U.S. patent number 3,579,829 [Application Number 05/004,904] was granted by the patent office on 1971-05-25 for pericortical dental implant and inserter therefor.
This patent grant is currently assigned to The Sampson Corporation. Invention is credited to Arnold Sampson.
United States Patent |
3,579,829 |
Sampson |
May 25, 1971 |
PERICORTICAL DENTAL IMPLANT AND INSERTER THEREFOR
Abstract
A pericortical implant for the retention of various dental
prosthetic replacements in the form of a two-part clamp adapted to
be placed about either the mandible or maxilla of the patient and
having a mounting post for reception of the dental prosthesis. An
inserter device including a force-applying screw for moving one
clamp half with respect to the other and having extendible arms for
temporarily retaining the clamp halves in position is provided for
rapid application of the clamp.
Inventors: |
Sampson; Arnold (Pittsburgh,
PA) |
Assignee: |
The Sampson Corporation
(Pittsburgh, PA)
|
Family
ID: |
21713103 |
Appl.
No.: |
05/004,904 |
Filed: |
January 22, 1970 |
Current U.S.
Class: |
433/158;
433/173 |
Current CPC
Class: |
A61C
8/0089 (20130101); A61C 8/0031 (20130101) |
Current International
Class: |
A61C
8/00 (20060101); A61c 013/00 () |
Field of
Search: |
;32/2,10,13 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Peshock; Robert
Claims
What I claim as my invention and desire to protect by Letters
Patent of the United States is:
1. A pericortical clamp to provide anchorage for artificial teeth
and adapted for application to the mandible or maxilla, comprising
a pair of clamp halves, each half having a relatively planar
vertical wall, means interconnecting said clamp halves so that said
walls are in adjustably spaced apart clamping relationship on
either side of a bone, and post means on one of said clamp halves
for mounting an artificial tooth.
2. A clamp as defined in claim 1, wherein said interconnecting
means comprises a pedestal extending inwardly from one clamp half
and a pair of straddle arms extending inwardly from the other clamp
half and adapted to fit about the sides of the pedestal.
3. A clamp as defined in claim 2, wherein said post means is
mounted on said pedestal.
4. A clamp as defined in claim 3, wherein said post means comprises
a screw secured on said pedestal and a mounting post threadedly
received on said screw.
5. A pericortical clamp as defined in claim 1, and further
including a plurality of bone-engaging spikes mounted on the inner
face of said vertical walls.
6. A clamp as defined in claim 2, wherein said pedestal and
straddle arms are interconnected in slidably adjustable
relationship by a tongue and groove interface.
7. A clamp as defined in claim 6 and further including adjustable
screw means for retaining a predetermined adjusted relationship of
said clamp halves.
8. A dental prosthetic appliance and inserter comprising a pair of
relatively movable clamp halves having flat inner faces and adapted
to be engaged about either the maxilla or mandible, means on one of
said clamp halves for mounting an artificial tooth, an inserter
having expandable arms adapted to temporarily retain said clamp
halves therebetween during installation on a bone, means on the
inserter for expanding and contracting said arms about said clamp
halves, mechanical force transmission means for moving one of said
clamp halves toward the other to clamp about the bone, and screw
means adjustably retaining said clamp halves in position about said
bone after removal of said inserter.
9. An appliance and inserter as defined in claim 8, and further
including means on the inserter engageable with one clamp half to
move said one clamp half away from said other clamp half.
10. An appliance and inserter as defined in claim 8, wherein said
expandable arms are stiff spring members normally parallel to each
other and said means for expanding and contracting the same
comprises a pair of toggle links commonly pivoted at one end to a
pusher bar and having their opposite ends pivotally mounted on one
of said arms, and power means for advancing said pusher bar to
expand said arms for the reception of said clamp halves.
11. An appliance and inserter as defined in claim 8, wherein said
force transmission means comprises a screw jackshaft on said
inserter, and nut means engageable with said screw jackshaft and in
contact with said one clamp half.
12. An appliance and inserter as defined in claim 8, and further
including screwdriver means on said inserter engageable with said
screw means.
13. A method of applying a dental prosthetic appliance to either
the mandible or maxilla comprising the steps of stripping the
periosteum from about the implant site on the bone, placing a
two-piece clamp over the bared bone portion, tightening said clamp
into firm bone contact, and securing the prosthetic appliance to
the clamp.
Description
This invention relates broadly to dental prosthetic devices and
more particularly to a pericortical dental prosthetic devices and
more particularly to a pericortical dental implant and an inserting
tool therefor. The pericortical dental implant is in the form of a
clamping device specifically adapted for attachment to either the
mandible or maxilla wherein the clamp may be securely fastened to
the bone structure to serve as a permanent base for the reception
and mounting of an artificial tooth or in conjunction with other
clamps to mount a partial or full denture.
In the field of prosthodontics, the ultimate objective is to
provide one or more artificial teeth which are firmly mounted
within the mouth which will remain firm under the normal oral
activities of the patient and which will appear natural to the
sight.
The use of full or partially removable dentures is the common
approach with most edentulous or partially edentulous patients.
These dentures are not actually implanted but are merely fitted to
the gums and may be held thereon as by adhesives or close
interfitting with the gum. Many oral activities such as are
frequently associated with eating of food substances such as corn
and sticky candy may cause the denture to become dislodged.
Discomfort and inconvenience in proper denture hygiene are other
common complaints lodged by denture wearers.
When only one or two teeth are to be replaced, it is conventional
to use a permanent bridge which consists of an artificial tooth
supported by inlays that are cemented to the healthy natural teeth
adjacent thereto. This bridge generally provides a reasonably firm
support for the artificial tooth, however it usually requires the
removal of portions of the adjacent healthy teeth in order to
provide the necessary structure for supporting the anchoring inlays
and is not, therefore, entirely desirable in all cases.
Due to the problems arising during utilization of dentures or
bridges, experimentation and research have progressed in recent
years in regard to the implanting of dental prosthetic appliances
within the tissue of the gum so as to provide an anchor for
dentures. The attempt to replace missing dentition by various
implant means has been practiced with fairly limited success for
somewhat over 100 years. Recent studies have indicated that there
are presently over 35 million partially or completely edentulous
people in the United States, 25 percent of whom cannot utilize
their maxillary or mandibular dentures with comfort or ease.
Studies also indicate that in Great Britain there are over 17
million partially or completely edentulous people and a similar
percentage who have problems with dentures. Due to discomfort of
dentures in such patients, many have not completely adapted to
wearing these appliances and remain edentulous. The present
invention overcomes the problems of denture fit and comfort.
PRIOR ART IMPLANTS
Many implant methods have been utilized in the past and are
presently being employed to replace missing dentition, either in
part or totally. It was not until Venable et al., in 1937 reported
on the use of certain electropassive metals that were tolerated by
human tissues that the field of implant research was truly placed
on a scientific footing. Their work not only explained previous
complications, but also lead to the development of the present day
metals which are biologically inert when imbedded in tissue,
examples being stainless steel and Vitallium.
Success of implants was also enhanced by the availability of
antibiotics which, when used prophylactically to prevent infection,
made intraoral procedures possible.
Indications for the use of implant dentures are:
1. cases of marked atrophy of the alveolus and jaw;
2. cases in which dentures cannot be worn because of painful
mucosa;
3. cases of soft tissue hypertrophy and flabby ridge caused by
denture irritation; and
4. cases with poor masticating function.
The individual replacement of missing teeth utilizing metals such
as gold, silver and platinum is one of the oldest methods and these
have failed primarily due to electrolytic reactions which develop
when saliva comes in contact with the metal, producing bone
resorption and loosening of the implant. Submucosal implants in the
form of "collar buttons" have been inserted directly beneath the
mucosa. These implants frequently loosen when secondary
inflammation and infection occur, resulting in the loss of the
retention of the dental prosthesis. Another method that has enjoyed
only a marginal degree of success is the supraperiosteal implant.
These implants generally in the form of polyethylene, silicone,
nylon and acrylic resins are placed beneath the mucosa but above
the periosteum. The major problem with this type of implant is the
high frequency of foreign body reaction followed by rejection of
the implanted substance. This rejection, coupled with the formation
of areas of pressure necrosis, has been cited as the principal
failure of the supraperiosteal implants.
Transosseous implants have also been used and these require
burrowing into and through the bone and utilizing screw or pin
fixation. The required drilling through the bone in this method
often produces an intense postsurgical inflammatory response and
accompanying bone resorption which may lead to the mobility of the
implant when the same is subjected to the high stress of
mastication, and consequently the following loss of the
implant.
Some limited degree of success has been achieved by the use of
endosseous implants which have taken various forms. The
intraosseous use of implants in the form of magnets has met with
little acceptance since the results have been questionable in view
of the fact that the magnetic field is somewhat diminished by the
overlying tissue coupled with the necessity of preparing a bed in
the bone for the reception of the magnet which sometimes is
followed by foreign body reaction. Here an intraoral incision is
made in the gum tissue and a magnetic insert is placed within the
tissue so as to be between the surface of the gum tissue and the
lower jaw bone after the incision is closed. The artificial tooth
is provided with a metallic plug cast therein which holds the tooth
to the gum tissue due to the magnetic attraction exerted by the
magnetic insert that has been implanted. The intraosseous use of
screws, pins, vent posts and vent blades requires that the same be
driven into the bone and then having severe pressures placed on
them which results in the rapid dissolution of bone around the
implant, followed by mobility of the implant and possible failure.
An example of a ring-type implant of this form is shown in the
Linkow U.S. Pat. No. 3,465,441, issued Sept. 9, 1969.
A final form of implant is the subperiosteal implant which is
applied beneath the mucosa in the periosteum which rests on the
bone but without intraosseous engagement. While these implants have
met with limited success, there are factors which mitigate against
total successful use thereof. Since these implants are dependent
upon fibrous tissue to hold them against the bone, and since
fibrous tissue possesses a degree of elasticity, the net result is
mobility of the implant when stress is applied thereto, thereafter
followed by rejection. Maxillary subperiosteal implants are
contraindicated in as much as the normal force of gravity will
frequently prevent retention. It is also contraindicated in the
maxilla because of the gross amount of cancellous bone present
therein which will not support a subperiosteal implant due to rapid
resorption of such cancellous bone. If a mandibular subperiosteal
implant is inserted on a mandible which has not fully resorbed to
dense cortical bone, the implant will become mobile and fail
secondary to resolution of the remaining cancellous bone which
produced a space defect between the base of the implant and the
residual bone. Additionally, periosteal implants usually required
multiple surgical procedures (i.e., initial surgery for exposure of
the mandible and obtaining an impression; followed by a healing
period of up to 6 weeks, than a second surgical procedure
consisting of reexposure of the mandible followed by implantation
of the subperiosteal device).
OBJECTS OF THE INVENTION
The pericortical clamp of the instant invention herein disclosed
obviates the difficulties inherent in the prior art methods
disclosed above. The clamp provides a firm, fixed base which more
easily, quickly, and effectively supports a total or partial dental
prosthesis.
A primary object of this invention is to provide means for mounting
a dental prosthetic replacement which means is in the form of a
clamp adapted to be fastened securely to either the mandible or
maxilla of the patient.
Another object of the invention is to avoid the disadvantages
common in the prior art of implantation by providing a clamping
device that prevents any movement of the implant either lateral,
torsional or longitudinal and yet will not place undue pressure
upon the bone surface.
Still another object of this invention is to provide an inserter
construction specifically adapted to place the implant clamp on the
mandible or maxilla of the patient in a quick and simple
operation.
Another object of the invention is to provide an implant device and
inserter which may be readily applied by any dental surgeon and
which includes a clamping device having two separate disengageable
sections.
Another object of the invention is to provide an implant device
formed of two sections, a clamp and an inserter, the latter being a
tool to be used in inserting and tightening the clamp on the bone
and which is then disengaged therefrom, leaving the implant clamp
on the bone and about which the wound is closed.
Another object of the invention is to provide a fixed implant clamp
which can be applied with minimum surgical dissection of soft
tissue.
Still another object of the invention is to provide a firm, fixed
implant base which can be attached to the maxilla.
Yet another object of the invention is to provide a dental implant
device which is simple in construction, relatively cheap to
manufacture and which is safe and efficient at all times and which
may be removed at a later date if desired.
Other objects and advantages will become apparent from the
following description of the exemplary forms of the invention
illustrated in the accompanying drawings.
DESCRIPTION OF THE VIEWS
FIG. 1 is a perspective view of the pericortical dental implant
clamp;
FIG. 2 is an exploded perspective view of the clamp in inverted
position;
FIG. 3 is a side elevation showing the pericortical dental implant
clamp secured to a human mandible;
FIG. 4 is an enlarged cross-sectional view taken along the line 4-4
of FIG. 3;
FIG. 5 is a perspective view of the inserter tool with portions
broken away to show detail, showing a pericortical dental implant
clamp attached thereto;
FIG. 6 is a perspective view similar to FIG. 5 but showing the
inserter inverted and without a clamp in place;
FIG. 7 is a sectional view of the inserter taken along the line 7-7
of FIG. 5;
FIG. 8 is a top plan view of the inserter in the closed
position;
FIG. 9 is a bottom plan of the inserter in the closed position with
the extended or open position shown in phantom lines;
FIG. 10 is a cross-sectional view through the inserter taken along
the line 10-10 of FIG. 8;
FIG. 11 is a partial exploded perspective of the front end portion
of the inserter showing the manner in which the pericortical clamp
is secured therein;
FIG. 12 is a perspective view similar to FIG. 11 showing the clamp
in place in the inserter with the two halves thereof separated;
and
FIG. 13 is a perspective view similar to FIG. 12 showing the clamp
portions being brought together.
Referring to the drawings in greater detail wherein like parts are
represented by like reference characters, the pericortical dental
implant clamp of the present invention is shown generally at 10,
and is formed in two pieces, the proximal half 11 and the distal
half 12. The clamp half portions are preferably formed from a
biologically inert metal suitable for implantation in the human
body. Stainless steel, tantalum, or a cobalt-chromium alloy
commonly sold under the trademark Vitallium, have been used as
implant materials in recent years and would be acceptable for this
particular application.
Each clamp half includes an upright vertical wall 13, 14 having a
planer inner face. The distal half 12 is provided with a pedestal
15 extending inwardly from the bottom of the vertical wall and the
pedestal has elongated grooves 16 on the side surfaces thereof. The
front face of the pedestal is drilled and tapped as at 17. The
proximal clamp half 11 is formed with straddle arms 18 and 19
extending therefrom in a manner such as to fit closely about the
pedestal 15 of the distal half 12. Each of the straddle arms are
tapered to an edge as at 19' and are formed on their inner surfaces
with a rounded elongated tongue 20 as shown in FIG. 2. It will be
evident that the straddle arms of the proximal half will engage
about the pedestal 15 of the distal half with the tongue portions
20 being received within the grooves 16. As best seen in FIG. 2,
each of the flat wall surfaces 13 and 14 are provided with
relatively sharp bone-engaging spikes 21.
The proximal clamp half is formed with a smooth bore hole 22
adapted for alignment with the tapped hole 17 of the distal half. A
machine screw 23 serves to connect the two clamp halves together in
a selected position of engagement about a bone as shown in FIG. 4.
The screw 23 passes through the hole 22 and into threaded
engagement with the tapped hole 17 in the distal half 12. Another
tapped hole 24 is placed centrally of the wall of the proximal half
11 for a purpose to be later described. A truncated conical
mounting post 25 is secured centrally on the bottom face of the
pedestal 15 by means of a mounting screw 26. (See FIG. 4). It will
be understood that if desired the mounting post could be formed
integrally with the pedestal although in the preferred embodiment
the same is removable since various configurations of posts could
be used if desired. For example, a square cross section post may be
found desirable in certain applications. An artificial tooth
structure T may be cemented onto the mounting post 25 with the use
of conventional dental cements. Alternatively, other means for
locking the tooth structure to the mounting post may be employed
such as a resilient detent member within the recess of the
artificial tooth adapted to snap into a groove provided on the
surface of the mounting post (not shown).
The clamp 10 may be applied to either the mandible or maxilla of
the patient and as shown in FIGS. 3 and 4 is placed on the mandible
for mounting of an artificial tooth to take the place of a tooth
that has been removed and is surrounded by natural teeth. The
detailed procedure for placing of the clamp will be described later
herein in greater detail, however generally the application
requires surgical procedures in order to expose the mandible and
requires some scraping of the periosteum in order to provide
intimate contact between the wall faces of the clamp and the bone
surface. The clamp is pushed down so that the face of the pedestal
15 is directly against the top surface of the bone and forces are
applied to cause a tight gripping of the bone by the wall faces 13
and 14. It will be noted that the spikes 21 will imbed themselves
into the bone in order to provide a tight purchase and to prevent
slippage of the clamp. The spikes are designed to be of a length as
not to interfere or impinge upon the neurovascular bundle which
runs through the mandible or maxilla. After placement of the clamp,
the normal restorative powers of the body cause rebuilding and
growth of the tissues and, as shown in FIG. 4, the normal gum line
G will extend around and above the clamp so as to completely cover
the same. The post 25 may be adjusted slightly in the vertical
direction after completion of the surgery in order to make proper
correction of the bite and proper mating with the teeth on the
opposite bone.
It is also contemplated that the clamp may be fabricated in various
widths in order to accommodate two or even more mounting posts.
Additionally, the mounting posts may be angled with respect to the
pedestal for areas such as the retromolar areas where curvature of
the ridge crest may dictate such use. Such angled posts may also be
useful in achieving parallelism with a mesially or distally tilted
tooth or implant abutment. Various combinations of one or more
implant clamps may be used for proper mounting of complete
dentures.
When a completely edentulous mandible or maxilla is to be fitted
with a prosthesis, at least four mounting posts are required for
proper support.
THE INSERTER
While the pericortical implant clamp 10 could be applied to the
bone by hand and the screw 23 tightened with a conventional
screwdriver, a novel inserting tool has been developed which
greatly speeds application of the clamp and achieves a tighter and
more secure purchase of the clamp on the bone. This inserter is a
modification of the bone clamp application tool shown in my earlier
U.S. Pat. No. 3,477,429. The improved inserter is shown in FIGS. 5
and 6 and is designated generally at 30. The various components of
the inserter may be formed of stainless steel or other suitable
metallic material that can easily be sterilized. The inserter
consists of a generally cylindrical, although slightly tapered,
barrel portion 31 having a flat end wall from which extend spring
arms 32 and 33. These arms may be part of a one-piece U-shaped
construction and due to their length and design, are resilient and
may be biased outwardly at their free end in a manner described in
greater detail later herein. The inner face of each of the spring
arms is provided with a V-groove or guide track 34 for a portion of
its length and terminating in a front shoulder stop 35.
The barrel has a through cutout 36 and the interior of the barrel
defined within the cutout has a rear wall 37 and a front wall 38.
The rear wall 37 is axially bored as at 39 and the front wall 38 is
bored at 40 to provide an opening coaxial with the opening 39 for
reception of a hollow jack shaft 41. The jack shaft is rotatable
within the barrel and is retained from axial movement with respect
to the barrel by means of retaining clips 42 and 43 received within
annular grooves in the shaft. A knurled hand knob 44 is secured to
the rear end of the jack shaft in order to provide a convenient
surface for manual rotation of the shaft. The forward portion of
the shaft is formed with screw threads 45.
A screwdriver 46 is received within the axial bore of the jack
shaft 41 and may be slid forwardly and rearwardly in an axial
direction but is frictionally held in position by means of a
friction grommet 47 mounted within the jack shaft 41. The rear end
of the shaft of the screwdriver is provided with a hand knob 48
having a knurled surface and being slightly smaller in diameter
than the knob 44. The forward end of the screwdriver is provided
with a conventional flat blade configuration as shown at 49.
The end 45 of the jack shaft having threads thereon is threadedly
received in a jack nut 50 located between the spring arms 32 and 33
and has an upstanding front flange 51 mounted at the front end
thereof which has flat, parallel side portions that are engageable
against the spring arms in order to prevent rotation of the jack
nut. A pusher plate 52 is mounted between the spring arms and
forwardly of the front flange of the jack nut and has guide
shoulders 53 engageable on the top faces of the spring arms. The
pusher plate is mechanically connected to the front upstanding
flange 51 by means of a flexible braided cable 54 which also serves
as a retention means for retraction of the proximal clamp half as
later described. The braided cable is adapted to transmit rotation
along its length and yet has a certain degree of flexibility as
shown in FIG. 7. A cutout 55 is provided in the barrel 31 in order
to house the rear end of the cable which terminates in a knurled
hand knob 56. The forward end of the cable is formed with a
screw-threaded portion 57 extending beyond the pusher plate and
adapted for insertion and attachment into the threaded tapped hole
24 of proximal clamp half 11. A flat retainer member 58 is mounted
on the cable in order to prevent retraction of the same through the
upstanding front flange 51.
In order to open and to retract the spring arms 32 and 33 for
insertion and retention of the clamp halves, means are provided on
the lower portion of the inserter for mechanically forcing the
spring arms into the dotted line clamp-receiving position of FIG.
9. For this purpose screw shaft 60 is mounted in the barrel
parallel to the jack shaft 41 and is provided intermediate its ends
with a thumb wheel 61 extending partially through the cutout
portion 36 of the barrel in order to be readily grasped by the
thumb of the operator. The shaft is retained in the barrel by means
of a flat retainer 62 mounted on the shaft 60. A push rod 63 is
mounted by means of a nut 64 on the threaded end of the screw shaft
60 and is located immediately below the jack nut 50. A pair of
toggle links 65 and 66 are pivotally mounted to the forward end of
the opening rod by means of a toggle link pin 67. The opposite ends
of the toggle links are pivoted to the respected spring arms by
means of link pivot pins 68 shown in FIG. 9. It will be understood
that rotation of the thumb wheel 61 in one direction will cause the
inserter opening rod 63 to move forwardly thereby acting on the
toggle links 65 and 66 to expand or extend thereby spreading the
spring arms 32 and 33 as shown in phantom lines in FIG. 9. This
position of extension is also shown in FIG. 11 wherein it will be
evident that the two clamp halves may be inserted with the tapered
shoulder portion 19' thereof being received in the V guide tracks
34 of the spring arms with the front shoulder stop 35 serving as an
end abutment for the clamp. Rotation of the thumb wheel 61 in the
opposite direction will cause retraction of the spring arms so that
the clamp halves are firmly held within the inserter but may be
moved with respect to each other as shown in FIGS. 12 and 13. By
application of rotary motion on the knob 56, the screw end 57 of
the flexible cable 54 may be secured within the tapped hole 24 of
the proximal clamp half 11. In this position, rotation of the
knurled hand knob 44 in a clockwise direction will cause retraction
of the jack nut 50 along with the pusher plate 52 and the proximal
clamp half 11 as shown in FIG. 12. In this retracted position, the
screwdriver 46 may be physically removed from the jack shaft 41.
The screw 23 has such a cross section that the same can be inserted
through the bore inside the jackshaft as later described.
In this position, the clamp and inserter are placed over the bare
bone portion previously prepared and counterclockwise rotation is
imparted to the hand knob 44 in order to move the jack nut
forwardly and along therewith the proximal clamp half through
action of the pusher plate 52 as shown in FIG. 13. Rotation is
continued until such time as a firm, secure purchase is applied to
the bone by the two clamp halves, and wherein the spikes 21 will
become engaged within the bone. At this point the screw is inserted
through the open end of the jack shaft and is followed by the
screwdriver 46 which as shown in FIG. 7 can be turned to insert the
screw through the hole 22 of the proximal clamp half and become
threadedly engaged in the tapped hole 17 in the distal half 12. As
soon as the screw is tightened to the desired degree, the
screwdriver is manually retracted and the knob 56 turned to release
the screw end 57 from engagement with the proximal clamp half 11.
Thereafter, the knob 44 may be turned slightly to retract the jack
nut and associated parts so that the thumb wheel 61 may be actuated
to expand the spring arms into the dotted line position of FIG. 9
so that the inserter may be manually removed.
As an aid to rotation of the thumb wheel, a leverage assist pin 69
which is normally housed on the barrel as shown in FIGS. 5 and 7
may be inserted into one of a plurality of pin receiving holes 70
on the barrel. See FIGS. 6 and 9. This pin permits additional
leverage to be applied to the thumb wheel when desired.
After insertion of the clamp, the mounting post 25 may be applied
over the threaded portion 26 and the prosthetic replacement is
subsequently emplaced. In a short period of time during the natural
healing process, gum tissue will completely cover the exposed
portions of the clamp and there will usually be no necessity for
ever removing the clamp from the bone.
While I have shown and described a preferred embodiment of the
invention, it is to be understood that the drawings and detailed
disclosure are to be construed in an illustrative rather than a
limiting sense since various modifications and substitutions of
equivalents may be made by those skilled in the art within the
spirit and scope of the invention.
* * * * *