The invention relates generally to a surgical instrument and a surgical method performed with the instrument. In particular, the invention is a device for acquiring tissue samples for cytology analyses and surgical procedures for using the tools to collect cytological samples.
Devices and methods for collecting tissue samples from a patient for cytological analysis in a laboratory are generally known. During a cytological sample acquisition procedure a sample collection device is typically delivered to a sample site within a body lumen through the use of an endoscope and/or catheter. Following the collection of the tissue sample the device is withdrawn. By way of example, the Sahatjian U.S. Pat. No. 5,409,012 and the Parasher U.S. Pat. No. 5,535,756 disclose instruments and surgical procedures for collecting cytological samples. There remains, however, a continuing need for enhanced cytological acquisition and sampling technologies.
One embodiment of the invention is a tissue collection device that includes a body, first and second diametrically expandable members at spaced-apart locations on the body, one or more actuating structures, and one or more collection structures on the body. The actuating structures cause the expandable members to move between expanded and collapsed states. The collection structures collect a tissue sample from a collection region between the first and second expandable members.
In another embodiment the expandable members include balloons, and the actuating structures include inflation lumens. The body is an elongated member and the balloons are fixedly mounted to the elongated member. The collection structures include one or more of an irrigation lumen and an aspiration lumen having one or more ports opening into the collection region.
Another embodiment of the invention is a method for acquiring a cytological sample using the tissue collection device. The method includes delivering the collection device to a sample site through a body lumen, expanding the first and second expandable members, and collecting a tissue sample from the collection site between the first and second expandable members. The expandable members can be collapsed, and the collection device withdrawn.
A cytological sample collection device 10 in accordance with one embodiment of the present invention is illustrated generally in
A cytological tissue acquisition procedure in accordance with one embodiment of the invention can be described with reference to
After the balloons 14 are expanded, saline or other collection fluid is delivered from a source (not shown) to the sample site through the irrigation lumen 20 and irrigation ports 22. The collection fluid can, for example, be delivered under high pressure. Alternatively or in addition, exfoliating agents or other substances that enhance cell release and collection can be delivered through the irrigation ports 22. The volume of the collection zone between the balloons 14 can be completely or partially filled with the collection fluid in this manner. After delivery to the sample site, the collection fluid (and tissue sample that has been suspended in the collection fluid) is aspirated through the suction ports 26 and aspiration lumen 24. In one embodiment of the invention 100-200 ml of collection fluid is retrieved, although more or less fluid can be used in other embodiments. In the illustrated embodiment having a separate irrigation lumen 20 and aspiration lumen 24, the collection fluid can be infused and aspirated separately or simultaneously. In other embodiments (not shown) having a common aspiration and collection lumen, the collection fluid is aspirated after being infused. In still other embodiments of the invention other tools or devices are delivered to the sample site through an accessory lumen in the collection device 10. For example, a brush or an abrasive or scraping tool can be inserted through the accessory lumen and used to enhance the removal of tissue from the sample site.
Following the sample collection and the removal of any tools inserted through the collection device 10, the balloons 14 can be collapsed and the collection device returned to the delivery state and withdrawn from the body lumen 12. The collection fluid will be processed and the samples analyzed in known or otherwise conventional manners (e.g., the fluid is centrifuged and the cell pellet analyzed).
During a cytological sample acquisition procedure the proximal component 116 is delivered to the sample site with the balloon 126 collapsed. The proximal component balloon 126 is then inflated by the introduction of fluid through the inflation lumen 128. The diametrically expanded balloon 126 thereby creates a seal that will prevent retrograde fluid flow through the body lumen 112. After placement of the proximal component 116, the distal component 114, in the delivery state, is inserted through the proximal component and the balloon 118 advanced to a position beyond balloon 116 of the proximal component. Balloon 118 of the distal component is then inflated by the introduction of fluid through inflation lumen 122.
After the collection device 110 is positioned at the sample site, it can be operated one of several different manners to collect a tissue sample. For example, collection fluid can be introduced and withdrawn through the irrigation/aspiration lumen 130 in the manner described above in connection with collection device 10. Alternatively, by manipulating the member 120, balloon 118 can be moved in a rotational or reciprocal manner to mechanically disrupt cells before the collection fluid is introduced and withdrawn to collect the sample. This mechanical disruption of the tissue at the sample site can be enhanced by the abrasive edge 123 on the balloon 118. In another alternative approach, the balloon 118 is deflated and the distal component 114 removed from the sample site before suction is applied to the irrigation/aspiration lumen 130 to remove the tissue sample. In another approach the balloon 118 in the distal component 114 can be filled with cell preservative solution (e.g., through the inflation lumen 122) and overfilled to burst and release the preservative. The preservative dispensing approach can but need not be done before the mechanical disruption but will typically be done before aspiration of the tissue sample. Following the collection of the tissue sample the components 114 and/or 116 can be returned to their delivery state and withdrawn from the sample site. The method described above can, for example, be used for indications in the bile duct, pancreatic duct, pancreatic cysts, gall bladder, urethra and uterine system.
Alternative versions of collection device 110 can include one or more other features described in connection with collection device 10. For example, collection device 110 can include separate irrigation and aspiration lumens and/or a guide wire lumen and/or one or more accessory lumens. Collection device 110 can also be delivered using any of the approaches described above in connection with collection device 10 (e.g., through an endoscope and/or over a guide wire). Although the embodiments of collection devices 10 and 110 described above have balloons, other diametrically expandable structures and associated expansion members can be used. For example, other embodiments (not shown) have a diametrically expandable umbrella-like structure and a mechanical expansion member.
In one embodiment of the invention, tool 200 is used in connection with the collection devices 10 and 110 described above. In particular, with the disruption member 204 retained in a retracted position within the sheath 202, the tool 200 is inserted through an accessory lumen in the collection device and advanced through the accessory lumen to position the distal end of the tool at the sample site. By manipulating the actuating member with respect to the delivery sheath 202 the disruption member 204 is extended from the tool 200. The delivery sheath 202 and/or the actuating member 206 can then be actuated (e.g., moved in a rotating or reciprocal manner) while the disruption member 204 is in contact with tissues at the sample site. By this motion the disruption member 204 enhances the mechanical release of cells from the sample site. Following the use of the tool 200 in this manner, the disruption member 204 can be retracted into the sheath 202 and the tool removed from the collection device and body lumen. In alternative embodiments (not shown) a motor is coupled to the disruption member 206 (e.g., through the actuating member 206) to rotate the disruption member during the sample acquisition process. In still other embodiments of the invention, tool 200 can be used with other tissue removal methods and/or with other devices. For example, the tool 200 can be delivered to a sample site through an endoscope or over a guide wire, and cells released by the abrasion process collected within the sheath 202 when the disruption member 204 is retracted into the sheath.
Although the present invention has been described with reference to preferred embodiments, those skilled in the art will recognize that changes can be made in form and detail without departing from the spirit and scope of the invention.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2012/022504 | 1/25/2012 | WO | 00 | 8/15/2013 |
Number | Date | Country | |
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61436837 | Jan 2011 | US |