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首页> 外文期刊>Journal of Emergencies, Trauma and Shock >Management of Ocular Trauma in Emergency (MOTE) Trial: A pilot randomized double-blinded trial comparing topical amethocaine with saline in the outpatient management of corneal trauma
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Management of Ocular Trauma in Emergency (MOTE) Trial: A pilot randomized double-blinded trial comparing topical amethocaine with saline in the outpatient management of corneal trauma

机译:在紧急情况下的眼外伤(MOTE)试验:试点随机双盲试验比较了角膜创伤门诊治疗盐水的外用氨基肽

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Background:It is unclear whether local anesthetic eye drops can be safely used for the topical anesthesia of patients with minor corneal injury who are discharged from the emergency department (ED).Objectives:To assess whether topical 0.4% amethocaine self-administered to a maximum recommended frequency of once every hour for 36–48 h is safe in the management of uncomplicated corneal injury in patients discharged from the ED.Patients and Methods:A pilot randomized double-blinded trial comparing topical 0.4% amethocaine with topical normal saline.Results:Forty-seven subjects were recruited, with 22 randomized to receive amethocaine and 25 to receive placebo (normal saline). Baseline characteristics, including corneal injury type, were similar in both groups. There were no significant functional or clinical adverse sequelae in the majority of enrolled patients who could be contacted at 2 weeks (17/22 for amethocaine and 21/25 for placebo). Follow-up for the primary study outcome was suboptimal, with only 7/22 from the amethocaine group and 9/25 from the saline group presenting for 36–48 h review; there was a statistically nonsignificant trend for persistence of the corneal defect in the amethocaine group as compared with the saline group (2/7 and 1/9, respectively).Conclusion:Compared with saline drops, amethocaine eye drops are not definitely safe but they are effective for topical analgesia in minor corneal injury. Until further definitive studies, topical nonsteroidal agents or long-lasting artificial tears may be preferred for the topical analgesia of minor corneal injury. Return for corneal re-evaluation will necessarily remain suboptimal in an otherwise self-limiting condition, leading to a bias even if study recruitment is good.
机译:背景:目前尚不清楚局部麻醉眼滴管是否可以安全地用于从急诊部(ED)中排出的轻微角膜损伤患者的局部麻醉。目的:评估局部0.4%的氨基肽自我管理到最大推荐频率每小时每小时36-48小时是在从ED.Pat.pat.pat.pater和方法出发的患者中的软复杂角膜损伤管理中是安全的招募了四十七个受试者,22例随机接受氨基肽和25次接受安慰剂(正常盐水)。两组中,包括角膜损伤类型的基线特征在内。在大多数读取患者中没有显着的功能或临床不良后遗症,可以在2周(17/22次Amethocaine,21/25为安慰剂)。初级研究结果的随访是次优,只有7/22来自氨基肽组,9/25来自盐碱的36-48 H审查;与盐水组(分别为2/7和1/9)相比,氨基肽组的角膜缺损持续存在统计学的态度。结论:与盐水下降相比,氨基妥氨疹滴眼液并不肯定是安全的对小角膜损伤的局部镇痛有效。直到进一步的确定性研究,局部非甾体试剂或长期的人工泪液对于轻微角膜损伤的局部镇痛可能是优选的。返回角膜重新评估将在其他自我限制条件下仍然次优,即使学习招聘也是好的偏见。

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