首页> 外文期刊>British journal of ophthalmology >A pilot randomised controlled trial comparing the post-operative pain experience following vitrectomy with a 20-gauge system and the 25-gauge transconjunctival system.
【24h】

A pilot randomised controlled trial comparing the post-operative pain experience following vitrectomy with a 20-gauge system and the 25-gauge transconjunctival system.

机译:一项前瞻性随机对照试验,比较了采用20规格和25规格经结膜系统的玻璃体切除术后的疼痛经历。

获取原文
获取原文并翻译 | 示例
           

摘要

AIMS: To compare post-operative pain following 25-gauge (25G) and 20-gauge (20G) vitrectomy in the first week following surgery. METHODS: The study was a pilot randomised controlled trial with patients masked to the treatment allocation. Post-operative pain was assessed using both a visual scale and verbal pain scores for 1 week following surgery. Additional data collected included intraocular pressure (IOP), time taken to perform the surgical procedure, per-operative and post-operative complications, and dropout rates. RESULTS: Forty patients were recruited for the study: 21 randomised to 20G vitrectomy and 19 to 25G. In the first 12 h following surgery, presence of significant post-operative pain (defined as >1 cm on a visual analogue scale) was similar in both 20G (50%) and 25G (53%) patients. In the first week following surgery, 38 of the 527 scores (7.2%) were >1 (median 2.1, IQR 1.3-3) cm; however, there was evidence that significant pain statistical difference in the time taken to complete the surgical procedure, although in the 25G group the time from first incision to the start of vitrectomy was significantly shorter (p = 0.043) and in the 20G group the time taken to complete the vitrectomy was less (p = 0.047). Post-operative hypotony (IOP <6 mmHg) was observed in 25% of patients in the 25G group. No patients required additional surgery for hypotony. CONCLUSION: There was evidence that 25G resulted in less patient discomfort. However, pain was not a prominent feature in either group. We failed to find a significant advantage in 25G for patients or surgeons.
机译:目的:比较在手术后第一周进行25规格(25G)和20规格(20G)玻璃体切割手术后的术后疼痛。方法:该研究是一项随机对照试验,其中患者掩盖了治疗分配。术后1周,使用视觉量表和言语疼痛评分评估术后疼痛。收集的其他数据包括眼内压(IOP),执行手术程序所需的时间,术中和术后并发症以及辍学率。结果:招募了40位患者进行研究:21位随机接受20G玻璃体切割术,19至25G。在手术后的前12小时内,在20G(50%)和25G(53%)的患者中,存在明显的术后疼痛(在视觉模拟量表上定义为> 1 cm)。在手术后的第一周,527个评分中有38个评分(7.2%)> 1(中位数2.1,IQR 1.3-3)cm。但是,有证据表明,完成手术过程所需的疼痛统计差异显着,尽管在25G组中,从第一次切开到开始玻璃体切除术的时间明显缩短了(p = 0.043),而在20G组中,完成玻璃体切除术所需的时间更少(p = 0.047)。 25G组中有25%的患者出现术后低渗(IOP <6 mmHg)。没有患者因低渗而需要额外的手术。结论:有证据表明25G可减少患者不适感。但是,疼痛在这两个组中都不是突出的特征。我们未能为患者或外科医生找到25G的显着优势。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号