Brain Shift during Staged Deep Brain Stimulation for Movement Disorders

被引:1
|
作者
Chee, Keanu [1 ]
Hirt, Lisa [1 ]
Mendlen, Madelyn [1 ]
Machnik, Jannika [1 ]
Razmara, Ashkaun [1 ]
Bayman, Eric [1 ]
Thompson, John A. [1 ,2 ,3 ]
Kramer, Daniel R. [1 ]
机构
[1] Univ Colorado, Sch Med, Dept Neurosurg, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Univ Colorado, Sch Med, Dept Neurol, Anschutz Med Campus, Aurora, CO USA
[3] Univ Colorado, Sch Med, Dept Psychiat, Anschutz Med Campus, Aurora, CO USA
关键词
Brain shift; Deep brain stimulation; Intracranial air; Pneumocephalus; PARKINSONS-DISEASE; FUNCTIONAL NEUROSURGERY; STEREOTACTIC ERROR; ACCURACY; SURGERY; DBS; DISPLACEMENT; IMPLANTATION; ELECTRODES; IMPACT;
D O I
10.1159/000535197
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction: Deep brain stimulation (DBS) is a routine neurosurgical procedure utilized to treat various movement disorders including Parkinson's disease (PD), essential tremor (ET), and dystonia. Treatment efficacy is dependent on stereotactic accuracy of lead placement into the deep brain target of interest. However, brain shift attributed to pneumocephalus can introduce unpredictable inaccuracies during DBS lead placement. This study aimed to determine whether intracranial air is associated with brain shift in patients undergoing staged DBS surgery. Methods: We retrospectively evaluated 46 patients who underwent staged DBS surgery for PD, ET, and dystonia. Due to the staged nature of DBS surgery at our institution, the first electrode placement is used as a concrete fiducial marker for movement in the target location. Postoperative computed tomography (CT) images after the first electrode implantation, as well as preoperative, and postoperative CT images after the second electrode implantation were collected. Images were analyzed in stereotactic targeting software (BrainLab); intracranial air was manually segmented, and electrode shift was measured in the x, y, and z plane, as well as a Euclidian distance on each set of merged CT scans. A Pearson correlation analysis was used to determine the relationship between intracranial air and brain shift, and student's t test was used to compare means between patients with and without radiographic evidence of intracranial air. Results: Thirty-six patients had pneumocephalus after the first electrode implantation, while 35 had pneumocephalus after the second electrode implantation. Accumulation of intracranial air following the first electrode implantation (4.49 +/- 6.05 cm(3)) was significantly correlated with brain shift along the y axis (0.04 +/- 0.35 mm; r (34) = 0.36; p = 0.03), as well as the Euclidean distance of deviation (0.57 +/- 0.33 mm; r (34) = 0.33; p = 0.05) indicating statistically significant shift on the ipsilateral side. However, there was no significant correlation between intracranial air and brain shift following the second electrode implantation, suggesting contralateral shift is minimal. Furthermore, there was no significant difference in brain shift between patients with and without radiographic evidence of intracranial air following both electrode implantation surgeries. Conclusion: Despite observing volumes as high as 22.0 cm(3) in patients with radiographic evidence of pneumocephalus, there was no significant difference in brain shift when compared to patients without pneumocephalus. Furthermore, the mean magnitude of brain shift was <1.0 mm regardless of whether pneumocephalus was presenting, suggesting that intracranial air accumulation may not produce clinical significant brain shift in our patients.
引用
收藏
页码:83 / 92
页数:10
相关论文
共 50 条
  • [21] Deep brain stimulation for hyperkinetic movement disorders
    Reich, M. M.
    Volkmann, J.
    NERVENARZT, 2014, 85 (02): : 147 - +
  • [22] Deep brain stimulation for the treatment of movement disorders
    Tronnier, VM
    Krause, M
    Heck, A
    Kronenbürger, M
    Bonsanto, MM
    Tronnier, J
    Fogel, W
    NEUROLOGY PSYCHIATRY AND BRAIN RESEARCH, 1999, 6 (04) : 199 - 212
  • [23] Deep Brain Stimulation in Hyperkinetic Movement Disorders
    Del Alamo, Marta
    Cabanes, Lidia
    Regidor, Ignacio
    STEREOTACTIC AND FUNCTIONAL NEUROSURGERY, 2013, 91 : 243 - 243
  • [24] Deep brain stimulation for movement disorders and pain
    Bittar, RG
    Burn, SC
    Bain, PG
    Owen, SL
    Joint, C
    Shlugman, D
    Aziz, TZ
    JOURNAL OF CLINICAL NEUROSCIENCE, 2005, 12 (04) : 457 - 463
  • [25] Deep brain stimulation for movement disorders before DBS for movement disorders
    Blomstedt, Patric
    Hariz, Marwan I.
    PARKINSONISM & RELATED DISORDERS, 2010, 16 (07) : 429 - 433
  • [26] Anatomical brain structures normalization for deep brain stimulation in movement disorders
    Vogel, Dorian
    Shah, Ashesh
    Coste, Jerome
    Lemaire, Jean-Jacques
    Wardell, Karin
    Hemm, Simone
    NEUROIMAGE-CLINICAL, 2020, 27
  • [27] Movement Disorders and Deep Brain Stimulation in the Middle East
    Siddiqui, Junaid H.
    Bhatti, Danish
    Alsubaie, Fahd
    Bajwa, Jawad A.
    WORLD NEUROSURGERY, 2018, 113 : E314 - E319
  • [28] Novel targets in deep brain stimulation for movement disorders
    Baumgartner, Alexander J.
    Thompson, John A.
    Kern, Drew S.
    Ojemann, Steven G.
    NEUROSURGICAL REVIEW, 2022, 45 (04) : 2593 - 2613
  • [29] Deep Brain Stimulation in the Treatment of Neurological Movement Disorders
    Volkmann, J.
    KLINISCHE NEUROPHYSIOLOGIE, 2009, 40 (02) : 119 - 125
  • [30] Mechanisms and targets of deep brain stimulation in movement disorders
    Johnson, Matthew D.
    Miocinovic, Svjetlana
    McIntyre, Cameron C.
    Vitek, Jerrold L.
    NEUROTHERAPEUTICS, 2008, 5 (02) : 294 - 308