Biopsy device with fluid delivery to tissue specimens

Information

  • Patent Grant
  • 10874381
  • Patent Number
    10,874,381
  • Date Filed
    Thursday, August 23, 2018
    6 years ago
  • Date Issued
    Tuesday, December 29, 2020
    3 years ago
Abstract
An apparatus for collecting one or more tissue specimens includes a tissue specimen collector having a cannula receiving opening, a vacuum opening, and an interior. The vacuum opening is on a first axis, and the cannula receiving opening is on a second axis. A removable tissue specimen retaining member is positioned within the interior of the tissue specimen collector. The removable tissue specimen retaining member has a plurality of openings that are interposed between the first axis of the vacuum opening and the second axis of the cannula receiving opening. The removable tissue specimen retaining member is movable along the second axis. An elongated tissue cutting member extends through the cannula receiving opening of the tissue specimen collector to position a proximal end of the elongated cutting member in the interior above the plurality of openings of the removable tissue specimen retaining member.
Description
FIELD OF THE INVENTION

The present invention relates generally to tissue removing devices such as biopsy devices and the methods of using such devices. More specifically, it is directed to an improved biopsy or other tissue removing device and method of using the device which includes flushing one or more specimens with suitable fluid within a tissue collector to remove blood, debris and the like from the specimen(s).


BACKGROUND OF THE INVENTION

In diagnosing and treating certain medical conditions, such as potentially cancerous tumors, it is usually desirable to perform a biopsy, in which a specimen of the suspicious tissue is removed for pathological examination and analysis. In many instances, the suspicious tissue is located in a subcutaneous site, such as inside a human breast. To minimize surgical intrusion into the patient's body, it is desirable to be able to insert a small instrument into the patient's body to access the targeted site and to extract the biopsy specimen therefrom.


A variety of tissue collecting components have been proposed for biopsy devices but they have not always been easy for the physician or other operating room personnel to separate or remove the specimen from the device. Needle like tip designs have been developed to aid in the accessing of intracorporeal sites for biopsy and other procedures.


SUMMARY OF THE INVENTION

This invention is directed to a system and method for collecting one or more severed tissue specimens from a target site which includes the application of a fluid such as saline to one or more collected tissue specimens. The fluid may be applied to the one or more tissue specimens to flush blood and other debris from the one or more collected tissue specimens and/or to apply one or more agents to the collected tissue specimens. The tissue specimens are preferably collected within a tissue collector associated with a biopsy system. The fluid is preferably applied to at least one tissue specimen after it has been collected within the tissue collector but fluid may be applied as the tissue is delivered into the tissue collector. A vacuum may be generated within the tissue collector to remove the fluid from the specimens. The tissue collector component is preferably part of the biopsy system and easily removable therefrom so that the specimens may be removed without interfering with the position of the biopsy device.


A biopsy system having the tissue collection and fluid applying features of the invention generally include an elongated, preferably disposable probe component having an elongated tubular shaft, an elongated cutting member within the inner lumen of the elongated tubular shaft, a proximal housing that is secured to the proximal portion of the elongated tubular shaft and a tissue collector secured to the proximal housing in fluid communication with the inner lumen of the cutting member. The tissue cutter has a distal cutting edge to separate a tissue specimen from supporting tissue at an intracorporeal target site, an inner lumen to withdraw one or more tissue specimens and a proximal end with a discharge port which is configured to discharge specimens into the interior of the tissue collector.


A fluid delivery conduit extends from a source of fluid and opens to the interior of the tissue collector to deliver fluid to one or more specimens in the interior of the tissue collector. Preferably the fluid delivery conduit has a valve to control the fluid flow therethrough so as to sequence the flow of fluid to the interior of the tissue collector after the delivery of a tissue specimen. The fluid is preferably sprayed onto the specimens, for example by one or more spray heads or nozzles that may be provided. A controller may be provided to control the operation of the valve in the fluid delivery conduit to control fluid flow thereto.


A vacuum conduit may extend from a lower portion of the tissue collector to generate a vacuum within the interior of the tissue collector to aid in the aspiration of fluid and debris from the specimens. The vacuum within the tissue collector interior may also be employed to facilitate aspiration of one or more tissue specimens through the inner lumen of the tubular cutter. The vacuum conduit preferably leads to a waste container which captures the waste (fluid and debris) from the interior of the tissue collector. Preferably, a second vacuum conduit leads from the waste container to a vacuum source such as a vacuum pump which maintains a vacuum within the waste container. A controller may be utilized to control the operation of the vacuum pump to control the level of vacuum in the waste container and the interior of the tissue collector. The controller controlling the vacuum pump may be the same controller controlling the fluid control valve referred to above.


A suitable biopsy device which may be utilized with specimen flushing features of the invention is described in co-pending application Ser. No. 11/014,413, filed on Dec. 16, 2004. The housing on the proximal end of the probe has driving elements for the tissue cutter and other operative elements such as described in the aforesaid co-pending application which is incorporated herein by reference.


The elongated probe component preferably has a distal shaft portion with a tissue penetrating distal tip, a tubular section proximal to the distal tip, an inner lumen extending within the tubular section and an open, tissue receiving aperture in the tubular section proximal to the distal tip which provides access to tissue at the targeted site. The probe component includes an elongated tissue-cutting member, which is preferably at least in part cylindrically shaped and slidably disposed within the inner lumen of the tubular section. The tissue cutting member is provided with at least one tissue cutting edge on its distal portion which is configured to sever tissue extending into the interior of the tubular section through the aperture thereof. The cutting edge on the tissue cutting member may be configured for longitudinal cutting movement and may include oscillating rotational motion and/or reciprocating longitudinal motion to sever specimen tissue extending through the aperture from supporting tissue at the targeted site. The cutting edges are radially spaced from a longitudinal axis of the probe component and are preferably transversely oriented with respect to the longitudinal axis of the probe component. The tissue cutter is preferably slidably disposed within the inner lumen of the tubular section, although it may be disposed about the tubular section. The probe component may also have a handle which releasably engages a driver component as described in the above referenced application.


The tissue cutting member has an inner lumen preferably extending to a discharge port in the proximal end thereof for tissue specimen removal. While mechanical withdrawal of the tissue specimen may be employed, it is preferred to provide a vacuum within the cutting member from the proximal end of the cutting member (via the tissue collector interior) to aspirate the severed tissue specimen through the inner lumen of the cutting member to a tissue collection station. A higher fluid pressure may be maintained in the inner lumen of the cutting member distal to the tissue specimen to aid in transporting the specimen proximally through the inner lumen. In this manner, the mechanical withdrawal and/or the vacuum on the proximal end of the specimen and a higher pressure on the distal end of the specimen can move the specimen through the inner lumen of the cutting member to the tissue collector station.


In at least one embodiment described in the above mentioned application, the handle of the probe component is secured, preferably releasably secured, to the driver provided to interconnect the various operative elements of the probe with operative elements of the driver component. The tissue cutting member is operatively connected to at least one driver to provide the desired cutting motion. The proximal end of the tubular section of the probe component is fixed within the handle housing so that the orientation thereof with respect to the longitudinal axis and therefore the orientation of the tissue receiving aperture within the tubular section, can be selected by rotation of the handle housing with respect to the driver component. The orientation of the aperture may be selected manually such as described in copending application Ser. No. 10/642,406, filed February Aug. 15, 2003 or it may be preset or selected electronically by a control module which also controls the operation of the cutting member and electrical power such as described in copending application Ser. No. 11/014,413, filed Dec. 16, 2004. The aperture orientation setting may be selected before or after the tubular section of the probe component is inserted into the patient.


A method of collecting one or more severed tissue specimens with a tissue collection device embodying features of the invention includes advancing a biopsy or other tissue removal system having such a tissue collecting device at least partially into tissue at a desired site within the patient's body with the tissue penetrating distal tip of the outer cannula disposed distal to the tissue specimen to be separated from the target site. A vacuum is established within the inner lumen of the tubular section to draw tissue through the aperture therein into the inner lumen of the tubular section. The cutting member, which is slidably disposed within the inner lumen of the tubular section, may then be moved, e.g. longitudinally, to cut a tissue specimen from supporting tissue at the target site by such cutter motion. The cutter motion preferably includes oscillating rotational movement and/or reciprocating longitudinal movement. The vacuum established within the inner lumen of the tubular section may be applied through the inner lumen of the tissue cutting member when the tissue cutting member is disposed within the tubular section. The applied vacuum within the inner lumen of the tissue cutting member from the vacuum of the tissue collector interior, may also be utilized to pull or aspirate the separated tissue sample proximally. In addition, or alternatively, a higher fluid pressure may be maintained in a distal part of the inner lumen of the tubular section, distal to the specimen, to push the tissue specimen proximally, Alternatively, the tissue specimen may be mechanically withdrawn. Fluid pressure may include pressure from a liquid delivered into the interior of the device, such as a physiological saline solution, and may include a gas, such as pressurized carbon dioxide, nitrogen or air, delivered into the interior of the device. Access to ambient air can also maintain a sufficiently high pressure differential to move the specimen through the inner lumen of the cutting member. Anesthetic may be injected to the target site through the outer cannula or the inner lumen of the cutting member.


The one or more tissue specimens are discharged into the interior of the tissue collector and preferably onto a tray provided therefore in the interior. The tray preferably has one or more openings which allow for drainage from the specimens on the tray. Irrigation (or other) fluid is applied to one or more specimens to remove blood or other debris. The periphery of the tissue collection tray is sealed within the interior of the tissue collector so that vacuum generated beneath the tray will aspirate fluid and debris from specimens on the tray to a vacuum conduit opening beneath the collector tray. The application of the irrigation fluid is preferably controlled to sequence after one or more tissue specimens are discharged onto the tissue collector tray from the discharge port in the proximal end of the tissue cutter. The fluid may contain or be a treating agent suitable for the subsequent evaluation of the specimens.


Upon removal from the patient, the tissue specimen may then be subjected to pathological examination. After acquisition of a tissue specimen or specimens, the tissue separation system may be repositioned for further tissue separation and collection or it may be withdrawn from the patient.


These and other advantages of the invention will become more apparent from the following detailed description of the invention and the accompanying exemplary drawings.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a schematic view of a biopsy system having a tissue specimen collector with flush and aspiration that embodies features of the invention.



FIG. 2 is an exploded perspective view of the elongated tissue biopsy system shown in FIG. 1.



FIG. 3 is a perspective view of the embodiment shown in FIG. 2 in an assembled condition without a cover for the probe component.



FIG. 4 is a side elevational view of the tissue biopsy system shown in FIG. 3.



FIG. 4A is a transverse cross-sectional view of the probe component taken along the lines 4A-4A shown in FIG. 4



FIG. 5A is a perspective view, with exterior portions partially in phantom, of a tissue collector shown in FIG. 4.



FIG. 5B is a longitudinal cross sectional view taken along lines 5B-5B shown in FIG. 5A.



FIG. 5C is a perspective view of the tissue receiving tray shown in FIG. 5A.



FIG. 5D is an exploded perspective view of tissue collector shown in FIG. 5A.



FIG. 5E is an end view in perspective of the tissue collector shown in FIG. 5A.



FIG. 6A is a perspective view, with exterior portions partially in phantom, of a modified tissue collector.



FIG. 6B is a longitudinal cross sectional view taken along lines 6B-6B shown in FIG. 6A.



FIG. 6C is a transverse cross-sectional view of the tissue receiving tray shown in FIG. 6B taken along the lines 6C-6C.



FIG. 6D is an end view of the tissue collector shown in FIG. 6B taken along the lines 6D-6D.



FIG. 6E is a transverse cross-sectional view of the tissue collector shown in FIG. 6B taken along the lines 6E-6E.



FIG. 6F is an exploded perspective view of tissue collector shown in FIG. 6A.



FIG. 6G is an end view in perspective of the tissue collector shown in FIG. 6A.





DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION


FIG. 1 schematically illustrates a biopsy system 10 embodying features of the invention. The system 10 includes a probe component 11 with an elongated tubular section 12, a proximal housing 13 and a tissue specimen collector 14 attached to the proximal housing. A first conduit 15 extends from fluid source 16 to the proximal end of the tissue collector 14 to deliver fluid to tissue specimens in the interior of the collector. A valve 17 is provided to control the fluid flow through the first conduit 15. A second conduit 18 extends to the tissue specimen collector 14 for application of a vacuum to the interior of the tissue specimen collector to aspirate fluid applied to one or more severed tissue specimens within the specimen collector. The second conduit 18 directs the aspirated fluid and debris to waste container 20. A third conduit 21 extends from the waste container 20 to a vacuum pump 22 which provides vacuum to the waste container and ultimately to the interior of the tissue specimen collector 14. The operation of the valve 17 in the fluid delivery conduit 15 and the vacuum pump 22 connected to the third conduit 21 may be controlled by controller 23.



FIGS. 2-5A-E illustrate the biopsy device 24 of the system 10 in further detail. The probe component 11 generally includes an elongated tubular section or cannula 12 with a tissue penetrating tip 25 on the distal end thereof and an open, tissue receiving aperture 26 proximally adjacent to the distal tip. The probe component 11 also includes a proximal housing 13 which contains the driving mechanisms for the various elements of the probe component. Probe housing cover 27 is configured to interfit with the driver component 28 so as to enclose the proximal housing 13 of the probe component 11. A tissue cutter 30 is slidably disposed within the probe component 11 and has a distal cutting edge 31 which severs tissue that extends through the tissue receiving aperture 26. An inner lumen 32 extends through the tissue cutter 30 to the tissue discharge port 33 in a proximal portion of the tissue cutter which discharges tissue specimen into the interior 34 of the tissue collector 14. The tissue discharge port 33 is preferably located at the proximal end of the tissue cutter 30.


The details of driver component 28 and the interaction between the driver component and the probe component 11 can be found in the above mentioned application Ser. No. 11/014,413.


The tissue specimen collector 14 (shown in more detail in FIGS. 5A-5E) is secured to the proximal end of the housing 13 of probe component 11 and has an interior 34 in fluid communication with the inner lumen 32 of the tissue cutter 30 through tissue discharge port 33. The tissue specimen collector 14 has a distal wall portion 14-2 with a cannula receiving opening 14-1 through which the tissue cutter 30 extends when the tissue biopsy system is assembled. The interior 34 of the specimen collector 14 has a specimen receiving basket or tray 35, preferably removable, which is configured to receive tissue specimens from the discharge port 33 which may have been drawn therein. The tray 35 (e.g. a removable tissue specimen retaining member) may have a grated portion 36 (or foraminous or is otherwise provided with a plurality of openings) to provide fluid communication with the vacuum chamber 37 provided under the tray. A vacuum is generated within the interior 34 by the vacuum within the vacuum chamber 37 to draw tissue specimens through the inner lumen 32 of the cutter 30 into the interior 34 of the tissue collector 14 and toward the floor 34-1 of the interior 34 of the tissue specimen collector 14. The second vacuum conduit 18 has a distal end, which is in fluid communication with the vacuum chamber 37 through the vacuum opening 37-1, and has a proximal end, which is configured to be connected to a waste container 20. Alternatively, the second vacuum conduit 18 may be directly connected to a vacuum source such as vacuum pump 22. The cannula receiving opening 14-1 is spaced apart from the vacuum opening 37-1 in a first direction 29A by an intermediate portion, which is located between the distal wall portion 14-2 and the proximal wall portion 14-3. The cannula receiving opening 14-1 is spaced apart from the vacuum opening 37-1 in a second direction 29B orthogonal to the first direction 29A. An intermediate portion 14-4 is located between the distal wall portion 14-2 and the proximal wall portion 14-3. The vacuum opening 37-1 is on a first axis 18-1, and the cannula receiving opening 14-1 is on a second axis 30-1. The first axis 18-1 and the second axis 30-1 are spaced apart, and the removable tissue specimen retaining member 35 is positioned between the first axis 18-1 and the second axis 30-1. The removable tissue specimen retaining member 35 is concave in a third direction 29C from the cannula receiving opening 14-1 toward the vacuum opening 37-1.


Application of a vacuum within the tubular section 12 aids in pulling tissue into the interior thereof through the tissue receiving aperture 26 and the transfer of the severed tissue specimen through the inner lumen 32 of the tissue cutter 30 and the deployment of the specimen onto the collection tray 35 within the tissue collector 14. Preferably, the vacuum is applied under the tray 35 in vacuum chamber 37 to facilitate removal of fluid and/or debris from the one or more specimens that may be on the upper surface of tray 35.


Fluid delivery conduit 15 has a spray head 38 which discharges into the interior 34 over the tray 35 so as to spray fluid onto one or more specimens located on the tray. The low pressures in the vacuum chamber 37 under the tray 35 aspirates fluid and debris through the openings of grated portion 36 of the tray. Fluids include blood from the specimen and fluids injected or sprayed into the chamber 34 of the tissue collector 14 through the spray head 38. The size of the debris aspirated into the vacuum chamber is limited for the most part by the size of the openings in grated portion 36. Preferably, the delivery of flushing fluid to the chamber 34 is controlled to sequence after aspiration of one or more tissue specimens onto the tray 35. Saline is a suitable fluid, but other fluids may be used. A variety of agents, such as thrombolytic agents, e.g heparin, may be incorporated into the fluid to break up thrombus which may have formed on the specimen. Treatment fluids may also be employed for the subsequent examination of the one or more specimens.


The tissue penetrating distal tip 25 may have a variety of tip shapes. Particularly suitable distal tips are disclosed in the above mentioned co-pending application Ser. No. 11/014,413.


In use, the distal end of the probe component 11 is advanced within the patient with the tissue cutter 30 in a forward position to close off the tissue receiving aperture 26 of the tubular section 12 until the aperture is located in a desired location within the patient for taking a tissue specimen. The tissue cutter 30 is then withdrawn proximally to an open position to open up the aperture 26. The withdrawal of the tissue cutter 30 can be used to control the length of the aperture which is opened in order to control the length of the specimen which is drawn into the interior of the tubular section 12 and severed from supporting tissue. A vacuum is applied to the inner lumen 32 of the tissue cutter 30 through the interior 34 of the tissue collector 14 to draw tissue at the site into the inner lumen of the tubular section 12 through the aperture 26. The tissue cutter 30 is then driven distally and rotated or oscillated to sever the aspirated tissue specimen from the supporting tissue at the target site with the tissue cutting edge 31. The vacuum within the inner lumen 32 of the tissue cutter 30 aids or causes the severed tissue specimen to be drawn through the inner lumen of the tissue cutter and into the interior 34 of specimen collector 14. Positive pressure or even ambient conditions distal to the tissue specimen in the lumen 32 can help tissue specimen passage through the inner lumen to the discharge port 33 of the tissue cutter 30. If another tissue specimen is desired, the tubular section 12 may be rotated in one or more steps to move the aperture 26 to another location and repeat obtaining another tissue specimen in the same manner without otherwise moving the biopsy device 24. Typically, tissue specimens are obtained sequentially with the aperture 26 of the probe 11 in the 12, 2, 4, 6, 8, 10 o-clock positions and then in the 1 3, 5, 7, 9 and 11 o-clock positions. Other sequences for obtaining tissue specimens may be employed. The position of the aperture 26 may be indicated by a marker arrow 39 at the distal end cap 40 (FIG. 2) of proximal housing 13 so that the physician or other operating personnel can readily determine what the orientation of the aperture 26 within the patient. The biopsy system 10 may be hand held for some biopsy procedures or the system may be mounted on a stereotactic mounting stage such as a shoe that is slidably mounted to a rail of a Fischer or Lorad stage as discussed in the above mentioned application Ser. No. 11/014,413.


Fluid from a source 16 may be delivered through first conduit 15 to the interior 34 of tissue collector 14 and sprayed onto the one or more specimens on the grated portion of the tray 35. Vacuum generated in the vacuum chamber 37 under the tray 35 aspirates fluid and small dimensioned debris through the grated openings of the tray into the vacuum chamber 37. Fluid and debris are aspirated from vacuum chamber 37 through second conduit 18 into the waste container 20. Third conduit 21 maintains vacuum conditions in the interior of waste container 20 by the vacuum pump 22.


An alternative tissue specimen collector 114 is shown in detail in FIGS. 6A-6G) which is secured to the proximal end of the housing 13 of probe component 11 and has an interior 134 in fluid communication with the inner lumen 32 of the tissue cutter 30 through tissue discharge port 33. The interior 134 of the specimen collector 114 has a specimen receiving basket or tray 135, preferably removable, which is configured to receive tissue specimens from the discharge port 33 which may have been drawn therein. The tray 135 has a grated portion 136 (or foraminous or is otherwise provided with a plurality of openings) to provide fluid communication with the vacuum chamber 137 provided under the tray. A vacuum is generated within the interior 134 by the vacuum within the vacuum chamber 137 to draw tissue specimens through the inner lumen 32 of the cutter 30 into the interior 134 of the tissue collector 114. The vacuum conduit 118 has a distal end which is in fluid communication with the vacuum chamber 137 and has a proximal end which is configured to be connected to a waste container 20. Alternatively, the vacuum conduit 115 may be directly connected to a vacuum source such as vacuum pump 22 as shown in FIG. 1.


Fluid delivery conduit 115 has a spray head 138 which discharges into the interior 134 over the tray 135 so as to spray fluid onto one or more specimens located on the tray. The low pressures in the vacuum chamber 137 under the tray 135 aspirates fluid and debris through the openings of grated portion 136 of the tray. Fluids include blood from the specimen and fluids injected or sprayed into the chamber 134 of the tissue collector 114 through the spray head 138, shown in detail in FIGS. 6B and 6C. The size of the debris aspirated into the vacuum chamber is limited for the most part by the size of the openings in grated portion 136. Preferably, the delivery of flushing fluid to the chamber 134 is controlled to sequence after aspiration of one or more tissue specimens onto the tray 135.


While particular forms of the invention have been illustrated and described herein, it will be apparent that various modifications and improvements can be made to the invention. For example, while the various embodiments of the invention have been described herein in terms of a biopsy device, it should be apparent that the tissue collector may be employed to remove tissue for purposes other than for biopsy, i.e. for treatment or other diagnoses. Alternatively, the tissue cutting element may be on the exterior of the probe device and the tubular component having the tissue receiving opening in the distal end may be disposed within the tissue cutting element. In the latter alternative embodiment, the tissue specimen may be transported through the tubular component having the tissue receiving opening.


Individual features of embodiments having features of the invention may be shown in some drawings and not in others, but those skilled in the art will recognize that individual features of one embodiment can be combined with any or all the features of another embodiment. Accordingly, it is not intended that the invention be limited to the specific embodiments illustrated.


Terms such a “element”, “member”, “device”, “section”, “component”, “portion”, “means”, “step” and words of similar import, when used in the following claims, shall not be construed as invoking the provisions of 35 U.S.C. § 112(6) unless the claims expressly use the term “means” followed by a particular function without specific structure or the term “step” or “steps” followed by a particular function without specific action. All patents and patent applications referred to herein are incorporated by reference in their entirety.

Claims
  • 1. An apparatus for collecting one or more tissue specimens, comprising: a tissue specimen collector having a cannula receiving opening, a vacuum opening, and an interior, the vacuum opening being on a first axis, the cannula receiving opening being on a second axis;a removable tissue specimen retaining member positioned within the interior of the tissue specimen collector, the removable tissue specimen retaining member having a plurality of openings configured to retain the one or more tissue specimens and to pass fluid, the plurality of openings being interposed between the first axis of the vacuum opening and the second axis of the cannula receiving opening, the removable tissue specimen retaining member being movable along the second axis; andan elongated tissue cutting member having a proximal end, a distal end, and an inner lumen that extends between the proximal end and the distal end, wherein the elongated cutting member extends through the cannula receiving opening of the tissue specimen collector to position the proximal end of the elongated cutting member in the interior above the plurality of openings of the removable tissue specimen retaining member.
  • 2. The apparatus of claim 1, further comprising a spray head positioned wherein the plurality of openings of the removable tissue specimen retaining member is interposed between the spray head and the vacuum opening of the tissue specimen collector.
  • 3. The apparatus of claim 1, comprising a spray head positioned to face toward the proximal end of the elongated tissue cutting member, and the spray head being positioned to be spaced apart and above the vacuum opening of the tissue specimen collector, and with the plurality of openings of the removable tissue specimen retaining member being interposed between the spray head and the vacuum opening of the tissue specimen collector.
  • 4. The apparatus of claim 1, wherein the removable tissue specimen retaining member is disposed between the proximal end of the elongated tissue cutting member and the vacuum opening.
  • 5. The apparatus of claim 1, comprising a fluid source, a spray head, a valve, and a controller, the valve being communicatively coupled to the controller to control a fluid flow of tissue washing fluid from the fluid source to the spray head, the spray head delivering the fluid flow of tissue washing fluid to the removable tissue specimen retaining member in the interior of the tissue specimen collector.
  • 6. The apparatus of claim 5, comprising a vacuum source in fluid communication with the vacuum opening, and wherein the delivery of the tissue washing fluid is controlled to occur after a tissue specimen has been drawn by vacuum onto the removable tissue specimen retaining member.
  • 7. The apparatus of claim 1, comprising a vacuum source and a waste container interposed between the vacuum source and the vacuum opening for collecting fluid from the interior of the tissue specimen collector.
  • 8. The apparatus of claim 1, comprising: a driver unit having a gear arrangement; andan elongated probe component having a tubular section, the elongated tissue cutting member being movably disposed within the tubular section, each of the elongated probe component and the elongated tissue cutting member having a respective gear drivably coupled to the gear arrangement of the driver unit.
  • 9. An apparatus for collecting one or more tissue specimens, comprising: a driver unit having a plurality of drive gears;an elongated probe component having a tubular section and a first driven gear drivably engaged with a respective drive gear of the plurality of drive gears of the driver unit;an elongated tissue cutting member having a proximal end, a distal end, and an inner lumen that extends between the proximal end and the distal end, the elongated tissue cutting member having a second driven gear drivably engaged with a respective drive gear of the plurality of drive gears of the driver unit, the elongated tissue cutting member being movably disposed within the tubular section;a tissue specimen collector having a cannula receiving opening, a vacuum opening, and an interior, the vacuum opening being on a first axis, the cannula receiving opening being on a second axis; anda removable tissue specimen tray positioned within the interior of the tissue specimen collector, the removable tissue specimen tray having a floor with a plurality of openings configured to retain the one or more tissue specimens and to pass fluid, the floor having the plurality of openings being interposed between the first axis of the vacuum opening and the second axis of the cannula receiving opening, the removable tissue specimen tray being movable along the second axis, wherein the elongated cutting member extends through the cannula receiving opening of the tissue specimen collector to position the proximal end of the elongated cutting member in the interior above the floor of the removable tissue specimen tray that has the plurality of openings.
  • 10. The apparatus of claim 9, further comprising a spray head positioned wherein the plurality of openings of the removable tissue receiving tray is interposed between the spray head and the vacuum opening of the tissue specimen collector.
  • 11. The apparatus of claim 9, comprising a spray head positioned to face toward the proximal end of the elongated tissue cutting member, and the spray head being positioned to be spaced apart and above the vacuum opening of the tissue specimen collector, and with the plurality of openings of the removable tissue receiving tray being interposed between the spray head and the vacuum opening of the tissue specimen collector.
  • 12. The apparatus of claim 9, wherein the removable tissue specimen tray is disposed between the proximal end of the elongated tissue cutting member and the vacuum opening.
  • 13. The apparatus of claim 9, comprising a fluid source, a spray head, a valve, and a controller, the valve being communicatively coupled to the controller to control a fluid flow of tissue washing fluid from the fluid source to the spray head, the spray head delivering the fluid flow of tissue washing fluid to the removable tissue specimen tray in the interior of the tissue specimen collector.
  • 14. The apparatus of claim 13, comprising a vacuum source in fluid communication with the vacuum opening, and wherein the delivery of the tissue washing fluid is controlled to occur after a tissue specimen has been drawn by vacuum onto the floor of the removable tissue specimen tray.
  • 15. The apparatus of claim 9, comprising a vacuum source and a waste container interposed between the vacuum source and the vacuum opening for collecting fluid from the interior of the tissue specimen collector.
RELATED APPLICATIONS

This application is a continuation of application Ser. No. 14/552,611, filed Nov. 25, 2014, now U.S. Pat. No. 10,064,609, which is a continuation of application Ser. No. 13/683,890, filed Nov. 21, 2012, now U.S. Pat. No. 8,915,864, which is a continuation of application Ser. No. 11/980,298, filed Oct. 30, 2007, now U.S. Pat. No. 8,317,725, which is a divisional of application Ser. No. 11/498,504, filed Aug. 3, 2006, now U.S. Pat. No. 7,572,236, which is a continuation-in-part of application Ser. No. 11/197,827 filed Aug. 5, 2005, now abandoned, each of which is incorporated herein in its entirety by reference.

US Referenced Citations (225)
Number Name Date Kind
2032860 Wappler et al. Mar 1936 A
2192270 McGowan Mar 1940 A
3341417 Sinaiko Sep 1967 A
3805791 Seuberth et al. Apr 1974 A
3815604 O'Malley et al. Jun 1974 A
3818894 Wichterle et al. Jun 1974 A
3823212 Chvapil Jul 1974 A
3844272 Banko Oct 1974 A
3847153 Weissman Nov 1974 A
3910279 Okada et al. Oct 1975 A
3945375 Banko Mar 1976 A
3955578 Chamness et al. May 1976 A
4007732 Kvavle et al. Feb 1977 A
4074562 North, Jr. Feb 1978 A
4172449 LeRoy et al. Oct 1979 A
4197846 Bucalo Apr 1980 A
4202338 Bitrolf May 1980 A
4243048 Griffin Jan 1981 A
4250892 Dolhay et al. Feb 1981 A
4276885 Tickner et al. Jul 1981 A
4294241 Miyata Oct 1981 A
4294254 Chamness Oct 1981 A
4311143 Komiya Jan 1982 A
4331654 Morris May 1982 A
4362160 Hiltebrandt Dec 1982 A
4418692 Guay Dec 1983 A
4503855 Maslanka Mar 1985 A
4545367 Tucci Oct 1985 A
4565200 Cosman Jan 1986 A
4576162 McCorkle Mar 1986 A
4638802 Okada Jan 1987 A
4643187 Okada Feb 1987 A
4647480 Ahmed Mar 1987 A
4682606 DeCaprio Jul 1987 A
4693237 Hoffman et al. Sep 1987 A
4718419 Okada Jan 1988 A
4724836 Okada Feb 1988 A
4729764 Gaultier Mar 1988 A
4813062 Gilpatrick Mar 1989 A
4847049 Yamamoto Jul 1989 A
4863470 Carter Sep 1989 A
4909250 Smith Mar 1990 A
4926858 Gifford, III et al. May 1990 A
5007908 Rydell Apr 1991 A
5024617 Karpiel Jun 1991 A
5035696 Rydell Jul 1991 A
5041124 Kensey Aug 1991 A
5047027 Rydell Sep 1991 A
5059204 Lawson et al. Oct 1991 A
5064424 Bitrolf Nov 1991 A
5066295 Kozak et al. Nov 1991 A
5078716 Doll Jan 1992 A
5080660 Buelna Jan 1992 A
5085659 Rydell Feb 1992 A
RE33925 Bales et al. May 1992 E
5111828 Komberg et al. May 1992 A
5133359 Kedem Jul 1992 A
5133360 Spears Jul 1992 A
RE34056 Lindgren et al. Sep 1992 E
5147307 Gluck Sep 1992 A
5158561 Rydell et al. Oct 1992 A
5163938 Kambara et al. Nov 1992 A
5196007 Ellman et al. Mar 1993 A
5201732 Parins et al. Apr 1993 A
5201741 Dulebohm Apr 1993 A
5207686 Dolgin May 1993 A
5217458 Parins Jun 1993 A
5224488 Neuffer Jul 1993 A
5236410 Granov et al. Aug 1993 A
5258006 Rydell et al. Nov 1993 A
5281218 Imran Jan 1994 A
5281408 Unger Jan 1994 A
5282781 Liprie Feb 1994 A
5312400 Bales et al. May 1994 A
5318564 Eggers Jun 1994 A
5320613 Houge et al. Jun 1994 A
5323768 Saito et al. Jun 1994 A
5324288 Billings et al. Jun 1994 A
5330471 Eggers Jul 1994 A
5334381 Unger Aug 1994 A
5335671 Clement Aug 1994 A
5344381 Cabrera y Lopez Caram Sep 1994 A
5344420 Hilal et al. Sep 1994 A
5368030 Zinreich et al. Nov 1994 A
5374188 Frank et al. Dec 1994 A
5376094 Kline Dec 1994 A
5380321 Yoon Jan 1995 A
5395312 Desai Mar 1995 A
5395319 Hirsch et al. Mar 1995 A
5401272 Perkins Mar 1995 A
5415656 Tihon et al. May 1995 A
5417687 Nardella et al. May 1995 A
5417697 Wilk May 1995 A
5422730 Barlow et al. Jun 1995 A
5423809 Klicek Jun 1995 A
5423814 Zhu et al. Jun 1995 A
5431649 Muller et al. Jul 1995 A
5433204 Olson Jul 1995 A
5437665 Munro Aug 1995 A
5441498 Perkins Aug 1995 A
5441503 Considine et al. Aug 1995 A
5462553 Dolgin Oct 1995 A
5470308 Edwards et al. Nov 1995 A
5477862 Haaga Dec 1995 A
5484436 Eggers et al. Jan 1996 A
5487385 Avitall Jan 1996 A
5488958 Topel et al. Feb 1996 A
5494030 Swartz et al. Feb 1996 A
5501654 Failla et al. Mar 1996 A
5507743 Edwards et al. Apr 1996 A
5526822 Burbank et al. Jun 1996 A
5527331 Kresch et al. Jun 1996 A
5536267 Edwards et al. Jul 1996 A
5538010 Darr et al. Jul 1996 A
5542948 Weaver et al. Aug 1996 A
5549560 Van de Wijdeven Aug 1996 A
5578030 Levin Nov 1996 A
5595185 Erlich Jan 1997 A
5599347 Hart et al. Feb 1997 A
5607389 Edwards et al. Mar 1997 A
5611803 Heaven et al. Mar 1997 A
5630939 Bulard et al. May 1997 A
5636255 Ellis Jun 1997 A
5643282 Kieturakis Jul 1997 A
5646146 Faarup et al. Jul 1997 A
5649547 Ritchart et al. Jul 1997 A
5653718 Yoon Aug 1997 A
5665085 Nardella Sep 1997 A
5672174 Gough et al. Sep 1997 A
5674184 Hassler, Jr. Oct 1997 A
5676663 Kim Oct 1997 A
5676925 Klaveness et al. Oct 1997 A
5683384 Gough et al. Nov 1997 A
5687739 McPherson et al. Nov 1997 A
5688490 Tournier et al. Nov 1997 A
5715825 Crowley Feb 1998 A
5720763 Tovey Feb 1998 A
5741225 Lax et al. Apr 1998 A
5749626 Yoshida May 1998 A
5766134 Lisak et al. Jun 1998 A
5766169 Fritzsch et al. Jun 1998 A
5769086 Ritchart et al. Jun 1998 A
5772660 Young et al. Jun 1998 A
5775333 Burbank et al. Jul 1998 A
5782764 Werne Jul 1998 A
5782775 Milliman et al. Jul 1998 A
5782827 Gough et al. Jul 1998 A
5786207 Katz et al. Jul 1998 A
5794626 Kieturakis Aug 1998 A
5797907 Clement Aug 1998 A
5800378 Edwards et al. Sep 1998 A
5810806 Ritchart et al. Sep 1998 A
5814044 Hooven Sep 1998 A
5846513 Carroll et al. Dec 1998 A
5848978 Cecchi Dec 1998 A
5853366 Dowlatshahi Dec 1998 A
5857981 Bucalo et al. Jan 1999 A
5857982 Milliman et al. Jan 1999 A
5876340 Tu et al. Mar 1999 A
5882316 Chu et al. Mar 1999 A
5902272 Eggers et al. May 1999 A
5913857 Ritchart et al. Jun 1999 A
5925044 Hoffman et al. Jul 1999 A
5928164 Burbank et al. Jul 1999 A
5938587 Taylor et al. Aug 1999 A
5941893 Saadat Aug 1999 A
5947964 Eggers et al. Sep 1999 A
5954670 Baker Sep 1999 A
5964716 Gregoire et al. Oct 1999 A
5972002 Bark et al. Oct 1999 A
5980469 Burbank et al. Nov 1999 A
5984919 Hilal et al. Nov 1999 A
5997560 Miller Dec 1999 A
6004269 Crowley et al. Dec 1999 A
6036681 Hooven Mar 2000 A
6050955 Bryan et al. Apr 2000 A
6050992 Nichols Apr 2000 A
6056700 Burney et al. May 2000 A
6059782 Novak et al. May 2000 A
6063082 DeVore et al. May 2000 A
6071280 Edwards et al. Jun 2000 A
6120462 Hibner et al. Sep 2000 A
6142955 Farascioni et al. Nov 2000 A
6161034 Burbank et al. Dec 2000 A
6203524 Burney et al. Mar 2001 B1
6220248 Voegele et al. Apr 2001 B1
6234177 Barsch May 2001 B1
6254601 Burbank et al. Jul 2001 B1
6261241 Burbank et al. Jul 2001 B1
6277083 Eggers et al. Aug 2001 B1
6312429 Burbank et al. Nov 2001 B1
6331166 Burbank et al. Dec 2001 B1
6344026 Burbank et al. Feb 2002 B1
6350244 Fisher Feb 2002 B1
6454727 Burbank et al. Sep 2002 B1
6485436 Truckai et al. Nov 2002 B1
6494881 Bales et al. Dec 2002 B1
6514215 Ouchi Feb 2003 B1
6514248 Eggers et al. Feb 2003 B1
6540695 Burbank et al. Apr 2003 B1
6679851 Burbank et al. Jan 2004 B2
6689145 Lee et al. Feb 2004 B2
6712775 Burbank et al. Mar 2004 B2
6758824 Miller et al. Jul 2004 B1
7189206 Quick et al. Mar 2007 B2
7226424 Ritchart et al. Jun 2007 B2
7572236 Quick et al. Aug 2009 B2
7621917 Geneve et al. Nov 2009 B2
7981051 Quick et al. Jul 2011 B2
8088079 Kaye et al. Jan 2012 B2
8109886 Miller et al. Feb 2012 B2
20010001811 Burney et al. May 2001 A1
20010002250 Burbank et al. May 2001 A1
20020016555 Ritchart et al. Feb 2002 A1
20020193705 Burbank et al. Dec 2002 A1
20030004407 Carroll et al. Jan 2003 A1
20030069543 Carpenter et al. Apr 2003 A1
20030125639 Fisher et al. Jul 2003 A1
20030130594 Hynes et al. Jul 2003 A1
20030199787 Schwindt Oct 2003 A1
20040019299 Ritchart et al. Jan 2004 A1
20040191897 Muschler Sep 2004 A1
20050065453 Shabaz et al. Mar 2005 A1
20080243030 Seibel et al. Oct 2008 A1
20110245715 Quick et al. Oct 2011 A1
Foreign Referenced Citations (36)
Number Date Country
19528440 Feb 1997 DE
0146699 Jul 1985 EP
0255123 Feb 1988 EP
0292936 Nov 1988 EP
0472368 Feb 1992 EP
0481685 Apr 1992 EP
0509670 Oct 1992 EP
0601709 Jun 1994 EP
0667126 Aug 1995 EP
0769281 Oct 1995 EP
0858774 Jan 1997 EP
0966925 Jun 1998 EP
0970658 Jun 1998 EP
1698283 Mar 2006 EP
2311468 Feb 1997 GB
9313718 Jul 1993 WO
9314712 Aug 1993 WO
9502370 Jan 1995 WO
9502371 Jan 1995 WO
9608208 Mar 1996 WO
9806346 Feb 1998 WO
9808441 Mar 1998 WO
9930764 Jun 1999 WO
9944506 Sep 1999 WO
0012009 Mar 2000 WO
0016697 Mar 2000 WO
0030531 Jun 2000 WO
0205717 Jan 2002 WO
0222023 Mar 2002 WO
02062228 Aug 2002 WO
02062232 Aug 2002 WO
2004043531 May 2004 WO
2004052212 Jun 2004 WO
2004075719 Sep 2004 WO
2005063126 Jul 2005 WO
2006049911 May 2006 WO
Non-Patent Literature Citations (7)
Entry
Armstrong, J.S. et al., “Differential marking of excision planes in screened breast lesions by organically coloured gelantins”, Journal of Clinical Pathology, (Jul. 1990), 43(7) 604-7, XP000971447 abstract; tables 1 and 2.
Burbank, F., M.D., Stereotactic Breast Biopsy: Its History, Its Present, and Its Future, The American Surgeon, Feb. 1996, vol. 62, pp. 128-150.
Fucci, V. et al., “Large Bowel Transit Times Using Radiopaque Markers in Normal Cats”, J. of Am. Animal Hospital Assn., Nov.-Dec. 1995 vol. 31 (6) 473-477.
Lorenzen,T. et al., The Loop Electrode: a New Device for US-guided Interstitial Tissue Ablation Using Radio frequency Electrosurgery—An Animal Study, 1996 Blackwell Science Ltd. Min Incas Ther & Allied Technol, pp. 6.511-516.
Micklos, Timothy J., Percutaneous Biopsy Techniques, Manual of Oncologic Therapeutics (1989/1990) pp. 39-42.
Schindlebeck, N.E., et al., “Measurement of Colon Transit Time”, J. of Gastroenterology, No. 28, pp. 399-404, 1990.
Whitman, et al., Coaxial Core Needle Biopsy Under Mammographic Guidance: Indications and Applications, AJR:171, Jul. 1998, pp. 67-70.
Related Publications (1)
Number Date Country
20190046167 A1 Feb 2019 US
Divisions (1)
Number Date Country
Parent 11498504 Aug 2006 US
Child 11980298 US
Continuations (3)
Number Date Country
Parent 14552611 Nov 2014 US
Child 16110472 US
Parent 13683890 Nov 2012 US
Child 14552611 US
Parent 11980298 Oct 2007 US
Child 13683890 US
Continuation in Parts (1)
Number Date Country
Parent 11197827 Aug 2005 US
Child 11498504 US