Skin foundation access portal

Disclosed herein are surgical access stabilization devices and related methods, such as methods for stabilizing a port or other surgical access device relative to a patient during a surgical procedure.

In many cases, it may be desirable to stabilize an instrument or object. In surgical applications, for example, it may be desirable to stabilize a surgical access device, such as a port, relative to a patient during a surgical procedure. As a further example, it may be desirable to establish, stabilize, and maintain a desired trajectory of the surgical access device during a surgical procedure to accommodate an instrument, object (e.g., an implant), or the like that is percutaneously passed through the access device toward a surgical site. Additionally, it may be desirable to stabilize the surgical access device in a manner that minimizes interference with the surgical procedure and allows for easy and rapid adjustment of the surgical access device during the procedure, if necessary.

In current practice, a surgical instrument or object is generally stabilized by connecting or coupling to another instrument or object. Often, a rigid connector is used to stabilize a surgical instrument by connecting or coupling it to a support. For example, a mechanical arm connector can be used to connect a surgical access device to a support, such as a surgical bed or a rigid implant post, to stabilize the access device during a surgical procedure. Prior art stabilization methods and devices rely on at least one additional stationary object at or near the surgical site to couple to the surgical access device. Such systems can be particularly cumbersome in minimally invasive surgical procedures, where the dimensions of the working envelope are small and the amount of space for maneuvering is limited.

Additionally, the use of rigid mechanical arm connectors to stabilize a surgical access device constrains the surgical procedure in several ways. For example, the position of the support (e.g., a surgical table or rigid implant post) dictates the position of the access device based on the size and configuration of the mechanical connector. Similarly, the rigid mechanical connectors of the prior art may limit the range of movement of the access device when connected to the support. Often, surgeons desire greater range of motion during surgery in at least one preferred direction based on the surgical anatomy. For example, in spinal surgery, surgeons often desire the ability to allow greater port movement in a direction transverse to the spinal column. Rigid connectors prevent this desired movement due to the physical constraints of the connector and associated support structures. Additionally, the flow of the surgical procedure may be determined by the prior art connector stabilization systems rather than a function of the surgeon's expertise. For example, when a surgical access device is stabilized by connection to a pedicle screw or other implant post, the contralateral screw may be used to stabilize the surgical access device. The endoscopic screw must first be placed in the patient prior to insertion and stabilization of the access device.

<p>Thus, a need remains for devices and techniques for establishing, stabilizing, and maintaining a desired trajectory and positioning of surgical instruments, particularly surgical access devices, during a surgical procedure in an easier and less restrictive manner.</p>

<p>The present invention generally provides devices and methods for stabilizing a surgical access device. Specifically, a surgical access device, such as a port, may be stabilized within a surgical incision against an anchor surface, such as the skin of a patient, using the devices and methods described herein. In one aspect of the invention, a surgical access stabilization device is provided that includes a pad having a proximal facing surface and an adhesive distal facing surface, a surgical access device coupled to the pad, and a locking mechanism that selectively locks the position of the surgical access device relative to the pad.</p><p>The surgical access stabilizer described above may have various modifications within the scope of the present invention. For example, in some embodiments, the pad may have an opening extending therethrough to receive the locking mechanism. Additionally, in some embodiments, the opening may be an elongated slot. In some embodiments, the opening may be centrally located on the pad. The pad may further include imaging features to aid in imaging of the pad. In some embodiments, the pad may include navigation features to aid in navigation of the surgical access device. In certain embodiments, the pad may have a central portion having at least one radial finger. In some embodiments, the pad may be made from any of a flexible fabric, an elastomer, and a polymer.</p><p>In some embodiments, the locking mechanism can selectively lock translational movement of the surgical access device in a direction along the proximal facing surface of the pad. In some embodiments, the locking mechanism can selectively lock translational movement of the surgical access device in a direction transverse to the proximal facing surface of the pad. Additionally, in some embodiments, the locking mechanism can selectively lock either rotational movement of the surgical access device or angular movement of the surgical access device. The locking mechanism of the present invention can take a variety of forms. For example, in some embodiments, the locking mechanism can include at least one locking ring. In yet other embodiments, the locking mechanism can include either a releasable adhesive or a hook and loop fastener.</p><p>In another aspect, a surgical access stabilization system is provided that includes a pad having a proximal facing surface and an adhesive distal facing surface, a surgical access device defining a working channel, and a connection mechanism coupled between the pad and the surgical access device to position the surgical access device at a location away from the pad.</p><p>The surgical access stabilization system described above can have various modifications within the scope of the present invention. For example, in some embodiments, the connection mechanism can include an arm coupled to the surgical access device at a first end and coupled to the pad at a second end. Additionally, in some embodiments, the arm can be bendable to adjust the placement of the first end relative to the second end.</p><p>In yet another aspect, a method of stabilizing a surgical access device is provided that includes making an incision in a patient, adhering a pad to the patient, inserting a surgical access device into the patient through the incision, coupling the surgical access device to the pad, and selectively locking a position of the surgical access device relative to the pad.</p><p>The above-described surgical access stabilization methods can have various modifications within the scope of the present invention. For example, in some embodiments, the method can further include positioning the surgical access device within the incision by at least one of translating, rotating, and angling the surgical access device relative to the pad.</p><p>In other embodiments, the position of the surgical access device can be selectively locked to prevent further translation, rotation, or angulation of the surgical access device relative to the pad.</p><p>In some embodiments, the pad may be adhered to the patient after the incision is made. In some embodiments, the pad may be adhered to the patient before the incision is made. In certain embodiments, the pad may be adhered to the patient at a location away from the incision.</p><p>In some embodiments, coupling the surgical access device to the pad can include positioning the surgical access device within an opening in the pad, hi other embodiments, coupling the surgical access device to the pad can include connecting the surgical access device to the pad with a connector arm.</p><p>In other embodiments, the surgical access device stabilization method may further include deploying at least a portion of the pad from the surgical access device after the surgical access device is inserted through the incision.</p><p>Any of the features or variations described above may be applied to any particular aspect or embodiment of the present disclosure in many different combinations, and no explicit description of any particular combination is provided, simply to avoid redundancy in this summary.</p>

The above-described aspects and embodiments of the present invention will be more fully understood from the following detailed description taken in conjunction with the accompanying drawings.

<figref num="1">1 is a perspective view of one embodiment of a surgical access stabilization device having an underlying pad and a locking mechanism with a surgical access device disposed therein; FIG.</figref><figref num="2">FIG. 2 is a perspective view of the surgical access stabilization device of FIG. 1.</figref><figref num="3">2 is a cross-sectional view of the surgical access stabilizer of FIG. 1 with a surgical access device disposed therein.</figref><figref num="4">2 is a perspective view of the surgical access stabilizer of FIG. 1 with a surgical access device disposed therein.</figref><figref num="5">FIG. 2 is a perspective view of the foundation pad of FIG. 1.</figref><figref num="6">FIG. 2 is a perspective view of the pad with the base of the locking mechanism of FIG. 1 engaged.</figref><figref num="7">FIG. 7 is an exploded view of the foundation with the base of FIG. 6 engaged.</figref><figref num="8">FIG. 7 is a perspective view of the base of FIG.</figref><figref num="9">FIG. 7 is a top view of the base of FIG. 6.</figref><figref num="10">2 is a perspective view of the foundation and base, skirt, and split ring of the locking mechanism of the surgical access stabilizer of FIG. 1 with a surgical access device disposed therein.</figref><figref num="11">FIG. 11 is a perspective view of the skirt of FIG.</figref><figref num="12">FIG. 11 is a perspective view of the split ring of FIG. 10.</figref><figref num="13">2 is a perspective view of the skirt and split ring of the locking mechanism of FIG. 1 with a surgical access device disposed therein.</figref><figref num="14">FIG. 2 is a perspective view of the base, skirt, split ring, and retaining ring of the locking mechanism of FIG.</figref><figref num="15">FIG. 15 is a cross-sectional view of the locking mechanism components of FIG.</figref><figref num="16">FIG. 15 is a top view of the retaining ring of FIG.</figref><figref num="17">FIG. 17 is a perspective view of the retaining ring of FIG. 16.</figref><figref num="18">FIG. 2 is a top view of a retaining ring engaged with the base of the locking mechanism of FIG. 1.</figref><figref num="19">FIG. 20 is a cross-sectional view of FIG. 19.</figref><figref num="20">2 is a perspective view of the surgical access stabilizer of FIG. 1 with a surgical access device disposed therein.</figref><figref num="21">FIG. 21 is a cross-sectional view of the locking mechanism of FIG. 20.</figref><figref num="22">FIG. 2 is a perspective view of one embodiment of a first locking part.</figref><figref num="23">FIG. 13 is a perspective view of one embodiment of a second locking part.</figref><figref num="24">FIG. 24 is a cross-sectional view of the second locking component of FIG. 23.</figref><figref num="25">23 is a cross-sectional view of the second locking component of FIG. 22 engaged with the skirt. FIG.</figref><figref num="26">1 depicts an exemplary surgical application of one embodiment of a surgical access stabilization device.</figref><figref num="27">1 depicts an exemplary surgical application of another embodiment of a surgical access stabilization device.</figref><figref num="28">1 illustrates a surgical access stabilization device of the present invention in use in a spinal procedure with a rigid port tube disposed therein.</figref><figref num="29">1 illustrates a surgical access stabilization device of the present invention in use in spinal surgery with a flexible barrier port disposed therein.</figref><figref num="30">1 depicts an exemplary surgical application of another embodiment of a surgical access stabilization device.</figref><figref num="31">1 depicts an exemplary surgical application of another embodiment of a surgical access stabilization device.</figref><figref num="32">1 depicts an exemplary surgical application of another embodiment of a surgical access stabilization device.</figref><figref num="33">13 is a perspective view of another embodiment of a surgical access stabilizer having a surgical access device therein. FIG.</figref><figref num="34">34 illustrates an exemplary base pad for the surgical access stabilization device of FIG. 33. </figref><figref num="35">1 depicts another embodiment of a surgical access stabilizer having a surgical access device therein.</figref><figref num="36">FIG. 36 is another view of the surgical access stabilizer of FIG. 35.</figref><figref num="37">36 depicts another exemplary surgical application of the surgical access stabilization device of FIG. 35. </figref><figref num="38">36 depicts another exemplary surgical application of the surgical access stabilization device shown in FIG. 35. </figref><figref num="39">11A-11C are views of another embodiment of the surgical access device of the surgical access stabilization apparatus of the present invention.</figref><figref num="40">13 is a perspective view of another embodiment of a handle of the surgical access stabilization apparatus of the present invention. FIG.</figref><figref num="41">FIG. 41 is an exploded view of the handle of FIG. 40.</figref><figref num="42">FIG. 41 is a perspective view of the body of the handle of FIG. 40.</figref>

Certain exemplary embodiments will now be described to provide an overall understanding of the principles of the structure, function, manufacture, and use of the devices, systems, and methods disclosed in this application. One or more examples of these embodiments are illustrated in the accompanying drawings. Those skilled in the art will appreciate that the devices, systems, and methods described in detail herein and illustrated in the accompanying drawings are non-limiting exemplary embodiments. Features illustrated or described in connection with one exemplary embodiment may be combined with features of other embodiments. Such modifications and variations are intended to be within the scope of the present disclosure.

Further, to the extent that linear or circular dimensions are used in describing the disclosed devices and methods, such dimensions are not intended to limit the types of shapes that may be used with such devices and methods. Those skilled in the art will recognize that equivalent dimensions for such linear and circular dimensions can be readily determined for any geometric shape. Furthermore, the size and shape of the device and its components may depend at least on the anatomy of the patient with whom the device will be used, the size and shape of the components with which the device will be used, and the method and procedure with which the device will be used.

Although the illustrated embodiments and accompanying description are intended for use in spinal surgical procedures, and in particular minimally invasive spinal surgery, the devices, systems, and methods described herein are not limited to these applications. Rather, the devices, systems, and methods described may be utilized in a variety of applications where stabilization of an object is required or beneficial, and are particularly suited for surgical applications to stabilize a surgical access device relative to a patient in one or more desired positions, trajectories, or orientations during the course of a surgical procedure.

1-4 show a first exemplary embodiment of a surgical access stabilizer 100. The device 100 can be used to stabilize a surgical access device, such as a port or access device 10 inserted through an incision in a patient. Preferably, the surgical access stabilizer of the present invention can be patient-mounted to stabilize the surgical access device relative to the patient. The device 100 can selectively limit any one of translational, rotational, or angular motion of the port relative to the patient. Additionally, the surgical access stabilizer 100 can be used to establish, stabilize, and maintain the surgical access device in a desired trajectory during a surgical procedure and provide easy adjustment as needed.

FIG. 1 illustrates a preferred embodiment of a surgical access stabilizer according to the present invention. The surgical access stabilizer 100 is shown with a surgical access device, such as a port or access device 10, engaged therein. The surgical access stabilizer 100 can include a base pad 102 and a locking mechanism 104, which will be described in more detail below. The locking mechanism 104 can be configured to couple and secure the port 10 to the pad 102. The locking mechanism can be further configured to facilitate positioning and adjustment of the port 10 and can selectively lock movement of the port relative to the pad. The pad 102 can have an adhesive distal facing surface configured to contact and adhere to an anchoring surface. In a preferred embodiment, the anchoring surface can be the patient's skin and the distal facing surface of the pad can be the patient contacting surface. The proximal facing surface of the pad can be exposed to a user and can include features to facilitate placement of the pad and adjustment of the port 10 during a surgical procedure.

FIG. 2 illustrates the surgical access stabilizer of FIG. 1 without a surgical access device disposed therein. A central opening 101 can extend through the surgical access stabilizer 100 and can be configured to receive the port 10. As shown in FIG. 2, in some embodiments, the central opening 101 can extend through the locking mechanism 104 and the pad 102. A central axis A1 of the surgical access stabilizer can extend through the central opening 101 perpendicular to a proximal facing surface of the pad. The port 10 can be inserted distally along the axis A1 through the central opening 101 such that the port 10 is received within the surgical access stabilizer. FIG. 3 illustrates a cross-sectional view of the surgical access stabilizer 100 of FIG. 1 with the port 10 inserted through the central opening 101. Here, the various components organizing one embodiment of the locking mechanism 104 can be seen in an assembled configuration. In one embodiment, the locking mechanism 104 can include a base 200, a retaining ring 202, a skirt 204, a split ring 206, a first locking piece 208, and a second locking piece 210, each of which is described in more detail with reference to additional figures below.

The port 10 can have a proximal end 10p and a distal end 10d between which extends an inner lumen 20 having a longitudinal axis A2. When the port 10 is inserted into the surgical access stabilizer 100, the proximal end 10p of the port 10 can remain proximal to the surgical access stabilizer, while the distal end 10d of the port 10 can extend distally beyond the surgical access stabilizer, through the incision in the patient, and to the surgical site. It will be appreciated that in the orientation shown in FIGS. 1 and 3, the longitudinal axis A1 of the surgical access stabilizer and the port axis A2 are collinear as a result of the depicted orientation of the port 10 relative to the surgical access device 100. More specifically, the port 10 is shown inserted into the surgical access device 100 without any angulation relative to the pad 102, such that the port axis A2 is aligned with the longitudinal axis A1 of the surgical access device 100. When the port 10 is angled relative to the surgical access device 100, the longitudinal port axis A2 can be offset or angled relative to the longitudinal axis A1 of the surgical access stabilizer. This is because movement of the port 10 relative to the pad 102 can adjust the angle between the port axis A2 and the stabilizer axis A1. For example, as seen in FIG. 4, the port 10 can be angled within the locking mechanism 104 relative to the pad 102 such that the port axis A2 moves from the longitudinal axis A1 of the surgical access stabilizer by an angle α. It will be understood that an angle α of zero degrees corresponds to a collinear orientation of the port 10 and the longitudinal axis of the surgical access stabilizer.

Returning to FIG. 3, the port 10 can have a handle 12 that allows an operator to manipulate the port 10 within the surgical access stabilizer. The handle 12 can include a gripping portion 14 and a port extension 16. The port extension 16 can extend axially to engage the proximal port end 10p such that the inner lumen of the port extension is aligned with the port lumen 20. Extending the lumen 20 by engaging the handle 12 can facilitate easier insertion of an instrument, such as an implant, through the inner lumen 20 of the port 10. In one embodiment, the outer surface of the port 10 can have an engagement feature 18 configured to mate with a complementary engagement feature of the handle 12 to secure the port in a desired longitudinal position. For example, the outer surface of the port 10 can have a plurality of longitudinally aligned grooves 18. In one embodiment, the port extension 16 of the handle 12 can have at least one inwardly extending protrusion configured to selectively engage at least one of the grooves 18 of the port 10. In this manner, the handle can be positioned at a desired location on the port 10 by adjusting the engagement between the port extension and the plurality of grooves 18. One skilled in the art will appreciate that alternative engagement methods are available for engaging the handle 12 with the port 10. With the handle 12 secured to the port 10, the grip 14 can be used to move the port 10 either rotationally, angularly, or translationally relative to the pad 102 and axis A1. Alternatively, the proximal end 10p of the port may be directly manipulated without the attachment of a handle to facilitate movement of the port.

The grip 14 can extend in a direction substantially transverse to the port axis A2 and can be configured to facilitate manipulation of the port by a user. The grip 14 can encompass any of a variety of shapes. In one embodiment shown in FIGS. 1 and 3, the grip 14 can have a tilted lever shape with semicircular ends. Preferably, the grip body can be tilted in the proximal direction. The grip 14 can be shaped to facilitate easy grasping and manipulation by a user. For example, the tilted portion of the grip 14 can have a contour that can comfortably receive a user's hand or fingers.

5-25 show various exemplary components of the stabilization device 100. FIG. 5 shows one exemplary embodiment of the base pad 102. The pad can have a proximal facing surface 102p and an adhesive distal facing surface, not shown. The adhesive distal facing surface can be adhered to an anchor surface such that the pad 102 is secured to the anchor surface. For example, the pad 102 can be adhered to the patient's skin such that the pad 102 is secured firmly to the patient. However, in other embodiments, the pad 102 can be adhered to any of a variety of surfaces. The pad 102 can preferably be made from a flexible material such that the pad can conform to the anchor surface. A flexible pad 102 can allow the pad to adhere to the patient's skin in any of a variety of application positions. The adhesive distal facing surface of the pad 102 can have a distal adhesive layer. For example, the adhesive layer can be a medical grade adhesive.

By way of non-limiting example, the pad 102 may be made from any of a flexible fabric, an elastomer, and a polymer. Exemplary materials include synthetic or natural rubber. In one embodiment, the pad 102 may be made from a thin polymer, such as, for example, rubber, neoprene, polytetrafluoroethylene (PTFE), etc. In some embodiments, the thin polymer pad may have a thickness of 1 mm to 5 mm. In other embodiments, the thin polymer pad may have a thickness of 1.5 mm to 3.5 mm.

The pad 102 can have any of a variety of sizes and shapes and can be tailored to suit a particular surgical procedure or application. For example, the shape of the pad 102 can be configured to cover the entire sterile drape opening. In one embodiment, the pad 102 can have a generally rectangular shape with rounded corners, as shown in FIG. 5. Alternatively, the pad can have a thin shape to fit within an anatomical structure, such as the lower back of a small patient. Additionally, the pad 102 can be cut, trimmed, or otherwise shaped to aid in placement for a particular application or surgical procedure. For example, the pad 102 can be cut to fit an obstacle or object that may be placed at or near the surgical site.

The pad 102 may have an opening 106 extending through the pad from the proximal facing surface 102p to the distal facing surface. It will be appreciated that the opening 106 may be any of a variety of different shapes and sizes. Additionally, the opening 106 may be located at a variety of different locations on the pad 102. For example, the opening 106 may be generally circular and located at a central portion of the pad 102 as shown in FIG. 5. Alternatively, the opening 106 may be located off-center or closer to the edge of the pad 102. The pad 102 may have a recess 108 surrounding the opening 106. The recess 108 may promote smoother engagement and relative movement between the locking mechanism 104 and the pad 102. In one embodiment, the recess 108 of the pad 102 may have a shape or curvature similar to the distal facing portion of the locking mechanism 104, as discussed in more detail herein.

The pad 102 may have one or more engagement features configured to removably attach the pad to the locking mechanism. In one embodiment, one or more protrusions 110 may extend proximally from a proximal facing surface of the pad 102. The protrusions 110 may be configured to engage complementary portions of the locking mechanism 104 to facilitate a secure connection between the pad 102 and the locking mechanism 104. In one embodiment, the protrusions 110 may be generally rectangular or oval and may extend apart on the proximal facing surface of the pad 102. In one embodiment, the pad 102 may include a plurality of protrusions 110 spaced apart about the periphery of the opening 106. Any number of protrusions 110 may be formed on the pad 102 to enable the locking mechanism 104 to stably mate with the pad 102. Although the protrusions 110 are shown disposed about the periphery of the opening 106, the protrusions 110 may be disposed at any of a variety of locations on the pad 102. Those skilled in the art will recognize that other engagement features and methods can be used to secure the locking mechanism 104 to the pad 102. Non-limiting examples of engagement features include snap mechanisms, key lock mechanisms, any of a variety of screws or other thread features, and the like.

The pad may further include various features to assist or aid the user. The pad may have imaging features to aid imaging of the pad during positioning. For example, the pad 102 may include radiopaque markings 112 to aid in fluoroscope identification during positioning. The radiopaque markings may be identified by an imaging system to provide accurate feedback regarding the placement of the pad 102. In one embodiment, the markings 112 may aid in positioning a locking mechanism engaged within the pad 102 or an opening 106 in the pad 102 a specific known distance away from the midline of the patient. The pad 102 may include navigation features to aid navigation of a surgical access device coupled to the pad. For example, the pad may have reflective fiducials or markers to aid surgical navigation of the trajectory or axial placement of the coupled surgical access device.

In one embodiment, the locking mechanism 104 can be attached to the pad 102 through the opening 106 such that a portion of the opening 106 and the central opening of the locking mechanism 104 are aligned to form the central opening 101 of the surgical access stabilizer. In an exemplary embodiment, a base 200 of the locking mechanism 104 can be connected to the pad 102 as shown in FIG. 6. The base 200 can serve as a primary contact between the locking mechanism 104 and the pad 102. The base 200 can include an opening 216 that can align with at least a portion of the pad opening 106. Although the base 200 is shown as having a generally ring shape, it will be understood that the base 200 can have any of a variety of shapes. The base 200 and pad 102 can be preassembled as a single unit prior to a surgical procedure. Alternatively, the pad 102 and base 200 can be configured as two separate components that can be attached during a surgical procedure, either before or after adhering the pad 102 to the anchor surface. For example, the pad 102 can be adhered to the anchor surface at a desired location. With the pad secured in place, engagement features of the base 200 can engage with engagement features of the pad 102 such that the base 200 is securely attached to the pad 102.

As a non-limiting example, as shown in FIG. 7, the engagement feature of the base 200 may be configured as a slot 209. The slot 209 may extend through the base 200 and may be configured to receive the protrusion 110 of the pad 102. The base 200 may be securely attached to the pad 102 by placing the protrusion 110 of the pad into the slot 209 of the base to form a snap fit between the base and the pad. It will be understood that alternative attachment mechanisms may be utilized to secure the base 200 to the pad 102. The base 200 may have a tapered portion 218 that extends inwardly from an outer portion of the base 200 to the opening 216. Preferably, the tapered portion 218 may have a shape complementary to the shape of the recess 108 of the pad 102. When the base 200 is attached to the pad 102 , the tapered portion 218 of the base 200 and the recess 108 of the pad 102 may be aligned to seat the base 200 within the pad 102 .

FIG. 8 shows a perspective view of the base 200. A plateau 220 may be formed between the tapered portion 218 and an outer rim wall 222. The outer rim 222 may extend proximally from the plateau 220 to create a ring around the outer edge of the base. In one embodiment, the outer rim 222 may taper from a distal end to an opposing proximal end at the junction with the plateau 220. The outer rim 222 may have an upper lip at a proximal end of the rim 222 and include one or more extensions 224 extending radially inwardly over the plateau 220 such that a groove 225 is formed between the upper lip of the extension 224 and a surface of the plateau 220. A transition 226 may be formed at one end of each extension 224. In a preferred embodiment, the transition 226 may be formed at a distal end of each extension 224 as measured in a clockwise direction along the circumference of the base 200. The transition portion 226 may be a solid portion that extends distally from the upper lip to the plateau 220. In other words, the transition portion 226 forms a stop within the circumferential groove 225. The transition portion 226 may also define a transition between the extension 224 and the recess 228. The recess 228 does not have any portion that extends radially inward beyond the outer rim 222. Thus, the transition portion 226 may have an outer edge that slopes radially outward from a radially inner location of the extension 224 to a location on the inner surface of the rim. The recess 228 may form a concave or pocket-like region between the two extensions 224.

As can be seen from the top view of the base 200 in FIG. 9, one embodiment of the base 200 may include three extensions 224 separated by three recesses. Preferably, one of the recesses may be a deformation recess 229. The tabs 230 may be biased radially outward by an object inserted into the base 200 and rotated in a clockwise direction. The tabs 230 may return to a neutral position once the outward force is removed, as shown in FIG. 9. The tabs 230 may be formed by a channel 232 that extends radially inward from the outer edge of the rim 222 and continues a circumferential distance along the plateau 220. The tabs 230 may be formed to include a stop 227 that extends distally to the plateau 220, similar to the transition portion 226 described above. As will be described below, the retaining ring 202 may be rotatably received within the base 200 such that the retaining ring can be rotated between a locked state and an unlocked state. The tabs 230 can secure the retaining ring in the locked position and can prevent unwanted rotation of the retaining ring back to the unlocked state. The identification feature 234 can extend from a portion of the tabs 230 to assist the user in orienting and assembling the surgical access stabilizer. For example, the identification structure 234 can extend proximally from the stop 227 of the tab portion 230. In one embodiment, to return the retaining ring from the locked state to the unlocked state, the user can position the tabs 230 by the identification structure 234 and simultaneously apply a force to the tabs 230 to urge the tabs 230 outwardly and rotate the retaining ring 202 to the unlocked position.

Additional exemplary features of the locking mechanism 104 will now be described. FIG. 10 is a perspective view of the pad 102 with several components of the locking mechanism 104 that couple the port 10 to the pad. In addition to the base 200, FIG. 10 shows the skirt 204 and split ring 206 of the locking mechanism 104. With the base 200 coupled to the pad 102, the skirt 204 can be placed on top of the proximal facing surface of the base 200. As best shown in FIGS. 11 and 15, the skirt 204 can preferably have a tapered surface 318. The surface 318 can have a surface taper that is complementary to the tapered surface 218 of the base 200. The skirt 204 can be positioned such that the tapered surface 318 of the skirt 204 seats within the tapered surface 218 of the base 200. The tapered surface 318 of the skirt 204 can extend inward from the outer edge of the skirt 204 toward the opening 316. In one embodiment, the tapered surface 318 may be generally ring-shaped and form the body of the skirt 204. It will be appreciated that the skirt 204 may have any of a variety of shapes. When the skirt 204 is seated within the base 200, the opening 316 in the skirt 204 may align with at least a portion of the opening 216 in the base 200 and the opening 106 in the pad 102.

The skirt 204 may have an extension 320 extending proximally from the surface 318 to define the opening 316. In one embodiment, the inner surface 324 of the extension 320 defining the opening 316 may preferably be a smooth surface tapered from the proximal end of the opening to the distal end of the opening. As described below, the smooth tapered surface 324 may facilitate rotational and angular movement of the split ring 206 relative to the skirt 204, and of the surgical access device received therein. The extension 320 may include an engagement feature configured to engage another portion of the locking mechanism 104, and preferably to engage a locking component of the locking mechanism 104. In one embodiment, the engagement feature may be male threads 322 formed on the outer surface of the extension 320. Other means for engaging the skirt 204 with the locking component of the locking mechanism 104 are also contemplated within the scope of the present invention.

The skirt 204 may preferably be made from a polymer or other flexible material. The skirt 204 is configured such that the skirt can translate in accordance with the translational motion of a surgical access device received by the surgical access stabilizer 100. The thickness of the skirt 204 may preferably be slightly less than the height of the cavity formed between the base 200 and the retaining ring 202. As described in more detail below, an outer portion of the skirt 204 may be slidably received within the cavity such that the skirt 204 can translate in any radial direction along the base 200.

FIG. 12 illustrates a split ring 206 that can be received within the opening 316 of the skirt 204 to facilitate coupling of a surgical access device to the pad 102 via the locking mechanism 104. The split ring 206 can have an opening 416 configured to receive a surgical access device. The opening 416 can be defined by a circumferential wall 400 having an outer surface 402 and an inner surface 404. In one embodiment, the outer surface 402 and the inner surface 404 can have different shapes such that the circumferential wall 400 has a non-uniform thickness. As a non-limiting example, the outer surface 402 can be generally circular and the inner surface 404 can be elliptical or oval. In a preferred embodiment, the inner surface can have a perimeter that corresponds to the shape of the surgical access device received therein. The outer surface 402 of the split ring 206 can have a curved contour and the inner surface 404 can have a linear contour. The curved contour of the outer surface 402 can allow the split ring 206 to move more easily relative to the skirt opening 316. In this manner, the split ring 206 can be rotated or angled relative to the longitudinal axis A1 of the skirt and the surgical access stabilizer. Figure 13 shows a skirt 204 with a split ring 206 having a port 10 received through an opening 416 in the split ring. As can be seen, the port has an oval shaped outer surface that is mirrored in the shape of the inner surface 404 of the split ring 206.

Returning to FIG. 12 , a channel 410 can be formed extending through the peripheral wall 400. The channel 410 can provide flexibility to the split ring 206 so that it can expand to accommodate a greater number of surgical access devices within the opening 416. The split ring 206 can have one or more engagement features configured to aid in selective longitudinal positioning of the surgical access device 10 received within the opening 416. In one embodiment, at least one inwardly projecting protrusion 408 can be formed on the inner surface 404 to engage with a complementary feature formed on an outer surface of the surgical access device, such as a plurality of grooves 18. Interaction of the split ring engagement feature with the complementary feature formed on the outer surface of the surgical access device can provide easier alignment and longitudinal adjustment of the surgical access device relative to the inner ring as the surgical access device passes distally through the opening 416. Engagement of the engagement features of the split ring 206 with an inserted surgical access device can provide a secure connection between the two components, allowing the split ring 206 to move in accordance with the application of force to the surgical access device. Additionally, the complementary engagement features of the split ring and the surgical access device can provide beneficial tactile feedback to the user regarding the alignment and engagement of the surgical access device with the inner ring.

FIG. 14 shows a perspective view of the locking mechanism, including the assembled base 200, skirt 204, split ring 206, and retaining ring 202. As shown, the opening 416 of the split ring 206 can extend through the various components of the assembled locking mechanism. The cross-sectional view of FIG. 15 shows how the various components of the locking mechanism 104 can be assembled relative to one another. The skirt 204 can be positioned such that an outer portion of the skirt is slidably received within a cavity 212 formed between a proximal facing surface of the base 200 and the retaining ring 202. The skirt 204 can thus translate within the cavity 212 with a force applied by a user. The split ring 206 can be positioned within an opening defined by the extension 320 of the skirt 204. As discussed above, the outer curved surface 402 of the split ring 206 can be rotatably received by the inner surface 324 of the extension 320. Thus, the split ring 206 can be angled or rotated through a full range of motion within the opening 316 in the skirt 204 .

The retaining ring 202 will now be described in more detail with reference to Figures 15-19. Figure 16 shows a top view of one embodiment of the retaining ring of the present invention. In one embodiment, the retaining ring 202 can have an annular body 500 with a rim 504 having at least one radially extending projection 502. The retaining ring 202 can be configured such that the retaining ring can be positioned and secured within the base 200. In one embodiment, the radially extending projection can engage features of the base 200 to secure the placement of the retaining ring within the base 200. The body 500 can define an opening 516, at least a portion of which can be aligned with other components of the locking mechanism to form the central through opening 101. The retaining ring 202 can be sized such that the retaining ring fits within the base. Additionally, the retaining ring body 500 extends radially inward a distance away from the surface of the base 200 to form a circumferential cavity 212 between the base 200 and the body 500 and is configured to slidably receive the skirt 204. In one embodiment, the opening 516 may be generally circular and formed at a central location of the retaining ring 202. Preferably, the opening 516 may have a diameter larger than the diameter of the opening 216 in the base 200 and larger than the diameter of the opening 316 in the skirt 204.

The body 500 may have a generally stepped profile formed from an outer rim 504, a proximally extending portion 506, and a laterally extending portion 510. The proximally extending portion 506 may extend proximally from the rim 504. As best seen in FIG. 15, the proximally extending portion 506 may form a circumferential ring of the body 500 having a radial thickness less than the radial thickness of the body 500. The laterally extending portion 510 may extend radially inward from a proximal end of the proximally extending portion 508 toward an opening 516. Specifically, the laterally extending portion 510 may be elevated a distance from a distal end of the proximally extending portion 508 such that a cavity 212 is formed below the laterally extending portion 510 from an inner radial point of the body 500 to an inner facing surface of the proximally extending portion 506.

In other words, the body 500 can have a solid walled circumference, i.e., a proximally extending portion 508, and a flared, i.e., laterally extending portion 510, which does not extend the full distal length of the solid walled circumference, but rather creates a radial gap at the distal portion of the retaining ring 202. The laterally extending portion 510 can have a tapered shape such that the height of the laterally extending portion 510 increases along a radially inward direction. Preferably, the taper of the laterally extending portion 510 can be complementary to the tapered portion 218 of the base 200. In this manner, the radial cavity 212 formed between the distally facing surface of the laterally extending portion 510 and the proximal facing surface of the base 200, particularly the proximal facing surface of the tapered portion 218 of the base 200, can maintain a constant height along the radial direction. The radial cavity 212 is formed by disposing the retaining ring 202 within the base 200. The components of the locking mechanism 104 may be sized to allow the skirt 204 to slidably fit within the cavity 212 .

A radially inwardly facing surface of the laterally extending portion 510 may have threads 512 configured to engage another component of the locking mechanism 104. As described in detail below, the threads 512 may preferably engage with threads of the first locking piece 208. It will be appreciated that alternative engagement mechanisms between the retaining ring 202 and the first locking piece 208 are possible, so long as the first locking piece 208 can be selectively tightened or locked relative to the retaining ring 202.

17, the radially extending projections 502 may extend radially outward from the rim 504 and may be configured to engage the grooves 225 of the base 200. Inserting the retaining ring 202 into the base 200 may include aligning the radially extending projections 502 with the recesses 228 of the base 200 such that the projections 502 are aligned with the grooves 225. Once inserted, the retaining ring 202 may be secured within the base 200 by rotating the retaining ring 202 such that the leading edge 518 of the radially extending projections 502 abuts the edge of the transition portion 226 of the base 200. The proximal facing surface of the primarily laterally extending portion 510 may have at least one projection 514 to aid in gripping and rotating the retaining ring 202 from the proximal facing surface. In this manner, the projections 502 may be received within the extensions 224. 18, leading edge 518 and transition portion 226 may have complementary shapes such that leading edge 518 mates with transition portion 226. When leading edge 518 abuts transition portion 226, extension 224 of base 200 extends over radially extending protrusion 502, thereby constraining longitudinal movement of retaining ring 202 relative to base 200. In a preferred embodiment, extension 224 of base 200 may extend inwardly a radial distance such that a small gap 240 may be formed between an inner facing surface of extension 224 and an outer facing surface of body 500.

Figure 19 is the cross-sectional top view of Figure 18 showing the retaining ring 202 engaged with the base 200 and rotated so that the projections 502 are aligned with the extensions 224. In this locked position, the leading edge 518 of each projection 502 is seen to abut the transition portion 226 of the base 200. A cavity 212 configured to slidably receive the skirt 204 is seen between the inner surface of the laterally extending portion 510 and the base 200.

FIG. 20 illustrates a surgical access stabilizer 100 having a locking mechanism 104 having a first locking part 208 and a second locking part 210. In the illustrated embodiment, the locking mechanism 104 can include first and second locking parts for selectively locking the position of the surgical access device relative to the underlying pad. In a preferred embodiment, the first and second locking parts, e.g., 208 and 210, can be locking rings. In other embodiments, the locking mechanism 104 can include, for example, at least one peelable adhesive site, a threaded locking knob, or a lever-operated tightening wheel. It will be understood that any of the locking components disclosed herein are contemplated for use alone or in combination to selectively lock the movement of the surgical access device relative to the pad. In an exemplary embodiment, as shown in the cross-sectional view of FIG. 21, the first locking part 208 can be a locking ring configured to engage with the retaining ring 202 to selectively lock the translational movement of an inserted surgical access device, such as the port 10. The second locking component 210 may be a locking ring configured to engage with the skirt 204 to selectively lock rotational, angular, and translational movement of a surgical access device, such as the port 10, inserted within the split ring 206.

FIG. 22 is a perspective view of one embodiment of the first locking part 208. Preferably, in one embodiment, the first locking part may be generally ring-shaped having a wall 602 and an opening 608. The outer diameter of the first locking part may preferably be substantially the same as or slightly smaller than the inner diameter of the retaining ring 202. The outer surface of the wall 602 may have an engagement feature 604 configured to engage with a complementary engagement feature of the retaining ring 202. Preferably, the engagement feature may be a thread 604 formed on the outer surface of the wall 602. A tab 606 may extend radially from the top of the wall 602 to aid in rotating or otherwise moving the first locking part 208. In one embodiment, the tab 606 may be sized and shaped to facilitate a user to grip the tab 606 and rotate the first locking part 208.

21 shows a cross-sectional view of the first and second locking parts 208, 210 engaged with the retaining ring 202 and skirt 204, respectively. The base 200 and split ring 206 are also shown. The first locking part 208 can be rotated in a first direction relative to the retaining ring 202 to move the first locking part 208 distally toward the base 200. The first locking part 208 can be rotated in a second direction relative to the retaining ring 202 to move the first locking part 208 proximally away from the base 200. As the first locking part 208 moves distally toward the base 200, the skirt 204, disposed within the cavity 212, can be clamped between the base 200 and the first locking part 208 such that translational movement of the skirt 204 is restricted. On the other hand, when first locking component 208 is rotated in a second direction and moves proximally away from base 200 along the inner circumference of retaining ring 202, the compressive force on skirt 204 is released, allowing skirt 204 to translate in any radial direction relative to base 200. More specifically, when skirt 204 is not clamped by first locking component 208, a force can be applied by the surgeon or user to skirt 204 such that an outer portion of skirt 204 can move within cavity 212. In this configuration, movement of skirt 204 is constrained by the radial depth of cavity 212 and the dimensions of skirt 204.

FIG. 23 illustrates an exemplary embodiment of the second locking component 210 configured as a locking ring formed by a wall 702 having a central opening 706. The outer surface of the wall 702 may be shaped to have a curved lower portion and a tapered upper portion. With reference to FIG. 24, the wall 702 may have a radially inwardly extending upper portion 708 that forms a hood over the inner surface 704 of the second locking component 210. The opening 706 may be defined by the inner surface of the upper portion 708 at a proximal end and by the inner surface 704 at a distal end. In this manner, the opening 706 may have a first diameter at the proximal end that is smaller than a second diameter of the opening 706 at the distal end. As described in more detail below, the larger diameter opening at the distal end of the opening 706 may allow radial movement of an object, i.e., the extension 320 of the skirt 204 engaged with the second locking component, and may selectively limit movement of a surgical access device received within the surgical access stabilizer 100.

Preferably, the inner surface 704 can have an engagement feature 712 configured to engage with a complementary engagement feature of the skirt 204. In one embodiment, the second locking part can have internal threads 712 formed along the inner surface 704 configured to engage with threads 322 on the outer surface of the skirt extension 320. The second locking part 210 can be rotated in a first direction relative to the skirt 204 to move the second locking part 210 distally relative to the skirt 204. The second locking part 210 can be rotated in a second direction relative to the skirt 204 to move the second locking part 210 proximally relative to the skirt 204. The tab 710 can extend proximally from the outer surface of the wall 702. Similar to the tab 606 of the first locking part, the tab 710 can aid in the rotation or movement of the second locking part 210 by a user. Preferably, the tab 710 can be sized and shaped to facilitate a user's gripping of the tab 710.

FIG. 25 illustrates a cross-sectional view of one embodiment of the second locking component 210 engaging the skirt 204. As can be seen, the internal female threads 712 of the second locking component 210 can engage with the external threads 322 of the extension 320 of the skirt 204. When the second locking component 210 is rotated in a first direction, the second locking component 210 moves distally relative to the skirt 204, which exerts a radially inward compressive force biasing the extension 320 of the skirt 204 radially inward. On the other hand, when the second locking component 210 is rotated in a second direction, the second locking component moves proximally relative to the skirt, thereby reducing any inward compressive force exerted by the second locking component on the skirt 204. In this manner, when a surgical access device is received within the opening formed by the skirt 204, the second locking component can selectively limit movement between the surgical access device and the skirt by selectively applying and removing an inward compressive force on the skirt extension 320. As can be seen in FIG. 25 , the tapered inner surface 324 defining the opening of the skirt 204 is tapered such that a radially inward compressive force can cause the upper portion of the tapered surface 324 to move radially inward toward a straighter profile and abut against the outer surface of an instrument or object received therein. In an exemplary embodiment, referring again to FIG. 21 , the split ring 206 can be retained within the tapered surface 324 to receive a surgical access device. The radial compressive force applied to the skirt extension 320 by the second locking component 210 can cause the extension 320 to compress inwardly relative to the split ring 206. This inward compression can limit the movement of the split ring 206, and thus the movement of the received surgical access device, relative to the skirt 204.

Figure 26 illustrates a first exemplary surgical application of the surgical access stabilizer 100 of the present invention. Figure 26 illustrates the surgical stabilizer 100 fully assembled with the port 10 received therein. The distal facing surface of the pad 102 is adhered to the patient's skin. In this embodiment, the pad 102 is formed as a complete patch having a generally elliptical or egg shape.

FIG. 27 illustrates a portion of an exemplary method of use of the surgical access stabilizer 100. In FIG. 27, the pad 102 is shown attached to an anchor surface, such as the patient's skin, in a position such that the surgical incision 120 is located within the opening 106 of the pad 102. A base 200 is shown secured to the pad 102. In one embodiment, the pad 102 can be attached to the anchor surface as a stand-alone component. Once attached, the base 200 can be secured to the proximal facing surface of the pad 102 by a user. For example, the surgeon can first select, cut, or manipulate the pad 102 into the desired shape and dimensions for a particular surgical application. The adhesive distal facing side of the pad 102 can then be placed in the desired location on the patient's skin. With the pad securely attached, the base 200 can be moved distally on the pad 102 and secured to the pad 102 by engaging complementary engagement features on the base and pad. For example, the slots 209 of the base 200 can be aligned with the protrusions 110 of the pad 102. The base can then be secured to the pad 102 with a snap fit.

Alternatively, the base 200 can be secured to the pad 102 prior to adhering the pad 102 to the anchor surface. In one embodiment, the pad and base may be pre-assembled as a single, integral component for use in a surgical procedure. Alternatively, the pad and base may be constructed as two separate components that are attached prior to a surgical procedure. In this manner, the pad and base may be positioned during a surgical procedure as a single, assembled unit.

As shown in FIG. 27, with the pad 102 secured to the engagement surface and the base 200 attached to the pad 102, the surgeon is manipulating tissue (e.g., navigating to a surgical site, widening the incision 120, etc.) using an instrument 15 inserted through the incision 120. It will be appreciated that the incision 120 may be made either before or after the pad 102 is secured to the anchoring surface. Additionally, the incision 120 may be widened to accommodate various instruments either before or after the pad 102 is secured to the engagement surface and either before or after the base 200 is attached to the pad 102. Once the incision is widened to accommodate a surgical access device, such as the port 10, the port may be inserted through the incision. Again, insertion of the surgical access device may occur either before or after the pad 102 is secured to the engagement surface and either before or after the base 200 or any other components of the locking mechanism 104 are attached.

In one exemplary method, the incision 120 can be made at a desired location on the patient. The pad 102, pre-sized and shaped to meet the requirements of a particular surgical procedure or application, can then be secured to the patient's skin by placing the adhesive distal surface of the pad 102 against the surface of the skin. In other embodiments, a standard sized and shaped pad can be cut or otherwise manipulated during surgery to meet the requirements of a particular surgical procedure or application. The pad 102 can be pre-assembled with the base 200 attached. Alternatively, the base 200 can be attached to the pad 102 once the pad 102 is secured to the patient's skin. In a preferred embodiment, the pad 102 can be aligned such that the incision 120 is centered within the opening 106 of the pad 102. With the pad and base surrounding the incision 120, the incision 120 can be prepared to receive the port 10. For example, the incision 120 can be dilated using a set of dilator tubes to obtain the desired incision opening. Alternatively, incision 120 may be prepared to receive a surgical access device using other methods known in the art. Port 10 may then be inserted into incision 120 using standard surgical techniques.

With the port 10 inserted and the base 200 secured on the pad 102, the locking mechanism 104 can be positioned within the base 200. The locking mechanism 104 can be comprised of a retaining ring 202, a skirt 204, a split ring 206, a first locking part 208 configured to engage the retaining ring 202, and a second locking part 210 configured to engage the skirt 204. The port 10 can be positioned in the opening 416 of the split ring 206, and the locking mechanism 104 can be moved distally along the port 10 until a distal facing surface of the locking mechanism 104 contacts a proximal facing surface of the base 200. In one embodiment, the distal facing surface of the skirt 204 can contact a proximal facing surface of the base 200, and the retaining ring 202 can be aligned with the base 200 in an unlocked position. To secure the locking mechanism 104, the retaining ring 202 can be rotated from the unlocked position to the locked position. In the unlocked position, the radially extending protrusions 502 of the retaining ring may be aligned with the recesses 228 of the base, as described above. The retaining ring 202 may then be rotated in a first direction such that the protrusions 502 rotate into engagement with the transition portion 226 of the base extension 224. The tab portions 530 of the base 200 may be biased radially outward by the retaining ring protrusions 502 and may remain in an outward position as the protrusions 502 pass completely into the extension 224. The retaining ring 202 and base 200 may be configured such that in the locked position, i.e., when the leading edge of the protrusions 502 engages the transition portion 226, the protrusions 502 clear the tab portions 230 such that the tabs 230 are no longer biased radially outward and may return to their neutral configuration. In this manner, because the tabs 230 and transition portions 226 are located on either end of the protrusions 502 in the locked position, the tab portions 230 can function as a securing mechanism to prevent the retaining ring 202 from rotating out of the locked position during surgical application. A user can grasp the feature 514 to facilitate smooth and easy rotation of the retaining ring relative to the base. Although the above description is provided in the context of assembly of various components, such as the locking mechanism 104 after insertion of the port, it should be understood that in some embodiments, the port may be inserted through an existing locking mechanism while in the unlocked configuration.

With the locking mechanism 104 disposed within the base and the port 10 extending therethrough, the port 10 may be adjusted to a desired trajectory, orientation, and position. The port 10 may be adjusted relative to the pad 102 with multiple degrees of freedom. For example, the port 10 may translate in any radial direction relative to the pad 102. In one embodiment, a surgeon may apply a translational force to a proximal portion of the port 10 by grasping and moving the proximal portion of the port 10 or a handle attached thereto. The skirt 204 may move according to the translational force applied to the port 10. The skirt 204 may translate or slide within the cavity 212 between the base 200 and the retaining ring 202. After achieving the desired positioning of the port 10, the first locking component 208 may be rotated in a first direction to clamp the skirt 204 in the desired position within the cavity 212, thereby restricting further radial translation of the skirt, and thus the attached port 10. By rotating the first locking part 208 in a second direction, the first locking part can be moved proximally from the base, thereby releasing the clamped skirt 204, thereby allowing translational movement of the skirt, and thus the attached port 10.

The port 10 can also be angled, rotated, or translated longitudinally relative to the pad 102. For example, the port 10 can be rotated 360 degrees by grasping a proximal portion of the port 10 and rotating the port. The split ring 206 having a rounded outer edge 402 can be rotated 360 degrees within the tapered inner surface 324 of the opening 316 of the skirt 204. Additionally, the port 10 can be angled to a variety of desired orientations by grasping a proximal portion of the port 10 and angling the port relative to the pad 102. Again, the rounded outer edge 402 of the split ring 206 can be angled relative to the tapered inner surface 324 of the opening 316 of the skirt 204.

The port 10 can also be translated longitudinally relative to the pad 102 by applying a force in a proximal or distal direction to the proximal end of the port 10 such that the port 10 translates proximally or distally relative to the pad 102. Once the desired orientation and positioning of the port 10 is achieved relative to the pad 102, the second locking component can be rotated in a first direction to limit further rotational, angular, or translational motion. In one embodiment, as the second locking component rotates in a first direction, it moves distally and applies an inward compressive force to the skirt extension 320. As the skirt extension 320 compresses radially inward, the skirt extension is compressed onto the split ring 206 with the port 10 disposed therein. After rotating the second locking component a first amount, the compressive force applied by the second locking component limits the longitudinal translational motion of the port. After rotating the second locking component further a second amount, the compressive force applied by the second locking component can limit the rotational movement of the port relative to the pad by limiting the ability of the inner ring 206 to rotate relative to the inner extension 320 of the skirt 204. After rotating the second locking component further a third amount, the compressive force applied by the second locking component can limit the angular movement of the port relative to the pad by limiting the ability of the split ring 206 to angle relative to the extension 320 of the skirt 204. Rotating the second locking component in a second direction moves the second locking mechanism proximally relative to the inner extension 320 of the skirt 304 and reduces the inner compressive force received on the skirt 204, and thus on the split ring 206 and the port 10. As the second locking component rotates in the second direction, the port 10 can move relative to the pad 102. In this manner, the second locking component can be used to selectively limit translational, rotational, and angular movement of the port relative to the pad. The locking mechanism 104 allows adjustment of the port 10 during a surgical procedure by leaving it in an unlocked state, and can be relocked, if desired, to secure the port in a different position or trajectory.

With the port 10 established and stabilized in a desired position and trajectory, various instruments, implants, etc. can be passed percutaneously through the port 10 to the surgical site. For example, as shown in FIG. 28, the surgical access device can be a port tube 30 used to access a surgical site located in the spinal region 32. An instrument 34 can be inserted through the port tube 30. The instrument 34 can be any of a variety of instruments, such as a camera or an implant. In one embodiment, the port tube 30 can be, for example, a 15 mm rigid port sized to accommodate any of a variety of objects, including larger implants. The inner lumen of the port tube 30 can be sized to facilitate the insertion of a variety of instruments, implants, etc. having a variety of shapes. Thus, non-circular lumen shapes may be preferred.

FIG. 29 illustrates an exemplary application of the surgical access stabilizer 100 configured to receive a flexible mesh port 40. In the embodiment of FIG. 29, the locking mechanism 104 may be adapted to receive a flexible port or other surgical access device by including a cap member 44 for securing and selectively closing the opening to the surgical access device. The cap member 44 may be removable from the proximal end of the surgical access device to allow instruments, implants, and the like to be passed percutaneously to the surgical site 42. In some procedures, it may be desirable to use a flexible port to minimize trauma to the surrounding tissue. In one embodiment, the flexible port may be a 5 mm flexible port and may be sized and configured to receive visualization instruments, optical trocars, and medium-sized implants, among others. In another embodiment, the flexible port may be a 4 mm flexible port and may be sized and configured to receive small dilating implants, optical trocars, and visualization instruments, among others.

Modifications may be made to the above-described methods and devices and are considered within the scope of the present invention. For example, the locking mechanism 104 may be disposed within the base 200 and secured therein before the port 10 is inserted into the incision 120. In such an embodiment, the port 10 may be inserted into the incision 120 by moving the port distally through the central opening 101 of the surgical access device. As a further example, the first and second locking components may take forms other than locking rings and may selectively lock the port relative to the pad by means other than rotation to operate the first and second locking mechanisms. As non-limiting examples, the locking mechanisms of the present invention may include any number of removable adhesive adjustment sites, threaded locking knobs, or lever-operated tightening wheels. Furthermore, as referenced above, the locking mechanism 104 need not have separate first and second locking components. In one embodiment, a single locking component may be used to selectively limit movement of the port 10 relative to the pad 102. Regardless of the configuration used, the locking mechanism 104 is configured to couple and selectively lock the surgical access device relative to the pad.

In the surgical access stabilizer of the present invention, the foundation pad can have various shapes and sizes depending on the geometry of the application area or the needs of the user. In a surgical application, the specific shape and size of the pad can depend on various factors including the size of the patient, the location of the surgical site, the size of the incision, the size of the area to be treated, the range of motion required for the surgeon to complete the procedure, etc. FIG. 30 shows an embodiment of a surgical access stabilizer 1000 including a pad 1002 and a locking mechanism 1014 (not shown) located at a central portion of the pad 1002. The pad 1002 can have at least one radial finger 1004 extending from the central portion. The navigation marking 1008 can be included on one of the at least one radial finger 1004. In the embodiment shown, the pad 1002 has eight radial fingers 1004. Each radial finger 1004 can be sized and shaped as desired or needed by a particular application.

In another exemplary embodiment shown in FIG. 31, the surgical access device 1020 can include a pad 1022 formed from a thin polymer having an adhesive distal facing surface. In one embodiment, the thin polymer pad can be rubber, neoprene, PTFE, or the like. The pad 1022 can have a thickness of about 1 mm to about 5 mm, and in some embodiments, can have a thickness of about 1.5 mm to about 3.5 mm. In the embodiment shown in FIG. 31, at least a portion of the locking mechanism 1024 can be disposed between the anchor surface, i.e., the patient's skin, and the adhesive distal facing surface of the pad 1022. For example, the base 1026 of the locking mechanism 1024 can be disposed such that the distal surface of the base 1026 contacts the anchor surface. The pad 1022 can then be disposed over the anchor surface and the base 1026 such that the base 1026 is held fixed to the anchor surface by the pad 1022. The locking mechanism 1024 can be attached to the base 1026 in the manner described above.

32 illustrates yet another exemplary embodiment of a surgical stabilizer 1030 of the present invention. The surgical access stabilizer 1030 includes a pad 1032 configured as a complete patch having a generally rectangular shape. A locking mechanism 1034 is shown in a central location on the pad 1032. Alternatively, the locking mechanism 1034 may be received anywhere on the pad 1032. The pad 1032 can include navigational markings, such as marking 1036, to aid in alignment and placement of the pad 1032 relative to surgical or anatomical structures.

33 and 34 illustrate a second exemplary embodiment of the surgical access stabilizer of the present invention. As shown in FIG. 33, the surgical access stabilizer 1100 can include a pad 1102 configured to receive a surgical access device, such as a port 1110. A locking mechanism can couple the port 1110 to the pad 1102 and selectively lock movement therebetween. The pad 1102 can have an adhesive distal facing surface configured to contact an anchor surface. In a preferred embodiment, the adhesive distal facing surface of the pad 1102 can include a medical adhesive contact layer that contacts the patient's skin.

The pad 1102 can have an opening 1106 configured to receive a surgical access device. In a preferred embodiment, the opening 1106 can be an elongated slot extending along the pad 1102. For example, with reference to FIG. 34, the pad 1102 can have an opening 1106 extending along the longitudinal axis of the pad. In one embodiment, the pad 1102 can be generally rectangular in shape. As shown in FIG. 34, the opening 1106 can have a shape similar to or complementary to the pad 1102. Alternatively, the opening 1106 can have a shape different from the shape of the pad 1102. One of ordinary skill in the art will appreciate that the pad 1102 and the opening 1106 can have any of a variety of shapes.

The elongated slot opening 1106 can beneficially facilitate adjustment of the surgical access device in the transverse plane during a surgical procedure. Such adjustment allows for global changes to the angulation of the surgical access device. For example, in spinal surgery applications, it may be desirable to move the surgical access device in the transverse direction. Thus, the pad 1102 can be positioned such that the elongated opening 1106 extends in the transverse plane (e.g., extends medially laterally). In this manner, the port can be adjusted to allow for global changes in angulation. For example, the port can be positioned for 25 degree TLIF access or 45 degree Kambin access to a spinal surgical site.

The base 1108 can be configured to receive the port 1110 through a central opening in the base. Alternatively, the base 1108 can be integrally formed with the port 1110 in the form of a flange extending from a proximal end of the port 1110. Additionally, the base 1108 can be a single component, such as shown in FIG. 33, or the base 1108 can be multiple components. For example, the base 1108 can be configured similar to the skirt 104 described above and can be configured to receive the port 1110 using a split ring similar to the inner split ring 106 described above.

The locking mechanism can be configured to selectively limit movement of the port 1110 relative to the pad 1102. In one embodiment, the locking mechanism 1104 can be a removable adhesive. As a non-limiting example, the locking mechanism can be a hook and eye closure. For example, one side of the hook and eye closure can be disposed on a proximal facing surface of the pad 1102 near at least a portion of the opening 1106. A corresponding side of the hook and eye closure can be disposed on a distal facing surface of the base 1108. In this manner, the base 1108 can be removably secured to the pad 1102 by engaging two corresponding portions of the hook and eye closure. The base 1108 with the port 1110 inserted therein can be repeatably positioned and removed at multiple positions along the opening 1106 as desired. It will be appreciated that any other form of removable adhesive can be used in a similar manner.

In some embodiments, at least one additional locking component 1112 can be used to further selectively limit movement of the port 1110 relative to the pad 1102. In one embodiment, the locking component 1112 can be a locking ring having external threads 1114 configured to engage corresponding threads on the inner surface of the base 1108. A gripping portion 1116 can extend proximally from the locking component such that a user can rotate the locking component 1112 to selectively limit rotation, angulation, and longitudinal translation of the port relative to the pad 1102. It will be appreciated that the locking component 1112 can be configured similarly to one of the first and second locking components, as previously described herein.

FIG. 34 illustrates an exemplary positioning of the surgical access stabilizer of the second embodiment. The pad 1102 can be positioned such that the pad 1102 extends laterally along the transverse axis of the patient. In one application involving a spinal surgical site, the pad 1102 can be positioned laterally within the patient's lower back. The opening 1106 can extend laterally along the pad 1102 such that the base 1108, within which the port is received, can be selectively moved and adjusted along the transverse plane. In this manner, the surgeon can achieve global changes to change the angle of the port during surgery without having to remove the stabilizer or make additional incisions.

Another exemplary embodiment of the surgical access stabilizer of the present invention is shown in Figures 35 and 36. In some applications, it may not be desirable to place an adhesive pad close to the surgical site, or even close to the incision used to access it. For such situations, the surgical access stabilizer of the present invention can be used to couple the surgical access device to a remotely located underlying pad to position the surgical access device at a distance from the pad.

The surgical access stabilizer 1200 can have a connection mechanism 1204 configured to connect a surgical access device, such as a port 1210, to the pad 1202. In one embodiment, the connection mechanism 1204 can include an arm 1206 having a connector 1208 and an attachment component 1214. The attachment component 1214 can have a central opening that receives the surgical access device 1210. The connector 1208 can be located at a first end of the arm 1206 and can be configured to engage a portion of the attachment component 1214. A second end of the arm 1206 can be attached to the pad 1202 such that the arm 1206 couples the surgical access device to the pad.

As shown in FIG. 36, the pad 1202 may be similar to the pads described above. In one embodiment, the pad 1202 may be an expandable flexible pad having an adhesive distal facing surface. The pad 1202 may have an attachment portion 1212 configured to couple with a portion of the connection mechanism 1204, as described below. The pad 1202 and the arm 1206 may be integrally formed as one component or may be configured to be connected via one or more connection features. In one embodiment, an opening 1216 may be formed in the attachment portion 1212 and may be configured to receive a fastener 1218 of the arm 1206. It will be appreciated that the pad 1202 and the opening 1216 may take on any of a variety of shapes and dimensions as required by a particular application. The pad 1202 may be coupled to the arm 1206 by any number of known coupling methods. In one embodiment, the fastener 1218 may be a threaded screw fastener, as shown in FIG. 36. The fastener 1218 may be placed into the opening 1216 and engaged therein using thread features on the fastener 1218. Non-limiting examples of alternative fasteners include snap mechanisms, an interference fit of complementary male and female components, screws, threaded fasteners, and the like.

The arm 1206 can be made of a malleable material such that the arm can bend to adjust the positioning of the first end relative to the second end. In this manner, a surgical access device connected to the first end of the arm can be positioned in a desired position relative to a pad coupled to the second end of the arm by bending the arm to a desired configuration. In one embodiment, a connector 1208 can be located at the first end of the arm 1206 and engage a mounting piece 1214 to couple the port 1210 to the first end of the arm. The connector 1208 can engage the mounting piece 1214 by any connection means as known in the art. For example, in one embodiment, the connector 1208 can be a ball joint connector and an extension of the mounting piece 1214 can be received within a recess of the ball joint connector to secure the mounting piece 1214 to the arm 1206.

A handle 1220 can be associated with the port 1210 to aid in movement, e.g., rotational movement, of the port. In one embodiment, the port 1210 can be inserted through an opening in the handle 1220. The handle can have a gripping portion 1222 that extends radially outward from the opening. The gripping portion 1222 can include features to facilitate rotational movement of the port 1210. For example, the gripping portion can have a slot for an instrument or tab for a user to grasp. The rotational movement of the gripping portion can translate to a concomitant rotational movement of the inserted port.

37 and 38 show an exemplary use of the port after it has been placed in a stabilized position using the surgical access stabilizer of the present invention. Although FIGS. 37 and 38 show an embodiment of the surgical access stabilizer having bendable arms connected to the port, it will be understood that any of the embodiments described herein may be used to stabilize the port. FIGS. 37 and 38 show that the port may be used to pass any of a variety of instruments, implants, or objects percutaneously through the stabilized port to the target surgical site. For example, as shown in FIG. 37, the port 1310 may be secured by the surgical access stabilizer 1300. With the port 1310 stabilized, an elongated tool or other instrument having a navigation array 1350 may be inserted percutaneously through the port 1310 to the target site. As a further non-limiting example, FIG. 38 shows the port 1410 secured by the surgical access stabilizer 1400. With the port 1410 secured, a protective mesh 1450 may be inserted through the port to the target site to reduce trauma to the surrounding tissue. An additional instrument, such as a needle 1460 or other object, may then be passed percutaneously through the port 1410 and mesh 1450.

In another possible variation of the above-described method and device, the surgical access device can have a pad attached to a proximal portion of the surgical access device such that the pad can be deployed to adhere to an anchor surface. In one embodiment, as shown in FIG. 39, a surgical access device port 1510 can have an adhesive pad 1520 attached to a proximal end 1512 of the port. The adhesive pad 1520 can be attached to the proximal portion 1512 of the port such that after the port is inserted into a patient's incision, the pad can be deployed from the proximal portion of the port to adhere to an anchor surface, such as the patient's skin. The adhesive pad 1520 can be any of the pads described above. For example, in one embodiment, the pad 1520 can be a continuous pad such that, in a deployed state, the pad can cover the entire sterile drape opening. In other embodiments, the adhesive pad can include one or more extensions, fingers, or tethers that can be positioned in a deployed or undeployed state.

In the undeployed or inserted state, the adhesive pad can be compactly positioned and attached or secured to the proximal portion of the port while the port is being inserted through the incision. Alternatively, the pad can be attached or secured to the proximal portion of the port in the undeployed state after the port is inserted into the incision. For example, the pad can be snapped onto the proximal portion of the port in the undeployed state before or after the port is inserted into the incision. The pad can then be deployed so that the distal facing adhesive side of the pad can be adhered to the anchor surface. In one embodiment, the pad can be deployed by rotating or moving the pad or a portion of the pad distally toward the anchor surface. Alternatively, the engagement mechanism between the pad and the port can be released such that the pad or a portion of the pad is no longer secured to the port and can be manipulated by the surgeon to secure the distal facing adhesive side of the pad to the anchor surface. As a non-limiting example, the engagement mechanism can be a snap, screw, lever, tension member, or other engagement mechanism known in the art.

40-42 illustrate another embodiment of a handle 1600 of the surgical access stabilizer of the present invention. For example, the handle of FIGS. 40-42 can be associated with a surgical access device similar to that shown and described with respect to the port 1210 in FIGS. 35-36 where the handle 1220 is shown. The handle 1600 can include a body portion 1610 having an extension 1620 and a lever 1630. In one embodiment, the extension 1620 can be generally cylindrical and can extend distally from the handle body 1610. The extension 1620 can define a through hole 1640 through which a surgical access device, such as, for example, a port, can be inserted. It will be appreciated that the through hole 1640 can have any of a variety of shapes to allow a desired surgical access device to pass therethrough. As best seen in FIG. 42, the handle 1600 can include a locking portion 1650 that can engage with a feature of a surgical access device to selectively maintain relative positioning between the surgical access device and the handle 1600. In one embodiment, the locking portion 1650 can be a zip tie or ratchet/pawl style snap lever having one or more teeth 1652 that can engage with a feature on an outer surface of the surgical access device. For example, in one embodiment, the one or more teeth 1652 of the locking portion 1650 can selectively engage with one or more grooves formed on the outer surface of the surgical access device when the surgical access device is disposed within the through hole 1640. In some embodiments, the locking portion 1650 can include a tab or lever that is biased to engage the surgical access device without user interaction. Also, in some embodiments, one or more teeth 1652 can be configured to allow movement in a first direction while preventing movement in a second direction (e.g., allowing distal advancement of a surgical access device through the through hole 1640 while preventing proximal retraction).

FIG. 41 illustrates the lever 1630 of FIG. 40 separated from the body 1610. The lever 1630 can be selectively engaged with the locking portion 1650 to move the locking portion out of engagement with the surgical access device within the throughbore 1640 of the handle 1600, thereby acting as a release to allow adjustment of the surgical access device relative to the handle. In one embodiment, the lever 1630 can be a generally planar element having at least one engagement feature extending from its distally facing surface. In the embodiment illustrated in FIG. 41, a first post 1632 can extend from a distally facing surface of the first planar portion 1636 and can be received within a slot 1612 in the body 1610. A second post 1634 can extend from a distally facing surface of the second planar portion 1638 and can be received within a bore 1614 of the body. To insert the lever 1630 into the body 1610, lever engagement features such as posts 1632, 1634 can be moved into body receiving features such as slot 1612 and hole 1614. In one embodiment, the lever engagement features can snap into the body receiving features. The body slot 1612 can have a first end 1616 and a second end 1618. The first end 1616 of the slot 1612 can be located closer to the edge of the body 1610 than the second end 1618 of the slot. In other words, the slot 1612 can extend laterally inward from a location closer to the edge of the body 1610 toward the center of the body. While the embodiment of the handle 1600 shown in FIG. 41 has two engagement features and corresponding receiving features, it will be understood that the lever and body of the handle can have any number of engagement features and receiving features.

For example, as shown in FIG. 40, with the lever 1630 inserted into the body 1610, a user can engage the lever such that the lever moves the locking portion 1650 to selectively engage a surgical access device disposed within the through hole 1640. For example, a force can be applied to the lever 1630 such that the first post 1632 translates within the slot 1612. The second post 1634 of the lever can remain fixed within the body hole 1614 such that the lever can pivot about the second post as the first post 1632 translates within the slot 1612 in the body 1610. In one embodiment, a user can depress the lever by applying a force to the first planar portion 1636 of the lever in an inward direction, i.e., toward the centerline of the body 1610, causing the first post 1632 to translate within the slot 1612 and pivot the lever about the second post 1634. With the lever depressed, the second planar portion 1638 of the lever may engage a locking portion 1650 of the body 1610 to bias the locking portion to a position where the one or more teeth 1652 are disengaged from one or more grooves formed on the surgical access device disposed within the through hole 1640. In one embodiment, the lever 1630 may return to the position shown in FIG. 40 when the user releases the force described above. That is, the lever 1630 may pivot about the post 1634 such that the first planar portion 1636 moves radially outward. Such movement allows the locking portion 1650 to return (e.g., via a biasing force, etc.) to a position where the one or more teeth 1652 engage one or more grooves or other features formed on the surgical access device disposed within the through hole 1640.

It will be appreciated that the handle 1600 of Figures 40-42, and its various components, may be associated with a port in a number of different ways within the scope of the present invention. For example, a zip tie or ratchet/pawl style snap lever may be used as a component of the locking mechanism of the present invention in place of a split ring to selectively limit axial movement of a surgical access device. As a further example, the handle 1600 may be used in any of the various embodiments described herein. Additionally, the lever engagement feature and the body receiving feature may be formed as any complementary features such that the lever is coupled to the body of the handle and may be movable between an open position in which the locking portion of the handle is not engaged and a closed position in which the locking portion of the handle is engaged.

The exemplary embodiment above describes a spinal surgical application. While this is one contemplated use, the methods and devices of the present invention can be equally adapted for use in other areas of a patient's body. Thus, the devices described herein can be made in a variety of sizes and materials suitable for use in various areas of a patient's body.

Those skilled in the art will appreciate further features and advantages based on the above-described embodiments. Therefore, the present disclosure is not limited by what has been particularly shown and described. All publications and documents cited herein are expressly incorporated by reference in their entirety.

[Embodiments] (1) A surgical access stabilization device comprising: a pad having a proximal facing surface and an adhesive distal facing surface; a surgical access device coupled to the pad; and a locking mechanism configured to selectively lock the position of the surgical access device relative to the pad.

(2) The device of embodiment 1, wherein the pad has an opening extending therethrough configured to receive the locking mechanism.

(3) The device of embodiment 2, wherein the opening is an elongated slot.

(4) The device of any one of claims 2 to 3, wherein the opening is located in the center of the pad.

(5) The device of any one of claims 1 to 4, wherein the pad includes an imaging feature to assist in imaging the pad.

(6) The device of any one of embodiments 1 to 5, wherein the pad includes a navigation feature for assisting in navigation of the surgical access device.

(7) The device of any one of the preceding claims, wherein the pad has a central portion having at least one radial finger.

(8) The device of any one of embodiments 1 to 7, wherein the pad is made of any one of a flexible fabric, an elastomer, and a polymer.

(9) The device of any one of claims 1 to 8, wherein the locking mechanism is capable of selectively locking translational movement of the surgical access device in a direction along the proximal facing surface of the pad.

(10) The device of any one of claims 1 to 9, wherein the locking mechanism is capable of selectively locking translational movement of the surgical access device in a direction transverse to the proximal facing surface of the pad.

(11) The device of any one of embodiments 1 to 10, wherein the locking mechanism is capable of selectively locking either rotational motion of the surgical access device or angular motion of the surgical access device.

(12) The device described in any one of embodiments 1 to 11, wherein the locking mechanism further comprises at least one locking ring.

(13) The device described in any one of embodiments 1 to 11, wherein the locking mechanism further comprises one of a peelable adhesive and a hook-and-loop fastener.

(14) A surgical access stabilization system comprising: a pad having a proximal facing surface and an adhesive distal facing surface; a surgical access device defining a working channel; and a connection mechanism coupled between the pad and the surgical access device to position the surgical access device at a location away from the pad.

(15) The system of embodiment 14, wherein the connection mechanism further comprises an arm coupled at a first end to the surgical access device and coupled at a second end to the pad.

(16) The system of embodiment 15, wherein the arm is bendable to adjust the positioning of the first end relative to the second end.

(17) A method of stabilizing a surgical access device, the method comprising: making an incision in a patient; adhering a pad to the patient; inserting the surgical access device into the patient through the incision; coupling the surgical access device to the pad; and selectively locking a position of the surgical access device relative to the pad.

(18) The method of embodiment 17, further comprising positioning the surgical access device within the incision by at least one of translating, rotating, and angling the surgical access device relative to the pad.

(19) The method of claim 18, further comprising selectively locking the position of the surgical access device to prevent further translation, rotation, or angulation of the surgical access device relative to the pad.

(20) The method of any one of claims 17 to 19, wherein the pad is adhered to the patient after making the incision.

(21) The method of any one of claims 17 to 19, wherein the pad is adhered to the patient prior to making the incision.

(22) The method of any one of claims 17 to 21, wherein the pad is adhered to the patient at a location away from the incision.

(23) The method of any one of embodiments 17 to 22, wherein coupling the surgical access device to the pad further comprises positioning the surgical access device within an opening in the pad.

(24) The method of any one of embodiments 17 to 23, wherein coupling the surgical access device to the pad further comprises connecting the surgical access device to the pad using a connector arm.

(25) The method of any one of claims 17 to 24, further comprising deploying at least a portion of the pad from the surgical access device after the surgical access device is inserted through the incision.