Nepafenac punctal plug reduces Postop Pain After Cataract Surgery

Dr Eric D. Donnenfeld and the team conducted a phase 2 study to evaluate the safety and efficacy of a nepafenac punctal plug delivery system (N-PPDS) after cataract surgery.

It was a prospective, multicenter, randomized (2:1), parallel-arm, double-masked, placebo-controlled, phase II pilot study of 56 patients. Researchers randomly assigned them to receive either experimental N-PPDS (n=38) or placebo (n=18). All eyes underwent routine unilateral cataract surgery with intraocular lens implantation. The major outcomes assessed were postoperative ocular pain and inflammation.

Key findings of the study were:

• Upon evaluation, researchers found that the N-PPDS group had a significantly higher percentage of pain-free patients than that in the p-PPDS group (22/32 [69%] vs 6/16 [38%] at 3days; and 24/36 [67%] vs 5/16 [31%] at 7days).

• They also found that about 52% of patients in the N-PPDS cohort were pain-free at all postoperative visits compared with 0% in the placebo group.

• On day 7, they noted that the anterior chamber cell scores were better in the N-PPDS group.

• They also noted that the plug retention rate in the overall group was 98.2%, with plug extrusion occurring in one patient in the N-PPDS group who was excluded from the analysis.

The authors concluded, "The Evolute punctal plug delivery system for sustained drug delivery of nepafenac during cataract surgery is safe and effective in controlling postoperative pain and inflammation associated with surgery."

For further information:

https://journals.lww.com/jcrs/Abstract/2021/02000/Safety_and_efficacy_of_nepafenac_punctal_plug.4.aspx