All patents, patent applications and publications cited herein are hereby incorporated by reference in their entirety. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art as known to those skilled therein as of the date of the invention described and claimed herein.
This patent disclosure contains material that is subject to copyright protection. The copyright owner has no objection to the facsimile reproduction by anyone of the patent document or the patent disclosure as it appears in the U.S. Patent and Trademark Office patent file or records, but otherwise reserves any and all copyright rights.
This application claims the benefit of the filing of U.S. Provisional Patent Application No. 63/463,857 filed on May 3, 2023, which is incorporated by reference herein.
The present disclosure relates to orthopedic devices and related methods of use. More specifically, the present disclosure relates to devices and methods to alleviate detrimental changes in gait patterns that are frequently observed following surgery or injury.
Treatment of and recovery from orthopedic injuries or orthopedic procedures such as knee surgery present significant medical challenges, particularly in light of changes in a subject's gait that can be observed following the injury or procedure.
Of particular importance are the effects of the injury or procedure on the “loading response” phase of a subject's gait cycle. Briefly, the loading response phase occurs at the point in the gait cycle when the heel of the leading foot touches the ground, and the weight of the body begins to shift to a single leg. As this phase progresses, the leading foot rocks forward along the heel, and the foot flattens to make full contact with the ground, allowing for a wide base of support. During a normal gait cycle, the knee on the leading foot flexes to a certain degree to absorb the shock of impact as weight is shifted to the leading leg. As such, the loading response phase is critical for establishing a stable base of support and preparing the body for the propulsion phase of the gait cycle.
Pain or mechanical instability following a knee injury or a medical procedure involving the knee often disrupts this important phase. Namely, subjects suffering from such a condition tend to exhibit reduced knee flexion during the loading response phase. For example, one study has shown that, following a knee injury, subjects can develop “quadriceps avoidance” or a “stiffening strategy” that is characterized by a knee flexion angle of under 15° during the loading response phase. See Park et al. Knee Surgery & Related Research (2021) 33:45. This stiffening strategy is used to reduce pain and discomfort by shifting body weight towards the unaffected leg to minimize weight on the affected leg.
However, the quadriceps avoidance gait can lead to several complications, including, but not necessarily limited to, muscle atrophy, joint stiffness, and altered gait mechanics. Such a stiffening strategy can delay healing of the injured knee and reduce blood flow to the injured area. Compensatory gait mechanics following injury can also contribute to reduced confidence and fear of reinjury, which can further delay healing and delay the individual's ability to return to their normal activities and daily life.
As such, there is a significant need for methods and devices that promote a normal gait pattern and faster healing during recovery from a knee injury.
The problems expounded above, as well as others, are addressed by the following inventions, although it is to be understood that not every embodiment of the inventions described herein will address each of the problems described above.
In one aspect, an orthopedic device for offloading weight from a subject's knee is disclosed. Certain embodiments comprise a continuous main shaft that further comprises a superior vertical extension, a curved portion, and an inferior vertical extension. In one embodiment, the curved portion is disposed between the superior vertical extension and the inferior vertical extension. The curved portion can comprise a substantially parabolic shape.
In embodiments, the superior vertical extension and the inferior vertical extension are colinear with one another along the vertical axis of the orthopedic device.
In various embodiments, the curved portion comprises a degree of curvature that is substantially equal to at least the minimum knee flexion angle that is observed during the loading phase of the normal human gait cycle. The curved portion can comprise a degree of curvature that is substantially equal to at least the maximum knee flexion angle that is observed during the loading phase of the normal gait cycle. In some embodiments, the curved portion comprises a radius of curvature of between about 10 inches and about 20 inches. The radius of curvature can be about 14 inches. In some embodiments, the curved portion comprises a longitudinal length, and the curved portion is defined by a plurality of bends along the longitudinal length of the curved portion. At least one of the plurality of bends has an angle of between about 20° to about 25°. In one embodiment, at least one of the plurality of bends is a 22° bend that has an angle of about 22°. The 22° bend can comprise a plurality of minor angular changes. At least one of the plurality of minor angular changes can comprise an angle of about 7.33°. In an embodiment, the plurality of minor angular changes comprises at least six minor angular changes.
In various embodiments, the orthopedic device further comprises a handle portion, a foot, or a combination thereof, wherein the handle portion is disposed along at least a portion of the superior vertical extension and the foot is disposed along the bottommost portion of the inferior vertical extension. The handle portion can comprise a grip and a handle shaft. In embodiments, the handle shaft further comprises one or more adjustment positions that are configured to permit adjustment of the longitudinal length of the orthopedic device along its vertical axis.
Another aspect of the present disclosure relates to a method of off-loading weight from a subject's knee wherein the subject is afflicted with a knee condition. In various embodiments, the method comprises providing the subject with any of the orthopedic device embodiments disclosed herein and instructing the subject to utilize the orthopedic device for a given amount of time.
Yet another aspect relates to a method of promoting a normal gait cycle in a subject afflicted with a knee condition, comprising providing the subject with any of the orthopedic devices disclosed herein and instructing the subject to utilize the orthopedic device for a given amount of time.
In various embodiments, the knee condition comprises an anterior cruciate ligament injury, a medial collateral ligament injury, a meniscus tear, patellar tendinitis, chondromalacia patellae, osteoarthritis of the knee, rheumatoid arthritis of the knee, bursitis, patellofemoral pain syndrome, iliotibial band syndrome, a surgical procedure involving the knee, an infection of the knee, or a combination thereof.
Other objects and advantages of this invention will become readily apparent from the ensuing description.
Certain illustrations, charts, or flow charts are provided to allow for a better understanding of the present invention. It is to be noted, however, that the drawings illustrate only selected embodiments and are therefore not to be considered limiting of scope. Additional and equally effective embodiments and applications of the present invention exist.
Detailed descriptions of one or more preferred embodiments are provided herein. It is to be understood, however, that the present invention may be embodied in various forms. Therefore, specific details disclosed herein are not to be interpreted as limiting, but rather as a basis for the claims and as a representative basis for teaching one skilled in the art to employ the present invention in any appropriate manner.
The singular forms “a”, “an” and “the” include plural reference unless the context clearly dictates otherwise. The use of the word “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “one or more than one.”
Wherever any of the phrases “for example,” “such as,” “including” and the like are used herein, the phrase “and without limitation” is understood to follow unless explicitly stated otherwise. Similarly, “an example,” “exemplary” and the like are understood to be nonlimiting.
The term “substantially” allows for deviations from the descriptor that do not negatively impact the intended purpose. Descriptive terms are understood to be modified by the term “substantially” even if the word “substantially” is not explicitly recited. Therefore, for example, the phrase “wherein the lever extends vertically” means “wherein the lever extends substantially vertically” so long as a precise vertical arrangement is not necessary for the lever to perform its function.
The terms “comprising” and “including” and “having” and “involving” (and similarly “comprises”, “includes,” “has,” and “involves”) and the like are used interchangeably and have the same meaning. Specifically, each of the terms is defined consistent with the common United States patent law definition of “comprising” and is therefore interpreted to be an open term meaning “at least the following,” and is also interpreted not to exclude additional features, limitations, aspects, etc. Thus, for example, “a process involving steps a, b, and c” means that the process includes at least steps a, b, and c. Wherever the terms “a” or “an” are used, “one or more” is understood, unless such interpretation is nonsensical in context.
As used herein the term “about” is used herein to mean approximately, roughly, around, or in the region of. When the term “about” is used in conjunction with a numerical range, it modifies that range by extending the boundaries above and below the numerical values set forth. In general, the term “about” is used herein to modify a numerical value above and below the stated value by a variance of 20 percent up or down (higher or lower)
For purposes of the present disclosure, it is noted that spatially relative terms, such as “up,” “down,” “right,” “left,” “beneath,” “below,” “lower,” “above,” “upper” and the like, can be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. It will be understood that the spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is turned over or rotated, elements described as “below” or “beneath” other elements or features would then be oriented “above” the other elements or features. Thus, the exemplary term “below” can encompass both an orientation of above and below. The device can be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly.
The terms “subject” and “patient,” as used herein, can be used interchangeably and include any individual who suffers from is likely to suffer from a knee injury or knee condition.
The term “condition,” whether inflicted via a surgical procedure or naturally from an environmental occurrence or genetic predisposition, as used herein can mean any wound, injury, pathology, infection, infirmity, malady, or any other ailment, particularly those affecting at least one knee of a subject. By way of non-limiting example, the presently disclosed orthopedic device can be used to assist with or promote recovery from any one or more of the following knee conditions: anterior cruciate ligament (ACL) injury, medial collateral ligament (MCL) injury, meniscus tear, patellar tendinitis, chondromalacia patellae, osteoarthritis of the knee, rheumatoid arthritis of the knee, bursitis, patellofemoral pain syndrome, iliotibial band syndrome, a surgical procedure involving the knee, and an infection of the knee.
As used herein, the phrase “injured leg” refers to the subject's leg that is afflicted with a knee condition or any other injury or condition that may be located on the leg of a subject.
Disclosed herein is an orthopedic device configured to promote normal walking gait following an injury or surgical procedure involving a subject's knee. Embodiments of the present disclosure provide ongoing and continuous support to a subject while avoiding the deleterious effects of compensatory gait mechanisms that are typically observed in subjects suffering from a knee condition. The orthopedic device disclosed herein can be configured to permit external bracing that compensates for an internal deficit of the knee in a subject who suffers from a knee condition. In embodiments, the device is configured to offload weight or pressure from a subject's injured knee while permitting the patient to ambulate with a normal working pattern to promote healing and recovery from the knee condition. Embodiments of the orthopedic device comprise a curved portion that is designed to mimic the expected maximum knee flexion angle that is typically observed during the end of the loading phase of a healthy individual's normal gait cycle.
Generally speaking, the presently disclosed orthopedic device offers the advantage of providing external bracing to address the internal deficit of an injured knee. This, in turn, facilitates early initiation of strength training and promotes a healthy, more controlled gait. In various exemplary embodiments, the presently disclosed orthopedic device allows for greater force absorption, as the curvature of the main shaft transfers impact forces from the tip, foot, or boot of the orthopedic device throughout the subject's upper body.
As shown in
The main shaft 120 can comprise three sections. In the pictured embodiment, the main shaft 120 comprises a superior vertical extension 122, a curved portion 124, an inferior vertical extension 126, or a combination thereof. The curved portion 124 can comprise a generally parabolic shape such that the curvature extends outward in the walking direction until reaching an apex at the foremost location and then returning to the same longitudinal plane. When so configured, the superior vertical extension 122 and the inferior vertical extension 126 are substantially colinear with one another. As shown the main shaft 120 can have only a single curved portion 124.
As can be seen, the superior vertical extension 122 can comprise a section at the uppermost point of the main shaft 120 that extends substantially vertically with little to no curvature therein. Similarly, the inferior vertical extension 126 can comprise a section at the lowermost point of the main shaft 120 that extends substantially vertically with little to no curvature therein. In embodiments, the curved portion 124 is disposed along the main shaft 120 between the superior vertical extension 122 and the inferior vertical extension 126. In embodiments, the curved portion 124 can be substantially centrally disposed between the superior vertical extension 122 and the inferior vertical extension 126. In such embodiments, the superior vertical extension 122 and the inferior vertical extension 126 can be about the same longitudinal length. In certain embodiments, the curved portion 124 can be disposed along the body of the main shaft 120 in a manner that places the curved portion closer to the top of the superior vertical extension 122. In such embodiments, the longitudinal length of the superior vertical extension 122 can be less than the longitudinal length of the inferior vertical extension 126. In an alternate embodiment, the curved portion 124 can be disposed along the body of the main shaft 120 in a manner that places the curved portion 124 closer to the inferior vertical extension 126. In such exemplary embodiments, the longitudinal length of the inferior vertical extension 126 can be less than that of the superior vertical extension 122.
As most clearly shown in
As can be seen in
The orthopedic device 100 can comprise a mechanism or means for adjusting the height of the device. As shown in
As will be understood by one of skill in the art, the second embodiment of the push-button spring clip 145 is shown adjacent to the orthopedic device 100 throughout the drawings merely as an exemplary reference of an alternative embodiment and can be used in place of (as opposed to in addition to) the first embodiment of the push-button spring clip 140. As such, to the extent that the drawings suggest that both the first embodiment and the second embodiment of the push-button spring clip 140, 145 are required, such a suggestion is expressly renounced.
In embodiments, the boot or foot 132 can be frictionally attached to the bottom-most portion of the inferior vertical extension 126. In alternate embodiments, the boot or foot 132 can be glued, adhered, or otherwise joined to the main shaft 120. In embodiments, the boot or foot 132 is integral with the main shaft 120. As will be understood by one of skill in the art, the third embodiment of the boot or foot 132 is shown adjacent to the orthopedic device in
As shown in
The main shaft 220 can comprise three sections. In the pictured embodiment, the main shaft 220 comprises a superior vertical extension 222, a curved portion 224, an inferior vertical extension 226, or a combination thereof. As can be seen, the superior vertical extension 222 can comprise a section at the uppermost point of the main shaft 220 that extends substantially vertically with little to no curvature therein. Similarly, the inferior vertical extension 226 can comprise a section at the lowermost point of the main shaft 220 that extends substantially vertically with little to no curvature therein. In embodiments, the curved portion 224 is disposed along the main shaft 220 between the superior vertical extension 222 and the inferior vertical extension 226. As shown in the present embodiment of the orthopedic devices 200, the curved portion 224 can be disposed along the body of the main shaft 220 in a manner that places the curved portion 224 closer to the top of the main shaft 220. In such embodiments, the longitudinal length of the superior vertical extension 222 can be less than the longitudinal length of the inferior vertical extension 226. In embodiments, the curved portion 224 can be substantially centrally disposed between the superior vertical extension 222 and the inferior vertical extension 226. In such embodiments, the superior vertical extension 222 and the inferior vertical extension 226 can be about the same longitudinal length. In an alternate embodiment, the curved portion 224 can be disposed along the body of the main shaft 220 in a manner that places the curved portion 224 closer to the base of the main shaft 220. In such exemplary embodiments, the longitudinal length of the inferior vertical extension 226 can be less than that of the superior vertical extension 222.
As can be seen in
In embodiments, the boot or foot 230, 231, 232 can be frictionally attached to the bottom-most portion of the inferior vertical extension 226. In alternate embodiments, the boot or foot 230, 231, 232 can be glued, adhered, or otherwise joined to the main shaft 220. In embodiments, the boot or foot 230, 231, 232 is integral with the main shaft 220. As will be understood by one of skill in the art, the second embodiment of the boot or foot 231 and the third embodiment of the boot or foot 232 are shown adjacent to the orthopedic device merely as an exemplary reference of an alternative embodiment and can be used in place of (as opposed to in addition to) the first embodiment of the boot or foot 230. As such, to the extent that the drawings suggest that both the first embodiment, the second embodiment, and the third embodiment of the boot or foot 230, 231, 232 are required, such a suggestion is expressly renounced.
The orthopedic device 200 can comprise a mechanism or means for adjusting the height of the device. As shown in
As will be understood by one of skill in the art, the second embodiment of the push-button spring clip 245 is shown adjacent to the orthopedic device 200 merely as an exemplary reference of an alternative embodiment and can be used in place of (as opposed to in addition to) the first embodiment of the push-button spring clip 240. As such, to the extent that the drawings suggest that both the first embodiment and the second embodiment of the push-button spring clip 240, 245 are required, such a suggestion is expressly renounced.
In the embodiment of
As discussed above and shown within the drawings, the superior vertical extension 222 can be shortened as compared to the inferior vertical extension 226 (see, for example,
In embodiments, the longitudinal length of the curved portion 124, 224, 324 is at least about twice that of the superior vertical extension 122, 222, 322, the inferior vertical extension 126, 226, 326, or both. The curved portion 124, 224, 324 can comprise a length that that is about three times that of the superior vertical extension 122, 222, 322, the inferior vertical extension 126, 226, 326, or both. In various embodiments, the longitudinal length of the curved portion 124, 224, 324 is at least about one and one-half that of the superior vertical extension 122, 222, 322, the inferior vertical extension 126, 226, 326, or both.
In various embodiments, the curved portion 124, 224, 324 of the main shaft 120, 220, 320 can comprise a fixed length and can be placed vertically at any position of the main shaft. The main shaft 120, 220, 320 can have a fixed length, and the curved portion 124, 224, 324 can have a fixed length across various embodiments. Thus, in such embodiments, the longitudinal length of the superior vertical extension 122, 222, 322 and the inferior vertical extension 126, 226, 326 can vary between alternate iterations. For exemplary purposes only, the main shaft 120, 220, 320 can have an entire longitudinal length of about 36 inches, and the curved portion 124, 224, 324 can have a longitudinal length of about 21 inches across various embodiments such that the remaining 15 inches of the main shaft 120, 220, 320 can be split between the superior vertical extension 122, 222, 322 and the inferior vertical extension 126, 226, 326 in any conceivable manner. Thus, under one embodiment of the presently discussed example, the superior vertical extension 122, 222, 322 has a longitudinal length of about 7 inches, and the inferior vertical extension 126, 226, 326 has a longitudinal length of about 8 inches. In another embodiment using the present example, the superior vertical extension 122, 222, 322 has a longitudinal length of about 4 inches, and the inferior vertical extension 126, 226, 326 has a longitudinal length of about 11 inches. Thus, as can be seen, the entire longitudinal length of the main shaft 120, 220, 320 and the curved portion 124, 224, 324 can be fixed such that the longitudinal lengths of the superior vertical extension 122, 222, 322 and the inferior vertical extension 126, 226, 326 vary across embodiments depending on the disposition of the curved portion 124, 224, 324 therebetween. As stated above, any specific values provided herein are merely for exemplary purposes only and should not be interpreted as limiting. The recited values can be any value that permits any of the orthopedic devices described herein to retain physiological utility in promoting a normal gait in a subject afflicted with a knee condition.
As can be seen in
In certain embodiments, each of the bends or major angular changes can be formed by a “bump bend” that is made up of a plurality of minor angular changes in the main shaft 120, 220, 320. For instance, a single 22° bend or major angular change can comprise a plurality of minor angular changes that sum to about 22° in total. By way of nonlimiting example, a single 22° bend can be comprised of six minor angular changes that are each equal to about 7.33°.
Although a plurality of 22° major angles are shown in the embodiments of
In embodiments, the orthopedic device 100 can comprise any device that is known in the art to be useful in providing support and stability to a subject while walking. Although a cane is shown in the pictured embodiments, the presently disclosed main shaft 120, 220, 320 can be applied to any orthopedic device that is capable of assisting a subject who is suffering from a knee condition with ambulation. By way of non-limiting example, additional orthopedic devices that comprise a shaft with the curvature disclosed herein comprise auxilia crutches (also referred to as underarm crutches), forearm crutches (also referred to as loft strand or elbow crutches), gutter crutches (also referred to as adjustable arthritic crutches, forearm support crutches), or a combination thereof.
As can be seen from the various embodiments depicted herein, the handle shaft 114, 214, the main shaft 120, 220, or both can comprise hollow tubing. In such embodiments, the tubing comprises an inner diameter that is defined by the hollow interior space of the tube and an outer diameter that is defined by the exterior walls of the tube. Alternatively, the handle shaft 114, 214, main shaft 120, 220, or both can comprise a substantially solid tube with no interior space. In embodiments wherein the handle shaft 114, 214 and the main shaft 120, 220 are substantially solid, the handle shaft 114, 214 and the main shaft 120, 220 can comprise a single, continuous material.
Further, as shown in the present embodiments, one or both of the main shaft 120 and the handle shaft 114 have a substantially circular cross-section. However, it should be understood that the cross-section of the main shaft 120, the handle shaft 114, or both can comprise any shape. By way of non-limiting example, the cross-section of the main shaft 120, the handle shaft 114, or both can comprise a triangle, square, rectangle, pentagon, hexagon, heptagon, octagon, nonagon, decagon, circle, oval, half circle, quarter circle, or a combination thereof.
The main shaft 120, handle shaft 114, or both can comprise any material suitable for use in a lightweight orthopedic device. By way of non-limiting example, the main shaft 120, handle shaft 114, or both can comprise metal, carbon fiber, wood, resin, or any other material having a strength that is sufficient to support the weight of at least a large adult human male during use thereof. In certain embodiments, the material of the main shaft 120, handle shaft 114, or both comprises steel. Such material can comprise chrome-moly steel. In embodiments, the material of the main shaft 120, handle shaft 114, or both can support at least 600 pounds of downward force without experiencing a structural failure. The main shaft 120, handle shaft 114, or both can comprise a material that is sufficient to support at least 400 pounds without experiencing a structural failure. In one embodiment, the main shaft 120, handle shaft 114, or both comprise a material that is sufficient to support up to 1,000 pounds without experiencing a structural failure.
The height or the length in the longitudinal direction can be in a plurality of sizes depending on the height of the user or the age of the user. For instance, the height can be configured for use by an average-sized human child of 12 years or younger. The height can be configured for use by an average-sized human male between the ages of 13 and 18. The height can be configured for use by an average-sized human female between the ages of 13 and 18. In embodiments, the height of the orthopedic device is configured for use by an average-sized adult human male over the age of 18, an average-sized adult human female over the age of 18, or a combination thereof. In certain embodiments, the height of the orthopedic device is configured for use by human individuals with a height between the 5th percentile of females and the 95th percentile of males, inclusive according to any commonly referenced anthropometric standards. The height of the orthopedic device can be configured for use with subjects who are up to 7 feet tall. In certain embodiments, the height of the orthopedic device can be configured for use with subjects who are at least 40 inches tall.
In specific embodiments, the height or longitudinal length of the main shaft 120, 220, 320 is as small as 25 inches. The height or longitudinal length of the main shaft 120, 220, 320 can be as long as 35 inches. The longitudinal length of the main shaft 120, 220, 320 can be any value between about 28 inches to about 32.5 inches, inclusive. In certain embodiments, the height or longitudinal length of the main shaft 120, 220, 320 is about 28.0 inches, about 28.5 inches, about 29.0 inches, about 29.5 inches, about 30.0 inches, about 30.5 inches, about 31.0 inches, about 31.5 inches, about 32.0 inches, about 32.5 inches, or any value between any of the foregoing.
Additionally and as discussed herein, the orthopedic device 100, 200 can include a mechanism for modifying its height, such as altering its longitudinal length. For instance, the orthopedic device 100, 200 may feature one or multiple adjustable height configurations to cater to individuals of varying statures or to enable adaptations as the user's mobility requirements evolve over time. The orthopedic device 100, 200 can comprise a means for adjusting the height within a given range. The means for adjusting the height can comprise a locking mechanism for locking the device at a given height. By way non-limiting example, the device can comprise a push-button spring clip 140, 145 that is configured to cooperatively interact with one or more height adjustment positions 118, 218 and at least one spring retention hole 128, 228. In embodiments, each of the one or more height adjustment positions 118, 218 comprises a hole, gap, notch, indenture, or pass-through in the handle shaft 114. In operation, the height adjustment positions 118, 218 permit the device to be reversibly secured at a preferred height. In such embodiments, height adjustment positions 118, 218 can be so dimensioned to receive a component of the locking mechanism therein. For example, one or more of the height adjustment positions 118, 218 can comprise a diameter that is configured to receive the push-button or cap 142, 147 of a spring clip 140, 145, such that, when depressed, the handle shaft 114, 214 can move vertically along the superior vertical extension 122, 222 of the main shaft 120 until a desired overall height of the orthopedic device 100, 200 is achieved.
The handle portion 110 of the cane can be ergonomically designed to provide a comfortable grip 112, 212 and minimize strain on the hand and wrist. The grip 112, 212 can comprise a soft, non-slip material. In certain embodiments, the grip comprises rubber, foam, or any other material known in the art to provide added grip and prevent slipping.
The bottom of the cane can be fitted with a tip, boot, or foot 130, 131, 132, 230, 231, 232 to provide traction and prevent slipping on certain surfaces. In embodiments, the tip or boot comprises rubber or plastic.
In certain aspects, the present disclosure relates to a method of transferring the force of impact during the loading response phase of the gait cycle away from an injured knee and to the upper body of the user.
The present disclosure further relates to methods of promoting recovery from a knee condition, methods of treating a knee condition, or methods of promoting a healthy walking gait. In embodiments, any of the various methods disclosed herein are accomplished through use of any one or more of the orthopedic devices disclosed herein.
In certain embodiments, the presently disclosed device is positioned in tandem with the injured leg such that the impact during walking can be absorbed through the orthopedic device and the supporting arm of the individual rather than through the injured knee. By way of example when the orthopedic device 100, 200 is a cane, as the subject initiates the loading phase by placing the heal on the injured leg on the ground, the subject will simultaneously (or near simultaneously) place the foot, boot, or tip of the cane on the ground at about the same distance in front of the subject as the subject's heel. As the subject rocks his or her heel forward, the subject will begin transitioning his or her weight to the orthopedic device 100, 200 rather than the injured leg such that, towards the end of the loading phase, the knee on the injured leg can bend normally along the curved portion 124, 224, 324 of the cane (as if there were little or no injury to knee) while all weight is supported on the orthopedic device 100, 200. This allows the subject to continue with a normal gait without the injured knee absorbing the shock of the body's contact with the ground. Such embodiments can promote a healthy gait and more rapid muscle recovery.
Non-limiting, exemplary dimensions, and design aspects are provided in this example. It should be noted any dimensions recited in this example are merely exemplary and can vary above or below the described value by any range that still permits the orthopedic device to provide support to a human subject. In certain embodiments, the measurements vary above or below the recited value by up to 20%, up to 15%, up to 10%, or up to 5%. The values can vary up to 1%, up to 2%, up to 3%, or up to 4%.
The material for the tube or shaft 114, 120 utilized in any of the various embodiments disclosed herein can be about ¾″ (about 0.750″) OD Chrome-Moly steel or any other material known in the art. In one embodiment, the inner diameter of the material is about 19/32″ (about 0.614″).
The handle portion 110, 210 as used in certain embodiments can comprise a handle shaft 114, 214 with two or more adjustment positions 118, 218. In one embodiment the handle shaft 114 is configured to “sleeve” over the top of the superior vertical extension 122, 222 the main shaft 120, 220. The adjustment positions 118, 128 can comprise holes, gaps, notches, indentures, or pass-throughs within the handle shaft 114, 214. The first of such adjustment positions can begin at about 1 inch from the bottom of the handle shaft. In certain embodiments, there is about 1 inch between each adjustment position.
In one embodiment the handle design comprises an “offset T” design. The handle shaft can further comprise a locking collet or collar 160, 260 configured to reversibly lock the vertical position of the handle, whereby locking the vertical position of the handle reversibly establishes the height of the orthopedic device 100, 200.
In one embodiment, the handle shaft 114, 214 dimensions are as follows: the inner diameter of the shaft is about 0.751 inches and the outer diameter of the shaft is about 0.839 inches. The handle shaft 114, 214 can have a length of about 7 inches extending from the base of the handle grip 112 regions. The bottom of the handle shaft 114, 214 can comprise a threaded portion comprising threads that can reversibly receive and secure the collet/collar 160, 260 thereon. In one embodiment the locking collet or collar 160, 260 is about 0.896 inches long.
In embodiments, the orthopedic device 100, 200 comprises a foot 130, 230 that can be secured to the inferior vertical extension 126, 226 of the main shaft. The foot 130, 230 can be reversibly secured to the bottom portion of the main shaft 120, 220. The foot 130, 230 can be configured to friction fit over the bottommost portion of the main shaft 120, 220. In one embodiment, the foot 130, 230 comprises a rubber material. In one embodiment, the foot comprises a length of about 1.159 inches. The inner diameter of the foot can be about 0.77 inches.
As stated herein the height adjustment mechanism can comprise a push-button spring clip 140, 145, 24, 245. In such embodiments, the spring can be a compression spring such as a looped compression spring 140, 240 or a V-shaped compression spring 145, 245, wherein at least one end of the spring comprises an extension that is attached to the button or a flanged spring retainer cap 142, 147, 242, 247. In one embodiment, a compression portion of the spring is configured to reside within at least one of the adjustment positions 118, 218. A button end of the spring can be attached to the button or spring retainer cap.
The button or cap 142, 147, 242, 247 can be thimble-shaped with a flange that extends at least partially around the diameter of the cap. The top of the button or cap 142, 147, 242, 247 can be the portion of the button or cap 142, 147, 242, 247 that faces away from the spring, while the bottom of the button or cap 142, 147, 242, 247 can be the portion of the button or cap 142, 147, 242, 247 that faces the spring. The body of the button or cap 142, 147, 242, 247 can comprise the portion of the button or cap 142, 147, 242, 247 that is disposed between the top and the bottom of the button or cap 142, 147, 242, 247. In embodiments, the bottom of the button or cap 142, 147, 242, 247 comprises an opening that is configured to receive and secure at least a portion of the spring (such as the button end) therein.
In certain embodiments, the flange is disposed at the bottom of the button or cap 142, 147, 242, 247. The flange can have a diameter that is greater than that of the body of the button or cap 142, 147, 242, 247. In one embodiment, the body of the button or cap 142, 147, 242, 247 has a diameter that is so dimensioned to pass through the one or more adjustment positions 118, 218 and the spring retention hole 128, 228, and the diameter of the flange is larger than that of the one or more adjustment positions 118, 218 and the spring retention hole 128, 228. Therefore, when inserted through the adjustment position 118, 218 and the spring retention hole 128, 228 from the interior of the shaft, the body of the button or cap 142, 147, 242, 247 can pass therethrough but the bottom portion of the button or cap 142, 147, 242, 247 is prevented from passing through the spring retention hole 128, 228, the adjustment position 118, 218, or both by the flange. Thus, when attached to the spring and the button is positioned within one of the at least one adjustment positions, the push-button spring clip 140, 145, 240, 245 snaps into place such that the button or cap 142, 147, 242, 247 extends at least partially through the adjustment position 118, 218 and the spring retention hole 128, 228, and is retained in the inner diameter of the adjustment position 118, 218 and the spring retention hole 128, 228 by the cooperative actions of the flange and the expansive force of the compressed spring.
In one embodiment, the outer diameter of the flange is about 0.477 inches. The height of the cap can be about 0.398 inches. In one embodiment, the cap 142, 147, 242, 247 can comprise a taper from about 0.377 inches to about 0.397 inches.
One or more of the adjustment positions can comprise a spring retention hole 128, 228 with a diameter that is about 0.3975 inches. The diameter can be as small as 0.3155 inches.
Those skilled in the art will recognize, or be able to ascertain, using no more than routine experimentation, numerous equivalents to the specific substances and procedures described herein. Such equivalents are considered to be within the scope of this disclosure and are covered by the following exemplary claims.
| Number | Date | Country | |
|---|---|---|---|
| 63463857 | May 2023 | US |