Emergency Department, University Hospital, Galway, Ireland.
Emergency Department, Midland Regional Hospital, Tullamore, Co Offaly, Ireland.
Emerg Med J. 2014 Jun;31(6):463-6. doi: 10.1136/emermed-2012-201447. Epub 2013 Mar 29.
Patients with corneal foreign bodies (CFBs) often present to the emergency department (ED). However, removal techniques vary among emergency physicians (EPs). A prospective, single-blinded, observational study was performed to compare slit-lamp-aided (SLA) versus non-slit-lamp-aided (NSLA) CFB removal by EPs.
Five EPs enrolled consecutive patients with a CFB over 3 months. One blinded EP reviewed patients after 3 days. The study end points were: change in visual acuity; visual analogue pain scale (VAS) score at 12 and 24 h; satisfaction rating; symptoms at follow-up; and rate of complications.
54 patients were enrolled: 28 had SLA removal and 26 NSLA removal; 52 were male; 22 had undergone previous CFB removal; six were wearing eye protection at the time of injury. Forty-three patients were reviewed: 26 by attendance and 18 by telephone. There was no difference in any end points at review. However, patients in the SLA group had median VAS scores that were 1.5 cm lower after 24 h than patients in the NSLA group (p=0.43, 95% CI -2.0 to 1.0). One patient in the SLA group developed keratitis.
We show that patient satisfaction ratings, complications and visual acuity were similar for the two methods. There was a trend for increased pain in the NSLA group at 12 and 24 h. Slit-lamp biomicroscopy and the use of magnification to remove CFBs remains the gold standard of care, and more intensive training should be given to EPs at the departmental level, particularly in EDs that receive patients with eye injuries.
患有角膜异物(CFB)的患者常到急诊科(ED)就诊。然而,急诊医师(EP)的清除技术各不相同。进行了一项前瞻性、单盲、观察性研究,比较了 EP 采用裂隙灯辅助(SLA)与非裂隙灯辅助(NSLA)清除 CFB 的效果。
5 位 EP 连续纳入 3 个月以上 CFB 的患者。1 位盲法 EP 在 3 天后对患者进行评估。研究终点为:视力变化;12 小时和 24 小时时视觉模拟疼痛量表(VAS)评分;满意度评分;随访时症状;以及并发症发生率。
共纳入 54 例患者:28 例采用 SLA 清除,26 例采用 NSLA 清除;52 例男性;22 例曾行 CFB 清除;6 例在受伤时戴有眼部防护装置。43 例患者接受了评估:26 例为就诊,18 例为电话评估。评估时各终点无差异。然而,SLA 组患者 24 小时 VAS 评分中位数比 NSLA 组低 1.5cm(p=0.43,95%CI-2.0 至 1.0)。SLA 组 1 例患者发生角膜炎。
我们表明,两种方法的患者满意度评分、并发症和视力均相似。NSLA 组在 12 小时和 24 小时时疼痛有增加趋势。裂隙灯生物显微镜检查和使用放大设备清除 CFB 仍然是护理的金标准,应在部门层面为 EP 提供更强化的培训,特别是在接收眼部受伤患者的 ED。