• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

丘脑前核深部脑刺激与颞叶反应性神经刺激治疗颞叶癫痫的比较。

Anterior nucleus of the thalamus deep brain stimulation vs temporal lobe responsive neurostimulation for temporal lobe epilepsy.

机构信息

Department of Neurosurgery, Emory University School of Medicine, Atlanta, Georgia, USA.

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, USA.

出版信息

Epilepsia. 2022 Sep;63(9):2290-2300. doi: 10.1111/epi.17331. Epub 2022 Jul 5.

DOI:10.1111/epi.17331
PMID:35704344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9675907/
Abstract

OBJECTIVE

Based on the promising results of randomized controlled trials, deep brain stimulation (DBS) and responsive neurostimulation (RNS) are used increasingly in the treatment of patients with drug-resistant epilepsy. Drug-resistant temporal lobe epilepsy (TLE) is an indication for either DBS of the anterior nucleus of the thalamus (ANT) or temporal lobe (TL) RNS, but there are no studies that directly compare the seizure benefits and adverse effects associated with these therapies in this patient population. We, therefore, examined all patients who underwent ANT-DBS or TL-RNS for drug-resistant TLE at our center.

METHODS

We performed a retrospective review of patients who were treated with either ANT-DBS or TL-RNS for drug-resistant TLE with at least 12 months of follow-up. Along with the clinical characteristics of each patient's epilepsy, seizure frequency was recorded throughout each patient's postoperative clinical course.

RESULTS

Twenty-six patients underwent ANT-DBS implantation and 32 patients underwent TL-RNS for drug-resistant TLE. The epilepsy characteristics of both groups were similar. Patients who underwent ANT-DBS demonstrated a median seizure reduction of 58% at 12-15 months, compared to a median seizure reduction of 70% at 12-15 months in patients treated with TL-RNS (p > .05). The responder rate (percentage of patients with a 50% decrease or more in seizure frequency) was 54% for ANT-DBS and 56% for TL-RNS (p > .05). The incidence of complications and stimulation-related side effects did not significantly differ between therapies.

SIGNIFICANCE

We demonstrate in our single-center experience that patients with drug-resistant TLE benefit similarly from either ANT-DBS or TL-RNS. Selection of either ANT-DBS or TL-RNS may, therefore, depend more heavily on patient and provider preference, as each has unique capabilities and configurations. Future studies will consider subgroup analyses to determine if specific patients have greater seizure frequency reduction from one form of neuromodulation strategy over another.

摘要

目的

基于随机对照试验的良好结果,深部脑刺激(DBS)和反应性神经刺激(RNS)越来越多地用于治疗耐药性癫痫患者。耐药性颞叶癫痫(TLE)是丘脑前核(ANT)DBS 或颞叶(TL)RNS 的适应证,但没有研究直接比较这些治疗方法在该患者人群中的癫痫获益和不良反应。因此,我们检查了在我们中心接受 ANT-DBS 或 TL-RNS 治疗耐药性 TLE 的所有患者。

方法

我们对在我们中心接受 ANT-DBS 或 TL-RNS 治疗耐药性 TLE 且至少有 12 个月随访的患者进行了回顾性研究。除了每位患者癫痫的临床特征外,还记录了每位患者术后临床过程中的癫痫发作频率。

结果

26 例患者接受 ANT-DBS 植入,32 例患者接受 TL-RNS 治疗耐药性 TLE。两组患者的癫痫特征相似。接受 ANT-DBS 的患者在 12-15 个月时癫痫发作减少了 58%,而接受 TL-RNS 治疗的患者在 12-15 个月时癫痫发作减少了 70%(p>.05)。ANT-DBS 的应答率(癫痫发作频率降低 50%或更多的患者百分比)为 54%,TL-RNS 为 56%(p>.05)。并发症和刺激相关副作用的发生率在两种治疗方法之间无显著差异。

意义

我们在单中心经验中证明,耐药性 TLE 患者从 ANT-DBS 或 TL-RNS 中获益相似。因此,ANT-DBS 或 TL-RNS 的选择可能更多地取决于患者和提供者的偏好,因为每种方法都具有独特的功能和配置。未来的研究将考虑亚组分析,以确定是否特定患者从一种神经调节策略中获得更大的癫痫发作频率降低。

相似文献

1
Anterior nucleus of the thalamus deep brain stimulation vs temporal lobe responsive neurostimulation for temporal lobe epilepsy.丘脑前核深部脑刺激与颞叶反应性神经刺激治疗颞叶癫痫的比较。
Epilepsia. 2022 Sep;63(9):2290-2300. doi: 10.1111/epi.17331. Epub 2022 Jul 5.
2
Distinct Biomarkers of ANT Stimulation and Seizure Freedom in an Epilepsy Patient with Ambulatory Hippocampal Electrocorticography.癫痫患者动态海马脑电监测下抗癫痫药物刺激和无癫痫发作的生物标志物明显不同。
Stereotact Funct Neurosurg. 2023;101(6):349-358. doi: 10.1159/000533680. Epub 2023 Sep 22.
3
Invasive neuromodulation for epilepsy: Comparison of multiple approaches from a single center.癫痫的侵袭性神经调节:来自单一中心的多种方法比较。
Epilepsy Behav. 2022 Dec;137(Pt A):108951. doi: 10.1016/j.yebeh.2022.108951. Epub 2022 Oct 27.
4
Clinical efficacy and safety of anterior thalamic deep brain stimulation for intractable drug resistant epilepsy.丘脑前核电刺激治疗耐药性癫痫的临床疗效和安全性。
Epilepsy Res. 2023 Sep;195:107199. doi: 10.1016/j.eplepsyres.2023.107199. Epub 2023 Jul 27.
5
Deep brain and cortical stimulation for epilepsy.用于癫痫治疗的深部脑刺激和皮层刺激
Cochrane Database Syst Rev. 2017 Jul 18;7(7):CD008497. doi: 10.1002/14651858.CD008497.pub3.
6
Neurostimulation in generalized epilepsy: A systematic review and meta-analysis.全身性癫痫中的神经刺激:一项系统评价和荟萃分析。
Epilepsia. 2023 Apr;64(4):811-820. doi: 10.1111/epi.17524. Epub 2023 Feb 16.
7
Deep brain stimulation for seizure control in drug-resistant epilepsy.深部脑刺激治疗耐药性癫痫的癫痫发作控制。
Neurosurg Focus. 2018 Aug;45(2):E4. doi: 10.3171/2018.4.FOCUS1872.
8
Practical considerations in epilepsy neurostimulation.癫痫神经刺激的实际考虑因素。
Epilepsia. 2022 Oct;63(10):2445-2460. doi: 10.1111/epi.17329. Epub 2022 Aug 9.
9
Deep brain stimulation targets in epilepsy: Systematic review and meta-analysis of anterior and centromedian thalamic nuclei and hippocampus.癫痫的脑深部刺激靶点:丘脑前核、中央中核及海马的系统评价与荟萃分析
Epilepsia. 2022 Mar;63(3):513-524. doi: 10.1111/epi.17157. Epub 2022 Jan 3.
10
Deep brain stimulation for drug-resistant epilepsy.脑深部电刺激治疗耐药性癫痫。
Epilepsia. 2018 Feb;59(2):273-290. doi: 10.1111/epi.13964. Epub 2017 Dec 7.

引用本文的文献

1
Deep Brain Stimulation Therapy for Drug-Resistant Epilepsy: Present and Future Perspectives.用于耐药性癫痫的深部脑刺激疗法:现状与未来展望
J Epilepsy Res. 2025 Jun 10;15(1):33-41. doi: 10.14581/jer.25004. eCollection 2025 Jun.
2
Intracranial stimulation for pediatric refractory epilepsy: A single institutional experience using evolving therapies.小儿难治性癫痫的颅内刺激:采用不断发展的疗法的单机构经验。
Epilepsia Open. 2025 Jun;10(3):694-704. doi: 10.1002/epi4.70006. Epub 2025 Apr 1.
3
The Role of Neuroinflammation and Network Anomalies in Drug-Resistant Epilepsy.神经炎症和网络异常在耐药性癫痫中的作用
Neurosci Bull. 2025 May;41(5):881-905. doi: 10.1007/s12264-025-01348-w. Epub 2025 Feb 24.
4
Decreased Structural Connectivity Between Thalamic Nuclei and Hippocampus in Temporal Lobe Epilepsy-A Diffusion Tensor Imaging-Based Study.基于扩散张量成像的颞叶癫痫患者丘脑核与海马之间结构连接性降低的研究
Eur J Neurol. 2025 Jan;32(1):e70040. doi: 10.1111/ene.70040.
5
The Best Things Happen When You Least Expect Them: Responsive Neurostimulation During Low-Risk Brain States is Associated with Improved Long-Term Seizure Suppression.当你最不经意时,最美好的事情就会发生:低风险脑状态下的反应性神经刺激与长期癫痫发作抑制改善有关。
Epilepsy Curr. 2024 Jun 14;24(5):350-352. doi: 10.1177/15357597241258287. eCollection 2024 Sep-Oct.
6
The Neurostimulationist will see you now: prescribing direct electrical stimulation therapies for the human brain in epilepsy and beyond.神经刺激专家现在将为您诊治:为癫痫及其他病症的人脑开具直接电刺激疗法的处方。
Front Hum Neurosci. 2024 Sep 4;18:1439541. doi: 10.3389/fnhum.2024.1439541. eCollection 2024.
7
Therapeutic approaches targeting seizure networks.针对癫痫发作网络的治疗方法。
Front Netw Physiol. 2024 Aug 7;4:1441983. doi: 10.3389/fnetp.2024.1441983. eCollection 2024.
8
Deep Brain Stimulation Inhibits Epileptic Seizures via Increase of Adenosine Release and Inhibition of ENT1, CD39, and CD73 Expression.深部脑刺激通过增加腺苷释放及抑制ENT1、CD39和CD73的表达来抑制癫痫发作。
Mol Neurobiol. 2025 Feb;62(2):1800-1812. doi: 10.1007/s12035-024-04374-3. Epub 2024 Jul 23.
9
Exploring the Role of the Pulvinar Nucleus of the Thalamus in Occipital Lobe Epilepsy: A Case Report.探索丘脑枕核在枕叶癫痫中的作用:一例报告
Cureus. 2024 Jan 18;16(1):e52534. doi: 10.7759/cureus.52534. eCollection 2024 Jan.
10
Closed-loop stimulation in periods with less epileptiform activity drives improved epilepsy outcomes.在癫痫样活动较少的时期进行闭环刺激可改善癫痫治疗效果。
Brain. 2024 Feb 1;147(2):521-531. doi: 10.1093/brain/awad343.

本文引用的文献

1
Anterior nucleus of the thalamus seizure detection in ambulatory humans.丘脑前核癫痫发作在活动状态下的人类中的检测。
Epilepsia. 2021 Oct;62(10):e158-e164. doi: 10.1111/epi.17047. Epub 2021 Aug 21.
2
The SANTÉ study at 10 years of follow-up: Effectiveness, safety, and sudden unexpected death in epilepsy.SANTÉ 研究 10 年随访结果:癫痫的疗效、安全性和突发性意外死亡。
Epilepsia. 2021 Jun;62(6):1306-1317. doi: 10.1111/epi.16895. Epub 2021 Apr 8.
3
Nine-year prospective efficacy and safety of brain-responsive neurostimulation for focal epilepsy.脑反应性神经刺激治疗局灶性癫痫的 9 年疗效和安全性前瞻性研究。
Neurology. 2020 Sep 1;95(9):e1244-e1256. doi: 10.1212/WNL.0000000000010154. Epub 2020 Jul 20.
4
Real-world experience with direct brain-responsive neurostimulation for focal onset seizures.直接针对大脑反应的神经刺激治疗局灶性发作性癫痫的真实世界经验。
Epilepsia. 2020 Aug;61(8):1749-1757. doi: 10.1111/epi.16593. Epub 2020 Jul 13.
5
Mesial temporal resection following long-term ambulatory intracranial EEG monitoring with a direct brain-responsive neurostimulation system.经长期颅内脑电监测和直接脑反应性神经刺激系统引导行颞叶内侧切除术。
Epilepsia. 2020 Mar;61(3):408-420. doi: 10.1111/epi.16442. Epub 2020 Feb 18.
6
Early detection rate changes from a brain-responsive neurostimulation system predict efficacy of newly added antiseizure drugs.脑反应性神经刺激系统的早期检测率变化可预测新添加的抗癫痫药物的疗效。
Epilepsia. 2020 Jan;61(1):138-148. doi: 10.1111/epi.16412. Epub 2019 Dec 17.
7
Probing circuit of Papez with stimulation of anterior nucleus of the thalamus and hippocampal evoked potentials.用丘脑前核刺激和海马诱发电位探测帕佩兹环路。
Epilepsy Res. 2020 Jan;159:106248. doi: 10.1016/j.eplepsyres.2019.106248. Epub 2019 Nov 29.
8
Responsive neurostimulation targeting anterior thalamic nucleus in generalized epilepsy.针对全面性癫痫的前丘脑核的反应性神经刺激。
Ann Clin Transl Neurol. 2019 Oct;6(10):2104-2109. doi: 10.1002/acn3.50858. Epub 2019 Sep 11.
9
Effects of surgical targeting in laser interstitial thermal therapy for mesial temporal lobe epilepsy: A multicenter study of 234 patients.手术靶向在激光间质热疗治疗内侧颞叶癫痫中的作用:234 例多中心研究。
Epilepsia. 2019 Jun;60(6):1171-1183. doi: 10.1111/epi.15565. Epub 2019 May 21.
10
Comparison and Selection of Current Implantable Anti-Epileptic Devices.当前可植入抗癫痫装置的比较与选择。
Neurotherapeutics. 2019 Apr;16(2):369-380. doi: 10.1007/s13311-019-00727-2.