NZ612526B2 - Orthotic device and method of making an orthotic device - Google Patents
Orthotic device and method of making an orthotic device Download PDFInfo
- Publication number
- NZ612526B2 NZ612526B2 NZ612526A NZ61252612A NZ612526B2 NZ 612526 B2 NZ612526 B2 NZ 612526B2 NZ 612526 A NZ612526 A NZ 612526A NZ 61252612 A NZ61252612 A NZ 61252612A NZ 612526 B2 NZ612526 B2 NZ 612526B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- torso
- attachment point
- torso section
- reinforcement
- wearer
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices ; Anti-rape devices
- A61F5/01—Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
- A61F5/02—Orthopaedic corsets
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices ; Anti-rape devices
- A61F5/01—Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
- A61F5/02—Orthopaedic corsets
- A61F5/024—Orthopaedic corsets having pressure pads connected in a frame for reduction or correction of the curvature of the spine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices ; Anti-rape devices
- A61F5/01—Orthopaedic devices, e.g. long-term immobilising or pressure directing devices for treating broken or deformed bones such as splints, casts or braces
- A61F5/02—Orthopaedic corsets
- A61F5/026—Back straightening devices with shoulder braces to force back the shoulder to obtain a correct curvature of the spine
Abstract
612526 An orthotic device (10) that may be particularly effective in the treatment of scoliosis comprises a torso section and a resilient reinforcement (40) attached to the torso section. The reinforcement extends diagonally across a front and/or a rear portion of the torso section between a first attachment point (51) at a first side of the torso section and a second attachment point (52) at a second side of the torso section. At least one of the first attachment point and the second attachment point is locally indented into the torso section such that the reinforcement is stretched when device is donned a patient, thereby applying a force to the patient's torso. attachment point (51) at a first side of the torso section and a second attachment point (52) at a second side of the torso section. At least one of the first attachment point and the second attachment point is locally indented into the torso section such that the reinforcement is stretched when device is donned a patient, thereby applying a force to the patient's torso.
Description
Orthotic Device And Method Of Making An Orthotic Device
New Zealand patent application 709234 (NZ 709234) has been divided out of the present
application. In the description in this present specification reference may be made to
subject matter which is not within the scope of the appended claims and which may be
claimed in NZ 709234. That subject matter should be readily identifiable by a person
skilled in the art and may assist in putting into practice the invention as defined in the
presently appended claims.
The invention relates to an orthotic device and a method of making an orthotic device. The
device may be particularly suitable for use in the treatment of scoliosis.
Background to the invention
Scoliosis is a condition involving a lateral curvature of the spine, often coupled with
vertebral rotation. Untreated scoliosis can cause problems with respiratory and cardiac
functions, as well as pain, and restricted mobility and limb functions. The treatment of
scoliosis varies depending on the severity of the spinal curvature, and may involve
physiotherapy, bracing or, in severe cases, surgery.
A typical non-surgical treatment of scoliosis involves the use of a rigid thoraco-lumbar
brace to hold the spine in a preferential position, thereby enabling a wearer to experience
improved posture and limb functionality. An example of such a rigid thoracic brace is the
Boston brace developed in 1976. Typically, rigid brace treatment involves the wearing of a
brace for up to 23 hours in a day. Studies have shown that such treatment may have a
positive effect when the brace is worn for the prescribed periods of time. However,
compliance with the prescribed treatment regimen may often be poor due to the
inconvenience of wearing a rigid brace for long periods of time. Studies have shown that in
some cases a brace was only worn 20% of the prescribed time, resulting in the treatment
having little effect on prognosis of the scoliosis (Howton et al. 1987 orthopaedic
transactions 11: 125-126).
Other methods of bracing have been used in the treatment of scoliosis. For example, the
SpineCor brace is a dynamic brace that relies on elastic bands to apply a dynamic
corrective force to a patient’s trunk to correct spinal curvature. There may be patient
comfort issues such as abrasion involved in use of the SpineCor brace, but overall patient
40 compliance appears to be increased compared with a rigid brace system.
5596593_2.docx
Matthews and Crawford (Prosthetics and Orthotics International August 2006; 30(2): 174-
181) describe the use of a dynamic elastomeric fabric orthosis consisting of a Lycra
body-suit with the addition of elastomeric panels that act to counter thoracic spine rotation
and lateral curvature. Patient compliance and comfort were improved with respect to a
rigid brace, and the orthosis did not have the same abrasion issues as the SpineCor
dynamic brace. The suit also appeared to provide beneficial proprioceptive effects and the
visual appearance of the suit was improved compared with previously known braces. The
orthosis described by Matthews and Crawford may be limited in the force that can be
provided by the elastomeric panels, however, which may limit the situations in which the
suit is applicable.
Summary of invention
The invention provides an orthotic device and a method of making an orthotic device
according to the appended independent claims to which reference should now be made.
Preferred and/or advantageous features of the invention are set out in various dependent
sub-claims.
Thus, the invention may provide an orthotic device comprising a torso section fabricated
from a material for conforming to at least a portion of a wearer’s torso and a reinforcement
for applying a force to the wearer’s torso to urge a portion of the wearer’s spine in a
substantially lateral direction. The reinforcement comprises resilient material attached to
the torso section, preferably in the form of a strip or panel, that extends diagonally across
a front portion, and/or a rear portion, of the torso section between a first attachment point
at a first side of the torso section and a second attachment point at a second side of the
torso section. The first attachment point is locally indented into the first side of the torso
section, and/or the second attachment point is locally indented into the second side of the
torso section, such that the resilient material attached to the torso section is stretched
when the orthotic device is donned by the wearer, thereby applying the force to the
wearer’s torso.
A resilient material is a material that can elastically deform under load and return to its
original shape when the load is removed, for example rubber materials or elastomeric
fabric materials.
The material forming the torso section of the device, which may be termed an underlying
40 material, is preferably a resilient or elastomeric material that is capable of conforming to
the wearer’s body without generating substantial directional forces, or giving rise to lines of
tension or compression in any specific direction. Suitable materials are readily available,
5596593_2.docx
for example elastomeric materials comprising a polyurethane-polyurea copolymer such as
® ® ®
Dorlastan , Spandex , or Lycra . A particularly suitable material may be a polyamide-
cotton-Dorlastan material, for example a material comprising 51% polyamide, 17% cotton
and 32% Dorlastan .
The reinforcement that is attached to the torso section to form the device includes one or
more sections of resilient material. The purpose of the resilient material in the
reinforcement is to apply a force acting in one or more predetermined directions to assist
and/or restrict movement of the wearer’s torso. Particularly preferably, the resilient
material is in the form of one or more strips or panels of resilient or elastic material that are
attached to the torso section to produce a lateral force that acts on the wearer’s spine.
It is preferable that the resilient material forming the reinforcement is a different material
from the underlying material forming the torso section. For example, the reinforcement
may comprise one or more elongated strips or panels of a resilient material such as a
nylon/cotton material or a nylon/ Lycra material, for example a material comprising 81%
polyamide and 19% Lycra .
When the device is worn, the reinforcement may provide a constant force to the wearer’s
torso that urges the wearer’s spine in a specific direction. The reinforcement may also
provide a force that resists movement of the wearer’s torso and spine when the wearer
moves their torso in a specific direction.
The torso section is indented at the first attachment point, the second attachment point, or
both first and second attachment points. The circumference of the torso section at the
indent or the indents is reduced. Thus, when the device is worn, the material at the indents
needs to stretch more than the rest of the material in order to conform to the wearer’s
torso. By stretching when the device is worn, the resilient material is placed under tension.
This tension applies a compressive force to the user. The depth of the indent or indents
controls the tension that the resilient material is placed under and, thereby, the power of
the device.
By attaching the reinforcement to the torso section at one or more indents, the
reinforcement material (i.e. the resilient material) may be attached to the first portion in a
non-tensioned condition, only becoming tensioned when the device is worn. Thus, the
40 strips or panels of resilient material forming the reinforcement need not have a force
applied to them when they are attached to the underlying resilient material of the torso
section. It is not easy to pre-tension a resilient material and then attach it to an underlying
5596593_2.docx
orthotic device, for example by stitching. It also becomes more difficult to pre-tension a
resilient material as the force the material is required to produce increases. By attaching
the reinforcement at an indent, these problems may be overcome.
An indent may locally reduce the circumference of the torso section by greater than 2%.
Preferably the circumference is reduced by between 3% and 30%, preferably between 5%
and 25%, preferably between 7.5 % and 20%. The circumference may be reduced by
about 10% or about 15%.
The indents cause the reinforcement material to stretch when the device is worn. The
reinforcement material preferably stretches by between 2% and 25% of its length, for
example between 5% and 20%, or between 10% and 15%. The more the reinforcement
stretches, the greater the force exerted by the reinforcement.
It is preferred that one of the first or second attachment points is located level with a
patient’s hip on one side of the torso section and that the other of the first or second
attachment points is located between the hip and the armpit on the other side of the torso
section. The reinforcement extends diagonally between the first and second attachment
points. For the avoidance of doubt, the assignment of the terms first attachment point,
second attachment point, and, where needed, third attachment point, has no bearing on
the function of the device. For the purposes of the following discussion, an attachment
point that is level with the hip is referred to as the second attachment point and an
attachment point located between the hip and the armpit on the opposing side of the torso
section to the second attachment point is referred to as the first attachment point. An
attachment point located between the hip and the armpit on the same side of the torso
section as the second attachment point is referred to as a third attachment point.
While either or both of the first and second attachment points may be locally indented, it is
preferred that an attachment point located at the hip, i.e. the second attachment point in
the convention adopted for the purposes of this description, is not indented, or is only
indented to a small degree compared with the first attachment point. There may be some
wearer discomfort if a hip attachment point is locally indented to a great degree.
In preferred embodiments of the orthotic device, the second attachment point is located
level with a patient’s hip, or at the lowest point on one side of the torso section, and is not
40 locally indented, whereas the first attachment point is located between the hip and armpit
on the opposite side of the torso section and is locally indented,
5596593_2.docx
Advantageously, the reinforcement may comprise a further section of resilient material
extending laterally or diagonally across a front portion, and/or a rear portion, of the torso
section between the first attachment point and a third attachment point that is vertically
spaced from the second attachment point on the second side of the torso section. The
third attachment point may be locally indented relative to the torso section. The
reinforcement applies a compressive force that urges a wearer’s torso in a lateral direction
towards the second side of the torso section.
Where the reinforcement comprises sections of resilient material that attach to a first
attachment point on one side of the torso section, and second and third attachment points
on a second side of the torso section, the reinforcement may be described as being “V-
shaped”, although the “V” is on its side when the device is worn. The first attachment point
forms the apex of the “V”, and the second and third attachment points are at the end of
each of the legs of the “V”.
Where the reinforcement is “V-shaped” in the front view or rear view (or both) as described
above, the first attachment point refers to the point on one side of the torso section that the
reinforcement contacts, and the second and third attachment points refer to points on the
opposite side of the torso section that the reinforcement contacts. When the resilient
material forming the reinforcement is stretched, lines of tension are produced between the
first attachment point and the second attachment point and between the first attachment
point and the third attachment point.
It is preferable that the reinforcement extends across both front and rear portions of the
torso section. Thus, in a preferred configuration the device may have reinforcement
material attached at a first attachment point on, say, a left side of the torso section, and at
second and third attachment points on a right side of the torso section. Sections of
reinforcement material may extend across both the front and rear of the torso section
between the first attachment point and the second attachment point and between the first
attachment point and the third attachment point. It is preferred that the torso section is
indented at the first attachment point, and there may be further indents at one or both of
the second and third attachment points. The effect of the indents is to reduce the length of
the sections of resilient material that form the reinforcement when the device in not worn.
Thus, when the device is worn and the material at the indents is stretched (i.e. both the
underlying resilient material and the reinforcement material) the reinforcement material
40 causes a force to be applied to the wearer’s torso.
5596593_2.docx
Where the reinforcement is applied to the device in a “V-shape” to the front and/or rear of
the torso section, a force is applied to the wearer’s torso in a lateral direction from the first
attachment point, or apex of the “V”, toward the second side of the torso section. Thus, if
the first attachment point is on the left side of the device, the lateral force acts in a left to
right direction. If the first attachment point is on the right of the device, the lateral force
acts in a right to left direction.
It is preferred that the second attachment point is fixed to be level with a patient’s hip on
either the left side or right side, as required. The first attachment point may be located at
any point above the hip on the opposite side to the second attachment point, as
determined by a medical practitioner. By moving the location of the first attachment point
vertically up or down, the point at which the lateral force has maximum effect may be
moved up or down. Scoliosis may result from curvature low in the spinal column or high in
the spinal column. Typically the curvature will result in a “C-shape” to the spine when
viewed from the rear. A double curvature may also cause an “S-shape” in the spine when
viewed from the rear. By moving the first attachment point up or down, the device may be
tailored to provide a corrective force at the appropriate point for a particular patient.
Preferably, the position of the first attachment point is determined by reference to an x-ray
of the wearer’s spine. Such an x-ray will show the position and extent of the scoliotic curve
and allow the first attachment point to be chosen for most effective treatment. The process
of preparing an orthotic device using x-ray information is known as x-ray blueprinting.
The height of the third attachment point may also be determined by x-ray blueprinting.
Preferably the second attachment point, however, is determined by the position of the
wearer’s hip, i.e. without reference to the patient’s condition.
Typically scoliosis patients have a lateral curvature of the spine of between 10 degrees
and 60 degrees or more. A low degree of scoliosis may not require a high applied force for
treatment, whereas a more severe scoliosis may require treatment using an orthotic
device that exerts a greater corrective force. The use of indents at attachment points for
the reinforcement provides a simple means to tailor the corrective force provided by the
device to a patient’s needs. A shallow indent means that the reinforcement only needs to
stretch a small amount in order for the device to conform to a patient’s torso. Thus, the
elastic force urging the reinforcement back towards its un-stretched state is low, and the
40 corrective force transmitted to the patient is correspondingly low. By forming a device with
an increased indent, the corrective force applied to the patient may be increased. In
combination with the selection of different resilient materials having different degrees of
5596593_2.docx
elasticity to form the reinforcement, the corrective force transmitted to a patient may be
carefully controlled to provide appropriate treatment.
An orthotic device according to embodiments of the invention may comprise additional
reinforcement panels to exert forces in other directions to those described above. For
example, the device may additionally comprise a reinforcement consisting of a section of a
resilient material that extends from a central point on a front side of the torso section to a
centre point on a rear side of the torso section. Such a reinforcement panel is preferably
situated on the side of the wearer’s body at which the spinal curve is convex and may
provide a resistance to the curve via the wearer’s thoracic cage.
In a further example of an optional reinforcement panel, embodiments of an orthotic device
may comprise a section of reinforcement material that acts as a reinforcement to counter
thoracic spine rotation. Such reinforcement may be termed spinal de-rotation
reinforcement.
In a first configuration, a spinal de-rotation reinforcement may comprise a strip of resilient
material that has a first end located on the torso section at an anterior portion of a
shoulder. In most circumstances, the shoulder is the shoulder located on the same side of
the torso section as the first attachment point described above. In some unusual
circumstances, the shoulder may be on the opposite side of the torso section as the first
attachment point. The strip of material extends over the shoulder and then downwards
until clear of the axilla area. The strip then extends diagonally across the front of the chest
and terminates at a second end located at a portion of the torso section near to the
anterior superior iliac spine, i.e. near the hip. The second end is at approximately the
same location as the second location point described above.
In a second configuration, a spinal de-rotation reinforcement may comprise a strip of
resilient material that has a first end located on the torso section at an posterior portion of
a shoulder. The shoulder is the shoulder located on the same side of the torso section as
the first attachment point described above. The strip of material extends over the shoulder
and then downwards until clear of the axilla area. The strip then extends diagonally across
the rear of the torso section and terminates at a second end located at a portion of the
torso section near to the anterior superior iliac spine, i.e. near the hip. The second end is
at approximately the same location as the second location point described above.
The strip of resilient material may be any suitable material, and may be multiple strips of
material. The action of a spinal de-rotation reinforcement is to compress the convex side
5596593_2.docx
of the spinal curvature in a patient suffering from scoliosis, thus countering the natural
progression of the scoliotic curve rotation, and to provide either a posterior or anterior
acting force on the shoulder.
The orthotic device may take the form of a vest. The device may, however, be in the form
of a body suit. In this case the device may have arm sections and leg sections in addition
to the torso section. Leg sections may assist the anchoring of a lower portion of the device
so that the attachment points do not stray from their intended position with respect to the
wearer.
Fasteners such as zips may cut through reinforcement materials. The functionality of the
reinforcement material, i.e. a strip or panel of a resilient material, should not be affected as
long as a secure attachment is made on either side of the fastener. Forces generated by
the reinforcement are transmitted through the fastener when it is closed. It is preferred that
the fastener is a zip fastener.
The orthotic device may further comprise a reinforcement for applying a compressive force
to a first shoulder of the wearer, the reinforcement for applying a compressive force to the
first shoulder comprising a resilient material attached to the torso section and extending
from a first end located on the front or rear portion of the torso section, over a first
shoulder portion, downward and beneath an armpit portion of the first side of the torso
section, and diagonally downwards across the front or rear portion of the torso section to a
second end located at a hip portion on the second side of the torso section, in which there
is no arm portion extending from the second side of the torso section.
The invention may also provide a method of making an orthotic device as described above
comprising the steps of determining the vertical position of the first attachment point based
on x-rays of the wearer’s torso (blueprinting), producing a torso section for substantially-
conforming to the wearer’s body, the torso section being indented at the first attachment
point, and attaching the reinforcement for applying a force to the wearer’s torso to the
torso section such that it is stretched when worn by the wearer. Advantageously, the
reinforcement material is attached in an un-stretched condition. It is preferred that the
location of the second attachment point is determined by the position of a patient’s hip.
The method may further comprise the vertical position of a third attachment point being
40 determined from x-rays of the wearer’s torso.
5596593_2.docx
The method may involve a further step of determining the corrective force desired from the
device and selecting the reinforcement material and/or the indent depth to achieve this
force.
There is also disclosed herein an orthotic device comprising a torso section fabricated
from a material for conforming to at least a portion of a wearer’s torso and reinforcement
for applying a force to a first shoulder of the wearer to provide a posterior or anterior acting
force on the shoulder. The reinforcement comprises resilient material attached to the torso
section, preferably in the form of a strip or panel. The resilient material extends upwardly
from an anterior or posterior shoulder position on a first side of the torso section, upwardly
over the first shoulder and then downward over the shoulder-blade until clear of the axilla.
The resilient material then extends diagonally downwards across the front or rear of the
torso section and is attached to the torso section at a position approximately at the anterior
superior iliac spine or upper trochanter (i.e. at the hip) on a second side of the torso
section opposite the first side of the torso section. The orthotic device comprises an arm
section that encapsulates the first shoulder. The arm section may extend as required, and
preferably covers at least an upper portion of the arm. There is no arm section on
extending from the second side of the torso section. This orthotic device provides a spinal
de-rotation effect, and pulls the first shoulder either backwards and down or forwards and
down.
If used on a scoliosis patient, this device is preferably configured such that the first
shoulder is the shoulder on the convex side of the patient’s scoliosis curve.
The presence of the arm section on the same side as the first shoulder, but not on the side
of the second shoulder, provides a counter-rotational force on the first shoulder.
Preferably, the orthotic device includes a pressure relief panel located at a second
shoulder of the torso section. The pressure relief panel is a fastenable flap that can be
opened to allow the wearer’s second shoulder to be free of the orthotic device. The flap
may be fastened once the wearer has donned the device.
An orthotic device comprising a spinal de-rotation reinforcement may comprise any other
reinforcements described above in relation to other orthotic devices.
5596593_2.docx
Specific embodiment of the invention
A specific, non-limiting embodiment of the invention will now be described with reference
to the figures, in which;
Figure 1 illustrates a frontal view of an orthotic device according to an embodiment of the
invention;
Figure 2 is a schematic illustration showing the indent in the embodiment as illustrated in
figure 1;
Figure 3 illustrates front and rear views of a wearer of an orthotic device according to an
embodiment of the invention and illustrates the position of translational reinforcement
panels; and
Figure 4 illustrates front and rear views of a wearer of an orthotic device according to an
embodiment of the invention and illustrates the position of spinal de-rotational
reinforcement panels.
Figure 1 illustrates an orthotic body-suit 10 for the treatment of scoliosis. The frontal view
of the suit is illustrated. The body-suit 10 is an orthotic device and comprises a torso
section 20 for covering a wearer’s torso and pelvis, and leg sections 31, 32 that extend
down an upper portion of a wearer’s right and left leg respectively. The torso section 20
and the leg sections 31, 32 are formed from an elastomeric material having a composition
of 51% polyamide, 17% cotton and 32% Dorlastan . This material is a lightweight,
breathable, elastomeric fabric and is suitable for forming the underlying material of the
body-suit 10. Other suitable fabrics are available, for example under the trade names
Spandex or Lycra .
The body-suit 10 has a first reinforcement panel 40 that is v-shaped when viewed from the
front. This reinforcement panel may also be termed a translatory panel, as it provides a
translation force to the wearer’s torso. This panel extends from a first attachment point 51
on a right side of the torso section 20, where the apex of the “V” 41 is attached, to second
and third attachment points 52, 53 on a left side of the torso section, where lower and
upper portions of the “V” 42, 43 are attached. The first reinforcement panel 40 extends
around the rear of the suit in the same way as it extends across the front of the suit. Thus,
40 in a rear view the reinforcement panel would also appear to be v-shaped.
5596593_2.docx
Effectively, the first reinforcement panel provides two bands of reinforcement. A first band
encircles the torso section and extends diagonally upwards from the first attachment point
51 to the third attachment point 53, and a second band encircles the torso section and
extends diagonally downwards from the first attachment point 51 to the second attachment
point 52.
The first reinforcement panel 40 is formed from a resilient material having a composition of
81% polyamide and 19% Lycra , which is an elastomeric material that offers greater
resistance to deformation than the underlying elastomeric material.
The first reinforcement panel 40 is attached to the underlying resilient material of the body-
suit by means of stitching. This stitching follows the edges of the panel. Thus, the first
reinforcement panel 40 is not only attached to the body-suit at the designated attachment
points.
It is noted that the first reinforcement need not be a single v-shaped panel as illustrated in
figure one. A plurality of strips of resilient material may be attached to the torso section in
order to produce lines of tension between the first attachment point and the second
attachment point and between the first attachment point and the third attachment point.
The first attachment point 51 is indented into the right side 21 of the torso section 20. This
is more clearly illustrated by figure 2. In figure 2, a dotted line 100 shows the position the
right side of the torso section would take if there was no indent. This is also the line that
the right side of the torso section has when the device is worn, as the wearer’s body
stretches the fabric forming the device and eliminates the indents. The depth of the indent
may be defined as the distance between the actual position of the material at a point of
attachment and the position the material would be in if there was no indent. This is shown
as the distance “d” in figure 2.
The position of the second attachment point is determined by reference to the position of a
patient’s hip. The positions of the first and third attachments points are determined by
reference to the patient’s condition. The strength of the correctional force applied by the
orthotic device may depend in part on the resilience of the reinforcement panel 40, and in
part on the depth of the indent at the first attachment point 51.
40 Figure 3 is a schematic diagram illustrating the position of the first reinforcement panel 40
on a wearer of the suit. The position of the first attachment point 51, the second
attachment point 52, and the third attachment point 53, is shown in both front and rear
5596593_2.docx
views. While the second attachment point 52 is preferably fixed with respect to a wearer’s
hip, the first and third attachment points may vary depending on the wearer’s condition.
The body suit of this specific embodiment also comprises a second spinal de-rotation
reinforcement panel 90. This second reinforcement panel originates at a first end 97
located at an anterior portion of the torso section adjacent to the right shoulder. The panel
then extends over the shoulder and downwards beneath the right armpit of the torso
section. The panel 90 then extends diagonally downwards across the front of the body-
suit, to a second end 92 located at a left hip portion of the torso section. The second
reinforcement panel 90 lies beneath the first reinforcement panel 40 in this embodiment.
The second reinforcement panel 90 generates a strong compressive force to the right side
of the wearer’s torso. The suit incorporates a pressure relief panel 95 at a left shoulder of
the torso section to compensate for this pressure. The pressure relief panel 95 is an
adjustable Velcro fastened flap. When donning the suit, the pressure relief panel is the
final component to be fastened.
Figure 4 is a schematic illustration showing in front and rear views the position of the
second reinforcement panel (spinal de-rotation panel) on a wearer when the suit is worn.
The panel 90 can be seen to extend from a first end 97 on an anterior portion of the
wearer’s shoulder, downwardly over the wearer’s right shoulder blade 98 and underneath
the right armpit 99. The panel 90 then extends diagonally downwards across the wearer’s
chest and terminates at a second end 92 located at the anterior superior iliac spine.
When the body-suit 10 is worn, the suit conforms to the wearer’s body. At the first
attachment point 51 the suit needs to stretch in order to eliminate the indent and conform
to the wearer’s body. The first reinforcement panel 40 is, therefore, stretched and elastic
forces are generated between the first attachment point and the second attachment point,
and between the first attachment point and the third attachment point. These forces are
illustrated in figure 1 as double-headed arrows extending along the upper and lower
portions 43, 42 of the first reinforcement panel 40. The result of the forces generated in the
upper and lower portions 43,42 of the first reinforcement panel 40 is that a force is
generated that urges the wearer’s torso from right to left as indicated by arrow 110 in
figure 1. The second reinforcement panel 90 simultaneously acts to compress the spine
and prevent thoracic spine rotation.
In alternative embodiments, the suit may have an arm section, for covering a wearer’s
arm, on the same side as the first end of the second reinforcement panel. For example, if
5596593_2.docx
an arm section were attached to the suit of figure 1 it would be a right arm section. An arm
section may act to prevent the shoulder from coming forward.
To treat a scoliosis sufferer, the first attachment point would be provided on the convex
side of the scoliotic curve, so that the force provided by the panel urges the spine towards
a more normal curvature. The vertical position of the first attachment point and the vertical
position of the second attachment point would be determined by reference to x-rays
showing the abnormal curvature of the spine.
For example, the apex of the first reinforcement panel (the first attachment point) may be
vertically positioned to apply a force to the rib below the vertebral angle lower “null” point
of the scoliotic curve. The pressure from the reinforcement is thus applied, via the rib, to
the vertebra at the lower “null” point of the scoliotic curve. The first attachment point
should not be positioned higher than this, as pressure applied incorrectly may have
detrimental results for the patient.
The vertical position of the third attachment point may likewise be determined from the
patient’s x-rays. The third attachment point may, for example, apply pressure to the rib
below the vertebral angle upper “null” point of the scoliotic curve.
The magnitude of the corrective force may be tailored by altering the depth of the indent.
The term ‘comprising’ as used in this specification and claims means ‘consisting at least in
part of’. When interpreting statements in this specification and claims which include the
term ‘comprising’, other features besides the features prefaced by this term in each
statement can also be present. Related terms such as ‘comprise’ and ‘comprised’ are to
be interpreted in similar manner.
5596593_2.docx
Claims (15)
1. An orthotic device comprising; a torso section fabricated from a first material for conforming to at least a portion of a wearer’s torso, and 10 a reinforcement for applying a force to the wearer’s torso to urge a portion of the wearer’s spine in a lateral direction, the reinforcement comprising resilient material attached to the torso section and extending diagonally across a front portion, and/or a rear portion, of the torso section between a first attachment point at a first side of the torso section and a second attachment point at a second side of the torso section, 15 in which the first attachment point is locally indented into the first side of the torso section, and/or the second attachment point is locally indented into the second side of the torso section, such that the resilient material attached to the torso section is stretched when the orthotic device is donned by the wearer, thereby applying the force to the wearer’s torso.
2. An orthotic device according to claim 1 in which the reinforcement further comprises resilient material extending diagonally across a front portion, and/or a rear portion, of the torso section between the first attachment point and a third attachment point vertically spaced from the second attachment point on the second side of the torso 25 section, the reinforcement applying a lateral compressive force that urges a wearer’s torso in a lateral direction towards the second side of the torso section.
3. An orthotic device according to claim 2 in which the third attachment point is locally indented into the second side of the torso section.
4. An orthotic device according to claim 2 or claim 3 in which the first attachment point is situated vertically higher than the second attachment point and vertically lower than the third attachment point. 35
5. An orthotic device according to any preceding claim in which the reinforcement is a first reinforcement, further comprising a second reinforcement, the second reinforcement comprising resilient material attached to the torso section such that it applies a rotational force that acts to rotate the torso of a wearer. 40
6. An orthotic device according to any preceding claim in which the first material forming the torso section is a lightweight resilient material that can conform to the wearer’s body without giving rise to lines of tension or compression in any specific direction. 5596593_2.docx
7. An orthotic device according to claim 6 in which the reinforcement comprises a different resilient material.
8. An orthotic device according to claim 6 or claim 7 in which the reinforcement 10 comprises sections of a resilient material capable of providing a constant force to urge the wearer’s torso in a specific direction, the sections of the resilient material being applied to the torso section in the form of panels or strips of material.
9. An orthotic device according to any preceding claim in which the magnitude of the 15 force generated by the reinforcement when the device is worn is related to the depth that the, or each, attachment point is indented into the first and/or second side of the torso section.
10. An orthotic device according to any preceding claim in which the second 20 attachment point is located at a wearer’s hip on the second side of the torso section and the third attachment point is located below an arm opening on the second side of the torso section, the first attachment point being located between the hip and the arm-opening on the first side of the torso section. 25
11. An orthotic device according to any preceding claim comprising a reinforcement for applying a compressive force to a first shoulder of the wearer, the reinforcement for applying a compressive force to the first shoulder comprising a resilient material attached to the torso section and extending from a first end located on the front or rear portion of the torso section, over a first shoulder portion, downward and beneath an armpit portion 30 of the first side of the torso section, and diagonally downwards across the front or rear portion of the torso section to a second end located at a hip portion on the second side of the torso section, in which there is no arm portion extending from the second side of the torso section. 35
12. A method of making an orthotic device according to any preceding claim comprising the steps of, determining the vertical position of the first attachment point based on x-rays of the wearer’s torso, producing a torso section for substantially-conforming to the wearer’s body, the 40 torso section being indented at the first attachment point, and 5596593_2.docx 5 attaching the reinforcement for applying a force to the wearer’s torso to the torso section such that the reinforcement for applying a force to the wearer’s torso is stretched when the device is worn.
13. A method according to claim 12 in which the vertical position of a third attachment 10 point is determined from x-rays of the wearer’s torso.
14. An orthotic device according to claim 1, the orthotic device being substantially as hereinbefore described with reference to the accompanying drawings. 15
15. A method according to claim 12, the method being substantially as hereinbefore described with reference to the accompanying drawings. 5596593_2.docx
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NZ709234A NZ709234B2 (en) | 2011-03-10 | 2012-03-12 | Orthotic device |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1104074.8A GB2488824B (en) | 2011-03-10 | 2011-03-10 | Orthotic device and method of making an orthotic device |
| GB1104074.8 | 2011-03-10 | ||
| PCT/GB2012/050543 WO2012120316A2 (en) | 2011-03-10 | 2012-03-12 | Orthotic device and method of making an orthotic device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ612526A NZ612526A (en) | 2015-07-31 |
| NZ612526B2 true NZ612526B2 (en) | 2015-11-03 |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US12514733B2 (en) | Orthotic device and method of making an orthotic device | |
| CN204744527U (en) | Brace is rescued to backbone | |
| KR101821869B1 (en) | Functional Brassiere | |
| KR101801868B1 (en) | Scoliosis brace | |
| US2871850A (en) | Orthopedic spinal brace | |
| CN210114545U (en) | A dynamic rehabilitation brace for relieving back pain | |
| NZ612526B2 (en) | Orthotic device and method of making an orthotic device | |
| NZ709234B2 (en) | Orthotic device | |
| CN111432673A (en) | Sports bra for postural recovery and chest mobility | |
| HK1193739B (en) | Orthotic device and method of making an orthotic device | |
| KR200323715Y1 (en) | Scoliosis brace of open type | |
| KR101895004B1 (en) | Scoliosis brace | |
| CN117860456B (en) | Flexible spine orthosis | |
| HK1238120A1 (en) | Orthotic device | |
| TR202014265A2 (en) | Posture Supporting Garment | |
| KR20150030943A (en) | A comfortable pants |