别在有效性方面是否有任何作用。使用 Microsoft Excel 版本 16.0 和 IBM SPSS 版本 27 分析数据。

结果

在分析的 161 名患者的 240 只眼中,男性 114 只(47.5%),平均年龄为 57.89±14.32 岁,女性 126 只(52.5%),平均年龄为 58.02±10.85 岁。总体而言,2 名(1.75%)男性和 1 名(0.8%)女性在手术后一周内出现突破性炎症。他们接受了抗炎滴眼液治疗,在 1 例(33%)中接受了 1 周的抗生素滴眼液治疗。在第 90 天,没有患者有残留炎症或新出现的炎症。此外,15 名(6.25%)患者在第 7 天至第 30 天期间出现眼压升高。大多数病例(66.7%)在使用降眼压滴眼液 1 周内得到解决。没有患者在术后发生眼内炎。

结论

无滴剂白内障方案被发现是一种有效且安全的替代方案,易于管理。

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