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多焦点人工晶状体植入术后6个月手术性眼内炎的发生率

Incidence of Postsurgical Intraocular Inflammation 6 Months After Implantation with a Multifocal Intraocular Lens.

作者信息

Paauw James, Caplan Michael B, Gallardo Mark, Rushin Kristi, Horn Jeffrey D

机构信息

Department of Ophthalmology, Piedmont Eye Center, Lynchburg, VA, USA.

Berkeley Eye Center, Houston, TX, USA.

出版信息

Clin Ophthalmol. 2024 Jul 9;18:1971-1980. doi: 10.2147/OPTH.S458130. eCollection 2024.

Abstract

PURPOSE

This study assessed the incidence of postsurgical intraocular inflammation after cataract extraction by phacoemulsification and implantation with AcrySof IQ ReSTOR intraocular lenses (IOLs) produced using an updated manufacturing process. Incidence rates were compared with historical rates of postsurgical intraocular inflammation.

METHODS

This was a prospective, multicenter, post-approval study at 34 sites. Patients aged ≥22 years received a study lens in at least 1 eye. Postsurgical intraocular inflammation (aqueous cell grade ≥3+ within 14 days after surgery, aqueous cell ≥2+ at 14 to ≤60 days after surgery, or aqueous cell ≥1+ at >60 days) was assessed within a 180-day period after implantation. Rates of toxic anterior segment syndrome (TASS), acute postoperative endophthalmitis, chronic postoperative endophthalmitis, and uncategorized cases of postsurgical intraocular inflammation were assessed. Ocular adverse events (AEs) and ocular adverse device effects (ADEs) were evaluated. Historical rates of postsurgical intraocular inflammation were determined from the 2011-2013 Medicare Limited Data Set files (a 5% sample of the Medicare data set representative of patients aged ≥65 years).

RESULTS

Final safety analysis set included 3357 eyes (1792 patients; mean age, 68.6 ± 7.9 years). Postsurgical intraocular inflammation (any type) rate was 5.1 per 1000 attempted IOL implants (95% CI, 2.95, 8.10). TASS, acute postoperative endophthalmitis, and uncategorized inflammation rates were 0.6 (95% CI, 0.07, 2.15), 0.3 (95% CI, 0.01, 1.66), and 4.2 (95% CI, 2.28, 6.99) per 1000 attempted IOL implants, respectively. There were no events of chronic postoperative endophthalmitis. Ocular AEs and ADEs were reported in 17% and 1.5% of eyes, respectively. Most common ADEs were halo (0.63%) and glare (0.51%). The historical postsurgical inflammation rate from 221,519 cataract procedures was 10.3/1000 cataract surgeries, and the endophthalmitis rate was 1.2/1000 surgeries.

CONCLUSION

The updated IOL manufacturing process resulted in postoperative intraocular inflammation rates that were substantially lower than the historic rate.

摘要

目的

本研究评估了采用更新制造工艺生产的AcrySof IQ ReSTOR人工晶状体(IOL)进行白内障超声乳化吸除及植入术后眼内炎症的发生率。将发生率与既往术后眼内炎症发生率进行比较。

方法

这是一项在34个地点开展的前瞻性、多中心、上市后研究。年龄≥22岁的患者至少一只眼植入研究用晶状体。在植入后180天内评估术后眼内炎症(术后14天内房水细胞分级≥3+,术后14至≤60天房水细胞≥2+,或术后>60天房水细胞≥1+)。评估毒性前段综合征(TASS)、急性术后眼内炎、慢性术后眼内炎以及未分类的术后眼内炎症病例的发生率。评估眼部不良事件(AE)和眼部不良器械效应(ADE)。既往术后眼内炎症发生率根据2011 - 2013年医疗保险有限数据集文件(医疗保险数据集的5%样本,代表年龄≥65岁的患者)确定。

结果

最终安全性分析集包括3357只眼(1792例患者;平均年龄68.6±7.9岁)。每1000次人工晶状体植入尝试中,术后眼内炎症(任何类型)发生率为5.1(95%CI,2.95,8.10)。每1000次人工晶状体植入尝试中,TASS、急性术后眼内炎和未分类炎症的发生率分别为0.6(95%CI,0.07,2.15)、0.3(95%CI,0.01,1.66)和4.2(95%CI,2.28,6.99)。无慢性术后眼内炎事件。分别有17%和1.5%的眼报告了眼部AE和ADE。最常见的ADE是光晕(0.63%)和眩光(0.51%)。221,519例白内障手术的既往术后炎症发生率为10.3/1000白内障手术,眼内炎发生率为1.2/1000手术。

结论

更新后的人工晶状体制造工艺导致术后眼内炎症发生率显著低于既往发生率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b84/11246081/97c5057fa41f/OPTH-18-1971-g0001.jpg

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