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DOI: 10.1055/a-2707-0593
Half Burr-Hole Method: A Novel Surgical Technique for Reducing Brain Shift and Improving Electrode Placement Accuracy in Deep-Brain Stimulation
Authors
Abstract
Background
Deep-brain stimulation (DBS) is used to treat movement disorders and drug-resistant focal epilepsy. However, electrode placement accuracy is affected by brain shift caused by pneumocephalus and cerebrospinal fluid (CSF) leakage during surgery. We present the novel half burr-hole method for improved DBS electrode placement accuracy.
Case Description
This approach was used to treat a 28-year-old man with drug-resistant epilepsy in whom stereo-electroencephalography revealed bilateral seizure onset in the temporal lobes, precluding focal resection. The patient, under general anesthesia, was placed in the supine position. Using a ROSA robot-assisted surgical system, approximately 8-mm-deep “partial burr-holes” were created, with the deeper portion perforated using a 2.4-mm twist drill. Stimulation electrodes were placed bilaterally in the anterior thalamic nucleus. Directional leads were secured using standard burr-hole caps. Postoperative computed tomography confirmed a 0.46-cm3 pneumocephalus and electrode positioning with 0.47 mm (range: 0–1.62 mm) vector and 0.12 mm (range: 0.08–0.16 mm) axial errors relative to the target coordinates. Postoperative electrode impedance values were within the normal range.
Conclusion
The half burr-hole method effectively minimizes CSF leakage and pneumocephalus during DBS surgery, reducing brain shift and enhancing electrode placement accuracy, and is compatible with standard burr-hole caps for electrode fixation, minimally affecting impedance values.
Introduction
Deep-brain stimulation (DBS) is a standard treatment modality for movement disorders such as Parkinson's disease, tremor, dystonia, and drug-resistant epilepsy.[1] [2] [3] The success of DBS surgery depends on precise electrode placement at the tentative target, which is predetermined based on preoperative anatomical imaging. However, intraoperative brain shift—that is, brain tissue displacement owing to pneumocephalus and cerebrospinal fluid (CSF) loss during surgery—is a well-recognized cause of reduced targeting accuracy.[4] [5] While various approaches have been suggested,[6] [7] no definitive solution to this problem has been established in clinical practice.
Herein, we introduce the half burr-hole technique, a novel method developed to minimize brain shift during DBS targeting the anterior nucleus of the thalamus (ANT). In this technique, the burr-hole is drilled to half the normal skull thickness, followed by a twist-drill perforation and dural opening using monopolar cautery, which helps minimize CSF leakage. Furthermore, the Stimloc system is compatible with this technique, providing reliable postoperative electrode fixation.
Case Presentation
Case Illustration
The patient was a 28-year-old Japanese man with drug-resistant epilepsy who initially presented with focal impaired awareness seizures (FIAS) 20 years ago. The patient's clinical history is summarized in [Table 1]. Neurological examination revealed no abnormalities, and the patient's cognitive function was intact. There were no comorbid conditions, and the patient had no history of previous surgeries. Antiepileptic medication was initiated 12 years after onset, resulting in good seizure control after 1 year. However, FIAS recurred 5 years ago, prompting a referral to our hospital the following year. Weekly seizures persisted despite medication adjustments, prompting bilateral temporal lobe stereo-electroencephalography evaluation 6 months ago. Focal resection was deemed unfeasible based on the intracranial recordings, which indicated that seizure onset originated from the lateral aspects of both temporal lobes. Consequently, ANT-DBS was selected as the treatment approach. Since ANT-DBS electrodes are implanted via a transventricular approach, there is a high risk of brain shift due to CSF leakage, which may compromise the accuracy of electrode placement. Therefore, this technique was selected.
Abbreviations: ANT, anterior nucleus of the thalamus; DBS, deep-brain stimulation.
This study was approved by the Ethics Committee of Nishi-Niigata Chuo National Hospital. Written informed consent to participate in the study was obtained from the participant.
Technique
Preoperative determination of the tentative target (the ANT) and insertion trajectory was performed using the ROSA planning software (Zimmer Biomet, Warsaw, Indiana, United States; [Fig. 1]).


On the day of surgery, a Leksell frame was mounted on the patient's head using four pins, followed by cranial imaging using a computed tomography (CT) suite. In the operating room, the patient was positioned flat, and the cranial CT data were registered into the ROSA ONE robotic system (Zimmer Biomet).
Using the robotic arm of the system, the electrode insertion sites were marked bilaterally in the frontal region, 4-cm skin incisions were made, and the insertion points were re-marked on the exposed bone surface. Initial partial burr-holes were made to a planned depth of approximately 8 mm, with penetration controlled using a rubber ring attached to the drill adapter as a stopper, in tandem with a perforator guard (PG01: S & Brain Corporation, Tokyo, Japan; [Fig. 2A]). Subsequently, a specialized trephine (Rescue Round Cutter, SPD103: S & Brain Corporation) was used to contour the stepped floor of the initial holes, enabling the attachment of the Stimloc device (Medtronic, Minneapolis, Minnesota, United States; [Fig. 2B]).


Next, the ROSA guidance system was used again to mark the electrode insertion point. The skull was perforated using a 2.4-mm twist drill ([Fig. 2C]), and the dura mater and cortical surface were cauterized using a specialized electrosurgical scalpel. A catheter insertion needle (outer diameter: 2.1 mm; Elekta AB, Stockholm, Sweden) was advanced to the target point, and a biological tissue adhesive (BOLHEAL Tissue Sealant, KM Biologics, Kumamoto, Japan) was sprayed at the cortical entry point to prevent CSF leakage. Frontal and lateral radiographs were obtained to confirm that the position of the needle tip deviated < 1 mm from the tentative target. Subsequently, the inner catheter was removed, and a directional lead with integrated stylet was inserted (B33005M; Medtronic). The outer catheter was withdrawn, biological adhesive was reapplied, and the lead was secured using the Stimloc device ([Fig. 2D]). The appropriate placement of the electrodes was confirmed through a second series of intraoperative radiographs.
Following bilateral electrode placement, electrode impedance measurements and deep-brain recordings were performed. Magnetic resonance imaging was performed 6 days after the ANT-DBS surgery. Postoperative 3D-T1 images were imported into the ROSA planning software, and the deviation between the actual position of the electrode tip and its preoperatively planned position was measured. Postoperative CT examination revealed a pneumocephalus volume of 0.46 cm3, indicating minimal CSF leakage. The electrodes were accurately placed near the planned target coordinates.
Deviation measurements based on postoperative MRI showed that the right electrode deviated by 0.31 mm medial, 1.40 mm anterior, and 1.11 mm superior, while the left electrode deviated by 0.05 mm lateral, 0.16 mm anterior, and 0.21 mm inferior to the preoperative plan ([Fig. 3]). The total time from skin incision to the creation of bilateral half burr-holes was 32 minutes and from bilateral electrode placement to skin closure was 45 minutes. The patient was discharged on postoperative day 8. Stimulation was initiated on postoperative day 3 at 2(−)C(+) with 1.5 mA, 90 µs, and 145 Hz bilaterally. At the 3-month follow-up, the stimulation intensity was increased to 3.5 mA. No stimulation-related adverse effects, such as psychiatric symptoms or memory impairment, were observed. The surgical wound showed no abnormalities. Prior to surgery, the patient experienced FIAS 20 to 30 times per week. Following ANT-DBS, the seizure frequency decreased to approximately twice per week.


Discussion
The half burr-hole technique proposed in this study is designed to suppress brain shift by minimizing CSF leakage using a small-diameter cranial and dural perforation. In addition, by preserving the lower half of the skull at the burr-hole site, this method eliminates the need for extradural hemostasis and sealing procedures typically employed to prevent CSF leakage. Furthermore, lead fixation using the Stimloc system is feasible with this approach, offering greater postoperative stability compared to titanium microplates, thereby reducing the risk of electrode displacement.
DBS is commonly performed via the burr-hole technique, in which a cranial burr-hole is created coaxially to the planned electrode trajectory. After dural incision and visualization of the cortical surface, the electrode is inserted under stereotactic guidance. However, intracranial pneumocephalus occurring during DBS surgery can lead to brain shift, thereby impairing the precision of electrode placement.[8] Several factors have been implicated in brain shift, including CSF leakage, intraoperative changes in intracranial pressure, and air influx into the cranial cavity.[4]
To address these concerns, multiple technical refinements have been introduced. These include three-layer sealing of the arachnoid, pia, and cortex with fibrin glue,[8] burr-hole closure using polyethylene glycol-based sealants such as DuraSeal,[7] asleep DBS under general anesthesia,[9] [11] and twist-drill craniostomy with a reduced diameter of 5 mm.[12] These approaches have significantly decreased pneumocephalus volume from 8 to 44 mL using conventional methods to as little as 1.3 to 12 mL.[13] More recently, Zhang et al introduced a pneumocephalus-minimizing technique (PMT) in which the dural opening is minimized and the burr-hole is sealed dynamically during insertion using Gelfoam, resulting in a drastic reduction of pneumocephalus surface area from 5.91 to 0.21 cm2.[11] We performed the procedure under general anesthesia with the patient's head maintained in a flat position, limiting postoperative pneumocephalus to a minimal volume of 0.46 cm3.
We adopted a modified half burr-hole technique in which the lower portion of the skull bone is preserved, thereby eliminating the need for postoperative burr-hole sealing. This approach also simplifies extradural hemostasis and allows for accurate targeting, even in cases with thick cranial bone or eccentric lead trajectories. Unlike conventional methods requiring burr-hole enlargement in such situations,[10] [14] our method reduces the need for re-drilling by utilizing stereotactic twist drilling.
Electrode fixation is achieved using the Stimloc anchoring system, which offers superior stability compared to titanium microplate fixation, where greater postoperative displacement has been reported.[15] Thus, this technique ensures secure lead stabilization and minimizes the risk of migration.
As in Zhang's PMT,[11] direct visualization of cortical vasculature during lead insertion is not feasible. However, the safety of this approach is supported by data indicating that selecting an entry site more than 4 mm away from surface vasculature avoids hemorrhagic complications. Our method utilizes a conservative 5-mm safety margin, which we believe provides comparable safety. [Table 2] summarizes the technical differences between the conventional burr-hole, PMT, twist drill, and the present half burr-hole technique.
We set the twist-drill perforation depth at 8 mm to ensure compatibility with all lead clips currently approved in Japan. While the superficial diameter achieved by the perforator reaches 14 mm, the deep diameter is limited to 11 mm, which may interfere with the anchoring mechanism of some lead clips. To address this, a rescue cutter is used to expand the deep-bone cavity; alternatively, a steel bar may serve as a substitute when necessary.
This technique is suitable for cases in which the cranial bone is ≥ 10 mm thick and multi-track MER is not essential.
Limitation
This case highlights the potential utility of the half burr-hole technique in ANT-DBS; however, as a single case report, the findings should be interpreted with caution. Further large-scale studies should validate its reproducibility, safety, and long-term efficacy. If minor trajectory adjustments are required intraoperatively, they can be addressed either by additional twist-drill perforation or by creating a full burr-hole to the dura (PMT method).
Conclusion
The half burr-hole technique proposed in this study effectively suppresses CSF leakage and minimizes brain shift. By preserving the lower skull margin at the burr-hole site, this approach eliminates the need for extradural hemostasis and sealing procedures. Furthermore, this technique allows for lead fixation using the Stimloc system, reducing the risk of postoperative electrode displacement compared to titanium microplates.
Conflict of Interest
The authors declare that they have no conflict of interest.
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References
- 1 Fasano A, Aquino CC, Krauss JK, Honey CR, Bloem BR. Axial disability and deep brain stimulation in patients with Parkinson disease. Nat Rev Neurol 2015; 11 (02) 98-110
- 2 Moro E, LeReun C, Krauss JK. et al. Efficacy of pallidal stimulation in isolated dystonia: a systematic review and meta-analysis. Eur J Neurol 2017; 24 (04) 552-560
- 3 Ryvlin P, Rheims S, Hirsch LJ, Sokolov A, Jehi L. Neuromodulation in epilepsy: state-of-the-art approved therapies. Lancet Neurol 2021; 20 (12) 1038-1047
- 4 Halpern CH, Danish SF, Baltuch GH, Jaggi JL. Brain shift during deep brain stimulation surgery for Parkinson's disease. Stereotact Funct Neurosurg 2008; 86 (01) 37-43
- 5 Matias CM, Frizon LA, Asfahan F, Uribe JD, Machado AG. Brain shift and pneumocephalus assessment during frame-based deep brain stimulation implantation with intraoperative magnetic resonance imaging. Oper Neurosurg (Hagerstown) 2018; 14 (06) 668-674
- 6 Petersen EA, Holl EM, Martinez-Torres I. et al. Minimizing brain shift in stereotactic functional neurosurgery. Neurosurgery 2010; 67 (03, suppl operative): ons213-ons221 , discussion ons221
- 7 Takumi I, Mishina M, Hironaka K. et al. Simple solution for preventing cerebrospinal fluid loss and brain shift during multitrack deep brain stimulation surgery in the semisupine position: polyethylene glycol hydrogel dural sealant capping: rapid communication. Neurol Med Chir (Tokyo) 2013; 53 (01) 1-6
- 8 Chee K, Hirt L, Mendlen M. et al. Brain shift during staged deep brain stimulation for movement disorders. Stereotact Funct Neurosurg 2024; 102 (02) 83-92
- 9 Ko AL, Magown P, Ozpinar A, Hamzaoglu V, Burchiel KJ. A sleep deep brain stimulation reduces incidence of intracranial air during electrode implantation. Stereotact Funct Neurosurg 2018; 96 (02) 83-90
- 10 Toyoda K, Urasaki E, Umeno T. et al. The effectiveness of the stereotactic burr-hole technique for deep brain stimulation. Neurol Med Chir (Tokyo) 2015; 55 (09) 766-772
- 11 Zhang DY, Pearce JJ, Petrosyan E, Borghei A, Byrne RW, Sani S. Minimizing pneumocephalus during deep brain stimulation surgery. Clin Neurol Neurosurg 2024; 238: 108174
- 12 Sharim J, Pezeshkian P, DeSalles A, Pouratian N. Effect of cranial window diameter during deep brain stimulation surgery on volume of pneumocephalus. Neuromodulation 2015; 18 (07) 574-578 , discussion 578–579
- 13 Sasaki T, Agari T, Kuwahara K. et al. Efficacy of dural sealant system for preventing brain shift and improving accuracy in deep brain stimulation surgery. Neurol Med Chir (Tokyo) 2018; 58 (05) 199-205
- 14 Liu L, Mariani SG, De Schlichting E. et al. Frameless ROSA robot-assisted lead implantation for deep brain stimulation: technique and accuracy. Oper Neurosurg (Hagerstown) 2020; 19 (01) 57-64
- 15 Contarino MF, Bot M, Speelman JD. et al. Postoperative displacement of deep brain stimulation electrodes related to lead-anchoring technique. Neurosurgery 2013; 73 (04) 681-688
Correspondence
Publication History
Received: 16 May 2025
Accepted: 21 September 2025
Accepted Manuscript online:
23 September 2025
Article published online:
03 October 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
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References
- 1 Fasano A, Aquino CC, Krauss JK, Honey CR, Bloem BR. Axial disability and deep brain stimulation in patients with Parkinson disease. Nat Rev Neurol 2015; 11 (02) 98-110
- 2 Moro E, LeReun C, Krauss JK. et al. Efficacy of pallidal stimulation in isolated dystonia: a systematic review and meta-analysis. Eur J Neurol 2017; 24 (04) 552-560
- 3 Ryvlin P, Rheims S, Hirsch LJ, Sokolov A, Jehi L. Neuromodulation in epilepsy: state-of-the-art approved therapies. Lancet Neurol 2021; 20 (12) 1038-1047
- 4 Halpern CH, Danish SF, Baltuch GH, Jaggi JL. Brain shift during deep brain stimulation surgery for Parkinson's disease. Stereotact Funct Neurosurg 2008; 86 (01) 37-43
- 5 Matias CM, Frizon LA, Asfahan F, Uribe JD, Machado AG. Brain shift and pneumocephalus assessment during frame-based deep brain stimulation implantation with intraoperative magnetic resonance imaging. Oper Neurosurg (Hagerstown) 2018; 14 (06) 668-674
- 6 Petersen EA, Holl EM, Martinez-Torres I. et al. Minimizing brain shift in stereotactic functional neurosurgery. Neurosurgery 2010; 67 (03, suppl operative): ons213-ons221 , discussion ons221
- 7 Takumi I, Mishina M, Hironaka K. et al. Simple solution for preventing cerebrospinal fluid loss and brain shift during multitrack deep brain stimulation surgery in the semisupine position: polyethylene glycol hydrogel dural sealant capping: rapid communication. Neurol Med Chir (Tokyo) 2013; 53 (01) 1-6
- 8 Chee K, Hirt L, Mendlen M. et al. Brain shift during staged deep brain stimulation for movement disorders. Stereotact Funct Neurosurg 2024; 102 (02) 83-92
- 9 Ko AL, Magown P, Ozpinar A, Hamzaoglu V, Burchiel KJ. A sleep deep brain stimulation reduces incidence of intracranial air during electrode implantation. Stereotact Funct Neurosurg 2018; 96 (02) 83-90
- 10 Toyoda K, Urasaki E, Umeno T. et al. The effectiveness of the stereotactic burr-hole technique for deep brain stimulation. Neurol Med Chir (Tokyo) 2015; 55 (09) 766-772
- 11 Zhang DY, Pearce JJ, Petrosyan E, Borghei A, Byrne RW, Sani S. Minimizing pneumocephalus during deep brain stimulation surgery. Clin Neurol Neurosurg 2024; 238: 108174
- 12 Sharim J, Pezeshkian P, DeSalles A, Pouratian N. Effect of cranial window diameter during deep brain stimulation surgery on volume of pneumocephalus. Neuromodulation 2015; 18 (07) 574-578 , discussion 578–579
- 13 Sasaki T, Agari T, Kuwahara K. et al. Efficacy of dural sealant system for preventing brain shift and improving accuracy in deep brain stimulation surgery. Neurol Med Chir (Tokyo) 2018; 58 (05) 199-205
- 14 Liu L, Mariani SG, De Schlichting E. et al. Frameless ROSA robot-assisted lead implantation for deep brain stimulation: technique and accuracy. Oper Neurosurg (Hagerstown) 2020; 19 (01) 57-64
- 15 Contarino MF, Bot M, Speelman JD. et al. Postoperative displacement of deep brain stimulation electrodes related to lead-anchoring technique. Neurosurgery 2013; 73 (04) 681-688







