U.S. patent application number 12/911198 was filed with the patent office on 2011-04-14 for device for providing spongy bone with bone substitute and/or bone reinforcing material, bone substitute and/or bone reinforcing material and method.
This patent application is currently assigned to Bone Support AB. Invention is credited to Par Arvidsson, Sven Jonsson, Lars LIDGREN, Torgny Lundgren.
Application Number | 20110087161 12/911198 |
Document ID | / |
Family ID | 29707895 |
Filed Date | 2011-04-14 |
United States Patent
Application |
20110087161 |
Kind Code |
A1 |
LIDGREN; Lars ; et
al. |
April 14, 2011 |
DEVICE FOR PROVIDING SPONGY BONE WITH BONE SUBSTITUTE AND/OR BONE
REINFORCING MATERIAL, BONE SUBSTITUTE AND/OR BONE REINFORCING
MATERIAL AND METHOD
Abstract
The present invention relates to a device for providing spongy
bone with bone substitute and/or bone reinforcing material, wherein
at least one perforating device (4) is provided for making at least
one hole (5) in the spongy bone (1) and wherein at least one
flushing or rinsing device (6) is provided for flushing or rinsing
the hole (5) with a rinsing agent (7). At least one vacuum source
(9) is provided for generating a vacuum in the hole (5) in the
spongy bone (1) for sucking and/or facilitating insertion or
feeding of the bone substitute and/or bone reinforcing material (3)
into said spongy bone (1). The invention also relates to bone
substitute and/or bone reinforcing material and methods in
connection with the invention.
Inventors: |
LIDGREN; Lars; (Lund,
SE) ; Lundgren; Torgny; (Eslov, SE) ;
Arvidsson; Par; (Lund, SE) ; Jonsson; Sven;
(Staffanstorp, SE) |
Assignee: |
Bone Support AB
|
Family ID: |
29707895 |
Appl. No.: |
12/911198 |
Filed: |
October 25, 2010 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10578734 |
May 10, 2006 |
|
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PCT/SE2004/001626 |
Oct 10, 2004 |
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12911198 |
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Current U.S.
Class: |
604/28 ; 604/30;
604/35 |
Current CPC
Class: |
A61B 17/1615 20130101;
A61B 17/8822 20130101; A61F 2310/00293 20130101; A61F 2/4601
20130101; A61B 17/1637 20130101; A61B 17/8827 20130101; A61F 2/4675
20130101; A61F 2002/4685 20130101 |
Class at
Publication: |
604/28 ; 604/35;
604/30 |
International
Class: |
A61M 1/00 20060101
A61M001/00 |
Foreign Application Data
Date |
Code |
Application Number |
Nov 11, 2003 |
SE |
0302983-2 |
Claims
1. A device for providing spongy bone with bone substitute and/or
bone reinforcing material, including: at least one perforating
device (4) configured to make at least one hole (5) in the spongy
bone (1), at least one flushing or rinsing device (6) configured to
flush or rinse the hole (5) with a rinsing agent (7), at least one
supply device (8) configured to supply the bone substitute and/or
bone reinforcing material (3) to the hole (5) in the spongy bone
(1), and at least one vacuum source (9) configured to generate a
vacuum in the hole (5) in the spongy bone (1), suck the rinsing
agent (7) into the hole (5) in the spongy bone(1), and to suck
rinsing agent (7) and tissue material out of said hole (5), wherein
said vacuum source (9) is further configured to suck the bone
substitute and/or bone reinforcing material (3) into the hole (5)
in the spongy bone (1) by imparting pulse like suction and/or
insertion movements to the bone substitute and/or bone reinforcing
material.
2. (canceled)
3. The device according to claim 1, wherein the vacuum source (9)
is provided to generate a vacuum in the hole (5) of the spongy bone
(1) which is adapted such that the bone substitute and/or bone
reinforcing material (3) is sucked into said hole (5) and
distributed therein without substantial portions thereof being
sucked out of the hole (5).
4. The device according to claim 1, wherein the vacuum source (9)
is provided to suck tissue material out of the hole (5) of the
spongy bone (1) before bone substitute and/or bone reinforcing
material (3) is sucked into the spongy bone (1).
5. The device according to claim 1, further comprising a collecting
device (27) configured to collect tissue material which by the
vacuum source (9) has been sucked out of the hole (5) of the spongy
bone (1) for preventing tissue material from being sucked into the
vacuum source (9) and/or into a monomer filter (28) and/or into a
bacteria filter (29).
6. The device according to any preceding claim 1, further
comprising a monomer filter (28) configured to prevent poisonous
gases, which are generated during production of bone substitute
and/or bone reinforcing material (3) from being discharged into the
surroundings.
7. The device according to claim 1, further comprising a bacteria
filter (29) configured to prevent bacteria from getting into the
hole (5) of the spongy bone (1) if a connection between the vacuum
source (9) and the spongy bone (1) is opened unintentionally.
8. The device according to claim 1, further comprising a non-return
valve device (26) configured to prevent tissue material and/or any
other material and/or bacteria from being sucked into the hole (5)
of the spongy bone (1) if the connection between the vacuum source
(9) and the hole (5) in the spongy bone (1) is opened
unintentionally.
9. The device according to claim 5, further comprising a non-return
valve device (26) configured to be located between the hole (5) in
the spongy bone (1) and the collecting device (27).
10. The device according to claim 5, further including a non-return
valve device (26) configured to be located between the monomer
filter (28) and/or the bacteria filter (29) and the hole (5) in the
spongy bone (1).
11. The device according to claim 1, further comprising a container
(18) configured to produce and/or store bone substitute and/or bone
reinforcing material (3), wherein the container includes a feeding
device (30) configured to feed bone substitute and/or bone
reinforcing material (3) out of the container (18) and into the
hole (5) of the spongy bone (1) at the same time the vacuum source
(9) generates a vacuum therein.
12. The device according to claim 1, further comprising a container
(18) configured to produce and/or store bone substitute and/or bone
reinforcing material (3), wherein the container (18) includes a
feeding device (30) configured to feed bone substitute and/or bone
reinforcing material (3) into the hole (5) of the spongy bone (1)
after the vacuum source (9) has generated a vacuum therein.
13. The device according to claim 11, wherein the feeding device
(30) is manually operable.
14. The device according to claim 1, wherein the vacuum source (9)
is configured to generate a vacuum of between -0.5 bar and -0.92
bar in the hole (5) of the spongy bone (1).
15. The device according to claim 14, the vacuum source (9) is
configured to generate a vacuum of between -0.7 and -0.8 bar in the
hole (5) of the spongy bone (1).
16. The device according to claim 1, further comprising a valve
device (32) configured to close or interrupt the supply of bone
substitute and/or bone reinforcing material (3) to the hole (5) of
the spongy bone (1) until the vacuum source (9) has generated a
suitable vacuum therein, the valve device (32) being configured to
open and permit supply of bone substitute and/or bone reinforcing
material (3) such that said material is sucked into the hole (5) of
the spongy bone (1) when said suitable vacuum has been measured
therein.
17. The device according to claim 1, further comprising at least a
first cannula or needle and a second cannula or needle (19, 20)
configured to be insertable into the spongy bone (1) such that they
are simultaneously directed into the hole (5) thereof, wherein the
first cannula or needle (19) is connected to a container (18) for
producing and/or storing the bone substitute and/or bone
reinforcing material (3) while the second cannula or needle (20) is
connected to the vacuum source (9).
18. The device according to claim 17, wherein the flushing or
rinsing device (6) comprises a rinsing agent container (16) which
is connected to the first cannula or needle (19) for leading
rinsing agent (7) into the hole (5) of the spongy bone (1) through
said first cannula (19) and out of said hole (5) to the second
cannula or needle (20).
19. The device according to claim 18, further comprising a valve
device (32) configured to either open for supply of bone substitute
and/or bone reinforcing material (3) or of rinsing agent (7)
through the first cannula or needle (19).
20. The device according to claim 1, wherein the rinsing device (6)
is configured to flush or rinse the sides (5a) of the hole (5) so
that tissue material and other material are flushed away therefrom
such that depressions (5b) are formed therein, into which the bone
substitute and/or bone reinforcing material (3) can penetrate.
21. (canceled)
22. (canceled)
23. The device according to claim 1, wherein the perforating device
(4) includes an outer tube member (11) located at the spongy bone
(1), and a perforating means (12), wherein the perforating means
(12) is configured to be movable in said outer tube member (11) in
coaxial and/or rotary direction and includes and/or cooperates with
a perforating member (13) for making the hole (5) in the spongy
bone (1).
24. The device according to claim 23, wherein the perforating means
(12) further includes an inner tube member (15) configured to
direct rinsing agent (7) into or out of the hole (5) in the spongy
bone (1).
25. The device according to claim 23, wherein the outer or inner
tube member (11 or 15) is connected to a vacuum source (9) for
sucking rinsing agent (7) through the hole (5) in the spongy bone
(1) and out of said hole through the outer tube member (11).
26. The device according to claim 1, wherein the perforating device
(4) further includes several units for making at least two holes
(5) in the spongy bone (1), wherein the at least two holes are
configured to either extend into each other, or be separated from
one another with spongy bone (1) remaining therebetween, and
wherein the sponging bone (1) remaining between the at least two
holes (5) is penetrated by air and provided with bone substitute
and/or bone reinforcing material (3).
27. The device according to claim 1, wherein the vacuum source (9)
is an injector pump (21) operatable by a compressed medium.
28. The device according to claim 27, wherein the injector pump
(21) is connected to a compressed-medium device (22) which is
designed as a compressed-air device and is positionable in
localities in or close to which the vacuum source (9) shall be
used.
29. The device according to claim 28, wherein the injector pump
(21) is connected to a compressed-medium device (22) with
commercial gas.
30. The device according to claim 28, wherein the injector pump
(21) is connected to a compressed-medium device (22) which is
configured to operate said pump with a compressed-medium pressure
of 4.5-8.5 bar.
31. The device according to claim 1, wherein the vacuum source (9)
is an electrically operated vacuum pump.
32. The device according to claim 1, wherein the vacuum source (9)
is a pump operated by gas.
33. The device according to claim 1, wherein the vacuum source (9)
is operated by hand.
34. The device according to claim 1, characterized in that the
spongy bone (1) is a spongy vertebra (2).
35. The device according to claim 1, wherein the spongy bone (1) is
a fracture due to osteoporosis.
36. The device according to claim 1, wherein the spongy bone (1) is
a femoral or knee fracture.
37. The device according to claim 1, wherein the rinsing agent (7)
is a sodium chloride solution.
38. The device according to claim 1, wherein the rinsing agent (7)
contains a detergent.
39. The device according to claim 1, wherein the flushing or
rinsing device (6) contains the rinsing agent (7), and wherein the
rinsing agent (7) contains at least one trombolytic substance.
40. The device according to claim 1, wherein flushing or rinsing
device (6) contains the rinsing agent (7), and wherein the rinsing
agent (7) is distilled water.
41. (canceled)
42. The device according to claim 1, further including a secondary
device (9 and/or 30) configured to impart reciprocating suction
and/or insertion movements to the bone substitute and/or bone
reinforcing material (3) into the hole (5) in the spongy bone
(1).
43. The device according to claim 1, further including a secondary
device (9 and/or 30) configured to impart pulse like suction and/or
feeding of the rinsing agent (7) through the hole (5) in the spongy
bone (1).
44. The device according to claim 1, further including a bone
substitute and/or bone reinforcing material, wherein the bone
substitute and/or bone reinforcing material is at least one of a
mineral material, a substantially mineral material, a ceramic, and
a substantially ceramic material.
45. The device according to claim 44, wherein the mineral material
or ceramic material is a hardenable mineral or ceramic which can be
brought to harden in the spongy bone (1).
46. The device according to claim 45, wherein the mineral material
or ceramic can be brought to harden by being mixed with a hardening
agent.
47. The device according to claim 44, wherein the mineral material
or ceramic is selected from the group comprising calcium
sulphate-.alpha.-hemihydrate, calcium sulphate-.beta.-hemihydrate,
calcium sulphate-dihydrate, calcium carbonate, .alpha.-tricalcium
phosphate, hydroxyapatite, dicalcium phosphate-dihydrate, anhydrous
dicalcium phosphate, tetracalcium phosphate, .beta.-tricalcium
phosphate, calcium deficient hydroxyapatite, monocalcium
phosphate-monohydrate, monocalcium phosphate,
calcium-pyurophosphate, precipitated hydroxyapatite, carbonaceous
apatite (dahlite), octacalcium phosphate, amorphous calcium
phosphate, oxyapatite, carbonato apatite and calcium aluminate.
48. The device according to claim 44, wherein an X-ray contrast
agent is mixed with the ceramic material.
49. The device according to claim 48, wherein the X-ray contrast
agent is water soluble and non-ionic.
50. The device according to claim 49, wherein the water soluble,
non-ionic X-ray contrast agent is selected from the group
comprising iohexol, ioversol, iopamidol, iotrolan, metrizamide,
iodecimol, ioglucol, ioglucamide, ioglunide, iogulamide, iomeprol,
iopentol, iopromide, iosarcol, iosimide, iotusal, ioxilan, iofrotal
and iodecol.
51. The device according to claim 1, further including a bone
substitute and/or bone reinforcing material (3), wherein the bone
substitute and/or bone reinforcing material (3) is a bone cement
including a polymer component, and a monomer component, wherein the
polymer and monomer harden to bone cement after mixing with each
other and feeding into the hole (5) of the spongy bone (1).
52. The device according to claim 51, wherein the bone substitute
and/or bone reinforcing material (3) consists of mineral and/or
ceramic in combination with polymer material.
53. A method for providing spongy bone with bone substitute and/or
bone reinforcing material, wherein at least one hole (5) is made in
the spongy bone (1), the at least one hole (5) is flushed or rinsed
with rinsing agent (7), and a vacuum is generated in the hole (5)
for sucking and/or facilitating insertion or feeding of the bone
substitute and/or bone reinforcing material (3) into the hole
(5).
54. The method according to claim 53, wherein a vacuum is generated
in the hole (5) for sucking rinsing agent (7) through said hole
(5).
55. The method according to claim 53, wherein the rinsing agent (7)
is brought to flush tissue material and other material away from
the sides (5a) of the hole (5) such that depressions (5b) are
formed therein and that bone substitute and/or bone reinforcing
material (3) is brought to penetrate into said depressions
(5b).
56. A Method for providing spongy bone with bone substitute and/or
bone reinforcing material (3), which is applied or provided in at
least one hole (5) in the spongy bone (1) in which a vacuum is
generated, wherein the bone substitute and/or bone reinforcing
material (3) is brought to pulsate during its application in the
spongy bone (1).
57. The method according to claim 56, wherein reciprocating
movements are imparted to the bone substitute and/or bone
reinforcing material (3) during its application in the hole (5) in
the spongy bone (1).
58. A method for providing spongy bone with bone substitute and/or
bone reinforcing material (3), which is applied or provided in at
least one hole (5) in the spongy bone (1) in which a vacuum is
generated and wherein the hole (5) is flushed or rinsed with
rinsing agent (7) before application therein of the bone substitute
and/or bone reinforcing material (3), wherein the rinsing agent (7)
is sucked pulsatingly through the hole (5) in the spongy bone (1)
by generating a pulsating vacuum in said hole (5).
59. The device according to claim 39, wherein the at least one
trombolytic substance is chosen from heparin, streptokinase,
urokinase, TPA, and other substances dissolving coagulum and
thrombi, and mixtures thereof.
60. The device according to claim 51, wherein the polymer is
polymethyl-methacrylate (PMMA)-type, and the monomer is
methylmethacrylate (MMA)-type.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional of application Ser. No.
10/578,734, filed May 10, 2006, allowed July 27, 2010, which is a
National Stage Entry of PCT International Application No.
PCT/SE2004/001626, filed Nov. 10, 2004, which claims the benefit of
priority of Swedish Application No. 0302983-2, filed Nov. 11, 2003.
All of the above listed applications are hereby incorporated by
reference in their entirety.
FIELD OF THE INVENTION
[0002] The present invention relates to a device for providing
spongy bone with bone substitute and/or bone reinforcing material,
wherein at least one perforating device is provided for making at
least one hole in the spongy bone and wherein at least one flushing
or rinsing device is provided for flushing or rinsing the hole with
a rinsing agent. The invention further relates to a bone substitute
and/or bone reinforcing material and a method.
BACKGROUND OF THE INVENTION
[0003] Vertebroplasty is a technique according to which
biocompatible material is injected into a spongy vertebra. After
some time, the injected material hardens, whereby an inner support
is obtained for fixing the vertebra and thereby alleviate pain and
reduce the risk of vertebral collapse.
[0004] The material is injected into the vertebra through a needle
and in doing so, it is necessary to subject the material to high
pressure, often one or more MPa. Hereby, there is an obvious risk
that tissue material, e.g. blood and fat, in the vertebra is
pressed out into the blood vessels or into fracture gaps such that
said material can affect adjacent nerves. There is also an obvious
risk that the injected material is pressed out into fracture gaps
or into adjacent tissue. This is well known and the material and
fat being pressed out can reach the blood vessels and the lungs,
resulting in a poorer oxygenation, blood pressure reduction and, in
exceptional cases, death.
[0005] By inserting an extra needle into the vertebra, the risk of
leakage (note publications in the enclosed reference list, point 1
and 2, in the end of the description). Normally, this extra needle
is left open or preferably connected to a suction hose for
generating a suction effect (note publication in the enclosed
reference list, point 3). However, any decisive effect is not
reached with the prior art.
[0006] Various hole making and rinsing devices for making holes in
and rinsing of vertebrae are known from e.g. U.S. Pat. No.
6,440,138, U.S. Pat. 6,716,216, U.S. Pat. No. 6,719,761 and U.S.
6,740,090, but none of these publications describes generation of a
vacuum in the vertebrae for providing safe suction of bone
substitute and/or bone reinforcing material into said
vertebrae.
SUMMARY OF THE INVENTION
[0007] The object of the present invention has been to eliminate
the abovementioned problem and this is arrived at while the
invention has been given the characterizing features of each of the
subsequent claims.
[0008] By making a hole in the spongy bone and rinse it, tissue
material and other material can be flushed away from the hole and
the sides thereof, such that said sides get rough or uneven
surfaces with depressions into which the bone substitute and/or
bone reinforcing material can be brought to penetrate by generating
a vacuum in the hole and without risking that said bone substitute
and/or bone reinforcing material penetrates into the blood
paths.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] The invention will be further described below with reference
to the accompanying drawings, in which:
[0010] FIG. 1 is a schematic view of a device according to the
invention when making a hole in a spongy vertebra shown in
section;
[0011] FIG. 2 illustrates parts of the device of FIG. 1 during
flushing or rinsing of the hole made in the spongy vertebra;
[0012] FIG. 3 illustrates parts of the device according to the
invention during suction of bone substitute and/or bone reinforcing
material into the vertebra;
[0013] FIG. 4 is a sectional view of a spongy vertebra in which
bone substitute and/or bone reinforcing material has been injected
with pressure through a needle according to prior art; and
[0014] FIG. 5 is a sectional view of a spongy vertebra into which
bone substitute and/or bone reinforcing material has been sucked by
means of a device according to the invention.
[0015] In the figures, different parts of a device for preparing
spongy bone 1, e.g. a vertebra 2, to receive bone substitute and/or
bone reinforcing material 3, and for locating said material in said
vertebra is schematically illustrated. Said device comprises at
least one perforating device 4 for making at least one hole 5 in
the vertebra 2, at least one flushing or rinsing device 6 for
flushing or rinsing said hole with rinsing agent 7 and at least one
supply device 8 which permits suction and/or insertion of bone
substitute and/or bone reinforcing material 3 into the
vertebra.
[0016] At least one vacuum source 9 is provided to generate a
vacuum in the hole 5 in the vertebra 2 for sucking and/or
facilitate insertion of bone substitute and/or bone reinforcing
material 3 into said vertebra.
[0017] The perforating device 4 can be designed in many different
ways and so can also the rinsing device 6. At the exemplary
embodiment of FIGS. 1 and 2, the perforating and rinsing devices 4,
6 are combined to a device 10 including an outer tube member 11
which can be located at the vertebra 2. In the tube member 11 there
is provided a perforating means 12 which is movable relative to
said tube member in coaxial and/or rotary direction. The
perforating means 12 has and/or cooperates with a perforating
member 13 which can be designed in many ways. As an example of a
perforating member 13, it is shown an end portion of the
perforating means 12 which can be retracted into the outer tube
member 11 when this is located at the vertebra 2 and which is bent
when it is expelled out of said pipe member. When the perforating
means 12 is rotated, the bent perforating member 13 will make the
hole 5 in the vertebra 2.
[0018] The movements of the perforating means 12 can be obtained by
means of a drive unit 14 of a suitable type.
[0019] At the exemplary embodiment, the perforating means 12 is
designed as an inner tube member 15. A rinsing agent container 16
is connected to this inner tube member 15 through a connecting
device 17 which permits feeding of rinsing agent 7 from the
container 16 into the inner tube member 15 irrespective of whether
said inner tube member is rotatable or not. Alternatively, the
rinsing agent container 16 may be connected to the outer tube
member 11 and the collecting device 27 and the vacuum source 9 to
the inner tube member 15, such that the outer tube member 11 can
lead rinsing agent 7 into the hole 5 and be sucked out of said hole
through the inner tube member 15. The perforating device 4 is used
preferably for making at least two holes 5 in the vertebra 2. These
holes 5 are located such that they communicate with each other
either by extending into each other (as is illustrated in FIG. 3)
or by having spongy bone 1 between them since such bone is pervious
to air and can be provided with bone substitute and/or bone
reinforcing material 3.
[0020] The vacuum source 9 is provided to suck rinsing agent 7
through the hole 5 and it is preferably connected to the outer tube
member 11 for sucking, through said outer tube member, rinsing
agent 7 and tissue material and other material out of said hole
5.
[0021] Between the outer tube member 11 and the vacuum source 9
there is preferably a collecting device 27 for collecting rinsing
agent 7 and tissue material and other material brought along
therewith out of the hole 5.
[0022] The rinsing device 6 is preferably provided also to flush or
rinse the sides 5a of the hole 5 such that depressions 5b and
similar are formed therein while tissue material and other material
is flushed off said sides. This is advantageous since bone
substitute and/or bone reinforcing material 3, by means of the
vacuum generated in the hole 5, can be brought to penetrate into
the depressions 5b.
[0023] At the embodiment illustrated in FIG. 3, the outer tube
member 11 has its equivalent in a first cannula or needle 19 which
can cooperate with a perforating device (not shown) for making a
first hole 5 in the vertebra 2. A second cannula or needle 20 is
connected to a vacuum source 9 and this second cannula can also
cooperate with a perforating device (not shown) for making a second
hole 5 in the vertebra 2.
[0024] The supply device 8 illustrated in FIG. 3 may have a
container 18 for mixing various components for production of bone
substitute and/or bone reinforcing material 3 and/or for storage
thereof. The container 18 is connected or connectable to a first
cannula or needle 19 which can be inserted into the vertebra 2 and
which is adapted to lead bone substitute and/or bone reinforcing
material 3 into the holes 5 in the vertebra 2. A second cannula or
needle 20 can be inserted into the vertebra 2 and is connected to
the vacuum source 9, which is adapted to generate a vacuum in the
holes 5 such that bone substitute and/or bone reinforcing material
3 is sucked into said holes and/or for facilitating insertion or
feeding of said material into said holes.
[0025] The vacuum source 9 can be an injector pump 21 which is run
or driven by a suitable compressed medium from a compressed-medium
device 22. The injector pump 21 may e.g. be driven by compressed
air and connected, through a compressed-air conduit 23, to a
compressed-medium device 22 in the form of a compressed-air device.
This device may be built into a hospital or other locality in which
the injector pump 21 shall be used. Alternatively, the injector
pump 21 can be run or driven by another commercially available gas
as is indicated with broken lines in FIG. 3.
[0026] The compressed-medium device 22 can operate the injector
pump 21 with a compressed-medium pressure of 4, 5-8, 5 bar and the
injector pump 21 may be of a type which is placed on the floor and
which has a foot pedal 24 for its operation. Thus, the injector
pump 21 can be started by tilting the foot pedal 24 in one
direction and stopped by tilting the foot pedal 24 in the opposite
direction. As an example of a usable injector pump 21 in this
connection one can mention an injector pump of the type used for
producing bone cement as defined in U.S. patent specification
5,328,262 and sold under the product name Scan Vacuum Pump.TM. by
the company Scandimed International AB, Sjobo, Sweden.
[0027] The injector pump 21 is preferably provided to generate a
vacuum in all the holes 5 of the spongy bone 1 such that said holes
are filled or can be filled with bone substitute and/or bone
reinforcing material 3 and/or a vacuum such that the bone
substitute and/or bone reinforcing material 3 is distributed
therein, preferably without any or any substantial portions thereof
being sucked into the second cannula 20.
[0028] The injector pump 21 can be provided to generate a vacuum of
between -0.5 bar and -0, 92 bar in the spongy bone 1, which vacuum
corresponds to a 70% and 90% absolute vacuum. In many cases it is
sufficient that the injector pump 21 generates a vacuum of between
-0.7 bar and -0.8 bar in the spongy bone 1.
[0029] The injector pump 21 is preferably provided to suck tissue
material such as blood and fat out of the holes 5 of the spongy
bone 1 and into the second cannula 20 before bone substitute and/or
bone reinforcing material 3 is sucked into the spongy bone 1
through the first cannula 19.
[0030] In at least one connecting conduit 25 between the second
cannula 20 (the inlet end of which is the end which is inserted
into a hole 5 of the spongy bone 1) and the injector pump 21, there
may be provided a non-return valve device 26 and/or a collecting
device 27 and/or a monomer filter 28 (if the bone substitute and/or
bone reinforcing material 3 is of bone cement type) and/or a
bacteria filter 29.
[0031] The collecting device 27 may be a container which is placed
on the floor and closed or sealed by means of a cap. A portion of
the connecting conduit 25, which is connected to the second cannula
20, is directed through the cap and a small distance down into the
container. Another portion of the connecting conduit 25 is also
directed through the cap and a small distance down into the
container. When tissue material is sucked from the holes 5 of the
spongy bone 1 to the collecting device 27, said material is
collected down below in the container and is therefore prevented
from being sucked further towards the injector pump 21 and into
said pump. If there is a monomer filter 28 and/or a bacteria filter
29 between the collecting device 27 and the injector pump 21, the
tissue material is prevented also from being sucked thereto.
[0032] The monomer filter 28 may be a carbon filter and is adapted
to prevent monomer gases, generated during production of bone
substitute and/or bone reinforcing material 3 in the form of bone
cement, from being sucked into the injector pump 21 and discharged
to the surroundings. The advantages with such a monomer filter 28
are described in the publication according to the enclosed
reference list, point 4. The bacteria filter 29 is provided to
prevent bacteria from entering or getting into the holes 5 of the
spongy bone 1 if the connecting conduit 25 is opened or opens
unintentionally and air is sucked therethrough to the holes 5 if
there is a vacuum therein.
[0033] The monomer filter 28 and bacteria filter 29 may be provided
in that portion of the connecting conduit 25 which connects the
collecting device 27 with the injector pump 21.
[0034] The non-return valve device 26, which preferably can be
provided in the connecting conduit 25 between the collecting device
27 and the second cannula 20, is adapted to prevent tissue material
from being sucked out of the collecting device 27 and into the
holes 5 of the spongy bone 1 if the connecting conduit 25 is opened
or opens unintentionally such that a suction is generated therein
towards the holes 5 of the spongy bone 1 if there is a vacuum
therein.
[0035] The container 18 may include a feeding device 30 for feeding
bone substitute and/or bone reinforcing material 3 out of the
container 18 and into the holes 5 of the spongy bone 1 at the same
time the injector pump 21 generates a vacuum therein or
thereafter.
[0036] The feeding device 30 is schematically illustrated with a
feed means 31 which is displaceably mounted relative to the
container 18 and which can be displaced manually for discharge of
bone substitute and/or bone reinforcing material 3 from the
container 18 and through the first cannula 19 into the holes 5 of
the spongy bone 1.
[0037] The container 18 may eventually be used as mixing container
for mixing the components required for the production of such bone
substitute and/or bone reinforcing material 3 that can be brought
to harden after insertion thereof into the holes 5 of the spongy
bone 1. This mixing can occur with a mixing means or in any other
way. Such a mixing means can preferably be moved manually back and
forth in the container 18 and is eventually rotated relative
thereto for mixing the components.
[0038] A valve device 32 may be provided for, on one hand, close or
interrupt the supply of bone substitute and/or bone reinforcing
material 3 through the first cannula 19 to the holes 5 of the
spongy bone 1 until the injector pump 21 has generated a suitable
vacuum therein. When this is done, the valve device 32 may be
opened for permitting suction of bone substitute and/or bone
reinforcing material 3 into the holes 5 of the spongy bone 1 by
means of the injector pump 21. The valve device 32 may be located
on the first cannula 19 or on a connecting conduit between the
container 18 and the first cannula 19. The valve device 32 may be
manually operable by means of a control handle 33.
[0039] As an alternative to the embodiment of the flushing or
rinsing device 6 described above, said device may be combined with
the supply device 8. At this alternative, the rinsing agent
container 16 of the rinsing device 6 may be connected to the first
cannula 19 e.g. through the valve device 32 which in this case can
be a three way valve permitting either that the supply of rinsing
agent to the vertebra 2 is open and the supply of bone substitute
and/or bone reinforcing material 3 to the vertebra 2 is closed or
that said supply of rinsing agent is interrupted and said supply of
material open.
[0040] The rinsing agent 7 may be of different types and it may
e.g. be distilled water or a sodium chloride solution and/or be
detergent and/or include at least one trombolytic substance, e.g.
heparin, streptokinase, urokinase, TPA and/or other substances
dissolving coagulum and thrombi.
[0041] The bone substitute and/or bone reinforcing material 3 may
consist of primarily minerals or ceramics which can be mixed with a
hardener, e.g. water. These substances may be selected from the
group comprising calcium sulphate-.alpha.-hemihydrate, calcium
sulphate-.beta.-hemihydrate, calcium sulphate-dihydrate, calcium
carbonate, .alpha.-tricalcium phosphate, hydroxyapatite, dicalcium
phosphate-dihydrate, anhydrous dicalcium phosphate, tetracalcium
phosphate, .beta.-tricalcium phosphate, calcium deficient
hydroxyapatite, monocalcium phosphate-monohydrate, monocalcium
phosphate, calcium-pyurophosphate, precipitated hydroxyapatite,
carbonaceous apatite (dahlite), octacalcium phosphate, amorphous
calcium phosphate, oxyapatite, carbonato apatite and calcium
aluminate.
[0042] A ceramic material may be calcium aluminate, which forms
part of the product Doxa T from the company Doxa
(www.doxa.se/pdf/nyhet.sub.--1.pdf).
[0043] X-ray contrast agents can be added to said ceramic bone
substitute and/or bone reinforcing material 3, e.g. water soluble
non-ionic X-ray contrast agents selected from the group comprising
iohexol, ioversol, iopamidol, iotrolan, metrizamide, iodecimol,
ioglucol, ioglucamide, ioglunide, iogulamide, iomeprol, iopentol,
iopromide, iosarcol, iosimide, iotusal, ioxilan, iofrotal and
iodecol.
[0044] Alternatively, the bone substitute and/or bone reinforcing
material 3 can be a hardenable bone cement comprising polymer and
monomer components. The polymer may be polymethylmethacrylate
(PMMA) and the monomer methylmethacrylate (MMA). A polymer base
material can be the product Cortoss.TM. from the company Orthovita
in the U.S. For composition see
www.orthovita.com/products/cortoss/oustechspecs.html. Another
polymer base material can be the product SECOUR.RTM. Acrylic Resin
PMMA from parallax medical inc.
(www.parallax-medical.com/go/9192b550-56421157-a432-d7a2b98310fe).
[0045] The bone substitute and/or bone reinforcing material 3 may
consist of a mineral and/or a ceramic in combination with polymer
material.
[0046] The advantages with the invention is obvious when comparing
the degree or ratio of fullness of the vertebra 2 of FIGS. 4 and 5.
In the vertebra 2 of FIG. 4, the bone substitute and/or bone
reinforcing material 3 has been pressed into said vertebra 2
through a cannula or needle and it clearly appears from FIG. 4 that
only a part of the vertebra 2 is filled with bone substitute and/or
bone reinforcing material 3. In the vertebra 2 of FIG. 5 however,
the bone substitute and/or bone reinforcing material 3 has been
sucked into the vertebra 2 in accordance with the invention through
the cannula or needle and it is clearly evident from FIG. 5 that
substantially larger parts of the vertebra 2 are filled with bone
substitute and/or bone reinforcing material 3 without said material
having been pressed out into the blood paths.
[0047] It is also obvious from FIG. 5 that the negative pressure
generated by the vacuum source 9 has provided for a uniform and
complete distribution of the bone substitute and/or bone
reinforcing material 3 in the hole 5 and depressions 5b in the
sides 5a of the hole 5.
[0048] The invention is not limited to what is described above and
illustrated in the drawings, but may vary within the scope of
subsequent claims. Thus, the vacuum source 9 may instead of an
injector pump 21 be another vacuum pump which can be electrically
operated or operated by gas or by hand or operated in any other
way, that the hole 5 may be more than one hole and surrounding
parts thereto, that the rinsing agent 7 may be another than those
described and that the bone substitute and/or bone reinforcing
material 3 may be of another type than those described.
[0049] There may be a device for imparting pulse like suction
and/or insertion movements to the bone substitute and/or bone
reinforcing material 3 into the hole(s) 5 in the spongy bone 1.
Furthermore, there may be a device for imparting reciprocating
suction and/or insertion movements to the bone substitute and/or
bone reinforcing material 3 into the hole(s) 5 in the spongy bone
1.
[0050] There may also be a device for pulse like suction and/or
feeding of the rinsing agent 7 through the hole(s) 5 in the spongy
bone 1.
[0051] Said device may be defined by pulsating the vacuum source 9
and/or its vacuum generation and/or by generating pulses by means
of the feeding device 30.
REFERENCE LIST
[0052] 1) Aebli Nt Krebs J, Schwenke D, Davis G, Theis J C.
Cardiovascular charges during multiple vertebroplasty with and
without vent-hole: an experimental study in sheep. Spine
2003;28(14):1504-11. [0053] 2) Koessler M J, Aebli N, pitto R P.
Fat and Bone Marrow Embolism During Percutaneous Vertebroplasty.
Anesth Analg 2003;97:293-294. [0054] 3) Lidgren, Lars. Bone
Substitutes. Karger Gazette No. 65 2003; Bone and Joints. [0055] 4)
Kirby B S, Doyle A, Gilula L A. Acute bronchospasm due to exposure
to polymethacrylate vapours during percutaneous vertebroplasty. AJR
J Roentgenol. 2003 Feb; 180 (2) :543-4.
* * * * *
References