Introducer drill

Abstract

A steerable, or curveable, introducer drill to access a target treatment region within bone along a curved trajectory is disclosed. The drill may include a drive shaft including a proximal rotational member, a distal drill tip, and an elongate shaft portion extending from the proximal rotational member to the distal drill tip. The distal drill tip may be sharp and include cutting flutes. The drill may also include an outer tube surrounding the drive shaft. A distal end portion of the outer tube may include a segmented tube section configured to facilitate controlled bending of the segmented tube section of the outer tube. The drill may also include an actuator operably coupled to the drive shaft and adapted to apply tension to the drive shaft which, in turn, causes the segmented tube section of the outer tube to bend.

Description

FIELD

Described herein are various implementations of systems, devices and methods for accessing bone (e.g., vertebral bodies of the spine) using a curveable, or steerable, introducer drill to facilitate access to target treatment locations within bone along a curved trajectory, especially in “hard” bone, or bone having a high or normal (e.g., non-osteoporotic or non-osteopenic) bone mass density.

BACKGROUND

Back pain is a very common health problem worldwide and is a major cause for work-related disability benefits and compensation. At any given time, low back pain impacts nearly 30% of the US population, leading to 62 million annual visits to hospitals, emergency departments, outpatient clinics, and physician offices. Back pain may arise from strained muscles, ligaments, or tendons in the back and/or structural problems with bones or spinal discs. The back pain may be acute or chronic. Existing treatments for chronic back pain vary widely and include physical therapy and exercise, chiropractic treatments, injections, rest, pharmacological therapy such as opioids, pain relievers or anti-inflammatory medications, and surgical intervention such as vertebral fusion, discectomy (e.g., total disc replacement), or disc repair. Existing treatments can be costly, addictive, temporary, ineffective, and/or can increase the pain or require long recovery times. In addition, existing treatments do not provide adequate relief for the majority of patients and only a small percentage are surgically eligible.

SUMMARY

Applicant's existing technology (the Intracept® procedure by Relievant®) offers a safe and effective minimally invasive procedure that targets the basivertebral nerve for the relief of chronic vertebrogenic low back pain. As disclosed herein, several embodiments provide adjunct technologies to facilitate access to target treatment locations within bone (e.g., within one or more vertebral bodies of a spine of a human or veterinary subject) that are only accessible (or that are more feasibly accessible) using a curved trajectory, especially target treatment locations in “hard” bone, or bone having a high or normal (e.g., non-osteoporotic or non-osteopenic) bone mass density.

Several implementations described herein are directed to systems and methods for accessing target treatment or diagnostic locations within bone (e.g., a vertebral body). In some embodiments, an intraosseous nerve (e.g., basivertebral nerve) within a bone (e.g., vertebral body) of the spine is accessed using a steerable, or curveable, introducer drill so as to facilitate treatment, or prevention of, back pain (e.g., chronic low back pain, acute back pain, or other ailments or conditions associated with the spine (e.g., vertebral fractures, spinal tumors, scoliosis, spondylosis)). The introducer drill may advantageously form a passageway within bone to facilitate insertion of additional instruments to the target treatment location or diagnostic location within bone. However, the introducer drill may also advantageously function as both an access and treatment instrument in some embodiments. In some embodiments, the introducer drill may advantageously facilitate access to locations within bone (e.g., posterior portions of a vertebral body) that may be difficult to access using straight instruments alone or using pre-curved instruments.

In accordance with several embodiments, a kit or system of access tools (and optionally one or more treatment or diagnostic instruments) may include a steerable, or curveable, introducer drill. The steerable, or curveable, introducer drill may advantageously facilitate access to a target treatment location of a terminus of a basivertebral nerve located in a posterior half of the vertebral body and within a region approximately 0%-50% (e.g., 5%-15%, 5%-25%, 10%-30%, 10%-40%, 20%-50%, 10%-35%, 20%-40%, overlapping ranges thereof, or any value within the recited ranges) of the distance between posterior and anterior walls of the vertebral body and approximately aligned with a sagittal plane or a central spinous process of the vertebral body). The steerable, or curveable, introducer drill may access the target treatment location along a curved trajectory after using a transpedicular (i.e., through a pedicle) access approach. However, other approaches (e.g., anterior, lateral, posterior lateral, anterior lateral, non-transpedicular) are possible. The kit or system may include a radiofrequency energy delivery device (e.g., a bipolar radiofrequency energy delivery probe configured to be operatively coupled to a radiofrequency generator or a battery-operated radiofrequency energy delivery device).

The steerable, or curveable, introducer drill may advantageously be used in hard bone. Hard bone may be determined based on bone mass density testing, compressive strength determinations, compressive modulus determinations, imaging modalities, or based on tactile feel by the operator as access instruments are being advanced. In some implementations, hard bone may be determined as bone having a bone mineral density score within a standard deviation of a normal healthy young adult (e.g., a T score greater than or equal to −1). In some implementations, hard bone may be identified as bone having a compressive strength of greater than 4 MPa and/or a compressive modulus of greater than 80 MPa for cancellous bone and greater than 5.5 MPa and/or a compressive modulus of greater than 170 MPa for cortical bone.

In accordance with several embodiments, a curveable introducer drill configured to access a target treatment region within hard bone along a curved trajectory includes a drive shaft comprising a proximal rotational member (e.g., paddle, handle, knob, crank), a distal drill tip, and an elongate shaft portion extending from the proximal rotational member to the distal drill tip. The distal drill tip is sharp and includes cutting flutes (e.g., top and/or side cutting flutes). The curveable introducer drill further includes an outer tube surrounding the drive shaft. A distal end portion of the outer tube includes a segmented tube section configured to facilitate controlled bending of the segmented tube section of the outer tube. The introducer drill also includes an actuator operably coupled to the drive shaft and adapted to apply tension to the drive shaft which, in turn, causes the segmented tube section of the outer tube, and thus the entire distal end portion of the introducer drill, to bend.

The outer tube may comprise a shape memory material (e.g., nitinol or other metallic alloy or a shape-memory polymer) that is shape set to have a straight configuration when unconstrained. The outer tube may include a proximal housing at its proximal end and the proximal rotational member may extend out of a proximal end of the proximal housing of the outer tube. In some embodiments, one side (e.g., one and only one side) of a distal end portion of the outer tube comprises a segmented tube section or zone comprised of tube segments and slits, gaps, apertures, or slots configured to facilitate controlled bending of the segmented tube section of the outer tube in a single known direction (as opposed to uncontrolled bending in any direction). The slits, gaps, apertures, or slots may be formed by laser cutting, for example. In some implementations, the drive shaft (upon application of tension by the actuator) exerts a lateral force on the segmented tube section of the outer tube to cause the controlled bending of the segmented tube section in the single known direction. In some embodiments, the drive shaft can generate a lateral force of between 0.25 pounds and 10 pounds (between 0.25 pounds and 1.5 pounds, between 0.5 pounds and 2.5 pounds, between 1 pound and 5 pounds, between 2 pounds and 8 pounds, between 4 pounds and 10 pounds, overlapping ranges thereof, or any value within the recited ranges, such as 0.25 pounds, 0.5 pounds, 1 pound, 1.5 pounds, 2 pounds, 2.5 pounds, 3 pounds, 3.5 pounds, 4 pounds, 4.5 pounds, 5 pounds, 5.5 pounds, 6 pounds, 6.5 pounds, 7 pounds, 7.5 pounds, 8 pounds, 8.5 pounds, 9 pounds, 9.5 pounds, 10 pounds, or more) by activating the actuator.

The proximal housing of the outer tube may include an indicator (e.g., arrow, line, dot, or other visual indicia or marking) configured to indicate the single known direction of bending or curving. The introducer drill may further include a compression spring mechanically coupled to a proximal end of the outer tube. The introducer drill may also include a bushing and/or thrust bearing and/or roller bearing positioned between a distal edge of the outer tube and a proximal edge of the distal drill tip.

The actuator may include a lever. In such implementations, the lever may be operably coupled to the drive shaft (e.g., via a cam assembly) and be adapted to apply tension to the drive shaft which, in turn, exerts a lateral force on the segmented tube section of the outer tube to cause the controlled bending of the segmented tube section in the single known direction. The actuator may alternatively not include a lever actuator and may instead comprise a pull wire assembly, a slider, or a rotational member, such as a wheel, crank, or knob. The actuator may be actuated by a single finger (e.g., thumb, index, or middle finger) or multiple fingers working together. In several embodiments, the introducer drill may be adapted for single-hand operation (e.g., advancement and actuation using a single hand).

The outer tube may comprise a conductive portion configured or adapted to form a proximal electrode of a bipolar electrode pair with the drill tip functioning as a distal electrode of the bipolar electrode pair when radiofrequency energy is applied to the drill tip via one or more electrically conductive wires or leads coupled between the drill tip and a radiofrequency generator. At least a portion of the outer tube may comprise a conformal, anodized coating. The coating may not be electrically conductive (e.g., may provide an insulation function). The introducer drill may be configured to be advanced through a previously-introduced introducer cannula. The introducer cannula may have a distal opening at its tip. The distal opening may be an axial opening or a radial side window.

In some implementations, the introducer drill may include an inner tube coupled (e.g., attached, welded, bonded) to the distal end of the drive shaft and the inner tube may be configured to apply compressive force to cause lateral bending of the segmented tube section of the outer tube instead of the drive shaft, thereby allowing the drive shaft to be focused on controlling the distal drill tip and the drilling function. The inner tube may be comprised of shape memory material (e.g., nitinol or other metallic alloy).

In accordance with several embodiments, a method of accessing a target treatment location within a vertebral body includes inserting at least a distal drill tip of a steerable, or curveable, introducer drill along a straight path through at least a portion of a pedicle of the vertebral body. The introducer drill may include a drive shaft including a proximal rotational member, the distal drill tip, and an elongate shaft portion extending from the proximal rotational member to the distal drill tip. The introducer drill may also include an outer tube surrounding the drive shaft, the outer tube comprising a proximal housing, with the proximal rotational member extending out of a proximal end of the proximal housing of the outer tube. In some embodiments, one (e.g., one and only one) side of a distal end portion of the outer tube comprises a segmented tube section comprised of tube segments and slits configured to facilitate controlled bending of the segmented tube section of the outer tube in a single known direction. The introducer also includes an actuator operably coupled to the drive shaft and adapted to apply tension to the drive shaft which, in turn, causes the segmented tube section of the outer tube to bend in the single known direction. The method further includes advancing the introducer drill within the vertebral body while actuating the actuator so as to facilitate advancement of the distal drill tip along a curved trajectory toward a target treatment region within a posterior half of the vertebral body.

In some embodiments, inserting at least the distal drill tip of the curveable introducer drill along the straight path through at least the portion of the pedicle of the vertebral body comprises inserting the curveable introducer drill through a straight introducer cannula that was previously inserted. The method (or steps thereof) may be performed under fluoroscopy or other imaging modality. The further advancing step may include adjusting a radius of curvature using the actuator as the introducer drill is advanced. The method may further include applying radiofrequency energy to the target treatment region using the curveable introducer drill, wherein the distal drill tip is configured to act as a distal electrode of a bipolar electrode pair and a conductive portion of the outer tube is configured to act as a proximal electrode of the bipolar electrode pair. In some embodiments, the applied radiofrequency energy is sufficient to modulate (e.g., ablate, denervate) an intraosseous nerve (e.g., basivertebral nerve) within the vertebral body. In some embodiments, the radiofrequency energy is applied by a separate radiofrequency energy delivery probe (e.g., bipolar radiofrequency energy delivery device operatively coupled to a radiofrequency generator) that is inserted (e.g., through an introducer cannula) within the vertebral body along a path formed by the introducer drill after removal of the introducer drill.

The method may optionally include sensing or detecting the presence of nerves during insertion of the introducer drill via one or more sensors located along the introducer drill. For example, nerves within or adjacent a pedicle may be sensed upon insertion of the drill through a pedicle or through bone via another insertion approach. A basivertebral nerve location may be sensed or detected upon advancement of the drill within the cancellous bone portion of the vertebral body. The method may include determining whether ablation of a nerve within the bone (e.g., basivertebral nerve within a vertebral body) has been successful (e.g., through stimulation and monitoring via the one or more sensors, which may include one or more stimulation and/or sensory electrodes).

In some embodiments, the introducer drill may be operably coupled to a robotic system configured to control advancement and steering, or bending, of the introducer drill in a fully-automated or semi-automated manner. Fully-automated may mean without any physical user interaction (other than initiating the fully-automated procedure by starting a computer-executable program of stored instructions on a non-transitory storage medium) and semi-automated may mean that the movement is carried out by a user manipulating a controller (e.g., joystick) that directs or controls the robotic movement of the introducer drill.

Several embodiments of the invention have one or more of the following advantages: (i) increased treatment accuracy; (ii) increased efficacy and enhanced safety; (iii) increased efficiency as a result of fewer instruments to access and/or treat a target treatment location or ability to access vertebrae having differing bone anatomy or bone density; (iv) increased precision; (v) an integrated access and treatment instrument; (vi) ability to access locations in dense bone; and/or (vii) ease of use.

For purposes of summarizing the disclosure, certain aspects, advantages, and novel features of embodiments of the disclosure have been described herein. It is to be understood that not necessarily all such advantages may be achieved in accordance with any particular embodiment of the disclosure provided herein. Thus, the embodiments disclosed herein may be embodied or carried out in a manner that achieves or optimizes one advantage or group of advantages as taught or suggested herein without necessarily achieving other advantages as may be taught or suggested herein.

The methods summarized above and set forth in further detail below describe certain actions taken by a practitioner; however, it should be understood that they can also include the instruction of those actions by another party. For example, actions such as “applying thermal energy” include “instructing the applying of thermal energy.” Further aspects of embodiments of the disclosure will be discussed in the following portions of the specification. With respect to the drawings, elements from one figure may be combined with elements from the other figures.

BRIEF DESCRIPTION OF THE DRAWINGS

Several embodiments of the disclosure will be more fully understood by reference to the following drawings which are for illustrative purposes only:

FIG. 1 illustrates various vertebral levels and vertebrae that may be treated by the systems, devices and methods described herein.

FIG. 2 illustrates a schematic representation of a vertebra having a basivertebral nerve.

FIG. 3 illustrates an embodiment of an introducer drill.

FIG. 3A is a side view of a distal end portion of the introducer drill of FIG. 3.

FIG. 4 is a partial cross-section side view of a distal end portion of another embodiment of an introducer drill.

DETAILED DESCRIPTION

Several implementations described herein are directed to systems and methods for accessing target treatment and/or diagnostic locations within bone (e.g., a vertebral body). In some implementations, an intraosseous nerve (e.g., basivertebral nerve) within a bone (e.g., vertebral body) of the spine is accessed so as to facilitate treatment, or prevention of, back pain or other ailments or conditions associated with the spine (e.g., vertebral fractures, spinal tumors, scoliosis, spondylosis). The vertebral body may be located in any level of the vertebral column (e.g., cervical, thoracic, lumbar and/or sacral). FIG. 1 schematically illustrates a vertebral column and the various vertebral segments or levels. Multiple vertebral bodies may be accessed in a single visit or procedure (simultaneously with multiple instruments or sequentially with the same instrument or different instruments). The multiple vertebral bodies may be located in a single spine segment (e.g., two adjacent vertebral bodies in the sacral spine segment (e.g., S1 and S2) or lumbar spine segment (e.g., L3. L4 and/or L5) or thoracic spine segment or cervical spine segment) or in different spine segments (e.g., an L5 vertebra in the lumbar spine segment and an S1 vertebra in the sacral spine segment). Target treatment and/or diagnostic locations within bones other than vertebral bodies may also be accessed. For example, target locations within a humerus, radius, femur, tibia, calcaneus, tarsal bones, hips, knees, and/or phalanges may be accessed.

In accordance with several implementations, the systems and methods of accessing target treatment locations within bone described herein can be performed without surgical resection, without general anesthesia, without cooling, without performing vertebroplasty or injecting flowable material such as bone cement, and/or with virtually no blood loss. In accordance with several implementations, successful treatment can be performed in challenging or difficult-to-access locations and access can be varied depending on bone structure (e.g., differing bone mass density) or differing bone anatomy. One or more of these advantages also apply to access within bone outside of the spine (e.g., other orthopedic applications or other tissue).

In some embodiments, cooling may be optionally used to, for example, reduce an extent of heating within the bone or within a device that is generated by friction from rotation of a component of the device within the bone or by application of energy using the device.

Various methods of access may be used to access a vertebral body or other bone. In some implementations, the vertebral body is accessed transpedicularly (through one or both pedicles). In other implementations, the vertebral body is accessed extrapedicularly (e.g., without traversing through a pedicle). In some implementations, the vertebral body is accessed using an extreme lateral approach or a transforaminal approach, such as used in XLIF and TLIF interbody fusion procedures. In some implementations, an anterior approach is used to access the vertebral body.

Access tools used in conjunction with the introducer drill may include an introducer assembly including an outer cannula and a sharpened stylet, an inner cannula configured to be introduced through the outer cannula, and/or one or more additional stylets, curettes, or drills to facilitate access to an intraosseous location within a vertebral body or other bone. The access tools (e.g., outer cannula, inner cannula, stylets, curettes, drills) may have pre-curved distal end portions or may be actively steerable or curveable. Any of the access tools may have beveled or otherwise sharp tips or they may have blunt or rounded, atraumatic distal tips. Any of the access tools may be inserted in a minimally-invasive manner (e.g., percutaneously or laparoscopically).

In some implementations, an outer cannula assembly (e.g., introducer assembly) includes a straight outer cannula and a straight stylet configured to be received within the outer cannula. The outer cannula assembly may be inserted first to penetrate an outer cortical shell of a bone and provide a conduit for further access tools (e.g., steerable, or curveable, introducer drill) to the inner cancellous bone. An inner cannula assembly may include a cannula having a pre-curved or steerable distal end portion and a stylet having a corresponding pre-curved or steerable distal end portion. Multiple stylets having distal end portions with different curvatures may be provided in a kit and selected from by a clinician. The inner cannula assembly may alternatively be configured to remain straight and non-curved.

In accordance with several embodiments, a kit or system of access tools may include a steerable, or curveable, introducer drill. The steerable, or curveable, introducer drill may advantageously facilitate access to a target treatment location of a terminus of a basivertebral nerve located approximately mid-body in a vertebral body (e.g., approximately 30%-50% across the sagittal vertebral body width and in a posterior half of the vertebral body or encompassing a geometric center of the vertebral body) along a curved trajectory after using a transpedicular access approach. The steerable, or curveable, introducer drill may advantageously be used in hard bone.

Hard bone may be determined based on bone mass density testing, compressive strength determinations, compressive modulus determinations, imaging modalities, or based on tactile feel by the operator as access instruments are being advanced. In some implementations, hard bone may be determined as bone having a bone mineral density score within a standard deviation of a normal healthy young adult (e.g., a T score greater than or equal to −1). In some implementations, hard bone may be identified as bone having a compressive strength of greater than 4 MPa and/or a compressive modulus of greater than 80 MPa for cancellous bone and greater than 5.5 MPa and/or a compressive modulus of greater than 170 MPa for cortical bone. Hard bone may be defined as non-osteopenic bone or non-osteoporotic bone.

FIG. 2 illustrates a cross-sectional view of a vertebra 120. The vertebra 120 includes a vertebral body 126, a vertebral foramen 132 posterior to the vertebral body 120, a transverse process 134 on each side of the vertebral foramen 132, a central spinous process 136 posterior to the vertebral foramen 132, and a pedicle 138 on each side of the vertebral foramen 132. The vertebral body 126 includes an inner cancellous bone region 124 and an outer cortical bone region 128. The vertebral body 126 also includes a basivertebral nerves 122. The basivertebral nerve 122 has at least one exit point 142 at a location along the basivertebral nerve 122 where the basivertebral nerve 122 exits the vertebral body 126 into the vertebral foramen 132. The basivertebral nerve 122 includes multiple branches 130 extending from a trunk or terminus throughout the cancellous bone region 124 of the vertebral body 126.

In accordance with several embodiments, a target treatment region to be accessed for modulation (e.g., ablation, denervation, stimulation) of the basivertebral nerve 122 is located within the cancellous bone region 124 at a location posterior to a terminus or trunk (labeled as point “A” in FIG. 2). In some embodiments, the target treatment region is not too close to the posterior border of the vertebral body 126. For example, the target treatment region may be at least 0.5 cm away (e.g., at least 1 cm away) from the posterior border (such as a distance away schematically represented by the point labeled “B” in FIG. 2). However, in other implementations, there is no posterior limit or boundary of the target treatment region. In accordance with several embodiments, the target treatment region to be accessed may be in a posterior half of the vertebral body 126 (e.g., posterior of the terminus or trunk of the basivertebral nerve). Treatment in this target treatment region may be advantageous because only a single portion of the basivertebral nerve 122 need be effectively treated to denervate or affect the entire system including the branches 130. The target treatment region may be located approximately mid-body in a vertebral body (e.g., approximately 30%-50% across the sagittal vertebral body width). The lateral-lateral center of the target treatment region may generally be aligned with the spinous process 136.

In one approach for accessing the basivertebral nerve, the patient's skin is penetrated with a surgical instrument which is then used to access the desired basivertebral nerves, i.e., percutaneously. In one embodiment, a transpedicular approach is used for penetrating the vertebral cortex to access the basivertebral nerve 122. A passageway 140 is created between one of the transverse processes 134 and the spinous process 136 through the pedicle 138 into the cancellous bone region 124 of the vertebral body 126 to access the target treatment region at or proximate to the terminus of the basivertebral nerve 122. In some vertebral bodies (e.g., vertebral bodies having hard bone or high-density bone or vertebral bodies at the lower lumbar levels or sacral levels) accessed transpedicularly, it may be difficult to obtain a curved trajectory to get to a desired target treatment region of the vertebral body 124 with instruments having pre-curved distal ends that are advanced through straight introducers and that cannot be actively steered or with straight access instruments. Accordingly, it may be advantageous according to several embodiments to include a steerable or curveable drill in a kit or system of access instruments to facilitate steeper curved trajectories to the targeted treatment region (for example, if the operator can tell that the density of the bone is going to be sufficiently dense or hard that additional steps and/or tools will be needed to obtain a desired curved trajectory to access a posterior portion (e.g., posterior half) of the vertebral body).

FIG. 3 illustrates an embodiment of a steerable, or curveable, introducer drill 350 configured to access a desired target treatment location in bone (e.g., a vertebral body having hard or dense cancellous bone regions and/or a vertebral body in a spine region that may be difficult to access via a straight access tool, such as an L5, S1, or S2 vertebral body). For example, for a vertebral body, the desired target treatment location may be in a posterior half of the vertebral body 126 (e.g., posterior of the terminus or trunk of the basivertebral nerve 122) as described in connection with FIG. 2. In some implementations, the desired target treatment location may correspond to a geometric center of the vertebral body 126.

In accordance with several embodiments, the introducer drill 350 may comprise a single device configured to both penetrate a cortical outer shell of a bone along a straight trajectory and channel a path toward a target treatment location within an inner cancellous bone portion along a curved trajectory that can be adjusted or manipulated in real time. The illustrated embodiment of the drill 350 comprises a drill tip 352, a bushing 354, an outer tube 355, a drive shaft 356, a compression spring 357, an actuator 358, a rotational member 359, and a proximal housing 360. The illustrated drill tip 352 is pointed and includes top and/or side cutting flutes. The cutting flutes may have varying spacing, pitch, and widths as desired and/or required to facilitate bone drilling. A proximal end of the drill tip 352 is connected to the drive shaft 356. The drill tip 352 and drive shaft 256 may be made as a single integrated unitary component so as to prevent likelihood of separation or may comprise two separate components that are coupled or connected to each other during manufacturing (e.g., via welding, adhesive, and/or the like). The flutes may advantageously provide open volume for bone chips, fragments, or shards to be received therein. In some embodiments, the distal drill tip 352 is not a blade.

The bushing 354 is positioned between a proximal edge or surface of the drill tip 352 and a distal edge or surface of the outer tube 355. The bushing 354 may be adapted to guide, position and support the drive shaft 356 as it is rotated and curved, or bent, under compression and to protect the drive shaft 356 and pointed drill tip 352 from abrasion during bending and rotating. The drive shaft 356 may have a circular cross-sectional shape. The drive shaft 356 may have an elliptical cross-sectional shape. The bushing 354 may be made of steel or other high carbon metal or bronze or plastic (e.g., nylon). In some embodiments, the bushing 354 is substituted by or replaced with (or included in addition to) a thrust bearing and/or roller bearing. A thrust bearing (e.g., thrust ball bearing) may facilitate reduced wear on adjacent components and may help support axial loads. A roller bearing may include cylindrical- or barrel-shaped rolling elements as opposed to ball bearings to support loads (e.g., radial loads) and reduce friction. In some embodiments, the roller bearing comprises any cylindrical or spherical object that facilitates movement of and/or reduces wear from two adjacent components. The bushing 354 may cause rotation of the drive shaft 356 or may remain stationary with respect to rotation of the drive shaft 356.

The outer tube 355 concentrically and/or coaxially surrounds the drive shaft 356. A distal end portion 362 of the outer tube 355 comprises a segmented tube profile. The segmented tube portion 362 of the distal end portion of the outer tube 355 may include notches, slits, slots or apertures aligned on one side of the outer tube 355 and spaced apart and arranged so as to facilitate bending, steering, or articulating in a single, known, controlled direction. Accordingly, the outer tube 355 may advantageously bend or arc in one and only one lateral direction and such that the segmented tube portion 365 bends or arcs in a distal to proximal direction. The slots or slits may comprise transverse slots or slits. In other embodiments, the notches or slits or slots may be aligned on more than one side to facilitate bending in multiple directions (e.g., 2 opposite directions or omnidirectionally).

The proximal housing 360 of the outer tube 355 may include a visible indicator 361 (e.g., arrow head, marking) to indicate to the operator the single, known direction that the drill will bend or curve. A close-up side view of the segmented tube profile of the segmented tube portion 362 of the outer tube 355 is illustrated in FIG. 3A. The notches or slits or slots may be perpendicular or generally perpendicular to a central longitudinal axis of the outer tube 355 and may allow for adjacent segments to overlap or collapse on each other to facilitate bending of the outer tube 355. The number of, pitch, and spacing between the notches, slits, or slots may vary as desired and/or required. The length of the segmented tube portion 362 may also vary as desired and/or required. The outer tube 355 may be formed of nitinol material or another flexible metallic alloy or flexible shape-memory material. The outer tube 355 may be shape-set during manufacturing to remain in a straight configuration when in a default resting (or unconstrained) state or configuration, even once deployed from the constraint of an introducer cannula (not shown). In accordance with several embodiments, the outer tube 355 does not require multiple concentric tubes moving relative to each other, thereby reducing overall device diameter.

The compression spring 357 surrounds the drive shaft 356 and is mechanically coupled to the proximal end of the outer tube 355 and may be located within the housing 360 attached to the proximal end of the outer tube 355. The housing 360 may also include at least a portion of the actuator 358 operatively coupled to the drive shaft 356 that is adapted to add tension to or remove tension from the drive shaft 356. The actuator 358 may comprise a lever or other mechanism (e.g., pull wire assembly, slider, trigger, rotational member), adapted to add or remove tension to facilitate bending or curving of the segmented tube portion 362 of the outer tube 355, and thus the entire drill 350.

A pull wire assembly may include one or more pull wires extending from the proximal handle 360 to a distal end of the outer tube 355. The one or more pull wires may be tensioned to cause bending and relaxed to allow the outer tube 355 to straighten. The pull wires may provide axial force toward the proximal handle 360. The one or more pull wires may be adhered or welded to the distal end of the outer tube 355. A slider may be operably coupled to the segmented tube portion 362 such that sliding of the slide in one direction causes bending of the segmented tube portion 362 and sliding of the slider in the opposite direction causes straightening of the segmented tube portion 362. A trigger may be operably coupled to the segmented tube portion 362 such that actuation of the trigger (e.g., pressing or pulling the trigger) causes bending of the segmented tube portion 362 and releasing the trigger causes straightening of the segmented tube portion 362. A rotational member (e.g. thumb or finger wheel, crank, or knob) may be operably coupled to the segmented tube portion 362 such that rotation of the rotational member in a first rotational direction (e.g., clockwise) causes bending of the segmented tube portion 362 and rotation of the rotational member in an opposite rotational direction (e.g., counter-clockwise) causes straightening of the segmented tube portion 362. In some implementations, the slider, trigger, or rotational member may be used in conjunction with a pull wire assembly.

The proximal end of the drive shaft 356 is mechanically coupled to the rotational paddle 359 or other structural member adapted to be acted upon to cause rotation of the drive shaft 356. The rotational member 359 may comprise a paddle, wheel, crank, knob, handle, enlarged tip, or other structure adapted to be rotated manually by an operator (e.g., a clinician or surgeon) or automatically (e.g., via a motor of a robotic system) without manual operator contact. In some embodiments, the drive shaft 356 does not have a lumen and does not include a stiffening wire adapted for insertion within the lumen of the drive shaft. In some embodiments, the drive shaft has a lumen to facilitate introduction or circulation of cooling fluid via closed loop fluid circulation system.

The drill 350 may be initially inserted into bone (e.g., a vertebral body) through an introducer cannula (not shown) in a default straight configuration with no tension applied on the drive shaft 356. The insertion may be performed while rotating the rotational member 359. Because the outer tube 355 is shape set in a straight configuration, the drill 350 should naturally hold this straight configuration even when unconstrained. Once the drill tip 352 has been initially inserted into the bone (e.g., vertebral body), the actuator 358 may be actuated to provide tension on the drive shaft 356, which causes compression on the segmented tube portion 362 of the outer tube 355. This action causes the drill 350 to attempt to collapse the segments of the segmented tube portion 362 of the outer tube 355 and lean (e.g., bend, arc, steer, or articulate) into a curved shape (e.g., in a distal-to-proximal configuration). The compression spring 357 takes up lateral forces that are unable to be used to curve the drill 350 (such as because the drill 350 is constricted in an introducer cannula or in hard, high-density bone). The fully curved angle may be in a range between 20 degrees and 90 degrees (e.g., between 20 degrees and 60 degrees, between 40 degrees and 70 degrees, between 30 degrees and 80 degrees, between 35 degrees and 75 degrees, between 50 degrees and 90 degrees, between 30 degrees and 70 degrees, between 45 degrees and 65 degrees, overlapping ranges thereof, or any value within the recited ranges).

In some embodiments, the drill 350 may optionally include a second tube 353 (e.g., inner tube) attached (e.g., welded or bonded) to the distal end of the drive shaft 356. The second tube 353 is illustrated with dotted lines in FIG. 3. The second tube 353 may be used to apply compression to the outer tube 355 and force the outer tube 355 to bend or arc. In accordance with several embodiments, inclusion of the second tube 353 (e.g., inner tube) may allow the drive shaft 356 to solely function for the drill function (e.g., transmitting torque to the drill tip) and not for both drilling and application of compression to the outer tube 355. The second tube 353 (e.g., inner tube) may be formed of nitinol material or another flexible metallic alloy or flexible shape-memory material (e.g., similar to the outer tube 355). The second tube 353 may extend from the drill tip 352 and extend along any length or portion of the outer tube 355. For example, the second tube 353 may extend to just cover the segmented tube portion 362 or may extend to the proximal handle 360 or may extend proximal to the segmented tube portion 362 but distal to the proximal handle 360. The second tube 353 may or may not include a segmented tube portion corresponding to the segmented tube portion 362 of the outer tube 355. The inner tube 353 may advantageously apply compression to the outer tube 355 without compromising the structural integrity of the drive shaft 356 (such as by requiring an internal lumen in the drive shaft for insertion of a stiffening element for imparting rigidity). In some embodiments, the drill 350 does not include any components configured for insertion through the drive shaft 356.

The drill 350 may then either be manually advanced forward with axial pressure while the drive shaft 356 is rotated or an automated separate mechanism (such as a robotic surgical system) can provide the axial pressure. As the drill 350 advances within the bone, the drill 350 moves forward and reduces its radius of curvature as it is deployed (and as a result, the compression spring 357 relaxes). The actuator 358 may be adjusted to adjust the radius of curvature during advancement. The radius of curvature may be actively controlled and monitored under visualization. In accordance with several embodiments, advancement may be performed while using fluoroscopy or other imaging modalities to facilitate access along a desired trajectory to the desired target treatment and/or diagnostic location.

Once fully deployed, the actuator 358 can be caused to relieve tension on the drive shaft 356, thereby allowing the outer tube 355 to straighten as the drill 350 is removed from the bone (e.g., vertebral body). This straightening may advantageously help prevent, or reduce the likelihood of, the segments of the segmented tube portion 362 of the outer tube 355 from catching on the introducer cannula as force is applied on the opposite side of the outer tube 355. In some embodiments, the compression spring 357 may be replaced with a hydraulic or pneumatic mechanism. The hydraulic or pneumatic mechanism may serve to provide a similar function as the mechanical compression spring 357.

FIG. 4 illustrates an alternative design of a distal end portion that could optionally be incorporated into the steerable drill 350 of FIG. 3. In this embodiment, the drill 350′ may advantageously function as both an access instrument and a treatment instrument. In this embodiment, the drill tip 352 could function as a distal electrode of a bipolar electrode pair and a conductive portion 363 of the outer tube 355 may function as a proximal electrode of the bipolar electrode pair, with proper masking or electrical isolation being achieved by appropriate insulation structures or materials positioned between the distal electrode and proximal electrode portions. In one implementation, at least a portion of the outer tube 355 (e.g., a portion proximal of the conductive portion 363) could be coated with a conformal, anodized, and/or other non-electrically conductive coating to help with surface friction and concentrated electrode operation. The outer tube 355 could be masked to provide a 4×2×4 mm electrode spacing or other suitable electrode spacing geometry. In some embodiments, the bushing 354 may function as an insulator between the conductive portion 363 of the outer tube 355 and the drill tip 352.

The drill tip 352 may or may not include cutting flutes. A distal end portion of the outer tube 355 of the drill 350′ may include the segmented tube portion 362 described in connection with FIGS. 3 and 3A.

The drill 350 may include one or more electrical leads or wires electrically coupled between a connector adapted to electrically interface with a radiofrequency generator and the drill tip 352 so as to allow for the drill 350 to deliver radiofrequency energy sufficient to modulate (e.g., ablate, stimulate, denervate) tissue (e.g., bone tissue, nerves, tumor tissue). For example, the drill 350 may advantageously be used to both access a desired target treatment location within bone and ablate nerves or tumors within the bone.

Applying ablative radiofrequency energy to the target treatment location within the bone may be performed according to the following example treatment parameters: a frequency between 400 kHz and 600 kHz (e.g., between 400 kHz and 500 kHz, between 450 kHz and 500 kHz, between 470 kHz and 490 kHz, between 500 kHz and 600 kHz, overlapping ranges thereof, or any value within the recited ranges); a target temperature of between 60 degrees Celsius and 90 degrees Celsius (e.g., between 60 degrees Celsius and 80 degrees Celsius, between 65 degrees Celsius and 75 degrees Celsius, between 70 degrees Celsius and 80 degrees Celsius, between 80 degrees Celsius and 90 degrees Celsius, overlapping ranges thereof, 70 degrees Celsius, 75 degrees Celsius, 80 degrees Celsius, 85 degrees Celsius, 90 degrees Celsius or any other value within the recited ranges); a temperature ramp of between 0.5 and 3 degrees Celsius per second (e.g., 0.5 degree Celsius per second, 1 degree Celsius per second, 1.5 degrees Celsius per second, 2 degrees Celsius per second, 2.5 degrees Celsius per second, 3 degrees Celsius per second); and an active energy delivery time of between 1 minute and 20 minutes (e.g., between 1 minute and 5 minutes, between 2 minutes and 10 minutes, between 4 minutes and 8 minutes, between 5 minutes and 10 minutes, between 5 minutes and 15 minutes, between 10 minutes and 20 minutes, overlapping ranges thereof, 5 minutes, 10 minutes, 12, minutes, 14 minutes, 15 minutes, 16 minutes, 18 minutes, 20 minutes, or any value within the recited ranges).

In some implementations, a target ablation zone has a major diameter along a long axis of between 20 mm and 30 mm and a minor diameter along a short axis of between 5 mm and 15 mm. In some implementations, the target ablation zone generally comprises a 1 cm sphere. The lesion may form an elliptical shape or other controlled lesion shape as desired and/or required.

In some implementations, no active cooling is provided. In other implementations, cooling fluid may be circulated through one or more internal lumens surrounding the drive shaft 356. The drill 350′ may include one or more temperature sensors (e.g., thermocouples, thermistors) configured to monitor temperature at one or more locations along the drill 350′. The drills 350, 350′ may include one or more sensors configured to provide stimulation to sense a presence or location of nerves within bone (e.g., basivertebral nerve within a vertebral body or nerves adjacent a pedicle of a vertebra).

In some implementations, the drill 350′ is configured to operate as a monopolar electrode. For example, an electrical lead may only be coupled to the conductive portion 363 and not to the drill tip 352 and a ground pad may be used as the second electrode. The drill 350 may additionally or alternatively be used to provide stimulation energy to facilitate confirmation of nerve ablation or to help identify locations of nerves within the bone to facilitate identification of the desired target treatment region.

In some implementations, the steerable drill comprises various features that are present as single features (as opposed to multiple features). For example, in one embodiment, the drill includes a single electrode. A single thermocouple (or other means for measuring temperature) may also be included. Multiple features or components are provided in alternate embodiments.

Although certain embodiments and examples have been described herein, aspects of the methods and devices shown and described in the present disclosure may be differently combined and/or modified to form still further embodiments. Additionally, the methods described herein may be practiced using any device suitable for performing the recited steps. Further, the disclosure (including the figures) herein of any particular feature, aspect, method, property, characteristic, quality, attribute, element, or the like in connection with various embodiments can be used in all other embodiments set forth herein. Any section headings used herein are merely provided to enhance readability and are not intended to limit the scope of the embodiments disclosed in a particular section to the features or elements disclosed in that section.

While the embodiments are susceptible to various modifications, and alternative forms, specific examples thereof have been shown in the drawings and are herein described in detail. It should be understood, however, that the embodiments are not to be limited to the particular forms or methods disclosed, but to the contrary, the embodiments are to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the various embodiments described and the appended claims. Any methods disclosed herein need not be performed in the order recited. The methods disclosed herein include certain actions taken by a practitioner; however, they can also include any third-party instruction of those actions, either expressly or by implication.

The terms “top,” “bottom,” “first.” “second.” “upper.” “lower,” “height.” “width,” “length,” “end,” “side,” “horizontal,” “vertical,” and similar terms may be used herein; it should be understood that these terms have reference only to the structures shown in the figures and are utilized only to facilitate describing embodiments of the disclosure. Various embodiments of the disclosure have been presented in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the invention. The ranges disclosed herein encompass any and all overlap, sub-ranges, and combinations thereof, as well as individual numerical values within that range. For example, description of a range such as from 20 to 90 degrees should be considered to have specifically disclosed subranges such as from 20 to 40 degrees, from 30 to 60 degrees, from 45 to 75 degrees, from 80 to 90 degrees etc., as well as individual numbers within that range, for example, 20, 30, 40, 45, 90, 40.5, 60.5 and any whole and partial increments therebetween. Language such as “up to,” “at least,” “greater than,” “less than,” “between,” and the like includes the number recited. Numbers preceded by a term such as “about” or “approximately” include the recited numbers. For example, “approximately 30-50%” includes 30% and 50%. The terms “generally” and “substantially” as used herein represent an amount close to the stated amount that still performs a desired function or achieves a desired result.

Claims

1. A curveable introducer drill configured to access a target treatment region within hard bone along a curved trajectory, the drill comprising: a drive shaft comprising a proximal rotational paddle, a distal drill tip, and an elongate shaft portion extending from the proximal rotational paddle to the distal drill tip,wherein the distal drill tip is pointed and comprises top and side cutting flutes;an outer tube surrounding the drive shaft, the outer tube comprising a proximal housing at its proximal end,wherein the outer tube comprises a shape memory material that is shape set to have a straight configuration when unconstrained,wherein the proximal rotational paddle extends out of a proximal end of the proximal housing of the outer tube;wherein one and only one side of a distal end portion of the outer tube comprises a segmented tube section comprised of tube segments and slits configured to facilitate controlled bending of the segmented tube section of the outer tube in a single known direction;a lever operably coupled to the drive shaft and adapted to apply tension to the drive shaft which, in turn, exerts a lateral force on the segmented tube section of the outer tube to cause the controlled bending of the segmented tube section in the single known direction;a compression spring mechanically coupled to a proximal end of the outer tube; anda bushing positioned between a distal edge of the outer tube and a proximal edge of the distal drill tip.

2. The drill of claim 1, wherein the outer tube comprises a shape memory material that is shape set to have a straight configuration when unconstrained.

3. The drill of claim 1, wherein the proximal housing of the outer tube comprises an indicator configured to indicate the single known direction.

4. The drill of claim 1, further comprising an inner tube within the outer tube and surrounding the drive shaft, wherein the inner tube is attached to the distal end of the drive shaft, and wherein the inner tube is configured to apply compression to the outer tube and force it to apply lateral force.

5. The drill of claim 1, wherein the distal drill tip is configured to form a distal electrode of a bipolar electrode pair and a conductive portion of the outer tube is configured to form a proximal electrode of the bipolar electrode pair.

6. The drill of claim 5, further comprising at least one electrically conductive wire coupled between the distal drill tip and a radiofrequency generator.

7. The drill of claim 1, wherein at least a portion of the outer tube comprises a non-electrically conductive coating.

8. The drill of claim 1, further comprising one or more sensors configured to sense a presence or location of nerves within bone.

9. A steerable introducer drill comprising: a drive shaft comprising a proximal rotational member and a distal drill tip;an outer tube surrounding the drive shaft, the outer tube comprising a proximal housing and a distal end portion, wherein the distal end portion includes a segmented tube section configured to facilitate controlled bending;an actuator operably coupled to the drive shaft and adapted to apply tension to the drive shaft to cause the segmented tube section to bend;a lever operably coupled to the actuator to control the tension applied to the drive shaft; anda bushing positioned between a distal edge of the outer tube and a proximal edge of the distal drill tip.

10. The drill of claim 9, wherein the outer tube comprises a shape memory material that is shape set to have a straight configuration when unconstrained.

11. The drill of claim 9, wherein the proximal housing of the outer tube comprises an indicator configured to indicate a direction of bending of the segmented tube section.

12. The drill of claim 9, further comprising an inner tube within the outer tube and surrounding the drive shaft, wherein the inner tube is coupled to a distal end of the drive shaft, and wherein the inner tube is configured to apply compression to the outer tube to facilitate bending of the segmented tube section.

13. The drill of claim 9, wherein the distal drill tip comprises top and side cutting flutes.

14. The drill of claim 9, wherein the actuator is configured to apply tension to the drive shaft to cause the segmented tube section to bend in a single known direction.

15. The drill of claim 9, further comprising a compression spring mechanically coupled to a proximal end of the outer tube.

16. The drill of claim 9, wherein the distal drill tip is configured to form a distal electrode of a bipolar electrode pair and a conductive portion of the outer tube is configured to form a proximal electrode of the bipolar electrode pair.