硅水凝胶隐形眼镜在特定临床病例中的治疗应用。

Therapeutic use of a silicone hydrogel contact lens in selected clinical cases.

作者信息

Ambroziak Anna M, Szaflik Jacek P, Szaflik Jerzy

机构信息

Department of Ophthalmology, Medical University of Warsaw, Warsaw, Poland.

出版信息

Eye Contact Lens. 2004 Jan;30(1):63-7. doi: 10.1097/01.ICL.0000105563.54932.44.

DOI:10.1097/01.ICL.0000105563.54932.44

PMID:14722474

Abstract

PURPOSE

To evaluate a silicone hydrogel contact lens as a continuous-wear bandage in selected clinical cases, a prospective, open, nonrandomized clinical study was conducted.

METHODS

Seventy eyes from 70 patients with anterior segment conditions for which therapeutic lenses were indicated were enrolled in the study. In most patients (47 eyes, 67%), the presenting condition was bullous keratopathy. Patients were fitted with a lotrafilcon A silicone hydrogel lens (Focus Night & Day) that was worn continuously for 7 to 30 days, and the concomitant therapies were used. The corneal condition was assessed, and subjective comfort was recorded for 7 days to 18 months after fitting (mean follow-up, 69 days).

RESULTS

Of 70 eyes, 64 (91%) showed improvement in the clinical condition of the eye, and 66 (94%) rated comfort when wearing the lens as very good or good.

CONCLUSIONS

The study lens was found to be an effective and well-tolerated bandage lens in these selected patients.

摘要

目的

为了在特定临床病例中评估一种硅水凝胶隐形眼镜作为连续佩戴绷带的效果，开展了一项前瞻性、开放性、非随机临床研究。

方法

70例患有需要治疗性镜片的眼前节疾病患者的70只眼睛纳入研究。大多数患者（47只眼睛，67%）的主要病症为大泡性角膜病变。为患者佩戴lotrafilcon A硅水凝胶镜片（日夜型焦点镜片），连续佩戴7至30天，并采用相应的辅助治疗。评估角膜状况，并记录配镜后7天至18个月的主观舒适度（平均随访69天）。