The disclosure relates to the field of prosthetic devices, and more particularly to a prosthetic device, system and method for increasing vacuum in a vacuum assisted suspension system.
With advancements in prosthetic components, improved suspension solutions have become a pressing need. Elevated vacuum suspension has been around for nearly a decade, and improves proprioception and volume control. The concept is well accepted and has gained many users.
Many known elevated vacuum solutions on the market rely solely on sleeves or reflecting liners for placement over a socket to achieve an airtight seal necessary for an effective vacuum. This mode of sealing, particularly sleeves, adds to material thickness over the knee and constrains knee bending dramatically for trans-tibial amputees.
A vacuum in the sense of elevated vacuum solutions refers to creating pressure significantly lower than atmospheric pressure. In prosthetic systems, a vacuum is not applied directly to the skin, but typically between the hard socket and the skin interface. The vacuum system is adapted to stabilize soft tissue volume at the residuum that the liner and hard socket surround and maintain more effective suspension of a prosthetic system.
A significant drawback to known elevated vacuum solutions is they fail to adapt to limb volume change which occurs particularly when a user is walking. Yet another drawback is that many known systems have a tendency to lose suction due to the method used to seal the socket and hence the vacuum formed. Many of such vacuum systems are bulky and significantly contribute to the weight of the prosthetic device, wherein the hard socket may be oversized to accommodate vacuum chambers, or additional attachments are used to supply or assist in vacuum generation.
In sleeve based systems, a sleeve is applied at the proximal end of the hard socket and the vacuum is often formed along the entirety or near entirety of residual limb covered by the hard socket. The vacuum is formed along the length of the covered residual (i.e., “above-knee” vacuum systems) and does not account for areas of the residual limb more or less prone to volume change. When the sleeve is removed, the seal is broken and the vacuum is lost. While valves may be used in combination with vacuum suspension, these solutions often lack means to quickly release the vacuum.
There is a need for a prosthetic device, system and method that provides freedom of vacuum suspension for a prosthetic system with no sleeve. There is also a call to provide a prosthetic device, system and method to minimize changes in the volume of a residual limb with vacuum suspension, providing secure vacuum without losing suction and confidence to the user over a period of use. There is a demand for applying a vacuum where it is needed, while still stabilizing volume and maintaining vacuum suspension. It is desirable for prosthetic devices to draw a vacuum while being lightweight and streamlined.
Embodiments of the prosthetic device, system and method provide the security and freedom of vacuum suspension without the sensation and restrictions of a sleeve, or the accompanying bulk and complicated features and attachments. Without a sleeve, range-of-motion can be less restricted and the vacuum can be released quickly and easily by a release valve.
The embodiments address volume fluctuation for effective volume stabilization. The embodiments have a capacity to create a distal vacuum and stabilize soft tissue volume and maintain effective suspension. By locating distal suspension, the embodiments avoid the risk of proximal vacuum leakage and any puncture issues that may arise with full vacuum systems.
The embodiments are preferably but not limited to forming a distal vacuum around the distal part of the limb to stabilize volume while creating effective and sleeveless vacuum suspension. The embodiments rely on the understanding that the distal end of the limb, where there is typically more soft tissue, is the area most susceptible to volume fluctuations and the area which requires efficient stabilization to maintain good suspension and prosthetic function. The area closer to the knee containing bones and tendons is relatively stable over the day and do not fluctuate significantly in volume, thereby removing the necessity for negative pressure to be formed throughout the entirety of the prosthetic socket.
The embodiments comprise a mechanical vacuum pump or mechanism providing vacuum assisted suspension by generating negative pressure inside a prosthetic socket worn over a residual limb, and reducing sliding movement between the liner and the socket. The function of the embodiments is automatic as it is activated during gait; the weight placed on the heel of a prosthetic foot expands the vacuum pump which efficiently draws air out from the socket in each step, and expels it into the atmosphere during swing phase as the reservoir compresses again. The pump mechanism creates a negative pressure inside the socket, resulting in secure and reliable elevated vacuum suspension. The vacuum assisted suspension enables intimate suspension as the negative pressure formed inside the socket holds the liner and residuum firmly against the socket wall.
According to an embodiment, a prosthetic system has a prosthetic foot, a pump mechanism defining first and second sides, a first member connected to the prosthetic foot and the first side of the pump mechanism, and a second member carrying the pump mechanism and engaging the prosthetic foot. The second side of the pump mechanism is connected to the second member. The first and second members are movable relative to one another upon movement of the prosthetic foot such that the pump mechanism varies in volume as the first and second members move relative to one another.
The prosthetic system includes a prosthetic socket in fluid communication with the pump mechanism and connected to the prosthetic foot. A tube connects an interior of the prosthetic socket to a first port of the pump mechanism. The pump mechanism is arranged to draw air from the prosthetic socket interior upon expansion of the pump mechanism. The pump mechanism has a second port including a one-way valve arranged for expelling air drawn from the prosthetic socket interior.
A suspension liner has a seal component adapted to engage at least an interior wall of the prosthetic socket. The seal component is located on a distal end of the suspension liner and circumferentially engages the interior wall of the prosthetic socket defining an interior of the prosthetic socket. The area distally below the seal component forms a vacuum zone within the prosthetic socket. The tube connects the prosthetic socket interior within the vacuum zone to the first port of the pump mechanism.
A valve may be secured to the socket and connect the prosthetic socket interior to the tube. The valve is arranged to permit expulsion, vacuum bypass and vacuum release.
A second end of the first member is secured to the second member, and the first member has a first end secured to the prosthetic foot, and a second end extending freely over a surface of the prosthetic foot. A compressible heel element may be connected to the second member and extend between upper and lower sections of the prosthetic foot.
According to the embodiments of the prosthetic system, a method for using the embodiments provides vacuum suspension. The method may include the steps of locating the seal component at a distal area of the suspension liner, forming a vacuum zone at a distal area of the prosthetic socket from the seal component to the distal end of the prosthetic socket, connecting the pump mechanism to the vacuum zone, and articulating the prosthetic foot to actuate the pump mechanism to draw a vacuum from the vacuum zone during gait of a user.
The method may further comprise the steps of connecting the pump mechanism to the prosthetic socket via a tube arranged for drawing a vacuum from the interior of the prosthetic socket and through a first port on the pump mechanism depending on movement of the prosthetic foot during gait, and expelling air drawn by the pump mechanism through a second port on the pump mechanism on movement of the prosthetic foot during gait.
In another embodiment, a prosthetic device is arranged for securing to a prosthetic foot. The prosthetic device includes a pump mechanism defining first and second sides, a first member arranged for securing to a prosthetic foot and connected to the first side of the pump mechanism, and a second member carrying the pump mechanism and engaging the prosthetic foot. The second side of the pump mechanism is connected to the second member. The first and second members are movable relative to one another upon movement of the prosthetic foot such that the pump mechanism varies in volume as the first and second members move relative to one another.
The pump mechanism includes first and second ports, where the first port is arranged to draw fluid due to the increase of volume of the membrane, and the second port includes a one-way valve is adapted to expel fluid upon relaxation of the membrane.
The first side of the pump mechanism may be pivotally coupled to the first member.
A compressible heel element may be securable to a prosthetic foot, and the first member extends over the heel element. A connector secures to a first side of the pump mechanism to the first member.
In an embodiment of the pump mechanism, it may include a housing having first and second ports, a fluid chamber with a volume defined by an enclosure at least partially formed from a flexible material where an upper side of the fluid chamber is in fluid communication with the first and second ports, and a connector connected to a lower side of the enclosure. A portion of the enclosure is shifted to increase the volume of the fluid chamber.
The pump mechanism may include a tube connected to the first port. The first port is arranged to draw fluid through the tube due to the increase of volume of the fluid chamber. The second port may include a one-way valve. The increase in the volume of the fluid chamber preferably occurs by deforming or extending a wall of the enclosure.
The enclosure may have two opposing walls connected by at least one side wall. The connector is formed of an insert attached to the enclosure, and may include a fastener securing to the insert. In an alternative embodiment, the connector has a pivotable coupling part.
In a variation, the housing includes an arm section having first and second ends, a plate section extending from the first end of the arm section, and a bumper secured to a second end of the arm section. The first and second ports are located over the plate section of the housing. The bumper may include a roller element.
The pump mechanism may be combined in a prosthetic system including a prosthetic component. The pump mechanism includes a connector connected to a lower side of the enclosure and the prosthetic component, such that a portion of the enclosure is shifted due to movement of the prosthetic component to increase the volume of the fluid chamber.
The prosthetic component may be a prosthetic foot. In an embodiment, a first member connects the pump mechanism to a portion of the prosthetic foot. The first member has an extending section movable relative to the prosthetic foot such that when weight of a user is applied to the prosthetic foot causing motion of the member, a portion of the enclosure is shifted to increase the volume of the fluid chamber. The first member may secure to a proximal end of the prosthetic foot, and the extending section extends freely over at least an ankle portion of a front surface of the prosthetic foot.
The embodiment may include a second member connected to the first member and extending thereover. The pump mechanism is preferably mounted to the second member and the connector mounted to the first member. The fluid chamber changes in volume between the first and second members upon action of the prosthetic foot.
According to a variation, the housing of the pump mechanism further includes an arm section having first and second ends, a plate section extending from the first end of the arm section, and a bumper secured to a second end of the arm section. The bumper is arranged to engage the prosthetic foot.
Embodiments of the disclosure are preferably arranged to apply an elevated vacuum with a sealing suspension liner, for example a seal component extending from the suspension and arranged to engage an inner wall of a socket. The embodiments preferably employ a single pump mechanism mounted on and having minimal impact on the function of a prosthetic foot.
The prosthetic device is described referring to the accompanying drawings which show preferred embodiments according to the device described. The device, system and method as disclosed in the accompanying drawings are illustrated for example only. The elements and combinations of elements described below and illustrated in the drawings can be arranged and organized differently to result in embodiments still within the spirit and scope of the device described.
A better understanding of different embodiments of the prosthetic device may be gained from the following description read with the accompanying drawings in which like reference characters refer to like elements.
While the disclosure is susceptible to various modifications and alternative constructions, certain illustrative embodiments are in the drawings and will be described below. It should be understood, however, there is no intention to limit the disclosure to the specific embodiments disclosed, but on the contrary, the intention covers all modifications, alternative constructions, combinations, and equivalents falling within the spirit and scope of the disclosure and defined by the appended claims.
It will be understood that, unless a term is expressly defined in this disclosure to possess a described meaning, there is no intent to limit the meaning of such term, either expressly or indirectly, beyond its plain or ordinary meaning.
Any element in a claim that does not explicitly state “means for” performing a specified function, or “step for” performing a specific function, is not to be interpreted as a “means” or “step” clause as specified in 35 U.S.C. §112, paragraph 6.
The embodiments of a prosthetic device will be described which form part of a vacuum system. A vacuum pump mechanism having a fluid connection with a socket assists in creating a vacuum between a residual limb and the socket by pumping fluid out of the socket. The fluid is pumped out of the socket when the user puts his weight on a prosthetic foot such as upon a heel strike. The compressive force of the heel strike causes the pump to increase the volume of a fluid chamber in the pump. The increase in volume of the pump draws in fluid from the vacuum space between the residual limb and the socket of a prosthetic limb. In this manner, the pump decreases the air pressure within the vacuum space causing a vacuum effect.
After the compressive force is removed during toe-off and the swing phase of gait, the volume of the fluid chamber in the pump is decreased. The connection between the vacuum space and the pump may have a one-way valve, so all of the air within the volume of the pump is expelled out of an outlet to another space or to atmosphere. The outlet is provided with a one-way valve so the vacuum space is the only source of air.
This method of producing a vacuum effect in the prosthetic socket is advantageous over prior methods of compressing the pump to expel air and decompressing the pump to draw in air. The method described achieves smaller fluctuations in air pressure than the prior method, so the difference between the greatest pressure and lowest pressure in the vacuum space is less in the method described compared to the prior method.
The efficiency of the pump is determined partially by how effectively the volume of the fluid chamber is reduced. Since the pump returns to the original state of zero or near-zero volume at the beginning or end of each cycle, the volume of the fluid chamber is determined by the compressive force applied to the pump. In the method described, all fluid drawn into the pump is expelled afterwards fully utilizing each cycle. The method described may be implemented using a pump that has no spring type elements which may affect the bio-mechanical function of the prosthetic device.
In the prior methods, the system relies on a complete compression of the pump in expelling air in each cycle to use the pump to its maximum capacity. It is difficult for complete compression to occur in every cycle using the gait of a user as the compressive force since the impact and displacement of the pump is not consistent and varies between users.
The vacuum suspension system also reduces volume fluctuations of the residual limb and allows for increased proprioception and reduced pistoning since there is a better attachment between the socket and the residual limb. It may also be beneficial to produce hypobaric pressure below a certain level in the socket. This may be achieved using a sealing membrane or seal component between the residual limb and the socket, instead of the conventional sealing method of using a sleeve to form an airtight connection between the residual limb and the proximal end of the socket. The sealing membrane may be on a prosthetic liner as described in U.S. Pat. No. 8,034,120 incorporated by reference and belonging to the assignee of this disclosure.
The benefit of using a liner having a seal or seal component reduces the volume of air to be drawn out of the socket and therefore, a better suspension may be achieved in a shorter time period. Using a silicone liner with integrated seal also provides the added benefit that the hypobaric region is not directly applied to the skin.
The vacuum pump mechanisms in the embodiments of the prosthetic device described are generally described as a pump mechanism. A bladder-type pump may be used in the embodiments in place of a membrane-type pump, and a skilled person would understand that the pump mechanisms described may also be used with a bladder-type pump and vice versa.
A bladder-type pump has an interior fluid chamber surrounded by an airtight material. When the interior chamber is expanded, the opposing walls are moved away from each other by extending at least one side wall of the pump. The side walls of the bladder-type pump may have an accordion-like shape or be formed of a polymeric material which allow for the increase in distance between the opposing walls.
A membrane-type pump has at least one wall of flexible material and a second opposing wall which may be rigid or flexible. The edges of the two walls are attached to each other such that when a force applies to the pump to expand the interior fluid chamber, the force deforms at least the flexible wall, and the flexible wall arcs outward to form an interior fluid chamber. To allow for deformation, the flexible wall may be made of a polymeric material including elastomeric material such as rubber or plastic.
The bladder-type pump and membrane-type pump are arranged so that when no force applies to the pump or no weight is placed on the prosthetic device the volume of the interior fluid chamber is zero or near-zero. The pumps described and shown have a cylindrical shape. A skilled person would understand that the pumps may have a variety of shapes, for example, a diamond, rectangular, or triangular shape.
The specific embodiments of the prosthetic device will now be described regarding the figures.
The pump mechanism 2 may be a bladder-type pump or a membrane-type pump as discussed above.
When a user steps, such as a heel strike, weight is placed on the heel of the foot 4 and the moveable member 12 moves away from the foot 4 pulling the attached wall and causing the volume of the internal fluid chamber of the pump mechanism 2 to increase. The increase in volume of the fluid chamber draws fluid into the interior fluid chamber. During the stance phase or toe-off, the moveable member 12 compresses the pump mechanism 2 decreasing the volume of the internal chamber and causing the pump mechanism 2 to expel fluid within the fluid chamber. The pump mechanism 2 may be fitted with one-way valves to control the direction of fluid flow so that fluid is not drawn from the atmosphere when the volume of the internal chamber is increased, and the fluid is not expelled into the socket when the pump mechanism 2 is compressed.
The vacuum pump mechanism 2 can be placed in various areas of the prosthetic foot 4 along the front of the foot. As shown in
The moveable member 12 and pieces 14, 16 may be formed of many materials including carbon fiber, plastic, and metal. The moveable member 12 may take a variety of forms including a plate, wire, or arm.
In this embodiment, as used in others, the moveable member 12 connects to the proximal end 5 of the prosthetic foot 4, whereat a connector 7 carries a male pyramid adapter 9.
A moveable member 30 is attached at one end to the prosthetic foot 4 in the midfoot area with a pivoting attachment 28, and the moveable member 30 wraps around the heel area 10 of the foot 4. The portion of the moveable member 30 located within the heel area 10 maintains contact with the heel portion of the foot 4 such that on a heel strike the heel portion of the foot 4 rotates the arm upward and pulls the rigid wall 24 causing a deformation of the flexible membrane 22. Simultaneous to the upward movement of the moveable member 30, the ankle portion of the foot 4 moves downwards.
The total deformation of the flexible membrane 22 combines the displacement of the rigid wall 24 caused by the upward movement of the moveable member 30 and the downward movement of the ankle portion to which the flexible membrane 22 is attached. The flexible membrane 22 and rigid wall 24 are simultaneously pulled away from each other, and the displacement between the bottom of the flexible membrane 22 and the rigid wall 24 corresponds to the displacement between ankle and heel portions of the prosthetic foot 4.
During displacement of the flexible membrane 22 and the rigid wall 24, a fluid chamber is formed or the volume of an existing fluid chamber is increased to draw in air through a one-way valve 26 by deforming the flexible membrane 22. In the embodiment in
Once weight is removed from the heel portion of the prosthetic foot 4, the flexible membrane 22 and rigid wall 24 move towards each other and fluid within the fluid chamber is expelled out of a one-way valve 26.
The top plate 32 is present between the ankle area and the midfoot area of the foot 4 and is partially parallel to the bottom plate 34. The top plate 32 and the bottom plate 34 meet in the midfoot area and form a firm connection at a common attachment point. The top plate 32 has two arms 42 which extend down each side of the foot 4 from the top plate 32 to the heel area of the prosthetic foot 4. A heel cylinder 36 is connected between the arms 42 and rests on the heel of the foot 4.
Similar to a previous embodiment, the vacuum pump mechanism 2 in the embodiment in
The pump mechanism 2 can be arranged at a variety of points on the front of the prosthetic foot in combination with different angles of the arms 42 to maximize the length of the displacement between the stationary position of the pump and compressed position.
The membrane used in the embodiments described can vary in thickness in different areas and in shape. The thickness of the membrane may be thicker at the portions attached to the rigid wall to create a stronger connection and greater deformation of the membrane wall. Similarly, the membrane wall may be thinner than the attachment portions to allow for greater displacement with less force. The membrane may a cylindrical shape or a tapered shape as shown in
The pump mechanism 2 in
Upon a heel strike, the interior wall 60 is deformed due to stress placed on the edges of the interior wall 60 and an interior fluid chamber is formed or expanded. The ankle and heel of the foot 4 compress the housing 46 and shift the housing 46 outwards which causes the housing 46 to push the edges of the flexible enclosure 44 outwards. Meanwhile, the anchor member 48 is firmly attached to the interior enclosure wall, preferably near the center of the interior enclosure wall, and since the interior enclosure wall remains stationary, the outward movement of housing 46 causes at least the interior wall to deform and increase the volume of an interior fluid chamber.
The compressive force on the housing 46 is provided along a first axis 56, and the resulting expansion of the fluid chamber is along a second axis 58 substantially perpendicular to the first axis 56.
The anchor member 48 preferably ends with an arm plate 50 attached to the interior enclosure wall. The arm plate 50 is semi-rigid so that once the compressive force is removed from the housing 46, the housing 46 and the flexible enclosure 44 return to their unextended state which causes the fluid drawn into the interior fluid chamber to be expelled.
The anchor member 48 may be attached to the interior wall using hooks or adhesive or some other form of mechanical connection. The arm plate 50 may be provided with hooks which attached to the interior wall of the enclosure 44. The hooks may also fit within a groove along the interior circumference of the wall such that when the housing shifts outward the hooks remain in the groove causing the attachment point of the wall to remain stationary while the edges around the interior wall shift outward.
In another embodiment, the enclosure 44 is formed of two separate opposing walls. The opposing walls are attached to each other using a mechanical connection such as a screw. A seal is formed between the opposing walls through the strength of the mechanical connection.
The flexible enclosure 44 is described as operating as a membrane-type pump, and a skilled person would understand that the flexible enclosure 44 may also be in a bladder-type pump having a reciprocating wall.
In this embodiment, the housing 46 remains stationary while the cylindrical block 54 is pushed outwards when weight applies to the heel of the foot 4. The interior flexible enclosure wall is pulled due to a pulley effect create by the outward movement of the cylindrical block 54 on the anchor member 48 to which the interior wall is attached. When the anchor member is pulled outwards, the interior wall flexes or deforms starting at the attachment point of the interior wall and the anchor member to cause the interior fluid chamber to expand. For an embodiment using a bladder pump, the interior wall may reciprocate within the housing.
The anchor member may be a cable or wire made of a flexible material such as an elastomeric material, metal, or plastic.
The sixth embodiment of the prosthetic device in
The prosthetic foot 4 has a vacuum pump mechanism 65 attached to the foot 4 through two plates 32, 34. The pump mechanism 65 is placed on a top surface 31 of top plate 32 and operable between the two plates as shown in more detail in
Similar to the third embodiment, upon a heel strike, the force on the heel of the foot 4 and a heel element 76 in the direction of arrow 96 in
As discussed, the pump mechanism 65 relies upon deformation of a membrane 22 to increase the volume of a fluid chamber located between the bottom surface of the housing 66 and the top surface of the membrane 22. The housing 66 surrounds the outer edge of the membrane 22 and creates an airtight seal with the membrane 22. The membrane and surrounding portion of the housing 66 rest within an opening in the top plate 32. The housing 66 has a lip which extends beyond the membrane 22 and surrounding portion of the housing to rest on the top surface of the top plate 32 and allows the top plate 32 to pull the housing 66 away from the membrane 22 when flexed.
The bottom surface of the housing 66 has two openings which extend into the housing to form internal passageways 84 to provide fluid communication between the internal fluid chamber and the two one-way valves 68, 70. The bottom surface of the housing 66 complements the top surface of the membrane 22 such that when no force is exerted on the pump mechanism 65 to expand the fluid chamber, the volume of the fluid chamber is zero or near-zero. As shown in
The pump mechanism 65 may be easily removed and reattached with no tools through a connector 86 on the membrane 22. The connector 86 is formed of an insert 88 having a circular end embedded in the membrane 22 and a fastener, such as a screw 90. The connector 86 anchors the membrane 22 to the bottom plate 34. The screw 90 having a circular end is used with the insert 88 to form the connector 86. The bottom plate 32 has two partially overlapping circular openings. The first circular opening is larger than the circular end of the screw 90 while the second circular opening is smaller than the circular end of the screw 90. To fixedly attach the pump mechanism 65 to the plates 32, 34 the screw 90 is inserted through the opening of the top plate 32 and then the first opening of the bottom plate 34 such that the lip of the housing 66 rests on the top plate 32. The user then slides the pump mechanism 65 into the smaller second circular opening and snaps the pump mechanism 65 into place. The insert 88 and the screw 90 may be formed of metal. Through the structure of the pump mechanism 65 and the plates 32, 34, the pump mechanism 65 has the benefit of being easily and quickly replaced.
The top plate 32 is provided with an opening 82 to enable easier flexion of the top blade near the attachment point 80. The size and shape of the opening 82 may be adjusted to change the force needed on the heel strike to flex the top plate 32. The attachment at attachment point 80 may be in a screw.
The heel element 76 is located between and attached to the two arms 42 of the top plate 32 which extend down either side of the foot 4, and the heel element 76 rests on the heel portion of the foot 4. The heel element 76 is preferably contoured such that the entirety of at least the outer edges of the bottom surface of the heel element 76 are in contact with the surface of the heel portion of the foot 4 upon which the heel element 76 rests. Through the contoured shape of the heel element 76 and the length and material of the top plate 32 and its two arms 42, the heel element 76 is held in place on the heel of the foot with no mechanical attachment between the heel element 76 and the heel of the foot.
To provide a lightweight pump mechanism 65 and pump mechanism on the prosthetic foot 4, the heel element 76 has an upper recess surrounded by raised edges 92. The raised edges 92 are formed such that the edges 92 provide a supporting surface for the curved ankle area of the foot 4. The edges 92 also control the maximum flexion of the top plate 32 and therefore, expansion of the pump mechanism 65.
As seen in
An insert, which may have an “H” shape (not shown), fits between the blades of the heel and extends between the lower recess 94 of the heel element 76 and the blades of the heel. The insert may be formed of rubber and is used to provide a uniform pressure distribution from the heel of the foot 4 to the heel element 76. If the force on heel strike is only placed on one blade of the heel, some force is distributed to the other side and blade of the heel.
The embodiments described may be used with a prosthetic socket as described in U.S. Pat. No. 6,589,289 incorporated by reference and belonging to the assignee of this disclosure.
The embodiments described may be used with a prosthetic foot as described in U.S. Pat. No. 6,969,408 incorporated by reference and belonging to the assignee of this disclosure.
The vacuum suspension system 100 provides improved proprioception and volume control. The vacuum suspension system 100 includes the pump mechanism 65, as discussed in earlier embodiments, which provides a vacuum assisted suspension by generating a negative pressure (vacuum) inside the socket 102. The function of the vacuum suspension system is fully automatic. The weight of the user is placed on the heel of the prosthetic foot 114 and expands the vacuum pump to efficiently draw air out of the socket in each step and expel it into the atmosphere during swing phase as the reservoir compresses again. The pump mechanism 65 creates a negative pressure inside the socket, resulting in a secure and reliable elevated vacuum suspension. The vacuum assisted suspension results in a secure and intimate suspension as the negative pressure formed inside the socket 102 within a vacuum zone 107 holds the liner 104 and the residuum firmly to the socket wall.
The vacuum suspension system 100 in combination with the liner 104 having a seal component 106 preferably at the proximal portion of the line allows for a transtibial amputee to move freely without pulling on the knee joint. This provides better comfort during daily activities and when sitting or driving.
The liner 104 may be of type including a seal component, preferably the liner with a seal component described in U.S. patent application publication no. 2013/0053982, published on Feb. 28, 2013, incorporated by reference, and sold as the ICEROSS SEAL-IN V LINER by Össur hf. Other liners having a seal component may likewise be used including liners disclosed in U.S. Pat. No. 7,025,793, granted on Apr. 11, 2006, U.S. Pat. No. 7,909,884, granted on Mar. 22, 2011, U.S. Pat. No. 8,034,120, granted on Oct. 11, 2011, U.S. Pat. No. 8,052,760, granted on Nov. 8, 2011, and U.S. Pat. No. 8,097,043, granted on Jan. 17, 2012, and U.S. patent application Ser. No. 13/589,415, filed on Aug. 20, 2012. Each of these references is incorporated by reference. The vacuum suspension system is not limited to the liners mentioned above, and other liners whether with or without a seal may be employed.
The shock absorption from the rotation/shock module is independent of the pump module 4 which harvests a small amount of the heel motion for efficient vacuum generation. A rotation/shock module useable with the vacuum suspension system 100 is found in at least U.S. Pat. No. 6,478,826, granted on Nov. 12, 2002, U.S. Pat. No. 6,969,408, granted on Nov. 29, 2005, and U.S. Pat. No. 7,371,262, granted on May 13, 2008, incorporated by reference and belonging to the assignee of this disclosure. A commercial example of the foot and shock module may be the RE-FLEX SHOCK or RE-FLEX ROTATE sold by Össur hf of Reykjavik, Iceland.
A second ring or gasket 132 and a third ring or gasket 134 are inserted into an interior groove 154 on a valve outer housing 136. A check valve 144 is inserted into an aperture 156 on the valve outer housing 136 and is interlocked with a tube connector 146.
The valve foam 138, screw 140 and valve insert 142 are used for mounting the valve 108 onto a socket. While the valve foam 138 and screw 140 may be removed after the socket is formed, the valve insert 142 remains on the socket and is used for coupling the valve 108 thereto. The shaft 148 of the valve inner housing 130 extends through an opening 158 of the valve insert 142 and into the socket 102 for fluid communication therewith for forming the vacuum.
The valve inner housing 130 is inserted into the valve outer housing 136. This arrangement of the valve outer housing 136 in combination with the gaskets used therewith is that the valve inner housing 130 and associated parts can be tightened or rotated regardless of the direction of the valve outer housing 136. The valve outer housing 136 can rotate relative to the socket with no loss of vacuum. This allows for accommodating any movement from the tube 110 coupled to the pump module 4 and the prosthetic foot 114.
As exemplified in
As shown in
One will understand that the vacuum of this embodiment can be opposite of that of the embodiment depicted in
In
The embodiments described may be used with a pressure regulator to insure the safety and comfort of the user which may be achieved using mechanical and/or electronic methods known in the industry.
While the foregoing embodiments have been described and shown, alternatives and modifications of these embodiments, such as those suggested by others, may be made to fall within the scope of the invention. The principles described may be extended to other types of prosthetic or orthopedic devices.
Number | Name | Date | Kind |
---|---|---|---|
708685 | White | Sep 1902 | A |
980457 | Toles | Jan 1911 | A |
1288803 | Beck | Dec 1918 | A |
1586015 | Underwood | May 1926 | A |
2424278 | Kunkel | Jul 1947 | A |
2464443 | Ganoe et al. | Mar 1949 | A |
2530285 | Catranis | Nov 1950 | A |
2533404 | Sharp et al. | Dec 1950 | A |
2606325 | Nielson et al. | Aug 1952 | A |
2664572 | Blevens | Jan 1954 | A |
2671225 | Schoene et al. | Mar 1954 | A |
2696010 | Robinson | Dec 1954 | A |
2696011 | Galdik | Dec 1954 | A |
2790180 | Hauser | Apr 1957 | A |
2808593 | Anderson | Oct 1957 | A |
3253600 | Scholl | May 1966 | A |
3322873 | Hitchcock | May 1967 | A |
3377416 | Kandel | Apr 1968 | A |
3557387 | Ohlenbusch et al. | Jan 1971 | A |
3631542 | Potter | Jan 1972 | A |
3712298 | Snowdon et al. | Jan 1973 | A |
3732578 | Pollack | May 1973 | A |
3751733 | Fletcher et al. | Aug 1973 | A |
3806958 | Gusev | Apr 1974 | A |
3858379 | Graves et al. | Jan 1975 | A |
3889301 | Bonner, Sr. | Jun 1975 | A |
3895405 | Edwards | Jul 1975 | A |
3922727 | Bianco | Dec 1975 | A |
3975350 | Hudgin et al. | Aug 1976 | A |
3991424 | Prahl | Nov 1976 | A |
4010052 | Edwards | Mar 1977 | A |
4106745 | Carrow | Aug 1978 | A |
4133776 | Pruett et al. | Jan 1979 | A |
4282325 | Rubenstein et al. | Aug 1981 | A |
4283800 | Wilson | Aug 1981 | A |
4314398 | Pettersson | Feb 1982 | A |
4381768 | Erichsen et al. | May 1983 | A |
4404296 | Schapel | Sep 1983 | A |
4456642 | Burgdorfer et al. | Jun 1984 | A |
4466936 | Schapel | Aug 1984 | A |
4479272 | Beldzisky | Oct 1984 | A |
4623354 | Childress et al. | Nov 1986 | A |
4634446 | Kristinsson | Jan 1987 | A |
4635626 | Lerman | Jan 1987 | A |
4655779 | Janowiak | Apr 1987 | A |
4704129 | Massey | Nov 1987 | A |
4822371 | Jolly et al. | Apr 1989 | A |
4828325 | Brooks | May 1989 | A |
4888829 | Kleinerman et al. | Dec 1989 | A |
4908037 | Ross | Mar 1990 | A |
4923475 | Gosthnian et al. | May 1990 | A |
5007937 | Fishman et al. | Apr 1991 | A |
5108455 | Telikicherla | Apr 1992 | A |
5108456 | Coonan, III | Apr 1992 | A |
5133776 | Crowder | Jul 1992 | A |
5139523 | Paton et al. | Aug 1992 | A |
5163965 | Rasmusson et al. | Nov 1992 | A |
5201774 | Greene | Apr 1993 | A |
5211667 | Danforth | May 1993 | A |
5221222 | Townes | Jun 1993 | A |
5258037 | Caspers | Nov 1993 | A |
5314497 | Fay et al. | May 1994 | A |
5353525 | Grim | Oct 1994 | A |
5362834 | Schapel et al. | Nov 1994 | A |
5376129 | Faulkner et al. | Dec 1994 | A |
5376131 | Lenze et al. | Dec 1994 | A |
5376132 | Caspers | Dec 1994 | A |
5397628 | Crawley et al. | Mar 1995 | A |
5405407 | Kodama et al. | Apr 1995 | A |
5480455 | Norvell | Jan 1996 | A |
5490537 | Hill | Feb 1996 | A |
5507834 | Laghi | Apr 1996 | A |
5534034 | Caspers | Jul 1996 | A |
5549709 | Caspers | Aug 1996 | A |
5555216 | Drouot | Sep 1996 | A |
5571208 | Caspers | Nov 1996 | A |
5593454 | Helmy | Jan 1997 | A |
D379845 | Lee | Jun 1997 | S |
5658353 | Layton | Aug 1997 | A |
5658354 | Norvell | Aug 1997 | A |
5702488 | Wood et al. | Dec 1997 | A |
5702489 | Slemker | Dec 1997 | A |
5709017 | Hill | Jan 1998 | A |
5728166 | Slemker | Mar 1998 | A |
5728167 | Lohmann | Mar 1998 | A |
5728168 | Laghi et al. | Mar 1998 | A |
5728169 | Norvell | Mar 1998 | A |
5728170 | Becker et al. | Mar 1998 | A |
5732578 | Kang | Mar 1998 | A |
5735906 | Caspers | Apr 1998 | A |
5807303 | Bays | Sep 1998 | A |
5830237 | Kania | Nov 1998 | A |
5846063 | Lakic | Dec 1998 | A |
5888216 | Haberman | Mar 1999 | A |
5888230 | Helmy | Mar 1999 | A |
5888231 | Sandvig et al. | Mar 1999 | A |
5904721 | Henry et al. | May 1999 | A |
5904722 | Caspers | May 1999 | A |
5931872 | Lohmann | Aug 1999 | A |
5944760 | Christensen | Aug 1999 | A |
5980577 | Radis et al. | Nov 1999 | A |
5984972 | Huston et al. | Nov 1999 | A |
6007582 | May | Dec 1999 | A |
6063125 | Arbogast et al. | May 2000 | A |
6066107 | Habermeyer | May 2000 | A |
D429335 | Caspers et al. | Aug 2000 | S |
6117117 | Mauch | Sep 2000 | A |
6149691 | Fay et al. | Nov 2000 | A |
6231616 | Helmy | May 2001 | B1 |
6231617 | Fay | May 2001 | B1 |
6273918 | Yuhasz et al. | Aug 2001 | B1 |
6287345 | Slemker et al. | Sep 2001 | B1 |
6296669 | Thorn et al. | Oct 2001 | B1 |
6334876 | Perkins | Jan 2002 | B1 |
6361568 | Hoerner | Mar 2002 | B1 |
6362387 | Carlson et al. | Mar 2002 | B1 |
6402788 | Wood et al. | Jun 2002 | B1 |
6406499 | Kania | Jun 2002 | B1 |
6478826 | Phillips et al. | Nov 2002 | B1 |
6508842 | Caspers | Jan 2003 | B1 |
6544292 | Laghi | Apr 2003 | B1 |
6554868 | Caspers | Apr 2003 | B1 |
6589289 | Ingimarsson | Jul 2003 | B2 |
6602295 | Doddroe et al. | Aug 2003 | B1 |
6613096 | Shirvis | Sep 2003 | B1 |
6626952 | Janusson et al. | Sep 2003 | B2 |
6645253 | Caspers | Nov 2003 | B2 |
6673117 | Soss et al. | Jan 2004 | B1 |
6702858 | Christensen | Mar 2004 | B2 |
6706364 | Janusson et al. | Mar 2004 | B2 |
6726726 | Caspers | Apr 2004 | B2 |
6761742 | Caspers | Jul 2004 | B2 |
6767370 | Mosler et al. | Jul 2004 | B1 |
6797008 | Arbogast et al. | Sep 2004 | B1 |
D499794 | Comer | Dec 2004 | S |
6855170 | Gramnas | Feb 2005 | B2 |
6863695 | Doddroe et al. | Mar 2005 | B2 |
6926742 | Caspers et al. | Aug 2005 | B2 |
6964688 | Kania | Nov 2005 | B1 |
6969408 | Lecomte et al. | Nov 2005 | B2 |
6974484 | Caspers | Dec 2005 | B2 |
7025792 | Collier | Apr 2006 | B2 |
7025793 | Egilsson | Apr 2006 | B2 |
D526046 | Lin | Aug 2006 | S |
7255131 | Paper et al. | Aug 2007 | B2 |
7371262 | Lecomte et al. | May 2008 | B2 |
7427297 | Patterson et al. | Sep 2008 | B2 |
7448407 | Alley et al. | Nov 2008 | B2 |
7468079 | Collier | Dec 2008 | B2 |
7686848 | Christensen | Mar 2010 | B2 |
7744653 | Rush et al. | Jun 2010 | B2 |
D634813 | Hernandez, IV | Mar 2011 | S |
7909884 | Egilsson et al. | Mar 2011 | B2 |
7922775 | Caspers | Apr 2011 | B2 |
7947085 | Haines et al. | May 2011 | B2 |
D639825 | Murakami et al. | Jun 2011 | S |
7993413 | Perkins et al. | Aug 2011 | B2 |
8007543 | Martin | Aug 2011 | B2 |
8034120 | Egilsson et al. | Oct 2011 | B2 |
8052760 | Egilsson et al. | Nov 2011 | B2 |
8080065 | Scussel et al. | Dec 2011 | B2 |
8097043 | Egilsson | Jan 2012 | B2 |
8097766 | Carlson et al. | Jan 2012 | B2 |
8114167 | Caspers | Feb 2012 | B2 |
D655393 | Whitaker | Mar 2012 | S |
D656223 | Cronje et al. | Mar 2012 | S |
8298294 | Kaltenborn et al. | Oct 2012 | B2 |
8317876 | Mosler | Nov 2012 | B2 |
8343233 | Perkins et al. | Jan 2013 | B2 |
D675714 | Nguyen | Feb 2013 | S |
D681782 | Bohm et al. | May 2013 | S |
8523951 | Kania | Sep 2013 | B2 |
D691240 | Iranyi et al. | Oct 2013 | S |
D691701 | Iranyi et al. | Oct 2013 | S |
D691702 | Iranyi et al. | Oct 2013 | S |
D691703 | Iranyi et al. | Oct 2013 | S |
D702320 | Pifer | Apr 2014 | S |
8956422 | Halldorsson | Feb 2015 | B2 |
8961618 | Lecomte et al. | Feb 2015 | B2 |
9044348 | Halldorsson et al. | Jun 2015 | B2 |
9066822 | Caldwell et al. | Jun 2015 | B2 |
9072617 | Halldorsson et al. | Jul 2015 | B2 |
9198790 | Babkes et al. | Dec 2015 | B2 |
20010005798 | Caspers | Jun 2001 | A1 |
20010016781 | Caspers | Aug 2001 | A1 |
20020087215 | Caspers | Jul 2002 | A1 |
20020091449 | Caspers et al. | Jul 2002 | A1 |
20020103545 | Arbogast et al. | Aug 2002 | A1 |
20020128580 | Carlson et al. | Sep 2002 | A1 |
20030191539 | Caspers | Oct 2003 | A1 |
20040024322 | Caspers | Feb 2004 | A1 |
20040030411 | Caspers | Feb 2004 | A1 |
20040064195 | Herr | Apr 2004 | A1 |
20040122528 | Egilsson | Jun 2004 | A1 |
20040163278 | Caspers et al. | Aug 2004 | A1 |
20040181290 | Caspers | Sep 2004 | A1 |
20040236434 | Carstens | Nov 2004 | A1 |
20040260403 | Patterson et al. | Dec 2004 | A1 |
20050131324 | Bledsoe | Jun 2005 | A1 |
20050131549 | Caspers | Jun 2005 | A1 |
20050143838 | Collier | Jun 2005 | A1 |
20050240282 | Rush et al. | Oct 2005 | A1 |
20050267603 | Lecomte et al. | Dec 2005 | A1 |
20060212130 | Collier | Sep 2006 | A1 |
20060212131 | Curtis | Sep 2006 | A1 |
20070005149 | Egilsson et al. | Jan 2007 | A1 |
20070043316 | Carlson et al. | Feb 2007 | A1 |
20070055383 | King | Mar 2007 | A1 |
20070112440 | Perkins et al. | May 2007 | A1 |
20070196222 | Mosler et al. | Aug 2007 | A1 |
20070204487 | Clough | Sep 2007 | A1 |
20080086218 | Egilsson | Apr 2008 | A1 |
20080243266 | Haynes et al. | Oct 2008 | A1 |
20080269911 | Street et al. | Oct 2008 | A1 |
20080269912 | Gobbers et al. | Oct 2008 | A1 |
20090036998 | Finlinson et al. | Feb 2009 | A1 |
20090132056 | Kania | May 2009 | A1 |
20090157196 | Danzig et al. | Jun 2009 | A1 |
20090198346 | Perkins et al. | Aug 2009 | A1 |
20090204229 | Mosler et al. | Aug 2009 | A1 |
20100070051 | Carstens | Mar 2010 | A1 |
20100087931 | Bogue | Apr 2010 | A1 |
20100106260 | Phillips | Apr 2010 | A1 |
20100262261 | Laghi | Oct 2010 | A1 |
20100312359 | Caspers | Dec 2010 | A1 |
20100312360 | Caspers | Dec 2010 | A1 |
20100331749 | Powaser | Dec 2010 | A1 |
20110035027 | McCarthy | Feb 2011 | A1 |
20110060421 | Martin et al. | Mar 2011 | A1 |
20110071649 | McKinney | Mar 2011 | A1 |
20110087142 | Ravikumar et al. | Apr 2011 | A1 |
20110130846 | Kampas et al. | Jun 2011 | A1 |
20110202143 | Caspers | Aug 2011 | A1 |
20110270413 | Haynes | Nov 2011 | A1 |
20110295386 | Perkins et al. | Dec 2011 | A1 |
20120000092 | Ingvarsson et al. | Jan 2012 | A1 |
20120035520 | Ingimundarson et al. | Feb 2012 | A1 |
20120123559 | Mosler et al. | May 2012 | A1 |
20120173000 | Caspers | Jul 2012 | A1 |
20120173001 | Caspers | Jul 2012 | A1 |
20120191217 | Mackenzie | Jul 2012 | A1 |
20130053982 | Halldorsson | Feb 2013 | A1 |
20130096694 | Caldwell et al. | Apr 2013 | A1 |
20130211544 | Jonsson et al. | Aug 2013 | A1 |
20130282142 | Perkins et al. | Oct 2013 | A1 |
20130289741 | Halldorsson et al. | Oct 2013 | A1 |
20140249648 | Sandahl | Sep 2014 | A1 |
20160120665 | Muller | May 2016 | A1 |
Number | Date | Country |
---|---|---|
670631 | Jul 1996 | AU |
675 386 | May 1966 | BE |
2 098 945 | Jul 1997 | CA |
1946358 | Apr 2007 | CN |
1989342 | Jun 2007 | CN |
101815870 | Aug 2010 | CN |
685 861 | Dec 1939 | DE |
745 981 | May 1944 | DE |
27 12 342 | Sep 1977 | DE |
27 29 800 | Jan 1979 | DE |
32 21 920 | Apr 1983 | DE |
42 17 877 | Dec 1992 | DE |
43 21 182 | Dec 1994 | DE |
94 18 210 | Jan 1995 | DE |
94 19 211 | Feb 1995 | DE |
94 17 913 | Mar 1995 | DE |
299 05 020 | Jul 1999 | DE |
29823435 | Jul 1999 | DE |
0 019 612 | Nov 1980 | EP |
0 057 838 | Aug 1982 | EP |
0 057 839 | Aug 1982 | EP |
0 086 147 | Aug 1983 | EP |
0 261 884 | Mar 1988 | EP |
0 320 170 | Jun 1989 | EP |
0 363 654 | Apr 1990 | EP |
0 631 765 | Jan 1995 | EP |
0 650 708 | May 1995 | EP |
0 870 485 | Oct 1998 | EP |
1 509 176 | Mar 2005 | EP |
1 875 881 | Jan 2008 | EP |
2816978 | Dec 2014 | EP |
1 135 516 | Apr 1957 | FR |
1 532 625 | Jul 1968 | FR |
2 420 035 | Oct 1979 | FR |
2 501 999 | Sep 1982 | FR |
136 504 | Dec 1919 | GB |
267 988 | Mar 1927 | GB |
2 069 847 | Sep 1981 | GB |
2 149 309 | Jun 1985 | GB |
7155343 | Jun 1995 | JP |
1771722 | Oct 1992 | RU |
1812982 | Apr 1993 | RU |
1821177 | Jun 1993 | RU |
8801686 | Mar 1989 | SE |
1667855 | Aug 1991 | SU |
8400881 | Mar 1984 | WO |
9505792 | Mar 1995 | WO |
9621405 | Jul 1996 | WO |
9804218 | Feb 1998 | WO |
9855055 | Dec 1998 | WO |
9905991 | Feb 1999 | WO |
9965434 | Dec 1999 | WO |
0003665 | Jan 2000 | WO |
0074611 | Dec 2000 | WO |
0154631 | Aug 2001 | WO |
0170147 | Sep 2001 | WO |
0226158 | Apr 2002 | WO |
02065958 | Aug 2002 | WO |
02067825 | Sep 2002 | WO |
02080813 | Oct 2002 | WO |
03077797 | Sep 2003 | WO |
03099173 | Dec 2003 | WO |
03099188 | Dec 2003 | WO |
2005039444 | May 2005 | WO |
2005105000 | Nov 2005 | WO |
2006012820 | Feb 2006 | WO |
2010141960 | Dec 2010 | WO |
2011035099 | Mar 2011 | WO |
2012010309 | Jan 2012 | WO |
2012177965 | Dec 2012 | WO |
2014194998 | Dec 2014 | WO |
Entry |
---|
Chinese Examination Report from Chinese Application No. 201380022874.0, Aug. 25, 2015. |
International Search Report from corresponding International PCT Application No. PCT/US2015/037204, Sep. 25, 2015. |
International Search Report from corresponding PCT Application No. PCT/US2016/033915, Jul. 29, 2016. |
International Search Report and Written Opinion from corresponding International PCT Application No. PCT/US2014/019218, May 9, 2014. |
International Search Report from PCT Application No. PCT/US2015/044434, Oct. 8, 2015. |
International Search Report from PCT Application No. PCT/US2015/041089, Oct. 5, 2015. |
International Search Report from PCT Application No. PCT/US2016/012215, May 23, 2016. |
International Search Report from PCT Application No. PCT/US2016/033707, Jul. 29, 2016. |
Brochure, “Sometimes Less is More, Harmony P3” Otto Bock, 12 pages. Available at, http://www.ottobock.com/cps/rde/xbcr/ob—es/646A303-EN-01-1001w.pdf, dated 2012. |
Information Guide, “Harmony Users Guide Otto Bock, 9 pages, available at http://media.ottobock.com/Prosthetics/Socket-Technologies/Harmony/—Genreal/Files/12072403.1—OB-Harmony-UsersGuide-9-10-12.pdf”, dated 2012. |
Brochure,“Harmony Certification Course Manual, Original Harmony Pump, 42 pages. Availiable at, http://academy.ottobockus.com/videos/harmony/data/downloads/harmony%20course%20manual%202013.pdf.” Dated 2013. |
Brochure, Harmony P2 & Hd, 2 pages. Available at http://www.ottobock.com/cps/rde/xchg/ob—us—en/hs.xsl/14904.html?id=4641. Dated 2012. |
International Search Report from corresponding PCT Application No. PCT/US2013/025849, Jun. 4, 2013. |
International Search Report and Written Opinion Regarding Application No. PCT/US2013/038668, Aug. 7, 2013. |
Haberman, Louis J., “Silicone-Only Suspension (SOS) with Socket-Loc and the Ring for the Lower Limb”, found at, http://www.oandp.org/jpo/library/1995—01—002.asp. Journal of Prosthetics and Orthotics 1995; vol. 7, No. 1, p. 2, 19 pages, dated 2012. |
Number | Date | Country | |
---|---|---|---|
20150282954 A1 | Oct 2015 | US |
Number | Date | Country | |
---|---|---|---|
61762097 | Feb 2013 | US | |
61683245 | Aug 2012 | US | |
61640056 | Apr 2012 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 13873315 | Apr 2013 | US |
Child | 14743340 | US |