EP3793475A1 - Method for producing bite splints - Google Patents
Method for producing bite splintsInfo
- Publication number
- EP3793475A1 EP3793475A1 EP19723825.6A EP19723825A EP3793475A1 EP 3793475 A1 EP3793475 A1 EP 3793475A1 EP 19723825 A EP19723825 A EP 19723825A EP 3793475 A1 EP3793475 A1 EP 3793475A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- bite
- positions
- patient
- splints
- jaw
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 238000000034 method Methods 0.000 claims abstract description 82
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 59
- 238000011282 treatment Methods 0.000 claims abstract description 45
- 210000000056 organ Anatomy 0.000 claims abstract description 36
- 201000010099 disease Diseases 0.000 claims abstract description 34
- 230000004064 dysfunction Effects 0.000 claims abstract description 29
- 210000000515 tooth Anatomy 0.000 claims description 79
- 230000036544 posture Effects 0.000 claims description 53
- 230000003068 static effect Effects 0.000 claims description 38
- 230000001055 chewing effect Effects 0.000 claims description 35
- 210000001738 temporomandibular joint Anatomy 0.000 claims description 33
- FGUUSXIOTUKUDN-IBGZPJMESA-N C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 Chemical compound C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 FGUUSXIOTUKUDN-IBGZPJMESA-N 0.000 claims description 29
- GNFTZDOKVXKIBK-UHFFFAOYSA-N 3-(2-methoxyethoxy)benzohydrazide Chemical compound COCCOC1=CC=CC(C(=O)NN)=C1 GNFTZDOKVXKIBK-UHFFFAOYSA-N 0.000 claims description 28
- 230000033001 locomotion Effects 0.000 claims description 13
- 230000001225 therapeutic effect Effects 0.000 claims description 11
- 230000008901 benefit Effects 0.000 claims description 7
- 230000000399 orthopedic effect Effects 0.000 claims description 6
- 230000035807 sensation Effects 0.000 claims description 5
- 230000037361 pathway Effects 0.000 claims description 3
- 238000004364 calculation method Methods 0.000 claims description 2
- 210000004907 gland Anatomy 0.000 claims 1
- 230000018984 mastication Effects 0.000 abstract 1
- 238000010077 mastication Methods 0.000 abstract 1
- 210000001847 jaw Anatomy 0.000 description 71
- 210000003128 head Anatomy 0.000 description 32
- 208000035475 disorder Diseases 0.000 description 20
- 238000002560 therapeutic procedure Methods 0.000 description 18
- 201000005973 campomelic dysplasia Diseases 0.000 description 15
- 201000006815 congenital muscular dystrophy Diseases 0.000 description 15
- 208000019484 coronary microvascular disease Diseases 0.000 description 15
- 238000003384 imaging method Methods 0.000 description 9
- 241000282465 Canis Species 0.000 description 7
- 208000024891 symptom Diseases 0.000 description 7
- 230000008569 process Effects 0.000 description 6
- 238000013459 approach Methods 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 238000004590 computer program Methods 0.000 description 5
- 210000003205 muscle Anatomy 0.000 description 5
- 230000006978 adaptation Effects 0.000 description 4
- 206010006514 bruxism Diseases 0.000 description 4
- 238000002591 computed tomography Methods 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 210000004373 mandible Anatomy 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000001575 pathological effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 208000012639 Balance disease Diseases 0.000 description 3
- 208000009205 Tinnitus Diseases 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 210000000845 cartilage Anatomy 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 210000003041 ligament Anatomy 0.000 description 3
- 238000002595 magnetic resonance imaging Methods 0.000 description 3
- 210000002050 maxilla Anatomy 0.000 description 3
- 230000003387 muscular Effects 0.000 description 3
- 210000002346 musculoskeletal system Anatomy 0.000 description 3
- 230000036961 partial effect Effects 0.000 description 3
- 238000000554 physical therapy Methods 0.000 description 3
- 231100000886 tinnitus Toxicity 0.000 description 3
- 238000003325 tomography Methods 0.000 description 3
- 206010047571 Visual impairment Diseases 0.000 description 2
- 210000003484 anatomy Anatomy 0.000 description 2
- 230000002146 bilateral effect Effects 0.000 description 2
- 230000017531 blood circulation Effects 0.000 description 2
- 210000004556 brain Anatomy 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- 238000002219 manual therapy Methods 0.000 description 2
- 210000003784 masticatory muscle Anatomy 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 210000000214 mouth Anatomy 0.000 description 2
- 210000004237 neck muscle Anatomy 0.000 description 2
- 230000000422 nocturnal effect Effects 0.000 description 2
- 238000002611 posturography Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 230000011514 reflex Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 210000003625 skull Anatomy 0.000 description 2
- 238000002630 speech therapy Methods 0.000 description 2
- 230000002123 temporal effect Effects 0.000 description 2
- 238000010146 3D printing Methods 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- 208000020084 Bone disease Diseases 0.000 description 1
- 206010052804 Drug tolerance Diseases 0.000 description 1
- 206010014020 Ear pain Diseases 0.000 description 1
- 241000283073 Equus caballus Species 0.000 description 1
- 206010016059 Facial pain Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 206010061274 Malocclusion Diseases 0.000 description 1
- 206010049816 Muscle tightness Diseases 0.000 description 1
- 208000025747 Rheumatic disease Diseases 0.000 description 1
- 206010041235 Snoring Diseases 0.000 description 1
- 208000008312 Tooth Loss Diseases 0.000 description 1
- 208000012886 Vertigo Diseases 0.000 description 1
- 241000596212 Vulpes lagopus Species 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 208000008784 apnea Diseases 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 230000001364 causal effect Effects 0.000 description 1
- 238000009232 chiropractic Methods 0.000 description 1
- 230000001447 compensatory effect Effects 0.000 description 1
- 238000011960 computer-aided design Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011982 device technology Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 230000026781 habituation Effects 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 210000002414 leg Anatomy 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 230000002232 neuromuscular Effects 0.000 description 1
- 230000004768 organ dysfunction Effects 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 230000001144 postural effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 206010039722 scoliosis Diseases 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 208000019116 sleep disease Diseases 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 230000009747 swallowing Effects 0.000 description 1
- 210000003582 temporal bone Anatomy 0.000 description 1
- 210000002435 tendon Anatomy 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 231100000889 vertigo Toxicity 0.000 description 1
- 230000001720 vestibular Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
- A61C13/00—Dental prostheses; Making same
- A61C13/0003—Making bridge-work, inlays, implants or the like
- A61C13/0004—Computer-assisted sizing or machining of dental prostheses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
- A61C19/00—Dental auxiliary appliances
- A61C19/04—Measuring instruments specially adapted for dentistry
- A61C19/05—Measuring instruments specially adapted for dentistry for determining occlusion
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
- A61C9/00—Impression cups, i.e. impression trays; Impression methods
- A61C9/004—Means or methods for taking digitized impressions
- A61C9/0046—Data acquisition means or methods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices ; Anti-rape devices
- A61F5/56—Devices for preventing snoring
- A61F5/566—Intra-oral devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices ; Anti-rape devices
- A61F5/56—Devices for preventing snoring
- A61F2005/563—Anti-bruxisme
Definitions
- the present invention relates to a method for producing occlusal splints and follow-on splints for use in the treatment of a patient with at least one disease resulting from a functional disorder of the chewing organ, in particular craniomandibular dysfunctions, as well as bite splints and subsequent bite splints be prepared by this method.
- CMD craniomandibular dysfunction
- cranium cranium
- Mandibula Lower jaw
- myoarthropathy myoarthropathy
- a temporomandibular joint essentially consists of a condyle (condyle with caput mandibulae) of the lower jaw, which is movably arranged in a fossa (Fossa articularis) of the temporal bone.
- the lower jaw is suspended by a complex system of cartilage, muscles and ligaments, especially the bilaminar zone on the skull, whereby the position of the temporomandibular joint and the occlusion, i. the final bite of the teeth of the upper and lower jaw, influence each other in statics and dynamics.
- An ideal occlusion is when the teeth are in a physiological position and the jaw can maintain its physiological position.
- the Kaumuskellage is essentially involved in the head posture in statics and dynamics.
- the head posture in turn has a significant influence on the entire posture. This often results in interactions of the muscular mass with the appendage in the neck area, while the latter interacts with the entire body statics.
- the frequently occurring craniomandibular dysfunction is a pathological and thus non-physiological position of the condyle in the joint pit and a concomitant over- or Friedbelastung the entire anatomical structures involved, such as ligaments, cartilage, muscles, teeth and temporomandibular joints.
- this leads to painful tension in the masticatory muscles leading to permanent damage to ligaments, tendons and cartilage and to the destruction of bony structures involved.
- Symptoms of CMD include headache, ear or face pain, as well as nocturnal crunching and grinding of the teeth.
- CMD bite splints hereinafter also referred to as a splint or dental splint
- the aim of the use of such Aufbiss rails is to prevent the patient from a pathological occlusion and / or chewing or wean him.
- This is intended to at least partially eliminate the over- and underloading of the teeth and temporomandibular joints, which generally leads to improved positioning of the temporomandibular joints and relaxation of the jaw musculature. This can reduce inflammation, remodel bone structures and recalibrate the musculoskeletal system.
- bite rails with unadjusted i. occlusal surface not adapted to the chewing profile of the patient
- bite rails with adjusted occlusal surfaces may cover parts of the row of teeth (individual teeth) or extend over all the teeth of a jaw.
- the prior art discloses various bite splints for the treatment of craniandibular dysfunction and corresponding methods for producing such bite splints.
- the utility model DE202004020196 U1 describes a maxillary bite splint with a receiving area for maxillary teeth as well as with a lower side directed towards the lower jaw teeth in the inserted state of the bite splint, wherein the underside of the bite splint in the anterior region is formed as a plateau (anterior splint splint plateau). which prevents the complete closing of the jaws, ie leaves the jaw in a slightly open state.
- the receiving area for the maxillary teeth is designed such that the plateau forms an angle in the range of 0 ° to 10 ° or, in another embodiment, an angle in the range of 5 ° to 30 ° with the occlusal plane in the inserted state of the bite splint.
- the rails have no canine guidance and posterior contacts.
- the easy opening of the temporomandibular joints and the missing canine guidance and posterior contacts are intended to restore the physiological center of the temporomandibular joints (CR position) and to achieve a neuromuscular relaxation of the temporomandibular joints and jaw musculature.
- the utility model DE202009003999 U1 describes a bite splint for the upper or lower jaw, consisting of a base plate with precisely fitting tooth support elements, wherein the tooth support elements have a first surface, which is occlusally adapted to the teeth, and have a second surface which is vestibular to the second Plane and ensure posterior guidance, and where In the case of the tooth support elements, a cranial concave dome shape is overall present.
- the bite splints may also have compensating elements which allow adaptation of the occlusion during the treatment of a patient with CMD via the course of the therapy.
- DE1020131 12032A1 describes a method of constructing an adjusted bite splint for use in treating a patient having at least one craniomandibular dysfunction from an existing bite splint.
- This method includes the computer-assisted steps of acquiring data to uniquely define a shape of the existing bite splint, an actual morphology of the teeth of the second jaw, and a location of the second jaw, the contact area of the existing bite splint, and patient's temporomandibular joints relative to each other; Simulating an occlusion of a patient's craniomandibular system comprising the existing bite splint inserted into the patient; Identifying spurious contacts between the contact area of the existing bite rail and the teeth of the second jaw; and constructing the adjusted bite bar from the acquired data and data obtained from the simulation such that the identified interfering contacts are eliminated. Furthermore, it is proposed to repeat the above-mentioned steps in order to construct a series of bite splints for iter
- the prior art methods of making occlusal splints for treating CMD typically start from an ideal bite position, i. a bite position with a dental-defined occlusion, position of the lower jaw or the rod ends as well as a tooth-defined muscular posture.
- This "ideal bite position” generally refers to the physiological bite position, which is also referred to as a centric condylar position or “centric relation position” (CR position) or as a “stable condyle position” (SCP).
- the ideal (physiological) bite position may change over the period of treatment of the chewing organ dysfunction.
- the ideal bite position can vary depending on the head and body postures or the patient's body position (eg standing, lying, sitting) and whether the patient is in a resting position or in motion (statics versus dynamics), ie Depending on the individual application areas of the bite splints by the patient, several ideal bite positions may exist.
- the inventive method is characterized in particular by the fact that due to the consideration of several bite positions bite splint (s), which largely eliminate or at least reduce the complaints of the patient, can be found faster and more effectively.
- bite splint due to the consideration of several bite positions bite splint (s), which largely eliminate or at least reduce the complaints of the patient, can be found faster and more effectively.
- the consideration of different patient-specific head and body postures or body positions in statics as well as in dynamics also makes it possible to treat the CMD specifically tailored to the individual needs of the patient.
- the result of the treatment can be further improved, i. the patient's complaints are reduced even more efficiently and far-reaching.
- the bite splints can be produced inexpensively and reproducibly with the method according to the invention.
- the present invention relates to a method of making occlusal splints for use in the treatment of a patient having at least one disease, starting from a functional disturbance of the chewing organ, in particular cranio-mandibular dysfunctions, comprising the following steps: a) gathering data on the position of the jaws, the temporomandibular joints, the movement paths of the lower jaw and the current morphology of the patient's teeth (starting point); State),
- step c) computer-assisted merging of the data acquired in step a) (initial state) and the bite positions (target states To) determined in step b) for calculating in each case a temporary model of a bite rail for two or more than two of the steps in step b ) certain bite positions,
- step d) Generation of one bite splint each for two or more than two of the bite positions determined in step b), based on the temporal models calculated in step c).
- the invention relates to a method for the production of follow-on bite bars, comprising the steps a) to d) as described above and below, the method additionally comprising the following steps: e) checking the bite positions determined in step b),
- step f) selecting one or more of the bite positions determined in step b) or rejecting all bite positions determined in step b),
- the present invention relates to occlusal splints and follow-on splints for use in the treatment of a patient with at least one disease that results from a functional disorder of the chewing organ, in particular craniomandibular dysfunctions obtainable by a method as described above and below.
- a further aspect of the invention relates to bite splints for use in the treatment of a patient with at least one disease which is based on a functional disorder of the chewing organ, in particular craniomandibular dysfunctions, comprising a receiving area for receiving teeth of a first jaw of the patient and a contact area for Contacting teeth of a second jaw of the patient opposite the first jaw, the at least one receiving area having at least one means for guiding the teeth and being profiled so as to ensure a sufficiently secure hold of the rails even under load, and wherein the contact area is only slightly profiled, characterized that the configuration of the means for guiding the teeth and the profiling of the contact areas of the bite splints and follow bite rails at bite positions with different head and body postures in statics and dynamics oriented, and that the distance of the receiving area or contact area for the first jaw to the receiving area or contact area for the second jaw of the bite splints and subsequent bite splints opposite the first jaw on the therapeutically desired bite increase (jaw opening
- the present invention relates to a set of occlusal splints for use in the treatment of a patient having at least one disease emanating from a functional disorder of the chewing organ, in particular craniomandibular dysfunctions consisting of two or more than two occlusal splints as before and within As defined below, each of these two or more bite splints is used in a different head and posture in statics and dynamics.
- biting off the upper jaw and / or lower jaw designate a means for biting off the upper jaw and / or lower jaw, the at least one receiving area for receiving the teeth of the upper jaw and / or lower jaw and / or at least one contact area for contacting the teeth of the upper jaw and / or the lower jaw.
- a "follow-on bite splint" can actually follow as a replacement for the first splint in the sense of a total replacement of the first splint, for example if the first splint has been modified for therapeutic reasons or had to be completely discarded.
- follow-on bite splint is also used for tracks which follow in production, but which at the same time come into therapeutic use, for example in combinations such as day / night splints, sports / work splints, hard - / soft rails and the like.
- the receiving area of the bite splints and the subsequent bite splints can not be profiled, ie not adapted to the respective tooth morphology (chewing profile) of the patient, slightly profiled, ie slightly or roughly adapted to the respective tooth morphology of the patient, or else strong profiled, ie be fully adapted to the particular tooth morphology of the patient.
- the contact area in turn, can either not be profiled, ie not adapted to the respective tooth morphology (chewing profile) of the patient, so that a complete freedom of movement of the jaws to each other in the maximum contact position remains, or slightly profiled, ie slightly or roughly to the be adapted to the particular tooth morphology of the patient, so that the freedom of movement of the jaw to each other in the final Bite position is restricted.
- occlusion splints such as equilibration rails, reduction rails, vertical rails, decompression rails and protrusion rails; as well as reflex rails, z. B. with bilateral bite or anterior bite.
- the profiling does not represent a form-fitting negative image (impression) of the contact areas of the teeth with the bite splint, but rather that the profiling consists of Surface of the bite splint to extended wells or pits and / or ramps in the contact area of the teeth is (occlusal impressions). In other words, these are smoothed impressions of the contact areas of the teeth.
- the smoothing of the contact areas can be more or less pronounced, depending on how large the desired freedom of movement of the jaw in the final bite position should be.
- the expressions "strongly profiled” or “completely adapted to the dental morphology of the patient” mean that the profiling represents an essentially positive negative impression (impression) of the contact area of the teeth of the patient, which determines the freedom of movement of the jaw in the end Bite severely restricts or even completely inhibits.
- the at least one receiving area for receiving the teeth of the upper jaw and / or lower jaw preferably has a low to strong profiling.
- the at least one receiving area is strongly profiled, i. completely adapted to the respective tooth morphology (chewing profile) of the patient.
- the receiving area may additionally comprise means for guiding the teeth.
- the receiving area has at least one means for guiding the teeth.
- the means for guiding the teeth may, for example, be anterior tooth guidance, canine guidance, group guidance (for example in the case of malocclusions), balanced occlusions (for example in dentures) or posterior guidance and combinations thereof.
- the means for guiding the teeth is preferably selected from a front tooth guide, canine guide and a front canine guide, in particular a front canine guide.
- the contact region has a slight profiling, i. the contact area is slightly or roughly matched to the particular tooth morphology of the patient. This will allow the jaws to be directed to a desired position in the end bite position.
- the bite rails and subsequent bite splints obtainable by the method according to the invention have a receiving area for receiving Teeth of a first jaw of the patient and a contact area for contacting teeth of the first jaw opposite arranged second jaw of the patient.
- the receiving area of these bite splints and subsequent bite splints is profiled in such a way that a sufficiently secure hold of the splints is ensured even under load (eg biting, speaking, bruxism).
- the support of the rails can be improved with conventional holding means (eg button anchors).
- the contact area is preferably slightly or roughly adapted to the particular tooth morphology of the patient.
- these bite rails and follower bite rails preferably have means for guiding the teeth, as defined above, eg a front canine guide.
- the strength of the bite splint or follower splint i.
- the distance of the receiving area or area of contact for the first jaw to the receiving area or contact area for the second jaw opposite the first jaw can vary widely and is based on the extent of the therapeutically desired bite increase through the jaw opening or mouth when needed with or without change of position by eg Protrusion and / or laterotrusion.
- end bite position also referred to as centric occlusion, refers to the end point of the jaw closure movement with maximum multi-point contact of the teeth with the opposing teeth or the material to which the teeth bite.
- both rod ends should sit centrally in the respective joint pits.
- the left and right temporomandibular joint should each be centrically located in their joint pits, the masticatory muscles should have physiological tension and length on both sides, and the rows of teeth in the lateral tooth area should show uniform multi-point contacts on the right and left.
- jaw position refers to a position of the mandible and maxilla with respect to one another, encompassing both physiological and pathologic positions.
- Pathological jaw positions may be primarily or secondarily caused by other disorders, e.g. a malposition of the teeth.
- initial state and "actual state” as used herein refer to the measured or actual anatomical positions of the jaws, temporomandibular joints and the present tooth morphology.
- desired state denotes a desired anatomical position of the jaws, the temporomandibular joints and the present the tooth morphology z. B. corresponds to the physiological state.
- the desired state can be calculated from the anatomical conditions of the patient, for example based on tabular values (eg cephalometric measurements, building material tables, gnatological standard values, etc.) or also determined clinically and empirically as explained below.
- the individual method steps for the production the bite splints and follow-on bite splints are computer-supported, if possible, using suitable computer programs (software) for this purpose.
- a first step of the method according to the invention data on the position of the jaws, temporomandibular joints, trajectories of the lower jaw and the current morphology of the teeth of the patient are recorded.
- three-dimensional imaging method refers to any pictorial representation of a real object in three to four dimensions, e.g. By x, y, z and time coordinates.
- Three-dimensional imaging methods include, for example, three-dimensional X-ray, magnetic resonance tomography or magnetic resonance tomography (MRT), three-dimensional computed tomography (CT) or digital X-ray tomography and / or surface scanning by incident light scanning.
- the image data can be reproduced both analog and digital, e.g.
- three-dimensional imaging method also encompasses superimposing and processing of image data, eg. by means of computer programs such as coDiagnostiX @ (Chemnitz, Germany), Onyx-Ceph (Image Instruments GmbH), 3shape (3Shape, Copenhagen, Denmark) or implant3D (med3D GmbH, Heidelberg, Germany). From the image data, actual values can be measured as coordinates, length, volume and angle dimensions.
- the skilled person has specific methods for describing the positional relationship of the anatomical structures in statics and dynamics (eg, detection of the trajectories of the lower jaw by the occlusion analysis and achsiographic examination methods), which make up for the temporomandibular joints and the temporomandibular joints Trajectories of the mandible relevant biomechanical parameters, such as the hinge axis, centric, Kondylenbahnne Trent, Bennett angle or Bennett movement can be determined.
- step a) serve as the basis for the construction of the bite rail and follow-on bite bar according to the method of the invention. From this it is possible to calculate the parameters that are essential for the therapy, which must be taken into account in the construction of the splints, such as the material thickness, type of material, surface structure in adaptation to the jaw position in statics and dynamics and the like. For subsequent rails, the exact metric change required can be calculated from the output rail (initial rail).
- step a) of the method according to the invention is additionally recorded in step a) of the method according to the invention by means of the methods described above. These data are taken into account in the design of the new bite bars and follower bite bars.
- two or more than two different bite positions of the patient are determined, whereby the bite positions are determined with different head and body postures in statics and dynamics.
- bite position or “therapeutic bite position”, which are used interchangeably here, refer to a disease relevant for the therapy of the disease (in particular craniomandibular dysfunctions) resulting from a functional disorder of the chewing organ. potentially / presumably relevant position of the maxilla and mandible relative to each other.
- the bite position thus represents a desired state, ie, a desired anatomical position of the jaws and temporomandibular joints.
- bite position as used herein is to be distinguished from the term “ideal bite position” as defined above.
- the bite positions determined in step b) can contain the ideal (physiological) bite position, but also include other bite positions, which generally differ from the ideal bite position. For example, due to different body positions and body positions in statics and dynamics and / or by the inclusion of examination findings from different from orthodontics medical areas.
- bite positions relevant for the therapy of the disease resulting from a functional disorder of the chewing organ can take place in various ways.
- the determination of the bite positions relevant to a disease that results from a functional disorder of the chewing organ takes place in step b) using the methods described above under step a), and via further empirical and clinical methods.
- the determination of the bite position is made for the body positions that are relevant for the patient, i.e. in different head and body postures in statics as well as dynamics (such as standing, sitting, lying but also running, walking, etc.).
- body positions that are relevant for the patient, i.e. in different head and body postures in statics as well as dynamics (such as standing, sitting, lying but also running, walking, etc.).
- MRI magnetic resonance imaging
- different bite positions can be determined, which from an anatomical or biomechanical point of view should have positive effects on the patient's complaints (for example relief of inflammatory areas, sufficiently large temporomandibular joint width, etc.).
- step a further empirical and clinical methods can be used to determine the relevant bite positions.
- the determination of the bite positions is carried out, for example, by inserting spacers or partial rails between the upper and lower jaw, support partial rails, which can possibly be slipped over (any) existing initial rail (s) for a short time, or with the aid of (bite). Registrations that temporarily fix the jaws in a specific position that at least partially reduces patient discomfort.
- This empirical determination also takes place in the case of different head and body postures or at different body positions in statics and dynamics (such as standing, sitting, lying, but also running, walking, etc.).
- This empirical and clinical determination of the bite position is particularly suitable for complaints or symptoms that can be after an at least partial correction of the cause quickly, eg within a few minutes to a few hours, diminish or largely disappear and are objectively measurable.
- These complaints or symptoms may be, for example, the following symptoms: Balance disorders, such as vertigo, caused by the interaction of the collarbone group with the neck muscles and cervical spine load, which are objectively determined by measuring and analyzing body fluctuations, eg with posturography equipment (eg the Tetraax posturography machine from BeamMed Ltd., Israel) to let;
- Muscle tension such as tension in the muscles of the muscles, neck or back muscles, which can be objectively determined by measurements of muscle tone.
- the determination of the bite positions in step b) therefore takes place with inclusion of one or more examination findings from medical fields that are different from orthodontics.
- osteopathic whole body findings can be used to determine the bite position relevant for the treatment of the functional disease of the chewing organ. be involved.
- the osteopathic view of favorable overall body posture are recorded while controlling the jaw.
- one or more bite positions can be ascertained.
- the optimal jaw position for total body posture determined from the osteopathic point of view is registered and included in the determination of the bite positions relevant for the therapy of the functional disease of the chewing organ.
- whole body orthopedic findings can be included in the determination of the bite positions relevant for the treatment of the functional disease of the chewing organ.
- the orthopedic whole body findings for example by means of treadmill analysis, analysis of posture such as with the Diers device technology or by means of X-ray, CT, MRI, recorded while controlling the jaw.
- relevant conditions for the total body posture such as joint and postural changes in the context of rheumatic diseases, foot vaulting disorders, spinal column deficiencies and the like, as well as planned and / or existing therapies or interventions, such as, for example, the construction of shoe inserts, planning of posture when inserting artificial joints or scoliosis therapy included.
- the optimal jaw position for total body posture determined from an orthopedic point of view is registered and included in the determination of the bite positions relevant for the treatment of the functional disease of the masticatory organ.
- ENT whole body findings can be included in the determination of the bite positions relevant for the treatment of the functional disease of the chewing organ.
- the interaction between the functional disease of the chewing organ and the ENT medical area often results in the above-mentioned symptoms or symptoms such as tinnitus, blood flow noise or balance disorders.
- the ENT whole-body findings are recorded, while the jaw position is checked.
- the optimum jaw position determined from the ENT-medical point of view is registered and included in the determination of the bite positions relevant for the therapy of the functional disease of the chewing organ.
- the registration of the jaw position can be achieved by conventional dental methods for producing impressions by means of registries, such as waxes, silicone bites (for example of vinylpolysiloxane), fast-curing polymer foams and the like.
- registries such as waxes, silicone bites (for example of vinylpolysiloxane), fast-curing polymer foams and the like.
- three-dimensional imaging methods as defined above, can also be used.
- surface rastering of the oral cavity by incident light scanning be used for registration of the jaw position.
- the above methods of determining the relevant bite positions can be combined as desired.
- the ideal bite position which has been determined from a biomechanical point of view, and which has been determined by means of imaging methods, can be combined with empirically and clinically determined bite positions from a medical range different from orthodontics.
- the bite positions relevant for the therapy of the functional disease of the chewing organ are calculated from the data acquired in step a), such as, for example, cranial CT, DVT, MRT. It is not necessarily assumed that a very specific ideal bite position, which usually corresponds to the biomechanically ideal bite position, exists, but rather on the basis of various medical assumptions (eg about the height of the bite splint or the form of the impressions) For example, based on the experience of the treating physician, several possible bite positions relevant to the therapy are calculated exclusively. Also in this second embodiment of the method according to the invention different head and body postures or different body positions are taken into account.
- the particular bite positions thus determined in step b) of the present invention represent a bite library of the patient.
- Each individual bite position from this bite library determined for a specific head and body posture in terms of statics and dynamics can be used as a starting point for the production of an or several Aufbissschie- nen be used for a particular purpose.
- further bite positions from this bite library which were determined in statics and dynamics for head and body postures deviating therefrom, can be used to produce so-called "companion rails" for further purposes or to produce a set of bite splints for respectively different ones Uses (day rail, night rail, work rail, sports rail, etc.) can be used.
- the computer-assisted merging of the data acquired in step a) and the bite positions determined in step b) takes place for calculating a temporary model of a bite rail for two or more more than two of the bite positions determined in step b).
- the data acquired in step a) and the bite positions determined in step b) are depicted using suitable computer software.
- suitable computer software In principle, all programs with which three-dimensional (image) data can be processed, ie displayed, processed and calculated, such as, for example, programs for computer-aided design or computer-aided manufacturing (CAD / CAM - Programs).
- CAD / CAM - Programs programs for computer-aided design or computer-aided manufacturing
- the teeth of the patient and motion paths or movement clouds of the lower jaw (initial state) and the determined in step b) bite positions (target states T o ) in an overall view together - led, such. B. by the superimposition of image data.
- This overlay can be performed manually by the attending physician or with the help of suitable software (virtual matching).
- Abnormalities of the teeth, the jaw and the jawbone are visualized by the imaging and can be quantified using anatomical fixed points, which serve as reference points. Subsequently, the bite positions (desired states To) determined in step b) are compared with the initial state to provide a measure of a deviation of the actual state from the respective desired desired states and thus a measure of a therapeutic repositioning into the respective desired target To determine conditions.
- bite positions which are based on different examination findings, e.g. based on various examination results from medical fields other than orthodontics, are brought together to form a bite position.
- the merged bite positions can be weighted equally (averaging) or, depending on relevance, to different degrees.
- a virtual articulator is synonymous with software that processes 3-dimensional data.
- the desired bite positions it is of course also possible to transfer the desired bite positions to a physical articulator.
- the temporary models which represent negative images of the desired bite positions, for example, by means of 3D printing process printed and attached to the physical articulator in the correct position.
- a bite splint is respectively generated for two or more than two of the bite positions determined in step b), based on the temporal models calculated in step c).
- a bite rail is generated for each of the bite positions determined in step b).
- the dispensing of the bite splints is advantageously done with 3D forming equipment, such as e.g. 3D printers and 3D milling units.
- 3D printers and 3D milling units the procedure is usually to first print a positive model of the dental morphology with the temporary ideal positions of the jaws and temporomandibular joints, from which then the rails, for example by deep drawing of a suitable polymer material , can be made.
- the bite splints thus produced, the patient's discomfort can be quickly and effectively reduced, or even largely eliminated, and thus advantageous in the treatment of diseases that emanate from a functional disorder of the chewing organ, in particular craniomandibular dysfunctions.
- bite splints In addition, special circumstances or changes may occur over the course of the treatment which necessitate the adaptation or rebuilding of the initially produced bite splints and / or the creation of additional bite splints, such as operations, accidents, tooth loss or illnesses which cause a direct or indirect influence on the jaw position, the tooth morphology, the head and body posture and / or the musculoskeletal system.
- a further aspect of the invention relates to a method for the production of subsequent bite bars, comprising the steps a) to d) as defined above and in the following, the method additionally comprising the following steps: e) checking that in step b ) certain bite positions,
- step f) selecting one or more of the bite positions determined in step b) or rejecting all bite positions determined in step b),
- the examination of the bite positions determined in step b) takes place within the framework of a treatment of the CMD within a period of a few weeks to several months after the preparation of the previous bite bars.
- step b) The examination of the initial bite positions is carried out according to the methods described above under step b) for determining the bite positions with different head and posture in statics and dynamics, whereby usually the method (s) is used, with which the check is as efficient as possible according to the situation.
- the empirical and clinical methods described above can be used advantageously for this purpose.
- the checking of the bite positions determined in step b) therefore takes place using empirical or clinical methods, as described above.
- one or more of the bite positions determined in step b) is / are selected or, if appropriate, all bite positions determined in step b) are discarded.
- the selection of the bite splint (s) is usually made on the basis of the examination performed in step e), as well as on the basis of the objective patient-specific benefit and / or on the basis of the subjective sensation of the patient.
- step (e) The selection of the splint (s) on the basis of the test carried out in step (e) is usually based on the following criteria:
- step e) If it is determined in step e) that a certain bite position (initial bite position) determined in step b) does not correspond or no longer corresponds to the desired therapeutic bite position for the relevant head and body posture in terms of statics and dynamics, this bite position is discarded. However, if this initial bite position still corresponds to the desired therapeutic bite position for the head and body posture concerned in statics and dynamics, or comes very close to it, the bite position is retained.
- the retained bite positions are then additionally selected on the basis of the objective patient-specific benefit and / or on the basis of the subjective sensation of the patient.
- the assessment of the objective patient-specific benefit is usually carried out by the orthodontist via a manual examination of findings using empirical and clinical examination methods, as described above. Additionally or alternatively, data on the current position of the jaws, temporomandibular joints and the tooth morphology can be obtained by means of three-dimensional imaging techniques. collected for the respective worn bite splints and included in the assessment of the objective patient-specific benefit. For example, the anatomical effects caused by wearing a specific bite splint, such as the relief of inflammatory areas or the temporomandibular joint width, can be specifically checked by MRI.
- the selection of the bite positions or rejection of all bite positions in step f) comprises the following steps: f.1) acquisition of data for determining the current position of the jaws, the temporomandibular joints and the tooth morphology for the in Step b) certain bite positions (current as-is condition), f.2) selection of one or more of the bite positions determined in step b) or rejection of all of the bite positions determined in step b) on the basis of the test performed in step e), and on the basis of the data collected from the data acquired in step f.1) for determining specific patient-specific benefit and / or based on the subjective sensation of the patient.
- the determination of the current actual state according to step f.1) is usually carried out with inserted rail.
- the rail is used, which was previously manufactured for the relevant bite position (initial rail). Based on this data, the current position of the jaws and temporomandibular joints can be compared with the desired bite position when the splint is inserted.
- the selection of the bite splint (s) takes place predominantly on the basis of the examination made in step e) as well as on the basis of the subjective sensation of the patient, optionally including orthodontic aspects.
- step g) of the method according to the invention successive bite splints are produced for the bite positions selected in step f). This can be done in different ways depending on the present situation and feasibility.
- one subsequent track can be generated for each of the selected bite positions.
- follower rails which differ slightly from one another. These slight modifications may be in the form of the rails (eg thickness of the rail, enhancement of impressions / profiling or rail-mounted means of toothing, and the like) and / or the material of which the rails are constructed (eg, to modify bite resistance or the plasticity of the rail).
- the mentioned following rails can then be worn as an alternative to the previously produced rails or replace the previously produced rails. The latter applies in particular in the case of an iterative approach to a desired bite position through the use of several intermediate stages (intermediate rails).
- the previously created bite bars are replaced by the follower bite bars.
- step f In the event that all initial bite positions are discarded in step f), usually the discarded bite positions must be redetermined and / or additional bite positions must be determined which better take into account the individual needs of the patient. Based on these new bite positions, the subsequent rails are then produced.
- step f) In a next step, if necessary, one or more of the bite positions rejected in step f) are redetermined and / or one or more additional bite positions are determined for different head and body postures in statics and dynamics.
- step b) all methods described under step b) can be used to determine the new bite positions.
- empirical and clinical methods are preferably used.
- the new bite positions can be calculated.
- the previously collected data for determining the current position of the jaw, the Temporomandibular joints as well as tooth morphology and / or examination findings from medical fields other than orthodontics can be calculated.
- a subsequent step the data recorded at the beginning (current actual state) and the bite positions newly or additionally determined in the previous step are combined and a respective temporary model of a bite splint is calculated for the previously determined and / or calculated new bite positions. From the temporary models, the follow-up bite splints are then created.
- the calculation of the models or the generation of the sequence bite splints is analogous to the steps c) and d) described above.
- step f) If, in step f), one or more of the bite position (s) determined in step b) has been selected (initial bite positions), the generation of the bite splints in step g) preferably comprises the following steps: g.1a) the collection of data for determining the current position of the jaws, the jaw joints and the dental morphology of the patient (current actual state), g.2a) possibly redetermining one or more of the bite positions discarded in step f) and / or determining one or more additional bite positions with different head and body postures in statics and dynamics, g.3a) computer-assisted merging of the data acquired in step g.1 a) (current actual state) and the one selected in step f) and optionally in step g.2a) new or additionally determined bite positions for calculating in each case a temporary model of a bite splint for two or more than two of the ones selected in step f) g.4a) Generation of a respective consecutive bite splint for
- step f) If none of the bite positions initially determined in step b) were found to be good and therefore discarded in step f), one or more of the bite positions rejected in step f) must be redetermined and / or one or more additional bite positions must be added Different head and body postures in statics and dynamics are determined, which better meet the requirements of the patient.
- the generation of subsequent bite bars preferably comprises the following steps: g.1 b) the acquisition of data to determine the current position of the jaws, the jaw joints and the dental morphology of the patient (actual status), g.2b) redetermination of one or more of the bite poses discarded in step f) and / or the determination of one or more additional bite positions with different head and body postures in statics and dynamics, g.3b) computer-assisted merging of the data acquired in step g.1 b) (current actual state) and that in step g .2b) certain new bite positions for calculating each a temporary model of a bite splint for two or more than two of the bite positions determined in step g.2b), and g.4b) generating one subsequent bite splice for two or more than two of the ones in step g .2b) determined bite positions, based on the temporary models calculated in step g.3b).
- step g.2b takes place as described above under step b).
- steps g.3b) and g.4b) are carried out analogously to the above-described steps c) and d).
- CMD therapy often occurs over an extended period of time in which the body responds in the sense of a control loop, which may require multiple adjustments to the bite splint until all functional symptoms have disappeared and a stable physiological position of the condyle reached in the joint pits.
- relapses recurrences
- a change to an alternative bite position-based bite splint may be required, for example, when new findings arise over time, for example, from medical fields other than orthodontics, as discussed above, or the existing findings due to interactions in the field Change control loop.
- the treatment of CMD is generally more tolerable for the patient if the approach to the respective therapeutic position (s) of the jaws and temporomandibular joints of the respective bite position (s) (therapy goal (s )) stepwise, ie on the creation of one or more, for example, about 1 to 10, so-called intermediate rails takes place.
- steps e) to g) are repeated once or several times until one or more final bite splines are obtained, with which the therapy goal is essentially achieved or until the patient-specific ones Complaints are largely eliminated, in which case, instead of the bite positions determined in step b), the bite positions selected in step f) and, if appropriate, those newly determined in step g) occur. If, from a therapeutic point of view, a bite position is required for which no (initial) bite splint has yet been created, it can be included as a new bite position in step g) to produce a corresponding subsequent bite splint.
- the steps e) to g) of the process according to the invention are preferably repeated 1 to 10 times.
- a further subject of the present invention relates to occlusal splints and follow-on splints for use in the treatment of a patient with at least one disease resulting from a functional disorder of the chewing organ, in particular craniomandibular dysfunctions produced by the process described herein ,
- these bite splints and follow-on bite splints are particularly suitable for the treatment of patients suffering from a disorder that results from a functional disorder of the masticatory organ, such as bruxism and craniomandibular dysfunctions.
- the bite splints and subsequent bite splints obtainable by the method according to the invention are suitable for the treatment of craniomandibular dysfunctions.
- a further aspect of the present invention therefore relates to bite splints for use in the treatment of a patient with at least one disease which is based on a functional disorder of the chewing organ, in particular craniandibular dysfunctions, comprising a receiving area for receiving teeth of a first jaw of the patient and one Contact area for contacting teeth of the second jaw of the patient opposite the first jaw, wherein the at least one receiving area has at least one means for guiding the teeth and is profiled so that a sufficiently secure hold of the rails is ensured even under load, and wherein Contact area is only slightly profiled,
- bite splints are preferably a set of two or more bite splints, each bite splint being inserted in the splint set for a different use (day rail, night rail, work rail, rail, sports rail, etc.).
- a preferred embodiment of the invention relates to a set of occlusal splints for use in the treatment of a patient with at least one disease which is based on a functional disorder of the chewing organ, in particular craniomandibular dysfunctions consisting of two or more than two bite splints as defined above, whereby each of these two or more bite splints is used in a different head and posture in statics and dynamics.
- FIG. 1 is a diagrammatic representation of FIG. 1:
- FIG. 1 shows the method according to the invention for the production of bite splints.
- a first step a data on the position of the jaws, the jaw joints, the movement pathways of the lower jaw and the current morphology of the patient's teeth are acquired (initial state).
- a step b two or more than two bite positions of the patient, i. for the treatment of craniomandibular dysfunctions relevant or potentially / presumably relevant positions of the maxilla and mandible relative to each other, determined in different head and body postures in statics and dynamics (target states or bite library).
- one bite splint is produced from two or more than two of the bite positions determined in step b) in accordance with steps c) and d) (2 to n bite splints produced).
- FIG. 2 is a diagrammatic representation of FIG. 1
- FIG. 2 shows a preferred embodiment of the method according to the invention for producing follow-on bite splints, starting from the bite splints produced in steps a) to d) or bite positions (initial bite positions) determined for this in step b).
- the initial bite positions are first checked to see if they still correspond to the currently desired therapeutic bite positions (step e)). Subsequently, in a subsequent Step f) selects one or more of the bite positions determined in step b). Thereafter, if necessary, one or more of the bite positions discarded in step f) are redetermined and / or one or more additional bite positions are determined for different head and body postures in statics and dynamics (step g.2)).
- the subsequent bite splints are then generated (2 to m generated consecutive bite splints).
- the steps e) to g) can be repeated until final bite splints are obtained with which the desired therapeutic goal is achieved.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Dentistry (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Otolaryngology (AREA)
- Pulmonology (AREA)
- Nursing (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Dental Tools And Instruments Or Auxiliary Dental Instruments (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP18173249.6A EP3569187A1 (en) | 2018-05-18 | 2018-05-18 | Method for the preparation of removable bite-raisers |
PCT/EP2019/062861 WO2019219937A1 (en) | 2018-05-18 | 2019-05-17 | Method for producing bite splints |
Publications (1)
Publication Number | Publication Date |
---|---|
EP3793475A1 true EP3793475A1 (en) | 2021-03-24 |
Family
ID=62217842
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP18173249.6A Withdrawn EP3569187A1 (en) | 2018-05-18 | 2018-05-18 | Method for the preparation of removable bite-raisers |
EP19723825.6A Ceased EP3793475A1 (en) | 2018-05-18 | 2019-05-17 | Method for producing bite splints |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP18173249.6A Withdrawn EP3569187A1 (en) | 2018-05-18 | 2018-05-18 | Method for the preparation of removable bite-raisers |
Country Status (3)
Country | Link |
---|---|
EP (2) | EP3569187A1 (en) |
DE (1) | DE102019207271A1 (en) |
WO (1) | WO2019219937A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20220226074A1 (en) * | 2021-01-19 | 2022-07-21 | Dang Ha | System for body alignment through correction of malocclusions |
US20230240804A1 (en) * | 2022-01-31 | 2023-08-03 | 1092228 B.C. Ltd | Orthodontic appliance |
CN114041894B (en) * | 2021-11-16 | 2024-12-27 | 北京大学口腔医学院 | Dental occlusal recording device and method for manufacturing the same |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE202004020196U1 (en) | 2004-12-30 | 2005-05-04 | Weiss, Franz | Bite splint for upper jaw, used for treatment of craniomandibular dysfunction, has plate on underside and specially configured space for upper jawbone teeth |
DE202009003999U1 (en) | 2009-03-25 | 2009-07-30 | Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts Universitätsmedizin | Bite splint and bite splint system |
DE102010037075B3 (en) * | 2010-08-19 | 2012-01-26 | Steffen G. Tschackert | Dental splint, method for its production and use |
US20120115107A1 (en) * | 2010-11-04 | 2012-05-10 | Adams Bruce W | System and method for automated manufacturing of dental orthotics |
DE102013110427A1 (en) * | 2013-09-20 | 2015-04-16 | Alexander Berka | dental splint |
DE102013112032B4 (en) | 2013-10-31 | 2018-10-31 | Bernhard Egger | Method of constructing a bite splint |
DE102014117080A1 (en) * | 2014-11-21 | 2016-05-25 | Hicat Gmbh | A method for determining a therapy position or a group of therapy positions and a method for producing a protrusion splint |
DE102014019464A1 (en) * | 2014-12-23 | 2016-06-23 | Franz Weiss | Maxillary occlusal splint |
US11779437B2 (en) * | 2017-06-30 | 2023-10-10 | Align Technology, Inc. | Treatment of temperomandibular joint dysfunction with aligner therapy |
-
2018
- 2018-05-18 EP EP18173249.6A patent/EP3569187A1/en not_active Withdrawn
-
2019
- 2019-05-17 WO PCT/EP2019/062861 patent/WO2019219937A1/en active Application Filing
- 2019-05-17 DE DE102019207271.2A patent/DE102019207271A1/en not_active Withdrawn
- 2019-05-17 EP EP19723825.6A patent/EP3793475A1/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
WO2019219937A1 (en) | 2019-11-21 |
EP3569187A1 (en) | 2019-11-20 |
DE102019207271A1 (en) | 2019-11-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Kinzinger et al. | Effects of fixed appliances in correcting Angle Class II on the depth of the posterior airway space. | |
DE69317912T2 (en) | DENTAL DEVICE FOR TREATING SNORING AND OBSTRUCTIVE SLEEPING | |
RU2657195C1 (en) | Method of diagnosing the musculoskeletal system in planning and conducting dental treatment | |
EP2282693B1 (en) | Method for manufacturing a bite guard | |
EP3793475A1 (en) | Method for producing bite splints | |
Clark | Diagnosis and treatment of painful temporomandibular disorders | |
WO2020141134A1 (en) | Biomechanical training device for the temporomandibular joint | |
Trawitzki et al. | Effect of treatment of dentofacial deformity on masseter muscle thickness | |
DE102013112032B4 (en) | Method of constructing a bite splint | |
Eriksson et al. | Instant reduction in postural sway during quiet standing by intraoral dental appliance in patients with Whiplash associated Disorders and non-trauma neck pain | |
EP3808267A1 (en) | Method for determining anatomical symmetry elements | |
Algabri et al. | Patient's satisfaction and muscles activity after management of temporomandibular disorders patients using computer-aided design/computer-aided manufacturing versus conventional occlusal splints (randomized clinical trial) | |
Gomi et al. | Electromyographic activity of masseter muscles after complete denture rehabilitation in edentulous participants. | |
EP2967971B1 (en) | Method for producing a protrusion splint | |
Khuman et al. | Physical Therapy in Temporomandibular Dysfunction Following Maxillo–Mandibular Fixation in Sub-Condylar Mandibular Fracture—A Single Case Study | |
DE102019106141A1 (en) | Biomechanical device for the temporomandibular joint | |
RU2778839C1 (en) | Method for complex rehabilitation of patients with partial loss of teeth and symptoms of temporomandibular joint dysfunction, occlusion problems and facial pain | |
RU2806492C1 (en) | Neuromuscular method of obtaining central jaw relationship in a patient | |
RU2779362C1 (en) | Method for diagnosing a person's health when planning and conducting osteopathic functional dental treatment by doctor datsenko's method | |
CN111031898A (en) | Methods for the identification and planning of corrections of occlusal-related body system-specific features | |
Kares | Therapeutische Kieferrelation in der zahnärztlichen Schlafmedizin. | |
Lou | Effect of Clear Aligner Therapy on Jaw Motor Function | |
Lu et al. | Using double occlusion checking system and Bi-digital O-Ring Test to determine the vertical dimension of occlusion for maxillofacial prosthodontics for patients with long-term pathophysiological condition | |
Husejko et al. | Rehabilitation in scoliosis-an overview of the most important procedures | |
Al-Ani et al. | TMD current concepts: 2. Imaging and treatment options. An update |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20201215 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
DAV | Request for validation of the european patent (deleted) | ||
DAX | Request for extension of the european patent (deleted) | ||
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20211115 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R003 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED |
|
18R | Application refused |
Effective date: 20231110 |