OCCIPITAL NEUROMODULATION METHOD

• US 20130023951A1
• Filed: 10/01/2012
• Published: 01/24/2013
• Est. Priority Date: 09/16/2008
• Status: Active Grant

• Current Assignee: Joshua Greenspan
• Original Assignee: Joshua Greenspan
• Inventors: Greenspan, Joshua
• Granted Patent: US 8,843,202 B2
• Time in Patent Office: Days
• US Class Current: 607/46
• CPC Class Codes: A61N 1/0504 Subcutaneous electrodes
• CPC Class Codes: A61N 1/0534 Electrodes for deep brain stimulation
• CPC Class Codes: A61N 1/36017 with leads or electrodes penetrating the skin
• CPC Class Codes: A61N 1/36025 for treating a mental or cerebral condition
• CPC Class Codes: A61N 1/36071 Pain
• CPC Class Codes: A61N 1/36075 Headache or migraine
• CPC Class Codes: A61N 1/36082 Cognitive or psychiatric applications, e.g. dementia or Alzheimer's disease
• CPC Class Codes: A61N 1/36157 Current A61N1/3616 takes precedence
• CPC Class Codes: A61N 1/36171 Frequency
• CPC Class Codes: A61N 1/36175 Pulse width or duty cycle

Abstract

A method of treating pain in a subject includes the step of positioning a tip of one or more leads subcutaneously in the occipital region of a subject'"'"'s scalp, where the leads are configured to conduct an electrical signal along an occipital nerve into the brain. The leads are energized to conduct the electrical signal along the occipital nerve and the electrical signal is adjusted to a level effective to decrease the subject'"'"'s pain over time and so that the subject cannot feel the lead being energized.

Claims

1. A method of treating pain in a subject comprising the steps of:

positioning a tip of at least one lead subcutaneously in an occipital region of a subject'"'"'s scalp, the at least one lead configured to conduct an electrical signal along an occipital nerve into the brain; and

energizing the at least one lead to conduct the electrical signal along the occipital nerve into the brain; and

adjusting the electrical signal to a level effective to decrease the subject'"'"'s pain over time and wherein the subject cannot feel the lead being energized.

2. The method of claim 1, wherein the at least one lead comprises:

a first pair of leads having a first left lead and a first right lead, wherein the first left lead and the second left lead are positioned in opposite lateral occipital portions of the occipital region of the subject'"'"'s scalp and along an imaginary line connecting the tops of the subject'"'"'s ears; and

a second pair of leads having a second left lead and a second right lead, the second pair of leads positioned below and substantially parallel to the imaginary line and wherein the second left lead and the second right lead are positioned in opposite lateral occipital portions of the occipital region of the subject'"'"'s scalp.

3. The method of claim 1 wherein the electrical signal comprises:

a current between 0.1 mA and 8 mA;

a frequency between 4 Hz and 96 Hz; and

a pulse width between 50 msec and 100 msec.

4. The method of claim 3, wherein the current is 0.6 mA or below.

5. The method of claim 4, wherein the frequency is 16 Hz and the pulse width is 100 msec.

6. The method of claim 4, wherein the frequency is 96 Hz and the pulse width is 100 msec.

7. The method of claim 1, wherein the electrical signal alters the release of one or more neurotransmitters within the brain, the one or more neurotransmitters selected from the group consisting of dopamine, serotonin, GABA, acetylcholine, and substance P.

8. The method of claim 1, wherein the pain is one selected from the group consisting of migraine pain, fibromyalgia pain, neuropathic pain, and traumatic brain injury pain.

9. The method of claim 3, further comprising the step of:

coupling a programmer to the at least one lead, the programmer being capable of delivering the electrical signal to the occipital nerve, thereby enabling the subject to adjust the electrical signal to a level such that the subject experiences a decrease in pain over time although not being able to feel the lead being energized; and

wherein the at least one lead comprises;

a first temporary lead positioned in a first lateral occipital region substantially along an imaginary line connecting the tops of the subject'"'"'s ears; and

a second temporary lead positioned in a second lateral occipital region opposing the first lateral occipital region and substantially along the imaginary line.

10. The method of claim 9, further comprising the steps of:

implanting a first pair of permanent leads having a first left lead and a first right lead, wherein the first left lead and the first right lead are positioned in opposite lateral portions of the occipital region of the subject'"'"'s scalp and along an imaginary line connecting the tops of the subject'"'"'s ears; and

implanting a second pair of permanent leads having a second left lead and a second right lead, the second pair of permanent leads positioned below and substantially parallel to the imaginary line and wherein the second left lead and the second right lead are positioned in opposite lateral occipital portions of the occipital region of the subject'"'"'s scalp.

implanting an internal pulse generator subcutaneously; and

coupling the first pair of permanent leads and the second pair of permanent leads to the implanted internal pulse generator.

12. The method of claim 9, further comprising the steps of:

conducting a PET scan prior to the energizing step to establish a first metabolic activity level for pain centers within the brain;

conducting a subsequent PET scan after the energizing step to determine a second metabolic activity level for pain centers within the brain;

comparing the second metabolic activity level with the first metabolic activity level to determine a change in metabolic activity.

13. A neuromodulation kit for treating pain without neurostimulation, the kit comprising:

at least one pair of leads configured to conduct an electrical signal along an occipital nerve to alter the release of neurotransmitters within the brain, wherein the signal is adjusted to a level below where the subject can feel the at least one pair of leads being energized;

a pulse generator capable of energizing the leads with an neuromodulation signal comprising an amplitude between 0.1 mA and 8 mA, a frequency from about 4 Hz to about 96 Hz, and a pulse width from 50 msec to 100 msec; and

instructions for programming the pulse generator to generate an electrical signal effective to treat pain using neuromodulation and below the level where the subject can feel the lead being energized, and for implanting the at least one pair of leads subcutaneously in respective opposite lateral portions of an occipital region of a subject'"'"'s scalp.

14. The kit of claim 13, wherein the at least one pair of leads and the pulse generator comprise a single unit.

15. The kit of claim 14, wherein the single unit further comprises a battery.