WO2013021348A1 - Kit for percutaneous removal of body tissues - Google Patents
Kit for percutaneous removal of body tissues Download PDFInfo
- Publication number
- WO2013021348A1 WO2013021348A1 PCT/IB2012/054026 IB2012054026W WO2013021348A1 WO 2013021348 A1 WO2013021348 A1 WO 2013021348A1 IB 2012054026 W IB2012054026 W IB 2012054026W WO 2013021348 A1 WO2013021348 A1 WO 2013021348A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cannula
- organism
- conveyor shaft
- kit
- shaft
- Prior art date
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
- A61B10/02—Instruments for taking cell samples or for biopsy
- A61B10/0233—Pointed or sharp biopsy instruments
- A61B10/0266—Pointed or sharp biopsy instruments means for severing sample
- A61B10/0275—Pointed or sharp biopsy instruments means for severing sample with sample notch, e.g. on the side of inner stylet
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/32—Surgical cutting instruments
- A61B17/3205—Excision instruments
- A61B17/3207—Atherectomy devices working by cutting or abrading; Similar devices specially adapted for non-vascular obstructions
- A61B17/320783—Atherectomy devices working by cutting or abrading; Similar devices specially adapted for non-vascular obstructions through side-hole, e.g. sliding or rotating cutter inside catheter
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00681—Aspects not otherwise provided for
- A61B2017/00685—Archimedes screw
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/28—Surgical forceps
- A61B17/29—Forceps for use in minimally invasive surgery
- A61B2017/2901—Details of shaft
- A61B2017/2904—Details of shaft curved, but rigid
-
- 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
- A61B90/03—Automatic limiting or abutting means, e.g. for safety
- A61B2090/037—Automatic limiting or abutting means, e.g. for safety with a frangible part, e.g. by reduced diameter
Definitions
- the present invention relates to the field of devices for percutaneous removal of body tissues from an organism. More specifically, the invention relates to a percutaneous removal of soft tissues (liver, breast, kidney biopsies, etc.), of neoformations (nodules, cysts, masses) or hernias, in particular hernias of the disc.
- soft tissues live, breast, kidney biopsies, etc.
- neoformations nodules, cysts, masses
- hernias in particular hernias of the disc.
- Laparoscopic removal requires an incision of the tissues of sufficient dimensions for insertion of a laporoscope into the organism and therefore much smaller than an incision required for a classic surgical removal.
- tissue performed percutaneously is still less invasive and typically is done with a sharp instrument able to penetrate the tissue up to the removal site; therefore no actual incision is required.
- a device is used for biopsies known as "aspiration needle" which can remove small quantities of tissues, especially liquids.
- a method for percutaneous removal of semisolid or cartilaginous tissues that can be actuated such as to perform nucleotomy or discectomy interventions (i.e. removal of the hernia of the pulpy nucleus of the intervertebral disc), in which the aspiration needles cannot be used as they are not suitable for aspirating the semi-solid and cartilaginous material of the pulpy nucleus.
- these methods comprise insertion, with ecographic control, of a coaxial needle 10 introducible percutaneously into an organism up to the removal site 20, i.e. up to when the distal end 1 1 of the coaxial needle 10 has penetrated into a removal site 20, meaning in an intervertebral disc at the hernia to be removed.
- the coaxial needle 10 is composed of a cannula 30 provided at a distal end thereof with means 32 for coupling with a handgrip 40, and a chuck 50 (also known as a blade or needle) slidably inserted in the cannula 30.
- a chuck 50 also known as a blade or needle
- the chuck 50 is extracted from the cannula 30 in direction X indicated by the arrow of figure 2.
- the cannula, decoupled from the chuck will therefore exhibit, at a distal end thereof, an opening 31 positioned in the removal site 20 for enabling introduction of a portion of tissue to be removed in a housing defined by the internal wall 33 of the cannula 30.
- a conveyor shaft 60 is inserted into the cannula, which shaft 60 has a longitudinal extension that is greater than that of the cannula 30.
- the conveyor shaft 60 is couplable at a relative proximal end 61 to the handgrip 40 and is provided, at a distal end thereof, with a threaded portion 62 that, when the conveyor shaft 60 is inserted in the cannula 30, projects partially from the opening 31 of the cannula 30 (as can be observed in figure 3).
- the threaded portion when the conveyor shaft 60 is set in rotation about the relative longitudinal axis Y by an actuator positioned internally of the handgrip 40, the threaded portion, which is in contact with the semi-solid tissue internally of the disc nucleus, cooperates with the cannula, functioning as an Archimedes screw and enabling removal of a portion of the tissue and the subsequent conveying thereof internally of the cannula 30 towards the handgrip 40.
- the threaded portion in rotation causes the movement of the semi-solid tissue of the pulpy nucleus in the direction K indicated in figure 3.
- the cannula 30 cannot have an internal diameter, and consequently an external diameter, that are too small.
- each insertion of the coaxial needle comprising the cannula 30 bears a not insignificant risk of damaging tissues, in particular nervous tissues. This might happen either during the first introduction of the coaxial needle 10 or during the successive introductions.
- the successive introductions might be necessary in a case in which the first attempt at introducing the coaxial needle 10 is not suitable for positioning the distal end in the hernia or in a case in which it is necessary to perform the removal a plurality of points of the hernia.
- the main aim of the present invention is to provide means for performing a removal of a body tissue percutaneously, in shorter times with respect to the prior art, in particular, in a case of removals of solid tissues, or semi-solid tissues and more in particular for performing nucleotomy or herniotomy of the intervertebral disc.
- a further aim of the present invention is to provide means for performing a removal of a body tissues percutaneously, which involves a lower residual risk of involuntarily cause lesions of the other body tissues, in particular in the case of nucleotomy or herniotomy of the intervertebral disc.
- kits for percutaneous removal of body tissues from an organism comprising: a first cannula percutaneously insertable in an organism and provided with a relative lateral surface; and a shaft for conveying body tissue, which shaft is insertable in the first cannula, is rotatable in the first cannula, and comprises a threaded portion, coaxial with an axis of the conveyor shaft, for conveying body tissues when the conveyor shaft rotates; characterised in that the first cannula is provided with a lateral through-hole afforded on a relative lateral surface in proximity of a relative distal end; and in that the first cannula and the conveyor shaft are conformed with respect to one another such that when the conveyor shaft is inserted internally of the first cannula, the threaded portion of the conveyor shaft is positioned at the through hole of the first cannula such as to convey body tissue from an organism consequently to activation in rotation of the conveyor shaft.
- the kit of the invention comprises the first cannula and the conveying shaft, which are couplable to a grip of a known type and, in the case of the shaft, to actuating means for setting the shaft of known type in rotation, with known coupling modes.
- the first cannula and the shaft can advantageously be of a single-use type, while the grip and the actuating means can be re-usable.
- the through-hole in the first cannula, comprised in the kit of the invention, can advantageously have a considerably larger dimension than that of the opening 31 afforded in the known-type cannula 30 (figures 1 , 2).
- This opening has dimensions correlated to the internal diameter of the cannula 30.
- the hole is a through-hole enables the first cannula to maintain, when coupled to the conveyor shaft, a structural rigidity which is sufficient to enable removal and conveying of the tissues at the through-hole, even when the through-hole has a considerably larger dimension than the distal opening 31 afforded in the cannulas 30 of known type.
- the quantity of tissue to be removed, in contact with the threaded portion of the shaft (which is arranged at the through-hole of the first cannula) is greater than the prior art. This involves shorter removal time and/or the possibility of reducing the external diameter of the first cannula, and therefore the risk connected with the insertion thereof in the organism, without this leading to an increase in the removal time with respect to the prior art.
- figure 1 is a section view of a coaxial needle of known type
- figure 2 is a longitudinal view of a cannula of known type comprised in the coaxial needle of figure 1
- figure 3 is a longitudinal view of a device for percutaneous removal of tissues of known type and insertable in the cannula of figure 2
- figure 4 is a longitudinal view, partially cutaway, of the device of figure 3 inserted in and coupled to the cannula of figure 2
- figure 5 is a longitudinal view, partially cutaway, of an embodiment of the kit of the invention
- figure 6 is a longitudinal view, partially cutaway, of a further embodiment of the kit of the invention
- figures 7 and 8 are larger-scale views, respective lateral and from above, of the discal end of an embodiment of the new cannula comprised
- numeral 100 denotes a kit for percutaneous removal of body tissues from an organism of the invention, comprising: a first cannula 80 percutaneously insertable in an organism and provided with a relative lateral surface; and a shaft 90 for conveying body tissue, which shaft 90 is insertable in the first cannula 80, is rotatable in the first cannula 80, and comprises a threaded portion 92, coaxial with an axis of the conveyor shaft 90, for conveying body tissues when the conveyor shaft 90 rotates.
- the first cannula 80 is provided with a lateral through-hole 84 afforded on a relative lateral surface in proximity of a relative distal end 81.
- the first cannula 80 and the conveyor shaft 90 are conformed with respect to one another such that when the conveyor shaft 90 is inserted internally of the first cannula 80, the threaded portion 92 of the conveyor shaft 90 is positioned at the through hole 84 of the first cannula 80 such as to convey body tissue from an organism consequently to activation in rotation of the conveyor shaft 90.
- the conveyor shaft 90 is preferably flexible and the first cannula 80 comprises a proximal portion 82 having a straight development; and a remaining distal portion 87 having a straight development and comprising the distal end 81 of the first cannula 80 and the through-hole 84, the distal portion 87 being inclined by an angle with respect to the proximal portion 82 (figure 5).
- the distal portion 87 of the first cannula 80 is inclined with respect to the proximal portion 82 of the first cannula 80 by an angle comprised between 1 and 30 degrees, advantageously between 5 and 25 degrees, more advantageously between 15 and 25 degrees.
- kits 100 in which the conveyor shaft 90 is flexible and the first cannula 80 comprises: a proximal portion 82 having a straight development; and a remaining distal portion 87, comprising the distal end 81 of the first cannula 80 and the through-hole 84, the distal portion 87' having a curved development (figure 6).
- the inclined or curved distal portion 87, 87' of the first cannula 80 enables manoeuvring around any obstacles present in the percutaneous insertion trajectory of the cannula.
- the curved-developing distal portion 87' of the first cannula 80 is preferably conformed as an arc of circumference which extends to an angle of up to 180°.
- the inclined or curved distal portion 87, 87' of the first cannula 80 enables, following a rotation of the first cannula 80 along a longitudinal axis X of the remaining proximal portion 82, positioning the through-hole 84 in a plurality of positions of the removal site, arranged along the arc of circumference described by the through-hole 84 during the rotation of the first cannula 80.
- This is particularly preferable in a case in which the removal site is a pulpy nucleus, and more preferably in a discal hernia.
- the rotation of the first cannula 80 can be performed by rotating the handgrip 40 to which both the cannula 80 and the conveyor shaft 80 comprised in the kit 100 of the invention have been coupled.
- the distal portion, inclined or curved 87, 87' of the first cannula 80 preferably has a length comprised between 2 and 6 cm, more preferably between 2.5 and 4.5 mm, advantageously between 2.5 and 4 mm. These lengths enable the through-hole 84 to describe an arc of circumference during the rotation of the first cannula 80 which falls in the removal point or enables the through- hole to be arranged on a further removal site arranged on the described arc.
- the distal portion of the first cannula 80 is inclined or curved, the risk connected with the percutaneous removal is further reduced and the quantity of tissue that can be removed with a single percutaneous introduction of the first cannula 80 is increased.
- the first cannula 80 is advantageously made of a memory shape material, especially when the cannula 80 comprises a distal portion 87, 87' that is inclined or curved.
- the through-hole 84 made on the first cannula 80 preferably has a longitudinal development comprised between 3 and 30 mm, more preferably between 10 and 30 mm, advantageously between 10 and 25 mm.
- the transversal development of the through-hole 84 is determined by the relative maximum depth (figure 8).
- Kits 100 according to the invention are preferred in which the through-hole 84 is obtainable by making a lateral undercut on the lateral surface of the first cannula 80, the undercut having a maximum depth P, measured along an external diameter of the first cannula 80, comprised between 45% and 60% of the external diameter D of the first cannula 80.
- the maximum depth is preferably comprised between 50 and 60% of the external diameter D of the cannula 80.
- the distal end 81 of the first cannula 80 is closed and sharpened such as to facilitate the percutaneous insertion into the organism.
- This embodiment of the first cannula is particularly preferable when the cannula has an external diameter comprised between 0.72 mm and 2.5 mm as this means that a chuck is no longer needed to be inserted in the first cannula, which closes the distal end during the percutaneous insertion of the cannula in the organism.
- the kit 100 of the invention preferably comprises an element 76 for percutaneous introduction having a longitudinal development and percutaneously insertable in an organism and having a relative longitudinal development that is greater than the longitudinal development of the first cannula 80.
- the element 76 for percutaneous introduction is entirely and slidably insertable in the first cannula 80, such as to guide the insertion of the first cannula 80 into the organism when the element 76 is percutaneously inserted in the organism.
- the percutaneous introduction element 76 can have an external diameter that is smaller by at least 0.1 mm than the internal diameter of the first cannula 80.
- This enables actuating a new removal method which comprises the following steps: predisposing a percutaneous introduction element 76 percutaneously and having a longitudinal development inserted percutaneously in an organism with a relative distal end inserted in a removal point internally of the organism and a relative distal end external of the organism; the percutaneous introduction element 76 having a relative longitudinal development that is greater than the longitudinal development of the first cannula 80 and being entirely and slidably insertable in the first cannula 80; percutaneously inserting the first cannula 80 into the organism using as a guide the percutaneous introduction element 76, inserted into the organism, realising a relative sliding between the percutaneous introduction element 76 and the first cannula and with the percutaneous introduction element 76 inserted internally of the first cannula 80.
- This method exhibits the indisputable advantage of using the percutaneous introduction element 76 in the first percutaneous insertion.
- this element has an external diameter that is smaller than that of the first cannula 80, with this method the risk of lesions during the positioning step of the first cannula 80 are further reduced.
- the method of the invention comprises following steps: predisposing a second cannula 70 percutaneously insertable into an organism, comprising: a butt 72, at a proximal end thereof; a pre-fracture line 74 arranged in proximity of the butt 72, preferably adjacent to the butt 72; a distal portion 76 thereof, having a longitudinal development originating from the pre-facture line 74 and being percutaneously insertable in an organism; the distal portion 76 of the second cannula 70 having a relative longitudinal development that is greater than the longitudinal development of the first cannula 80 and being entirely and slidably insertable in the first cannula 80; percutaneously inserting the distal portion 76 of the second cannula in an organism in such a way that a relative proximal end 71 is at a removal point internally of the organism and the pre-fracture line is external of the organism; separating the butt 72 from the distal portion 76 of the second cannula 70
- This method enables using, for assisted localisation of the removal point, a coaxial needle 75 (see figure 9) comprising: the second cannula 70 with an external diameter that is smaller than that of the first cannula 80 and provided with the pre-fracture line 74, and a butt 72; and a chuck 73 insertable in the second cannula 70.
- the kit 100 comprises: a second cannula 70 percutaneously inserted in an organism, provided: at a proximal end of a butt 72; with a pre-fracture line 74 arranged in proximity of the butt 72, preferably adjacent to the butt 72; with a distal portion 76 having a longitudinal development that originates from the pre-fracture line 74 and is percutaneously insertabie in an organism; the distal portion 76 of the second cannula 70 having a longitudinal development that is greater than the longitudinal development of the first cannula 80 and entirely and slidably insertabie in the first cannula 80 such as, when the distal portion is inserted percutaneously in the organism, to be a guide for the percutaneous insertion of the first cannula 80 into the organism.
- the last above embodiment of the kit 100 advantageously further comprises the chuck 73, insertabie in the second cannula and provided with a further butt 74.
- kit 100 further comprising a handgrip 40 bearing activating means for activating the conveyor shaft 90 in rotation, the grip being conformed such as to couple with a first cannula 80 and with the conveyor shaft 90 in such a way that when the conveyor shaft 90 is inserted internally of the first cannula 80 the threaded portion 92 of the conveyor shaft 90 is at the through-hole 84 of the first cannula 80 in order to convey body tissues from an organism consequently to the activation in rotation of the conveyor shaft 90 by the activating means.
- kit 100 enables assembling a new device for percutaneous removal of body tissues comprising: any embodiment of the first cannula 80 that is percutaneously insertabie in a previously-described organism and provided with a lateral through-hole 84 made on the relative lateral surface in proximity of a distal end 81 thereof; and a shaft 90 for conveying body tissue, which shaft 90 is insertabie in the first cannula 80, is rotatable in the first cannula 80, and comprises a threaded portion 92, coaxial with an axis of the conveyor shaft 90, for conveying body tissues when the conveyor shaft 90 rotates; and a handgrip 40 bearing activating means for activating the conveyor shaft 90 in rotation, the handgrip 40 being conformed such as to couple with the first cannula 80 and with the conveyor shaft 90 in such a way that when the conveyor shaft 90 is inserted internally of the first cannula 80, the threaded portion 92 of the conveyor shaft 90 is positioned at the through-hole 84 of the
- the handgrip 40 can be advantageously single-use in order to limit danger of infections caused by a careless etherisation, necessary in a case where a same handgrip is used several times.
- the handgrip 40 preferably comprises a command button 41 of the activating means positioned at a first opposite end of the end provided for coupling with the conveyor shaft 90 and the first cannula 80.
- the longitudinal development of the first cannula 80 can be comprised between 5 and 30 cm, preferably between 5 and 25 cm and advantageously * between 10 and 25 cm.
- the external diameter of the first cannula 80 which is percutaneously insertable in an organism, can be comprised between 0.72 mm (21 gauge) and 3.70 mm (7 gauge), preferably between 0.72 mm and 3 mm, more preferably between 1 mm and 2.5 mm.
- the threaded portion 92 of the conveyor shaft 90 can extend longitudinally for the whole longitudinal development of the first cannula 80 or have a longitudinal development that is less than the longitudinal development of the first cannula 80.
- the conveyor shaft 90 advantageously comprises at least a further threaded portion (not shown) arranged at an intermediate position between the threaded portion 92 and the proximal end of the conveyor shaft 90 in order to cooperate with the conveying of the tissues removed along the first cannula 80.
- the threaded portion 92 preferably comprises a helical cutting profile.
- the conveyor shaft 90 in the portions thereof not involved with the threaded portion 92 or the further threaded portion, exhibits a transversal section that is smaller than a transversal section of the threaded portions 92.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medical Informatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pathology (AREA)
- Molecular Biology (AREA)
- Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Surgical Instruments (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITBO2011A000493 | 2011-08-08 | ||
IT000493A ITBO20110493A1 (it) | 2011-08-08 | 2011-08-08 | Kit per il prelievo percutaneo di tessuti corporei |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013021348A1 true WO2013021348A1 (en) | 2013-02-14 |
Family
ID=44720943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2012/054026 WO2013021348A1 (en) | 2011-08-08 | 2012-08-07 | Kit for percutaneous removal of body tissues |
Country Status (2)
Country | Link |
---|---|
IT (1) | ITBO20110493A1 (it) |
WO (1) | WO2013021348A1 (it) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3945375A (en) * | 1972-04-04 | 1976-03-23 | Surgical Design Corporation | Rotatable surgical instrument |
US20020143270A1 (en) * | 2001-04-02 | 2002-10-03 | Temple University Of The Commonwealth System Of Higher Education | Multiple biopsy device |
WO2006015302A1 (en) * | 2004-07-29 | 2006-02-09 | X-Sten, Corp. | Spinal ligament modification devices |
US20080249553A1 (en) * | 2007-04-06 | 2008-10-09 | William Harwick Gruber | Method, system and device for tissue removal |
-
2011
- 2011-08-08 IT IT000493A patent/ITBO20110493A1/it unknown
-
2012
- 2012-08-07 WO PCT/IB2012/054026 patent/WO2013021348A1/en active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3945375A (en) * | 1972-04-04 | 1976-03-23 | Surgical Design Corporation | Rotatable surgical instrument |
US20020143270A1 (en) * | 2001-04-02 | 2002-10-03 | Temple University Of The Commonwealth System Of Higher Education | Multiple biopsy device |
WO2006015302A1 (en) * | 2004-07-29 | 2006-02-09 | X-Sten, Corp. | Spinal ligament modification devices |
US20080249553A1 (en) * | 2007-04-06 | 2008-10-09 | William Harwick Gruber | Method, system and device for tissue removal |
Also Published As
Publication number | Publication date |
---|---|
ITBO20110493A1 (it) | 2013-02-09 |
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