Coil design considerations for deep transcranial magnetic stimulation.

Published

Journal Article

OBJECTIVES: To explore the field characteristics and design tradeoffs of coils for deep transcranial magnetic stimulation (dTMS). METHODS: We simulated parametrically two dTMS coil designs on a spherical head model using the finite element method, and compare them with five commercial TMS coils, including two that are FDA approved for the treatment of depression (ferromagnetic-core figure-8 and H1 coil). RESULTS: Smaller coils have a focality advantage over larger coils; however, this advantage diminishes with increasing target depth. Smaller coils have the disadvantage of producing stronger field in the superficial cortex and requiring more energy. When the coil dimensions are large relative to the head size, the electric field decay in depth becomes linear, indicating that, at best, the electric field attenuation is directly proportional to the depth of the target. Ferromagnetic cores improve electrical efficiency for targeting superficial brain areas; however magnetic saturation reduces the effectiveness of the core for deeper targets, especially for highly focal coils. Distancing winding segments from the head, as in the H1 coil, increases the required stimulation energy. CONCLUSIONS: Among standard commercial coils, the double cone coil offers high energy efficiency and balance between stimulated volume and superficial field strength. Direct TMS of targets at depths of ~4 cm or more results in superficial stimulation strength that exceeds the upper limit in current rTMS safety guidelines. Approaching depths of ~6 cm is almost certainly unsafe considering the excessive superficial stimulation strength and activated brain volume. SIGNIFICANCE: Coil design limitations and tradeoffs are important for rational and safe exploration of dTMS.

Full Text

Duke Authors

Cited Authors

  • Deng, Z-D; Lisanby, SH; Peterchev, AV

Published Date

  • June 2014

Published In

Volume / Issue

  • 125 / 6

Start / End Page

  • 1202 - 1212

PubMed ID

  • 24411523

Pubmed Central ID

  • 24411523

Electronic International Standard Serial Number (EISSN)

  • 1872-8952

Digital Object Identifier (DOI)

  • 10.1016/j.clinph.2013.11.038

Language

  • eng

Conference Location

  • Netherlands