Department of Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, 252-0374, Japan.
Department of Anaesthesiology, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, 252-0374, Japan.
Eur Spine J. 2019 Feb;28(2):250-258. doi: 10.1007/s00586-018-5801-z. Epub 2018 Oct 26.
To investigate the safety and efficacy of intrathecal injection as an alternative to epidural injection for analgesia.
Seventy consecutive outpatients with chronic low back and lower extremity pain received lumbar intrathecal injection of low-dose isobaric bupivacaine using a 25-gauge pencil-point needle. The patients received 0.5, 1.0, and 1.5 mg of bupivacaine at 1-week intervals to determine the optimal dose. Thereafter, they received two more weekly injections with the optimal dose. The safety and efficacy of the treatment were assessed over a 1-year period.
No serious adverse events were encountered. The optimal dose of bupivacaine (1.0 mg in 60% of patients) alleviated pain and disability (both, p < 0.0001) and provided anesthesia below L1 (L5-T6). Motor block was negligible, and balance impairment improved relative to baseline (p < 0.0001).
Intrathecal injection of low-dose bupivacaine offers a safe and effective treatment for chronic low back and lower extremity pain.
The study was approved by the Kitasato University Hospital Ethics Committee, and written informed consent was obtained from all individual participants included in the study. This trial was registered with the University Hospital Medical Information Network (UMIN000008670). These slides can be retrieved under electronic supplementary material.
研究鞘内注射作为硬膜外注射镇痛替代方法的安全性和有效性。
70 例连续的慢性腰腿痛门诊患者使用 25 号笔尖式针进行鞘内注射低剂量等比重布比卡因。患者每 1 周接受 0.5、1.0 和 1.5 mg 布比卡因注射,以确定最佳剂量。此后,他们接受了两次每周最佳剂量的注射。在 1 年的时间内评估治疗的安全性和有效性。
未发生严重不良事件。最佳布比卡因剂量(60%的患者为 1.0 mg)缓解了疼痛和残疾(均,p < 0.0001),并提供了 L1 以下的麻醉(L5-T6)。运动阻滞可忽略不计,与基线相比平衡障碍有所改善(p < 0.0001)。
鞘内注射低剂量布比卡因可为慢性腰腿痛提供安全有效的治疗。
该研究得到了北里大学医院伦理委员会的批准,并从所有纳入研究的个体参与者处获得了书面知情同意。该试验在大学医院医疗信息网络(UMIN000008670)上进行了注册。这些幻灯片可在电子补充材料中检索。