WO1993012724A1 - Dispositif a fibre optique destine a la reparation des fibres nerveuses lesees - Google Patents
Dispositif a fibre optique destine a la reparation des fibres nerveuses lesees Download PDFInfo
- Publication number
- WO1993012724A1 WO1993012724A1 PCT/FR1992/001244 FR9201244W WO9312724A1 WO 1993012724 A1 WO1993012724 A1 WO 1993012724A1 FR 9201244 W FR9201244 W FR 9201244W WO 9312724 A1 WO9312724 A1 WO 9312724A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- nerve
- optical fiber
- sleeve
- fiber
- fibers
- Prior art date
Links
- 239000013307 optical fiber Substances 0.000 title claims abstract description 38
- 210000005036 nerve Anatomy 0.000 title abstract description 14
- 230000008439 repair process Effects 0.000 title description 3
- 210000004126 nerve fiber Anatomy 0.000 claims description 38
- 229920004934 Dacron® Polymers 0.000 claims description 3
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 3
- 230000000926 neurological effect Effects 0.000 abstract description 8
- 210000000278 spinal cord Anatomy 0.000 abstract description 7
- 230000003287 optical effect Effects 0.000 abstract description 5
- 239000000835 fiber Substances 0.000 description 16
- 230000003902 lesion Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 210000004556 brain Anatomy 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 230000000243 photosynthetic effect Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 206010033799 Paralysis Diseases 0.000 description 2
- 206010033892 Paraplegia Diseases 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 230000005693 optoelectronics Effects 0.000 description 2
- 210000000578 peripheral nerve Anatomy 0.000 description 2
- 230000035479 physiological effects, processes and functions Effects 0.000 description 2
- 230000001902 propagating effect Effects 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- -1 silver halides Chemical class 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 206010010356 Congenital anomaly Diseases 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 206010029174 Nerve compression Diseases 0.000 description 1
- 208000008765 Sciatica Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 210000003484 anatomy Anatomy 0.000 description 1
- 210000003461 brachial plexus Anatomy 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000007831 electrophysiology Effects 0.000 description 1
- 238000002001 electrophysiology Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000004941 influx Effects 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002406 microsurgery Methods 0.000 description 1
- 230000007659 motor function Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000005622 photoelectricity Effects 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000003016 quadriplegic effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 210000003594 spinal ganglia Anatomy 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/11—Surgical instruments, devices or methods for performing anastomosis; Buttons for anastomosis
- A61B17/1128—Surgical instruments, devices or methods for performing anastomosis; Buttons for anastomosis of nerves
Definitions
- Fiber optic device for repairing damaged nerve fibers
- the present invention relates to a fiber optic device (s) intended for the repair of damaged nerve fibers in human organisms.
- the intervention must be very early.
- the nerve fiber lesions are older or of a different nature than the blunt-tearing, crushing section - attempts at suturing are often unsuccessful.
- this electrical stimulation cannot recreate the junction between the nervous centers and the periphery because it can in no way correspond to a physiological message.
- the solution consists in restoring the relationships and messages between the nerve centers or the brain and the periphery. It suffices to insert a simple mechanism at the level of the damaged nerve fibers in order to reinstate a physiological conduction which is mainly motor and probably also sensitive.
- the restoration of the physiological conduction of the nerve impulse can be carried out by a method of connection or even an exogenous neurological bypass thanks to the interposition of a simple conducting mechanism, in place of the injured part of the nerve fiber in the cases of unitary, radicular or trunk lesions, or of nerve fibers in the case of plurifocal lesions of a nervous plexus and especially of the fibers of the spinal cord.
- This photosynthetic theory concerns all the cells and tissues of the organism, both on the physiology and cell biology scale.
- this theory leads to two particularly important conclusions: the first relates to the birth of nerve impulses; this nerve impulse propagating along the nerve fibers, relayed by the spinal ganglia and reaching the upper nervous centers and the brain is clearly demonstrated by electrophysiology experiments. All books on physiology and medical biophysics are Agree to conclude that the nerve impulses are transmitted electrically along the nerve fibers, but the problem of the birth of this nerve impulse remains a mystery.
- the birth of nerve impulses can be explained by a mechanism of photoelectricity and photoconductivity.
- the nerve fiber is the perfect analog of an optical fiber.
- the nervous system by its complexity and its extreme degree of performance has often been compared to a telephone system. It would in fact be a cable telecommunications network, the cabling consisting of optical fibers which we know can carry, in particular when they correspond to the wavelength of the infrared, thousands or even millions. information simultaneously.
- the comparative anatomy of the nerve fiber and an optical fiber therefore leads to the notion of an almost perfect structural equivalence, a simple reminder of the physics of light then allows to broaden the notion of nerve impulse in its informative component.
- Light whether wave or corpuscular, decomposes in the direction of its propagation according to a triple field equivalent to a trihedron: a light field accompanied by an electric field and a magnetic field, these three fields propagating along of three perpendicular plants to one another .
- the perfect complementarity of these three energy components leads to formulate the hypothesis according to which these three fields are inseparable. It is well known that an electric field induces a magnetic field and vice versa. It is also known that electronic agitation generates photons.
- the nerve impulse would not be a purely electrical conduction but makes it an optoelectronic and incidentally magnetic conduction.
- the present invention provides a solution to this problem and proposes to reconstitute the light of the nerve fiber by interposition, at the level of the lesion, of an optical fiber.
- fiber optic device at the level of the nerve fibers makes it possible to hope not only for the rehabilitation of motor function, even sensitivity, but also in the direction of physiological continuity by allowing information to be taken up. between the brain or nerve centers and the periphery.
- the device according to the invention intended for neurological bypass comprises two versions depending on whether the bypass involves a nerve fiber or the spinal cord.
- the description which follows concerns first of all the first version which aims at bridging a single nerve fiber.
- the device consists of a cylindrical sleeve inside which is the fiber optics to be inserted at the proximal and distal ends of the injured nerve fiber; this optical fiber, of length greater than that of the sleeve, is held in place inside the sleeve by means of two removable solid plugs, pierced in their center with a hole intended to receive and protect the ends of the fiber optical.
- the cylindrical sleeve further comprises at each of its ends two open articulated arms, semi-cylindrical, the articulation being ensured by an area of lesser thickness.
- These two articulated arms - semicylindrical - can be closed at the end of the intervention in order to sheath on both sides the terminal parts of the bridged nerve fiber, the central cylindrical sleeve covering the bridging itself, ie optical fiber.
- the closure of the two articulated arms can be ensured by an asynchronous oppositional toothing system, the final compression being able to be obtained by a gluing system.
- the optical fiber carried by the apparatus will advantageously have a diameter just smaller than that of the nerve fiber into which it will be introduced.
- the cylindrical sleeve will advantageously have a diameter slightly greater than the nerve fiber to be bridged. In this way as soon as the two ends of the optical fiber are inserted into the two ends of the nerve fiber, the sleeve can slide along the latter so that a possible fascial suture joins the ends of the fibers around the optical fiber. nervous that might break apart due to their retractability. Once the suture has been performed, the sleeve covers the optical fiber and the articulated arms are closed at each end in order to cover the distal and proximal parts of the nerve fiber.
- the variant of the device described uses the same apparatus which, instead of a single optical fiber, will comprise between the two plugs several tens of these same fibers.
- the same process can thus be applied to the spinal cord with the only difference being the reinsertion of multiple optical fibers.
- the diameter of the cylindrical sleeve is slightly greater than the diameter of the cord.
- Figure 1 shows, in section, the device according to the invention in its first version with an optical fiber.
- Figures 2 and 3 show, in section, the main bridging times.
- the optical fiber is fixed in the two ends of the nerve fiber and the cylindrical sleeve has been moved laterally on the nerve fiber in order to practice a possible suture of the two ends.
- FIG. 4 shows the coaptative toothing closure of the two articulated arms. a collage can permanently secure these two articulated arms which will thus reconstitute a sheathing tunnel.
- FIG. 5 represents, in section, the variant of the device of FIG. 1. its only difference is to include several tens of optical fibers.
- the device represented in FIG. 1 comprises a cylindrical sleeve (1) the lumen of which is closed at both ends by a removable plug (2) and (2 *), carrying a hole (3) and (3 ') now in places the optical fiber (4), the free ends of the cylindrical sleeve (1) comprise on both sides two articulated arms (5, 5 ') and (6, 6') whose lower right part is toothed (7) .
- each end of the optical fiber 4 will be inserted into each of the two ends of the nerve fiber 9 and 9 ′ as shown in FIGS. 2 and 3.
- the device shown in FIG. 5 is a variant with several optical fibers of the device shown in FIG. 1. The main difference will therefore lie in the removable plugs holding the optical fibers in place and which must have several holes in this variant.
- All of the component parts of the unitary device or its variant can be produced on an industrial scale.
- the ends of the optical fiber may also be butted at each end of the nerve fiber, that is to say without there being insertion of the optical fiber into the nerve fiber. such a possibility could thus be implemented according to the diagram in FIG. 6.
- a sleeve provided with articulated and toothed arms, as described above can advantageously be used to hold together the optical fiber-nerve fiber assembly and ensure the abutment.
- the main part of the device which includes the sleeve and the four articulated arms can be made in .dacron in a single molding operation.
- the removable caps can also be made of dacron.
- the optical fiber it will preferably be made of flexible material. It will operate preferentially in the range of 1 • infrared.
- the material composing it can be any material having the physical characteristics of optical and biocompatible fibers. It is preferably flexible glass.
- the preferred optical fibers are fibers made of silica dioxide, fibers monocrystalline based on sodium chloride and polycrystalline fibers based on silver halides or thallium halides.
- the diameter of the optical fibers will depend on that of the nerve fibers which one wishes to bridge.
- optical fibers will advantageously be full but may also be in the form of a hollow cylinder.
Landscapes
- Health & Medical Sciences (AREA)
- Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medical Informatics (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Neurology (AREA)
- Molecular Biology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Radiation-Therapy Devices (AREA)
- Prostheses (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Electrotherapy Devices (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP93911659A EP0619721A1 (fr) | 1991-12-30 | 1992-12-30 | Dispositif a fibre optique destine a la reparation des fibres nerveuses lesees |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR91/16465 | 1991-12-30 | ||
FR9116465A FR2685628B1 (fr) | 1991-12-30 | 1991-12-30 | Dispositif a fibre(s) optique(s) destine a la reparation des fibres nerveuses lesees. |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993012724A1 true WO1993012724A1 (fr) | 1993-07-08 |
Family
ID=9420779
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR1992/001244 WO1993012724A1 (fr) | 1991-12-30 | 1992-12-30 | Dispositif a fibre optique destine a la reparation des fibres nerveuses lesees |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0619721A1 (fr) |
AU (1) | AU3455193A (fr) |
CA (1) | CA2127118A1 (fr) |
FR (1) | FR2685628B1 (fr) |
WO (1) | WO1993012724A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7076292B2 (en) | 2002-04-25 | 2006-07-11 | Medtronic, Inc. | Optical communication of neurostimulation-system information |
US7147647B2 (en) | 2002-04-26 | 2006-12-12 | Medtronic, Inc. | Sintered titanium tube for the management of spinal cord injury |
JP2015061604A (ja) * | 2009-03-10 | 2015-04-02 | ザ ジョーンズ ホプキンズ ユニバーシティThe Johns Hopkins University | 生物学的組織結合及び修復装置及びその使用方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3833002A (en) * | 1973-09-10 | 1974-09-03 | J Palma | Apparatus for aiding severed nerves to join |
US4412825A (en) * | 1981-09-17 | 1983-11-01 | Tokarz Richard D | Medical entry connector for teeth bearing animals |
US4432363A (en) * | 1980-01-31 | 1984-02-21 | Tokyo Shibaura Denki Kabushiki Kaisha | Apparatus for transmitting energy to a device implanted in a living body |
US4534349A (en) * | 1983-02-02 | 1985-08-13 | Minnesota Mining And Manufacturing Company | Absorbable sutureless nerve repair device |
US4863668A (en) * | 1988-09-22 | 1989-09-05 | University Of Utah | Method of forming fibrin-collagen nerve and body tissue repair material |
-
1991
- 1991-12-30 FR FR9116465A patent/FR2685628B1/fr not_active Expired - Fee Related
-
1992
- 1992-12-30 CA CA 2127118 patent/CA2127118A1/fr not_active Abandoned
- 1992-12-30 WO PCT/FR1992/001244 patent/WO1993012724A1/fr not_active Application Discontinuation
- 1992-12-30 EP EP93911659A patent/EP0619721A1/fr not_active Withdrawn
- 1992-12-30 AU AU34551/93A patent/AU3455193A/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3833002A (en) * | 1973-09-10 | 1974-09-03 | J Palma | Apparatus for aiding severed nerves to join |
US4432363A (en) * | 1980-01-31 | 1984-02-21 | Tokyo Shibaura Denki Kabushiki Kaisha | Apparatus for transmitting energy to a device implanted in a living body |
US4412825A (en) * | 1981-09-17 | 1983-11-01 | Tokarz Richard D | Medical entry connector for teeth bearing animals |
US4534349A (en) * | 1983-02-02 | 1985-08-13 | Minnesota Mining And Manufacturing Company | Absorbable sutureless nerve repair device |
US4863668A (en) * | 1988-09-22 | 1989-09-05 | University Of Utah | Method of forming fibrin-collagen nerve and body tissue repair material |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7076292B2 (en) | 2002-04-25 | 2006-07-11 | Medtronic, Inc. | Optical communication of neurostimulation-system information |
US7865246B2 (en) | 2002-04-25 | 2011-01-04 | Medtronic, Inc. | Optical communication of neurostimulation-system information |
US7147647B2 (en) | 2002-04-26 | 2006-12-12 | Medtronic, Inc. | Sintered titanium tube for the management of spinal cord injury |
JP2015061604A (ja) * | 2009-03-10 | 2015-04-02 | ザ ジョーンズ ホプキンズ ユニバーシティThe Johns Hopkins University | 生物学的組織結合及び修復装置及びその使用方法 |
US9539009B2 (en) | 2009-03-10 | 2017-01-10 | The Johns Hopkins University | Biological tissue connection and repair devices and methods of using same |
Also Published As
Publication number | Publication date |
---|---|
CA2127118A1 (fr) | 1993-07-08 |
EP0619721A1 (fr) | 1994-10-19 |
FR2685628B1 (fr) | 1994-02-11 |
FR2685628A1 (fr) | 1993-07-02 |
AU3455193A (en) | 1993-07-28 |
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