胃下上神经丛阻滞治疗癌症相关性慢性盆腔疼痛。

Regional anesthesia Pub Date : 1997-11-01
R Plancarte, O A de Leon-Casasola, M El-Helaly, S Allende, M J Lema
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引用次数: 0

摘要

背景和目的:神经溶解性胃下上神经丛阻滞在特定的癌症患者中是安全有效的。研究人员对大量患者进行了队列研究,以评估该阻断剂在晚期癌症患者中的持续有效性和安全性。方法:在为期3年的研究中,共有227名患有妇科、结直肠或泌尿生殖系统癌的骨盆疼痛患者,由于疾病进展或不良副作用而经历疼痛控制不良。所有接受口服阿片类药物治疗的疼痛患者均符合参与条件。在0.25%布比卡因诊断阻滞成功后1天,采用10%苯酚进行双侧经皮胃下上神经丛阻滞。结果:所有患者在手术前均报告视觉模拟评分(VAS)疼痛评分为7-10/10。159名患者(79%)对诊断阻断有积极反应。总体而言,159名患者中有115名对诊断阻断有反应(72%,95%可信区间为65-79%)的患者疼痛缓解满意(VAS < 4/10),一次阻断后99名(62%),第二次阻断后16名(10%)。其余44例(28%)患者经2个阻滞后疼痛得到中度控制(VAS 4-7/10),并接受口服药物治疗和硬膜外镇痛治疗,效果良好。两组在神经溶解阻滞后口服阿片类药物治疗均显著减少。在3个月的随访期间有良好反应的患者不需要额外的阻滞。未发现与阻滞相关的并发症。结论:在接受神经溶解阻滞的72%的患者中,神经溶解性胃下上神经丛阻滞既能有效缓解疼痛,又能显著减少阿片类药物的使用(43%)。总的来说,这代表了参与研究的51%的患者。由于神经溶解剂的扩散不足,对于覆盖神经丛的广泛腹膜后疾病患者,预期结果不佳。
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Neurolytic superior hypogastric plexus block for chronic pelvic pain associated with cancer.

Background and objectives: Neurolytic superior hypogastric plexus block has been shown to be safe and effective in selected cancer patients. A large cohort of patients was studied to evaluate the continued efficacy and safety of this block in cancer patients with advanced disease.

Methods: A total of 227 pelvic pain patients with gynecological, colorectal, or genitourinary cancer who experienced poor pain control due to either progression of disease or to untoward side effects were enrolled in this study during a 3-year period. All pain patients receiving oral opioids were eligible to participate. A bilateral percutaneous neurolytic superior hypogastric plexus block with 10% phenol was performed 1 day after a successful diagnostic block with 0.25% bupivacaine.

Results: All patients reported a visual analog scale (VAS) pain score of 7-10/10 before the block. A positive response to a diagnostic block was obtained in 159 patients (79%). Overall, 115 patients of the 159 patients who responded to a diagnostic block (72%, 95% confidence interval of 65-79%) had satisfactory pain relief (VAS < 4/10), 99 (62%) after one block, and 16 (10%) after a second block. The remaining 44 patients (28%) had moderate pain control (VAS 4-7/10) after two blocks and received oral pharmacological therapy and epidural analgesic therapy with good results. Both groups experienced significant reductions in oral opioid therapy after the neurolytic blocks. No additional blocks were required by patients who had a good response during a follow-up period of 3 months. No complications related to the block were detected.

Conclusions: Neurolytic superior hypogastric plexus block provided both effective pain relief and a significant reduction in opioid usage (43%) in 72% of the patients who received a neurolytic block. Overall, this represents 51% of the patients enrolled in the study. Poor results should be expected in patients with extensive retroperitoneal disease overlying the plexus because of inadequate spread of the neurolytic agent.

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