Department of Anaesthesiology and Intensive Care, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.
Clinical Department of Internal Medicine, Dermatology and Allergology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.
Anaesthesiol Intensive Ther. 2024;56(2):98-107. doi: 10.5114/ait.2024.141279.
This study, conducted between December 2015 and March 2018 at a single university hospital, explored the feasibility and safety of opioid-free anesthesia combined with preoperative thoracic paravertebral block (ThPVB) for patients undergoing elective video-assisted thoracoscopic surgery (VATS). The aim was to assess the impact of this approach on postoperative pain levels and opioid consumption.
Sixty-four patients scheduled for elective VATS were randomly assigned to either the intervention group, receiving opioid-free anesthesia with ThPVB, or the control group, managed with standard general anesthesia. Postoperatively, both groups received oxycodone patient-controlled analgesia along with non-opioid analgesics. Pain intensity was measured using the Numeric Pain Rating Scale (NRS) and Prince Henry Hospital Pain Score (PHHPS). The total dose of postoperative oxycodone and the occurrence of opioid-related adverse events were recorded during the 24-hour follow-up period.
Patients in the intervention group showed significantly lower pain levels at 20 and 24 hours post-procedure ( P = 0.015, P = 0.021, respectively) compared to the control group. Notably, oxycodone consumption at 24 hours was significantly higher in the control group ( p < 0.0001). No serious adverse events were observed during the study period.
This study demonstrates the feasibility and safety of opioid-free anesthesia combined with ThPVB for elective VATS. The approach significantly reduces postoperative pain and the need for opioids, supporting its potential as an effective and balanced perioperative anesthetic strategy.
本研究于 2015 年 12 月至 2018 年 3 月在一家大学附属医院进行,旨在探讨在择期电视辅助胸腔镜手术(VATS)中应用无阿片类麻醉联合术前胸椎旁阻滞(ThPVB)的可行性和安全性。目的是评估这种方法对术后疼痛水平和阿片类药物消耗的影响。
64 例行择期 VATS 的患者被随机分为干预组(接受无阿片类麻醉联合 ThPVB)和对照组(接受标准全身麻醉)。术后两组均接受羟考酮患者自控镇痛联合非阿片类镇痛药。采用数字疼痛评分量表(NRS)和亨利王子医院疼痛评分(PHHPS)评估疼痛强度。记录术后 24 小时内羟考酮的总剂量和阿片类相关不良反应的发生情况。
与对照组相比,干预组患者术后 20 小时和 24 小时的疼痛水平显著降低(P=0.015,P=0.021)。值得注意的是,对照组在 24 小时内羟考酮的消耗量显著更高(p<0.0001)。研究期间未观察到严重不良事件。
本研究表明,无阿片类麻醉联合 ThPVB 用于择期 VATS 是可行且安全的。该方法显著降低了术后疼痛和阿片类药物的需求,支持其作为一种有效和平衡的围手术期麻醉策略的潜力。