Patent Grant
11759390
Chronic respiratory diseases, such as Chronic Obstructive Pulmonary Disease (COPD), affect at least twelve million people in the United States. Chronic respiratory diseases are characterized by obstruction to airflow that interferes with normal breathing. Patients with severe chronic respiratory disease are disabled by the inability of their diseased lungs to efficiently perform gas exchange. Of those affected, over half report that symptoms impair their ability to perform activities of daily living.
COPD is a disease state where gas exchange, including both oxygen absorption and carbon-dioxide elimination, is reduced. COPD typically worsens over time, further reducing the ability of a patient's lungs to exchange gas. As a patient's disease worsens, it limits their ability to function in daily life. Once a patient's lung function drops below 30%, his or her quality of life can significantly decline, making it difficult to even walk down the street or carry things without running out of breath. Eventually, a patient will be unable to even get up and move around. At around 15% lung function, patients have extreme increased work in breathing and the disease quickly becomes non-survivable.
COPD is the third most common cause of death in the United States and the cause of a substantial economic burden on individuals and society. As explained in “The Clinical and Economic Burden of Chronic Obstructive Pulmonary Disease in the USA,” by Anthony J Guarascio, Shaunta M. Ray, Christopher K. Finch, and Timothy H. Self (published online Jun. 17, 2013), the cost of COPD in the USA was projected to be approximately $50 billion in 2010, which included $20 billion in indirect costs and $30 billion in direct health care expenditures.
It is believed that in patients with COPD, carbon dioxide aggregates form in poorly stirred alveoli. These aggregates are believed to form from weak dipole-dipole interactions between carbon dioxide molecules. Such aggregates, particularly if left undisturbed by mechanical forces, could form progressively deepening confluent layers resting on the inner surface of the alveolus, increasingly widening the diffusion barrier. Vibration of the alveoli and the gas being exchanged is known to improve gas exchange in the lung. Known devices for improving gas exchange by vibration, however, are inconvenient to use, expensive, and do not effectively vibrate both the alveoli and the gas being exchanged.
For example, a high-frequency chest wall oscillation device, such as a ThAlRaphy Vest, has been used to oscillate the chest to help gas exchange. The device is a pneumatic vest that can be placed around a patient's chest to rapidly oscillate pressure to help vibrate the alveoli to increase gas exchange. But while the pneumatic vest vibrates the alveoli, it does not significantly vibrate the gas being exchanged. Further, the tissue surrounding the chest, such as muscle and fat, dampens the oscillation, thus limiting the amount that the oscillation results in vibration of the alveoli. In addition to being uncomfortable, the pneumatic vest requires an air compressor to pneumatically drive the vest and is thus inconvenient for patients due to its lack of portability. Because of the requirement of an air compressor to drive the vest, they are typically used in hospital or clinical settings.
As an alternative, oral high-frequency oscillation devices have been developed to oscillate the air column and thus the air within the lungs. To give patients the benefit of the oscillating air column, such devices typically also require a ventilator attached to a mask that fits over the patient's face or a tube inserted in a patient's throat to provide a sealed air system. Such devices are thus uncomfortable for patients and inconvenient because a patient cannot eat, drink, or effectively talk while using the ventilator. Additionally, such devices are inconvenient because they require a compressed air source and a motor to produce oscillations that can be superimposed on top of a patient's normal breathing. Further, the effectiveness of such devices is limited because they only vibrate the gas being exchanged and do not directly vibrate the alveoli.
Known respiratory assisting devices have low portability and are invasive, uncomfortable, and expensive. Additionally, no known respiratory assisting device effectively vibrates both the alveoli and the gas being exchanged. There is a need for an improved device that facilitates lung gas exchange.
Embodiments of a lung gas exchange device are described herein by way of example. Those skilled in the art recognize that lung gas exchange devices according to the present invention are not limited to the embodiments or drawings described herein. It should be understood that the drawings and description are not intended to be limited to the particular form disclosed. Rather, the intention is to cover all modifications, equivalents and alternatives falling within the spirit and scope of the disclosed embodiments. Any headings used herein are for organizational purposes only and are not meant to limit the scope of the description or the claims. As used herein, the word “may” is used in a permissive sense (i.e., meaning having the potential to) rather than the mandatory sense (i.e., meaning must). Similarly, the words “include,” “including,” and “includes” mean including, but not limited to.
Embodiments of the present invention provide a device that vibrates a user's, such as a patient's, trachea, thus effectively vibrating both the alveoli and the gas being exchanged to improve lung function. Embodiments include a portable device that may be conveniently and non-invasively affixed to a patient's neck, thus allowing a patient to walk, talk, eat, drink, and perform other routine tasks while having improved lung function. By improving gas exchange with a portable external device, patients with severe respiratory disease will become more active and thereby improve their health.
As illustrated in
The wear plate 34 may be curved and optimally sized to focus vibration on the trachea 34. The wear plate 34 may be patient specific and formed to the contours and length of the patient's neck to maximize transfer of the vibration from the vibrating device to the patient's trachea 34. The wear plate 34 may be securely affixed to front housing 10 and the vibrating device. In some embodiments, the wear plate 34 may be removably affixed to the front housing 10 to allow for attachment of alternative wear plates. The one wear plate 24 may be made from a metal material. Alternatively, the wear plate 24 may be made of a non-rigid, semi-elastic material configured to maintain pressure from the wear plate 24 on the anterior neck of a user. In some embodiments, wear plate 24 may be made from a metal material but covered in a less rigid material to increase comfort for a patient.
The front housing 10 may include at least one control mechanism 12. In certain embodiments, the at least one control mechanism 12 may be one or more buttons. The at least one control mechanism 12 may also include one or more dials or other controls configured to allow for variable adjustments. The at least one control mechanism 12 may be connected to the front side of the front housing 10. The control mechanism 12 may include an on/off control to allow a patient to turn on or turn off the vibration device. The control mechanism 12 may also include controls to allow a user, such as a doctor, to optimally set various aspects of the vibration, such as the frequency and the amplitude. In certain embodiments, control mechanism 12 may also allow a user to control the direction or axis of vibration, or control whether the vibration is periodic, random, or follows a predetermined pattern. In some embodiments, control mechanism 12 may include a single control to allow a user, such as a patient, to turn on and off the vibration device and include an interface, such as a wired or wireless interface, to allow a user, such as a doctor, to optimally tune the vibration device for a patient.
As shown in
At least one sensor 26 may attach to the wear plate 24. The gas exchange device may include one or more of a sensor for measuring a patient's oxygen saturation, carbon dioxide in the blood stream, heart rate, respiratory rate, and temperature. Embodiments may include a memory device 100 configured to store sensor measurements over time and an interface 150, such as a wireless interface, to allow a user, such as a patient or doctor, to access saved sensor measurements. In certain embodiments, the central processing board 28 may include a wireless interface and the gas exchange device may be configured to transmit sensor measurements to an external device, such as a smartphone or personal computer, with software configured to store the sensor data.
Embodiments may also include one or more sensors 26 configured to measure movement, such as sensors for measuring location based on GPS and/or a multi-direction accelerometer. Embodiments including sensors configured to measure movement may also capture data correlating a patient's health parameters, such as heart rate, oxygen saturation, carbon dioxide level, and respiratory rate with their movement.
In certain embodiments, the vibrator may be able to self-adjust to optimize the vibration parameters to enhance vibration and gas exchange dynamically. The central processing board 28 may include feedback controls that use data from the at least one sensor 26 to alter parameters of the vibration device to maintain optimal performance. In such embodiments, central processing board 28 may include a storage device with a vibration parameters map, such as a multi-variable vibration parameters map, to allow vibration parameters to be dynamically selected based on sensor feedback.
Embodiments may include a power source 16 positioned at the posterior or a user's neck. The power source 16 may be attached to the front housing 10 via one or more straps 14. The straps 14 may be configured such that the wear plate 24 exerts firm and consistent pressure on the anterior neck 32. A connecting cable 18 may connect the front housing 10 and the components within and along the front housing 10 to the power source 16. The at least one strap 14 may include a first end and a second end. The first end of the at least one strap 14 may connect to the front cover 10 and the second end of the at least one strap 14 may connect to the power source 16. The power source 16 may be at least one battery. The power source may rest on the back of the neck 32 and serve to counterbalance the vibrator as well as allow for more tracheal contact with the vibrator wear plate and greater power capacity. In alternative embodiments, the power source 16 may be integrated within front housing 10 and both ends of one or more straps 14 may connect to the front cover 10. The power source may also include a power wire, or an adaptor to which a power wire can be connected, to allow for connection to an external power source to allow for longer run time. The external power source may be, for example, an outlet or an extended battery pack. The at least one strap 14 may be connected by fastener or the like.
The motor 20 may be of a variable speed variety. The motor 20 may act like a vibrator, providing a rotary axis 36 while an offset weight 22 may help to provide rotational momentum. Those of skill in the art understand that the vibration device may take alternative forms. For example, alternative embodiments may include linear, rather than rotational, actuation to provide an alternative direction of vibration. Embodiments may also include more than one vibration device, thereby allowing for additional control of the vibration parameters, including the frequency, amplitude, and direction of the vibration. Certain embodiments may include multiple vibration devices each mounted in an orientation selected to provide a desired direction of vibration.
In certain embodiments, additional vibrating wear plate(s) may be added to vibrate a portion of the chest bony wall, for example the sternal notch. By applying vibration directly to the bony chest wall, as opposed to the exterior of the chest where users typically have greater tissue mass, embodiments may further increase vibration of the alveoli to further improve gas transfer. An extended wear plate 38 may conform to the part of or the entire chest. In certain embodiments, at least one extended wear plate 38 may be used instead of the at least one wear plate 24. A strap loop 40 may be used with the at least one extended wear plate 38 to help secure the at least one extended wear plate 38 in the proper location. For example, straps 41 attached to strap loop 40 may extend under a user's armpits and around a user's back such that two ends of a strap attach to the strap loops 40 shown in
In certain embodiments, the posterior battery pack serves and may be constructed as to counterweight to the vibrator portion to maintain wear plate pressure against the anterior neck and chest. Additionally, there may be additional weight(s) and/or components added to the posterior compartment 130 if the battery weight is not sufficient.
It should be understood that the foregoing relates to exemplary embodiments of the invention and that modifications may be made without departing from the spirit and scope of the invention as set forth in the following claims.
This application is a Continuation of U.S. application Ser. No. 15/072,695, filed Mar. 17, 2016 which claims the benefit of U.S. Provisional Application No. 62/134,385, filed Mar. 17, 2015, the disclosure of which is incorporated herein by reference in its entirety.
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| Number | Date | Country | |
|---|---|---|---|
| 20210186804 A1 | Jun 2021 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62134385 | Mar 2015 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15072695 | Mar 2016 | US |
| Child | 17175134 | US |
