1. Field of the Invention
The present invention relates to ablation device placement during targeted ablation and more particularly to a spacer for establishing the spacing between ablation devices during such ablation procedures.
2. Description of the Related Art
Cryosurgical probes are used to destroy living tissue by thermally manipulating a cryoprobe to extreme temperatures by using freezing and heating cycles. Similarly, other ablative devices such as RF probes are used to ablate the tissue. Currently cryosurgical probes are incorporated into computer guided cryosurgery systems wherein the systems calculate the optimal placement for the cryoprobes into diseased tissue. Entry position grids are typically utilized for aiding the user in locating the approximate entry point of cryoprobe into the patient during a cryosurgical procedure. U.S. Pat. No. 6,036,632, issued to W. F. Whitmore III, for example, discloses an example of a sterile disposable template grid system for positioning and implanting medical implants.
However, there are certain deficiencies with respect to the use of such entry position grids. These grids define fixed patterns for probe placement and therefore restrict the user to a limited number of insertion distances. As a result, anatomy is not accounted for such as adjacent organs, blood vessels and bone.
There is a need to provide greater flexibility in spacing ablation devices so as to be commensurate with recent improvements in computer guided cryosurgery systems.
In one broad aspect, the present invention is an ablation device placement spacer for use with a patient undergoing a targeted ablation procedure utilizing elongated ablation devices insertable into treatment zones of the patient. The ablation device placement spacer includes an elongated spacing member and at least one ablation device engaging element positioned on the elongated spacing member. During use, an ablation device is releasably engageable with the ablation device engaging element, a spacing portion of the elongated spacing member being spaced from the ablation device engaging element at a desired distance so as to provide the user with an indication of a desired spacing for a subsequent ablation device to be inserted into its respect treatment zone.
Preferably, the elongated spacing member includes a plurality of spaced openings formed along a side edge thereof. The openings function as the ablation device engaging elements.
As opposed to placing additional probes only based on visual guidance (using CT, MRI, ultrasound or other visual imaging means) the present invention provides enhanced placement distances to optimize the treatment.
Fixed grids provide preset orientation and distance parameters between ablation devices. The present invention, on the other hand, is not orientation dependent while still providing optimal distance parameters. Use of the present invention with its engaging element minimizes handling requirements during the placement of additional ablation devices.
Referring now to the drawings and the characters of reference marked thereon,
Each recess 14 is preferably formed of relatively large arcuate surfaces 18 for accommodating a relatively large diameter ablation device and progressively smaller arcuate surfaces 20, 22 formed in the relatively large arcuate surfaces 18 for accommodating progressively smaller diameter ablation devices. Surfaces 18, 20, 22 are arcuate so as to provide a complementary fit with an outer surface of an ablation device, which typically has a circular cross-section. They may be sufficiently closed to provide a snap fit with an ablation device. Or, the releasable engagement may be very loose, i.e. merely an abutting engagement.
The elongated spacing member 12 preferably includes measuring indicia 24 for indicating the distance from an ablation device to a subsequent ablation device to be inserted. The elongated spacing member 12 is preferably formed of a rigid plastic; however, it may be formed of other suitable materials such as metal, etc.
Referring now to
The placement spacer 10 is particularly adapted for use with ablation devices such as cryosurgical probes or RF probes. Additionally, the ablation device may include components such as temperature sensors that may use the present placement spacer. Present assignee, Endocare, Inc. of Irvine, Calif. manufactures and markets a cryosurgical system under the trademark CryoCare® including its newly enhanced automated feedback, marketed under the trademark AutoFreeze™. The CryoCare® surgical system® provides a treatment guidance plan for placing the ablative devices. Guidance as to recommended ablative element placement within a prostate is provided based on images of the prostate acquired from an imaging system, such as an ultrasound system.
The openings 18, 20, 22 provided allow for differing ablative device diameters. For example, for typical cryosurgical probes, openings may be 1.5 mm, 2.4 mm and 3.4 mm in diameter.
The present ablative element placement spacer 10 is useful in various types of surgeries, including open surgery, endoscopic surgery and percutaneous surgery.
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Other embodiments and configurations may be devised without departing from the spirit of the invention and the scope of the appended claims.
Number | Name | Date | Kind |
---|---|---|---|
5868673 | Vesely | Feb 1999 | A |
5961527 | Whitmore | Oct 1999 | A |
6010446 | Grimm | Jan 2000 | A |
6036632 | Whitmore | Mar 2000 | A |
6206832 | Downey | Mar 2001 | B1 |
6554759 | Fontayne | Apr 2003 | B2 |
6572525 | Yoshizumi | Jun 2003 | B1 |
Number | Date | Country | |
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20050059961 A1 | Mar 2005 | US |