不同类型后房型眼内透镜植入术后患者满意度的比较。

ISRN surgery Pub Date : 2012-01-01 Epub Date: 2012-06-19 DOI:10.5402/2012/629158
Muhammad Waseem, Sadia Humayun, Omer Farooq, Quratulain Humayun, Sana Sadiq Sheikh
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引用次数: 0

摘要

目的比较在不顺利的白内障手术中植入硬性、可折叠或可滚动的后房型眼内人工晶体后,患者对白天日常活动和夜间视力的满意程度。设计。回顾性横断面研究。研究地点和时间。卡拉奇 PNS SHIFA 医院,2009 年 11 月至 2010 年 11 月。研究方法。研究对象包括 91 名白内障手术患者,这些患者均顺利进行了乳化手术,在袋内植入了眼内晶状体,最佳矫正视力达到 6/9 或更高。排除了术后出现并发症的患者。对至少 3 个月前接受过白内障手术的患者进行了专门设计的问卷调查,以评估患者对视力的满意度。最后,他们被分为 "非常好 "到 "非常差 "五个组别。结果采用 SPSS 16 版进行分析。结果三个组别的满意度存在差异。佩戴可折叠后房型眼内透镜后,白天和晚上的视力都很好。结论。与植入硬性或可滚动后房型眼内晶状体的患者相比,植入可折叠后房型眼内晶状体的患者白天和夜间的视力满意度更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Patient's Satisfaction Level after Different Types of Posterior Chamber Intraocular Lens Implantation.

Objective. To compare patient's satisfaction level in performing routine activities during daylight and night vision after implantation with rigid, foldable, or rollable posterior chamber intraocular lens implants in uneventful cataract surgery. Design. Retrospective, cross-sectional. Place and Duration of Study. PNS SHIFA Hospital, Karachi, from Nov. 2009 to Nov. 2010. Methodology. 91 cataract surgery patients who had uneventful phacoemulsification, within the bag placement of intraocular lens and achieved best corrected visual acuity 6/9 or better were included in the study. Patients who developed postoperative complications were excluded. A specially designed questionnaire was used to assess patient's satisfaction level of vision for those who underwent cataract surgery at least 3 months ago. Finally, they were categorized into five groups ranging from "very good" to "very poor." SPSS version 16 was used to analyze the results. Results. There was a difference in satisfaction level between three groups. Vision was good in the day and the night with foldable posterior chamber intraocular lens implants. Conclusion. It was concluded that visual satisfaction level of patients who had foldable posterior chamber intraocular lens implantation was better during the day and night as compared to patients who had rigid or rollable posterior chamber intraocular lenses implantation.

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