CA1273068A - Self-actuating breast lesion probe and method - Google Patents
Self-actuating breast lesion probe and methodInfo
- Publication number
- CA1273068A CA1273068A CA000504390A CA504390A CA1273068A CA 1273068 A CA1273068 A CA 1273068A CA 000504390 A CA000504390 A CA 000504390A CA 504390 A CA504390 A CA 504390A CA 1273068 A CA1273068 A CA 1273068A
- Authority
- CA
- Canada
- Prior art keywords
- wire
- probe
- lesion
- cannula
- probe wire
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B10/00—Other methods or instruments for diagnosis, e.g. instruments for taking a cell sample, for biopsy, for vaccination diagnosis; Sex determination; Ovulation-period determination; Throat striking implements
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/39—Markers, e.g. radio-opaque or breast lesions markers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/34—Trocars; Puncturing needles
- A61B17/3403—Needle locating or guiding means
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00867—Material properties shape memory effect
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/06—Measuring instruments not otherwise provided for
- A61B2090/062—Measuring instruments not otherwise provided for penetration depth
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/39—Markers, e.g. radio-opaque or breast lesions markers
- A61B2090/3904—Markers, e.g. radio-opaque or breast lesions markers specially adapted for marking specified tissue
- A61B2090/3908—Soft tissue, e.g. breast tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2210/00—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2210/0014—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof using shape memory or superelastic materials, e.g. nitinol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2210/00—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2210/0014—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof using shape memory or superelastic materials, e.g. nitinol
- A61F2210/0019—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof using shape memory or superelastic materials, e.g. nitinol operated at only one temperature whilst inside or touching the human body, e.g. constrained in a non-operative shape during surgery, another temperature only occurring before the operation
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Molecular Biology (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Public Health (AREA)
- Medical Informatics (AREA)
- Pathology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Surgical Instruments (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
The present invention relates to lesion location within the body and is especially adapted to detection and location of a presymptomatic, non-palpable lesion within the female breast.
The present invention relates to lesion location within the body and is especially adapted to detection and location of a presymptomatic, non-palpable lesion within the female breast.
Description
~'7;~
-2--T~ C~L FI~LD
~ e prese1lt invention relates to ]esion 10cati.on within the hx1y and is especially adapted to cletection and location of a presymptomatic, non-pa~pable lesion wlthin the fenale breast.
L~ACI~GRoU~D OE` TE~ INVENTI~N
It is kncwn to rely on mar~ncgraphy in conjunction with a nee~le cannu]a llaving a probe wire therein for localization of a presymptomatic, non-palpable breast lesion. In such procedure, a needle cannula having a wire ~sheathe~
therein is inserted so that the distal end of the needle is located at ahout thetissue area of pathological alteration; desirably at J.ess than 2 crn frc~n the lesion. A mammogram is then talcen to confirm the probe position. If the probedoes not accurately relate to the lesion, then the probe is relocateA, or an additional probe may be inserted, and a further marnmogram is ta]cen. When the probe location is acceptable, then the cannula needle is removed and the patienttransferred to surgery for lesion excision.
Obviously, removal of -t~e lesion with minunal tissue datnage will relate to maintenance of the wire's distal end as detennined by the fi.nal mammographic examination.
In the instance of a straight wire probe, as for instace the ~ueno Probe manufactured by Micro-Machining of Claremont, New Tlampshire, taping-dc~n or otherwise fixing an extending portion of the wire does not prevent movement oF
the wire's distal end upon breast movement and expansion after the initial probeprocedure.
It is knc~n to use a probe wire having a bend at its Aista]. end whereby when the cannula neecl].e is r~movecd, the bend or hook portion anchors in the tissue. Such knc~n bent or hooked probe wires are for instance the Frank Breast Biopsy Probe manufactured by Ranclall-Faichney of Avon, Massachusetts, and the Kopans Probe manufactured by Cook, Inc. of Bloomington, Incliana. These kncxh~, hookecl type localization probes have a clisac3vantage in that once the wire is anchored it can only be rernoved by resection. Thus, the Kopans Probe w~uldhave to be marnmographically final].y positionecl while its wire element is comple-tely sheathed in the cannula needle. If, after cannula removal, the resultant hook ].ocation is unsatisfactory, then another probe means must be in3erted.
Elence, the knc~n bent or hookecl probe wlres have in e~fect a one-time anc11orincJ use. Further, if more than one wire is reliecl on, then eacll anchored ,~r"~
, ~'
~ e prese1lt invention relates to ]esion 10cati.on within the hx1y and is especially adapted to cletection and location of a presymptomatic, non-pa~pable lesion wlthin the fenale breast.
L~ACI~GRoU~D OE` TE~ INVENTI~N
It is kncwn to rely on mar~ncgraphy in conjunction with a nee~le cannu]a llaving a probe wire therein for localization of a presymptomatic, non-palpable breast lesion. In such procedure, a needle cannula having a wire ~sheathe~
therein is inserted so that the distal end of the needle is located at ahout thetissue area of pathological alteration; desirably at J.ess than 2 crn frc~n the lesion. A mammogram is then talcen to confirm the probe position. If the probedoes not accurately relate to the lesion, then the probe is relocateA, or an additional probe may be inserted, and a further marnmogram is ta]cen. When the probe location is acceptable, then the cannula needle is removed and the patienttransferred to surgery for lesion excision.
Obviously, removal of -t~e lesion with minunal tissue datnage will relate to maintenance of the wire's distal end as detennined by the fi.nal mammographic examination.
In the instance of a straight wire probe, as for instace the ~ueno Probe manufactured by Micro-Machining of Claremont, New Tlampshire, taping-dc~n or otherwise fixing an extending portion of the wire does not prevent movement oF
the wire's distal end upon breast movement and expansion after the initial probeprocedure.
It is knc~n to use a probe wire having a bend at its Aista]. end whereby when the cannula neecl].e is r~movecd, the bend or hook portion anchors in the tissue. Such knc~n bent or hooked probe wires are for instance the Frank Breast Biopsy Probe manufactured by Ranclall-Faichney of Avon, Massachusetts, and the Kopans Probe manufactured by Cook, Inc. of Bloomington, Incliana. These kncxh~, hookecl type localization probes have a clisac3vantage in that once the wire is anchored it can only be rernoved by resection. Thus, the Kopans Probe w~uldhave to be marnmographically final].y positionecl while its wire element is comple-tely sheathed in the cannula needle. If, after cannula removal, the resultant hook ].ocation is unsatisfactory, then another probe means must be in3erted.
Elence, the knc~n bent or hookecl probe wlres have in e~fect a one-time anc11orincJ use. Further, if more than one wire is reliecl on, then eacll anchored ,~r"~
, ~'
3;.
... .
~3~
wirt~ IS~ b~' s~rgically r~novr~<l w;th coll~eq~ient r?x-:ision.o.E t.isslle in adclitir.~n to that of ~le lesion.
SU~ ~ OF THE INVE~IO~
The present invention is especially dj.rectr~d to improved mealls and met~orl for confirJning location of a pres~np-tcrnatic, non-palpable breast lesion byplac~nent and manip~llati.on of a probe comprised of a cannu]a needle and pro~e wire there~ith.
It is an object of the present invention that the probe wire be of novel construction.
It is a further object of the invention that the novel probe wire cc~nprise inherent anchoring means that inhibit accidenta]. dislodgement of the wire upon ordinary and conventional movement of thr bcdy containing the lesi.on.
It is another object of the invention that the anchoring means cc~mprise a yieldable memory device that is manually retractable from an anchored location to a sheathed location within the cannula; as for re].ocation with respect to the lesion.
It is a further object of the invention that the novel probe wire bear graduated scale markings at its distc~l and proximal end portions.
It is yet ~nother object of the invention that a positive loc.k means be provided at the proxirnal end of the probe wire.
It i9 an object of thr-3 invention that the novel and improvred cannula neerlle and wire probe therewith be an uncomplicated combination of s:imple structural elements, inexI~ensive and easy to rnanufacture and simple to rnanipulate in lesion localization.
For a m.ore fully developr~ presentation of the invention, and a preferrecl ~mbodimen-t -thereof, reference is made to the follc~ing descriptive matter and attached drawings.
BRIEF DESCRIPTION OF T~E DRAh~NGS
FIG. 1 is ca view of the probe wire of the invention assembled with a longitudinal section of the carmula and, for c].arity of display, in an exaggerated dimr.?nsional rel.ati.onship.
FIG. 2 is a view of the self-a.ctuating hook or memory portion of the prohe wire pushed through the cannula as at an ancllored location;
FIG. 3 is a view of a preferred embodiment of the prob~3 wire shc~w;.ng graduated scale rnarkings thereon; and FIG. 4 is an explod~d view of a probe wire clamp m~nber.
'~
4_ D~TAlLED DESCR~PTI~ OF T~ LNTIO~I
Referrinc3 to ~he drawings w~lich shc~ a preferred ~nb~liment o~ the inven~ion ~u~d wherein like n~mlerals indicate like eleMents of structure, thereis shc~n in ~IG. 1 a conventional probe cannula 10 and an improv~l prohe wire 12in assenbled relationship preparatory to insertion of the unit into the bcdy tissue for lesion location. For purposes of clarity, the dimensional relationship of the cannula and probe wire are exaggerated. In actuality, the wire has a close but easily slidable fit; the wire beiny for instanceappro~imately 0.015 inches in diameter and the cannu a be~ng of 20 gauge.
Preferably, the wire is coated, as witll a silicone or ~a~r, for purposes of lubricity and electrical insuJation.
As shc~n in FIG. 1, the probe wire lies straight in its cannula sheathing and as so assembled, the unit is inserted into the body;tissue to a location whereat the distal end lies hopefully at about 2 cm fran the lesion as previously detennined by mamnography. The latter is repeated to confinn the accuracy of the probe location. If the desired accuracy is not confirmed, then the probe unit is repositioned and the steps repeated until the desirec confirmation is attained.
Follc~ing such confir~ation, the wire probe end is pushed forward of its sheathed position as illustrated in FIG. 2. Note that the freed wire end 14 hasassumed the shape of a relatively small curl or hook whereby the probe wire anchors itself in the tissue at the lesion site.
The probe wire is preferably manufactured of a material having the memory characteristic of such relatively small curl or hco}; at its fre~l distal end.
Materials broadly possessing such a memory characteristic an~ suitable for the inventive purpose are knc~n; as for instance Ni-tinol, a NiTi alloy producedby Raychem Corp. of Menlo Park, California. Such titaniun or ti-taniurn allo~materials have adclitional characteristics of being suf~iciently rigid whereby to inllibit dislodyement upon subsequent normal and ordinary rnovemen-t and handling o~ t~.e kxxly portion in which the lesion is loeated; are difficult to cut; an~
will not easily break whereas aceiclen-tal rupture of the probe wire, as is knc~n to occur wlth prior c~rt wires, ~ould severely complicate -the procedure of lesion excision with minimal darnage to the containing tissue. The probe wire eoulcl also be formed of a bimetal material that is normally straight but is responsiveto Lxxly heat for actuation to the hook Eormation.
T~lo~ Is c~ t~'RGte- --~AC~fi2
... .
~3~
wirt~ IS~ b~' s~rgically r~novr~<l w;th coll~eq~ient r?x-:ision.o.E t.isslle in adclitir.~n to that of ~le lesion.
SU~ ~ OF THE INVE~IO~
The present invention is especially dj.rectr~d to improved mealls and met~orl for confirJning location of a pres~np-tcrnatic, non-palpable breast lesion byplac~nent and manip~llati.on of a probe comprised of a cannu]a needle and pro~e wire there~ith.
It is an object of the present invention that the probe wire be of novel construction.
It is a further object of the invention that the novel probe wire cc~nprise inherent anchoring means that inhibit accidenta]. dislodgement of the wire upon ordinary and conventional movement of thr bcdy containing the lesi.on.
It is another object of the invention that the anchoring means cc~mprise a yieldable memory device that is manually retractable from an anchored location to a sheathed location within the cannula; as for re].ocation with respect to the lesion.
It is a further object of the invention that the novel probe wire bear graduated scale markings at its distc~l and proximal end portions.
It is yet ~nother object of the invention that a positive loc.k means be provided at the proxirnal end of the probe wire.
It i9 an object of thr-3 invention that the novel and improvred cannula neerlle and wire probe therewith be an uncomplicated combination of s:imple structural elements, inexI~ensive and easy to rnanufacture and simple to rnanipulate in lesion localization.
For a m.ore fully developr~ presentation of the invention, and a preferrecl ~mbodimen-t -thereof, reference is made to the follc~ing descriptive matter and attached drawings.
BRIEF DESCRIPTION OF T~E DRAh~NGS
FIG. 1 is ca view of the probe wire of the invention assembled with a longitudinal section of the carmula and, for c].arity of display, in an exaggerated dimr.?nsional rel.ati.onship.
FIG. 2 is a view of the self-a.ctuating hook or memory portion of the prohe wire pushed through the cannula as at an ancllored location;
FIG. 3 is a view of a preferred embodiment of the prob~3 wire shc~w;.ng graduated scale rnarkings thereon; and FIG. 4 is an explod~d view of a probe wire clamp m~nber.
'~
4_ D~TAlLED DESCR~PTI~ OF T~ LNTIO~I
Referrinc3 to ~he drawings w~lich shc~ a preferred ~nb~liment o~ the inven~ion ~u~d wherein like n~mlerals indicate like eleMents of structure, thereis shc~n in ~IG. 1 a conventional probe cannula 10 and an improv~l prohe wire 12in assenbled relationship preparatory to insertion of the unit into the bcdy tissue for lesion location. For purposes of clarity, the dimensional relationship of the cannula and probe wire are exaggerated. In actuality, the wire has a close but easily slidable fit; the wire beiny for instanceappro~imately 0.015 inches in diameter and the cannu a be~ng of 20 gauge.
Preferably, the wire is coated, as witll a silicone or ~a~r, for purposes of lubricity and electrical insuJation.
As shc~n in FIG. 1, the probe wire lies straight in its cannula sheathing and as so assembled, the unit is inserted into the body;tissue to a location whereat the distal end lies hopefully at about 2 cm fran the lesion as previously detennined by mamnography. The latter is repeated to confinn the accuracy of the probe location. If the desired accuracy is not confirmed, then the probe unit is repositioned and the steps repeated until the desirec confirmation is attained.
Follc~ing such confir~ation, the wire probe end is pushed forward of its sheathed position as illustrated in FIG. 2. Note that the freed wire end 14 hasassumed the shape of a relatively small curl or hook whereby the probe wire anchors itself in the tissue at the lesion site.
The probe wire is preferably manufactured of a material having the memory characteristic of such relatively small curl or hco}; at its fre~l distal end.
Materials broadly possessing such a memory characteristic an~ suitable for the inventive purpose are knc~n; as for instance Ni-tinol, a NiTi alloy producedby Raychem Corp. of Menlo Park, California. Such titaniun or ti-taniurn allo~materials have adclitional characteristics of being suf~iciently rigid whereby to inllibit dislodyement upon subsequent normal and ordinary rnovemen-t and handling o~ t~.e kxxly portion in which the lesion is loeated; are difficult to cut; an~
will not easily break whereas aceiclen-tal rupture of the probe wire, as is knc~n to occur wlth prior c~rt wires, ~ould severely complicate -the procedure of lesion excision with minimal darnage to the containing tissue. The probe wire eoulcl also be formed of a bimetal material that is normally straight but is responsiveto Lxxly heat for actuation to the hook Eormation.
T~lo~ Is c~ t~'RGte- --~AC~fi2
4 ;1~, ~L~73~168 In continuation of the localiz.~tiol~ pr-x-e(1~1re, s mal~lK~r;l~hi.c clete~ni~ tion is made to confirsn accuracy of the ancl)ored distal end of the prohe ~1i.re to less an 2 cm fr~m tl~e lesion site.
Ass~ning U~at such accuracy is not confi~ned, a relocation of the prohe wire is desirable in order to effect an optim-~ surgical result. Obviously, with prior art one-t~ne anchoring usage, such relocation is impossible; either the surgeoll proceeds with the less than optimally desirable locater guicJe or anew round of pro~e unit insertion/mclmmo~raphic confirmation is initiated.
~ lowever, in the instant case such relocation is possible. The aforedescribed probe wire which is strong enough to prevent accidental dislodgemellt and breaking, and is tough to cut also has an addi.tional and critical chc~-acteristic of being flexibly soft and responsive to manual urging whereby the anchorecl distal end will release and easily slide frcm its grasp oftissue and retract into its fully sheathe~ location within the cannula without further tissue clamage.
It is precisely such latter characteristic that most significantly distinguishes the instant probe wire frc~m the prior art. In this connection, it is of interest that the U.S. Patents to Finney--4,307,723 and Tafeen--3,539,034 each disclose a catheter whose dista]. end ~ossesses a memory harac-teristic, that Woo--3,943,932 discloses an acupuncture needle that may possess a memory characteristic and that Hawkins--4,230,123 discloses what is descri~ as a J-wire which is inserted through a cannula for fixing the clistal end of said cannula.
Having finally located the probe wire with confirmed accuracy, -the cannula is removed. As is ~Icwn in the art, one may then tape clc~n the proximal portion of the probe wire that extends from the body to thereby Eur-ther inhibit wire displacernent upon subse~uent kcxly handling and transportion. ~Ic~ever, it is preferred that a more positi.ve means b~ relied on to both fur-ther inhibit wiredisplacement and to prevent tissue Eram rising over a section of such extenclingproximal wire that due to prior mani.pulatiorl may have become non-sterile.
Such a more positive means may cc~nprise a biased clip typ~ member but a preferred clc~mp means is illustrated in F'IG. 4 where.in member 16 has an aperture 18 axially therethrough and a threadecl aperture 20 extending normal to aperture18 and intersecting same. A threadecl clamp-screw 22 operatively associates with aperture 20. The cross-sectional configuration of said clclmp means is broadly no-t material excel~t that, to facilitate hanclling, the peripheral surface may be $ .' ~ 73~)6~
ri~b~d or ~lurled or, as shc~n, mcly be provid~l witll flange porti.ons 30. lnuse, the clamp means is positialed with the proximal portion aE the fina]].y anchored probe wire ext~nding t}~ough the axially dis~osed apertur2, the end face 24 of the clamp is brought to bear on the bcKly surface, whereby to preventbody tissue from rising over any of such proximal portion extencling frcsm the body, and the screw tightened -to thereby fix the parts.
Graduations 26 are provided on the proximal extent of the probe wire.
These mar~ings indicate both the depth of the probe wire's distal end when anchored and the depth of ~le probe uni-t's distal end when the wire is properlysheathed in the ca~mula.
Graduations 28 on the extended distal portion of _he probe wire are an indication to the surgeon as to relation of incision to the distal end of the wire. SUC]1 graduations 28 may extend further along the distal end than is illustrated in FIG. 3.
Graduations 11 on the cannula are provided whereby to indicate the depth of cannula penetration into the bcdy.
Such graduations may be etchings ancd may be colcsr coded.
The e~bodiments shown and described are only illustrative of the present invention and are not to be construed as being delimitive thereo:E; since once apprised of the invention, changes in structure w~uld be readily apparent to oneskill~d in the art. E-lence, the present invention includes all.rrodifications of structure encanpassed within the spirit and scope of the following claims.
~ ~,
Ass~ning U~at such accuracy is not confi~ned, a relocation of the prohe wire is desirable in order to effect an optim-~ surgical result. Obviously, with prior art one-t~ne anchoring usage, such relocation is impossible; either the surgeoll proceeds with the less than optimally desirable locater guicJe or anew round of pro~e unit insertion/mclmmo~raphic confirmation is initiated.
~ lowever, in the instant case such relocation is possible. The aforedescribed probe wire which is strong enough to prevent accidental dislodgemellt and breaking, and is tough to cut also has an addi.tional and critical chc~-acteristic of being flexibly soft and responsive to manual urging whereby the anchorecl distal end will release and easily slide frcm its grasp oftissue and retract into its fully sheathe~ location within the cannula without further tissue clamage.
It is precisely such latter characteristic that most significantly distinguishes the instant probe wire frc~m the prior art. In this connection, it is of interest that the U.S. Patents to Finney--4,307,723 and Tafeen--3,539,034 each disclose a catheter whose dista]. end ~ossesses a memory harac-teristic, that Woo--3,943,932 discloses an acupuncture needle that may possess a memory characteristic and that Hawkins--4,230,123 discloses what is descri~ as a J-wire which is inserted through a cannula for fixing the clistal end of said cannula.
Having finally located the probe wire with confirmed accuracy, -the cannula is removed. As is ~Icwn in the art, one may then tape clc~n the proximal portion of the probe wire that extends from the body to thereby Eur-ther inhibit wire displacernent upon subse~uent kcxly handling and transportion. ~Ic~ever, it is preferred that a more positi.ve means b~ relied on to both fur-ther inhibit wiredisplacement and to prevent tissue Eram rising over a section of such extenclingproximal wire that due to prior mani.pulatiorl may have become non-sterile.
Such a more positive means may cc~nprise a biased clip typ~ member but a preferred clc~mp means is illustrated in F'IG. 4 where.in member 16 has an aperture 18 axially therethrough and a threadecl aperture 20 extending normal to aperture18 and intersecting same. A threadecl clamp-screw 22 operatively associates with aperture 20. The cross-sectional configuration of said clclmp means is broadly no-t material excel~t that, to facilitate hanclling, the peripheral surface may be $ .' ~ 73~)6~
ri~b~d or ~lurled or, as shc~n, mcly be provid~l witll flange porti.ons 30. lnuse, the clamp means is positialed with the proximal portion aE the fina]].y anchored probe wire ext~nding t}~ough the axially dis~osed apertur2, the end face 24 of the clamp is brought to bear on the bcKly surface, whereby to preventbody tissue from rising over any of such proximal portion extencling frcsm the body, and the screw tightened -to thereby fix the parts.
Graduations 26 are provided on the proximal extent of the probe wire.
These mar~ings indicate both the depth of the probe wire's distal end when anchored and the depth of ~le probe uni-t's distal end when the wire is properlysheathed in the ca~mula.
Graduations 28 on the extended distal portion of _he probe wire are an indication to the surgeon as to relation of incision to the distal end of the wire. SUC]1 graduations 28 may extend further along the distal end than is illustrated in FIG. 3.
Graduations 11 on the cannula are provided whereby to indicate the depth of cannula penetration into the bcdy.
Such graduations may be etchings ancd may be colcsr coded.
The e~bodiments shown and described are only illustrative of the present invention and are not to be construed as being delimitive thereo:E; since once apprised of the invention, changes in structure w~uld be readily apparent to oneskill~d in the art. E-lence, the present invention includes all.rrodifications of structure encanpassed within the spirit and scope of the following claims.
~ ~,
Claims (27)
1. A method of locating a lesion, especially a method for locating .
presymptomatic, non-palpable breast lesion, comprising the steps of:
(A) mammographically determing the probable location of such lesion;
(B) selecting a probe wire that has at its distal end a relatively small memory hook and a predetermined degree of soft flexibility;
(C) sheathing the probe wire in a needle cannula whereat the wire assumes the straight configuration of the cannula and the distal ends of the wire and cannula are in a predetermined relationship as evidenced by observationof graduated scale markings on the proximal portion of the wire;
(D) maintaining such predetermined relationship and initially inserting the assembled cannula and probe wire unit into the body tissue to a depth whereat said distal ends are at about the site of said lesion;
(E) mammographically determining if placement of such distal ends is within a predetermined spacing with regard to the lesion;
(F) repositioning the unit and mammographically determining each aforedescribed placement of said unit until the desired accuracy is achieved;
(G) solely moving the probe wire forwardly to an extent, as determined by further observation of said graduated scale markings, whereby to only free the distal end portion having the memory hook and whereby the distal end of the probe wire assumes the hook configuration to thereby anchor itself in the tissue;
(H) mammographically determining the spatial relationship of the anchored end of the probe wire to the lesion with regard to a desired accuracy thereof;
(I) relying on said characteristic of soft flexibility of the probe wire, manually actuating the probe wire to release and easily slide from its anchored position in the tissue to a fully sheathed location within the cannula at said predetennined relationship of the distal ends without injury to the tissue when said desired accuracy has not been effected; and (J) repositioning the unit as aforedescribed, reanchoring the probe wire as aforedescribed, and repeating the aforedescribed mammographic determinations until the desire accuracy of the spatial relationship of the anchored end of the probe wire to the lesion site is effected.
presymptomatic, non-palpable breast lesion, comprising the steps of:
(A) mammographically determing the probable location of such lesion;
(B) selecting a probe wire that has at its distal end a relatively small memory hook and a predetermined degree of soft flexibility;
(C) sheathing the probe wire in a needle cannula whereat the wire assumes the straight configuration of the cannula and the distal ends of the wire and cannula are in a predetermined relationship as evidenced by observationof graduated scale markings on the proximal portion of the wire;
(D) maintaining such predetermined relationship and initially inserting the assembled cannula and probe wire unit into the body tissue to a depth whereat said distal ends are at about the site of said lesion;
(E) mammographically determining if placement of such distal ends is within a predetermined spacing with regard to the lesion;
(F) repositioning the unit and mammographically determining each aforedescribed placement of said unit until the desired accuracy is achieved;
(G) solely moving the probe wire forwardly to an extent, as determined by further observation of said graduated scale markings, whereby to only free the distal end portion having the memory hook and whereby the distal end of the probe wire assumes the hook configuration to thereby anchor itself in the tissue;
(H) mammographically determining the spatial relationship of the anchored end of the probe wire to the lesion with regard to a desired accuracy thereof;
(I) relying on said characteristic of soft flexibility of the probe wire, manually actuating the probe wire to release and easily slide from its anchored position in the tissue to a fully sheathed location within the cannula at said predetennined relationship of the distal ends without injury to the tissue when said desired accuracy has not been effected; and (J) repositioning the unit as aforedescribed, reanchoring the probe wire as aforedescribed, and repeating the aforedescribed mammographic determinations until the desire accuracy of the spatial relationship of the anchored end of the probe wire to the lesion site is effected.
2. The method of claim 1 comprising the additional steps of:
(K) completely withdrawing and removing the cannula needle; and (L) fixing the probe wire by clamping a lock means onto the wire and simultaneously in a position whereat one surface of the lock means bears on the body containing the lesion;
whereby, during subsequent transportation and handling of the body, to further inhibit dislodgement of the probe wire and to prevent the body tissue from covering the proximal portion of the probe wire that may have become non-sterile.
(K) completely withdrawing and removing the cannula needle; and (L) fixing the probe wire by clamping a lock means onto the wire and simultaneously in a position whereat one surface of the lock means bears on the body containing the lesion;
whereby, during subsequent transportation and handling of the body, to further inhibit dislodgement of the probe wire and to prevent the body tissue from covering the proximal portion of the probe wire that may have become non-sterile.
3. The method of claim 1 wherein the depth of unit insertion, as described in (D), is guided by observation of graduated scale markings on the cannula needle.
4. A method of lesion excision comprising:
locating the lesion by the method of claim 1; and during surgical removal of the lesion, being guided by observation of graduated scale markings on the distal portion of the anchored probe wire.
locating the lesion by the method of claim 1; and during surgical removal of the lesion, being guided by observation of graduated scale markings on the distal portion of the anchored probe wire.
5. A probe unit adapted for location of a lesion, and especially for location of a presymptomatic, non-palpable breast lesion, comprising:
(A) a tubular needle cannula adapted for insertion into a body to the site of said lesion;
(B) a probe wire adapted to closely fit and be freely slidable through the cannula;
(C) said probe wire possessing a memory hook at its distal end whereby such end assumes the straight configuration of the cannula when sheathed thereinbut assumes the hook configuration when pushed through the cannula to thereby anchor itself in the tissue at the lesion when the probe unit of cannula and probe wire therein has previously been inserted into the body at about the lesion site;
(D) said probe wire possessing the further characteristic of a predetermined degree of soft flexibility whereby said wire is adapted to be manually actuated to release and easily slide from a said anchored location to afully sheathed disposition within the cannula and without undue destruction of surrounding tissue;
(E) whereby the probe unit may be relocated within the body and the probe wire reanchored within the tissue until a desired accuracy is attained with respect to lesion location; and (F) the cannula needle being completely withdrawable from the body and operative association with the probe wire.
(A) a tubular needle cannula adapted for insertion into a body to the site of said lesion;
(B) a probe wire adapted to closely fit and be freely slidable through the cannula;
(C) said probe wire possessing a memory hook at its distal end whereby such end assumes the straight configuration of the cannula when sheathed thereinbut assumes the hook configuration when pushed through the cannula to thereby anchor itself in the tissue at the lesion when the probe unit of cannula and probe wire therein has previously been inserted into the body at about the lesion site;
(D) said probe wire possessing the further characteristic of a predetermined degree of soft flexibility whereby said wire is adapted to be manually actuated to release and easily slide from a said anchored location to afully sheathed disposition within the cannula and without undue destruction of surrounding tissue;
(E) whereby the probe unit may be relocated within the body and the probe wire reanchored within the tissue until a desired accuracy is attained with respect to lesion location; and (F) the cannula needle being completely withdrawable from the body and operative association with the probe wire.
6. A probe unit as in claim 5 having in combination therewith a fixing clamp comprised of:
(G) a member having a first aperture axially therethrough and adapted to accommodate the proximal portion of an anchored probe wire when a cannula needle is withdrawn from the body and removed from operative association with the wire;
(H) a threaded aperture disposed generally normal to and intersecting the first aperture;
(I) a clamping screw operatively associated with the threaded aperture; and (J) a distal face of the member adapted to bear against the body surface through which the anchored probe wire would extend whereupon the clamp screw would be adapted to lock the proximal portion of said wire and the body surface would be prevented from rising over said extending proximal probe wire portion that may have become non-sterile.
(G) a member having a first aperture axially therethrough and adapted to accommodate the proximal portion of an anchored probe wire when a cannula needle is withdrawn from the body and removed from operative association with the wire;
(H) a threaded aperture disposed generally normal to and intersecting the first aperture;
(I) a clamping screw operatively associated with the threaded aperture; and (J) a distal face of the member adapted to bear against the body surface through which the anchored probe wire would extend whereupon the clamp screw would be adapted to lock the proximal portion of said wire and the body surface would be prevented from rising over said extending proximal probe wire portion that may have become non-sterile.
7. A probe unit as in claim 5 wherein the cannula needle has graduated scale markings thereon whereby to determine depth of cannula or probe unit insertion into the body.
8. A probe unit as in claim 6 wherein the cannula needle has graduated scale markings thereon whereby to determine depth of cannula or probe unit insertion into the body.
9. A probe unit as in claim 5 wherein the probe wire has graduated scale markings on the proximal portion thereof whereby to determine alignment of the distal ends of the assembled cannula and probe wire and whereby to determine theextent to which the probe wire need be pushed through the cannula to only free the memory hook portion for its anchoring function.
10. A probe unit as in claim 6 wherein the probe wire has graduated scale markings on the proximal portion thereof whereby to determine alignment of the distal ends of the assembled cannula and probe wire and whereby to determine theextent to which the probe wire need be pushed through the cannula to only free the memory hook portion for its anchoring function.
11. A probe unit as in claim 7 wherein the probe wire has graduated scale markings on the proximal portion thereof whereby to determine alignment of the distal ends of the assembled cannula a and probe wire and whereby to determine the extent to which the probe wire need be pushed through the cannula to only free the memory hook portion for its anchoring function.
12. A probe unit as in claim 5 wherein the probe wire has graduated scale markings on the distal portion thereof whereby during excision of a lesion the surgeon is guided.
13. A probe unit as in claim 6 wherein the probe wire has graduated scale markings on the distal portion thereof whereby during excision of a lesion the surgeon is guided.
14. A probe unit as in claim 7 wherein the probe wire has graduated scale markings on the distal portion thereof whereby during excision of a lesion the surgeon is guided.
15. A probe unit as in claim 9 wherein the probe wire has graduated scale markings on the distal portion thereof whereby during excision of a lesion the surgeon is guided.
16. A probe unit as in claim 5 wherein the probe wire is coated with an inert material having predetermined lubricity and electrically insulativevalues.
17. A probe unit as in claim 7 wherein the probe wire is coated with an inert material having predetermined lubricity and electrically insulativevalues.
18. A probe unit as in claim 9 wherein the probe wire is coated with an inert material having predetermined lubricity and electrically insulativevalues.
19. A probe unit as in claim 12 wherein the probe wire is coated with an inert material having predetermined lubricity and electrically insulativevalues.
20. A probe wire adapted for use with a cannula needle for location of a lesion and especially for location of a presymptomatic, non-palpable breast lesion, comprising:
a wire of the type possessing a relatively small memory hook at its distal end whereby being adapted to anchor in tissue at a lesion site when such end is pushed from a sheathing cannula needle that has been inserted into abody containing such lesion; and said wire having a relatively soft flexibility characteristic whereby said distal end when anchored is adapted to be manually actuated to release and slide from such an anchored position to a sheathed location in said cannula without undue damage to the tissue.
a wire of the type possessing a relatively small memory hook at its distal end whereby being adapted to anchor in tissue at a lesion site when such end is pushed from a sheathing cannula needle that has been inserted into abody containing such lesion; and said wire having a relatively soft flexibility characteristic whereby said distal end when anchored is adapted to be manually actuated to release and slide from such an anchored position to a sheathed location in said cannula without undue damage to the tissue.
21. A probe wire as in claim 20 wherein graduated scale markings are disposed at the proximal portion of the wire whereby to facilitate location of the wire's distal end with respect to the distal end of a cannula needle to be used therewith and whereby to determine the extent to which the wire need be pushed through a said cannula needle in order to free only the memory hook portion for its anchoring function.
22. A probe wire as in claim 20 wherein graduated scale markings are disposed at the distal portion of the wire whereby with the wire properly located and anchored, the markings are adapted to guide a surgeon during excision of a lesion.
23. A probe wire as in claim 21 wherein graduated scale markings are disposed at the distal portion of the wire whereby with the wire properly located and anchored, the markings are adapted to guide a surgeon during excision of a lesion.
24. A probe wire as in claim 20 being coated with an inert material having predetermined lubricity and insulative values.
25. A probe wire adapted for use with a cannula needle for location of a lesion, and especially for location of a presymtomatic, non-palpable breast lesion, comprising:
a wire of the type possessing a relatively small memory hook at its distal end whereby being adapted to anchor in tissue at a lesion site when such end is pushed from a sheathing cannula needle that has been inserted into abody containing such lesion; and said wire having graduated scale markings at its proximal portion whereby to facilitate location of the wire's distal end with respect to the distal end of a cannula needle to be used therewith and whereby to determine theextent to which the wire need be pushed through a said cannula needle in order to free only the memory hook portion for its anchoring function.
a wire of the type possessing a relatively small memory hook at its distal end whereby being adapted to anchor in tissue at a lesion site when such end is pushed from a sheathing cannula needle that has been inserted into abody containing such lesion; and said wire having graduated scale markings at its proximal portion whereby to facilitate location of the wire's distal end with respect to the distal end of a cannula needle to be used therewith and whereby to determine theextent to which the wire need be pushed through a said cannula needle in order to free only the memory hook portion for its anchoring function.
26. A probe wire as in claim 25 wherein graduated scale markings are disposed at the wire's distal portion whereby with the wire properly located andanchored, the markings are adapted to guide a surgeon during excision of a said lesion.
27. A probe wire as in claim 25 that is coated with an inert material having predetermined lubricity and insulative values.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US713,613 | 1985-03-19 | ||
| US06/713,613 US4616656A (en) | 1985-03-19 | 1985-03-19 | Self-actuating breast lesion probe and method of using |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1273068A true CA1273068A (en) | 1990-08-21 |
Family
ID=24866800
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000504390A Expired CA1273068A (en) | 1985-03-19 | 1986-03-18 | Self-actuating breast lesion probe and method |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4616656A (en) |
| EP (1) | EP0217858A4 (en) |
| JP (1) | JPS62502244A (en) |
| AU (1) | AU599908B2 (en) |
| CA (1) | CA1273068A (en) |
| DE (1) | DE3690135T (en) |
| GB (1) | GB2180760B (en) |
| WO (1) | WO1986005378A1 (en) |
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- 1985-03-19 US US06/713,613 patent/US4616656A/en not_active Expired - Lifetime
-
1986
- 1986-03-11 DE DE19863690135 patent/DE3690135T/de active Pending
- 1986-03-11 WO PCT/US1986/000509 patent/WO1986005378A1/en not_active Application Discontinuation
- 1986-03-11 EP EP19860902160 patent/EP0217858A4/en not_active Ceased
- 1986-03-11 AU AU56260/86A patent/AU599908B2/en not_active Expired
- 1986-03-11 JP JP61501749A patent/JPS62502244A/en active Granted
- 1986-03-11 GB GB8625454A patent/GB2180760B/en not_active Expired
- 1986-03-18 CA CA000504390A patent/CA1273068A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| WO1986005378A1 (en) | 1986-09-25 |
| EP0217858A1 (en) | 1987-04-15 |
| JPS62502244A (en) | 1987-09-03 |
| EP0217858A4 (en) | 1988-06-08 |
| GB8625454D0 (en) | 1986-11-26 |
| US4616656A (en) | 1986-10-14 |
| GB2180760A (en) | 1987-04-08 |
| AU5626086A (en) | 1986-10-13 |
| AU599908B2 (en) | 1990-08-02 |
| GB2180760B (en) | 1989-04-19 |
| DE3690135T (en) | 1987-05-14 |
| JPH0418861B2 (en) | 1992-03-27 |
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