Surgery – Instruments – Orthopedic instrumentation
Reexamination Certificate
2000-07-24
2004-01-13
Robert, Eduardo C. (Department: 3732)
Surgery
Instruments
Orthopedic instrumentation
C606S092000
Reexamination Certificate
active
06676664
ABSTRACT:
The present invention relates to a device for metering hardenable mass for applications of vertebroplastia and other similar bone treatments, achieving significant improvements with respect to the prior art in this field.
As is known, in different pathological states of diverse origin which affect the bone structures (trauma, osteoporosis, bone tumours, bone metastases, osteoarticular implants, etc.), one of the forms of treating, stabilizing and consolidating said structures consists in the injection into their interior of biomaterials having cementing properties which may incorporate drugs having a curative effect.
Access to the interior of the bone structure may be provided by puncture of the bone once exposed in the surgical sphere by means of conventional surgical techniques, or by means of percutaneous puncture, a technique which does not require a surgical incision and in which, instead of this, minimally invasive access through the skin is effected.
Access to the interior of the bone structure may be effected with the operator viewing directly the bone being treated, if the latter has been exposed by means of open surgery. In the case of percutaneous access, the guiding of the puncture needle or needles and their accessories (stylets, fastenings, metallic guides) requires the use of complementary techniques used in medical diagnostics for imaging (fluoroscopy, Computerized Axial Tomography, Magnetic Resonance, etc.) which facilitate the viewing of the path followed by said puncture equipment until it reaches the target in the bone.
The injection of cementing biomaterials is customarily carried out conventionally with standard syringes in which the plunger moves longitudinally along the body of said syringe without there being any type of mechanical connection between the two components. The longitudinal force exerted by the operator is what permits the of the biomaterial, although if this is highly dense or is in a rapid hardening phase, the force to be applied to the plunger needs to be considerable. Owing to the density of the biomaterial to be injected, the conventional syringe is customarily connected directly to the puncture needle, already introduced into the interior of the bone structure. In this way, the distance travelled by the biomaterial between the syringe and its target is shortened, thus reducing as far as possible the force to be generated on the plunger in order for the injection to be effective. The puncture needles customarily used arc of large diameter (size or gauge 8, 9 or 10) facilitating the passage of the dense biomaterial through them.
If the biomaterial to be injected is rapid hardening, the procedure for the preparation, loading in the syringe and injection of said material needs to be carried out in a short time (a few minutes). In the contrary case, the hardening of the cement prevents its injection in spite of exerting considerable force on the plunger of the syringe, connecting the syringe directly to the puncture needle, and using large diameter needles.
The aim of the present invention is to improve the methods for injecting hardenable masses in vertebroplastia by facilitating the loading of the biomaterial into the interior of an injector device having special features, making it possible to work with greater injection pressure and to obtain a greater capacity of adjustment thereof, so that the time for which injection of the material is possible is extended.
A further aim of the present invention consists in facilitating access by puncture in the interior of the bone structure by the use of a combination of stylets and needles having special features.
A further aim of the present invention consists in avoiding direct connection between the injection device and the puncture needle in order to avoid excessive exposure of the surgeon to X-rays.
In order to fulfil these aims, the present invention is based on an assembly of two stylets which have the same diameter adapted to the interior of the puncture needle.
The length ratio between the stylets may be variable, as a non-limiting example, from 1:1.5 to 1:3. The long stylet acts as a guide for the needle, which can move along said stylet. The length of the long stylet is such that, once its distal end reaches the outer surface of the bone being treated, the longitudinal portion which remains outside the body of the patient is greater than that introduced into said body.
The short stylet, once introduced completely into the needle, extends beyond the distal end of the latter for a distance of between 1 and 10 mm. That is to say, the length of the needle is slightly less than that of the short stylet.
The present invention also provides for the use of a tube of high pressure flexible plastics material, with connections at both ends adapted to the connections provided on the needle and the device for injecting the biomaterials. The device for injecting biomaterials according to the present invention has a plunger with screw-threaded shaft for exerting high injection pressures, and the body of the device incorporates a lateral entry connection adapted to the connection of conventional syringes, permitting the loading of the biomaterial from a conventional syringe into the body of the injection device.
According to the present invention, the method of introduction of the hardenable mass is characterized by the following operations:
1. Percutaneous Puncture and Access:
Using some diagnostic imaging technology (fluoroscopy, Computerized Axial Tomography, Magnetic Resonance, etc.) for guiding the introduction of the needle within the body of the patient and before initiating the percutaneous puncture, the operator introduces the long stylet completely through the needle.
By manual puncture, the distal end of the stylet is now introduced into the body of the patient. The stylet is advanced while controlling its path with the imaging system selected for the procedure, until the outer surface of the bone being treated is reached. The puncture needle and the proximal portion of the long stylet still remain outside the body of the patient.
The target having been reached with the distal end of the stylet, the puncture needle advances over the latter and is introduced into the inside of the body of the patient until its distal end reaches the distal end of the stylet. The long stylet has been used as described as a guiding element for the needle.
At that moment, the long stylet is substituted by the short stylet, so that the distal end of the latter will project a few millimetres beyond the end of the needle. By means of manual pressure, rotation or percussion, the needle/short stylet assembly is introduced into the interior of the bone to be treated. To inject the biomaterial, the short stylet must be withdrawn.
2. Injection of the Biomaterial:
The body of the injection device must be loaded with the biomaterial as described previously. The high pressure flexible tube will be connected to the body of the device and the rotatable plunger will be advanced until the biomaterial completely occupies the interior of the pressure tube, thus displacing the air which it contained previously.
At that moment the distal end of the pressure tube will be attached to the connection of the needle.
By rotating the plunger of the device in a clockwise direction, the biomaterial will be introduced into the interior of the bone. The system of rotation of the plunger permits controlled, accurate injection, while at the same time allowing the use of different biomaterials even though the latter may be in an advanced state of hardening.
By means of the application of the present invention it is possible to obtain the following advantages compared with the processes known at present.
A. Puncture and Access:
The method proposed is less aggressive or traumatic for the patient. By initially introducing only the stylet, the diameter of the puncture path created is less than that which would be produced if the needle were to be introduced directly. Moreover, in many cases various punctures have to be carried out to reach the t
Comstock David C
Darby & Darby
Grupo Grifols, S.A.
Robert Eduardo C.
LandOfFree
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