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用于白内障手术的眼内类固醇给药系统的II期研究结果。

Phase II results of an intraocular steroid delivery system for cataract surgery.

作者信息

Chang D F, Garcia I H, Hunkeler J D, Minas T

机构信息

Altos Eye Physicians, Los Altos, California, USA.

出版信息

Ophthalmology. 1999 Jun;106(6):1172-7. doi: 10.1016/S0161-6420(99)90262-2.

Abstract

OBJECTIVE

To evaluate the safety and efficacy of an intraocular biodegradable polymer dexamethasone drug delivery system (DEX DDS) in treating postoperative inflammation after cataract surgery.

STUDY DESIGN

Multicenter, randomized, double-masked, parallel group study comparing two dose levels of the DEX DDS to concurrent placebo and no treatment control subjects.

PARTICIPANTS

Ninety patients scheduled to undergo extracapsular cataract extraction with phacoemulsification and intraocular lens implantation participated in the study.

INTERVENTION

One or two DEX DDSs, each containing 60 microg of dexamethasone, were placed in the posterior chamber after cataract surgery. Patients receiving the placebo received a DDS composed of the same matrix with no active drug. In vivo rabbit studies have determined that the DEX DDS releases dexamethasone into the anterior chamber (AC) for approximately 7 to 10 days.

MAIN OUTCOME MEASURES

The AC cells and the AC flare were assessed over a 60-day postoperative period using slit-lamp examination by masked observers. The number and percent of patients in each treatment group requiring additional postoperative topical anti-inflammatory medication were compared.

RESULTS

Ninety patients were randomized into 4 treatment groups (30 to the 2 DEX DDS group, 30 to the 1 DEX DDS group, 15 to the placebo DDS group, and 15 to the no treatment group). The control patients required the addition of topical steroids as rescue medication more frequently and sooner than patients receiving DEX DDS (80% vs. 7% at week 2) (P < 0.001). Patients receiving DEX DDS showed a significant reduction in postoperative inflammation as assessed by the combined AC cell and flare scores when compared to the control group from day 3 (P = 0.002) through week 3. The DEX DDS was well tolerated. No clinically significant difference in any safety evaluations, including intraocular pressure, was seen between the DEX DDS-treated and control groups.

CONCLUSION

The DEX DDS was safe and effective in suppressing postoperative inflammation after uncomplicated cataract surgery. Additional topical anti-inflammatory drops were not needed for most patients.

摘要

目的

评估眼内可生物降解聚合物地塞米松药物递送系统(DEX DDS)在治疗白内障手术后炎症中的安全性和有效性。

研究设计

多中心、随机、双盲、平行组研究,比较两种剂量水平的DEX DDS与同期安慰剂及未治疗的对照受试者。

参与者

90例计划接受超声乳化白内障囊外摘除术和人工晶状体植入术的患者参与了该研究。

干预措施

白内障手术后,将一或两个DEX DDS(每个含60微克地塞米松)置于后房。接受安慰剂的患者接受由相同基质但无活性药物组成的DDS。体内兔研究已确定DEX DDS可将地塞米松释放到前房(AC)中约7至10天。

主要观察指标

术后60天内,由 masked 观察者使用裂隙灯检查评估前房细胞和前房闪光。比较各治疗组中需要额外术后局部抗炎药物治疗的患者数量和百分比。

结果

90例患者被随机分为4个治疗组(30例至2个DEX DDS组,30例至1个DEX DDS组,15例至安慰剂DDS组,15例至未治疗组)。与接受DEX DDS的患者相比,对照组患者更频繁且更早需要添加局部类固醇作为抢救药物(第2周时分别为80%对7%)(P < 0.001)。与对照组相比,从第3天(P = 0.002)至第3周,接受DEX DDS的患者经前房细胞和闪光综合评分评估显示术后炎症显著减轻。DEX DDS耐受性良好。DEX DDS治疗组与对照组在包括眼压在内的任何安全性评估中均未观察到临床显著差异。

结论

DEX DDS在抑制单纯性白内障手术后的术后炎症方面安全有效。大多数患者无需额外的局部抗炎滴眼液。

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