Department of Emergency Medicine, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Orthopedic Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
Am J Emerg Med. 2018 Oct;36(10):1766-1770. doi: 10.1016/j.ajem.2018.01.080. Epub 2018 Feb 4.
Many procedures performed in emergency department are stressful and painful, and creating proper and timely analgesia and early and effective assessment are the challenges in this department. This study has been conducted in order to compare the efficacy of propofol and fentanyl combination with propofol and ketamine combination for procedural sedation and analgesia (PSA) in trauma patients in the emergency department.
This is a randomized prospective double-blind clinical trial conducted in the emergency department of Imam Khomeini Hospital, a tertiary academic trauma center in northern Iran. Patients with trauma presenting to the emergency department who needed PSA were included in study. Patients were divided into two groups of propofol fentanyl (PF) and propofol ketamine (PK). Pain score and sedation depth were set as primary outcome measures and were recorded.
Out of about 379 patients with trauma, who needed PSA, 253 met the criteria to be included in the study, 117 of which were excluded. The remaining 136 patients were randomly allocated to either PF group (n = 70) or PK group (n = 66). Pain management after drug administration was significantly different between the groups and the analgesia caused by fentanyl was significantly higher than ketamine. The sedation score after 15 min of PSA in the group PF was significantly higher than the group PK.
It seems that regarding PSA in the emergency department, PF caused better analgesia and deeper sedation and it is recommended to use PF for PSA in the emergency departments.
急诊科的许多操作都具有压力和痛苦,因此,在该科室,恰当及时的镇痛以及早期和有效的评估是面临的挑战。本研究旨在比较在急诊科对创伤患者进行镇静和镇痛时,使用丙泊酚和芬太尼联合与使用丙泊酚和氯胺酮联合的效果。
这是一项在伊朗北部三级学术创伤中心伊玛目霍梅尼医院的急诊科进行的随机前瞻性双盲临床试验。本研究纳入了因需要镇静和镇痛而到急诊科就诊的创伤患者。患者被分为丙泊酚芬太尼(PF)组和丙泊酚氯胺酮(PK)组。疼痛评分和镇静深度被设定为主要观察指标并进行记录。
约有 379 名需要 PSA 的创伤患者,其中有 253 名符合纳入研究的标准,117 名被排除。其余 136 名患者被随机分配到 PF 组(n=70)或 PK 组(n=66)。给药后疼痛管理在两组之间存在显著差异,且芬太尼引起的镇痛效果明显高于氯胺酮。PF 组 PSA 后 15 分钟的镇静评分明显高于 PK 组。
在急诊科进行 PSA 时,PF 可产生更好的镇痛效果和更深的镇静作用,因此建议在急诊科使用 PF 进行 PSA。