Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul, 120-752, Republic of Korea.
Support Care Cancer. 2018 Jun;26(6):2023-2030. doi: 10.1007/s00520-018-4043-2. Epub 2018 Jan 17.
Neurolytic celiac plexus block (NCPB) is a safe and effective method for reducing abdominal cancer pain. However, the analgesic efficacy of NCPB is not always guaranteed. The aim of this retrospective study was to identify predictors for the analgesic efficacy of NCPB in patients with unresectable pancreatic cancer.
Patients with unresectable pancreatic cancer who underwent NCPB from 2006 to 2015 were enrolled. Good analgesia after NCPB was defined as ≥ 50% reduction in pain score at day 30. Patient demographics, cancer characteristics, and pain-related factors were evaluated using a logistic regression analysis to identify predictors for good analgesia after NCPB. Additionally, survival outcomes were compared between patients with poor and good analgesia after NCPB.
A total of 112 patients satisfied the study protocol requirements. Forty-seven patients (41.9%) showed good analgesia after NCPB. Better performance status, lower serum CA 19-9 level, shorter pain duration, and lower opioid dose were observed in patients with good analgesia after NCPB. Good performance status (ECOG performance status 1 vs. 2 or 3, OR = 2.737, 95% CI = 1.149 to 6.518, P = 0.023) and low daily opioid use (< 150 vs. ≥ 150 mg, OR = 2.813, 95% CI = 1.159 to 6.831, P = 0.022) before NCPB were independent predictors of good analgesia after NCPB. The median survival was significantly lower for patients with poor analgesia after NCPB (68 vs. 150 days, P < 0.001).
NCPB should be offered early to selected patients to improve its analgesic efficacy in advance of deterioration from disease and pain in this population.
神经松解腹腔神经丛阻滞(NCPB)是一种安全有效的减轻腹部癌痛的方法。然而,NCPB 的镇痛效果并不总是得到保证。本回顾性研究旨在确定无法切除的胰腺癌患者行 NCPB 后的镇痛效果的预测因素。
纳入 2006 年至 2015 年间接受 NCPB 的无法切除的胰腺癌患者。NCPB 后 30 天疼痛评分至少降低 50%定义为良好镇痛。使用逻辑回归分析评估患者的人口统计学、癌症特征和疼痛相关因素,以确定 NCPB 后良好镇痛的预测因素。此外,比较 NCPB 后镇痛效果差和效果好的患者的生存结局。
共 112 例患者符合研究方案要求。47 例(41.9%)患者 NCPB 后镇痛效果良好。NCPB 后镇痛效果良好的患者表现出更好的一般状况、更低的血清 CA 19-9 水平、更短的疼痛持续时间和更低的阿片类药物剂量。NCPB 后良好的一般状况(ECOG 体力状况 1 比 2 或 3,OR=2.737,95%CI=1.149 至 6.518,P=0.023)和 NCPB 前较低的每日阿片类药物用量(<150 比≥150mg,OR=2.813,95%CI=1.159 至 6.831,P=0.022)是 NCPB 后良好镇痛的独立预测因素。NCPB 后镇痛效果差的患者中位生存时间显著降低(68 比 150 天,P<0.001)。
对于该人群,在疾病恶化和疼痛加重之前,应尽早为选择的患者提供 NCPB,以提前提高其镇痛效果。