This invention relates to a device for taking samples of biological tissue for subsequent cytological/histological tests.
This method is nowadays increasingly used in the routine practice of performing clinical tests on the human body.
For the analysis of internal organs, instruments commonly known as endoscopes are used for this purpose, such as, for example, may be seen in publication U.S. Pat. No. 5,861,002 or US-2005/0090842.
The samples are normally taken by using needles which can be inserted and housed inside the endoscope, and activated when the sample is taken.
To perform a needle biopsy echo-endoscopically, a flexible endoscope is used, fitted with an ultrasound probe which is inserted in the hollow organ to be examined.
In the case of an examination relating to the esophagus, stomach and/or duodenum and nearby organs (pancreas, bile ducts and lymph nodes), it is introduced through the oral cavity (as with the gastroscope), whilst in the case of an examination of the anal canal and/or rectum/sigmoid colon, it is introduced through the anus as far as necessary.
The ultrasound images obtained are displayed on a special screen which helps the operator to better maneuver the endoscopic instrument and position it appropriately in the immediate vicinity of the portion from which the sample is then taken.
During the examination it is therefore possible to carry out maneuvers such as the one indicated above, by using a needle which is placed in the operating channel of the instrument, to drain cysts or administer anesthetic at the solar plexus.
When a biopsy is being taken, to obtain correct tissue sampling, it may be necessary to operate the needle several times.
Note the end of the instrument from which a needle 2 for FNA (Fine Needle Aspiration) projects from the operating channel and which is manoeuvred, at the appropriate moment, by the operator.
To perform the FNA, it is necessary to insert the needle in the endoscope channel until it protrudes from the distal portion of the endoscope.
The movements of the needle are then guided by the proximal end (not illustrated) of the handle which is equipped with a grip and controls associated with the various operating elements forming part of the endoscope.
In particular, the procedures which allow samples to be taken consist of:
- positioning the needle inside the instrument;
- inserting the needle in the lesion with a firm movement of the handle;
- modulating the excursion of the needle;
- aspiration of the material;
- removal of the needle by continuous movements;
- finally, withdrawing and removing the needle, and emptying of the needle to collect the sample.
The problem of the prior art is due to the limited possibility of altering the size and structure of the needle because of the need to pass through an endoscopic channel which, moreover, during the examination, adopts angled and curved positions not really suited for the transit of a needle-system, in one direction or another, inside it.
To have some idea of the shape and of functionalities of a needle-system, see, for example, the publication U.S. Pat. No. 5,199,441, whose main Figure is included as FIG. 2 of prior art in the accompanying drawings.
This solution clearly shows that the aspiration/sample taking needle is internally hollow so that this internal space can hold the tissue samples removed by insertion of the needle in the body part to be analysed.
To favour detachment and retention of the sample, the distal part of the outer surface of the needle is provided with holes passing through the thickness of the needle.
In addition, also to favour the retention of the tissue samples inside the needle, the cavity presents different thicknesses, thus creating a non-linear or undulating inner surface.
The drawbacks of the prior art consist therefore mainly in the fact that the needles used do not allow the removal of sufficient amounts of samples for in-depth analysis of the part under examination.
The aim of this invention is to provide a device for taking samples of tissue for cytological/histological tests which overcomes the above-mentioned disadvantages of the prior art.
More specifically, the aim of this invention is to provide a device for taking samples of tissue for cytological/histological tests which can be associated with instruments of examination such as endoscopes, and is able to withdraw sufficient amounts of samples to allow completeness of the subsequent step of cytological/histological examination.
A further aim of this invention is propose a device for taking samples of tissue for cytological/histological tests capable of using, for its operation, the usual instruments and commands of traditional endoscopes, not requiring therefore particular designs, on one hand, or different instruments in the operating room, on the other.
This and other features of the invention will become more apparent from the following detailed description of a preferred, non-limiting example embodiment of it, with reference to the accompanying drawings, in which:
With reference to the accompanying drawings, and in particular to
The device comprises a body (1) provided with means (2) for reversible association with the distal portion (3d) of the instrument (3).
These means are, in
The body (1) houses a needle (5) for taking a tissue (6) sample, movable between a proximal back, non-operating position (5p), inside the body and a distal, operating position (5d) partly outside the body (1), for penetrating the tissue (6) to be tested.
The device is equipped with first control means (10) associated with said needle, being positioned and slidable inside said analysis instrument (controlled by a handle that can be attached to the handgrip positioned on the proximal part of the endoscope), and designed to allow the movement, in both directions, between said proximal position and said distal position.
In a preferred embodiment of the device according to the invention, the needle has a portion (5s) with reduced thickness to form a seat (7) for receiving said tissue sample.
In a preferred embodiment of the device according to the invention it comprises further movement means (better referred to below) designed to modify the orientation of the above-mentioned body (1).
The body also houses a first protection element (8) of the needle, surrounding the needle by at least a surface portion (8s) which is cylindrical and opposite the portion with reduced thickness (5s).
This first protection element is also positioned inside the body and is mobile, in both directions, parallel to a line of movement (9) of the needle, between a proximal, back, non-operating position (8p) and a distal, operating position (8d), in which the needle and first protection element are facing one another.
To realize this preferred combination of elements, the body (1) comprises, according to the solution illustrated in
The cavities are tubular and are connected to one another by relative longitudinal grooves (30, 31) cut in their lateral surface close to that of the adjacent cavity.
The groove (30) connects the side cavity (17) with the central cavity (16), whilst the groove (31) connects the remaining side cavity (15) with the central cavity (16).
The latter therefore has two longitudinal cavities opposite one another at 180°.
The central cavity (16) houses the needle (5) which is associated at the rear with a cylindrical support (51), said support forming the portion for needle coupling and sliding inside the cavity (16); see in particular
The support (51) and the needle (5) comprise said portion (5s) with reduced thickness.
In
The side cavity (15) is internally provided with first actuator means (20) acting on the needle (5) to define its movement along the line of movement (9).
These first actuator means (20) are formed by a first cylindrical tubular body (20t), see
To complete the first actuator means (20), the device is provided with an elastic element, in the shape of a first spring (12), positioned at the back of the cavity (15) and acting on the back of said first cylindrical tubular body (20t); see also
The second side cavity (17) is internally provided with second actuator means (21) acting on the first protection element (8) to define its movement between the two positions, respectively proximal and distal.
These second actuator means (21) are formed by a second cylindrical tubular body (21t), see
To complete the second means actuators (21), the device is provided with an elastic element, in the shape of a second spring (13), positioned at the back of the cavity (17) and acting on the back of said second cylindrical tubular body (21t); see also
The reference numbers (40) and (41) denote first and second operating cables which slide inside the entire endoscope, usually using the existing ducts therein and which lead distally to said first spring (12) and said second spring (13) respectively, whilst proximally they are connected the handgrip (100) shown in
More exactly, during the step of preparation of the endoscope instrument, the above-mentioned operating cables (40) and (41) are pulled taut in a distal-proximal direction, in such a way that they contribute to the compression of the first and second springs (12) and (13), this position of “arming” the device being made possible by blocking the proximal ends of the cables at the grip (100).
The aforesaid cables (40) and (41) pass through corresponding cable-holes denoted with (42) and (43), visible in
The first actuator means (20), the first cylindrical tubular body (20t), the support (51) of the needle (5), the elastic element, in the shape of a first spring (12) and the first cable (40) define first control means labelled (10).
The second actuator means (21), the second cylindrical tubular body (21t), the first protection element (8) of the needle (5), the elastic element, in the shape of a second spring (13) and the second cable (41) define second control means labelled (11). We have seen that the device comprises the body (1) which is associated with the underlying cradle (2c).
In a preferred embodiment, shown in
By means of this solution it is possible to move the body (1), and with it also the associated needle, between a lowered position of
In this case too, the movement of the ramp is carried out by means of a third cable (45), passing, like the previous ones, through a third hole (46), as shown in
The functioning of the device according to the invention will now be briefly described.
During the preparation step, the body (1) is associated with, that is to say firmly attached to, the distal end of the endoscope, using the means (2v).
The first and second cables, (40) and (41), are pulled taut towards the handgrip (100) in such a way that the first and second springs (12) and (13) are compressed (loaded) with the needle (5) in a withdrawn position inside the relative cavity (16), see
The first cylindrical tubular body (20t), (which is securely connected to the support (51) of the needle (5)) and the second cylindrical tubular body (21t), (which is securely connected to the first protection element (8) of the needle (5)) are also pulled taut and are located inside the respective cavities (15) and (17).
This static arrangement is due to the fact that the proximal end of the cables (40) and (41) is firmly fixed to the handgrip (100) of the endoscope by means of the usual locking techniques, for example with a choker and/or trigger.
At this point the endoscope is inserted in the relative orifice of the patient.
Once the correct position has been reached, the operator can activate the third cable (44) in such a way as to position the ramp at the right height, see
By means of the trigger located on the handgrip, the operator can release the first cable (40), which leads to the protrusion, from the respective cavity (16), of the support (51) and needle (5), see
The needle will penetrate the tissue to be examined, removing a certain amount of tissue which fills the seat (7) with reduced thickness (5s).
By means of the trigger on the handgrip, the operator then releases the second cable (41) with consequent expulsion from the respective cavity (17) of the protective element (8) which then covers and protects the needle (5) in such a way that the needle, but above all the zone of the seat (7), is partly enclosed, see
The tissue sample taken from the patient is thus safely preserved.
The subsequent step consists of the operator applying traction on both of the cables (40) and (41) simultaneously, until all the movable parts are returned to their respective cavities: it should be noted that at this stage, the retraction of the needle-protective ensures preservation of the tissue sample taken, this being further protected inside the cavity (16), see
At this point the entire endoscope can be withdrawn in order to remove the sample of tissue.
It is interesting to note that the device according to the invention can have different constructional types; the fundamental element consists of the independent body that can be associated with an analysis instrument. This embodiment allows the use of particular needles both in terms of size and shape, which cannot be used in traditional types of endoscope instruments. In a basic solution, the body might also have a single cavity inside which the needle is positioned. This may be the type indicated above (that is with a portion with reduced thickness) or the traditional type, that is with a hollow body, even if it has a large diameter.
The device according to this invention therefore achieves the preset aims since:
| Number | Date | Country | Kind |
|---|---|---|---|
| BO2014A000437 | Jul 2014 | IT | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2015/055560 | 7/22/2015 | WO | 00 |