#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Vaskulární koridor pro implantaci stimulační elektrody do nucleus anterior thalami – experimentální studie


Authors: D. Hrabovský 1;  M. Joukal 2;  M. Baláž 3;  J. Kunst 3;  J. Chrastina 1
Authors place of work: Neurochirurgická klinika LF MU a FN U sv. Anny v Brně 1;  Anatomický ústav LF MU, Brno 2;  I. neurologická klinika LF MU a FN u sv. Anny v Brně 3
Published in the journal: Cesk Slov Neurol N 2023; 86(2): 140-145
Category: Original Paper
doi: https://doi.org/10.48095/cccsnn2023140

Summary

Aim: Stimulation of the anterior thalamic nucleus (ATN) is considered for patients with refractory epilepsy if there is no other surgical option. The target structure, the ATN, protrudes to the lateral brain ventricle as a thalamic tubercle, bordered by the thalamostriate vein laterally and the choroid plexus with the superior choroidal vein medially. The study aim was to analyze this vascular corridor for electrode implantation considering both surgical safety and possible association with stimulation outcomes. The best results are achieved when the anterior part of the ATN is stimulated. Materials and methods: The thalamic tubercle and its vascular borders were identified in dissection of both brain hemispheres of cadaveric specimens with intracranial vessel injections. The width of the vascular corridor was measured at distances of 2, 4, and 6 mm from the covering spot of the thalamostriate vein and choroid plexus or from the junction of these veins. Results: Six cadaveric specimens were measured. The median widths of the vascular corridor were 2.5–3 mm at the 2 mm, and 4–4.5 mm at the 4 mm, and 6 mm measures from the junction points, respectively. A small inconstant venous structure was observed in the dorsal part of the thalamic tubercle. After subtracting 1.3 mm (the diameter of a stimulation electrode) from the corridor width, the reserve space was 1.2–1.8 mm at the distance of 2 mm, and 2.7–3.2 mm at distances of 4 mm, and 6 mm from the junction, respectively. Conclusions: The narrow vascular corridor for electrode implantation (particularly in the anterior part of the thalamic tubercle) requires meticulous presurgical planning and precise implantation to maximize the effect of stimulation treatment while avoiding the risk of vascular conflict.

Keywords:

deep brain stimulation – Epilepsy – stereotaxic techniques – anterior thalamic nucleus – thalamostriate vein


Zdroje

1. Elliott RE, Morsi A, Kalhorn SP et al. Vagus nerve stimulation in 436 consecutive patients with treatment-resistant epilepsy: long term outcomes and predictors of response. Epilepsy Behav 2011; 20 (1): 57–63. doi: 10.1016/j.yebeh.2010.10.017.

2. Fisher R, Salanova V, Witt T et al. Electrical stimulation of the anterior nucleus of thalamus for treatment of refractory epilepsy. Epilepsia 2010; 51 (5): 899–908. doi: 10.1111/j.1528-1167.2010.02536.x.

3. Lehtimäki K, Möttönen K, Järventausta K et al. Outcome based definition of the anterior thalamic deep braion stimulation target in refractory epilepsy. Brain Stimul 2016; 9 (2): 268–275. doi: 10.1016/j.brs.2015.09.014.

4. Mullan S, Vailati G, Karasick J et al. Thalamic lesions for the control of epilepsy. A study of nine cases. Arch Neurol 1967; 16 (3): 277–285. doi: 10.1001/archneur.1967.00470210053006.

5. Upton AR, Cooper IS, Springman M et al. Supression of seizures and psychosis of limbic system origin by chronic stimulation of anterior nucleus of the thalamus. Int J Neurol 1985; 19–20: 223–230.

6. Hodaie M, Wennberg RA, Dostrovsky JO et al. Chronic anterior thalamic stimulation for intractable epilepsy. Epilepsia 2002; 43 (6): 603–608. doi: 10.1046/j.1528-1157.2002.26001.x.

7. Herrman H, Egge A, Konglund AE et al. Anterior thalamic deep brain stimulation in refractory epilepsy: a randomized, double blinded study. Acta Neurol Scand 2019; 139 (3): 294–304. doi: 10.1111/ane.13047.

8. Perez-Malagon CD, Lopez-Gonzales MA. Epilepsy and deep brain stimulation of anterior thalamic nucleus. Cureus 2021; 13 (9): e18199. doi: 10.7759/cureus.18 199.

9. Sanan A, Abdel Aziz KM, Janjua RM et al. Colored silicone injection for use in neurosurgical dissections: anatomic technical note. Neurosurgery 1999; 45 (5): 1267–1271. doi: 10.1097/00006123-199911000-00058.

10. Binder DK, Rau G, Starr PA. Haemorrhagic complications of microelectrode-guided deep brain stimulation. Stereotact Funct Neurosurg 2003; 80 (1–4): 28–31. doi: 10.1159/000075156.

11. Elias WJ, Sansur CA, Frysinger RC. Sulcal and ventricular trajectories in stereotactic surgery. J Neurosurg 2009; 110 (2): 201–207. doi: 10.3171/2008.7.17625.

12. Nowinski WL, Chua BC, Volkau I et al. Simulation and assessment of cerebrovascular damage in deep brain stimulation using a stereotactic atlas of vasculature and structure derived from multiple 3- and 7-tesla scans. J Neurosurg 2010; 113 (6): 1234–1241. doi: 10.3171/2010.2.JNS091528.

13. Möttönen T, Katisko J, Haapasalo T et al. Defining the anterior nucleus of the thalamus (ANT) as a deep brain stimulation target in refraktory epilepsy: delineation using 3T MRI and intraoperative microelectrode recording. Neuroimage Clin 2015; 7: 823–829. doi: 10.1016/j.nicl.2015.03.001.

14. Lehtimäki K, Möttönen K, Järventausta K et al. Outcome based definition of the anterior thalamic deep brain stimulation target in refractory epilepsy. Brain Stimul 2016; 9 (2): 268–275. doi: 10.1016/j.brs.2015.09. 014.

15. Wu Ch, D’Haese P-F, Pallavaram S et al. Variation in thalamic anatomy affect targeting in deep brain stimulation for epilepsy. Stereotactic Funct Neurosurg 2016; 94 (6): 387–396. doi: 10.1159/000449009.

16. Wang S, Wu DC, Fan XN et al. Mediodorsal thalamic stimulation is not protective against seizures induced by amyloid kindling in rats. Neurosci Lett 2010; 481 (2): 97–101. doi: 10.1016/j.neulet.2010.06.060.

17. Son BC, Shon YM, Kim SH et al. Technical implications in revision surgery for deep brain stimulation (DBS) of the thalamus for refractory epilepsy. J Epilepsy Res 2018; 8 (1): 12–19. doi: 10.14581/jer.18003.

18. Lehtimäki K, Coenen VA, Ferreira AG et al. The surgical approach to the anterior nucleus of thalamus in patients with refractory epilepsy: experience from the international multicenter registry (MORE). Neurosurgery 2019; 84 (1): 141–150. doi: 10.1093/neuros/nyy023.

19. Hughes EJ, Bond J, Svrckova P et al. Regional changes in thalamic shape and volume with increasing age. Neuroimage 2012; 63 (3): 1134–1142. doi: 10.1016/j.neuroimage.2012.07.043.

Štítky
Paediatric neurology Neurosurgery Neurology

Článok vyšiel v časopise

Czech and Slovak Neurology and Neurosurgery

Číslo 2

2023 Číslo 2
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#