US20070197935A1

US20070197935A1 - Hand-held instruments that access interior body regions

Info

Publication number: US20070197935A1
Application number: US11/789,244
Authority: US
Inventors: Mark Reiley; Michael Reo; Robert Scribner; Arthur Ferdinand
Original assignee: Kyphon Inc
Current assignee: Orthophoenix LLC
Priority date: 1999-10-19
Filing date: 2007-04-24
Publication date: 2007-08-23
Also published as: US6575919B1; WO2002041796A2; KR20030068141A; ES2304400T3; US7399306B2; JP4410229B2; JP3980481B2; CN1319493C; JP2004513741A; ATE385408T1; EP1925261A1; EP1328201B1; KR100882363B1; CN1630488A; KR20060126842A; AU2002239469A1; CN101045010A; JP2007021243A; WO2002041796A3; US20030191414A1

Abstract

A first instrument having a distal end is sized and configured to penetrate tissue and a proximal end comprising a first handle assembly. A second instrument including an interior lumen is sized and configured to accept passage of the first instrument. The second instrument has a proximal end comprising a second handle assembly sized and configured to releasably interlock with the first handle assembly to form a composite instrument sized and configured to provide percutaneous access to a cancellous bone region. The second handle assembly is also sized and configured to permit controllably release by a user of the first handle assembly from the second handle assembly to allow removal of the first instrument from the interior lumen. At least one additional instrument is sized and configured for passage through the interior lumen of the second instrument upon removal of the first instrument.

Description

RELATED APPLICATIONS

This application is a divisional of copending U.S. patent application Ser. No. 10/431,681, filed May 8, 2003 and entitled “Hand-Held Instruments that Access Interior Body Regions,” which is a divisional of U.S. patent application Ser. No. 09/695,566, filed Oct. 24, 2000, and entitled “Hand-Held Instruments that Access Interior Body Regions” (now U.S. Pat. No. 6,575,919), which is a continuation-in-part of U.S. patent application Ser. No. 09/421,635, filed Oct. 19, 1999, and entitled “Hand-Held Instruments that Access Interior Body Regions” (now U.S. Pat. No. 7,081,122), all of which are incorporated herein by reference.

FIELD OF THE INVENTION

The invention generally relates to hand-held tools and instruments and to procedures that deploy these instruments through tissue to access interior regions of the body.

BACKGROUND OF THE INVENTION

There are many different types and styles of hand-held surgical instruments that physicians use to gain access into interior body regions. These instruments are intended to penetrate tissue by the application of pushing forces, twisting forces, or both in combination.
Often, a single surgical procedure will require the physician to employ different surgical instruments, each possessing a different shape, size, and function. Often, the procedure will require the physician to deploy these instruments in both soft and hard tissue to meet the diagnostic or therapeutic objectives of the procedure. The physician will often need an enhanced mechanical advantage to advance an instrument through tissue, particularly through dense or hard tissue, such as bone.
The common need to use different instruments in a given procedure, coupled with the need to accurately and reliably deploy each of these different instruments through both soft and hard tissue, often with an enhanced mechanical advantage, complicate the physician's already difficult task. The need to handle different instruments in different ways for different purposes can distract the physician and lead to wasted effort, which can lengthen the overall time of the procedure.

SUMMARY OF THE INVENTION

The invention provides systems and methods for accessing body region such as bones.
One aspect of the invention provides systems and methods comprising a first instrument having a distal end sized and configured to penetrate tissue and a proximal end comprising a first handle assembly. The systems and methods include a second instrument including an interior lumen sized and configured to accept passage of the first instrument. The second instrument has a proximal end comprising a second handle assembly sized and configured to releasably interlock with the first handle assembly to form a composite instrument sized and configured to provide percutaneous access to a cancellous bone region. The second handle assembly is also sized and configured to permit controllably release by a user of the first handle assembly from the second handle assembly to allow removal of the first instrument from the interior lumen. The systems and methods include at least one additional instrument sized and configured for passage through the interior lumen of the second instrument upon removal of the first instrument.
The additional instrument can comprise, e.g., a delivery tube sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument. The delivery tube has a proximal end including a connector for coupling the delivery tube to an injector of bone filling material to convey the bone filling material into the cancellous bone region.
The additional instrument can comprise, e.g., a third instrument sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument. The third instrument can have a distal region sized and configured to treat the cancellous bone region. The distal region can be sized and configured, e.g., to biopsy cancellous bone, and/or to harvest cancellous bone, and/or to introduce a therapeutic material, and/or to modify the cancellous bone region to receive a bone filling material.
Features and advantages of the inventions are set forth in the following Description and Drawings, as well as in the appended Claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a perspective view of a first functional instrument engaging a second functional instrument to form a composite tool having a composite handle that the handles of the first and second instruments form.
FIG. 2 is a perspective view of the first instrument separated from the second instrument.
FIG. 3 is a perspective view of a hand engaging the composite handle of the tool shown in FIG. 1.
FIG. 4 is a perspective view of a hand engaging the handle of the second functional instrument when separated from the first functional instrument.
FIG. 5 is an enlarged perspective view of the handles of the first and second functional instruments, when separated, showing a coupling system than resists relative rotation between the functional instrument when the composite tool is formed.
FIG. 6A is an enlarged side view of the handles shown in FIG. 5, when separated.
FIG. 6B is an enlarged side view of the handles shown in FIG. 5, when mated together to form the composite handle.
FIG. 6C is a side view of a trocar suited for use with the composite handle of FIG. 6B.
FIG. 6D is a side view of a cannula suited for use with the composite handle of FIG. 6B.
FIG. 7A is a lateral view of a human spinal column.
FIG. 7B is a coronal view, with portions broken away and in section, of a human vertebral body, which is part of the spinal column.
FIG. 8 is a lateral view, with portions broken away and in section, of several vertebral bodies, which are part of the spinal column.
FIG. 9 is a perspective view showing advancement of the composite instrument through tissue, by using the composite handle to supply a twisting and/or pushing force.
FIG. 10 is a top view showing deployment of the composite instrument in a vertebral body, by using the composite handle to apply an axial and/or torsional force.
FIG. 11 is a top view of the vertebral body, showing deployment of a drill bit through a cannula instrument, which forms a part of the composite tool shown in FIG. 9.
FIG. 12 is a top view of the vertebral body showing deployment of an expandable structure in a collapsed condition through the cannula instrument that forms a part of the composite tool shown in FIG. 9.
FIG. 13 is a top view of the vertebral body after the structure shown in FIG. 12 is expanded to compact cancellous bone and form a cavity.
FIG. 14 is a top view of a syringe and attached nozzle in use to inject material into the cannula instrument for passage into the cavity shown in FIG. 13.
FIG. 15 is a side view showing advancement of a tamping instrument in the cannula instrument to displace and distribute material from the cannula instrument into the cavity shown in FIG. 13.
FIG. 16 is a side view of a syringe attached to the cannula instrument that forms a part of the composite tool shown in FIG. 9, for the purpose of conveying material through the cannula instrument into bone.
FIGS. 17A and 17B are perspective views showing material deformation that occurs in each handle as a result of heat sterilization, to prevent subsequent formation of the composite handle.
FIG. 18 a perspective view of an alternative embodiment of a composite tool like that shown in FIG. 1, with an interior lumen to accommodate passage of a spinal needle assembly to aid deployment.
FIG. 19 is a front perspective view of another embodiment of a composite tool formed by a first functional instrument engaging a second functional instrument, and also having a composite handle that the handles of the first and second instruments form.
FIG. 20 is a rear elevation view of the composite tool shown in FIG. 19.
FIG. 21 is a perspective view of the composite tool shown in FIG. 10, as the first and second instruments are being separated.
FIG. 22 is a perspective view of the first instrument separated from the second instrument.
FIG. 23 is a section view of the latching mechanism for the composite tool, taken generally along line 23-23 in FIG. 20.
FIG. 24 is a section view of the latching mechanism shown in FIG. 23, with the associated latch finger moved out of its normal latching position by the application of an external force.
The invention may be embodied in several forms without departing from its spirit or essential characteristics. The scope of the invention is defined in the appended claims, rather than in the specific description preceding them. All embodiments that fall within the meaning and range of equivalency of the claims are therefore intended to be embraced by the claims.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

This Specification describes new instruments for penetrating tissue. This specification also describes systems and methods to treat bones using expandable bodies in conjunction with new instruments for penetrating tissue.
The use of expandable bodies to treat bones is generally disclosed in U.S. Pat. Nos. 4,969,888 and 5,108,404, which are incorporated herein by reference. Improvements in this regard are disclosed in U.S. patent application, Ser. No. 08/188,224, filed Jan. 26, 1994; U.S. patent application Ser. No. 08/485,394, filed Jun. 7, 1995; and U.S. patent application Ser. No. 08/659,678, filed Jun. 5, 1996, which are each incorporated herein by reference.
The new instruments, systems and methods will be described with regard to the treatment of vertebral bodies. It should be appreciated, however, that the handle configuration, instruments, systems and methods so described are not limited in their application to vertebrae. The systems and methods are applicable to the treatment of diverse bone types. Additionally, the handle configuration could be used with instruments other than a trocar and a cannula.
I. The Instruments
FIG. 1 shows a composite instrument 10 for penetrating tissue. The composite instrument 10 includes a first functional instrument 20 and a second functional instrument 40, and a composite handle 12 comprising a first handle 22 and a second handle 42. The composite handle 12 aids a physician in manipulating the composite instrument 10, but a physician can also desirably use the first handle 22 to independently manipulate the first instrument 20 or the second handle 42 to independently manipulate the second instrument 40 during use.
The number and type of instruments 20 and 40 can vary. FIG. 1 shows two representative instruments 20 and 40, each having a different size and function. In a preferred embodiment, the first functional instrument 20 is a trocar instrument, and the second functional instrument 40 is a cannula instrument.
A. The Trocar Instrument
Referring to FIGS. 1-4, the first instrument 20 functions as a trocar instrument to penetrate tissue. A trocar 30 has a proximal end 32 and a distal end 34. The distal end 34 is tapered to present a penetrating surface 35. In use, the penetrating surface 35 is intended to penetrate soft tissue and/or bone in response to pushing and/or twisting forces applied by the physician at the first handle 22, or the composite handle 12.
The first handle 22 is coupled to the trocar 30 at the proximal end of the trocar 32. As best seen in FIG. 6C, the proximal end 32 of the trocar 30 can be formed in a T-shape, with the first handle 22 being molded around the T-shaped end. This arrangement significantly increases the mechanical strength of the bond between the handle 22 and the trocar 30, and allows significant longitudinal and torsional forces to be transmitted from the handle 22 to the trocar 30 without bond failure. Alternatively, with or without a T-shaped end, the proximal end 32 of the trocar 30 can be scored (indicated by scored region 33 in FIG. 6C) to increase the mechanical strength of the bond between the trocar 30 and the handle 22, or various bonding adhesives could be used, with varying results.
The first handle 22 desirably includes a viewing window 24, an alignment ridge receiver 26, a handle bore receiver 28, and a handle key 36, the uses of which are described later.
In an alternative embodiment (see FIG. 18), the trocar 30 includes an interior lumen 21, which passes through the handle 22 and the body of the trocar 30. The interior lumen 21 accommodates passage of a stylet and/or conventional spinal needle assembly 23, to guide the deployment of the first instrument 20, by itself or nested with the second instrument 40 (as FIG. 18 shows), through soft tissue to a targeted bone treatment site.
B. The Cannula Instrument
The second instrument 40 functions as a cannula instrument or guide sheath, and includes a cannula 50. The cannula 50 of the second instrument 40 is desirably somewhat larger in diameter than and not as long as the trocar 30 of the first instrument 20. As best shown in FIGS. 1 and 2, the second instrument 40 includes an interior lumen 44 that extends through the instrument from its distal end 54 to its proximal end 52. The interior lumen 44 is sized to accept the trocar 30. The size of the interior lumen 44 desirably allows the second instrument 40 to slide and/or rotate relative to the first instrument 20, and vice versa, as will be described in greater detail later.
The distal end 54 of the second instrument 40 presents an end surface 60. In use, the end surface 60 of the second instrument 40 desirably presents a low-profile surface, which can penetrate soft tissue surrounding the first instrument 20 in response to pushing and/or twisting forces applied at the composite handle 12 or the second handle 42.
The proximal end 52 is coupled with the second handle 42. As best seen in FIG. 6D, the proximal end 52 of the cannula 50 desirably incorporates a flared and notched end “A” and a textured surface “B”, around which the second handle 42 is molded. The flared and notched end “A” and textured surface “B” serve to increase the mechanical strength of the bond between the cannula 50 and the second handle 42, allowing significant longitudinal and torsional forces to be transmitted between the second handle 42 and cannula 50 without bond failure. As with the trocar 30, however, alternative bonding methods such as scoring of the cannula 50 and/or the use of various adhesives could be employed, with varying results.
Extending from the interior lumen 44 at the proximal end 52 of the cannula 50, the second handle 42 desirably includes a handle bore 48, preferably co-circumferential with the cannula 50. The second handle 42 includes an alignment ridge 46, and a handle groove 56, the uses of which are described later.
C. The Drill Bit Instrument
As shown in FIG. 11, an optional third functional instrument 70 functions as a drill bit. The drill bit instrument 70, having a distal end 72 and a proximal end 74, typically is slightly longer than and has generally the same physical dimensions as, the trocar 30. Like the trocar 30, the drill bit instrument 70 is intended, in use, to fit for sliding and rotational movement within the interior lumen 44 of the second instrument 40.
The distal end 72 of the drill bit instrument 70 desirably includes cutting edges 76. In use, the cutting edges 76 are intended to penetrate hard tissue in response to rotation and longitudinal load forces applied at the proximal end 74 of the drill bit instrument 70.
The drill bit instrument 70 can be of known construction, and could vary widely. Desirably. the diameter of the drill bit instrument 70 is smaller than the interior lumen 44 of the second instrument 40, and the length is longer than the cannula 50, such that the drill bit instrument 70 can access tissue deeper than the cannula 50 when the cannula 50 is installed in a patient.
II. The Instrument Handles
The first handle 22 and the second handle 42 are designed to comfortably accommodate a hand, to desirably interlock to form a composite handle 12 that resists relative rotation between the first handle 22 and the second handle 42, and desirably to indicate whether the instruments have been reused and/or resterilized.
A. Hand Accommodation
As shown in FIGS. 1-4, the composite handle 12 is shaped to be comfortably and securely grasped by a normal human hand as shown in FIG. 3. Preferably, the contours of the composite handle 12 are rounded to provide a comfortable grip and to minimize surgical glove tears.
As shown in FIG. 3, in the preferred embodiment, the first handle 22 is desirably equipped with two finger receivers 38, intended to receive the index finger and the pinkie finger of a physician.
Shown in FIG. 4, in the preferred embodiment, the second handle 42 is desirably equipped with two finger receivers 58, intended to receive the middle finger and the ring finger of a physician.
The shape and size of the first handle 22 and second handle 42, of course, vary. In the embodiment shown in FIG. 1, the composite handle 12, and in particular the first handle 22, includes a striking plate 14, elongated to fit comfortably across the palm of the hand. The striking plate 14 is also configured to receive a striking blow, described later.
B. Interlocking Configuration
In order to properly interact when applying striking, pushing and/or twisting forces to the composite handle 12, the first handle 22 desirably will not rotate relative to the second handle 42. Referring now to FIGS. 5, 6A and 6B, to avoid relative rotation, the first handle 22 preferably includes the alignment ridge receiver 26 to receive the alignment ridge 46 of the second handle 42. Although described and pictured as a ridge, the alignment mechanism interaction between the first handle 22 and the second handle 42 could comprise any number of shapes other than an arcuate shape, for example a block shape or a star shape.
In use, when the trocar 30 of the first instrument 20 is slid through the cannula 50 of the second instrument 40, the first handle 22 and second handle 44 can fit together to form the composite handle 12. In addition to the alignment ridge 46 resisting rotation because of the alignment ridge receiver 26, the first handle 22 can include a handle key 36 for coupling with the handle groove 56 of the second handle 42.
If the handle groove 56 is not aligned with the handle key 36, and thus the alignment ridge 46 not aligned with the alignment ridge receiver 26, the handle bore 48 of the second handle 42 desirably will not fully insert into the handle bore receiver 28 of the first handle 22. In this alignment, the viewing window 24 will display the trocar 30, which preferably extends past the viewing window 24. Also in this alignment, the first handle 22 is desirably able to rotate independently of the second handle 42.
If, however, as shown in FIG. 6B, the handle groove 56 is aligned with the handle key 36, and thus the alignment ridge 46 is aligned with the alignment ridge receiver 26, the handle bore 48 of the second handle 42 can be fully inserted into the handle bore receiver 28 of the first handle 22.
In this operational alignment, the viewing window 24 displays the handle bore 48. Preferably, the handle bore 48 is a different color than the trocar 30 such that visualization would be simplified. Also in this alignment, the first handle 22 desirably does not rotate independently of the second handle 42. In this alignment, the composite handle 10 is sized and shaped to accommodate four fingers, two fingers each on the first handle 22 and the second handle 42.
Of course, its should be understood that the first and second handles 22 and 42 could be designed to engage in non-parallel orientations, such that the first and second handles 22 and 42 would not be parallel when properly engaged to form the composite handle 10. For example, the first handle 22 could incorporate a star or hexagonal shaped opening, into which a corresponding star or hexagonal shaped second handle 42 could engage in a multiplicity of orientations.
In use, various forces resist relative motion between the first instrument 20 and the second instrument 40. As shown in FIG. 3, when a hand grips the composite handle 10, the upward force supplied by the fingers, coupled with the downward force supplied by the palm, will compress the first instrument 20 and the second instrument 40 together. As previously noted, when properly configured, relative rotation of the instruments is desirably constrained as well.
C. Handle Materials
1. Structural Integrity
The material chosen for the first handle 22 and the second handle 42 desirably provides sufficient structural integrity to withstand manual manipulation and forces expected from manual striking blows. The first handle 22 and the second handle 42 are made from a molded or cast rigid material sufficient in strength to withstand the striking, pushing and twisting forces without significant deformation.
Another preferable characteristic of the handle composition is that the first handle 22 and the second handle 42 can be roughened or otherwise textured to provide a secure gripping surfaces.
2. Reuse
To encourage single use and discourage reuse and/or resterilization, it is preferable to differentiate between new hand tools and hand tools that have been reused and/or resterilized.
Striking and exertion of manual pressure on any of the instruments and structures described herein during first use generates stress on the material or materials which make up the instruments and/or structure. The material stress created by operational loads during first use can significantly alter the molded morphology of the structure, making future performance of the structure unpredictable.
For example, during advancement of the trocar and the cannula into the cancellous bone during a single use creates contact with surrounding cortical and cancellous bone. This contact can damage the structure, creating localized regions of weakness, which often can escape visual detection. The existence of localized regions of weakness can unpredictably cause structural failure during a subsequent use. Such contact can also cause flattening and/or curling of the end surface of the cannula, or dulling of the penetrating surface of the trocar.
In addition, exposure to blood and tissue during a single use can entrap biological components on or within the structure of the cannula or handles. Despite cleaning and subsequent sterilization, the presence of entrapped biological components can lead to unacceptable pyrogenic reactions.
As a result, following first use, the structure might not meet established performance and sterilization specifications. The effects of material stress and damage caused during a single use, coupled with the possibility of pyrogen reactions even after resterilization, reasonably justify and encourage single use for the instruments and handles that are deployed in tissue and bone.
To protect patients from the potential adverse consequences occasioned by multiple use, which include disease transmission, or material stress and instability, or decreased or unpredictable performance, various materials may be used to indicate and possibly prevent re-use and /or resterilization of the hand tools.
For example, a heat degradable material can be used to indicate, through deformation, whether a hand tool has been autoclaved. Additionally, chemical sensitive pigments, such as inks commercially available from Tempil, could be applied to the composite handle 12 to indicate, through a change of color, whether a hand tool has been chemically sterilized, for instance by use of ethylene oxide (ETO), as described in the requirements of ANSI/AAMI/ISO11135:1994 for sterilizing devices. In addition, various materials which change color and/or physical composition in the presence of other sterilization methods, such as radiation sterilization, can be incorporated into hand tools to indicate sterilization.
One material that provides sufficient structural rigidity and yet indicates whether an instrument has been exposed to heat common to sterilization is LUSTRAN™ material, which is commercially available from Bayer. As shown in FIGS. 17A and 17B, when this material is used in handle construction, the material will typically deform during heat sterilization, desirably preventing the handle groove 56 from aligning with the handle key 36, and thus preventing the alignment ridge 46 from aligning with the alignment ridge receiver 26. Additionally, following deformation, the handle bore 48 of the second handle 42 desirably cannot be fully inserted into the handle bore receiver 28 of the first handle 22.
III. Illustrative Use of the System
The following describes use of the composite instrument 10, instruments 20, 40, and 70, in conjunction with a catheter component 130, a diagnostic or therapeutic element 132, a syringe 136 and a tamping instrument 142 as shown in FIGS. 9-15 in the context of treating bones. This is because these items can be advantageously used for this purpose. Still, it should be appreciated that the composite instrument 10 is not limited to use in the treatment of bones, nor limited to instruments intended to contact tissue to perform a diagnostic or therapeutic function. The composite handle 12 configuration associating the first handle 22 and the second handle 42 can be used in association with various other hand-held instruments.
The composite instrument 10, handles 12, 22, and 42, and instruments 20, 40, 64 and 70 will now be described with regard to the treatment of human vertebra. It should be appreciated, however, their use is not limited to human vertebrae. The handle 18 can be used in association with hand-held instruments in the treatment of diverse human or animal bone types.
A. Vertebral Anatomy
One use of the system is to treat vertebral bodies. As FIG. 7A shows, the spinal column 80 comprises a number of uniquely shaped bones, called the vertebrae 82, a sacrum 84, and a coccyx 86 (also called the tail bone). The number of vertebrae 82 that make up the spinal column 80 depends upon the species of animal. In a human (which FIG. 7A shows), there are twenty-four vertebrae 82, comprising seven cervical vertebrae 88, twelve thoracic vertebrae 90, and five lumbar vertebrae 92.
When viewed from the side, as FIG. 7A shows, the spinal column 80 forms an S-shaped curve. The curve serves to support the head, which is heavy. In four-footed animals, the curve of the spine is simpler.
As FIGS. 7A, 7B and 8 show, each vertebra 82 includes a vertebral body 96, which extends on the anterior (i.e., front or chest) side of the vertebra 82. As FIGS. 7A, 7B and 8 show, the vertebral body 96 is in the shape of an oval disk. As FIGS. 7B and 8 show, the vertebral body 96 includes an exterior formed from compact cortical bone 98. The cortical bone 98 encloses an interior volume 100 of reticulated cancellous, or spongy, bone 102 (also called medullary bone or trabecular bone). A “cushion,” called an intervertebral disk 104, is located between adjacent vertebral bodies 96.
An opening, called the vertebral foramen 106, is located on the posterior (i.e., back) side of each vertebra 82. The spinal ganglion 109 pass through the foramen 106. The spinal cord 108 passes through the spinal canal 107.
The vertebral arch 110 surrounds the spinal canal 107. The pedicles 112 of the vertebral arch 110 adjoin the vertebral body 96. The spinous process 114 extends from the posterior of the vertebral arch 110, as do the left and right transverse processes 116.
B. Surgical Technique
In a typical procedure, a patient lies on an operating table, while the physician introduces the composite instrument 10 into soft tissue (designated S in FIG. 9) in the patient's back. The patient can lie face down on the table, or on either side, or at an oblique angle, depending upon the physician's preference. Moreover, the procedure can be performed through an open anterior procedure or an endoscopic anterior procedure.
1. Accessing Cancellous Bone
Under radiologic or CT monitoring, the physician advances the composite instrument 10 through soft tissue S down to and into the targeted vertebra 82, as FIG. 9 shows. The physician will typically administer a local anesthetic, for example, lidocaine, to the targeted region. In some cases, the physician may prefer other forms of anesthesia, such as general anesthesia.
As shown in FIG. 10, the physician directs the composite instrument 10 such that the trocar 30 of the first instrument 20 and the cannula 50 of the second instrument 40 penetrate the cortical bone 98 and the cancellous bone 102 of the targeted vertebra 82. If desired, the physician twists the composite handle 10 while applying longitudinal force to the handle 10. In response, the penetrating surface 35 of the trocar 30, and the end surface 60 of the cannula 50 rotate and penetrate soft tissue and/or bone.
Preferably the depth of penetration of the distal end 34 of the trocar 30 and the end surface 60 of the cannula 50 are through a first wall of the cortical bone 98 and into the cancellous bone 102. However, if the penetration through the first wall of the cortical bone 98 and into the cancellous bone 102 is not achievable by manual advancement of the composite instrument 10, a physician can continue penetration by gently striking the striking plate 14 with a blunt instrument such as a surgical hammer (not shown), or otherwise applying appropriate additional longitudinal force to the composite handle 12, to advance the distal end 34 of the trocar 30 and the end surface 60 of the cannula 50.
If desired, the physician can utilize a spinal needle assembly and stylet to initially access the vertebral body 82, and then utilize the alternative embodiment shown in FIG. 18 to complete the access procedure. The embodiment shown in FIG. 18 allows the physician to place a stylet 23 into the targeted vertebral body 82, and then guide the composite instrument 10 through soft tissue and into the targeted vertebra body 82 along the stylet 23, which passes through the trocar lumen 21 as the composite instrument 10 is advanced through soft tissue and into the vertebral body 82. Once the trocar 30 has sufficiently penetrated cortical bone, the physician can withdraw the spinal needle assembly 23.
After penetrating the cortical bone 98, if desired, the physician may continue advancing the composite instrument 10 through the cancellous bone 102 of the vertebral body 96, thereby forming a passage through the cancellous bone 102. Preferably this passage will extend no more than 95% across the vertebral body. The physician may then withdraw the instrument 10, such that the cannula 50 remains within the cortical bone 98 and/or extends only part-way into the cancellous bone 102. The trocar 30 may then be withdrawn from the cannula 50, allowing access to the passage formed in the interior of the vertebral body 82 through the cannula 50.
Alternatively, after penetrating the cortical bone 98, the physician may choose to withdraw the trocar 30 from the cannula 50 and form a passage in the cancellous bone 102 using a drill bit 70. In such a case, the physician removes the first functional instrument 20 by holding the second instrument 40 in place and manually withdrawing the first instrument 20.
Next, as shown in FIG. 11, the physician advances the drill bit 70 through the cannula 50. Under X-ray control (or using another external visualizing system), the physician applies appropriate twisting and longitudinal forces to the drill bit 70, to rotate and advance the cutting edge 76 of the drill bit 70 to open a passage through the bone tissue and completely into the cancellous bone 102. The drilled passage preferably extends no more than 95% across the vertebral body 96.
At this point in the procedure, access to the cancellous bone 102 has been accomplished and the end surface 60 of the cannula 50 extends into the interior volume 100, leaving only the cannula instrument 50 in place.
2. Bone Treatment
As shown in FIG. 12, the physician can now acquire the catheter component 130. The physician can advance the diagnostic or therapeutic element 132 carried by the catheter component 130 through the handle bore 48 and cannula 50 and into the interior volume 100 of the vertebral body 96.
The distal diagnostic or therapeutic element 132 of the catheter component 130 can be configured to perform various functions. For example, the element 132 can comprise a biopsy instrument, to obtain samples of cancellous bone or to harvest bone marrow. Alternatively, the distal element 132 can be a stylet to introduce a medication or the like into cancellous bone. Still alternatively (as shown in FIG. 13), the distal element 132 can comprise an expandable body to compact cancellous bone 102 and form a cavity 134 in the vertebral body 96, in the manner disclosed in U.S. Pat. Nos. 4,969,888, 5,108,404, and 5,827,289, which are incorporated herein by reference. Upon compaction of cancellous bone 102, the distal element 132 can also include a nozzle 140 to inject a material into the formed cavity.
Upon formation of the cavity 134, the physician acquires a syringe 136 and injection nozzle 140. As FIG. 14 shows, the nozzle 140 is sized to pass through the cannula 50, to thereby pass into the cavity 134. The nozzle 140 connects by a threaded connector 186 to a syringe 136. The nozzle 140 can be formed from a rigid metal material, e.g., stainless steel.
As FIG. 14 shows, the physician fills the syringe 136 with the desired volume of filling material 138. The physician attaches the nozzle 140 to the filled syringe 136. The physician inserts the nozzle 140 a selected distance beyond the distal end 54 of the cannula 50 and into the cavity, guided by markings 166 on the nozzle 140. Next, the physician operates the syringe 136 to expel the material 138 through the nozzle 140 into the cavity 134.
Desirably, the physician first introduces the material 138 into the region of the cavity 134 farthest from the distal end 54 of the cannula 54. The physician successively draws the nozzle 140 toward the distal end 54 of the cannula 50, while injecting the material 138, to fill the remainder of the cavity 54.
At this stage, the nozzle 180 is unthreaded from the syringe 104. As FIG. 15 shows, the physician next advances a tamping instrument 142 through the nozzle 140. The distal end of the tamping instrument 142 contacts the residual volume of material 138 in the nozzle 140. Advancement of the tamping instrument 142 displaces the residual material 138 from the nozzle 140, forcing it into the cavity 134. The flow of material 138 into the cavity 134, propelled by the advancement of the tamping instrument 142 in the nozzle 140 serves to uniformly distribute and compact the material 138 inside the cavity 134, without the application of undue pressure.
As shown in FIG. 16, as an alternative to attaching the nozzle 140 to the syringe 136, the physician can attach the syringe 136 directly to the handle bore 48 of the second instrument 40. As shown in the alternate embodiment in FIG. 16, the syringe 136 can have threads 137 or other fasteners, such as snap-sit fasteners or luer-lock fasteners. The threads 137 would match with bore threads 49 contained in the handle bore 48. Next, the physician operates the syringe 136 to expel the material 138 through the handle bore 48 and the cannula 50 and directly into the cavity 134. In this arrangement, the physician disconnects the syringe 136 and advances the tamping instrument 142 through the handle bore 48 and the cannula 50 to displace the residual material 138 from the cannula 50, forcing it into the cavity 134.
The use of the syringe 136 with or without nozzle 140, and the tamping instrument 142 allows the physician to exert precise control when filling the cavity 134 with material 138. The physician can immediately adjust the volume and rate of delivery according to the particular local physiological conditions encountered. The application of low pressure (i.e., desirably no greater than 360 psi at the distal end of the cannula, more desirably no greater that 190 psi at the distal end of the cannula, and most desirably no greater than 100 psi at the distal end of the cannula), which is uniformly applied by the tamping instrument 142, allows the physician to respond to fill volume, flow resistance, and flow path conditions quickly. The chance of overfilling and leakage of material 138 outside the cavity portion is thereby significantly reduced.
When the physician is satisfied that the material 138 has been amply distributed inside the cavity portion, the physician withdraws the tamping instrument 142 from the cannula 50 and handle bore 48. The physician preferably first twists the tamping instrument 142 to cleanly break contact with the material 138.
Of course, this procedure could be repeated to access and treat one vertebral body multiple times in multiple orientations to create multiple cavities that may or may not interconnect. After a cavity has been filled and tamped in the above described manner, the instruments can be withdrawn and the incision sites sutured closed. The bone treatment procedure is concluded.
C. Suggested Materials
Desirably, the material 138 will provide sufficient support within the vertebral body to prevent further fracture of the body. The capability of the vertebral bodies to withstand loads will have thereby been improved. The material may also facilitate healing of the vertebral body.
The selected material 138 can be a bone cement, or autograft or allograft bone graft tissue collected in conventional ways, e.g., in paste form (see Dick, “A Use of the Acetabular Reamer to Harvest Autogenic Bone Graft Material: A Simple Method for Producing Bone Paste,” Archives of Orthopaedic and Traumatic Surgery (1986), 105: 235-238), or in pellet form (see Bhan et al, “A Percutaneous Bone Grafting for Nonunion and Delayed Union of Fractures of the Tibial Shaft,” International Orthopaedics (SICOT) (1993) 17: 310-312). Alternatively, the bone graft tissue can be obtained using a Bone Graft Harvester, which is commercially available from SpineTech. Using a funnel, the paste or pellet graft tissue material is loaded into the cannula 50. The tamping instrument 142 is then advanced into the cannula 50 in the manner previously described, to displace the paste or pellet graft tissue material out of the cannula 50 and into the cavity 134.
The selected material 138 can also comprise a granular bone material harvested from coral, e.g., ProOsteon™ calcium carbonate granules, available from Interpore. The granules are loaded into the cannula 50 using a funnel and advanced into the cavity using the tamping instrument 142.
The selected material 138 can also comprise demineralized bone matrix suspended in glycerol (e.g., Grafton™ allograft material available from Osteotech), or SRS™ calcium phosphate cement available from Novian. These viscous materials, like the bone cement previously described, can be loaded into the syringe 136 and injected into the cavity directly or using the nozzle 140, which is inserted through the cannula 50 into the cavity 134. The tamping instrument 142 is used to displace residual material from the cannula 50 into the cavity 134, as before described.
The selected material 138 can also be in sheet form, e.g. Collagraft™ material made from calcium carbonate powder and collagen from bovine bone. The sheet can be rolled into a tube and loaded by hand into the cannula 50. The tamping instrument 142 is then advanced through the cannula 50, to push and compact the material in the cavity 134.
IV. Interlocking Hand Held Instruments
FIGS. 19 and 20 show an alternative embodiment for a composite instrument 210 for penetrating tissue, which shares many of the features of the composite instrument 10, previously described. As FIG. 22 shows, when disassembled, the composite instrument 210, like the composite instrument 10 previously described, includes a first functional instrument 220 and a second functional instrument 240. A composite handle 212 joins the two instruments 220 and 240, when assembled (as FIGS. 19 and 20 show). The composite handle 212 comprises a first handle 222 (associated with the first instrument 220) and a second handle 242 (associated with the second instrument 240) (as FIG. 22 also shows). Like the composite handle 12 for the composite instrument 10, the composite handle 212 for the instrument 210 aids a physician in manipulating the composite instrument 210, but a physician can also desirably use the first handle 222 to independently manipulate the first instrument 220 or the second handle 242 to independently manipulate the second instrument 240 during use.
As previously explained, the number and type of instruments 220 and 240 can, of course, vary. In the illustrated embodiment, each instrument 220 and 240 has a different size and function. In a preferred embodiment, the first functional instrument 220 is a trocar instrument, and the second functional instrument 240 is a cannula instrument.
A. The Trocar Instrument
Referring to FIG. 22, the first instrument 220 functions as a trocar instrument 230 to penetrate tissue. The trocar 230 has a proximal end 232 and a distal end 234. The distal end 234 is intended to penetrate soft tissue and/or bone in response to pushing and/or twisting forces applied by the physician at the first handle 222, or the composite handle 212. If desired, the distal end 234 can terminate in a substantially blunt and/or cannulated tip, or alternatively terminate in a sharpened tip for cutting through tissue, as known in the art.
The first handle 222 is coupled to proximal end 232 of the trocar 230. Similar to that shown in FIG. 6C for the trocar 30, the proximal end 232 of the trocar 230 can likewise be formed in a T-shape, with the first handle 222 being molded around the T-shaped end. As earlier described with reference to the trocar 30, this arrangement significantly increases the mechanical strength of the bond between the handle 222 and the trocar 230, and allows significant longitudinal and torsional forces to be transmitted from the handle 222 to the trocar 230 without bond failure. Alternatively, with or without a T-shaped end, the proximal end 232 of the trocar 230 can be scored (as shown, in relation to the trocar 32, by scored region 33 in FIG. 6C) to increase the mechanical strength of the bond between the trocar 230 and the handle 222, or various bonding adhesives could be used, with varying results.
The first handle 222 desirably includes a receiving channel 226 with a viewing window 224 and a latch mechanism 236 (also shown in FIGS. 23 and 24), the structure and function of which are described later.
Like the trocar 30, the trocar 230 may include an interior lumen (not shown), which passes through the handle 222 and the body of the trocar 230, to accommodate passage of a stylet and/or conventional spinal needle assembly, to guide the deployment of the first instrument 220, by itself or nested with the second instrument 240 (as FIG. 18 shows with respect to the first described embodiment), through soft tissue to a targeted bone treatment site.
B. The Cannula Instrument
Still referring principally to FIG. 22, the second instrument 240 functions as a cannula instrument or guide sheath, and includes a cannula 250. The cannula 250 of the second instrument 240 is desirably somewhat larger in diameter than and not as long as the trocar 230 of the first instrument 220. As best shown in FIG. 21, the second instrument 240 includes an interior lumen 244 that extends through the instrument from its distal end 254 to its proximal end 252. The interior lumen 244 is sized to accept the trocar 230 (as FIG. 21 shows). The size of the interior lumen 244 desirably allows the second instrument 240 to slide and/or rotate relative to the first instrument 220, and vice versa, unless the two handles 222 and 242 are locked together, as will be described later.
The distal end 254 of the second instrument 240 presents an end surface that desirably presents a low-profile surface, which can penetrate soft tissue surrounding the first instrument 220 in response to pushing and/or twisting forces applied at the composite handle 212 or the second handle 242.
The proximal end 252 is coupled with the second handle 242. As shown in FIG. 6D with respect to the cannula 50, the proximal end 252 of the cannula 250 can desirably incorporate a flared and notched end “A” and/or a textured surface “B”, around which the second handle 242 is molded. The flared and notched end “A” and/or textured surface “B” serve to increase the mechanical strength of the bond between the cannula 250 and the second handle 242, allowing significant longitudinal and torsional forces to be transmitted between the second handle 242 and cannula 250 without bond failure. As with the trocar 230, however, other bonding methods such as scoring of the cannula 250 and/or the use of various adhesives could be employed, with varying results.
Extending from the interior lumen 244 at the proximal end 252 of the cannula 250, the second handle 242 desirably includes a handle bore 248, preferably co-circumferential with the cannula 250. The second handle 242 includes a transverse shoulder 246 and at least one latch notch 256 on the shoulder 246, the structure and function of which are described later.
C. The Handles
The first handle 222 and the second handle 242 are designed to comfortably accommodate a hand, to desirably interlock to form a composite handle 212 that resists relative rotation between the first handle 222 and the second handle 242.
D. Hand Accommodation
Like the composite handle 12, the composite handle 212 is shaped to be comfortably and securely grasped by a normal human hand, as generally shown in FIG. 21. Preferably, the contours of the composite handle 212 are likewise rounded to provide a comfortable grip and to minimize surgical glove tears. The first handle 222 is desirably equipped with two finger receivers 238, intended to receive the index finger and the pinkie finger of a physician, in the same fashion shown for the handle 12 in FIG. 3.
The second handle 242 is desirably equipped with two finger receivers 258, intended to receive the middle finger and the ring finger of a physician, in the same fashion shown for the handle 42 in FIG. 4.
The shape and size of the first handle 222 and second handle 242, of course, vary. In the embodiment shown in FIGS. 19 to 21, the composite handle 212, and in particular the first handle 222, includes a striking plate 214, elongated to fit comfortably across the palm of the hand. The striking plate 214 is also configured to receive a striking blow, for the purposes described above.
The material chosen for the first handle 222 and the second handle 242 desirably provides sufficient structural integrity to withstand manual manipulation and forces expected from manual striking blows. The first handle 222 and the second handle 242 are made from a molded or cast rigid material sufficient in strength to withstand the striking, pushing and twisting forces without significant deformation. Representative materials for the first and second handles 222 and 242 can include various plastics, metals, and/or ceramics well known in the art. In one disclosed embodiment, the first and second handles 222 and 242 are formed from Lustran® ABS (acrylonitrile-butadiene-styrene) plastic, available commercially from Bayer Corporation.
Another preferable characteristic of the handle composition is that the first handle 222 and the second handle 242 can be roughened or otherwise textured to provide a secure gripping surfaces.
E. Interlocking Configuration
In order to properly interact when applying striking, pushing and/or twisting forces to the composite handle 212, the first handle 222 desirably will not rotate relative to the second handle 242 when the two handles 222 and 242 are secured together. To avoid relative rotation, the first handle 222 preferably includes the receiving channel 226 into which the shoulder 246 of the second handle 242 is advanced and nests (see FIGS. 23 and 24)
In use, when the trocar 230 of the first instrument 220 is slid through the cannula 250 of the second instrument 240 (see FIG. 21), the first handle 222 and second handle 244 fit together to form the composite handle 212 (as FIG. 19 shows). The shoulder 246 nests within the locking channel 226, resisting rotation of the first instrument 220 relative to the second instrument 240.
Furthermore, when the locking shoulder 246 is advanced a desired distance through the channel 226, the latch mechanism 236 on the first handle 222 engages the latch notch 256 on the second handle 242, to resist separation of the two instruments 220 and 240.
The latch mechanism 236 can be constructed in various ways. As shown in FIGS. 23 and 24, the latch mechanism 236 includes a latch finger 260 situated to engage the latch notch 256 on the second handle 242. The latch finger 260 is carried on a hinge 262 in the first handle 222. The hinge 262 is desirably made from resilient plastic material and possesses plastic memory, forming a so-called “living hinge.”
The latch finger 260 is cantilevered on the hinge 262 for pivoting movement within the first handle 222. The plastic memory of the hinge 262 normally biases the finger 260 toward a normal position, shown in FIG. 23, in which the finger 260 will rest within the notch 256, provided that the two parts are in alignment. The latch finger 260 can be displaced out of its normal position (as shown in FIG. 24) in response to an applied force F. Upon removal of the force F, the hinge 262 returns the finger 260 to its normal position.
In the illustrated embodiment, the force F is applied in at least two different ways. One works in response to advancement of the shoulder 246 through the channel 226 toward the latch mechanism 236. This serves to secure the two instruments 220 and 240 together, for use as a composite instrument 210. The other works in response to manual pressure exerted by an operator upon the latch mechanism 236. This serves to separate the two instruments 220 and 240, for use of the instruments 220 and 240 individually.
Regarding the first mechanism, the latch finger 260 includes a cam surface 264 (best shown in FIG. 24). The leading edge 266 of the locking shoulder 246 slides or rides along the cam surface 264 as the shoulder 246 progresses through the channel 226. Progressive advancement of the leading edge 266 of the shoulder 246 along the cam surface 264 will apply the force F, to cause the latch finger 260 to pivot on the hinge 262. When the locking notch 256 on the shoulder 246 is in mutual alignment with the latch finger 260, the force F is relieved, and the latch finger 260 resiliently returns toward its normal position. This moves the latch finger 260 into the notch 256, in a snap-fit. The plastic memory of the hinge resists movement of the notch 256 out of engagement with the latch finger 260, effectively locking the two handles 222 and 242 together as the composite handle 212.
The shoulder 246 desirably includes a locking notch 256 on reverse facing, opposite sides of the shoulder 246. In this way, the fitment of the shoulder 246 into the channel 226 is not sensitive to mutual orientation of the two handles 222 and 242.
The viewing window 224 on the first handle 222 reveals the advancement of the shoulder 246 through the channel 226 and into engagement with the latching mechanism 236. This provides visual confirmation of the locking fit. Preferably, the shoulder 246 is a different color than first handle 220, such that visualization would be further simplified.
When formed, the composite handle 210 is sized and shaped to accommodate four fingers, two fingers each on the first handle 222 and the second handle 242, in the same fashion shown for the composite handle 10 in FIG. 3.
Regarding the second mechanism for applying the force F to the latch finger 260, the latch mechanism 236 also includes a detent surface 268. Pressing against the detent surface 268 applies the force F to the latch finger 260, causing the finger 260 to pivot on the hinge 262. The latch mechanism 236 also desirably incorporates a stop 280, which limits the displacement of the latch mechanism during release. The force F frees the finger 260 from the notch 256, to allow the shoulder 246 to be withdrawn from the channel 226. The operator can thereby separate the two handles 222 and 224 (as FIG. 21 shows).
The composite instrument 210 and the instruments 220 and 240 can be used in conjunction with a catheter element 130, a diagnostic or therapeutic element 132, and other instruments in the same fashion as the composite instrument 10, previously described.
The disclosed composite instrument 210 also greatly facilitates manipulation and use of the instrument by a physician wearing leaded and/or lead-lined gloves during the surgical procedure. Because many procedures are performed under fluoroscopic visualization, physicians repeatedly performing these procedures often wear leaded gloves to minimize exposure of their hands to harmful radiation. Such gloves are often thick, uncomfortable, and incorporate radiopaque materials, such as lead, and typically negatively impact the ability of the surgeon to manipulate small objects or to “feel” the surgical instruments during the procedure. With the disclosed composite instrument 210, the physician can hold the instrument in a single hand, and can use a single finger to depress the detent surface 268 to separate the two handles 222 and 242. The detent surface 268 is desirably sized such that it can be easily felt and manipulated, even through leaded gloves.
Moreover, because the stop 280 desirably limits the displacement of the latch mechanism 236 during release, the latch mechanism 236 can withstand a significant amount of force F without damage to the hinge 262. This is especially important where the physician is wearing leaded gloves, because the physician may not be able to accurately gage the amount of force he or she is imparting to a given tool. Even where the physician uses an excessive amount of force to release the instrument, therefore, the disclosed composite instrument 210 is less likely to fail during the surgical procedure.
The features of the invention are set forth in the following claims.

Claims

1. A system comprising

a first instrument having a distal end sized and configured to penetrate tissue and a proximal end comprising a first handle assembly,

a second instrument including an interior lumen sized and configured to accept passage of the first instrument, the second instrument having a proximal end comprising a second handle assembly sized and configured to releasably interlock with the first handle assembly to form a composite instrument sized and configured to provide percutaneous access to a cancellous bone region, the second handle assembly also sized and configured to permit controllably release by a user of the first handle assembly from the second handle assembly to allow removal of the first instrument from the interior lumen, and

at least one additional instrument sized and configured for passage through the interior lumen of the second instrument upon removal of the first instrument.

2. A system according to claim 1

wherein the additional instrument comprises a delivery tube sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument, the delivery tube having a proximal end including a connector for coupling the delivery tube to an injector of bone filling material to convey the bone filling material into the cancellous bone region.

3. A system according to claim 1

wherein the additional instrument comprises a third instrument sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument, the third instrument having a distal region sized and configured to treat the cancellous bone region.

4. A system according to claim 3

wherein the distal region is sized and configured to biopsy cancellous bone.

5. A system according to claim 3

wherein the distal region is sized and configured to harvest cancellous bone.

6. A system according to claim 3

wherein the distal region is sized and configured to introduce a therapeutic material.

7. A system according to claim 3

wherein the distal region is sized and configured to modify the cancellous bone region to receive a bone filling material.

8. A system according to claim 3

wherein the distal region is sized and configured to modify the cancellous bone region to receive a bone filling material by contacting the cancellous bone region.

9. A system according to claim 8

wherein the distal region is capable of expansion into contact with the cancellous bone region.

10. A system according to claim 8

wherein the distal region is capable of inflation into contact with the cancellous bone region.

11. A system according to claim 3

wherein the distal region is sized and configured to modify the cancellous bone region to receive a bone filling material by creating a cavity in the cancellous bone region.

12. A system according to claim 1

wherein the distal region is sized and configured to move fractured cortical bone.

13. A system according to claim 1

wherein the second instrument comprises a cannula.

14. A system comprising

a second instrument including an interior lumen sized and configured to accept passage of the first instrument, the second instrument having a proximal end comprising a second handle assembly sized and configured to releasably interlock with the first handle assembly to form a composite instrument sized and configured to provide percutaneous access a cancellous bone region, the second handle assembly also sized and configured to permit controllably release by a user of the first handle assembly from the second handle assembly to allow removal of the first instrument from the interior lumen,

a third instrument sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument, the third instrument having a distal region sized and configured to treat the cancellous bone region, and

a delivery tube sized and configured to pass through the interior lumen of the second instrument upon removal of the third instrument, the delivery tube having a proximal end including a connector for coupling the delivery tube to an injector of bone filling material to convey the bone filling material into the cancellous bone region treated by the third instrument.

15. A system according to claim 14

wherein the distal region is sized and configured to biopsy cancellous bone.

16. A system according to claim 14

wherein the distal region is sized and configured to harvest cancellous bone.

17. A system according to claim 14

18. A system according to claim 14

19. A system according to claim 18

20. A system according to claim 19

21. A system according to claim 19

22. A system according to claim 18

23. A system according to claim 14

24. A system according to claim 14

wherein the second instrument comprises a cannula.

25. A system comprising

an injector tool to inject bone filling material, and

a delivery tube sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument, the delivery tube having a proximal end including a connector for coupling the delivery tube to the injector tool to convey bone filling material into the cancellous bone region.

26. A system according to claim 25

wherein the injector tool includes a reservoir for receiving a bone filling material and an ejector sized and configured to expel the bone filling material from the reservoir.

27. A system according to claim 25

wherein the injector tool includes a syringe.

28. A system according to claim 25

wherein the bone filling material comprises bone cement.

29. A system according to claim 25

wherein the bone filling material comprises bone graft tissue.

30. A system according to claim 25

wherein the second instrument comprises a cannula.

31. A system comprising

a third instrument sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument, the third instrument having a distal region sized and configured to treat the cancellous bone region,

an injector tool to inject bone filling material, and

a delivery tube sized and configured to pass through the interior lumen of the second instrument upon removal of the third instrument, the delivery tube having a proximal end including a connector for coupling the delivery tube to the injector tool to convey bone filling material into the cancellous bone region treated by the third instrument.

32. A system according to claim 31

wherein the distal region is sized and configured to biopsy cancellous bone.

33. A system according to claim 31

wherein the distal region is sized and configured to harvest cancellous bone.

34. A system according to claim 31

35. A system according to claim 31

36. A system according to claim 35

37. A system according to claim 36

38. A system according to claim 36

39. A system according to claim 35

40. A system according to claim 31

41. A system according to claim 31

42. A system according to claim 31

wherein the injector tool includes a syringe.

43. A system according to claim 31

wherein the bone filling material comprises bone cement.

44. A system according to claim 31

wherein the bone filling material comprises bone graft tissue.

45. A system according to claim 31

wherein the second instrument comprises a cannula.

46. A method comprising

providing a first instrument having a distal end sized and configured to penetrate tissue and a proximal end comprising a first handle assembly,

providing a second instrument including an interior lumen sized and configured to accept passage of the first instrument, the second instrument having a proximal end comprising a second handle assembly sized and configured to releasably interlock with the first handle assembly,

forming a composite instrument by interlocking the first and second handle assemblies,

manipulating the composite handle to through tissue to provide percutaneous access to a cancellous bone region,

releasing the first handle assembly from the second handle assembly to remove the first instrument from the interior lumen,

providing an additional instrument, and

passing the additional instrument through the interior lumen of the second instrument into the cancellous bone region.

47. A method according to claim 46

48. A method according to claim 46

wherein the additional instrument includes a third instrument sized and configured to pass through the interior lumen of the second instrument upon removal of the first instrument, the third instrument having a distal region sized and configured to treat the cancellous bone region.

49. A method according to claim 48

wherein the distal region is sized and configured to biopsy cancellous bone.

50. A method according to claim 48

wherein the distal region is sized and configured to harvest cancellous bone.

51. A method according to claim 48

52. A method according to claim 48

53. A method according to claim 52

54. A method according to claim 53

55. A method according to claim 53

56. A method according to claim 52

57. A system according to claim 48

58. A method according to claim 46

further including providing a delivery tube sized and configured to pass through the interior lumen of the second instrument upon removal of the third instrument,

coupling the delivery tube to an injector of bone filling material,

conveying the bone filling material from the injector through the delivery tube and into the cancellous bone region treated by the third instrument.