Olczak Bogumił, Kowalski Grzegorz, Leppert Wojciech, Zaporowska-Stachowiak Iwona, Wieczorowska-Tobis Katarzyna
Department of Anesthesiology, Józef Struś Multiprofile Municipal Hospital.
Department of Palliative Medicine, Poznan University of Medical Sciences.
J Pain Res. 2017 May 4;10:1027-1032. doi: 10.2147/JPR.S125449. eCollection 2017.
Total hip arthroplasty (THA) causes extensive tissue damage and severe pain. This study aimed to assess the analgesic efficacy, adverse effects (AEs), and safety of continuous intravenous (iv) oxycodone infusion with ketoprofen (injected into the iv line) in patients after THA, and to assay serum oxycodone levels.
Fourteen patients, aged 59‒82 years with American Society of Anesthesiologists (ASA) classification I or III, underwent THA with intrathecal analgesia and sedation induced by iv propofol. After the surgery, oxycodone (continuous iv infusion) at a dose of 1 mg/h (five patients) or 2 mg/h (nine patients) with 100 mg ketoprofen (injected into the iv line) was administered to each patient every 12 h. Pain was assessed using a numerical rating scale (NRS: 0 - no pain, 10 - the most severe pain) at rest and during movement. AEs, including hemodynamic unsteadiness, nausea, vomiting, pruritus, cognitive impairment, and respiratory depression, were registered during the first 24 h after surgery.
Oxycodone (continuous iv infusion) at a dose of 2 mg/h with ketoprofen (100 mg) administered every 12 h provided satisfactory analgesia in all nine patients without the need of rescue analgesics within the first 24 h after THA. In three out of five patients, oxycodone at 1 mg/h was effective. Oxycodone did not induce drowsiness, vomiting, pruritus, respiratory depression, or changes in blood pressure. Bradycardia appeared in two patients, and nausea was observed in one patient.
Oxycodone infusion with ketoprofen administered by iv is effective in patients after THA. Intravenous infusion of oxycodone is a predictable, stable, and safe method of drug administration.
全髋关节置换术(THA)会造成广泛的组织损伤和剧痛。本研究旨在评估连续静脉输注羟考酮联合酮洛芬(注入静脉输液管路)对THA术后患者的镇痛效果、不良反应(AEs)及安全性,并检测血清羟考酮水平。
14例年龄在59至82岁、美国麻醉医师协会(ASA)分级为I或III级的患者,接受了鞘内镇痛及丙泊酚静脉诱导镇静下的THA手术。术后,每例患者每12小时接受一次剂量为1毫克/小时(5例患者)或2毫克/小时(9例患者)的羟考酮(持续静脉输注)联合100毫克酮洛芬(注入静脉输液管路)治疗。采用数字评分量表(NRS:0 - 无疼痛,10 - 最剧烈疼痛)评估静息和活动时的疼痛情况。记录术后首24小时内的不良反应,包括血流动力学不稳定、恶心、呕吐、瘙痒、认知障碍及呼吸抑制。
在THA术后首24小时内,每12小时给予一次剂量为2毫克/小时的羟考酮联合100毫克酮洛芬,所有9例患者均获得了满意的镇痛效果,无需使用解救镇痛药。5例患者中有3例,1毫克/小时的羟考酮有效。羟考酮未引起嗜睡、呕吐、瘙痒、呼吸抑制或血压变化。2例患者出现心动过缓,1例患者出现恶心。
静脉输注羟考酮联合酮洛芬对THA术后患者有效。静脉输注羟考酮是一种可预测、稳定且安全的给药方法。