Comparison of Ultrasound-Guided Thoracic Paravertebral Block Versus Thoracic Paravertebral Block Combined With Serratus Anterior Plane Block or Erector Spinae Block Following Video-Assisted Thoracoscopic Lobectomy.

IF 2.8 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics
Therapeutics and Clinical Risk Management Pub Date : 2025-03-15 eCollection Date: 2025-01-01 DOI:10.2147/TCRM.S507154
Meng-Meng Zheng, Jue Xie, Wei Tan, Cong-Wang Yuan, Dun-Yi Qi, Jie Sun
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Abstract

Purpose: Compared the efficacy of ultrasound-guided thoracic paravertebral block (TPVB) and thoracic paravertebral combined with serratus anterior plane block (SAPB) or erector spinae block (ESPB) following video-assisted thoracoscopic lobectomy(VATL).

Patients and methods: This retrospective study analyzed the medical records of 295 patients who underwent VATL surgery between August 2021 and January 2023. Patients were divided into three groups: TPVB (92 patients), TPVB combined with SAPB (106 patients), and TPVB combined with ESPB (97 patients). The primary outcomes were postoperative pain levels, measured using an 11-point visual analogue scale (VAS) both at rest and during coughing at 2, 6, 12, 24, and 48 hours postoperatively, as well as cumulative oxycodone consumption within 24 and 48 hours postoperatively.

Results: Postoperative cumulative oxycodone consumption within 24 and 48 hours was significantly lower in the TPVB+SAPB and TPVB+ESPB groups compared to the TPVB group (P < 0.001), with no significant difference between the TPVB+SAPB and TPVB+ESPB groups. The TPVB group exhibited higher VAS pain scores both at rest and during coughing at 2 and 6 hours postoperatively compared to the other two groups (P < 0.005). Within 24 hours postoperatively, the Area Under Curve (AUC) for VAS scores at rest was significantly lower in the TPVB+SAPB group than in the other two groups (P < 0.05), while the AUC for coughing pain was significantly lower in the TPVB+ESPB group compared to the TPVB group (P = 0.049). Nausea or vomiting occurred more frequently in the TPVB group compared to the other groups (P = 0.016).

Conclusion: TPVB combined with SAPB or ESPB provides superior analgesic effects compared to TPVB alone after video-assisted thoracoscopic lobectomy, with both techniques showing comparable analgesic efficacy. However, TPVB+SAPB may offer slightly better analgesia at rest, while TPVB+ESPB may have a potential advantage in reducing postoperative nausea and vomiting.

超声引导下椎旁阻滞与胸腔镜肺叶切除术后椎旁阻滞联合锯肌前平面阻滞或竖脊肌阻滞的比较。
目的:比较超声引导下胸椎旁阻滞(TPVB)与胸椎旁联合锯肌前平面阻滞(SAPB)或竖脊肌阻滞(ESPB)在胸腔镜肺叶切除术(VATL)后的疗效。患者和方法:本回顾性研究分析了2021年8月至2023年1月期间接受VATL手术的295例患者的医疗记录。患者分为TPVB组(92例)、TPVB联合SAPB组(106例)、TPVB联合ESPB组(97例)。主要结果是术后疼痛水平,在术后2、6、12、24和48小时使用11点视觉模拟量表(VAS)测量休息和咳嗽时的疼痛水平,以及术后24和48小时内的累积羟考酮消耗。结果:与TPVB组相比,TPVB+SAPB组和TPVB+ESPB组术后24、48小时内氧可酮累积消耗量显著降低(P < 0.001), TPVB+SAPB组与TPVB+ESPB组之间无显著差异。与其他两组相比,TPVB组在术后2和6小时休息和咳嗽时的VAS疼痛评分均较高(P < 0.005)。术后24小时内,TPVB+SAPB组休息时VAS评分曲线下面积(AUC)显著低于其他两组(P < 0.05),而TPVB+ESPB组咳嗽疼痛AUC显著低于TPVB组(P = 0.049)。TPVB组恶心或呕吐发生率高于其他组(P = 0.016)。结论:电视胸腔镜肺叶切除术后,TPVB联合SAPB或ESPB的镇痛效果优于单独使用TPVB,两种技术的镇痛效果相当。然而,TPVB+SAPB可能提供稍好的静止镇痛,而TPVB+ESPB可能在减少术后恶心和呕吐方面具有潜在优势。
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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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