膝神经超声引导下低温镇痛治疗慢性膝关节疼痛:一项观察性回顾性研究。

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Giuliano Lo Bianco, Francesco Paolo D'angelo, Guillherme Ferreira Dos Santos, Agnes Stogicza, Matteo Luigi Giuseppe Leoni, Andrea M Trescot, Robert Jason Yong, Christopher L Robinson
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引用次数: 0

摘要

由骨关节炎(OA)引起的慢性膝关节疼痛是成年人残疾的普遍来源。全膝关节置换术(TKA)是一种有效的手术治疗晚期疾病,但许多患者仍然遭受慢性术后疼痛(CPSP)。近年来,针对周围神经的微创技术得到了探索。膝神经低温镇痛(GNCryo)就是这样一种干预,通过对目标神经施加极低的温度来破坏感觉输入,可能导致持续的疼痛缓解,而不需要神经破坏性热损伤。本研究旨在评估超声引导GNCryo在TKA后原发性OA或CPSP所致慢性膝关节疼痛患者中的疗效。方法:这项回顾性、单中心研究纳入了90例在2021年9月至2023年2月期间接受GNCryo的患者。纳入标准为18岁以上患者,TKA后有症状的膝关节OA或CPSP,对诊断性膝神经阻滞有积极反应(疼痛缓解≥50%)。超声引导可优化置针位置,减少并发症。临床结果在基线和术后1、3、6和9个月进行评估。结果测量包括疼痛强度的视觉模拟量表(VAS, 0-10),评估与OA相关的疼痛、僵硬和身体功能的西安大略和麦克马斯特大学关节炎指数(WOMAC, 0-100),神经性疼痛的Douleur神经性疼痛4题(DN4, 0-10)和生活质量的EuroQol 5维(EQ-5D, 0-100)。结果:90例患者完成9个月的随访。VAS评分中位数从基线时的7.0(6.0,8.0)下降到1个月时的4.0(3.0,5.0),3个月时保持在4.0(3.0,5.0),6个月时略微上升到5.0(4.0,5.0),9个月时5.0(4.0,6.0),但疼痛缓解仍然低于基线。WOMAC评分从基线时的65分(55,71分)下降到1个月时的35分(30,40分)和3个月时的35分(30,40分),6个月时增加到40分(35,50分),9个月时增加到55分(45,65分)。DN4评分从基线时的7分(5,8分)降至1个月时的4分(3,4分)和3个月时的3分(2,4分),6个月时升至3.5分(3,5分),9个月时升至5分(4,6分),但仍低于基线。EQ-5D评分从基线时的64.5分(47,84分)增加到1个月时的42分(32,58分),3个月时的43.5分(31,59分),6个月时的45.5分(35,60分),9个月时的52分(41,72分)。结论:超声引导GNCryo是一种很有前景的微创治疗慢性膝关节疼痛的方法,可缓解疼痛并改善长达9个月的生活质量。尽管一些结果显示随着时间的推移趋向于基线,但疼痛缓解仍低于基线,与潜在的神经再生或恢复一致。需要更大的前瞻性对照试验来证实这些发现,并改进患者选择和技术优化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genicular Nerve Ultrasound-Guided Cryoanalgesia for the Treatment of Chronic Knee Joint Pain: An Observational Retrospective Study.

Introduction: Chronic knee pain caused by osteoarthritis (OA) is a prevalent source of disability in the adult population. Total knee arthroplasty (TKA) is an effective surgical treatment for advanced disease, but many patients continue to suffer from chronic post-surgical pain (CPSP). In recent years, minimally invasive techniques targeting peripheral nerves have been explored. Cryoanalgesia of the genicular nerves (GNCryo) is one such intervention that disrupts sensory input by applying extremely low temperatures to the target nerves, potentially leading to sustained pain relief without the need for neurodestructive heat lesions. This study aims to evaluate the effectiveness of ultrasound-guided GNCryo in patients with chronic knee pain due to primary OA or CPSP after TKA.

Methods: This retrospective, single-center study included 90 patients who underwent GNCryo between September 2021 and February 2023. Inclusion criteria were patients over 18 years of age, symptomatic knee OA or CPSP after TKA, and a positive response (≥ 50% pain relief) to diagnostic genicular nerve blocks. Ultrasound guidance was used to optimize needle placement and reduce complications. Clinical outcomes were assessed at baseline and at 1, 3, 6, and 9 months post-procedure. Outcome measures included the Visual Analog Scale (VAS, 0-10) for pain intensity, the Western Ontario and McMaster Universities Arthritis Index (WOMAC, 0-100) for assessing pain, stiffness, and physical function related to OA, the Douleur Neuropathique en 4 Questions (DN4, 0-10) for neuropathic pain, and the EuroQol 5-Dimension (EQ-5D, 0-100) for quality of life.

Results: Ninety patients completed the 9 months follow-up. The median VAS score decreased from 7.0 (6.0, 8.0) at baseline to 4.0 (3.0, 5.0) at 1 month, remained at 4.0 (3.0, 5.0) at 3 months, and increased slightly to 5.0 (4.0, 5.0) at 6 months and 5.0 (4.0, 6.0) at 9 months, yet pain relief remained lower than baseline. WOMAC scores decreased from 65 (55, 71) at baseline to 35 (30, 40) at 1 month and 35 (30, 40) at 3 months, increased to 40 (35, 50) at 6 months and 55 (45, 65) at 9 months. DN4 scores decreased from 7 (5, 8) at baseline to 4 (3, 4) at 1 month and 3 (2, 4) at 3 months, increased to 3.5 (3, 5) at 6 months and 5 (4, 6) at 9 months, yet remained lower than baseline. EQ-5D scores increased from 64.5 (47, 84) at baseline to 42 (32, 58) at 1 month, 43.5 (31, 59) at 3 months, 45.5 (35, 60) at 6 months, and 52 (41, 72) at 9 months.

Conclusions: Ultrasound-guided GNCryo is a promising minimally invasive treatment for chronic knee pain, providing pain relief and improved quality of life for up to 9 months. Although some outcomes showed a trend toward baseline over time, pain relief remained lower than baseline, consistent with potential nerve regeneration or recovery. Larger prospective, controlled trials are necessary to confirm these findings and to refine patient selection and technique optimization.

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来源期刊
Pain and Therapy
Pain and Therapy CLINICAL NEUROLOGY-
CiteScore
6.60
自引率
5.00%
发文量
110
审稿时长
6 weeks
期刊介绍: Pain and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of pain therapies and pain-related devices. Studies relating to diagnosis, pharmacoeconomics, public health, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, acute pain, cancer pain, chronic pain, headache and migraine, neuropathic pain, opioids, palliative care and pain ethics, peri- and post-operative pain as well as rheumatic pain and fibromyalgia. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports, trial protocols, short communications such as commentaries and editorials, and letters. The journal is read by a global audience and receives submissions from around the world. Pain and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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