Intrathecal cervical analgesia for cancer pain: a 12-year follow-up study in a comprehensive cancer center

医学 癌症疼痛 养生 麻醉 鞘内 吗啡 导管 外科 癌症 内科学
作者
Denis Dupoiron,Florent Bienfait,Gabriel Carvajal,Valérie Seegers,Thomas Douillard,Sabrina Jubier-Hamon,Thierry Delorme,Arthur Julienne,Y.-M. Pluchon,Nicolas Ribault,E. Nader,Nathalie Lebrec
出处
期刊:Regional Anesthesia and Pain Medicine [BMJ]
卷期号:: rapm-104961 被引量:1
标识
DOI:10.1136/rapm-2023-104961
摘要

Background 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. Aims A monocentric retrospective follow-up study was designed to evaluate results of cervical IDDS for cancer pain. Patients and methods 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. Results 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. Conclusions 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.
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