Methods, systems, and apparatus for closed-loop neuromodulation
Systems, apparatus, and methods for treating medication refractory epilepsy are disclosed. In one embodiment, a method of treating epilepsy is disclosed comprising detecting, using a first electrode array coupled to a first endovascular carrier, an electrophysiological signal of a subject. The method further comprises analyzing the electrophysiological signal using a neuromodulation unit electrically coupled to the first electrode array and stimulating an intracorporeal target of the subject using a second electrode array coupled to a second endovascular carrier implanted within a part of a bodily vessel superior to a base of the skull of the subject.
1. A method of treating epilepsy, comprising:
detecting, using a first electrode array, an electrophysiological signal of a subject, wherein the electrophysiological signal is a signal associated with or correlated with the onset of an epileptic seizure, wherein the first electrode array is coupled to a first endovascular carrier implanted within the subject, wherein the first endovascular carrier is a coiled microwire and wherein the first electrode array comprises electrodes arranged along a length of the coiled microwire;
analyzing the electrophysiological signal using a neuromodulation unit implanted within the subject and electrically coupled to the first electrode array; and
stimulating an intracorporeal target of the subject using a second electrode array in response to the electrophysiological signal detected, wherein the intracorporeal target is stimulated as part of a treatment for epilepsy, wherein the second electrode array is electrically coupled to the neuromodulation unit, wherein the second electrode array is coupled to a second endovascular carrier implanted within the subject, wherein the second endovascular carrier is implanted within the internal jugular vein superior to a jugular foramen of the subject.
2. The method of claim 1 , wherein the intracorporeal target is part of a vagus nerve of the subject.
3. The method of claim 2 , wherein the intracorporeal target is a superior ganglion of the vagus nerve.
4. The method of claim 1 , wherein the intracorporeal target is a cerebellum of the subject.
5. The method of claim 1 , wherein the first endovascular carrier is implanted within at least one of a superior sagittal sinus, an inferior sagittal sinus, a sigmoid sinus, a transverse sinus, and a straight sinus of the subject.
6. The method of claim 1 , wherein the first endovascular carrier is implanted within at least one of a vein of Labbe, a vein of Trolard, a Sylvian vein, and a Rolandic vein.
7. The method of claim 1 , wherein the first endovascular carrier is implanted within at least one of a vein of Rosenthal, a vein of Galen, a superior thalamostriate vein, and an internal cerebral vein.
8. The method of claim 1 , wherein the first endovascular carrier is implanted within at least one of a central sulcal vein, a post-central sulcal vein, and a pre-central sulcal vein.
9. The method of claim 1 , wherein the first endovascular carrier is implanted within a vessel extending through a hippocampus of the subject.
10. The method of claim 1 , wherein the first endovascular carrier is implanted within a vessel extending through an amygdala of the subject.
11. The method of claim 1 , wherein the neuromodulation unit is implanted within a forearm of the subject.
12. The method of claim 1 , wherein the first electrode array is electrically coupled to the neuromodulation unit via a first transmission lead having a first lead diameter, wherein the first transmission lead extends through a neck of the subject, and wherein the first lead diameter is between about 0.5 mm and 1.5 mm.
13. The method of claim 1 , wherein the second electrode array is electrically coupled to the neuromodulation unit via a second transmission lead having a second lead diameter, wherein the second transmission lead extends through a neck of the subject, and wherein the second lead diameter is between about 0.5 mm and 1.5 mm.
14. The method of claim 1 , wherein the extracorporeal device is provided as part of an armband.
15. The method of claim 1 , further comprising generating the electrical impulse by increasing a current amplitude of the electrical impulse from 0 mA to up to 10 mA in 0.1 mA steps.
16. The method of claim 15 , further comprising increasing a voltage of the electrical impulse from 0 V to up to 10 V in 0.25 V steps.
17. The method of claim 1 , wherein a pulse width of the electrical impulse generated is configured to be between about 25 μS to about 600 μS.
18. The method of claim 1 , wherein a frequency of the electrical impulse generated is configured to be between 1 Hz and 400 Hz.