Patent Application
20100076518
The present disclosure is directed to systems and methods for relieving dyspnea, including via electrical signals delivered to breathing muscles and/or associated afferent neural pathways.
Dyspnea is the chief patient complaint in a variety of diseases of the pulmonary system. These diseases include chronic bronchitis (12.5 million US patients), emphysema (1.7 million US patients), and asthma (18 million US patients), collectively referred to as Chronic Obstructive Pulmonary Diseases, or COPD. Dyspnea is also reported by patients suffering from combinations of the foregoing diseases, and/or other pulmonary diseases, and non-pulmonary diseases (notably in heart failure). Dyspnea, while a common medical term, is actually poorly defined and ultimately subjective since it is generally the perception of difficulty breathing or difficulty catching one's breath, and more generally, an uncomfortable sensation of breathing.
The severity of pulmonary diseases can typically be measured using objective techniques, such as FEV1 (the patient's forced expiratory volume in the first second of exhalation), minute ventilation (the volume inhaled or exhaled by the patient in one minute), arterial blood gas levels (e.g., of oxygen or carbon dioxide), among others. By contrast, the patient's dyspnea experience can be simply one of difficulty breathing, ultimately leading to a reduction or elimination of physical activity due to this discomfort. That is, the patient complaint is of dyspnea and a loss of mobility or physical function, not of a decreased FEV1.
In many ways dyspnea can be analogous to the perception of pain. While an organic source of the pain may be present (a broken bone, for example), the pain itself can be a problem and may require palliative treatment. Furthermore, in the same way that an individual can suffer from chronic pain for which an organic cause is either absent or inadequate to cause the pain, some patients can suffer from severe dyspnea despite relatively normal objective measures of pulmonary performance.
The origins of dyspnea remain unclear. Studies and experience have yielded confusing and often seemingly contradictory results. Treatments for dyspnea range from supplemental oxygen therapy to sitting in front of a fan to systemic opiates. Furthermore, dyspnea can be experimentally induced by vigorous exercise, breath-holding, breathing through a restrictive mouthpiece, or breathing carbon dioxide in symptomatic pulmonary disease patients. A common, though unproven, theory is that dyspnea derives from a mismatch between outgoing motor signals to the respiratory muscles and incoming afferent information. In one example, under a give set of conditions, the brain can expect a certain pattern of ventilation and associated afferent feedback. Deviations from this pattern can cause or intensify the sensation of dyspnea.
While dyspnea is often the chief complaint of a patient, there is currently no pharmacologic agent that primarily treats dyspnea. That is, a variety of bronchodilators are used to treat asthma and other COPD, and while they demonstrably increase FEV1, their effects on dyspnea can be modest and can fall below that of clinical significance. Accordingly, there remains a need for methods and devices that effectively treat dyspnea.
In the drawings, which are not necessarily drawn to scale, like numerals may describe similar components in different views. Like numerals having different letter suffixes may represent different instances of similar components. The drawings illustrate generally, by way of example, but not by way of limitation, various embodiments discussed in the present document.
Table 1 is a table of various categories and therapeutic methods that can be used to affect the sensation of dyspnea.
Mechanical vibration of the chest wall can relieve the sensation of dyspnea. Mechanical “in phase” vibration (i.e., vibration applied to the contracting muscles, the inspiratory intercostal muscles during the inspiratory phase of breathing) reduces the sensation of dyspnea. “Out of phase” vibrations often have a detrimental effect, increasing the sensation of dyspnea.
Dyspnea can be relieved using mechanical vibrators applied to the external chest wall in an upper anterior (typically the 2nd or 3rd intercostal spaces) parasternal location. In one example, manual application of the vibrators during inspiration and not during exhalation reduces dyspnea. In some examples, semi-permanently applied vibrators with sensors and a control algorithm trigger the vibrators during the inspiratory phase. An example of semi-permanent application of the vibrators includes placing the vibrators in a vest worn by a patient. An example of a sensor for detecting the inspiratory phase of a patient includes a thermistor placed at or in the patient's nose to sense airflow associated with the patient's breath. It is understood that other applications of the vibrators and selection of sensors is possible without departing from the scope of the present subject matter.
Mechanical vibrators used for chest wall vibration are typically 25 mm in diameter with an amplitude of 2 mm at a 100-120 Hz frequency. Such a transducer is bulky, noisy, and consumes substantial energy. Thus, a practical solution utilizing such devices would also be bulky, requiring a vest or other means to clamp the device to the chest, an electrical power supply, a separate sensor to detect airflow (likely placed near the nose or mouth), and a control device. Such a practical solution can be bulky, heavy, inconvenient, and unsightly for the user and would not be highly desired.
The mechanical vibration functionally serves to stimulate the intercostal muscle fibers to provide additional afferent feedback from the skeletal muscles to “trick” the body into sensing that it is breathing more and easier. In other embodiments, other mechanisms provide additional afferent feedback from the intercostal muscles to provide the same benefit.
In one example, electrical stimulation of the intercostal muscles is used to produce contractions (i.e., TENS transcutaneous electrical nerve stimulation). Electrical stimulators are of lower bulk and power usage than mechanical vibrators. In various examples, a single chest “strap” (similar in outward design to an athletic pulse monitor) can be used to place and hold the electrodes as well as to sense chest wall expansion during inspiration. A control unit provides control of the TENS electrodes based upon sensing inspiration.
A battery pack to power the device can be located in a variety of places, including but not limited to, on the strap, remotely, such as on a belt holster, via a connecting power cord or a combination thereof.
In another example, electrical stimulation of the afferent nerves leading from the intercostal muscles can duplicate the effects (on the central sensory cortex) of mechanical vibration of those same intercostal muscles. Electrical stimulation of the afferent nerves leading from the intercostal muscles can use less electrical power than either mechanical vibration or TENS. In various examples, implanted electrodes are located to effectively inject appropriate electrical signals into the afferent nervous fibers. One example includes a fully implantable system where the electrodes, leads, signal generator and battery, and sensors are all permanently implanted under the skin.
In various examples, the sensors for identifying the inspiratory phase of breathing include, but are not limited to, an external chest strap (such as described above) communicating transcutaneously with the signal generator, a strain gage implanted on the chest wall to measure chest expansion directly, a temperature-based flow meter (thermistor or thermocouple) implanted in the mucosa of the respiratory tract to sense airflow, impedance plethysmography utilizing permanently implanted leads, including both electrodes and sensor placed on the chest wall, or sensing directly, either through mechanical or electrical means, the firing of the intercostal muscles.
The intercostal nerve carrying afferent signals from the intercostal muscles runs parallel to the intercostal space from the sternum back around to the sympathetic chain and then to the spinal cord. An electrical lead can be placed at a variety of locations ranging from anterior to posterior. The leads can be tunneled subcutaneously to a convenient location for the signal generator after one or more electrodes are placed on one or more intercostal nerves. Lead tunnel locations include, but are not limited to subclavicular, on the abdominal wall, and on the back over the kidney. Sensor leads (such as from impedance plethysmography) could be similarly tunneled.
Some examples include accommodations for percutaneous recharging of the battery and for programming/controlling of the signal generator.
While certain embodiments of this disclosure are directed to stimulating the inspiratory muscles, such as the external intercostals, during inspiration only (“in-phase” vibrations), in other embodiments, the expiratory muscles can be stimulated, in addition to or in lieu of stimulating the inspiratory muscles. In the case of the expiratory muscles, such as the internal intercostals and/or the abdominals, “in-phase” refers to stimulation during the expiratory phase of breathing only.
As illustrated in
The electrical signal can be delivered to the electrodes 210 in accordance with selected stimulation parameters. For example, when the electrodes 210 are implanted and the signal is delivered to muscle tissue, it can be delivered at a current amplitude of up to 10 mA, a frequency of from about 0.1 Hz to about 50 Hz, and a pulsewidth of from about 0.05 milliseconds to about 5 milliseconds. The signal can be provided in bursts, timed to the patient's inspiration and/or expiration, lasting from about 0.1 seconds to about 5 seconds. When the signal is directed from an implanted electrode to neural tissue, the current amplitude can be up to about 10 mA, the frequency can range from about 1 Hz to about 100 Hz, with a pulsewidth of from about 25 microseconds to about 250 microseconds. Signal burst characteristics can be similar to those described above for muscle stimulation. Signals provided by an external electrode (e.g., placed on the patient's skin) can have a current amplitude of up to about 100 mA, a frequency of from about 0.1 Hz to about 150 Hz, a pulsewidth of from about 25 microseconds to about 1000 microseconds, and bursts having a timing and duration similar to those described above.
As discussed above, at least one advantage associated with one or more of the embodiments of the disclosed systems and methods is that they can provide the patient with relief from dyspnea. In particular embodiments that include electrical stimulation to achieve the foregoing results, the systems can be more effective, less bulky, and/or can consume less power than systems that mechanically stimulate the patient's muscles.
From the foregoing, it will be appreciated that specific embodiments of the subject technology have been described herein for purposes of illustration, but that various modifications may be made without deviating from the technology. For example, sensors other than those expressly disclosed above may be used to provide feedback to the controller. The electrodes used to provide stimulation to the patient can have any of a variety of configurations, including cuff electrodes for stimulating neural tissue, and disk-shaped electrodes for transcutaneously stimulating muscle tissue. Certain aspects of the disclosure described in the context of particular embodiments may be combined or eliminated in other embodiments. Further, while advantages associated with certain embodiments have been described in the context of those embodiments, other embodiments may also exhibit such advantages. Not all embodiments need necessarily exhibit such advantages to fall within the scope of the present technology. Accordingly, the present disclosure can include other embodiments not expressly shown or described above.
The present application claims priority to U.S. Provisional Application No. 61/098,198, filed Sep. 18, 2008 and incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61098198 | Sep 2008 | US |
