The present invention relates generally to medical devices, and more specifically to a balloon kyphoplasty surgical device.
In general, balloon kyphoplasty is a modified vertebroplasty technique. It is a minimally invasive procedure that aims to relieve pain, restore vertebral height, and correct kyphosis. During this procedure, an inflatable bone tamp is inserted into the collapsed vertebral body. Once inflated, the balloon elevates the end plates creating lift and thereby restores the height of the vertebral body. The balloon moves or shifts the pieces of broken or compressed vertebral bone and forms a space, i.e., a bony void when it is inflated. The balloon is deflated and removed, and the bony void is filled with bone cement.
The following presents a simplified summary of the innovation in order to provide a basic understanding of some aspects of the present disclosure. This summary is not an extensive overview of the present disclosure. It is intended to neither identify key or critical elements of the present disclosure nor delineate the scope of the present disclosure. Its sole purpose is to present some concepts of the present disclosure in a simplified form as a prelude to the more detailed description that is presented later.
In an aspect, an exemplary implementation in accordance with the present disclosure may feature a balloon kyphoplasty surgical device including an extrusion tube having internal fluid channels and a support wire, a port arrangement positioned on a proximal end of the extrusion tube and a balloon arrangement positioned on a distal end of the extrusion tube, the balloon arrangement resulting in a predetermined shape when inflated by the port arrangement. In an example illustrative of various implementations in accordance with the present disclosure, the inflated balloon arrangement's predetermined shape may be cubic, rectangular, or another shape.
In another aspect, an exemplary implementation in accordance with the present disclosure may feature a kyphoplasty balloon arrangement including inner balloons, and an outer balloon, the inner balloons being housed within the outer balloon.
In still another aspect, an exemplary implementation in accordance with the present disclosure may feature a kyphoplasty surgical method including placing a patient face down on a table, cleaning the patient's back, administering a local anesthesia, making a small incision in the patient's back, placing an extrusion tube through the incision, pushing the extrusion tube along a path through a pedicle of an involved vertebra and into a fractured area and inflating a balloon arrangement located on a distal end of the extrusion tube into a cubic shape.
Some exemplary implementations in accordance with the present disclosure may achieve one or more advantage. These and other such advantages will be further understood and appreciated by those skilled in the art by reference to the following written specification, claims and appended drawings.
It is to be understood that the specific devices and processes illustrated in the attached drawings and described in the following specification are exemplary embodiments of the inventive concepts defined in the appended claims. Hence, specific dimensions and other physical characteristics relating to the embodiments disclosed herein are not to be considered as limiting, unless the claims expressly state otherwise.
As shown in
With the balloon kyphoplasty surgical device 10, when the balloon arrangement 30 is inflated, the balloon arrangement 30 lifts with a predetermined shape resulting from the shapes of individual balloons comprising the balloon arrangement 30. In an example illustrative of various implementations in accordance with the present disclosure, the balloon arrangement 30 may comprise a plurality of individual balloons. The plurality of individual balloons may comprise an outer balloon. The outer balloon may be inflatable. The outer balloon may be manufactured to have a predetermined shape. The outer balloon may be manufactured to retain the predetermined outer balloon shape when the outer balloon is inflated. The outer balloon may retain one or more inner balloon. The one or more inner balloon may be inflatable. The one or more inner balloon may be manufactured to have a predetermined shape. The inner balloon may be manufactured to retain the predetermined inner balloon shape when the inner balloon is inflated. The outer balloon may be substantially cube-shaped. The outer balloon may be substantially cylindrical. The outer balloon bay be substantially spherical. The one or more inner balloon may be substantially spherical. The one or more inner balloon may be substantially cylindrical. The one or more inner balloon may be substantially cube shaped. The one or more inner balloon may be substantially pyramid-shaped. The one or more inner balloon may be substantially oval. The one or more inner balloon may be substantially elliptical. The one or more inner balloon may further comprise a plurality of inner balloons. One or more inner balloon of the plurality of inner balloons may have a shape different from another inner balloon of the plurality of inner balloons. The plurality of inner balloons may comprise inner balloons having a plurality of different shapes. The plurality of inner balloons may comprise inner balloons having a plurality of different sizes. The balloon arrangement may be inflated. A balloon arrangement's outer balloon may be inflated to a volume or pressure different from one or more inner balloon's volume or pressure. One or more inner balloon of a balloon arrangement's plurality of inner balloons may be inflated to a volume or pressure different from one or more other inner balloon's volume or pressure. The balloon arrangement may have a cubic or cubic-type shape, rather than a circular-type shape, as is found in prior kyphoplasty devices.
Referring now to
In an illustrative usage scenario of an exemplary kyphoplasty surgical device balloon arrangement 30 implementation configured with four balloons, after insertion into the fractured area, the inner balloons 110a, 110b, 110c, and 110d, and the outer balloon 100 are inflated. More specifically, the inner balloons 110a, 110b, 110c, and 110d are inflated to a size needed for the appropriate distance of lift, while the outer balloon 100 is inflated to have a volume of fluid added that is equal to the remaining volume needed to produce a cubic shape having 4 corners 100a,b,c,d for the inflated balloon arrangement 30. Inflation of the inner balloons 110a, 110b, 110c, and 110d and the outer balloon 100 is accomplished by the port arrangement 35.
In the exemplary balloon arrangement 30 implementation depicted by
In one embodiment and as shown in
In one embodiment and as illustrated in
The kyphoplasty surgical process 800 includes cleaning (810) the patient's back and administering (815) a local anesthesia.
The kyphoplasty surgical process 800 includes making (820) a small incision in the patient's back and placing (825) an exemplary kyphoplasty surgical device extrusion tube through the incision. The method may include positioning an exemplary kyphoplasty surgical device to ensure a balloon is aligned to be square with the vertebra so the flat surface is parallel to the vertebra.
The kyphoplasty surgical process 800 includes pushing (830) the extrusion tube along a path through a pedicle of an involved vertebra and into a fractured area.
Once in the fractured area, inner balloons retained within an outer balloon of a balloon arrangement are inflated (835). The inner balloons may be spherically shaped. The inner balloons may be cylindrically shaped. The outer balloon may be cubic shaped.
Once the inner balloons are inflated, the outer balloon in the balloon arrangement is inflated (840), resulting in the balloon arrangement having a cubic shape, lifting the target area such as a vertebrae or fracture.
The balloon arrangement is then deflated and removed (845), and the cavity is gradually filled (850) with a cement-like material and allowed to harden.
The balloon arrangement of the present invention creates a larger cavity and a more structurally sound structure after cementation. During compression of vertebra, the bone is grown to exert this force through flat surfaces, and the cubic cement structure enables a flat surface for the bone to compress on and for more cement to be packed in.
In one embodiment, the inflated balloon arrangement 30 is in place for 5 seconds to 30 minutes.
In one embodiment, the inflated balloon arrangement 30 is inserted with a 10f or 11f access needle or trocar that varies in length and size. The access needle or trocar are placed in the vertebral body and allows the balloon arrangement 30 to enter through the needle or the trocar into the vertebrae. The access needle and trocar are not shown.
In sum, the balloon kyphoplasty surgical device may be made up of multiple balloons, an extrusion tube, support wire, and a multichambered proximal port. The multiple balloons may be positioned as inner and outer balloons to produce a cubic shape when inflated. The one or more larger outer balloon may be manufactured to be cubic in shape, while the inner balloons have a standard cylindrical/spherical shape and support the corners to maintain the square geometry under pressure. The extrusion tube comprises multiple fluid channels so that the inner and outer balloons can be inflated at different volumes. The support wire will ensure the device does not get damaged while inserting into the vertebra. The multichambered proximal port may comprise multiple ports that attach to separate chambers. These chambers connect to different fluid routes keeping the inlets separate, this separation will allow for independent filling during use.
The goal of balloon kyphoplasty surgical device is to achieve lift with a cubic like balloon shape. The various components described herein achieve this shape. After insertion the inner and outer balloons are inflated, the inner balloons are inflated to the size needed for the appropriate distance of lift. The outer balloon will have a volume of fluid added to produce the cubic shape. The inflation is done using the multichambered ports and separate inflation device reservoirs to maintain the appropriate pressure/volume needed. The balloon material must be noncompliant enough to undergo a minimum of 400 PSI without losing the cubic shape or bursting while still being compliant enough to stretch to the appropriate size.
The predicate kyphoplastic balloons operate in a similar fashion but use a standard circular balloon. The circular cavity created has proven to work but the cement structure formed after use can have high single point pressure areas that can weaken the bone at these points, these devices can also not allow for enough bone cement to be added for proper support. The balloon kyphoplasty surgical device creates a larger boney void with a larger flat surface area producing a more structurally sound structure after cementation. During compression of vertebra the bone is grown to exert this force through flat surfaces, and the cubic cement structure allows for a flat surface for the bone to compress on and for more cement to be packed in.
While various embodiments of the present disclosure have been described above, it should be understood that they have been presented by way of example only, and not of limitation. Likewise, the various diagrams may depict an example architectural or other configuration for the present disclosure, which is provided to aid in understanding the features and functionality that may be included in an exemplary implementation in accordance with the present disclosure. An exemplary implementation in accordance with the present disclosure is not restricted to the illustrated example architectures or configurations, but the desired features can be implemented using a variety of alternative architectures and configurations.
Indeed, it will be apparent to one of skill in the art how alternative functional configurations can be implemented to implement the desired features of the present disclosure. Additionally, with regard to flow diagrams, operational descriptions and method claims, the order in which the steps are presented herein shall not mandate those various embodiments be implemented to perform the recited functionality in the same order unless the context dictates otherwise.
In the present disclosure, various features may be described as being optional, for example, through the use of the verb “may;” or, through the use of any of the phrases: “in some implementations,” “in some designs,” “in various implementations,” “in various designs,” “in an illustrative example,” or, “for example.” For the sake of brevity and legibility, the present disclosure does not explicitly recite each and every permutation that may be obtained by choosing from the set of optional features. However, the present disclosure is to be interpreted as explicitly disclosing all such permutations. For example, a system described as having three optional features may be implemented in seven different ways, namely with just one of the three possible features, with any two of the three possible features or with all three of the three possible features.
The phrases “connected to,” “coupled to” and “in communication with” refer to any form of interaction between two or more entities, including mechanical, electrical, magnetic, electromagnetic, fluid, and thermal interaction. Two or more components may be functionally coupled to each other even though they are not in direct contact with each other. The terms “abutting” or “in mechanical union” may refer to items that are in direct physical contact with each other, although the items may not necessarily be attached together. In various implementations, elements described herein as coupled or connected may have an effectual relationship realizable by a direct connection or indirectly with one or more other intervening elements.
Recitation in a claim of the term “first” with respect to a feature or element does not necessarily imply the existence of a second or additional such feature or element.
Although the disclosure is described above in terms of various exemplary embodiments and implementations, it should be understood that the various features, aspects and functionality described in one or more of the individual embodiments are not limited in their applicability to the particular embodiment with which they are described, but instead can be applied, alone or in various combinations, to one or more of the other embodiments of the disclosure, whether or not such embodiments are described and whether or not such features are presented as being a part of a described embodiment. Thus, the breadth and scope of the present invention should not be limited by any of the above-described exemplary embodiments.
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