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Under forty hours of laboratory training may be sufficient for teaching basic microsurgical skills to novices 不到40小时的实验室训练可能足以向新手教授基本的显微外科技术。
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-11-05 DOI: 10.1007/s00701-025-06704-3
Adam Yousfi, Ville Vasankari, Anni Pohjola, Anna Maria Auricchio, Francesco Calvanese, Ahmad Hafez, Martin Lehecka

Background

Structured laboratory-based microsurgical training is considered beneficial for junior residents before they begin to work in a neurosurgical operating room. The optimal duration of such training remains unclear. We studied the effect of a 40-h microsurgical laboratory course on the development of basic microsurgical skills among novices.

Methods

A total of 27 medical students participated in the study. Seven students (5 men, 2 women) underwent a structured microsurgical laboratory training program over four weeks. 20 students (10 women, 10 men) served as an untrained control group. None of the students had prior experience in microsuturing or working under magnification. The intervention group practiced for two hours per day, five days per week, over a four-week period. Skill development was assessed at baseline, after two weeks, and after four weeks of training with a microsuturing test task, and was monitored continuously throughout the training period with a microscraping test task. Microsurgical performance was compared between the intervention and the control groups using a test task performed under a surgical exoscope after two weeks of training. This task assessed complex depth perception and hand–eye coordination through the precise placement of a microneedle into small, concealed targets.

Results

For the microsuturing task the median time improved throughout the training (baseline: 44 min (interquartile range IQR = 22), 20 h training: 21 min (IQR = 6), 40 h training: 14 min (IQR = 4)). Similarly, the duration of the scraping task improved (baseline: 40 min (IQR 2), 20 h training: 15 min (IQR = 7), 40 h training: 13 min (IQR = 7)). The quality of work, including scraping accuracy, suture tightness and spacing, remained consistent in both tasks. In the exoscope task, the intervention group outperformed the control group (median task duration 6 min 54 s, IQR = 3 min vs 9 min 24 s, IQR = 6 min; p = 0.04).

Conclusions

Novices demonstrated rapid improvement during a 40-h microsurgical laboratory training course. Even less than 40 h of structured practice might be enough for surgical novices, such as neurosurgery residents, to learn the most basic microsurgical skills prior to assisting in the operating room.

背景:在初级住院医师开始在神经外科手术室工作之前,结构化的以实验室为基础的显微外科训练被认为是有益的。这种训练的最佳持续时间尚不清楚。我们研究了40小时显微外科实验课程对新手显微外科基本技能发展的影响。方法:共27名医学生参与研究。7名学生(5男2女)接受了为期四周的显微外科实验室训练计划。20名学生(10名女性,10名男性)作为未经训练的对照组。这些学生之前都没有显微缝合或在放大镜下工作的经验。干预组每天练习两小时,每周五天,为期四周。在基线、两周和四周训练后通过微缝合测试任务评估技能发展,并在整个训练期间通过微刮测试任务连续监测技能发展。在两周的训练后,通过在手术外窥镜下进行的测试任务,比较干预组和对照组的显微外科手术表现。这项任务通过将微针精确放置在隐蔽的小目标上来评估复杂的深度感知和手眼协调能力。结果:对于微缝合任务,在整个训练过程中,中位时间有所改善(基线:44 min(四分位间距IQR = 22),训练20 h: 21 min (IQR = 6),训练40 h: 14 min (IQR = 4))。同样,刮拭任务的持续时间也有所改善(基线:40分钟(IQR 2), 20小时训练:15分钟(IQR = 7), 40小时训练:13分钟(IQR = 7))。工作质量,包括刮刀精度、缝合紧密性和间距,在两项任务中保持一致。在外窥镜任务中,干预组优于对照组(中位任务持续时间6 min 54 s, IQR = 3 min vs 9 min 24 s, IQR = 6 min, p = 0.04)。结论:在40小时的显微外科实验室培训课程中,新手表现出快速的进步。即使不到40小时的结构化实践也足以让外科新手(如神经外科住院医师)在协助手术室之前学习最基本的显微外科技能。
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引用次数: 0
Evaluation of visual ergonomics in microsurgery: a real-time video processing solution 显微外科中视觉工效学的评价:实时视频处理解决方案。
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-11-05 DOI: 10.1007/s00701-025-06694-2
Gaukhar Mukash, Paavo Vartianen, Mastaneh Torkamani-Azar, Zeynel Karadis, Mehdi Faraz, Roman Bednarik, Pasi A. Karjalainen, Matti Iso-Mustajärvi, Ahmed Hussein

Purpose

Surgeons’ visual and ergonomical challenges are long-standing concerns since the use of microscopes in surgical procedures. Although devices have been improved in the last few decades, the problem of narrow visual fields in high magnification surgeries persists. This study aims to identify the visual ergonomics challenges among microsurgeons and assess the need for novel assistive surgical solutions.

Methods

The study consisted of two parts: a survey and a hands-on experiment. Sixteen surgeons from neurosurgery and otolaryngology (ENT) specialties were invited to semi-structured interviews on challenges encountered when using surgical microscopes and evaluation of the two proposed technological solutions: CPM (context-preserving magnification) and IT (instrument transparency). Following a demonstration of these software solutions, a survey utilizing a Likert scale was administered. The second part of the study involved twelve practicing neurosurgeons who performed a task using a novel solution and compared it to a standard operative microscope setting.

Results

The most common challenges reported were visual obstruction of field by instruments (93.75%), blurring of structures and light reflection (81.25%), and loss of context (68.75%). 50% of surgeons agreed that adjusting zoom and focus takes a considerable amount of time from surgery and 56% stated that they had at least one episode of difficulty seeing depth. Notably, 69% of respondents expressed interest in testing prototypes of both proposed solutions in real surgery, with a particular preference for instrument transparency. Furthermore, the context-preserving magnification solution hands-on trial demonstrated a 40% reduction in task completion time for 60% of participants. However, one participant found no advantage, and others took longer to complete tasks with the solution compared to standard settings.

Conclusion

Our solution addresses the top visual challenges and instrument obstruction remains a top challenge in high magnification microsurgery. We showed that surgeons are highly likely to use novel assistive technologies that provide wider visual field and transparent instruments.

目的:自从在外科手术中使用显微镜以来,外科医生的视觉和人体工程学挑战一直备受关注。虽然在过去的几十年里设备已经得到了改进,但在高倍手术中视野狭窄的问题仍然存在。本研究旨在确定显微外科医生在视觉工效学方面的挑战,并评估对新型辅助手术解决方案的需求。方法:本研究分为问卷调查和实践实验两部分。来自神经外科和耳鼻喉科(ENT)专业的16位外科医生被邀请参加半结构化访谈,讨论在使用手术显微镜时遇到的挑战,并评估两种拟议的技术解决方案:CPM(环境保留放大)和IT(仪器透明)。在演示了这些软件解决方案之后,使用李克特量表进行了调查。研究的第二部分涉及12名执业神经外科医生,他们使用一种新溶液完成一项任务,并将其与标准的手术显微镜环境进行比较。结果:最常见的视力障碍是仪器遮挡视野(93.75%)、结构和光反射模糊(81.25%)和环境丧失(68.75%)。50%的外科医生认为,调整变焦和对焦需要相当多的手术时间,56%的医生表示,他们至少有一次难以看清深度。值得注意的是,69%的受访者表示有兴趣在实际手术中测试这两种解决方案的原型,并特别偏好器械透明度。此外,情境保留放大解决方案的实践试验表明,60%的参与者完成任务的时间减少了40%。然而,一名参与者没有发现任何优势,而其他参与者用这个解决方案完成任务的时间比标准设置要长。结论:我们的解决方案解决了高倍显微手术中最大的视觉挑战,器械阻塞仍然是最大的挑战。我们发现外科医生很有可能使用新的辅助技术,提供更广阔的视野和透明的仪器。
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引用次数: 0
Continuous intracisternal nimodipine administration as rescue therapy for refractory vasospasm in patients with aneurysmal subarachnoid haemorrhage 颅内持续尼莫地平治疗动脉瘤性蛛网膜下腔出血难治性血管痉挛的疗效观察。
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-11-04 DOI: 10.1007/s00701-025-06702-5
Mandy D. Müller, Katharina Janosovits, David Bervini, Pasquale Mordasini, Tomas Dobrocky, Eike I. Piechowiak, Joerg C. Schefold, Michael Murek, Johannes Goldberg, Philippe Schucht, Andreas Raabe, Werner J. Z’Graggen

Purpose

Delayed cerebral ischaemia (DCI) and cerebral vasospasm (CVS) remain major causes of poor outcome in survivors of aneurysmal subarachnoid haemorrhage (aSAH). We aimed to investigate the safety and efficacy of intracisternal administration of nimodipine in patients suffering from symptomatic CVS refractory to treatment with induced hypertension and endovascular vasodilator therapy.

Methods

We performed a single-centre, retrospective, observational study including all patients diagnosed with refractory CVS after aSAH treated at our tertiary centre between January 2018 and December 2021 who received continuous intracisternal nimodipine. For nimodipine administration, a catheter was inserted in the optico-carotid cistern via supraorbital craniotomy. Our primary outcome was functional independence measured by the modified Rankin Scale (mRS) at 6 months. Secondary outcomes included treatment related complications and neurological outcome.

Results

We included 15 patients in total. Clinical outcome measured by the mRS at 6 months was good with 93.3% of patients showing mRS ≤ 1 (median mRS 1; range 1–4) Eight patients (53%) developed a new CVS-related neurological deficit during intrathecal nimodipine treatment and additionally received bolus intra-arterial nimodipine. Two patients (13%) developed acute subdural/epidural hematoma postoperatively, which was treated surgically in one patient. In two patients (13%), accidental dislocation of the intrathecal catheter occurred, which warranted re-operation.

Conclusion

Continuous intracisternal administration of nimodipine may be a viable rescue therapy option for patients with refractory CVS but is associated with an increased risk of treatment related complications.

目的:迟发性脑缺血(DCI)和脑血管痉挛(CVS)仍然是动脉瘤性蛛网膜下腔出血(aSAH)幸存者预后不良的主要原因。我们的目的是研究尼莫地平腹腔内给药对难治性CVS合并高血压和血管内扩张剂治疗的患者的安全性和有效性。方法:我们进行了一项单中心、回顾性、观察性研究,纳入了2018年1月至2021年12月在我们三级中心接受aSAH治疗后诊断为难治性CVS的所有患者,这些患者持续接受腹腔内尼莫地平治疗。尼莫地平给药时,经眶上开颅在颈光池内插入导管。我们的主要终点是6个月时用改良Rankin量表(mRS)测量的功能独立性。次要结局包括治疗相关并发症和神经预后。结果:共纳入15例患者。6个月mRS测量的临床结果良好,93.3%的患者mRS≤1(中位mRS 1;范围1-4)8例患者(53%)在鞘内尼莫地平治疗期间出现了新的cvs相关神经功能障碍,并在此基础上接受了动脉内尼莫地平。2例患者(13%)术后出现急性硬膜下/硬膜外血肿,1例患者接受手术治疗。2例患者(13%)发生鞘内导管意外脱位,需要再次手术。结论:对于难治性CVS患者,持续腹腔内给予尼莫地平可能是一种可行的抢救治疗选择,但与治疗相关并发症的风险增加有关。
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引用次数: 0
“Bonnet bypass” using a radial artery interposition graft—how I do it 用桡动脉间置移植术进行心脏搭桥,我就是这么做的
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-10-31 DOI: 10.1007/s00701-025-06700-7
Rajiv K. Khajuria, Milad Neyazi, Katharina Faust, Sajjad Muhammad

Background

Common carotid artery (CCA) occlusion frequently results in compromised hemodynamics of the ipsilateral hemisphere with risk of infarction but also a lack of blood flow in the ipsilateral superficial temporal artery (STA), requiring a more complex revascularization strategy than a standard extracranial-intracranial (EC-IC) bypass when indicated.

Method

We describe the performance of a “Bonnet bypass” using a radial artery interposition graft (RAIG) from the contralateral STA to the ipsilateral middle cerebral artery (MCA). A groove is drilled in the skullcap to position the RAIG and reduce risk of mobilization and compression.

Conclusion

The “Bonnet bypass” enables a revascularization procedure when the ipsilateral STA is not available as donor vessel.

背景:颈总动脉(CCA)闭塞经常导致同侧半球血流动力学受损,有梗死风险,但也会导致同侧颞浅动脉(STA)缺乏血流,需要比标准颅外-颅内(EC-IC)旁路手术更复杂的血运重建策略。方法我们描述了从对侧STA到同侧大脑中动脉(MCA)的桡动脉间置移植物(rag)的“Bonnet旁路”的表现。在头盖骨上钻孔以定位rag,减少活动和压迫的风险。结论当同侧STA不能作为供血管时,“帽状旁路”可以实现血运重建手术。
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引用次数: 0
Technical aspects of SEEG limitations and solutions using the Leksell Vantage frame 使用Leksell Vantage框架的SEEG限制和解决方案的技术方面。
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-10-27 DOI: 10.1007/s00701-025-06662-w
Insa Prilop, Stephan B. Sobottka, Georg K. Leonhardt, Ilker Y. Eyüpoglu, Witold H. Polanski

Background

Stereo-electroencephalography (SEEG) is an invasive electroencephalography method to precisely locate a seizure onset zone (SOZ). While today´s armamentarium allows any compromise between the historically strict orthogonal and oblique trajectories, the following aspects limit its effectiveness and safety. The shorter the distance from entry to the brain and target the less deviation of the electrode. The closer to orthogonal to the scull the more stable the anchor sits in the scull and deviation can be better controlled. Beyond that, limitations due to the stereotactic frame must be considered. In certain cases, a conflict between frame setup and entry point of the trajectory can arise. This conflict spurred us to explore the limits of stereotactic frame and the associated equipment needed for SEEG.

Methods

We utilize the Elekta Leksell Vantage frame (LVF) and surgical SEEG-instruments of the company AD-Tech. Planning of the trajectories is performed with a software based on MRI scans. After co-registration with stereotactical CT-angiogram coordinates for the centre-of-arc-principle to set up the LVF are generated. The frame setup focuses on the orientation of the ring-shaped z-axis, which impact SEEG electrode placement. Key factors, such as arc-angle and x-coordinate, influence instrument positioning and potential interference with the frame. Various combinations of ring-scale direction, arc alignment, arc-angle, and x-coordinate were attempted, along with the limitations of the ring angle in relation to y- and z-axis.

Results

Since 2018 our department performed 19 SEEG-implantations of in total 188 SEEG-electrodes. The average age at presentation of the 15 male and 4 female patients was 42 years (range 28 to 58). In 6 of the 19 implantation the ZD Inomed frame was used, while the other 13 cases were performed with the LVF. An average of 9 electrodes were applied using the ZD Inomed frame compared to 11 electrodes with the LVF. Both approaches aimed for bihemispheric targets. The average time of implantation of a single electrode using the ZD Inomed frame was 20,7 min, while the LVF took 4 min less (16,6 min). Other factors such as electrode repositioning or deviation and postoperative complications occurred very rarely. In at least 12 cases concerning 19 out of 188 (10.1%) electrodes an intraoperative trajectory replanning became necessary because of conflict between frame setup and entry point of the trajectory.

Conclusion

Our clinical experience confirmed that the complex planning of SEEG trajectories occasionally leads to a conflict between frame setup and entry points. The systematic analysis of the utilized stereotactic frame and SEEG-instruments can prevent replanning during surgery and improves patient’s safety and quality management.

背景:立体脑电图(SEEG)是一种精确定位癫痫发作区(SOZ)的侵入性脑电图方法。虽然今天的设备允许在历史上严格的正交和斜向轨迹之间进行任何妥协,但以下方面限制了其有效性和安全性。从入口到大脑和目标的距离越短,电极的偏差就越小。锚与桨越接近正交,锚在桨内的位置越稳定,偏离控制效果越好。除此之外,由于立体定向框架的限制必须考虑。在某些情况下,可能会出现框架设置和轨迹入口点之间的冲突。这种冲突促使我们探索立体定向框架的局限性以及SEEG所需的相关设备。方法:我们使用Elekta Leksell Vantage框架(LVF)和AD-Tech公司的外科seeg器械。轨迹规划是通过基于核磁共振扫描的软件进行的。在与立体定向ct血管造影共配准后,生成了圆心原理建立LVF的坐标。框架设置的重点是环形z轴的方向,它影响SEEG电极的放置。关键因素,如圆角和x坐标,影响仪器定位和对框架的潜在干扰。尝试了环尺度方向、圆弧对准、圆弧角和x坐标的各种组合,以及环角相对于y轴和z轴的限制。结果:2018年以来,我科共实施seeg植入19例,共植入188个seeg电极。15例男性和4例女性患者的平均发病年龄为42岁(28至58岁)。在19例植入中,有6例使用了ZD Inomed框架,而其他13例使用了LVF。使用ZD Inomed框架平均使用9个电极,而使用LVF则平均使用11个电极。这两种方法都针对双脑目标。使用ZD Inomed框架植入单个电极的平均时间为20.7 min,而LVF的平均时间为16.6 min。其他因素,如电极重新定位或偏差和术后并发症很少发生。在188个电极中有19个(10.1%)的至少12个病例中,由于框架设置和轨迹进入点之间的冲突,术中轨迹重新规划成为必要。结论:我们的临床经验证实,复杂的SEEG轨迹规划偶尔会导致框架设置和进入点之间的冲突。系统分析所使用的立体定向框架和seeg器械可以防止手术中重新规划,提高患者的安全性和质量管理。
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引用次数: 0
Microsurgical opening of the carotid dural rings: how I do it 显微外科打开颈动脉硬膜环:我是怎么做的。
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-10-27 DOI: 10.1007/s00701-025-06673-7
Edgar Nathal, Alejandro Serrano Rubio, Sharon Trujillo, Rodolfo Villalobos-Díaz, Julián Moisés Enríquez-Álvarez

Background

Paraclinoid aneurysms represent a challenge for neurosurgeons due to the anatomical complexity of this region and the technical difficulties involved in accessing this location.

Methods

In this work, we describe the surgical technique used to manage paraclinoid aneurysms, as exemplified through a clinical case. The distal dural ring (DDR) is exposed after the anterior clinoid process is resected extradurally. Then, the DDR is cut around the dorsal part of the carotid artery, moving toward the dura covering the optic nerve (ON). After, the lateral and ventral part of the ring is cut until the artery is freed from the dural attachment. The space between the proximal and DDR is visible and can be used as a proximal vascular control site if needed.

Conclusion

Microsurgical clipping of paraclinoid aneurysms through a pterional or a keyhole approach, combined with a systematic technique for opening the carotid rings, is an excellent strategy for exposing and clipping paraclinoid aneurysms, yielding favorable clinical and surgical outcomes.

背景:由于该区域的解剖复杂性和进入该位置的技术困难,类旁动脉瘤对神经外科医生来说是一个挑战。方法:在这项工作中,我们通过一个临床病例,描述了用于治疗类旁动脉瘤的手术技术。硬脑膜远端环(DDR)在前斜突外切除后暴露。然后,在颈动脉背侧切开DDR,向覆盖视神经(ON)的硬脑膜移动。之后,切开环的外侧和腹侧部分,直到动脉脱离硬脑膜附着。近端和DDR之间的空间是可见的,如果需要,可以用作近端血管控制部位。结论:经翼点或锁眼入路显微手术夹闭类旁动脉瘤,结合系统的打开颈动脉环技术,是一种很好的暴露和夹闭类旁动脉瘤的策略,具有良好的临床和手术效果。
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引用次数: 0
Intraoperative neurophysiological monitoring in surgery for intramedullary spinal cord lesions – workflow, setup and outcomes 髓内脊髓病变手术中的术中神经生理监测-工作流程,设置和结果
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-10-24 DOI: 10.1007/s00701-025-06697-z
Henrik Frisk, Gayane Margaryan, Ali Buwaider, Davit Sargsyan, Victor Gabriel El-Hajj, Tomas Majing, Aman Singh, Alexander Fletcher-Sandersjöö, Oscar Persson, Victor E. Staartjes, Jonas K. E. Persson, Erik Edström, Adrian Elmi-Terander

Objective

Gross total resection is strived for in intramedullary spinal cord lesion surgery. Intraoperative neurophysiological monitoring (IONM) is the gold standard, but there is no consensus on the optimal IONM workflow. This study details our institutional workflow.

Methods

We retrospectively reviewed all adults who underwent intramedullary resection at Karolinska University Hospital, 2007–2021 (n = 70). Continuous multimodal IONM (somatosensory-evoked potentials (SSEP), motor-evoked potentials (MEP) and epidural D-waves) was conducted by an in-room neurophysiologist. Alarm thresholds were preset (≥ 50% SSEP amplitude drop/10% latency rise; ≥ 80% MEP reduction; ≥ 50% D-wave loss) and triggered a standardized four-step rescue protocol (halt manipulation, raise MAP to 80–90 mm Hg, topical papaverine, observation). Motor/sensory function, modified McCormick (mMC) grade, pain, and sphincter control were documented pre-operatively, at 3 months, and ≥ 12 months.

Results

Seventy patients were included. Most harboured ependymoma (51%), hemangioblastoma (18%) and cavernoma (8.5%). A neurophysiologist was present during every procedure. A ≥ 50% intra-operative SSEP-amplitude decrease was not followed by a sensory deficit (OR:3.0, 95% CI 0.86–10.6; p = 0.085) or mMC deterioration (OR:1.6, 0.33–7.5; p = 0.57) at either short- or long-term follow-up. In contrast, complete SSEP loss markedly increased the risk of postoperative sensory deficit (3-months-OR:25.2, 4.7–135; p < 0.001; long-term-OR 11.0, 2.8–43.8; p < 0.001) and poorer mMC grade (3-months-OR:7.8, 2.0–31; p = 0.004; long-term-OR:11.0, 2.8–43.8; p < 0.001). Loss of MEPs predicted a decline in mMC at long-term follow-up (OR:4.0, 1.06–15.1; p = 0.041).

Conclusions

Live data from continuous intraoperative neurophysiological monitoring, expertly interpreted in the OR, could potentially be used to make surgical and anesthesiologic adjustments with the goal of minimizing the risk of negative neurological outcomes. Significant associations were found between decreased or lost IONM signals and poorer sensorimotor function and mMC score at short- and long-term follow-up. Implementation of the IONM workflow is suggested in all intramedullary surgery.

目的髓内脊髓病变手术力求大体全切除。术中神经生理监测(IONM)是金标准,但IONM的最佳工作流程尚未达成共识。本研究详细介绍了我们的机构工作流程。方法回顾性分析2007-2021年在卡罗林斯卡大学医院接受髓内切除术的所有成年人(n = 70)。连续多模态IONM(躯体感觉诱发电位(SSEP)、运动诱发电位(MEP)和硬膜外d波)由室内神经生理学家进行。预设报警阈值(SSEP幅度下降≥50% /潜伏期上升10%;MEP降低≥80%;d波损失≥50%),并触发标准化的四步抢救方案(暂停操作,将MAP升高至80-90 mm Hg,外用罂粟碱,观察)。术前、3个月和≥12个月记录运动/感觉功能、改良McCormick (mMC)分级、疼痛和括约肌控制。结果共纳入70例患者。大多数为室管膜瘤(51%)、血管母细胞瘤(18%)和海绵状瘤(8.5%)。每次手术都有一位神经生理学家在场。在短期或长期随访中,术中ssep幅度下降≥50%均未出现感觉缺陷(OR:3.0, 95% CI 0.86-10.6; p = 0.085)或mMC恶化(OR:1.6, 0.33-7.5; p = 0.57)。相比之下,完全SSEP丢失显著增加了术后感觉功能缺失的风险(3个月- or:25.2, 4.7-135; p < 0.001;长期- or:11.0, 2.8-43.8; p < 0.001)和mMC分级较差的风险(3个月- or:7.8, 2.0-31; p = 0.004;长期- or:11.0, 2.8-43.8; p < 0.001)。在长期随访中,mep的缺失预示着mMC的下降(OR:4.0, 1.06-15.1; p = 0.041)。结论术中连续神经生理监测的实时数据,在手术室中有专业的解释,可以潜在地用于外科和麻醉调整,以最大限度地减少神经系统不良预后的风险。在短期和长期随访中发现,IONM信号减少或丢失与感觉运动功能和mMC评分较差之间存在显著关联。建议在所有髓内手术中实施IONM工作流程。
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引用次数: 0
Nicotine replacement therapy during the acute phase of aneurysmal subarachnoid hemorrhage 动脉瘤性蛛网膜下腔出血急性期的尼古丁替代治疗
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-10-24 DOI: 10.1007/s00701-025-06698-y
H. Ghafaji, A. Sorteberg

Background

Many patients who suffer an aneurysmal subarachnoid hemorrhage (aSAH) are active smokers that may experience nicotine withdrawal following hospital admission. Nicotine replacement therapy (NRT) could alleviate abstinence and delirium but may have unwanted side-effects. Cerebral vasospasm (VS) is a feared complication of aSAH that can worsen outcome. The impact of NRT on VS, complications and outcome is still not fully delineated.

Methods

Retrospective study using anonymized data from a prospective quality registry. Patients smoking status, age, sex, comorbidities, along with aSAH severity were registered. Smokers were dichotomized into non-NRT and NRT groups depending on whether they had received a nicotine patch or not and subdivided into light smokers (≤ 10 cigarettes/day) and moderate to heavy smokers (> 10 cigarettes/day). We also registered radiological/sonological and clinical VS, delayed cerebral ischemia (DCI) related infarction and other common aSAH complications. Outcome was scored in terms of mortality and modified Rankin Score (mRS) at 90 days.

Results

495 patients were included; 220 received NRT. NRT was not a predictor of radiological/ultrasonological VS or DCI-related infarction. Poor outcome was more frequent in light smokers when they had received NRT (12.49% vs 29.31%) and their length of hospitalization was longer. Moderate to heavy smokers that had received NRT developed less frequently atrial fibrillation (3.4% vs 11.7%) and their length of stay at the ICU was shorter. There was no difference in thromboembolic or epileptic events, or respiratory failure between groups. There was no difference in smoking cessation at 90 days with or without NRT.

Conclusions

NRT had no impact on vasospasm or DCI-related infarction and it did not increase the frequency of complications. It seems advisable to abstain from NRT in light smokers.

背景:许多动脉瘤性蛛网膜下腔出血(aSAH)的患者是活跃的吸烟者,在入院后可能会出现尼古丁戒断。尼古丁替代疗法(NRT)可以缓解戒断和谵妄,但可能有不良的副作用。脑血管痉挛(VS)是aSAH的一种可怕的并发症,可使预后恶化。NRT对VS、并发症和结局的影响仍未完全描述。方法采用前瞻性质量注册中心匿名数据进行回顾性研究。记录患者的吸烟状况、年龄、性别、合并症以及aSAH严重程度。吸烟者根据是否接受尼古丁贴片分为非尼古丁贴片组和非尼古丁贴片组,并细分为轻度吸烟者(≤10支/天)和中度至重度吸烟者(≤10支/天)。我们还记录了影像学/超声和临床VS,延迟性脑缺血(DCI)相关梗死和其他常见aSAH并发症。根据90天的死亡率和修正兰金评分(mRS)对结果进行评分。结果共纳入495例患者;220人接受了NRT。NRT不是影像学/超声影像学VS或dci相关梗死的预测因子。接受NRT治疗的轻度吸烟者预后较差(12.49% vs 29.31%),住院时间较长。接受NRT的中度至重度吸烟者发生房颤的频率较低(3.4% vs 11.7%),他们在ICU的住院时间较短。两组之间血栓栓塞或癫痫事件或呼吸衰竭没有差异。在有或没有NRT的情况下,90天的戒烟效果没有差异。结论snrt对血管痉挛、dci相关梗死无影响,且未增加并发症发生频率。对于轻度吸烟者来说,戒掉NRT似乎是明智的。
{"title":"Nicotine replacement therapy during the acute phase of aneurysmal subarachnoid hemorrhage","authors":"H. Ghafaji,&nbsp;A. Sorteberg","doi":"10.1007/s00701-025-06698-y","DOIUrl":"10.1007/s00701-025-06698-y","url":null,"abstract":"<div><h3>Background</h3><p>Many patients who suffer an aneurysmal subarachnoid hemorrhage (aSAH) are active smokers that may experience nicotine withdrawal following hospital admission. Nicotine replacement therapy (NRT) could alleviate abstinence and delirium but may have unwanted side-effects. Cerebral vasospasm (VS) is a feared complication of aSAH that can worsen outcome. The impact of NRT on VS, complications and outcome is still not fully delineated.</p><h3>Methods</h3><p>Retrospective study using anonymized data from a prospective quality registry. Patients smoking status, age, sex, comorbidities, along with aSAH severity were registered. Smokers were dichotomized into non-NRT and NRT groups depending on whether they had received a nicotine patch or not and subdivided into light smokers (≤ 10 cigarettes/day) and moderate to heavy smokers (&gt; 10 cigarettes/day). We also registered radiological/sonological and clinical VS, delayed cerebral ischemia (DCI) related infarction and other common aSAH complications. Outcome was scored in terms of mortality and modified Rankin Score (mRS) at 90 days.</p><h3>Results</h3><p>495 patients were included; 220 received NRT. NRT was not a predictor of radiological/ultrasonological VS or DCI-related infarction. Poor outcome was more frequent in light smokers when they had received NRT (12.49% vs 29.31%) and their length of hospitalization was longer. Moderate to heavy smokers that had received NRT developed less frequently atrial fibrillation (3.4% vs 11.7%) and their length of stay at the ICU was shorter. There was no difference in thromboembolic or epileptic events, or respiratory failure between groups. There was no difference in smoking cessation at 90 days with or without NRT.</p><h3>Conclusions</h3><p>NRT had no impact on vasospasm or DCI-related infarction and it did not increase the frequency of complications. It seems advisable to abstain from NRT in light smokers.</p></div>","PeriodicalId":7370,"journal":{"name":"Acta Neurochirurgica","volume":"167 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00701-025-06698-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145352365","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Persistent primitive hypoglossal artery: a classification-based approach to understanding and managing a rare vascular anomaly 持久原始舌下动脉:一种基于分类的方法来理解和处理罕见的血管异常。
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-10-23 DOI: 10.1007/s00701-025-06654-w
Nshaat Abdrabou Elsayed, Ahmed Azhar Ali

Background

Persistent primitive hypoglossal artery (PPHA) is a rare embryological variant of the cerebral circulation in which the posterior circulation is supplied through a persistent embryonic carotid–basilar anastomosis. While often discovered incidentally, PPHA may have important clinical consequences when associated with atherosclerotic disease, aneurysms, or other cerebrovascular abnormalities.

Objective

To introduce a structured clinical classification system for PPHA that captures its anatomical spectrum, pathological associations, and symptomatic presentations, with the aim of improving diagnostic precision and procedural planning.

Methods

A six-category framework was developed to stratify PPHA according to its clinical and radiological features. This classification emphasizes anatomical distinctiveness and pathological relevance to facilitate risk stratification and therapeutic decision-making.

Results

The proposed classification defines six categories: (1) isolated asymptomatic PPHA, (2) PPHA with stenosis, (3) aneurysmal PPHA, (4) PPHA with carotid artery stenosis, (5) PPHA with cranial nerve compression, and (6) PPHA associated with other vascular anomalies. Organizing PPHA into these categories provides a practical system for clinical assessment and intervention planning.

Conclusion

This novel classification addresses the current absence of a standardized clinical framework for PPHA. Its adoption may enhance physician awareness, improve patient safety during cerebrovascular interventions, and aid multidisciplinary decision-making in complex neurovascular cases. Validation in clinical practice is warranted to establish its utility.

背景:持续性原始舌下动脉(PPHA)是脑循环的一种罕见的胚胎变异,其后循环是通过持续性胚胎颈动脉-基底动脉吻合提供的。虽然PPHA通常是偶然发现的,但当与动脉粥样硬化疾病、动脉瘤或其他脑血管异常相关时,PPHA可能具有重要的临床后果。目的:介绍一种结构化的PPHA临床分类系统,以捕获其解剖谱,病理关联和症状表现,以提高诊断精度和手术计划。方法:根据PPHA的临床和放射学特征,建立六类分类框架进行分层。这种分类强调解剖独特性和病理相关性,以促进风险分层和治疗决策。结果:提出的分类分为6类:(1)孤立性无症状PPHA,(2)合并狭窄的PPHA,(3)动脉瘤性PPHA,(4)合并颈动脉狭窄的PPHA,(5)合并颅神经压迫的PPHA,(6)合并其他血管异常的PPHA。将PPHA组织成这些类别为临床评估和干预计划提供了一个实用的系统。结论:这种新的分类解决了目前PPHA缺乏标准化临床框架的问题。它的采用可以提高医生的意识,提高脑血管干预期间患者的安全性,并有助于复杂神经血管病例的多学科决策。在临床实践中验证是必要的,以确定其实用性。
{"title":"Persistent primitive hypoglossal artery: a classification-based approach to understanding and managing a rare vascular anomaly","authors":"Nshaat Abdrabou Elsayed,&nbsp;Ahmed Azhar Ali","doi":"10.1007/s00701-025-06654-w","DOIUrl":"10.1007/s00701-025-06654-w","url":null,"abstract":"<div><h3>Background</h3><p>Persistent primitive hypoglossal artery (PPHA) is a rare embryological variant of the cerebral circulation in which the posterior circulation is supplied through a persistent embryonic carotid–basilar anastomosis. While often discovered incidentally, PPHA may have important clinical consequences when associated with atherosclerotic disease, aneurysms, or other cerebrovascular abnormalities.</p><h3>Objective</h3><p>To introduce a structured clinical classification system for PPHA that captures its anatomical spectrum, pathological associations, and symptomatic presentations, with the aim of improving diagnostic precision and procedural planning.</p><h3>Methods</h3><p>A six-category framework was developed to stratify PPHA according to its clinical and radiological features. This classification emphasizes anatomical distinctiveness and pathological relevance to facilitate risk stratification and therapeutic decision-making.</p><h3>Results</h3><p>The proposed classification defines six categories: (1) isolated asymptomatic PPHA, (2) PPHA with stenosis, (3) aneurysmal PPHA, (4) PPHA with carotid artery stenosis, (5) PPHA with cranial nerve compression, and (6) PPHA associated with other vascular anomalies. Organizing PPHA into these categories provides a practical system for clinical assessment and intervention planning.</p><h3>Conclusion</h3><p>This novel classification addresses the current absence of a standardized clinical framework for PPHA. Its adoption may enhance physician awareness, improve patient safety during cerebrovascular interventions, and aid multidisciplinary decision-making in complex neurovascular cases. Validation in clinical practice is warranted to establish its utility.</p></div>","PeriodicalId":7370,"journal":{"name":"Acta Neurochirurgica","volume":"167 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00701-025-06654-w.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145342737","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Outcome in adult patients with severe TBI, using a management protocol allowing a cerebral perfusion pressure ≤ 60 mmHg – a retrospective study over 10 years 一项超过10年的回顾性研究:使用允许脑灌注压≤60 mmHg的管理方案治疗成年严重TBI患者的结果。
IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY Pub Date : 2025-10-23 DOI: 10.1007/s00701-025-06701-6
Linus Réen, Anna Radman, Edward Visse, David Cederberg, Niklas Marklund, Peter Siesjö

Background

Current guidelines for the treatment of severe TBI recommend maintaining a cerebral perfusion pressure (CPP) at 60–70 mmHg. In our institution, as well as others, an alternative algorithm—originally named the Lund concept—has been used. This treatment algorithm employs metoprolol and clonidine to limit CPP, accepting levels below 60 mmHg, with the aim of reducing cerebral edema. Previous reports on this algorithm have shown promising outcome in severe TBI cohorts when compared with many contemporary practices; however, no population-based studies have been conducted to validate these findings.

Research Question:

What is the outcome in adult severe TBI using the Lund Concept algorithm in a population-based cohort and how are CPP levels lower than 60 mmHg tolerated?

Methods

The study included 135 evaluable adult patients out of 171 admitted with severe TBI over a ten-year period in the southern Swedish healthcare region. Baseline data, intracranial pressure (ICP), CPP, treatment duration, surgical interventions, and administered drugs were correlated to the Glasgow Outcome Scale Extended (GOSE).

Results

The 30-day and 6-month mortality rates were 16% and 20%, respectively. A favorable outcome (GOSE 5–8) was achieved in 48% of patients. Only increasing age was associated with inferior outcomes.

Conclusion

The use of a management protocol accepting lower CPP levels than those recommended in existing guidelines was generally well tolerated with outcome in line with comparable reports.

背景:目前治疗严重TBI的指南建议将脑灌注压(CPP)维持在60-70 mmHg。在我们的机构,以及其他机构,一种替代算法——最初被称为Lund概念——已经被使用。这种治疗方法使用美托洛尔和可乐定来限制CPP,接受低于60 mmHg的水平,目的是减少脑水肿。与许多当代实践相比,先前关于该算法的报告显示,在严重TBI队列中有很好的结果;然而,没有进行基于人群的研究来验证这些发现。研究问题:在以人群为基础的队列中,使用Lund概念算法治疗成人严重TBI的结果是什么? CPP水平低于60 mmHg是如何耐受的?方法:该研究纳入了瑞典南部医疗保健地区10年间入院的171例严重脑外伤患者中的135例可评估的成年患者。基线数据、颅内压(ICP)、CPP、治疗时间、手术干预和给药与格拉斯哥结局量表扩展(GOSE)相关。结果:30天死亡率为16%,6个月死亡率为20%。48%的患者获得了良好的结果(GOSE 5-8)。只有年龄的增长与不良结果有关。结论:采用比现有指南推荐的CPP水平更低的管理方案通常耐受良好,结果与可比报告一致。
{"title":"Outcome in adult patients with severe TBI, using a management protocol allowing a cerebral perfusion pressure ≤ 60 mmHg – a retrospective study over 10 years","authors":"Linus Réen,&nbsp;Anna Radman,&nbsp;Edward Visse,&nbsp;David Cederberg,&nbsp;Niklas Marklund,&nbsp;Peter Siesjö","doi":"10.1007/s00701-025-06701-6","DOIUrl":"10.1007/s00701-025-06701-6","url":null,"abstract":"<div><h3>Background</h3><p>Current guidelines for the treatment of severe TBI recommend maintaining a cerebral perfusion pressure (CPP) at 60–70 mmHg. In our institution, as well as others, an alternative algorithm—originally named the Lund concept—has been used. This treatment algorithm employs metoprolol and clonidine to limit CPP, accepting levels below 60 mmHg, with the aim of reducing cerebral edema. Previous reports on this algorithm have shown promising outcome in severe TBI cohorts when compared with many contemporary practices; however, no population-based studies have been conducted to validate these findings.</p><p>Research Question:</p><p>What is the outcome in adult severe TBI using the Lund Concept algorithm in a population-based cohort and how are CPP levels lower than 60 mmHg tolerated?</p><h3>Methods</h3><p>The study included 135 evaluable adult patients out of 171 admitted with severe TBI over a ten-year period in the southern Swedish healthcare region. Baseline data, intracranial pressure (ICP), CPP, treatment duration, surgical interventions, and administered drugs were correlated to the Glasgow Outcome Scale Extended (GOSE).</p><h3>Results</h3><p>The 30-day and 6-month mortality rates were 16% and 20%, respectively. A favorable outcome (GOSE 5–8) was achieved in 48% of patients. Only increasing age was associated with inferior outcomes.</p><h3>Conclusion</h3><p>The use of a management protocol accepting lower CPP levels than those recommended in existing guidelines was generally well tolerated with outcome in line with comparable reports.</p></div>","PeriodicalId":7370,"journal":{"name":"Acta Neurochirurgica","volume":"167 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00701-025-06701-6.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145342729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Acta Neurochirurgica
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