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Application Of 0.1% Bromfenac Sodium Hydrate After LASEK Operation Application Of 0.1% Bromfenac Sodium Hydrate After LASEK Operation

Recently, an ophthalmic researcher at Jianyang People's Hospital of Sichuan Province, China, published a paper aimed at observing partial replacement of sugar with 0.1% bromfenac sodium hydrate eye drops after laser subepithelial keratomileusis (LASEK) Effectiveness and tolerance of corticosteroids. The study pointed out that 0.1% bromfenac sodium hydrate eye drops in patients with LASEK can effectively stabilize intraocular pressure, patients can get better visual acuity and visual quality, and better tolerance, fewer complications, it is worth Promotion. This article was published in the 12th issue of 2015 International Journal of Ophthalmology.

180 cases of 180 patients undergoing LASEK surgery were divided into study group and control group according to different postoperative medication. The study group was given 0.1% bromfenac sodium hydrate eye drops combined with glucocorticoid, the control group given glucocorticoid. Visual acuity, intraocular pressure (IOP) changes and postoperative diffuse interocular keratitis were observed before and after surgery.

The visual acuity of the study group was 1.25 ± 0.22 at 1 month after surgery, and the visual acuity was 0.97 ± 0.23 at 1 month after surgery in the control group (P <0.05). The preoperative, postoperative 1, 10 and postoperative 3, 6, (P> 0.05). The IOP of the study group was 12.29 ± 2.71, 12.67 ± 2.33mm Hg at 1 and 3 months postoperatively, and the IOP of the control group was 14.26 ± 2.65 and 14.56 ± 2.61mm Hg, the difference was statistically significant (P <0.05); There was no significant difference in IOP between preoperative and postoperative 10d and 6mo (P> 0.05) In patients with ocular hypertension, intraocular pressure (IOP) was significantly decreased, and no discomfort occurred in the study group. The degree of diffuse larnellar keratitis (DLK) in the study group was 0, 1 and 2, respectively, 93.33% , 6.67%, 0, which was significantly better than that of the control group (75.56%, 17.78%, 6.67%, respectively). The difference was statistically significant (P <0.05).
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