Demmy Todd L, Nwogu Chukwumere, Solan Patrick, Yendamuri Saikrishna, Wilding Gregory, DeLeon Oscar
Department of Thoracic Surgery, Roswell Park Cancer Institute and State University of New York, Buffalo, New York 14263, USA.
Ann Thorac Surg. 2009 Apr;87(4):1040-6; discussion 1046-7. doi: 10.1016/j.athoracsur.2008.12.099.
This study compared a simplified method of intrapleural bupivacaine administration with traditional analgesic therapy to decrease postoperative pain and opioid usage in patients after thoracoscopy.
Thirty patients who had non-rib-spreading thoracoscopic operations under general anesthesia were prospectively randomized to no local anesthetic infusion (control), intermittent bolus (30 mL every 6 hours), or continuous infusion (5 mL/h). Bupivacaine (0.25%) was delivered through the pleural infusion channel of a specially designed single silicone 28F chest tube. Total intravenous fentanyl patient-controlled analgesia (boluses with basal rate) infused in the first 24 hours postoperatively was the designated primary study end point. Escalations of analgesic therapy, including ketorolac administration, were standardized across all groups. Nurses assessed pain control at onset and every 6 hours by visual analog pain scales (VAPS, 100 mm). VAPS were repeated 10 minutes later to assess any opioid or bupivacaine bolus effects.
No study-related adverse events occurred. Compared with controls, pooled VAPS scores and 24-hour fentanyl consumption were significantly lower for the intermittent and continuous administration groups (1753 vs 1180 vs 1177 microg/24 h, respective median; p = 0.04) Early (6-hour) VAPS analgesic responses were more certain for intermittent (10 of 10) and continuous (10 of 10) patients than controls (7 of 10, p = .04). Five continuous patients successfully maintained VAPS scores below 20 mm throughout the study vs 3 intermittent and 2 controls (p = .045).
Intermittent or continuous intrapleural bupivacaine infused through the chest tube reliably reduces postoperative pain and 24-hour opioid usage in thoracoscopy patients.
本研究比较了一种简化的胸膜内布比卡因给药方法与传统镇痛疗法,以减少胸腔镜检查术后患者的疼痛和阿片类药物使用量。
30例在全身麻醉下接受非肋骨撑开胸腔镜手术的患者被前瞻性随机分为不进行局部麻醉输注(对照组)、间歇性推注(每6小时30 mL)或持续输注(5 mL/h)。布比卡因(0.25%)通过专门设计的单硅胶28F胸管的胸膜输注通道给药。术后前24小时输注的静脉注射芬太尼总量(基础速率推注)是指定的主要研究终点。所有组的镇痛治疗升级,包括酮咯酸的给药,均标准化。护士在开始时和每6小时通过视觉模拟疼痛量表(VAPS,100 mm)评估疼痛控制情况。10分钟后重复VAPS以评估任何阿片类药物或布比卡因推注的效果。
未发生与研究相关的不良事件。与对照组相比,间歇性和持续给药组的VAPS总分和24小时芬太尼消耗量显著更低(分别为中位数1753 vs 1180 vs 1177 μg/24 h;p = 0.04)。间歇性(10/10)和持续性(10/10)患者的早期(6小时)VAPS镇痛反应比对照组(7/10,p = 0.04)更确切。5例持续给药患者在整个研究过程中成功将VAPS评分维持在20 mm以下,而间歇性给药组为3例,对照组为2例(p = 0.045)。
通过胸管间歇性或持续性胸膜内注入布比卡因可可靠地减轻胸腔镜检查患者的术后疼痛和24小时阿片类药物使用量。