DUAL PRESSURE RESPIRATORY ASSISTANCE DEVICE
20170312475 · 2017-11-02
Assignee
Inventors
- Peter Allen Gustafson (Schoolcraft, MI, US)
- Joseph David Hudson Taylor Barnett (Lawton, MI, US)
- Stephen Chiramukathu John (Ann Arbor, MI, US)
- Hoa Tri Le (Kentwood, MI, US)
Cpc classification
A61M16/208
HUMAN NECESSITIES
A61M16/024
HUMAN NECESSITIES
A61M16/0006
HUMAN NECESSITIES
International classification
Abstract
A dual pressure respiratory assistance device including a gas source which supplies a flow of gas into an air tube having a bubbler branch and a patient branch. A first tube that is connected to the bubbler branch is at least partially submerged in a fluid. An oscillatory relief valve cycles between first and second configurations. The relief valve includes an oscillating member which captures gas released through at least one hole in the first tube when the oscillating member is in a first position. The gas in the oscillating member causes the oscillating member to rise to a second position, wherein gas is released from the oscillating member and the at least one hole is blocked when the oscillating member reaches the second position.
Claims
1. A dual pressure respiratory assistance device, comprising: a gas source which supplies a flow of gas into an air tube, wherein the air tube has a patient branch and a bubbler branch that are fluidly interconnected; a first tube fluidly connected to the bubbler branch, wherein the first tube is at least partially submerged in a fluid; and an oscillatory relief assembly including an oscillating member that is configured to capture gas released through at least one hole in the first tube when the oscillating member is in a first position, and wherein the collection of gas in the oscillating member causes the oscillating member to rise through the fluid to a second position, and wherein the gas is released from the oscillating member when the oscillating member reaches the second position, whereby the oscillatory relief assembly causes the pressure in the patient branch to cycle between at least a first pressure range and a second pressure range.
2. The dual pressure respiratory assistance device of claim 1, wherein: the oscillatory relief assembly causes the pressure in the patient branch to remain at the first and second pressures for first and second periods of time, respectively.
3. The dual pressure respiratory assistance device of claim 2, wherein: the oscillatory relief assembly transitions from the first pressure to the second pressure in a period of time that is significantly less than the first and second periods of time.
4. The dual pressure respiratory assistance device of claim 3, wherein: the first pressure range is about 10 cm H.sub.2O or less.
5. The dual pressure respiratory assistance device of claim 4, wherein: the second pressure range is about 20 cm H.sub.2O or less.
6. The dual pressure respiratory assistance device of claim 3, wherein: the first and second pressures comprise first and second median pressures, respectively, and wherein a difference between the first and second median pressures is at least 1.0 cm H.sub.2O.
7. The dual pressure respiratory assistance device of claim 6, wherein: the difference between the first and second median pressures is about 3.0 cm H.sub.2O.
8. The dual pressure respiratory assistance device of claim 6, wherein: the difference between the first and second median pressures is about 15.0 cm H.sub.2O.
9. The dual pressure respiratory assistance device of claim 2, wherein: the first period of time is about 0.3 to about 3.0 seconds, and the second period of time is about 0.6 to about 6.0 seconds.
10. The dual pressure respiratory assistance device of claim 1, wherein: the pressure in the patient branch oscillates in a periodic manner to define a frequency.
11. The dual pressure respiratory assistance device of claim 9, wherein: the pressure oscillates at about 10-50 cycles per minute.
12. The dual pressure respiratory assistance device of claim 1, wherein: the gas source supplies a flow of gas at a constant pressure.
13. The dual pressure respiratory assistance device of claim 1 wherein: the oscillating member is slidably connected to the first tube.
14. The dual pressure respiratory assistance device of claim 13, wherein: the first tube includes a vertically-extending portion; the oscillating member is slidably connected to the vertically-extending portion.
15. The dual pressure respiratory assistance device of claim 14, wherein: the oscillatory relief assembly includes a shell disposed on the first tube, wherein the shell includes at least one passageway through a sidewall of the shell whereby gas is released through the passageway when the oscillating member reaches the second position.
16. The dual pressure respiratory assistance device of claim 15, wherein: the oscillating member includes an interior space having a partial or complete enclosure disposed above or around the at least one hole in the first tube whereby gas that is released through the at least one hole in the first tube travels upwardly through the fluid into the interior space of the oscillating member.
17. The dual pressure respiratory assistance device of claim 16, wherein: gas from the gas source flows through the first tube in a downstream direction; the at least one hole in the first tube comprises at least one upstream hole; the first tube including at least one downstream hole that is downstream of the at least one upstream hole, and wherein gas released from the at least one downstream hole moves upwardly through the fluid without entering the interior space of the oscillating member.
18. The dual pressure respiratory assistance device of claim 17, including: at least one adjustable stop member that limits movement of the oscillating member when the oscillating member is in a selected one of the first and second positions.
19. A kit for converting a bubble-CPAP machine to a dual pressure respiratory assistance device, the kit comprising: a shell having a side wall and having at least one window through the side wall, wherein the shell is sized to fit around a first tube which is at least partially submerged in a fluid; and an inverted basket attachment having a top portion which fits closely around the side wall of the shell and is able to slide with respect to the shell, and an upper wall extending from the top portion, wherein the upper wall is adapted to capture gas bubbles therein and thereby adjust the buoyancy of the inverted basket attachment.
20. A method of providing respiratory assistance to a patient, comprising the steps of: initiating a gas flow into a passageway, wherein the passageway branches into a bubbler branch and a patient branch; at least partially submerging a portion of the bubbler branch of the passageway with an oscillatory relief valve disposed thereon in a container of fluid; positioning a patient air supply interface on the patient, wherein the patient air supply interface is fluidly connected to the patient branch; and wherein the oscillatory relief valve causes gas pressure within the patient branch to oscillate between first and second magnitudes.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0011] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee;
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DETAILED DESCRIPTION
[0026] For purposes of description herein the terms “upper,” “lower,” “right,” “left,” “rear,” “front,” “vertical,” “horizontal,” and derivatives thereof shall relate to the variable/dual pressure respiratory assistance device and its components as shown in the side elevation view as shown in
[0027] As shown in the embodiment depicted in
[0028] The oscillatory relief valve mechanism 32, as further described herein, allows the oscillating dual pressure air supply to be maintained through a single power source, the gas source 12, and can be used to retrofit an existing bubble-CPAP device into the dual pressure respiratory device 10 described herein. The oscillating pressure of the dual pressure respiratory assistance device 10 functions to recruit and stabilize the functional units of the lungs, the alveoli. The modulating pressures are theorized to assist the patient's breathing, as well as reminding the patient to breathe, facilitating a more rapid recovery.
[0029] As shown in more detail in the embodiment depicted in
[0030] In greater detail, as shown in the embodiments depicted in
[0031] In operation, when the basket 42 is in the first (lower) position (
[0032] As shown in the embodiment depicted in
[0033] When the basket 42 is in the second (upper) peak position (
[0034] When the circumferential holes 58 are not covered, the effective length of the vertical tube 28 is X cm, where X is the depth of the circumferential holes 58 below the surface of the fluid 30. When the holes 58 are covered by the sleeve 54, the effective length of the tube 28 is X+L cm, where L is the distance between the circumferential holes 58 and the lowest point that the air must descend before traveling upward. Because hydrostatic pressure depends on the effective submerged depth that the air must travel, this change in the effective length through movement of the sleeve 54 results in a non-constant pressure waveform, as illustrated in
[0035] By changing the depth that the vertical tube 28 is submerged in the fluid 30 the pressure of the air supplied to the patient can be changed, while maintaining the same change in amplitude of the pressure (e.g. from 8 cm H.sub.2O/5 cm H.sub.2O to 10 cm H.sub.2O/7 cm H.sub.2O). By changing the effective length of the submerged vertical tube 28, such as through adding additional or longer tubing sections between the circumferential holes 58 and the maximum depth of the vertical tube 28, the amplitude of the pressure change can also be modified, allowing conversion between a BiPAP-like functionality and a NIPPV-like functionality (e.g., changing from 8 cm H.sub.2O/5 cm H.sub.2O to 20 cm H.sub.2O/5 cm H.sub.2O). Tubes of different lengths can be readily connected between the circumferential holes 58 and the lowest point that the air travels in the tubing. Increasing or decreasing the length of the tube 28 below holes 58 permits adjustment of the length of time t.sub.1 (
[0036] With low flow rates, a single first tube 28 can be used. The horizontal tube 38 is allows a bi-level waveform when higher flow rates are provided. Horizontal tube 38 also directs bubbles exiting outlet 31 away from inverted basket 42 such that bubbles exiting outlet 31 do not enter basket 42. By increasing the weight of the basket 42, the minimum flow rate at which the horizontal tube 38 is needed to modulate the bi-level waveform can be increased. At typical flow rates, as the flow rate is increased, the difference between the peak pressure 36 mean and the baseline pressure 34 mean can be increased, to the limiting pressure difference specified by the distance L (
[0037] In one preferred embodiment, the dual pressure respiratory assistance device 10 has a frequency of 10 to 45 cycles per minute. In such an embodiment, the amplitude and the pressure range can be adjusted through the use of different lengths of pipe for the first tube 28 or various levels of fluid 30 for submerging the first tube 28.
[0038] The inverted basket 42 and sleeve 54 for use herein can be manufactured in two or more portions, and fitted together around the cylindrical shell 44. Pins or tabs can be provided to aid in alignment of the portions of the inverted basket 42, and silicon O-rings can optionally be used to seal the portions of the inverted basket 42. In alternate embodiments, the inverted basket 42 can be formed from a single piece that can be slid along the length of the first tube 28 to position the basket 42. The tolerance between the cylindrical shell 44 and the inverted basket 42 is sized to reduce friction between the opening 49 in top wall 48 and the cylindrical shell 44, while still preventing air leakage between the top wall 48 and the cylindrical shell 44 until the basket 42 has risen to the level of the windows 60 in the cylindrical shell 44. The tolerance is determined with reference to the surface tension of the fluid 30. Therefore, the surface tension of the fluid 30 can be adjusted through addition of surface acting agents or use of different fluids 30 to optimize the operation of the basket 42 around the cylindrical shell 44.
[0039] In certain preferred embodiments, kits can be prepared to convert a bubble-CPAP device to a dual pressure respiratory assistance device 10 as described herein. Such a kit can include the cylindrical shell 44, the inverted basket 42 with attached sleeve 54, and optionally a replacement first tube 28. Conversion kits can also include varying lengths of first tube 28 or vertical tube 28 attachments, as well as horizontal tube 38 and vertical return tube 40 portions. In other preferred embodiments, the first tube 28 of a traditional bubble-CPAP device can be altered by adding circumferential holes 58 therearound, and used with the cylindrical shell 44 and inverted basket 42 with attached sleeve 54.
[0040] To use the dual pressure respiratory assistance device 10 described herein, a gas flow 14 is initiated into the air tube 16 which branches into the bubbler branch 24 and the patient branch 22. The first tube 28 attached to the terminal end of the bubbler branch 24, having the oscillatory relief valve 32 disposed thereon, is at least partially submerged in a container of fluid 30. The patient air supply interface 26 attached to the terminal end of the patient branch 22 is positioned for use on the patient. The gas flow 14 through the air tube 16 actuates the oscillatory relief valve 32 as described herein, resulting in dual pressure supply of air to the patient, at a baseline pressure 34 and a peak pressure 36.
[0041] With further reference to
[0042] With further reference to
[0043] The oscillatory relief valve mechanisms described herein have a low cost of manufacture, are reliable, inexpensive to operate, and is dependent only on pressurized air for power, and not an additional electrical current. Thus, users who currently employ bubble-CPAP could use the presently disclosed dual pressure respiratory assistance device 10 without any additional power requirements. The device 10 is also optimized as an add-on for the widely used bubble-CPAP technology, which facilitates widespread use. The presently disclosed dual pressure respiratory assistance device 10 has several adjustable parameters, including: the baseline pressure 34 and peak pressure 36 (by adjusting the submerged depth of the first tube 28 and the distance between the circumferential holes 58 and the lowest point that the air must descend before turning upward); the percentage of time at the peak pressure 36 at a desired airflow rate (by adjusting the mass of the basket 42); the percentage of time at the peak pressure 36 (by adjusting the air flow rate and/or the length of the sleeve); etc. Additionally, because the device is optimized for bubble-CPAP set-ups, it also provides a hydro-oscillatory effect, the quasi-random variation of back pressure due to bubble release, which may provide an advantage to the lungs over traditional BiPAP or NIPPY.
[0044] Referring again to
[0045] Also, in the illustrated example, the peak pressure 36 is maintained for a time t.sub.1 of about 0.6 seconds, and the base pressure 34 is maintained for a time t.sub.2 of about 1.3 seconds, such that the period P is about 1.9 seconds. Time t.sub.1 is preferably about 0.3 to 3.0 seconds, and time t.sub.2 is preferably about 0.6 to 6.0 seconds. The period P corresponds to the breathing frequency in cycles per minute. The frequency may be set to meet the requirements of a particular application or needs of a specific patient. Typically, the device 10 is configured (adjusted) to provide a frequency in the range of about 10 to 50 breaths per minute. For example, the device 10 may be configured to provide 15 breaths per minute, 30 breaths per minute, or 45 breaths per minute. The ratio of time t.sub.2 at the lower pressure to the time t.sub.1, at the higher pressure is preferably about 2.0, but may be less (e.g. 1.0) or larger (e.g. 3.0, 4.0, or greater). Thus, the period P is generally about 1.3 to 2.0 seconds. The transition times Δ.sub.1 and Δ.sub.2 from base pressure 34 to peak pressure 36 and from peak pressure 36 to base pressure 34, respectively, may be small. In the illustrated example transition time's Δ.sub.1 and Δ2 are about 0.1 seconds or less. However, larger transition times Δ.sub.1 and Δ.sub.2 may also be utilized. It will be understood that the peak pressures 36, 36A, 36B, and 36C, the base pressures 34, 34A, 34B, and 34C may be adjusted as required for a particular application by adjusting the configuration of device 10 of
[0046] With further reference to
[0047] An air supply tube 96 extends vertically through basket 84, tube 88, and through lower basket 86. A vent member 98 may be fixed to the air supply tube 96. The vent member 98 does not move relative to the air supply tube 96. However, the upper basket 84, lower basket 86, and tube 88 together form a moving assembly 100 that slides vertically along air supply tube 96 in a reciprocating manner as discussed in more detail below.
[0048] Referring to
[0049] Tube 96 may include one or more openings 114 that permit gas 14 to flow from inside tube 96 into cavity 84A of upper basket 84. Additional gas 14 may flow through tube 96 downwardly into cavity 86A of lower basket 86. When sufficient fluid 30 is displaced from cavities 84A and 86A, the buoyancy causes assembly 100 to shift upwardly, thereby shifting upper basket 84 upwardly a distance “B” to an upper position 184. The gas that was previously trapped in cavity 84A and 86A then flows outwardly through windows 116 of vent member 98 as shown by the arrow 14A (
[0050] With further reference to
[0051] The tapered/conical surfaces 125 and 126 promote self alignment of the upper basket 84 relative to the vent member 98 and tube 96. Also, because the basket 184 must travel a distance “D1” (
[0052] Referring again to
[0053] In use, a physician or other user may desire to be able to control cycle time, mean airway pressure (MAP), inspiratory and expiratory pressures, and the ratio of the pressures of the inspiratory and expiratory phases of the waveform (the I:E ratio). The device 10A provides for control of cycle time, waveform, MAP and I:E ratio, and further provides for control of inspiratory and expiratory pressures.
[0054] In the device 10A, the internal volume distribution of the device (as a function of depth) can be used for precise control of waveform (e.g.
[0055] In the device 10A, the ratio of the volumes (and the I:E ratio) is controlled by movement of the threaded tube 88. As discussed above, advancing the tube 88 upwards (from the lowest referenced position which has the maximum top basket volume), the tube location traps off a portion 124 of the top volume 84A so that gas 14 cannot be captured in the portion 124. Consequently, in order to be sufficiently buoyant to lift the moving assembly 100, more gas 14 must be pushed into the lower basket 86 through air supply tube 96. The volume ratio between the baskets 84 and 86 is thus changed, as is the I:E ratio and MAP. Other ways to change the volume ratio include providing an expandable top basket 84 having threaded, sliding, etc. portions that can be moved to adjust the volume of space 84A. Leak rate and weights 110 (
[0056] Also, as discussed above, the upper and lower walls 102 and 106, respectively, of upper basket 84 are generally conical. The conical inner surfaces 102A and 106A permit escape of gas 14 upwardly and water 30 downwardly, even if device 10A is misaligned from a vertical axis.
[0057] The use of two baskets (i.e. upper basket 84 and lower basket 86) creates a waveform in which two distinct (i.e. different) pressures are created. The waveform is well controlled in a substantially square waveform. However, other waveforms are also possible. The more general form has an arbitrary volume distribution as a function of depth. The integral of area over depth (∫Adh) controls the volume displaced as a function of depth (where depth is directly related to pressure). The volume displaced, times the density of the liquid, must exceed the weight (controllable) for the movable assembly 100 to lift, vent, and start a new cycle. Because the volumetric flow rate is relatively constant, each distribution of cross sectional area (as a function of depth) has a corresponding pressure vs time waveform. Thus, the volume distribution between upper basket 84 and lower basket 86 controls the waveform.
[0058] The following is a simplified mathematical model describing functioning of the device 10A.
[0059] Assume that overall friction and drag are negligible. Assume also that the system is quasi-static and the transitions occur quickly. (This is supported by experimental data.) Defined I/E ratio (φ) as a ratio of time at the different target pressures:
[0060] The relationship between flow rate and volume may be examined. First, flow is conserved:
{dot over (V)}.sub.flowthrough={dot over (V)}.sub.totalflow−{dot over (V)}.sub.leak
[0061] As air flows into the device 10A and becomes trapped, eventually a sufficient volume of water is displaced to cause buoyancy of the device. The total volume of air in a cycle is a combination of expiratory, inspiratory, tubing, and leaks volumes given by:
V.sub.exp={dot over (V)}.sub.flowthrought.sub.exp
V.sub.insp={dot over (V)}.sub.flowthrought.sub.insp
V.sub.tube={dot over (V)}.sub.flowthrought.sub.tube
V.sub.leak={dot over (V)}.sub.leakt.sub.cycle
[0062] The total trapped air (system) volume can be related to the flow rate through the system (not leaked):
V.sub.sys={dot over (V)}.sub.flowthrought.sub.cycle
[0063] The equations can be solved for time:
[0064] Total time and system volume are sums of flow rates for the different pressures:
t.sub.cycle=t.sub.tube+t.sub.insp+t.sub.exp
V.sub.sys=V.sub.tube+V.sub.insp+V.sub.exp
[0065] Substituting the time equations (2) into the I:E ratio equation (1):
[0066] The above is a significant result; that is, that the I:E ratio is the ratio of the air volumes trapped in the two baskets 84 and 86.
[0067] Equilibrium also holds:
W−F.sub.insp−F.sub.exp=0
W−gpV.sub.insp−gpV.sub.exp=0
[0068] Where: W is weight, F.sub.insp is the buoyancy contributed by the air trapped at the inspiratory pressure depth, and F.sub.exp is the buoyancy contributed by the air trapped at the expiratory depth.
[0069] Weight is mass times gravity:
gM−gpV.sub.insp−gpV.sub.exp=0
[0070] This is solved for the volume of the inspiratory depth air:
[0071] There are two equations. The equilibrium equation (4) and the derived of I:E ratio (3). Substituting one into the other:
[0072] The above equation (5) can be solved for the expiratory volume, which can be back substituted into inspiratory trapped air volume.
[0073] Thus, for any given system mass and desired I:E ratio, the target trapped air volumes can be determined.
[0074] Control of the cycle time is also possible. This may be done by controlling mass and flow rate. Total cycle time is:
t.sub.cycle=t.sub.tube+t.sub.insp+t.sub.exp
[0075] Where t.sub.tube is the time required to fill the down tube, t.sub.insp is the time to fill the inspiratory trapped air volume, and t.sub.exp is the time to fill the expiratory trapped air volume.
[0076] The times during any given phase are:
[0077] Thus:
[0078] In the above equation, r is the radius of the down tube 96 carrying air from top basket 84 to bottom basket 86, and h is the length of the down tube 96.
[0079] Substituting volumes:
[0080] Therefore the total cycle time is:
[0081] Thus, we have three summative equations.
[0082] Recall that the primary concerns are typically I:E, h, and cycle time (the inputs) and it may be important to determine is V.sub.exp and mass (M). It is noted that inspiratory volume is typically not critical for sizing. A large inspiratory basket that is open ended at the bottom may be utilized. The inspiratory trapped air volume will be automatically established within this bottom basket (because of the equilibrium relationship between total displaced volume and mass).
[0083] It is also noted that in the above equations (6), the “flow through volume”(V.sub.flowthrough) and its time derivative “flow through rate” ({dot over (V)}.sub.flowthrough) refers to the volume that goes through the system in a cycle (exclusive of leaks), not the volume which is available for the patient. As the system can be downstream of the patient, a portion of the patient volume can be leaked intentionally to control the cycle time. Thus, a dimensionless leak rate (γ) can be defined:
[0084] The third equation thus becomes:
[0085] For the system designer/user, the three equations can be solved to obtain desirable device values:
[0086] Note that V.sub.insp is the lower limit size of the open ended bottom basket 86. The other values set the required size of top basket 84 (which is adjustable as described previously) and the mass (ballast 110 can be added).
[0087] The above analysis is simplified, and ignores friction and dynamics. However, it provides guidance to a user of the system 10A the device 10A to provide the desired outcome. As a basic validation, a physical sizing calculation can be done. Assume some clinically relevant values:
[0088] In the above assumptions, r is the ratio of the source air tube which does not contribute to buoyancy under the assumption that the source air tube continues downward to the bottom basket. This source air tube is used for alignment, and is restrained in the exemplar embodiment.
[0089] These calculated assumptions lead to calculated sizes of:
V.sub.exp=52.15 cm.sup.3
M=78.22 grams
V.sub.insp=26.07 cm.sup.3
[0090] These volumes and the mass are consistent and within reasonable margins of error with a prototype device and laboratory data.
[0091] If a device 104 has already been set up, the three equations can also be solved for expected performance.
[0092] The derived equations can be used to set up a graphical performance charts (
[0093] Thus, the ability to control volume ratios in device 10A provides control of the I:E and MAP.
[0094] It is also noted that the construction and arrangement of the elements of the devices as shown and described in the exemplary embodiments is illustrative only. Although only a few embodiments of the present innovations have been described in detail in this disclosure, those skilled in the art who review this disclosure will readily appreciate that many modifications are possible (e.g., variations in sizes, dimensions, structures, shapes and proportions of the various elements, values of parameters, mounting arrangements, use of materials, colors, orientations, etc.) without materially departing from the novel teachings and advantages of the subject matter recited.
[0095] For example, first tube 28 is configured to provide a vertical slide/guide and to provide gas that is received in basket 42 to provide oscillating movement of basket 42. However, a separate guide structure such as a vertical rod or the like (not shown) may be utilized to guide basket 42, and tube 28 does not necessarily act as a guide. Elements shown as integrally formed may be constructed of multiple parts or elements shown as multiple parts may be integrally formed, the operation of the interfaces may be reversed or otherwise varied, the length or width of the structures and/or members or connector or other elements of the system may be varied, the nature or number of adjustment positions provided between the elements may be varied. It should be noted that the elements and/or assemblies of the system may be constructed from any of a wide variety of materials that provide sufficient strength, durability, or density in any of a wide variety of colors, textures, and combinations. Accordingly, all such modifications are intended to be included within the scope of the present innovations. Other substitutions, modifications, changes, and omissions may be made in the design, operating conditions, and arrangement of the desired and other exemplary embodiments without departing from the spirit of the present innovations.
[0096] It will be understood that any described processes or steps within described processes may be combined with other disclosed processes or steps to form structures within the scope of the present device. The exemplary structures and processes disclosed herein are for illustrative purposes and are not to be construed as limiting.
[0097] It is also to be understood that variations and modifications can be made on the aforementioned structures and methods without departing from the concepts of the present device, and further it is to be understood that such concepts are intended to be covered by the following claims unless these claims by their language expressly state otherwise.
[0098] The above description is considered that of the illustrated embodiments only. Modifications of the device will occur to those skilled in the art and to those who make or use the device. Therefore, it is understood that the embodiments shown in the drawings and described above is merely for illustrative purposes and not intended to limit the scope of the device, which is defined by the following claims as interpreted according to the principles of patent law, including the Doctrine of Equivalents.