36.腰椎管狭窄症腰椎手术术中硬膜外类固醇的影响

Q3 Medicine
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引用次数: 0

摘要

背景 CONTEXT脊柱手术后疼痛控制方法尚未标准化。术后止痛效果会影响患者满意度、术后康复和住院时间。术后止痛对老年患者尤为重要。虽然腰椎间盘突出症术后使用类固醇的效果已有报道,但其对腰椎管狭窄症的效果仍不明确。本研究旨在评估腰椎管狭窄症手术中硬膜外类固醇的疗效。纳入标准为年龄在 60-85 岁之间,减压范围在 1-3 个级别之间。排除标准为融合手术、再次手术、糖尿病、慢性炎症性疾病、慢性肾功能障碍、药物过敏、术后谵妄和痴呆。本研究是一项前瞻性双盲安慰剂随机对照研究。患者在术前通过随机数字表被分为两组(类固醇组和对照组)。在类固醇组,我们在手术减压后和伤口闭合前从硬膜外注射 6.6 毫克地塞米松。在对照组中,我们同样在伤口闭合前从硬膜外注射相同剂量的生理盐水。术后未使用阿片类药物。对照组口服Cox-2抑制剂5天,并根据需要使用双氯芬酸钠栓剂。我们调查了术后第 0、1、2、3、5、7 和 14 天(POD)背痛和腿痛的日平均疼痛程度和最大疼痛程度的 VAS 值。VAS 评估由一名护士进行,该护士不知道组别划分。术前以及 POD 1、3 和 7 日对 CRP 和 "起立行走时间测试 "进行了调查。结果类固醇组有 19 名患者(男性 11 名,女性 8 名),平均年龄为 72.9 岁,平均减压次数为 1.7 次。对照组有 21 名患者(男性 14 名,女性 7 名),平均年龄 74.2 岁,平均减压次数 1.8 次。两组患者的数据无明显差异。与对照组相比,类固醇组在 POD 0、1、2 和 3 的背痛(VAS)明显较轻。类固醇组术后 VAS(背痛/伤口疼痛)当天为 41.4 毫米,第一天为 43.8 毫米,第二天为 38.9 毫米,第三天为 27.6 毫米;对照组术后 VAS 当天为 62.8 毫米,第一天为 63.4 毫米,第二天为 55.9 毫米,第三天为 44.3 毫米。两组的腿部疼痛 VAS 无明显差异。引流液中的 IL-6 有明显差异:类固醇组为 29.8±22.6(ng/ml),对照组为 75.6±49.7。类固醇组的 CRP 结果在第三天明显降低。在 "计时前进 "测试中,对照组也明显慢于类固醇组。结论局部硬膜外注射类固醇可在术后数天内通过抑制局部炎症而明显减轻腰痛和伤口疼痛,对腰椎管狭窄术后的老年患者有立即止痛的作用。FDA设备/药物状态本摘要不讨论或包含任何适用的设备或药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
36. Effects of intraoperative epidural steroids for lumbar spine surgery in lumbar spinal canal stenosis

BACKGROUND CONTEXT

Pain control methods after spinal surgery are not yet standardized. Postoperative pain relief effects affect patient satisfaction and postoperative rehabilitation and hospital stay. Postoperative pain relief is especially important for elderly patients. Although the effects of steroids after lumbar disc herniation surgery have been reported, their effects on lumbar spinal stenosis are still unclear.

PURPOSE

The purpose of this study is to evaluate the efficacy of intraoperative epidural steroids in lumbar canal stenosis surgery.

STUDY DESIGN/SETTING

A randomized controlled trial.

PATIENT SAMPLE

We enrolled 40 adult patients scheduled for elective lumbar decompression surgery of lumbar canal stenosis. Inclusion criteria were 60-85 years old and decompression between 1 to 3 levels. Exclusion criteria were fusion surgery, reoperation surgery, diabetes mellitus, chronic inflammatory diseases, chronic renal dysfunction, drug allergy, postoperative delirium, and dementia.

OUTCOME MEASURES

We evaluated visual analog scale (VAS), Time Up and Go Test, C-reactive proteins (CRP) of blood data, The cytokines IL-6 of wound drainage and postoperative complications. The primary outcome is VAS of postoperatively, and the second outcomes are laboratory data, postoperative complication and walking ability.

METHODS

This study was a prospective double-blind placebo controlled randomized study. Patients were divided into two groups (steroid group, control group) using a random number table before surgery. In the steroid group, we injected 6.6 mg of dexamethasone epidurally after surgical decompression and before wound closure. In the control group we similarly injected the same volume of saline epidurally before wound closure. Opioids were not used postoperatively. A Cox-2 inhibitor was taken orally for 5 days, and Diclofenac Sodium suppositories were used as needed. We investigated the VAS of average daily pain and maximum pain of back pain and leg pain on postoperative days (POD) 0, 1, 2, 3, 5, 7, and 14. The VAS evaluation was performed by a nurse who was unaware of the group classification. CRP and Time Up and Go Test were investigated preoperatively and on POD 1, 3, and 7. IL-6 was investigated in drain fluid on POD 2.

RESULTS

The steroid group had 19 patients (male 11, female 8), with an average age of 72.9 years and an average number of decompressions of 1.7. The control group had 21 patients (male 14, female 7), with an average age 74.2 years and average number of decompressions of 1.8. There were no significant differences in patient data between the two groups. Back pain (VAS) on POD 0, 1, 2, and 3 were significantly lower in the steroid group compared to the control group. Postoperative VAS (back pain/wound pain) was 41.4 mm on the day of the steroid group, 43.8 on the first day, 38.9 on the second day, and 27.6 on the third day, and 62.8 mm on the day of the control group, 63.4 on the first day, and 55.9 on the second day, and 44.3 on the third day. There was no significant difference in VAS of leg pain between the two groups. There was a significant difference in IL-6 in the drain fluid: 29.8±22.6(ng/ml) in the steroid group and 75.6±49.7 in the control group. CRP results were significantly lower in the steroid group on the third day. The control group was also significantly slower than the steroid group in the Time Up and Go Test. As for postoperative complications, no postoperative wound infection was observed in either group.

CONCLUSIONS

Local epidural injection of steroids significantly reduced low back pain and wound pain by suppressing local inflammation for several days after surgery and was useful for pain relief immediately for elderly patients after surgery of lumbar canal stenosis. Therefore, it is effective in maintaining walking ability.

FDA Device/Drug Status

This abstract does not discuss or include any applicable devices or drugs.

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CiteScore
1.80
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