Zhang Jin, Zhang Fan, Zhang Hao, Yu Lei, Chen Jun, Wang Shaolin
Department of Anesthesiology, the Second People's Hospital of Wuhu, Wuhu, Anhui, 241000, People's Republic of China.
J Pain Res. 2025 Jan 3;18:11-19. doi: 10.2147/JPR.S493518. eCollection 2025.
The erector spinae plane block (ESPB) has been increasingly utilized for postoperative analgesia in thoracic, abdominal, and spinal surgeries. This study evaluated the postoperative analgesic outcomes of ESPB with nalbuphine as a ropivacaine adjuvant for lumbar trauma surgery.
This randomized double-blind clinical trial included 57 participants who underwent lumbar trauma surgery. Ultrasound-guided ESPB was performed with 0.375% ropivacaine (Group R) and 0.375% ropivacaine combined with 10 mg nalbuphine (Group N); 20 mL was used per side. The primary outcome measure was the time to first postoperative remedial analgesia. The secondary outcome measures included the Numerical Rating Scale (NRS) scores at rest and during movement, cumulative sufentanil consumption after surgery, intraoperative dosage of remifentanil and sufentanil, time to first off-bed, time to first flatus, and length of hospital stay.
The mean difference in the time to first postoperative remedial analgesia (Group N vs Group R, 489±52 min vs 391±23 min) was 98 min (95% CI, 76 to 119). Kaplan-Meier survival analysis revealed an increasing pain-free population in Group N and an increasing pain-free duration. The log-rank (Mantel-Cox) test showed that the hazard ratio (HR, Group N/Group R) was 0.225 (95% CI, 0.114 to 0.443). Group N showed decreased sufentanil consumption compared with Group R at 4-8 h, 8-12 h and 0-24 h after surgery (<0.001).
ESPB with nalbuphine in combination with ropivacaine significantly prolonged the duration of analgesia and reduced postoperative analgesic demands compared to ropivacaine alone.
竖脊肌平面阻滞(ESPB)已越来越多地用于胸科、腹部和脊柱手术的术后镇痛。本研究评估了以纳布啡作为罗哌卡因辅助药物用于腰椎创伤手术的ESPB术后镇痛效果。
这项随机双盲临床试验纳入了57例行腰椎创伤手术的参与者。采用超声引导下ESPB,分别给予0.375%罗哌卡因(R组)和0.375%罗哌卡因联合10 mg纳布啡(N组);每侧使用20 mL。主要结局指标为术后首次补救性镇痛的时间。次要结局指标包括静息和活动时的数字评定量表(NRS)评分、术后舒芬太尼累计用量、术中瑞芬太尼和舒芬太尼用量、首次离床时间、首次排气时间和住院时间。
术后首次补救性镇痛时间的平均差异(N组与R组,489±52分钟 vs 391±23分钟)为98分钟(95%CI,76至119)。Kaplan-Meier生存分析显示N组无痛人群增加,无痛持续时间延长。对数秩(Mantel-Cox)检验显示风险比(HR,N组/R组)为0.225(95%CI,0.114至0.443)。术后4 - 8小时、8 - 12小时和0 - 24小时,N组舒芬太尼用量较R组减少(<0.001)。
与单独使用罗哌卡因相比,纳布啡联合罗哌卡因的ESPB显著延长了镇痛时间,减少了术后镇痛需求。