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Chapter 4 - New Techniques for Deep Brain Stimulation Lead Implantation

Published online by Cambridge University Press:  09 June 2022

By
Paul S. Larson
Edited by
William J. Marks  and
Jill L. Ostrem
William J. Marks
Affiliation:
Stanford University, California
Jill L. Ostrem
Affiliation:
University of California, San Francisco
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Summary

Awake, physiologically guided surgery has long been considered the gold standard for deep brain stimulation (DBS) lead implantation.1–3 Most surgeons performing DBS have traditionally used a stereotactic frame such as the Leksell (Elekta, Stockholm, Sweden) or CRW (Integra, Plainsboro, NJ), although frameless systems such as the NexFrame (Medtronic, Minneapolis, MN) and the STarFix (FHC, Bowdoin, ME) are also available.

Type
Chapter
Information
Deep Brain Stimulation Management , pp. 33 - 46
Publisher: Cambridge University Press
Print publication year: 2022

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References

Starr, PA, Christine, CW, Theodosopoulos, PV, Lindsey, N, Byrd, D, Mosley, A, et al. Implantation of deep brain stimulators into the subthalamic nucleus: Technical approach and magnetic resonance imaging-verified lead locations. Journal of neurosurgery. 2002;97(2):370–387.Google Scholar
Starr, PA, Turner, RS, Rau, G, Lindsey, N, Heath, S, Volz, M, et al. Microelectrode-guided implantation of deep brain stimulators into the globus pallidus internus for dystonia: Techniques, electrode locations, and outcomes. Neurosurgical focus. 2004;17(1):E4.CrossRefGoogle ScholarPubMed
Machado, A, Rezai, AR, Kopell, BH, Gross, RE, Sharan, AD, Benabid, AL. Deep brain stimulation for Parkinson’s disease: Surgical technique and perioperative management. Movement disorders: Official journal of the Movement Disorder Society. 2006;21 Suppl 14:S247–S258.CrossRefGoogle ScholarPubMed
Holloway, KL, Gaede, SE, Starr, PA, Rosenow, JM, Ramakrishnan, V, Henderson, JM. Frameless stereotaxy using bone fiducial markers for deep brain stimulation. Journal of neurosurgery. 2005;103(3):404–413.Google Scholar
Henderson, JM, Holloway, KL. Achieving optimal accuracy in frameless functional neurosurgical procedures. Stereotactic and functional neurosurgery. 2008;86(5):332–333.Google Scholar
Konrad, PE, Neimat, JS, Yu, H, Kao, CC, Remple, MS, D’Haese, PF, et al. Customized, miniature rapid-prototype stereotactic frames for use in deep brain stimulator surgery: Initial clinical methodology and experience from 263 patients from 2002 to 2008. Stereotactic and functional neurosurgery. 2011;89(1):34–41.CrossRefGoogle ScholarPubMed
Ko, AL, Ibrahim, A, Magown, P, Macallum, R, Burchiel, KJ. Factors affecting stereotactic accuracy in image-guided deep brain stimulator electrode placement. Stereotactic and functional neurosurgery. 2017;95(5):315–324.Google Scholar
Bot, M, Van den Munckhof, P, Bakay, R, Sierens, D, Stebbins, G, Verhagen Metman, L. Analysis of stereotactic accuracy in patients undergoing deep brain stimulation using Nexframe and the Leksell frame. Stereotactic and functional neurosurgery. 2015;93(5):316–325.Google Scholar
Chen, CC, Pogosyan, A, Zrinzo, LU, Tisch, S, Limousin, P, Ashkan, K, et al. Intra-operative recordings of local field potentials can help localize the subthalamic nucleus in Parkinson’s disease surgery. Experimental neurology. 2006;198(1):214–221.Google Scholar
Kimmelman, J, Duckworth, K, Ramsay, T, Voss, T, Ravina, B, Emborg, ME. Risk of surgical delivery to deep nuclei: A meta-analysis. Movement disorders: Official journal of the Movement Disorder Society. 2011;26(8):1415–1421.Google Scholar
Tonge, M, Ackermans, L, Kocabicak, E, Van Kranen-Mastenbroek, V, Kuijf, M, Oosterloo, M, et al. A detailed analysis of intracerebral hemorrhages in DBS surgeries. Clinical neurology and neurosurgery. 2015;139:183–187.Google Scholar
LaHue, SC, Ostrem, JL, Galifianakis, NB, San Luciano, M, Ziman, N, Wang, S, et al. Parkinson’s disease patient preference and experience with various methods of DBS lead placement. Parkinsonism & related disorders. 2017;41:25–30.Google Scholar
Binder, DK, Rau, GM, Starr, PA. Risk factors for hemorrhage during microelectrode-guided deep brain stimulator implantation for movement disorders. Neurosurgery. 2005;56(4):722–732;discussion 32.CrossRefGoogle ScholarPubMed
Okun, MS, Tagliati, M, Pourfar, M, Fernandez, HH, Rodriguez, RL, Alterman, RL, et al. Management of referred deep brain stimulation failures: A retrospective analysis from 2 movement disorders centers. Archives of neurology. 2005;62(8):1250–1255.Google Scholar
Ellis, TM, Foote, KD, Fernandez, HH, Sudhyadhom, A, Rodriguez, RL, Zeilman, P, et al. Reoperation for suboptimal outcomes after deep brain stimulation surgery. Neurosurgery. 2008;63(4):754–60;discussion 60–1.CrossRefGoogle ScholarPubMed
Khan, MF, Mewes, K, Gross, RE, Skrinjar, O. Assessment of brain shift related to deep brain stimulation surgery. Stereotactic and functional neurosurgery. 2008;86(1):44–53.Google Scholar
Ivan, ME, Yarlagadda, J, Saxena, AP, Martin, AJ, Starr, PA, Sootsman, WK, et al. Brain shift during bur hole-based procedures using interventional MRI. Journal of neurosurgery. 2014;121(1):149–160.Google Scholar
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. Operative neurosurgery (Hagerstown). 2018;14(6):668–674.Google Scholar
Baizabal Carvallo, JF, Mostile, G, Almaguer, M, Davidson, A, Simpson, R, Jankovic, J. Deep brain stimulation hardware complications in patients with movement disorders: Risk factors and clinical correlations. Stereotactic and functional neurosurgery. 2012;90(5):300–306.Google Scholar
Flickinger, JC, Lunsford, LD, Kondziolka, D, Maitz, A. Potential human error in setting stereotactic coordinates for radiosurgery: Implications for quality assurance. International journal of radiation oncology biology physics. 1993;27(2):397–401.Google Scholar
McClelland, S, 3rd, Ford, B, Senatus, PB, Winfield, LM, Du, YE, Pullman, SL, et al. Subthalamic stimulation for Parkinson disease: Determination of electrode location necessary for clinical efficacy. Neurosurgical focus. 2005;19(5):E12.Google Scholar
Rolston, JD, Englot, DJ, Starr, PA, Larson, PS. An unexpectedly high rate of revisions and removals in deep brain stimulation surgery: Analysis of multiple databases. Parkinsonism & related disorders. 2016;33:72–77.Google Scholar
Starr, PA, Martin, AJ, Larson, PS. Implantation of deep brain stimulator electrodes using interventional MRI. Neurosurgery clinics of North America. 2009;20(2):193–203.Google Scholar
Starr, PA, Martin, AJ, Ostrem, JL, Talke, P, Levesque, N, Larson, PS. Subthalamic nucleus deep brain stimulator placement using high-field interventional magnetic resonance imaging and a skull-mounted aiming device: Technique and application accuracy. Journal of neurosurgery. 2010;112(3):479–490.CrossRefGoogle Scholar
Larson, PS, Starr, PA, Bates, G, Tansey, L, Richardson, RM, Martin, AJ. An optimized system for interventional magnetic resonance imaging-guided stereotactic surgery: Preliminary evaluation of targeting accuracy. Neurosurgery. 2012;70(1Suppl Operative):95–103; discussion 103.Google Scholar
Ostrem, JL, Ziman, N, Galifianakis, NB, Starr, PA, Luciano, MS, Katz, M, et al. Clinical outcomes using ClearPoint interventional MRI for deep brain stimulation lead placement in Parkinson’s disease. Journal of neurosurgery. 2016;124(4):908–916.Google Scholar
Ostrem, JL, Galifianakis, NB, Markun, LC, Grace, JK, Martin, AJ, Starr, PA, et al. Clinical outcomes of PD patients having bilateral STN DBS using high-field interventional MR-imaging for lead placement. Clinical neurology and neurosurgery. 2013;115(6):708–712.Google Scholar
Sillay, KA, Rusy, D, Buyan-Dent, L, Ninman, NL, Vigen, KK. Wide-bore 1.5 T MRI-guided deep brain stimulation surgery: Initial experience and technique comparison. Clinical neurology and neurosurgery. 2014;127:79–85.Google Scholar
Sidiropoulos, C, Rammo, R, Merker, B, Mahajan, A, LeWitt, P, Kaminski, P, et al. Intraoperative MRI for deep brain stimulation lead placement in Parkinson’s disease: 1 year motor and neuropsychological outcomes. Journal of neurology. 2016;263(6):1226–1231.CrossRefGoogle ScholarPubMed
Martin, AJ, Larson, PS, Ziman, N, Levesque, N, Volz, M, Ostrem, JL, et al. Deep brain stimulator implantation in a diagnostic MRI suite: Infection history over a 10-year period. Journal of neurosurgery. 2017;126(1):108–113.Google Scholar
Martin, AJ, Starr, PA, Ostrem, JL, Larson, PS. Hemorrhage detection and incidence during magnetic resonance-guided deep brain stimulator implantations. Stereotactic and functional neurosurgery. 2017;95(5):307–314.Google Scholar
Burchiel, KJ, McCartney, S, Lee, A, Raslan, AM. Accuracy of deep brain stimulation electrode placement using intraoperative computed tomography without microelectrode recording. Journal of neurosurgery. 2013;119(2):301–306.CrossRefGoogle ScholarPubMed
Vega, RA, Holloway, KL, Larson, PS. Image-guided deep brain stimulation. Neurosurgery clinics of North America. 2014;25(1):159–172.CrossRefGoogle ScholarPubMed
Mirzadeh, Z, Chapple, K, Lambert, M, Evidente, VG, Mahant, P, Ospina, MC, et al. Parkinson’s disease outcomes after intraoperative CT-guided “asleep” deep brain stimulation in the globus pallidus internus. Journal of neurosurgery. 2016;124(4):902–907.Google Scholar
Chen, T, Mirzadeh, Z, Chapple, K, Lambert, M, Dhall, R, Ponce, FA. “Asleep” deep brain stimulation for essential tremor. Journal of neurosurgery. 2016;124(6):1842–1849.CrossRefGoogle ScholarPubMed
Chen, T, Mirzadeh, Z, Ponce, FA. “Asleep” deep brain stimulation surgery: A critical review of the literature. World neurosurgery. 2017;105:191–198.Google Scholar
Kochanski, RB, Sani, S. Awake versus asleep deep brain stimulation surgery: Technical considerations and critical review of the literature. Brain science. 2018;8(1):17.Google Scholar
Liu, L, Mariani, SG, De Schlichting, E, Grand, S, Lefranc, M, Seigneuret, E, et al. Frameless ROSA(R) robot-assisted lead implantation for deep brain stimulation: Technique and accuracy. Operative neurosurgery (Hagerstown). 2010;19(1):57–64.Google Scholar
VanSickle, D, Volk, V, Freeman, P, Henry, J, Baldwin, M, Fitzpatrick, CK. Electrode placement accuracy in robot-assisted asleep deep brain stimulation. Annals of biomedical engineering. 2019;47(5):1212–1222.Google Scholar
Varma, TR, Eldridge, PR, Forster, A, Fox, S, Fletcher, N, Steiger, M, et al. Use of the NeuroMate stereotactic robot in a frameless mode for movement disorder surgery. Stereotactic and functional neurosurgery. 2003;80(1–4):132–135.Google Scholar
Faraji, AH, Kokkinos, V, Sweat, JC, Crammond, DJ, Richardson, RM. Robotic-assisted stereotaxy for deep brain stimulation lead implantation in awake patients. Operative neurosurgery (Hagerstown). 2020;19(4):444–452.Google Scholar
Paff, M, Wang, AS, Phielipp, N, Vadera, S, Morenkova, A, Hermanowicz, N, et al. Two-year clinical outcomes associated with robotic-assisted subthalamic lead implantation in patients with Parkinson’s disease. Journal of robotic surgery. 2019;14(4):559–565.Google Scholar
Fenoy, AJ, Schiess, MC. Deep brain stimulation of the Dentato-Rubro-Thalamic Tract: Outcomes of direct targeting for tremor. Neuromodulation: Journal of the International Neuromodulation Society. 2017;20(5):429–436.Google Scholar

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