髋关节置换术后阿片类联用与单用方案的疗效与安全性比较

    Comparison of the Efficacy and Safety of Opioid Combination Versus Single-agent Regimens After Hip Arthroplasty

    • 摘要:
      目的  比较髋关节置换术(hip arthroplasty,HA)后患者自控静脉镇痛(patient-controlled intravenous analgesia,PCIA)中阿片类药物联用与单用方案对术后早期疼痛及不良反应的影响。
      方法 采用回顾性队列研究,连续纳入2021年3月—6月及2025年3月—6月行单侧HA并使用PCIA的患者195例,根据PCIA方案分为联用组(n=86)和单用组(n=109)。收集包括人口学、术前疼痛、手术麻醉记录等变量。主要结局为术后(第0、1、2天)静息疼痛视觉模拟评分(visual analogue scale,VAS),次要结局为术后恶心呕吐(postoperative nausea and vomiting,PONV)及谵妄发生率。采用多因素回归分析,通过构建未调整、部分调整及完全调整模型,分析不同组别与结局的关联。
      结果 单因素分析显示,联用组术后各时间点疼痛VAS评分均低于单用组(P均<0.001)。在调整术前疼痛、手术时长、麻醉用药等因素后,多因素分析表明,2组在术后疼痛评分(术后当天:β=−0.32, P=0.123;术后第1天:β=−0.18, P=0.378;术后第2天:β=−0.21, P=0.236)及PONV风险(OR=1.39, P=0.833)上差异均无统计学意义。术后谵妄发生率组间差异无统计学意义。
      结论 HA术后PCIA采用阿片类药物联合或单用方案,在术后早期镇痛效果与安全性方面差异无统计学意义。在规范的多模式镇痛管理下,采用单用阿片类药物的PCIA方案可作为合理的临床选择。

       

      Abstract:
      OBJECTIVE To compare the effects of opioid combination versus single-agent regimens in patient-controlled intravenous analgesia(PCIA) on early postoperative pain and adverse reactions following hip arthroplasty(HA).
      METHODS A retrospective cohort study was conducted, continuously enrolling 195 patients who underwent unilateral HA and received PCIA from March to June 2021 and from March to June 2025. Based on the PCIA regiment, patients were divided into a combination group(n=86) and a single-agent group(n=109). Variables including demographics, preoperative pain, and surgical anesthesia records were collected. The primary outcomes were resting pain visual analogue scale(VAS) scores on postoperative days 0, 1, and 2. Secondary outcomes included the incidence of postoperative nausea and vomiting(PONV) and delirium. Multivariate regression analysis was performed by constructing unadjusted, partially adjusted, and fully adjusted models to analyze the association between different groups and outcomes.
      RESULTS Univariate analysis showed that the combination group had lower VAS pain scores at all postoperative time points compared to the single-agent group(all P<0.001). After adjusting for confounding factors such as preoperative pain, surgery duration, and anesthesia medications, multivariate analysis indicated no statistically significant differences between the 2 groups in postoperative pain scores(postoperative day 0: β=−0.32, P=0.123; postoperative day 1: β=−0.18, P=0.378; postoperative day 2: β=−0.21, P=0.236) and PONV risk(OR=1.39, P=0.833). There was also no significant difference in the incidence of postoperative delirium between the groups.
      CONCLUSION For HA patients receiving PCIA, no significant differences are observed in early postoperative analgesic efficacy and safety between opioid combination and single-agent regimens. A single-opioid PCIA regimen under standardized multimodal analgesia management can be a reasonable clinical option.

       

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