Device and implantation system for electrical stimulation of biological systems
The present specification discloses devices and methodologies for the treatment of transient lower esophageal sphincter relaxations (tLESRs). Individuals with tLESRs may be treated by implanting a stimulation device within the patient's lower esophageal sphincter and applying electrical stimulation to the patient's lower esophageal sphincter, in accordance with certain predefined protocols. The presently disclosed devices have a simplified design because they do not require sensing systems capable of sensing when a person is engaged in a wet swallow and have improved energy storage requirements.
1. A method of treating a patient with gastrointestinal reflux disease comprising:
implanting an electrical stimulator comprising an energy storage component, a non-volatile memory for storing programmatic code, and a pulse generator in electrical communication with at least one electrode, wherein said electrode is implanted such that said electrode is configured to be in electrical communication with a lower esophageal sphincter (LES) of the patient; and
programming said implanted electrical stimulator, wherein said electrical stimulator is programmed such that, when operated, the electrical stimulator generates a pulse stream, wherein said pulse stream comprises a pulse width having a range of 30 μsec to 5 msec, a pulse amplitude having a range of 2 to 15 mAmp, and a pulse frequency having a range of 2 to 80 Hz, wherein values for each of said pulse width, pulse amplitude, and pulse frequency are defined such that swallowing of the patient is not hindered by said stimulation while said stimulation is occurring.
2. The method of claim 1 , wherein the electrical stimulator comprises an accelerometer.
3. The method of claim 2 , further comprising programming the electrical stimulator to have a stimulation mode adapted to automatically stimulate the LES during time periods in which the patient is in a supine position as determined by said accelerometer.
4. The method of claim 3 , wherein said supine position is defined by a level of inclination relative to a vertical baseline and wherein said level is programmable and has a range of 50 to 80 degrees.
5. The method of claim 3 , further comprising programming the electrical stimulator such that said automatic stimulation occurs after the patient has been in the supine position for a predetermined period of time and wherein said predetermined period of time has a range of 1 minute to 60 minutes.
6. The method of claim 3 , further comprising programming the electrical stimulator such that said automatic stimulation occurs after a minimum percentage of data points occur within a predetermined period of time.
7. The method of claim 1 , wherein said electrical stimulator is not in communication with a sensor to determine when the patient is swallowing and does not modify said pulse stream based on said swallowing.
8. A method of treating a patient with gastrointestinal reflux disease comprising:
implanting an electrical stimulator comprising an energy storage component, an accelerometer, a non-volatile memory for storing programmatic code, and a pulse generator in electrical communication with at least one electrode, wherein said electrode is implanted such that said electrode is configured to be in electrical communication with a lower esophageal sphincter (LES) of the patient; and
programming said implanted electrical stimulator, wherein said electrical stimulator is programmed such that, when operated, the electrical stimulator generates a pulse stream, wherein said pulse stream comprises a pulse width having a range of 30 μsec to 5 msec, a pulse amplitude having a range of 2 to 15 mAmp, and a pulse frequency having a range of 2 to 80 Hz, wherein values for each of said pulse width, pulse amplitude, and pulse frequency are defined such that swallowing of the patient is not hindered by said stimulation while said stimulation is occurring.
9. The method of claim 8 , further comprising programming the electrical stimulator to automatically stimulate the LES based on whether the patient is in a supine position, as determined by data from said accelerometer.
10. The method of claim 9 , wherein said supine position is defined by a level of inclination relative to a vertical baseline and wherein said level is programmable and has a range of 50 to 80 degrees.
11. The method of claim 9 , further comprising programming the electrical stimulator such that automatic stimulation occurs after the patient has been in the supine position for a predetermined period of time and wherein said predetermined period of time has a range of 1 minute to 60 minutes.
12. The method of claim 9 , further comprising programming the electrical stimulator such that automatic stimulation occurs after a minimum percentage of data points occur within a predetermined period of time.