U.S. patent number 3,720,959 [Application Number 05/067,029] was granted by the patent office on 1973-03-20 for mandibular prosthetic apparatus.
Invention is credited to George W. Hahn.
United States Patent |
3,720,959 |
Hahn |
March 20, 1973 |
MANDIBULAR PROSTHETIC APPARATUS
Abstract
A kit for forming a number of different forms of prosthetic
devices to replace different portions of a mandible which have been
removed. The kit includes a number of prefabricated members,
fabricated from a malleable stainless steel mesh, including mating
inner and outer tubular sleeve portions for assembling adjoining
members, with the sleeve portions being crimped together to define
rigid couplings. Screws are used to attach the end member of an
assembled prosthetic device to the bone stump of the remaining
mandible.
Inventors: |
Hahn; George W. (Dallas,
TX) |
Family
ID: |
22073267 |
Appl.
No.: |
05/067,029 |
Filed: |
August 26, 1970 |
Current U.S.
Class: |
623/17.17 |
Current CPC
Class: |
A61F
2/3099 (20130101); A61F 2/2846 (20130101); A61F
2/2803 (20130101); A61F 2002/30593 (20130101); A61F
2230/0021 (20130101); A61F 2002/30154 (20130101); A61F
2002/30909 (20130101); A61F 2250/0062 (20130101); A61B
17/8085 (20130101); A61F 2230/0082 (20130101); A61F
2002/30607 (20130101); A61F 2002/30261 (20130101) |
Current International
Class: |
A61F
2/28 (20060101); A61F 2/30 (20060101); A61B
17/68 (20060101); A61B 17/80 (20060101); A61F
2/00 (20060101); A61f 001/24 () |
Field of
Search: |
;3/1
;128/92R,92C,89A,334R,334C ;32/1 ;29/515,516 |
References Cited
[Referenced By]
U.S. Patent Documents
Other References
"Chrome Cobalt Mesh Mandibular Prosthesis" by G. W. Hahn et al.,
Journal of Oral Surgery, Vol. 27, Jan. 1969, pages 5-10. .
"Vitallium Mesh Mandibular Prosthesis," by G. W. Hahn, Journal of
Prosthetic Dentistry, Vol. 14, No. 4, July-Aug. 1964, pages
777-784..
|
Primary Examiner: Gaudet; Richard A.
Assistant Examiner: Frinks; Ronald L.
Claims
What is claimed is:
1. Mandibular prosthetic apparatus comprising, in combination:
an assembly of members fabricated of a malleable mesh;
a bow member for replacing at least portions of the main body of a
mandible; said bow member comprising an elongated curved member,
elongated in cross section, and formed to include an elongated
cylindrical socket portion along one edge thereof defining an outer
mating circular sleeve;
a first bow support member comprising a body portion and a tubular
portion extending therefrom; said tubular portion defining an inner
mating circular sleeve dimensioned for sliding fit with the outer
mating circular sleeve of the bow member;
said bow member outer mating sleeve fully receiving and enclosing
said support member inner mating sleeve, for coupling said
members.
2. The invention set forth in claim 1
including an elongated curved lip member having a U-shaped cross
section; said lip member dimensioned to partially enclose the bow
member to define a lateral extension of the bow member cross
section in the bow area.
3. The invention set forth in claim 1
wherein said first bow support member defines a retention member
for securing the bow member to a mandible stump; said support
member body portion being formed to enclose a portion of the
mandible stump for attachment thereto.
4. The invention set forth in claim 1
wherein said first bow support member comprises a ramus-condyle
member for replacing the ramus and condyle of the mandible; the
body portion of said ramus-condyle member being elongated and
having means for attaching an artificial condyle at the end remote
from the tubular extension portion.
5. The invention set forth in claim 4
wherein said tubular extension portion extends at an angle relative
to said elongated body portion.
6. The invention set forth in claim 1
wherein said first bow support member comprises a ramus-condyle
assembly including a ramus member and a condyle member;
said ramus member comprising an elongated tubular body portion of
elongated cross section, defining an inner mating oval sleeve, and
said tubular extension portion, defining said inner mating circular
sleeve;
said condyle member comprising an elongated tubular body of
elongated cross section, defining an outer mating oval sleeve, and
an artificial condyle attached to one end of said tubular body;
said outer mating oval sleeve being dimensioned for a sliding fit
with said inner mating oval sleeve and receiving and enclosing said
inner oval sleeve to provide a rigid coupling between the ramus and
condyle members.
7. The invention set forth in claim 6
wherein said tubular extension portion of said ramus member extends
at an angle relative to the elongated tubular body portion of said
member; and wherein said outer and inner oval sleeves are deformed
in interfering relation to provide the rigid coupling between the
ramus and condyle members.
8. The invention set forth in claim 1
including a second bow support member defining a retention member
for securing the bow member to a mandible stump in the bow area of
a mandible;
said second bow support member comprising a body formed to enclose
a portion of the mandible stump for attachment thereto; said body
including a socket portion defining an outer mating circular
sleeve;
and a connector member comprising an elongated curved tubular
member of circular cross section, defining an inner mating circular
sleeve dimensioned for a sliding fit with the outer mating circular
sleeves of the bow member and the second support member; said
connector member being fully enclosed within said outer mating
sleeves to couple said bow member to said second support
member.
9. The invention set forth in claim 1
wherein said first bow support member defines a retention member
for securing the bow member to a bone stump in the bow area of the
mandible; said bow support member comprising a body formed to
enclose a portion of the mandible stump for attachment thereto;
said body including a socket portion defining an outer mating
circular sleeve;
and a connector member comprising an elongated curved tubular
member of circular cross section, defining an inner mating circular
sleeve dimensioned for a sliding fit with said socket portion outer
mating circular sleeve; said connector member defining said bow
support member tubular portion.
10. The invention set forth in claim 1
wherein said bow member is severed to provide two abutting
segments; and a curved connector member comprising an elongated
curved tubular member of circular cross section dimensioned to
define an inner mating circular sleeve for sliding fit with the
outer mating circular sleeves of the two bow member segments, with
the connector member being fully received in and enclosed by said
bow member segments to couple said segments.
11. The invention set forth in claim 1
said inner and outer mating sleeves being deformed in interfering
relation to provide a rigid coupling between the respective
members.
12. The invention set forth in claim 10
said curved connector member and said bow member segments being
deformed in interfering relation to provide a rigid coupling
between the bow member segments.
Description
BACKGROUND AND SUMMARY OF THE INVENTION
This invention relates to the field of mandibular prosthesis, and
more particularly to an apparatus for forming an artificial
mandible or part thereof.
The mandibular prosthetic apparatus of the present invention is an
improvement of apparatus described in an article entitled Chrome
Cobalt Mesh Mandibular Prosthesis published in Journal of Oral
Surgery, Vol. 27, Jan. 1969, by Donald A. Corgill, M.D., and the
inventor, George W. Hahn, D.D.S. In the apparatus described in that
publication, the various members of a prosthetic assembly were
attached together by means of screws which have the disadvantage of
producing protrusions in the prosthetic device which sometimes
caused exposures through the surface tissues of the face. Another
disadvantage of this apparatus was that adjustability was provided
in some cases by overlapping sleeve portions which produced abrupt
edges in the assembled prosthetic device, again sometimes piercing
the surface tissues.
An object of this invention is to provide an improved mandibular
prosthetic apparatus for restoration or replacement of all or a
part of a mandible.
Another object of this invention is to provide mandibular
prosthetic apparatus including a kit of prefabricated parts which
may be assembled in various combinations to replace substantially
all mandibles lost.
A further object of this invention is to provide mandibular
prosthetic apparatus consisting of a kit of prefabricated parts,
which may be assembled in various combinations and rigidly coupled
to provide a unitary prosthetic device without the use of screws
except at the point of attachment to the mandible bone stump.
Still another object of this invention is to provide a mandibular
prosthetic apparatus including a kit of prefabricated parts, which
may be assembled to form a desired prosthetic device having a
relatively smooth contour and eliminating sharp projections which
tend to pierce the facial tissues.
A still further object of this invention is to provide a mandibular
prosthetic apparatus which provides improved support for the facial
tissues.
Apparatus according to the invention for accomplishing these
objects includes, broadly, an assembly of members fabricated of
malleable mesh including, at least, a bow member for replacing
portions of the main body area of the mandible and a member for
supporting one end of the bow member consisting of a body portion
and an integral tubular extension. The bow member is elongated
vertically in cross section to define an outer, tissue supporting
wall. The bow member and the support member extension define
respective outer and inner mating circular sleeves adapted to be
crimped together to provide a rigid coupling between the members.
More specifically, the support member body may include a housing
for attachment to the bone stump by means of screws, or an oval
tubular portion angled relative to the tubular extension to define
a ramus portion of the prosthetic device. In another form the
support member is that of a body defining another mating outer
circular sleeve, whereby the support member and bow member may be
joined by a mating inner circular sleeve received in the adjoining
outer circular sleeves of the bow member and support member.
The novel features and the advantages of the invention, as well as
additional objects thereof, will be understood more fully from the
following description when read in connection with the accompanying
drawings.
DRAWINGS
FIGS. 1 and 2 are respective side and front views of a human skull
to illustrate the parts of the mandible;
FIG. 3 is an illustration of the several members which are
assembled in various combinations to form prosthetic devices;
FIG. 4 is a perspective view of a mandible consisting of the
natural posterior portions of the mandible and a prosthetic
anterior bow portion;
FIG. 5 is a perspective view of a mandible in which a relatively
small section of the main body and bow area is replaced with a
prosthetic device;
FIG. 6 is a perspective view of a mandible consisting of a right
half portion of the natural mandible and the left half portion
being a prosthetic device;
FIG. 7 is a perspective view of a mandible wherein only the
posterior portion on one side consists of the original mandible,
the remainder of the mandible consisting of a prosthetic
device;
FIGS. 8 and 9 are perspective views of two of the members
illustrated in FIG. 3;
FIGS. 10, 12, 13 and 14 are transverse sectional views of portions
of the prosthetic assemblies illustrated in FIGS. 4, 5 and 6, to
show the assembled relationship of certain of the members
illustrated in FIG. 3;
FIG. 11 is a sectional view taken along the line 11--11 of FIG. 7
illustrating structural details of the condyle member; and
FIGS. 15 and 16 are diagrammatic illustrations of means for
compensating for differences in the mandibular flair angle.
DESCRIPTION OF THE PREFERRED EMBODIMENT
Referring to FIGS. 1 and 2 for orientation, the portions of the
natural mandible which will be referred to are the main body, which
is the anterior portion of the mandible, and the ramus and condyle
which are the posterior portions of the mandible. The main body
includes a bow area which is the anterior relatively sharply curved
portion defining the chin, and posterior relatively straight
portions extending rearwardly from the bow area at a diverging
angle. The ramus extends upward from the main body, as viewed from
the side in FIG. 1, forming an angle with the main body. The
condyle at the upper end of the ramus includes an articulating
prominence forming a portion of the tempro-mandibular joint.
The mandibular flair is the angle defined by the straight portions
of the main body, and the angle of the main body bow area is a
complex angle, since it is a function both of the mandibular flair
and of the angle of the ramus relative to the main body, which
angle varies considerably with different individuals.
Referring now to FIG. 3, there are shown several members of a kit,
including different configurations of certain of these members.
These kit members are assembled in combinations to be described to
provide a variety of forms of prosthetic devices for restoring
various portions of a mandible which it is necessary to remove. All
the members to be described are fabricated of a malleable metal
mesh, particularly mesh fabricated, by casting, of No. 316
Stainless Steel. In general, the portions of the several members to
be described are hollow tubular members or hollow boxlike members
to encourage tissue retention to the prosthetic devices.
A bow member B-1 is an elongated tubular member curved in a
generally U-shaped form to replace the main body of the natural
mandible. This member has a fixed flair angle; and means will be
described subsequently for changing the flair angle. The cross
section of the bow member is best illustrated in FIG. 13 wherein it
is seen that the member has an elongated cross section, the major
axis of elongation being transverse to the plane of the member and,
therefore, generally vertical in use. As best seen in FIG. 13, the
bow member includes a relatively flat outer wall 10, with the
opposite inner wall being depressed inwardly to define a double
tube configuration which includes a lower socket portion 11, which
is circular in cross section and which is referred to as an "outer
mating circular sleeve." This socket portion 11 extends the entire
length of the bow member, since all or various portions thereof are
employed in the various forms of devices to be described. The upper
tubular rib portion 12 may be circular and may be smaller in cross
section.
A retention member A-1 is one form of bow support member for
supporting and attaching one end of a bow member to a remaining
bone stump of a mandible. This member is used for attaching the bow
member to a remaining straight portion of the main body; and the
configuration of the retention member A-1 is the same for use on
either side of the mandible. The structure of the retention member
A-1 is shown more clearly in FIG. 9 to include an elongated body
portion 14 defined by confronting side walls joined by a curved
bottom wall and one end wall. An elongated tubular portion 15
extends longitudinally from the end wall, and is attached
integrally to the end wall adjacent to the bottom wall. The tubular
portion 15 is circular in cross section and has an outer
predetermined diameter dimensioned for a sliding fit with the outer
mating circular sleeve 11 defined by the bow member B-1. This
tubular member will be referred to as "inner mating circular
sleeve;" and these inner and outer circular sleeves are dimensioned
to coact with each other in a manner that they may be crimped
together to define a rigid coupling or joint between the respective
bow and retention members.
Ramus members R-1, R-2, R-3 and R-4, as best shown in FIG. 3, are
members intended to replace the ramus portion of the natural
mandible; and these members differ from each other in the angle
between an upward extending, elongated tubular portion 19.
Referring to the ramus member R-2 for example, the tubular body
portion 18 has an elongated oval cross section, as best seen in
FIG. 10, and this portion has a predetermined configuration and
dimension to define an "inner mating oval sleeve." The tubular
portion 19 of circular cross section extends at a predetermined
angle relative to the body portion 18 to define the angle between
the ramus member and bow member for a particular prosthetic device.
A particular ramus member is selected relative to the desired
angle. The tubular projection 19 then defines an inner mating
circular sleeve for mating engagement with the outer mating
circular sleeve of the bow member B-1.
Condyle members C-1L and C-1R have similar and related
configurations corresponding to the natural left and right condyle
portions of the natural mandible. Referring particularly to the
member C-1L as illustrated in the drawings, this member includes a
tubular body 21 having an elongated oval cross section, as best
seen in FIG. 10. The upper end of the body 21 is enlarged, and
there is attached to the upper end adjacent the posterior edge
thereof an artificial condyle 22, which is preferably fabricated of
an acrylic resin, for example, and which corresponds to the natural
condyle or condyloid process which is a part of the
tempro-mandibular joint.
Another protuberance 23 is formed at the upper end of the body 21
adjacent to the anterior edge representing the coronoid process of
the natural mandible. The tubular body 21 has a predetermined
configuration and dimension for a sliding fit over the tubular body
portion 18 of a ramus member, and the tubular body 21 is further
referred to as "outer mating oval sleeve." The inner mating oval
sleeve of the ramus member and the outer mating oval sleeve of the
condyle member then are slidably related, as best seen in FIG. 10,
to adjust the length of the ramus condyle portion of a prosthetic
device, and these sleeves are crimped together to form a rigid
coupling between the respective members. Additionally, or
alternatively, these sleeves 18 and 21 may be secured together by
means of one or more metal screws.
FIG. 11 illustrates how the artificial acrylic resin condyle 22 is
formed about and thereby secured to a portion of the body 21 of the
condyle member C-1L.
Retention members A--2R and A-2L are examples of another form of
bow support member for securing the bow member to the stump of the
mandible bone. Referring particularly to the member A-2L, which is
more particularly illustrated in FIGS. 8 and 14 of the drawing,
this member consists of a boxlike elongated curved body 25 formed
of confronting side walls, a curved connecting bottom wall, and one
end wall. This member defines a box having one open end and an open
top for receiving a portion of the mandible bone stump in the bow
area, and to which the member is secured preferably by means of
tapered screws. The curved bottom wall of the body 25 is
particularly formed to define a socket 26 formed by walls of
circular cross section having an angular extent of approximately
180.degree.. Access to the socket 26 is provided through a circular
recess 27 provided in the body end wall and aligned with the
socket. The socket walls and the opening 27 have a predetermined
dimension to define an "outer mating circular sleeve," dimensioned
to correspond to that of the bow member B-1.
The bow member and the retention member A-2L are joined by a curved
connector member S-1 or S-2, as illustrated in the drawings. These
connector members are similar, differing only in length and degree
of curvature. The connector member S-2, for example, is a uniformly
curved tubular member of circular cross section having a diameter
corresponding to those of the circular tubular projections of the
ramus members and of the retention member A-1. The connector member
S-2 then may be referred to as an inner mating circular sleeve for
mating engagement with the outer mating circular sleeves of the
retention member A-2L and the bow member B-1 for example.
The lip member L-1, seen in FIGS. 3 and 12, is an elongated actuate
member of curved U-shaped cross section dimensioned to receive the
upper rib portion 12 of the bow member B-1 and to be crimped
thereto to define a rigid connection therewith. The lip member L-1
provides a flat forward or outer wall 29 which defines an upward
extension of the flat outer wall 10 of the bow member, to provide
additional support for the lip in the bow area of the prosthetic
device.
FIGS. 4, 5, 6 and 7 illustrate, by way of example, several forms of
mandibular prosthetic devices or apparatus which are formed from
various assemblies or combinations of the members illustrated in
FIG. 3.
Referring to FIG. 4, there is shown an anterior bow prosthetic
device to replace most of the main body portion of the mandible. As
seen in the drawing, the ramus-condyle portions of the natural
mandible remain with short posterior stumps of the straight
portions of the main body. The anterior bow prosthetic device
consists of two retention members A-1 which are secured to the two
main body stumps, a bow member B-1 which is fitted over the inner
mating circular sleeve 15 of the retention members A-1, and a lip
member L-1 forming an additional support for the lip of the patient
in the bow area. As seen in the drawing, the lower portions of the
mandible stumps are received within the bodies of the retention
members A-1; and these members are secured to the bone by means of
screws which are preferably tapered and fabricated of No. 316
Stainless Steel. The manner of coupling of the bow member B-1 to a
retention member A-1 is best seen in FIG. 13 wherein the inner
mating circular sleeve 15 of the retention member is slidably
received within the outer mating circular sleeve 11 of the bow B-1.
These circular sleeves are then crimped together to provide a rigid
joint or coupling between the members A-1 and B-1.
The assembled relation of the lip member L-1 to the bow member B-1
is best seen in FIG. 12, which is a transverse sectional view of
the assembled members. As seen in FIG. 12, the flat wall 29 of the
lip member defines an extension of the flat wall 10 of the bow
member, and the lip member is crimped over the rib section 12 of
the bow member to define a rigid coupling between these
members.
For the prosthetic device illustrated in FIG. 4, the bow member B-1
is formed to provide the correct configuration and flair angle for
this particular prosthetic device.
FIG. 5 illustrates a sectional prosthetic device for a relatively
small section of the main body of the mandible which has been
removed. This prosthetic device includes one of the above-described
retention members A-1 and a portion of a bow member B-1 which has
been cut to an appropriate size to include a straight portion and a
portion of the bow area of the main body of the mandible which has
been removed. The anterior end of the prosthetic device is secured
to the existing bow area portion of the mandible by means of a
retention member A-2L and a sleeve member S-2. The body portion 25
of the retention member A-2L is secured to the bone stump by means
of tapered screws in a manner similar to that of the member
A-1.
FIG. 14 of the drawing, which is a transverse sectional view
through the retention member A-2L adjacent to its end wall,
illustrates the manner in which the bow member is jointed to the
retention member. As seen in FIGS. 5 and 14, the sleeve member S-2,
which defines an inner mating cylindrical sleeve is received within
the sockets 11 and 26, respectively, of the bow member and
retention member which define outer mating circular sleeves; and
the sleeve member spans the sockets which are crimped around the
sleeve member to form the necessary rigid coupling between the bow
member B-1 and the retention member A-2L. As seen in FIG. 5, a
portion of the bone stump, within the body of the retention member
A-2L, is cut away to form a notch 28 for the purpose of
accommodating the end of the sleeve member S-2 which is received
within the retention member body.
Since the anterior end of this particular prosthetic device is
joined to the existing mandible in the bow area, the retention
member A-2L, along with a selection of sleeve members such as S-1
and S-2, provides greater flexibility in fitting the prosthetic
device to the particular patient.
FIG. 6 of the drawing illustrates a hemi-section prosthetic device
which replaces approximately one-half of the natural mandible. This
prosthetic device includes a retention member A-2L, a bow member
B-1 which is approximately one-half of the bow member illustrated
in FIG. 3 and which is joined to the retention member by a sleeve
member S-2, and a ramus member R-2 and a condyle member C-1L which
form the left side ramus-condyle portion of the prosthetic
device.
The anterior portion of this device is assembled and joined in the
same manner as the device of FIG. 5. The ramus portion of the
device which forms the angle of the prosthetic mandible is provided
by selecting a ramus member R-2 with an appropriate angle. This
member is joined to the bow member by inserting the inner mating
circular sleeve 19 into the outer mating circular sleeve of the bow
member B-1, these sleeves being crimped to define the rigid
coupling as above described. The tubular oval body portion 18
extends upwardly and defines the inner mating oval sleeve which is
received within the outer mating oval sleeve 21 of the condyle
member C-1L; and when these members are adjusted to provide the
desired length or height of the ramus-condyle section for the
particular patient, these sleeves are screwed or crimped together
to provide the rigid coupling. The sliding relation of the oval
sleeves is best illustrated in FIG. 10.
FIG. 7 of the drawing illustrates a three-quarter section
prosthetic device for replacing all of the natural mandible except
the right side ramus-condyle portion and the small stump of the
main body. For this device, the left hand ramus-condyle section is
formed in the same manner as described with respect to the device
of FIG. 6, a ramus member R-3 being shown to provide a slightly
different angle for the ramus portion. FIG. 11 is a sectional view
through the condyle member C-1L and illustrates the manner in which
the acrylic resin condyle 22 is secured to the body 21 of the
condyle member. The acrylic resin condyle 22 is preferably cast or
otherwise formed to duplicate as nearly as possible the
configuration of the natural condyle which is being replaced.
In the device of FIG. 7, a substantial length of the bow member B-1
is used, and since the bow member is secured to a straight portion
of the mandible main body on the right side, a retention member A-1
is used in the same manner as for the prosthetic device of FIG.
4.
It will become apparent, upon considering the three-quarter section
prosthetic device of FIG. 7, that a full prosthetic mandible can be
assembled by providing an additional artificial ramus-condyle
portion for the right hand side of the prosthetic device
illustrated in FIG. 7.
FIGS. 15 and 16 of the drawing are diagrammatic illustrations of an
anterior bow prosthetic device as illustrated in FIG. 4, composed
of a bow member B-1 and two retention members A-1. FIG. 15
illustrates the situation where the particular bow member B-1, as
fabricated, has a much smaller flair angle than that required for
the particular patient. FIG. 16 illustrates the manner of adjusting
the flair angle, which consists in severing the bow member B-1 at
the midline of the bow area, and then rejoining the abutting
severed ends at a different angle by providing a suitable sleeve
member S-2 which is received in the sockets 11 of the adjacent
abutting ends. These members are then crimped together, as
described previously, to provide a new rigid bow member assembly
having the desired flair angle.
A method for forming a mandibular prosthetic device, as described
above may include the steps:
providing an elongated curved bow member having an elongated socket
portion defining an outer mating circular sleeve, for replacing
various sections of the straight and curved areas of the main body
of the mandible;
providing a first support member, for one end of the bow member,
having a body and a projecting tubular portion defining an inner
mating circular sleeve for a sliding fit with the bow member outer
sleeve;
providing the first support member with a body for either anchoring
the support member to a bone stump or defining a ramus-condyle
portion of the prosthetic device for replacing the natural ramus
and condyle; wherein the anchoring body may be provided with a
socket portion defining an outer mating circular sleeve for
receiving a separate mating sleeve member, to define the projecting
inner mating circular sleeve;
providing a second support member, for the other end of the bow
member, having a body and a projecting tubular member defining an
inner mating circular sleeve for a sliding fit with the bow member
outer sleeve;
providing the second support member with a body for either
anchoring the support member to a bone stump or defining a
ramus-condyle portion of the device for replacing a natural ramus
and condyle; wherein the anchoring body may be provided with a
socket portion defining an outer mating circular sleeve for
receiving a separate mating sleeve member, to define the projecting
inner mating circular sleeve;
assembling the bow member mating sleeve with the respective support
member mating sleeves; and crimping the sleeves together to form a
rigid assembly of the members.
What has been described is a novel mandibular prosthetic apparatus,
and method for forming such apparatus, having a number of
advantages over devices and apparatus previously used for this
purpose. A particular feature and advantage of the apparatus and
method described is the mating sleeve construction wherein the
several members of a prosthetic device are assembled together by
means of mating inner and outer sleeves which may be crimped
together to provide the desired rigid coupling between adjoining
parts and, ultimately, a rigid integral prosthetic device suitably
formed to mate with the remaining portions of the natural
mandible.
A related feature and advantage of the described apparatus and
method is that the portions of the prosthetic devices to which the
facial tissue will adhere are the defined outer mating sleeve
portions, with the members being joined by the inner mating
sleeves, to minimize or eliminate sharp edges of the prosthetic
device which may pierce the surface tissues.
Another feature of the described apparatus is that the bow member
is formed to provide an elongated, or double tubular cross section,
thereby defining a flat outer wall surface for better support of
the tissues in the main body area. An ancilliary feature is the
provision of a lip member to provide additional tissue support area
in the bow area of the prosthetic device.
Another feature of the apparatus is that the bow member may be
severed and reassembled through the use of an interior joining
sleeve to adjust the flair angle of the bow member and thereby
adapt the device to the particular patient.
While a preferred embodiment of the invention has been illustrated
and described, it will be understood by those skilled in the art
that changes and modifications may be resorted to without departing
from the spirit of the invention or the scope of the appended
claims.
* * * * *