Anesthesiology and Pain Department, Institut de Cancérologie de l'Ouest, Angers, France
Anesthesiology and Pain Department, Institut de Cancérologie de l'Ouest, Angers, France.
Reg Anesth Pain Med. 2024 Oct 8;49(10):757-763. doi: 10.1136/rapm-2023-104961.
Intrathecal analgesia plays a key role for patients suffering refractory cancer pain. Nevertheless, intrathecal drug delivery systems (IDDS), requiring a cervical catheter tip implantation, have been poorly described in medical literature.
A monocentric retrospective follow-up study was designed to evaluate results of cervical IDDS for cancer pain.
From January 2010 to December 2022, all intrathecal-treated patients were prescribed a combined intrathecal analgesics regimen through a catheter placed in the cervical vertebral canal. Post-implant assessment of pain was determined using a numeric rating scale (NRS). Patients were followed via day-hospital visits and telephone calls at least monthly. Pain scores were compared using the Wilcoxon's signed rank test.
Ninety-eight patients were included in this study; all received intrathecal treatments. Implanted patients suffered from severe pain (mean presurgical maximum numerical rating score 8.02±0.24 despite a mean 562.56±127.72 mg of oral morphine equivalent daily dose). Mean survival time after intrathecal treatment start was 208.48±67 days. Intrathecal drug delivery systems provided pain relief compared with initial pain score with a significant statistical difference after 1 week, 1 month, 2 and 3 months (p<0.01). A 50% reduction in initial pain level was achieved in 93% of cases during the first week of intrathecal implant.
Results suggest that long-term intrathecal treatment using a multidrug regimen for cancer-related pain through cervical intrathecal catheters was suitable and safe in our study population. We demonstrated a clinically and statistically significant pain reduction in patients using mainly a percutaneous lumbar approach.
鞘内镇痛在治疗难治性癌痛患者中起着关键作用。然而,需要颈椎导管尖端植入的鞘内药物输送系统(IDDS)在医学文献中描述甚少。
本单中心回顾性随访研究旨在评估颈椎 IDDS 治疗癌症疼痛的结果。
2010 年 1 月至 2022 年 12 月,所有接受鞘内治疗的患者均通过放置在颈椎椎管内的导管给予联合鞘内镇痛药物治疗方案。通过数字评分量表(NRS)评估植入后的疼痛。通过日间医院就诊和每月至少一次的电话随访对患者进行随访。使用 Wilcoxon 符号秩检验比较疼痛评分。
本研究共纳入 98 例患者,均接受了鞘内治疗。植入患者患有严重疼痛(平均术前最大数字评分 8.02±0.24,尽管平均每日口服吗啡等效剂量为 562.56±127.72mg)。从鞘内治疗开始后,患者的平均生存时间为 208.48±67 天。与初始疼痛评分相比,鞘内药物输送系统提供了疼痛缓解,在第 1 周、第 1 个月、第 2 个月和第 3 个月时具有显著的统计学差异(p<0.01)。在鞘内植入的第 1 周内,93%的患者达到了初始疼痛水平的 50%降低。
研究结果表明,在我们的研究人群中,使用多药物方案通过颈椎鞘内导管进行长期鞘内治疗对于癌症相关疼痛是合适且安全的。我们主要通过经皮腰椎入路证明了患者的疼痛明显减轻,具有临床和统计学意义。