The disclosed invention relates to a dilator system and a method of using a dilator system.
A disc herniation may be removed through discectomy to relieve pain by removing pressure on a nerve.
A traditional method of discectomy requires an up to four inches long incision down the back and stripping of muscle from the spine to access the herniated disc. Microsurgery may be implemented with a one inch incision, but still requires cutting muscle and scraping it from the spine. The muscle damage causes post-operative pain and requires longer rehabilitation periods.
A surgical tool having metal tubes of various inner diameters has been proposed to create and maintain openings to access the spine. The metal tubes are called dilators, which progressively increase in diameter size. The dilators are inserted sequentially to gradually separate the muscle to create an opening large enough for surgical tools. Thus, a surgeon may avoid cutting the muscle fiber. The METRx system is an example of such a system. The use of such systems is discussed in Clinical Applications of the Tubular Refractor on Spinal Disorders, Kim et al., J Korean Neurosurgery Soc. 2007, October, 42(4) 245-250.
According to conventional art, a dilator tube 10 can be guided to the surgery site with a guide wire. The guide wire is secured to a spinal site using any known technique, for example, a known technique for the insertion of percutaneous screws. According to this known technique a dilator tube receives the secured guide wire in the interior space thereof and is guided to the surgery site.
An objective of a system according to the present invention is to facilitate performance of the posterior lumbar fusion based on a guidewire secured in order to insert percutaneous screws.
A system according to the present invention will use the secured guidewire as a reference point for the insertion of the dilators in order to appropriately locate the facet joint of interest in the lumbar and thoracic spine to allow for the percutaneous, automated preparation of the facet joint and the delivery of grafting material on various sources including but not limited to autograft, allograft, demineralized bone matrix, various ceramics, biologics, or variations thereof.
A system according to the present invention includes a novel dilation mechanism which will allow the tightening of the dilator based on an eccentrically positioned guidewire pathway on the outer periphery of a dilator, which will preferably serve as the surgical cannula. This is contrary to the conventional method in which the guidewire is centered in the middle of the dilator. The eccentric guidewire pathway allows for a lateral/medial/superior/inferior placement of the dilator (cannula) and access to the points of interest medial/lateral/superior/inferior to the guidewire entry site.
To perform a surgical method with a system according to the present invention, the guidewire may be secured through a conventional method, which could include the use of a needle to allow cannulation of the interested anatomy such as the pedicle in the case of the lumbar, and thoracic spine.
The guidewire, which may be a flexible body, can be placed for the purposes of the preparation and the insertion of the dilator (cannula) in question or for the placement of pedicle screws by the use of fluoroscopy, navigation of various sorts, direct visualization, and the like.
Once the guidewire is placed (for example, through the use of possible insertion needles), the guidewire is received in the eccentric guidewire pathway of the dilator (cannula), and the dilator (cannula) is guided to the desired site by sliding the eccentric guidewire pathway along the guidewire.
A dilator system according to the present invention includes a first tube having an eccentrically located guidewire opening radially spaced from a central longitudinal axis of the first tube, and having a first length, and a second tube being nestable inside the first tube and having a second length longer than the first length.
In the first embodiment, the first tube may have a first interior diameter, and a first exterior diameter, and the second tube may have a second interior diameter, and a second exterior diameter smaller than the first interior diameter. In the first embodiment, the first inner diameter may be dimensioned so that the first tube may serve as a cannula.
In a second embodiment, the first tube may be radially expandable to a first diameter to permit the nesting of the second tube therein. Thus, the first tube may include a plurality of pieces connected with a spring to become radially expandable. The plurality of pieces may be two semi-cylindrical pieces. In this embodiment, the second tube has a second inner diameter dimensioned so that the second tube may serve as a cannula.
A system according to the present invention may further include a third tube having a third interior diameter, a third exterior diameter smaller than the second interior diameter and a third length longer than the second length.
A lobe may be on an exterior surface of the first tube defining the guidewire opening.
A plurality of teeth may be located and extend from a distal end of the tube serving as the cannula.
A handle may be detachably attachable to the tube serving as the cannula.
A method according to the present invention includes dilating tissue with a dilator system according to the present invention by attaching a guide wire at a surgical area of interest within the human body, receiving the guidewire in the guidewire opening, and dilating the tissue by advancing the first tube along the guidewire toward the surgical area of interest.
The method may include nesting the second tube within the first tube prior to advancing the first tube toward the surgical area of interest, and dilating the tissue with the second tube prior to dilating the tissue with the first tube by advancing the second tube toward the surgical area of interest.
The first tube may be radially expandable to have a variable diameter, and the method may further include receiving the second tube inside the first tube and radially expanding the first tube prior to advancing the first tube toward the surgical area of interest, and dilating tissue by advancing the second tube toward the surgical area of interest prior to advancing the first tube.
The surgical area of interest may be the site of a facet joint, and the first tube or the second tube may be dimensioned to serve as a cannula, which is used for preparing the facet joint through the cannula.
The method may further include docking the cannula at the surgical area of interest and stabilizing the cannula with an arm or a handle prior to preparing the facet joint.
The method may further include dissecting the tissue with the first tube while advancing the first tube toward the surgical area of interest.
Other features and advantages of the present invention will become apparent from the following description of the invention which refers to the accompanying drawings.
Referring to
According to the present invention, the cannula 24 will have a guide hole (pathway) 26 sized to receive a guide wire 28 that is secured to a location on a vertebrae 14. The guide wire hole 26 may be defined in, for example, a lobe 30 extending radially away from the exterior surface of the cannula 24. Thus, the guide hole 26 is at an eccentric location outside of the interior space of the cannula 24.
The cannula 24 may also have a plurality of circumferentially spaced teeth 32 at its distal end 34 to engage the area on the vertebra around the site of operation.
The cannula 24 may also include a handle 25 (
As seen in
The first embodiment may include two or three dilator tubes 20, 22, 24, in which the dilator tube 24 with the largest diameter will have the eccentric guidewire pathway 26. The other one or two dilator tubes 20, 22 have smaller diameters and are receivable in the dilator tube 24 with the largest diameter and the eccentric guidewire pathway 26. The one or two internal dilators 20, 22 allow for dilatation of the muscle in sequence. Specifically, the narrowest tube 20 is inserted first. Then, the second tube 22 with the intermediate height and diameters is received over the narrowest tube 20. Thereafter, the widest tube 24 receives the guide wire 28 in pathway 26 and guided to the surgery site over the other two, already inserted, dilators 20, 22.
In the first embodiment, dilator 20 is inserted into dilator 22, and then the two dilators 20, 22 are inserted into dilator 24. In this assembled (nested) state, the guidewire is received in guidewire pathway 26 of dilator 24, and the assembly of the dilators 20, 22, 24 is guided, during the initial phase of the insertion, past skin, subcutaneous fat, and fascia. If necessary, with dilator 24 and its guide mechanism acting as a guide of general direction, dilators 20 and 22 will be advanced on to the area of special interest (the surgery area) in order to allow for a final muscle dissection. Once dilators 20, 22 have been advanced and docked, dilator 24 will be advanced over them and docked around the area of interest. Dilators 20 and 22 will be then removed. Once the muscle is properly dilated, and the internal dilators 20, 22 are removed, the largest diameter dilator 24 will now work as a working cannula. The internal dilators 20, 22 are longer than the cannula 24 so that once the initial fascia and musculature is centered the longer two dilators 20, 22 can be advanced to the facet joint or the area of interest and docked. The final working dilator 24 has teeth/structures 32 to allow for the engagement of the anatomy of interest and appropriate docking.
Referring to
In both embodiments, the final working dilator 24, which serves as the working cannula 24, would have an attached (which maybe detachable) handle (
Once docked onto the structure the soft tissue is removed if necessary. The drill guide with drill stops that are variable and can be adjusted based on the surgeons preference will work through the final working cannula 24 in order to appropriately decorticate and prepare the structure of interest such as a facet joint in the thoracic and lumbar spine.
The mechanism of the drill/mill will be such that a smooth operation will be allowed within the working cannula 24.
Various parts can be used to place fusion material onto the appropriately prepared facet joint in order to allow solid fusion.
Although the present invention has been described in relation to particular embodiments thereof, many other variations and modifications and other uses will become apparent to those skilled in the art. It is preferred, therefore, that the present invention be limited not by the specific disclosure herein, but only by the appended claims.
The present application claims priority to U.S. Provisional Application Ser. No. 62/817,721, filed Mar. 13, 2019, the entire disclosure of which is incorporated by reference herein.
Number | Date | Country | |
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62817721 | Mar 2019 | US |