Franzini Andrea, Attuati Luca, Zaed Ismail, Moosa Shayan, Stravato Antonella, Navarria Pierina, Picozzi Piero
1Department of Neurosurgery, Humanitas Clinical and Research Center-IRCCS, Rozzano (Milano), Italy.
2Department of Neurological Surgery, University of Virginia Health Science Center, Charlottesville, Virginia; and.
J Neurosurg. 2020 Jul 24;135(1):228-236. doi: 10.3171/2020.4.JNS20558. Print 2021 Jul 1.
The goal of this study was to assess the safety and efficacy of stereotactic central lateral thalamotomy with Gamma Knife radiosurgery in patients with neuropathic pain.
Clinical and radiosurgical data were prospectively collected and analyzed in patients with neuropathic pain who underwent Gamma Knife central lateral thalamotomy. The safety and efficacy of the lesioning procedure were evaluated by neurological examination and standardized scales for pain intensity and health-related quality of life. Visual analog scale (VAS) for pain, McGill Pain Questionnaire (MPQ), EuroQol-5 dimensions (EQ-5D), and the 36-Item Short Form Health Survey, version 2 (SF-36v2) were measured during baseline and postoperative follow-up evaluations at 3, 6, 12, 24, and 36 months.
Eight patients with neuropathic pain underwent Gamma Knife central lateral thalamotomy. Four patients suffered from trigeminal deafferentation pain, 2 from brachial plexus injury, 1 from central poststroke facial neuropathic pain, and 1 from postherpetic neuralgia. No lesioning-related adverse effect was recorded during the follow-up periods. All patients had pain reduction following thalamotomy. The mean follow-up time was 24 months. At the last follow-up visits, 5 patients reported ≥ 50% VAS pain reduction. The overall mean VAS pain score was 9.4 (range 8-10) before radiosurgery. After 1 year, the mean VAS pain score decreased significantly, from 9.4 (range 8-10) to 5.5 (mean -41.33%, p = 0.01). MPQ scores significantly decreased (mean -22.18%, p = 0.014). Statistically significant improvements of the SF-36v2 quality of life survey (mean +48.16%, p = 0.012) and EQ-5D (+45.16%, p = 0.012) were observed. At 2 years after radiosurgery, the VAS pain score remained significantly reduced to a mean value of 5.5 (p = 0.027). Statistically significant improvements were also observed for the MPQ (mean -16.05%, p = 0.034); the EQ-5D (mean +35.48%, p = 0.028); and the SF-36v2 (mean +35.84%, p = 0.043). At the last follow-up visits, pain had recurred in 2 patients, who were suffering from central poststroke neuropathic pain and brachial plexus injury, respectively.
Safe, nonpharmacological therapies are imperative for the management of refectory chronic pain conditions. The present series demonstrates that Gamma Knife central lateral thalamotomy is safe and potentially effective in the long term for relieving chronic neuropathic pain refractory to pharmacotherapy and for restoring quality of life.
本研究的目的是评估伽玛刀立体定向中央外侧丘脑切开术治疗神经性疼痛患者的安全性和有效性。
前瞻性收集并分析接受伽玛刀中央外侧丘脑切开术的神经性疼痛患者的临床和放射外科数据。通过神经学检查以及疼痛强度和健康相关生活质量的标准化量表评估损伤手术的安全性和有效性。在基线以及术后3、6、12、24和36个月的随访评估中,测量疼痛视觉模拟量表(VAS)、麦吉尔疼痛问卷(MPQ)、欧洲五维健康量表(EQ-5D)和简明健康调查问卷第2版(SF-36v2)。
8例神经性疼痛患者接受了伽玛刀中央外侧丘脑切开术。4例患有三叉神经去传入性疼痛,2例患有臂丛神经损伤,1例患有中风后中枢性面部神经性疼痛,1例患有带状疱疹后神经痛。随访期间未记录到与损伤相关的不良反应。所有患者丘脑切开术后疼痛均减轻。平均随访时间为24个月。在最后一次随访时,5例患者报告VAS疼痛评分降低≥50%。放射外科手术前VAS疼痛总体平均评分为9.4(范围8 - 10)。1年后,VAS疼痛平均评分显著下降,从9.4(范围8 - 10)降至5.5(平均降低41.33%,p = 0.01)。MPQ评分显著降低(平均降低22.18%,p = 0.014)。观察到SF-36v2生活质量调查有统计学意义的改善(平均提高48.16%,p = 0.012),EQ-5D评分也有改善(提高45.16%,p = 0.012)。放射外科手术后2年,VAS疼痛评分仍显著降低至平均值5.5(p = 0.027)。MPQ(平均降低16.05%,p = 0.034)、EQ-5D(平均提高35.48%,p = 0.028)和SF-36v2(平均提高35.84%,p = 0.043)也有统计学意义的改善。在最后一次随访时,2例患者疼痛复发,分别患有中风后中枢性神经性疼痛和臂丛神经损伤。
对于难治性慢性疼痛疾病的管理,安全的非药物治疗至关重要。本系列研究表明,伽玛刀中央外侧丘脑切开术在长期缓解药物治疗难治的慢性神经性疼痛和恢复生活质量方面是安全且可能有效的。