Yan Brian M, Myers Robert P
Division of Gastroenterology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
Am J Gastroenterol. 2007 Feb;102(2):430-8. doi: 10.1111/j.1572-0241.2006.00967.x. Epub 2006 Nov 13.
A major focus of palliation in patients with unresectable pancreatic cancer is pain control. The aim of this systematic review was to examine the efficacy and safety of neurolytic celiac plexus blockade (NCPB) compared with standard treatment in randomized controlled trials (RCTs) involving patients with unresectable pancreatic cancer.
An electronic search was completed (1966 through August, 2005) for RCTs comparing NCPB versus control (standard treatment and/or sham NCPB) in patients with unresectable pancreatic cancer. The primary outcome was pain measured on a 10-point visual analogue scale (VAS). Secondary outcomes included opioid usage, adverse effects, quality of life (QOL), and survival. All outcomes were assessed at 2, 4, and 8 wk.
Five RCTs involving 302 patients (NCPB, N = 147; control, N = 155) met the inclusion criteria. Mean age was 61.0 +/- 4.3 yr. Compared with control, NCPB was associated with lower VAS scores for pain at 2, 4, and 8 wk (weighted mean difference [WMD]-0.60, 95% CI -0.82 to -0.37). Opioid usage (in mg/d oral morphine) was also reduced at 2, 4, and 8 wk (WMD -85.9, 95% CI -144.0 to -27.9). NCPB was associated with a reduction in constipation (relative risk 0.67, 95% CI 0.49-0.91), but not other adverse events. No differences in survival were observed. QOL could not be adequately analyzed due to differences in outcome scales among studies.
In patients with unresectable pancreatic cancer, NCPB is associated with improved pain control, and reduced narcotic usage and constipation compared with standard treatment, albeit with minimal clinical significance.
不可切除胰腺癌患者姑息治疗的一个主要重点是疼痛控制。本系统评价的目的是在涉及不可切除胰腺癌患者的随机对照试验(RCT)中,研究与标准治疗相比,腹腔神经丛阻滞(NCPB)的疗效和安全性。
完成了一项电子检索(1966年至2005年8月),以查找比较不可切除胰腺癌患者中NCPB与对照(标准治疗和/或假NCPB)的RCT。主要结局是用10分视觉模拟量表(VAS)测量的疼痛。次要结局包括阿片类药物使用情况、不良反应、生活质量(QOL)和生存率。所有结局均在2、4和8周时进行评估。
五项涉及302例患者的RCT(NCPB组,N = 147;对照组,N = 155)符合纳入标准。平均年龄为61.0±4.3岁。与对照组相比,NCPB在2、4和8周时疼痛的VAS评分较低(加权平均差[WMD] -0.60,95%可信区间-0.82至-0.37)。在2、4和8周时阿片类药物使用量(以口服吗啡mg/d计)也有所减少(WMD -85.9,95%可信区间-144.0至-27.9)。NCPB与便秘减少相关(相对危险度0.67,95%可信区间0.49 - 0.91),但与其他不良事件无关。未观察到生存率的差异。由于各研究结局量表存在差异,无法对生活质量进行充分分析。
在不可切除胰腺癌患者中,与标准治疗相比,NCPB可改善疼痛控制,减少麻醉药物使用和便秘,尽管临床意义不大。