WO2012089317A1 - Percutaneous device for treating spinal fractures - Google Patents
Percutaneous device for treating spinal fractures Download PDFInfo
- Publication number
- WO2012089317A1 WO2012089317A1 PCT/EP2011/006441 EP2011006441W WO2012089317A1 WO 2012089317 A1 WO2012089317 A1 WO 2012089317A1 EP 2011006441 W EP2011006441 W EP 2011006441W WO 2012089317 A1 WO2012089317 A1 WO 2012089317A1
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- WIPO (PCT)
- Prior art keywords
- central
- constituted
- cylindrical body
- dilatable
- treating spinal
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/56—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
- A61B17/58—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
- A61B17/88—Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
- A61B17/885—Tools for expanding or compacting bones or discs or cavities therein
- A61B17/8852—Tools for expanding or compacting bones or discs or cavities therein capable of being assembled or enlarged, or changing shape, inside the bone or disc
- A61B17/8858—Tools for expanding or compacting bones or discs or cavities therein capable of being assembled or enlarged, or changing shape, inside the bone or disc laterally or radially expansible
Definitions
- the present invention relates to a percutaneous device for treating spinal fractures.
- a conventional device which is particularly adapted for treating osteoporotic compression fractures associated with pathological conditions of the spine caused by aging, is constituted by a sort of small dilatable or expandable metallic scaffold, similar to a stent, which can be inflated with a balloon from the inside of the vertebral body.
- the device is inserted in the vertebral body percutaneously, by means of a mini-incision which allows the insertion of the instrument.
- the device can be inserted laterally from either side of the spine and, after correct positioning, can be dilated by means of the balloon, reaching the sustainable height.
- the stents remain in place, maintaining the created cavity, while the balloons are removed in order to allow the insertion of the cement.
- Another conventional device is constituted by a titanium implant which is shaped like a jack and is inserted, with a mini-invasive procedure, in the vertebra by means of a transpeduncular approach.
- the device is provided with a set of adapted instruments for the guided insertion of one or two implants, depending on the anatomical configuration of the fracture and on the degree of reconstruction required.
- bone cement is injected in the vertebra so as to stabilize the structure and alleviate the pain of the patient.
- the procedure is typically completed in 20-30 minutes and entails for the patient an immediate relief from pain, allowing his discharge within one or two days.
- Another type of conventional device is constituted by a lattice-like body made of titanium, which is dilated within the collapsed vertebral body in order to restore the desired height and is subsequently filled with a bone cement that allows its stabilization.
- Such device is simple to use and the instruments are provided with a color code in order to streamline the surgical procedure, but it has drawbacks.
- the dilation of the implant is circumferential, with the risk of possible lateral breakthrough.
- WO2010/100287 and WO2007/028140 disclose widening devices consisting of a tube-shaped main body having elastic sections and which radially expands when the distance between a distal end and a proximal end is reduced.
- the aim of the present invention is to provide a percutaneous device for treating spinal fractures that overcomes the drawbacks of the cited prior art.
- an object of the invention is to provide a device that allows to treat different degrees of fracture with a single implant size.
- Another object of the invention is to provide a device that can be implanted with a procedure that is simple and safe.
- Another object is to provide a device which, by virtue of its particular constructive characteristics, is capable of giving the greatest assurances of reliability and safety in use.
- a percutaneous device for treating spinal fractures characterized in that it comprises a substantially cylindrical body, said cylindrical body being pre-cut so as to form a first end portion connected to a second end portion by a central dilatable portion; said central dilatable portion being constituted by two identical members, each of said identical members being constituted by a central body associated with said end portions by means of shaped bars; said bars having ends that are deformable along lines which are all mutually substantially parallel; said central bodies being movable between a closed position and a dilated position on a single vertical plane.
- Figure 1 is a side view of the device according to the invention, shown in the closed condition;
- Figure 2 is a longitudinally sectional side view of the device
- Figure 3 is a side view, similar to Figure 1 , which shows the device in the dilated condition
- Figure 4 is a perspective view of the device according to the invention, shown in the closed condition
- Figure 5 is a perspective view of the device in the dilated condition with a stabilization screw
- Figure 6 is a perspective view of the device of the preceding figure, taken from the opposite side;
- Figure 7 is a perspective view of a dedicated instrument for applying the device according to the present invention.
- Figure 8 is a schematic view showing the insertion of the device prior to its expansion
- Figure 9 is a view, similar to the preceding one, showing the step of expanding the device.
- the device according to the invention comprises a substantially cylindrical body, which is pre-cut so as to form a first end portion 2 which is connected to a second end portion 3 by means of a dilatable or expandable central portion.
- the dilatable central portion is constituted by two identical members, each of which is constituted by a central body 4 which is associated with the end portions 2 and 3 by means of two shaped bars: an inner bar 5 and an outer bar 6.
- the ends of the bars 5 and 6 can bend, with respect to the end portions 2 and 3 and to the central body 4, along lines which are all mutually substantially parallel, so that the two central bodies 4 dilate on a single vertical plane.
- the second portion 3 includes an internal thread 7 which is adapted to accommodate the end of a screw 8, the head 9 of which engages the first portion 2 of the device.
- the pre-cut cylindrical body is preferably made of titanium alloy and has a diameter, in the dilated position, that is approximately three times its diameter in the closed position.
- the inlet diameter is approximately 5 mm, while the central portion expands, within the soma, up to approximately 17 mm.
- the device is inserted within the vertebral body 10 and is then dilated by means of a dedicated instrument 11.
- the extent of the expansion is decided in the intraoperative period, depending on the degree of kyphotization of the vertebra.
- the instrument 1 1 also allows to remove the device in the intraoperative period, by virtue of the collapse of the device, which again assumes the initial cylindrical shape by means of the extension of the structure.
- the device is provided in two embodiments: standard and screw-in.
- the space created in the bone is filled with cement (PMMA).
- stabilization is performed not by injecting cement but by virtue of the screw 8, which is fixed to the second portion 3, i.e., the distal end, of the device 1.
- the device according to the present invention allows, by means of a percutaneous operating technique, to treat even old osteoporotic and traumatic spinal fractures.
- the device which is provided in a single size, can dilate to the height required to restore the vertebral collapse; the operator can block the dilation once the image intensifier, by means of an X-ray, confirms a satisfactory result.
- An important advantage of the present invention is constituted by the possibility to easily remove the device in the intraoperative period, making it return to its closed configuration by means of a dedicated instrument.
- the device according to the present invention has a dilation in a substantially vertical direction, without any lateral or circumferential dilation, avoiding the risk of lateral breakthrough.
- the device according to the present invention allows to choose the desired degree of dilation or expansion in the intraoperative period without forcing the surgeon to decide beforehand which type of implant to use, as in the case of traditional devices.
- the device according to the present invention may also be removed in the intraoperative period.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Surgery (AREA)
- Medical Informatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Prostheses (AREA)
- Surgical Instruments (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
A percutaneous device for treating spinal fractures, has a substantially cylindrical body, which is pre-cut so as to form a first end portion connected to a second end portion by a central dilatable portion; the central dilatable portion is constituted by two identical members, each of which is constituted by a central body associated with the end portions by means of shaped bars; the bars have ends that are deformable along lines which are all mutually substantially parallel; the central bodies are movable between a closed position and a dilated position on a single vertical plane.
Description
PERCUTANEOUS DEVICE FOR TREATING SPINAL FRACTURES
The present invention relates to a percutaneous device for treating spinal fractures.
Various devices for treating spinal fractures are known.
A conventional device, which is particularly adapted for treating osteoporotic compression fractures associated with pathological conditions of the spine caused by aging, is constituted by a sort of small dilatable or expandable metallic scaffold, similar to a stent, which can be inflated with a balloon from the inside of the vertebral body. The device is inserted in the vertebral body percutaneously, by means of a mini-incision which allows the insertion of the instrument. The device can be inserted laterally from either side of the spine and, after correct positioning, can be dilated by means of the balloon, reaching the sustainable height. The stents remain in place, maintaining the created cavity, while the balloons are removed in order to allow the insertion of the cement. The result is an immediate relief from pain and rapid mobilization of the patient. However, that type of device is not recommended for various types of fracture, such as fractures requiring internal fixation, split fractures, fractures due to a shearing force, complete compound fractures, and other fractures.
Another conventional device is constituted by a titanium implant which is shaped like a jack and is inserted, with a mini-invasive procedure, in the vertebra by means of a transpeduncular approach. The device is provided with a set of adapted instruments for the guided insertion of one or two implants, depending on the anatomical configuration of the fracture and on the degree of reconstruction required. Once insertion has been completed, bone cement is injected in the vertebra so as to stabilize the structure and alleviate the pain of the patient. The procedure is typically completed in 20-30 minutes and entails for the patient an immediate relief from pain, allowing his discharge within one or two days.
Another type of conventional device is constituted by a lattice-like body made of titanium, which is dilated within the collapsed vertebral body in order to restore the desired height and is subsequently filled with a bone cement that allows its stabilization. Such device is simple to use and the instruments are provided with a color code in order
to streamline the surgical procedure, but it has drawbacks. The dilation of the implant is circumferential, with the risk of possible lateral breakthrough. Moreover, it is necessary to establish beforehand the correct size of the implant to be used.
WO2010/100287 and WO2007/028140 disclose widening devices consisting of a tube-shaped main body having elastic sections and which radially expands when the distance between a distal end and a proximal end is reduced.
The aim of the present invention is to provide a percutaneous device for treating spinal fractures that overcomes the drawbacks of the cited prior art.
Within the scope of this aim, an object of the invention is to provide a device that allows to treat different degrees of fracture with a single implant size.
Another object of the invention is to provide a device that can be implanted with a procedure that is simple and safe.
Another object is to provide a device which, by virtue of its particular constructive characteristics, is capable of giving the greatest assurances of reliability and safety in use.
This aim and these and other objects that will become better apparent hereinafter are achieved by a percutaneous device for treating spinal fractures, characterized in that it comprises a substantially cylindrical body, said cylindrical body being pre-cut so as to form a first end portion connected to a second end portion by a central dilatable portion; said central dilatable portion being constituted by two identical members, each of said identical members being constituted by a central body associated with said end portions by means of shaped bars; said bars having ends that are deformable along lines which are all mutually substantially parallel; said central bodies being movable between a closed position and a dilated position on a single vertical plane.
Further characteristics and advantages will become better apparent from the description of preferred but not exclusive embodiments of the invention, illustrated by way of nonlimiting example in the accompanying drawings, wherein:
Figure 1 is a side view of the device according to the invention, shown in the closed condition;
Figure 2 is a longitudinally sectional side view of the device;
Figure 3 is a side view, similar to Figure 1 , which shows the device in the dilated condition;
Figure 4 is a perspective view of the device according to the invention, shown in the closed condition;
Figure 5 is a perspective view of the device in the dilated condition with a stabilization screw;
Figure 6 is a perspective view of the device of the preceding figure, taken from the opposite side;
Figure 7 is a perspective view of a dedicated instrument for applying the device according to the present invention;
Figure 8 is a schematic view showing the insertion of the device prior to its expansion;
Figure 9 is a view, similar to the preceding one, showing the step of expanding the device.
With reference to the cited figures, the device according to the invention, generally designated by the reference number 1 , comprises a substantially cylindrical body, which is pre-cut so as to form a first end portion 2 which is connected to a second end portion 3 by means of a dilatable or expandable central portion.
The dilatable central portion is constituted by two identical members, each of which is constituted by a central body 4 which is associated with the end portions 2 and 3 by means of two shaped bars: an inner bar 5 and an outer bar 6.
The ends of the bars 5 and 6 can bend, with respect to the end portions 2 and 3 and to the central body 4, along lines which are all mutually substantially parallel, so that the two central bodies 4 dilate on a single vertical plane.
The second portion 3 includes an internal thread 7 which is adapted to accommodate the end of a screw 8, the head 9 of which engages the first portion 2 of the device.
The pre-cut cylindrical body is preferably made of titanium alloy and has a diameter, in the dilated position, that is approximately three times its diameter in the closed position.
By way of example, the inlet diameter is approximately 5 mm, while the central portion expands, within the soma, up to approximately 17 mm.
The device is inserted within the vertebral body 10 and is then dilated by means of a dedicated instrument 11.
The extent of the expansion is decided in the intraoperative period, depending on the degree of kyphotization of the vertebra.
According to the present invention, with a single device it is thus possible to treat different degrees of fracture.
The instrument 1 1 also allows to remove the device in the intraoperative period, by virtue of the collapse of the device, which again assumes the initial cylindrical shape by means of the extension of the structure.
The device is provided in two embodiments: standard and screw-in.
In the standard embodiment, after implantation, the space created in the bone is filled with cement (PMMA).
In the screw-in embodiment, stabilization is performed not by injecting cement but by virtue of the screw 8, which is fixed to the second portion 3, i.e., the distal end, of the device 1.
The device according to the present invention allows, by means of a percutaneous operating technique, to treat even old osteoporotic and traumatic spinal fractures.
According to the present invention, the device, which is provided in a single size, can dilate to the height required to restore the vertebral collapse; the operator can block the dilation once the image intensifier, by means of an X-ray, confirms a satisfactory result.
An important advantage of the present invention is constituted by the possibility to easily remove the device in the intraoperative period, making it return to its closed configuration by means of a dedicated instrument.
The device according to the present invention has a dilation in a substantially vertical direction, without any lateral or circumferential dilation, avoiding the risk of lateral breakthrough.
The device according to the present invention allows to choose the desired degree of dilation or expansion in the intraoperative period without forcing the surgeon to decide beforehand which type of implant to use, as in the case of traditional devices.
The device according to the present invention may also be removed in the intraoperative period.
In practice it has been found that the invention achieves the intended aim and objects.
This application claims the priority of Italian Patent Application No. GE2010A000144, filed on December 29, 2010, the subject matter of which is incorporated herein by reference.
Claims
1. A percutaneous device for treating spinal fractures, characterized in that it comprises a substantially cylindrical body, said cylindrical body being pre-cut so as to form a first end portion connected to a second end portion by a central dilatable portion; said central dilatable portion being constituted by two identical members, each of said identical members being constituted by a central body associated with said end portions by means of shaped bars; said bars having ends that are deformable along lines which are all mutually substantially parallel; said central bodies being movable between a closed position and a dilated position on a single vertical plane.
2. The device according to claim 1 , characterized in that said shaped bars comprise an inner bar and an outer bar.
3. The device according to claim 1 or 2, characterized in that said second portion comprises an internal thread engaging the end of a screw; said screw having a head that engages said first portion.
4. The device according to one or more of the preceding claims, characterized in that said pre-cut cylindrical body is made of titanium alloy and has a diameter, in the dilated position, which is more than three times the diameter in the closed position.
5. The device according to one or more of the preceding claims, characterized in that it comprises a dedicated instrument for inserting said device inside the vertebral body and for dilating it.
6. The device according to one or more of the preceding claims, characterized in that it comprises a dedicated instrument for removing the device, in the intraoperative period, by collapsing or closing said device, which assumes the initial cylindrical shape by extension of the structure.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITGE2010A000144A IT1403237B1 (en) | 2010-12-29 | 2010-12-29 | PERCUTANEOUS DEVICE FOR TREATING VERTEBRAL FRACTURES |
ITGE2010A000144 | 2010-12-29 |
Publications (1)
Publication Number | Publication Date |
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WO2012089317A1 true WO2012089317A1 (en) | 2012-07-05 |
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ID=43736863
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2011/006441 WO2012089317A1 (en) | 2010-12-29 | 2011-12-20 | Percutaneous device for treating spinal fractures |
Country Status (2)
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IT (1) | IT1403237B1 (en) |
WO (1) | WO2012089317A1 (en) |
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JP2014097306A (en) * | 2012-11-13 | 2014-05-29 | Chang Gung Univ | Apparatus for strengthening bones and tool for mounting the apparatus |
US9295562B2 (en) | 2008-01-17 | 2016-03-29 | DePuy Synthes Products, Inc. | Expandable intervertebral implant and associated method of manufacturing the same |
US9320615B2 (en) | 2010-06-29 | 2016-04-26 | DePuy Synthes Products, Inc. | Distractible intervertebral implant |
US9402737B2 (en) | 2007-06-26 | 2016-08-02 | DePuy Synthes Products, Inc. | Highly lordosed fusion cage |
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US9750552B2 (en) | 2009-07-06 | 2017-09-05 | DePuy Synthes Products, Inc. | Expandable fixation assemblies |
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US9993349B2 (en) | 2002-06-27 | 2018-06-12 | DePuy Synthes Products, Inc. | Intervertebral disc |
US10390963B2 (en) | 2006-12-07 | 2019-08-27 | DePuy Synthes Products, Inc. | Intervertebral implant |
US10398563B2 (en) | 2017-05-08 | 2019-09-03 | Medos International Sarl | Expandable cage |
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