Koyyalagunta Dhanalakshmi, Mach Steven, Chung Matthew
Department of Pain Medicine, University of Texas, MD Anderson Cancer Center, Houston, TX.
Pain Physician. 2025 Jul;28(4):E403-E410.
Celiac plexus or splanchnic nerve neurolysis is a treatment modality commonly offered for cancer-related upper abdominal pain. The optimal spinal level for performing celiac/splanchnic sympathetic neurolysis remains unclear.
We aimed to assess the outcome, effectiveness, and complications associated with undergoing splanchnic sympathetic neurolysis at various spinal levels for treating intractable upper abdominal cancer pain.
This is an analysis of a retrospective cohort.
Pain management clinic at a large quaternary comprehensive cancer center.
A retrospective chart review of patients with unremitting cancer-related upper abdominal pain refractory to medical management was performed. Data were collected on pertinent demographic, clinical characteristics, cancer diagnosis and staging, location of abdominal pain, pain Numeric Rating Scale (NRS-11) scores, prior cancer treatments, level/laterality of splanchnic neurolysis, agents and volumes used for neurolysis, adverse events, pre- and postprocedure daily morphine milligram equivalents (MME), and symptom burden/quality-of-life outcomes.
A total of 254 patients treated with splanchnic sympathetic neurolysis for intractable upper abdominal cancer pain from July 2014 through June 2017 were included. Of the splanchnic sympathetic neurolysis procedures performed, most were done at T12 (44%) and L1 (54%)., The vast majority were bilateral (96%) using absolute alcohol (98%). There was no significant difference in MME requirements at postprocedure 6-months. Additionally, while NRS-11 scores improved at postprocedure one month and 6 months compared to baseline, there was no significant difference in NRS-11 scores based on the level at which the procedure was performed. A subgroup analysis of patients (n = 201 observations) with cancer pain related to intraabdominal viscera innervated by the splanchnic nerves (i.e., pancreatic, hepatobiliary, renal/adrenal, and gastrointestinal tract) also revealed that block level was not significantly associated with pain score. Time was a significant factor associated with NRS-11 score; patients had a significantly decreased pain score at postprocedure one month and 6 months. For patients with abdominal cancers of predominately splanchnic innervation, splanchnic sympathetic neurolysis also improved quality of life measures such as nausea, feeling of wellbeing, and mental clarity.
One-third of the patients in our study were lost to follow-up at 3 months, likely due to the patient population with end-stage cancer, the natural history of cancer disease progression, or death.
The majority of splanchnic sympathetic neurolysis were performed at L1 and T12. Improved pain scores were comparable between block levels and provided sustained pain relief for at least 6 months. Significant changes in daily MMEs were demonstrated with neurolysis in association with the one month follow-up. While we found that splanchnic sympathetic neurolysis was effective in reducing opioid requirements, larger randomized studies are needed to look for any meaningful difference in long-term efficacy for pain control and side effects for splanchnic nerve sympathetic neurolysis.
腹腔神经丛或内脏神经松解术是一种常用于治疗癌症相关上腹部疼痛的治疗方式。进行腹腔/内脏交感神经松解术的最佳脊柱水平仍不明确。
我们旨在评估在不同脊柱水平进行内脏交感神经松解术治疗顽固性上腹部癌症疼痛的疗效、有效性及并发症。
这是一项回顾性队列分析。
一家大型四级综合癌症中心的疼痛管理诊所。
对药物治疗无效的顽固性癌症相关上腹部疼痛患者进行回顾性病历审查。收集了相关人口统计学、临床特征、癌症诊断和分期、腹痛部位、疼痛数字评分量表(NRS-11)评分、既往癌症治疗情况、内脏神经松解术的水平/侧别、用于神经松解的药物和剂量、不良事件、术前和术后每日吗啡毫克当量(MME)以及症状负担/生活质量结果。
纳入了2014年7月至2017年6月期间接受内脏交感神经松解术治疗顽固性上腹部癌症疼痛的254例患者。在内脏交感神经松解术操作中,大多数在T12(44%)和L1(54%)水平进行。绝大多数为双侧(96%),使用无水乙醇(98%)。术后6个月时MME需求量无显著差异。此外,虽然术后1个月和6个月时NRS-11评分与基线相比有所改善,但基于手术操作水平的NRS-11评分无显著差异。对与内脏神经支配的腹腔内脏器相关的癌症疼痛患者(n = 201例观察对象)进行的亚组分析也显示,阻滞水平与疼痛评分无显著相关性。时间是与NRS-11评分相关的一个重要因素;患者在术后1个月和6个月时疼痛评分显著降低。对于主要由内脏神经支配的腹部癌症患者,内脏交感神经松解术还改善了生活质量指标,如恶心、幸福感和思维清晰度。
我们研究中三分之一的患者在3个月时失访,可能是由于患者为终末期癌症人群、癌症疾病进展的自然病程或死亡。
大多数内脏交感神经松解术在L1和T12水平进行。不同阻滞水平的疼痛评分改善情况相当,并提供了至少6个月的持续疼痛缓解。神经松解术与1个月随访相关的每日MME有显著变化。虽然我们发现内脏交感神经松解术在减少阿片类药物需求方面有效,但需要更大规模的随机研究来寻找内脏神经交感神经松解术在疼痛控制的长期疗效和副作用方面的任何有意义的差异。