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本文引用的文献

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Survival analysis of the Wallis interspinous spacer used as an augment to lumbar decompression.作为腰椎减压辅助手段的Wallis棘突间撑开器的生存分析。
Br J Neurosurg. 2017 Dec;31(6):688-694. doi: 10.1080/02688697.2017.1351522. Epub 2017 Jul 8.
2
Interspinous Process Decompression: Expanding Treatment Options for Lumbar Spinal Stenosis.棘突间减压术:拓展腰椎管狭窄症的治疗选择
Biomed Res Int. 2016;2016:3267307. doi: 10.1155/2016/3267307. Epub 2016 Oct 13.
3
Interspinous process spacers versus traditional decompression for lumbar spinal stenosis: systematic review and meta-analysis.腰椎管狭窄症的棘突间撑开器与传统减压术:系统评价与荟萃分析
J Spine Surg. 2016 Mar;2(1):31-40. doi: 10.21037/jss.2016.01.07.
4
IPD without bony decompression versus conventional surgical decompression for lumbar spinal stenosis: 2-year results of a double-blind randomized controlled trial.腰椎管狭窄症的非骨性减压与传统手术减压的比较:一项双盲随机对照试验的2年结果
Eur Spine J. 2015 Oct;24(10):2295-305. doi: 10.1007/s00586-014-3748-2. Epub 2015 Jan 14.
5
Superion interspinous process spacer for intermittent neurogenic claudication secondary to moderate lumbar spinal stenosis: two-year results from a randomized controlled FDA-IDE pivotal trial.用于中度腰椎管狭窄继发间歇性神经源性跛行的Superion棘突间撑开器:一项FDA-IDE随机对照关键试验的两年结果
Spine (Phila Pa 1976). 2015 Mar 1;40(5):275-82. doi: 10.1097/BRS.0000000000000735.
6
Biomechanics of interspinous devices.棘突间装置的生物力学
Biomed Res Int. 2014;2014:839325. doi: 10.1155/2014/839325. Epub 2014 Jul 9.
7
Percutaneous interspinous spacer versus open decompression: a 2-year follow-up of clinical outcome and quality of life.经皮棘突间撑开器与开放性减压术的比较:2 年临床疗效和生活质量随访。
Eur Spine J. 2013 Sep;22(9):2015-21. doi: 10.1007/s00586-013-2790-9. Epub 2013 Apr 27.
8
Clinical evaluation of the preliminary safety and effectiveness of a minimally invasive interspinous process device APERIUS(®) in degenerative lumbar spinal stenosis with symptomatic neurogenic intermittent claudication.APERIUS(®)微创棘突间装置治疗伴有症状性神经源性间歇性跛行的退变性腰椎管狭窄症的初步安全性和有效性的临床评估。
Eur Spine J. 2012 Dec;21(12):2565-72. doi: 10.1007/s00586-012-2330-z. Epub 2012 May 8.
9
Lumbar spinal stenosis treatment with Aperius perclid interspinous system.应用 Aperius 经皮棘突间系统治疗腰椎管狭窄症。
Eur Spine J. 2012 May;21 Suppl 1(Suppl 1):S69-74. doi: 10.1007/s00586-012-2222-2. Epub 2012 Mar 20.
10
Lumbar spinal stenosis.腰椎管狭窄症。
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经皮棘突间装置治疗神经源性间歇性跛行的长期疗效

Long-term results with percutaneous interspinous process devices in the treatment of neurogenic intermittent claudication.

作者信息

Fransen Patrick

机构信息

IM2S, Clinique Médico-Chirurgicale Orthopédique de Monaco, Monaco, Principality of Monaco.

出版信息

J Spine Surg. 2017 Dec;3(4):620-623. doi: 10.21037/jss.2017.11.07.

DOI:10.21037/jss.2017.11.07
PMID:29354740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5760401/
Abstract

BACKGROUND

Neurogenic intermittent claudication (NIC) is the main symptom of degenerative lumbar spinal stenosis. Percutaneous interspinous process decompression devices (IPDs) have been designed as an alternative therapy to conservative treatment and to open decompressive surgery for patients suffering from NIC. Initial short-term results were encouraging. We present the long-term results of a group of patients that we followed to provide insight on long-term outcomes and effectiveness of this technique compared to other decompression methods.

METHODS

Fifteen patients operated for NIC by implantation of percutaneous IPDs have been prospectively monitored for reoperations or complications. Follow-up (FU) was interrupted if the patient was reoperated. Results were considered poor if the patient had to be reoperated at any stage of the FU or if the treatment failed to alleviate the pain after 6 months. Results were considered average if the patient still suffered some pain but did not require reoperation.

RESULTS

The patients were followed up to 7 years after the initial surgery. The mean length of the FU was 3.53 years and all patients could be followed. At the end of the FU, the results were good in only 20.0% (3/15), average in 13.3% (2/15) and poor in 66.7% (10/15).

CONCLUSIONS

Despite initial satisfactory results, long-term FU is disappointing, with 80% poor or average results. The long-term reoperation rate is high (66.6%), increases over time and is higher than after implantation of IPDs for decompression augmentation. Although this technique is simple and safe, its effectiveness seems short-lived. We recommend cautious use and informing patients about the risk of relatively early failure and recurrence.

摘要

背景

神经源性间歇性跛行(NIC)是退行性腰椎管狭窄症的主要症状。经皮棘突间减压装置(IPD)已被设计为一种替代疗法,用于保守治疗以及为患有NIC的患者进行开放减压手术。最初的短期结果令人鼓舞。我们展示了一组患者的长期结果,以便与其他减压方法相比,深入了解该技术的长期疗效和有效性。

方法

前瞻性监测15例因植入经皮IPD治疗NIC而接受手术的患者的再次手术情况或并发症。如果患者接受再次手术,则随访(FU)中断。如果患者在随访的任何阶段必须接受再次手术,或者治疗在6个月后未能缓解疼痛,则结果被认为较差。如果患者仍有一些疼痛但不需要再次手术,则结果被认为一般。

结果

患者在初次手术后随访至7年。平均随访时间为3.53年,所有患者均能得到随访。随访结束时,结果仅20.0%(3/15)为良好,13.3%(2/15)为一般,66.7%(10/15)为较差。

结论

尽管最初结果令人满意,但长期随访结果令人失望,80%的结果为较差或一般。长期再次手术率较高(66.6%),且随时间增加,高于用于减压增强的IPD植入术后。虽然该技术简单且安全,但其有效性似乎是短暂的。我们建议谨慎使用,并告知患者相对早期失败和复发的风险。