Comparison of Effectiveness and Safety of Oxycodone Hydrochloride and Fentanyl for Post-operative Pain Following Total Hip Arthroplasty: A Randomized Triple-Blind Trial

Q2 Medicine
Neveen A. Kohaf, Salama A. Harby, Ahmed F. Abd-Ellatief, M. A. Elsaid, N. Abdelmottaleb, T. F. A. Abd Elsalam
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Abstract

Background: Total hip replacement (THR) is frequently associated with intense post-surgical pain. Effective pain management is of crucial importance to improving patient's condition and increasing his/her satisfaction in the post-operative time. Objectives: This study aimed to compare the analgesic effect and safety of oxycodone and fentanyl after THR. Methods: Seventy-two cases scheduled for elective THR were included in this randomized, triple-blind trial. The patients were equally randomized into 2 groups: fentanyl group (50 ug of fentanyl) and oxycodone group (oxycodone 4 mg). Drugs were received 20 min prior to the end of the operation. Results: Post-operative visual analog scale (VAS) measurements at rest and movement at the post-anesthesia care unit (PACU) and in the ward, 2 h, 4 h, and 8 h post-operatively exhibited a significantly reduced value in the oxycodone group compared to the fentanyl group (P-value < 0.05). Time to first rescue for analgesia was delayed significantly in the oxycodone compared to the fentanyl group (P-value < 0.001). Fentanyl consumption (ug) in the 1st post-operative 12 h, 24 h, and 48 h decreased significantly in the oxycodone group compared to the fentanyl group (P-value < 0.001). Post-operative nausea, vomiting, headache, and pruritus were matched between the 2 groups (P > 0.05). Conclusions: A bolus dose of 4 mg of oxycodone provided superior analgesic efficacy than 50 ug fentanyl as evidenced by significantly lower pain score, delayed onset to first request for analgesia, and the smaller amount of fentanyl consumption at 12, 24, and 48 h post-total hip arthroplasty compared to fentanyl. The incidence of adverse events was comparable between the 2 groups.
盐酸羟考酮和芬太尼治疗全髋关节置换术后疼痛的有效性和安全性比较:三盲随机试验
背景:全髋关节置换术(THR全髋关节置换术(THR)常伴有剧烈的术后疼痛。有效的疼痛管理对于改善患者的病情和提高其术后满意度至关重要。研究目的本研究旨在比较羟考酮和芬太尼在髋关节置换术后的镇痛效果和安全性。方法72例计划进行择期全脊椎十字路口置换术的患者被纳入这项随机三盲试验。患者被平均随机分为两组:芬太尼组(50 微克芬太尼)和羟考酮组(4 毫克羟考酮)。在手术结束前 20 分钟服药。结果术后 2 小时、4 小时和 8 小时在麻醉后护理病房(PACU)和病房休息和活动时的视觉模拟量表(VAS)测量结果显示,与芬太尼组相比,羟考酮组的数值明显降低(P 值 < 0.05)。与芬太尼组相比,羟考酮组首次镇痛抢救时间明显延迟(P 值 < 0.001)。与芬太尼组相比,羟考酮组在术后 12 小时、24 小时和 48 小时内的芬太尼消耗量(微克)明显减少(P 值 < 0.001)。两组患者术后恶心、呕吐、头痛和瘙痒的程度相当(P > 0.05)。结论与 50 ug 芬太尼相比,4 mg 羟考酮的栓塞剂量能提供更好的镇痛效果,具体表现在疼痛评分明显降低、从首次要求镇痛到起效时间延迟,以及与芬太尼相比,全髋关节置换术后 12、24 和 48 h 的芬太尼用量更少。两组的不良反应发生率相当。
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来源期刊
Anesthesiology and Pain Medicine
Anesthesiology and Pain Medicine Medicine-Anesthesiology and Pain Medicine
CiteScore
4.60
自引率
0.00%
发文量
49
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