Dexmedetomidine versus hyaluronidase along with lumbar transforaminal epidural steroid injection in failed back surgery: a randomized double-blind clinical trial.

Anesthesia and pain medicine Pub Date : 2025-01-01 Epub Date: 2024-11-27 DOI:10.17085/apm.24094
Mina Maher Raouf, Sherry Shehata Kyriacos, Manal Hassanein, Gehan Ibrahim Abdel-Razek Salem, Amira Elsonbaty, Sadik Abdel-Maseeh Sadik, Mohammad Awad
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Abstract

Background: Failed back surgery syndrome is a common problem faced by chronic pain management specialists. Steroid-only epidural injections have modest efficacy because of excessive scarring. Epidural hyaluronidase (HA), functions as a depolymerizing agent, successfully breaking down adhesions and collagen bundles, whereas dexmedetomidine (DEX) helps to reduce inflammation.

Methods: The current study is a randomized, double blind, clinical trial. The study cohort included population with persistent (> 6 months) back and/or radicular lower limb pain after laminectomy. Group I (HA group) received bupivacaine 0.5% (5 mg), triamcinolone 40 mg, sterile saline (2 ml), and HA (1500 IU) instilled in 1 mL of distilled water. Group II (DEX group) received bupivacaine 0.5% (5 mg), triamcinolone 40 mg (1 ml), DEX (0.5 mcg/kg), and sterile saline (2 ml).

Results: Both groups showed significant reductions in VAS scores at all follow-ups compared to the pre-injection values. At 6 months, the DEX group experienced a significantly greater reduction in pain scores than the HA group (P = 0.003). In terms of the MODI, both groups showed significant reductions in disability scores at all follow-ups relative to the pre-injection values. The DEX group showed greater improvement in MODI values than the HA group. No significant complications were reported.

Conclusions: Both DEX and HA yielded significant improvements in pain and disability scores compared with pre-injection levels. The DEX group showed a more substantial and long-term reduction in both pain scores and disability index than the HA group.

右美托咪定与透明质酸酶联合经椎间孔硬膜外类固醇注射治疗失败背部手术:一项随机双盲临床试验
背景:背部手术失败综合征是慢性疼痛管理专家面临的常见问题。由于瘢痕过多,仅使用硬膜外注射类固醇的疗效不高。硬膜外透明质酸酶(HA)作为一种解聚剂,能够成功地分解粘连和胶原蛋白束,而右美托咪定(DEX)则有助于减少炎症。方法:本研究为随机、双盲、临床试验。研究队列包括椎板切除术后持续(bbb6个月)背部和/或根性下肢疼痛的人群。ⅰ组(HA组)给予布比卡因0.5% (5 mg)、曲安奈德酮40 mg、无菌生理盐水2 ml、HA (1500 IU)灌注蒸馏水1 ml。II组(DEX组)给予布比卡因0.5% (5 mg)、曲安奈德酮40 mg (1 ml)、DEX (0.5 mcg/kg)、无菌生理盐水(2 ml)。结果:与注射前相比,两组在所有随访中VAS评分均显著降低。6个月时,与HA组相比,DEX组疼痛评分明显降低(P = 0.003)。就MODI而言,两组在所有随访中均显示相对于注射前值的残疾评分显著降低。DEX组的MODI值比HA组有更大的改善。无明显并发症报道。结论:与注射前水平相比,DEX和HA在疼痛和残疾评分方面均有显著改善。与HA组相比,DEX组在疼痛评分和残疾指数方面均表现出更显著和更长期的降低。
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