17 Lesioning versus Deep Brain Stimulation for Movement Disorders



10.1055/b-0039-171736

17 Lesioning versus Deep Brain Stimulation for Movement Disorders

Tony R. Wang, Robert F. Dallapiazza, Aaron E. Bond, Shayan Moosa, and W. Jeffrey Elias


Abstract


Deep brain stimulation and the creation of stereotactic lesions are both effective means of treating essential tremor (ET) and Parkinson’s disease (PD). DBS has largely supplanted lesion generation as the treatment of choice in movement disorders, since it is reversible, adjustable and can be used to safely treat bilateral disease. This chapter highlights differences in efficacy and safety along with the advantages and disadvantages for lesion generation and DBS in the treatment of movement disorders.




17.1 Historical Considerations


Although lesion generation and deep brain stimulation (DBS) are often viewed as competing procedures, they were at first complementary. In 1947 Spiegel and Wycis designed the first apparatus for accurate human lesion generation in deep brain targets. The device was used for medial thalamotomy for neuropsychiatric disorders as a surgical alternative treatment to lobotomy. 1 Subsequent work in the 1950s, relied on high frequency operative stimulation to identify subcortical targets for lesioning. 2 In the late 1980s, implanted high frequency stimulating electrodes were combined with battery-powered pulse generators as the first DBS devices. 3 DBS has since revolutionized the treatment of movement disorders. This chapter will focus on the use of lesion generation and DBS for treatment of ET and PD.



17.2 Effectiveness


In PD, subthalamic nucleus (STN) DBS may improve Unified Parkinson’s Disease Rating Scale, Part III (UPDRSIII) scores 25–89%. Average improvement is 45%. Quality of life measures improve as much as 35%, with an average improvement of 18%. 2 Globus pallidus interna (GPi) DBS leads to comparable improvements in UPDRSIII scores and quality of life measures with average improvements of 35% and 10%, respectively. 4 A recent meta-analysis of ten randomized controlled trials comparing STN-DBS to GPi-DBS for PD showed that STN and GPi were equally effective. STN-DBS, however led to greater decrease in levodopa equivalent daily dose (LEDD). 5 Ventral intermedius nucleus (Vim) DBS and RF Vim thalamotomy for PD improve tremor scores by up to 90%. 4 Both techniques may not address other symptoms of parkinsonism and are generally reserved for tremor dominant PD. STN-DBS, however will treat the other PD symptoms that are known to worsen over time.


For ET, Vim-DBS and RF lesioning have comparable reductions in tremor scores, ranging from 55–90% improvement. 6 A recent prospective trial for Gamma Knife thalamotomy demonstrated average tremor score improvement of 54% at one year blinded evaluation. 7 MRI-guided focused ultrasound (FUS) has recently been FDA-approved. With this technique, tremor scores improve an average of 40% at 12 months. 8 Long-term clinical data is not yet available. Several studies have compared RF lesioning to DBS at various subcortical targets for PD and ET (▶ Table 17.1). 9 , 10 , 11 , 12 , 13 , 14 , 15 Most of these studies showed no difference in tremors or functional outcome. The majority of the studies compared unilateral lesioning to unilateral or to bilateral DBS.











































































































Table 17.1 Studies that directly compared lesioning to DBS

           

Improvement percentages when compared to baseline


Study/year


Study Type


Target


Disease


N


Laterality


Follow-up


Tremor score/UPDRSIII


Functional status


Tasker et al., 1998 9


Retrospective


Vim


ET, PD


26 lesional 19 DBS


4 bilateral lesional, 2 bilateral DBS, otherwise unilateral


At least 3 mo for all


See Below


See below


Merello et al., 1999 10


Randomized


GPi


PD


7 lesional 6 DBS


Unilateral


3 mo


44 (lesional)


46 (DBS)


46 (lesional)


57.8 (DBS)


Schuurman et al., 2000 11


Randomized


Vim


ET, PD, MS #


34 lesional


34 DBS


Unilateral lesional,


unilateral or bilateral DBS *


6 mo


87 (lesional)


91.7 (DBS)


1.5 (lesional)


15.6 (DBS)


Pahwa et al. 2001 12


Retrospective matched cohort


Vim


ET


17 lesional


17 DBS


Unilateral


2.2 mo (lesional)


3.1 mo (DBS)


46 (lesional)


49.8 (DBS)


70 (lesional)


64 (DBS)


Esselink et al., 2004 13


Randomized


GPi (lesional)


STN (DBS)


PD


14 lesional


20 DBS


Unilateral pallidotomy


Bilateral STN-DBS


6 mo


20.4 (lesional)


48.5 (DBS)


34.5 (lesional)


46.3 (DBS)


Merello et al., 2008 14


Randomized


STN


PD


6 lesional


6 DBS


6


DBS + lesional


Bilateral DBS, bilateral lesioning, or unilateral lesion + contralateral DBS


12 mo


52.2 (lesional)


60.9 (DBS)


61.8 (lesional +DBS)


45.5 (lesional)


70.5 (DBS)


69.1 (lesional +DBS)


Anderson et al., 2009 15


Randomized


Vim


ET


10 lesional


10 DBS


Unilateral


6 mo


40 (lesional)


40 (DBS)


N/A


Tasker et al. do not report average (per patient) percentage improvements in tremor or functional status. They do report that 69% of lesional patients and 79% of DBS patients experienced “near abolition” of tremor. Regarding functional outcome, 48% of lesional paients and 49% of DBS patients had suppression of rigidity; 68% of lesional patients and 38% of DBS patients had improved dexterity. Little improvement in writing, speech, or gait was seen with either group.


# 55 PD patients, 13 ET patients, 10 MS patients


* For patients assigned to the lesional group if unilateral tremor was present, unilateral thalamotomy was performed, if bilateral tremor was present, thalamotomy was performed to treat the more symptomatic side, the contralateral side would receive thalamic DBS. All patients assigned to DBS group either underwent unilateral or bilateral thalamic stimulation based on symptoms.


denotes statistically significant improvement over lesioning



Vim DBS and RF Vim thalamotomy are generally reserved for tremor dominant PD.


STN DBS treats other PD symptoms that will likely emerge later.

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May 11, 2020 | Posted by in NEUROSURGERY | Comments Off on 17 Lesioning versus Deep Brain Stimulation for Movement Disorders

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