循环骶根神经调节:初步研究评估该模式在慢性盆腔疼痛综合征治疗中的神经调节剂规划的有效性

F. Cappellano, G. Ciotti, A. Tafuri, C. Munch, S. Bassi, M. Balzarro, A. Porcaro, E. Rubilotta, M. Wiesmayr, Cynthia Obrero, L. Metcalf, L. Mariani, W. Artibani, M. Cerruto
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引用次数: 4

摘要

目的:骶根神经调节(SNM)在慢性盆腔疼痛综合征(CPPS)治疗中的作用尚缺乏证据。我们评估了循环骶根神经调节(CSNM)在保守治疗无效患者的CPPS管理中的有效性。方法:在2012年2月至2016年3月期间,对所有常规治疗难治性CPPS患者进行了一项前瞻性、单中心、队列研究。在测试刺激期间,时间导线被放置在第三骶神经上,在他们报告疼痛更严重的一侧。成功定义为疼痛和并发泌尿系统症状改善>50%。在成功的4周SNM测试期后,患者接受永久种植体。我们还纳入了另外9名已经植入永久性植入物的患者,他们对神经调节剂编程的连续模式有部分反应。为了评估疼痛和生活质量,所有患者在基线、4周测试期和永久植入后填写了VAS量表、SF-36和McGill问卷。结果:22例连续成人患者适合进行循环试验刺激;其中19人(86.3%)在满意的测试阶段后接受了永久性植入,使用了程序化的循环模式。19名患者中有18名(94.7%)在平均21.3个月的随访中保持了测试刺激的益处。VAS量表、McGill量表和SF-36问卷评分在各领域均有显著提高,满意率达95%;9例已植入的患者中有7例(77.7%)疼痛控制明显改善。结论:CSRN对初次和既往植入部分应答者的CPPS治疗均有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cycling Sacral Root Neuromodulation: Pilot Study to Assess the Effectiveness of This Mode in Neuromodulator Programming for the Treatment of Chronic Pelvic Pain Syndrome
Aim: There is lack of evidence of the role of sacral root neuromodulation (SNM) in the management of chronic pelvic pain syndrome (CPPS). We evaluated the effectiveness of cycling sacral root neuromodulation (CSNM) in the management of CPPS in patients non responders to conservative treatment. Methods: A prospective, single center, cohort study was carried out on all patients with CPPS refractory to conventional treatment, who underwent test stimulation using the tined lead between February 2012 and March 2016. During test stimulation the tine lead was positioned along the third sacral nerve, on the side where they reported more pain. Success was defined as >50% improvement of pain and concurrent urinary symptoms. After a successful SNM test period of 4 weeks, patients received a permanent implant. We also included 9 more patients already with a permanent implant and partial responders to continuous mode in neuromodulator programming. To assess pain and quality of life, all patients filled-in a VAS scale and SF-36 and McGill questionnaires, at baseline, after the 4-week test period ad after the permanent implant. Results: Overall 22 consecutive adult patients were suitable to undergo a cycling test stimulation; 19 out of them (86.3%) underwent a permanent implant after a satisfactory test phase, using a codified cycling mode of programming. Eighteen naive patients out of nineteen (94.7%) maintained the benefits of the test stimulation at a mean follow up of 21.3 months. VAS scale, McGill and SF-36 questionnaires scores improved significantly in all domains with a 95% satisfaction rate; 7 out of the 9 already implanted patients (77.7%) significantly improved their pain control. Conclusion: CSRN appears to be effectiveness in treating CPPS in both naive and previous implanted partial responder patients.
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