U.S. patent application number 11/340268 was filed with the patent office on 2006-06-15 for transcutaneous inserter for low-profile infusion sets.
Invention is credited to Steven Wojcik.
Application Number | 20060129123 11/340268 |
Document ID | / |
Family ID | 26698999 |
Filed Date | 2006-06-15 |
United States Patent
Application |
20060129123 |
Kind Code |
A1 |
Wojcik; Steven |
June 15, 2006 |
Transcutaneous inserter for low-profile infusion sets
Abstract
A low-profile inserter for an angled infusion set comprises an
inserter housing having a bottom wall, a retainer slidably
connected to the inserter housing for movement between retracted
and extended positions in a direction substantially parallel with
the bottom wall, and a base member connected to the inserter
housing. The retainer is adapted to releasably receive a cannula
assembly, including a cannula connected to a cannula housing. The
base member has a lower surface that is adapted to contact a skin
outer surface. The lower surface and bottom wall together form an
acute angle. With this arrangement, the cannula can be inserted
subcutaneously at the acute angle with respect to the skin outer
surface.
Inventors: |
Wojcik; Steven; (Shoreline,
WA) |
Correspondence
Address: |
RATNERPRESTIA
P O BOX 980
VALLEY FORGE
PA
19482-0980
US
|
Family ID: |
26698999 |
Appl. No.: |
11/340268 |
Filed: |
January 25, 2006 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10024894 |
Dec 18, 2001 |
|
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|
11340268 |
Jan 25, 2006 |
|
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60256573 |
Dec 19, 2000 |
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Current U.S.
Class: |
604/506 ;
604/164.01; 604/93.01 |
Current CPC
Class: |
A61M 5/3287 20130101;
A61M 2005/1587 20130101; A61M 5/46 20130101; A61M 5/158 20130101;
A61M 2005/1585 20130101 |
Class at
Publication: |
604/506 ;
604/164.01; 604/093.01 |
International
Class: |
A61M 31/00 20060101
A61M031/00 |
Claims
1. An inserter for a low-profile angled infusion set, the
low-profile inserter comprising: an inserter housing having a
bottom wall, and a distal end defining an opening therein; a
retainer slideably mounted in the inserter housing for movement
between retracted and extended positions in a direction
substantially parallel with the bottom wall, the retainer being
adapted to releasably receive the infusion set, including a cannula
and an insertion needle, the cannula and insertion needle defining
an insertion axis; a tension spring for biasing said retainer
toward said extended position, said tension spring being movable
between an expanded position when said retainer is in said
retracted position, and a contracted position when said retainer is
in said extended position; a release lever releasably holding the
retainer in the retracted position; a first release button for
releasing said tension spring from said expanded position, said
first release button movable in a direction substantially normal to
said insertion axis; and a base member connected to the inserter
housing, the base member having a lower surface that is adapted to
contact a user's skin surface, the lower surface and the bottom
wall forming an acute angle, wherein the cannula and the insertion
needle are guided to be inserted subcutaneously along the insertion
axis at said acute angle with respect to the skin surface.
2. An inserter according to claim 1, and further comprising a
safety member slideably mounted to the inserter housing to prevent
inadvertent release of the retainer.
3. An inserter according to claim 2, wherein the release lever
includes a first end portion exposed through the housing for
manipulation by an operator and a second end portion for engagement
with the retainer to hold the retainer in the retraced position,
whereby pivotal movement of the release lever in a first rotational
direction causes disengagement of the second end portion and the
retainer to release the retainer.
4. An inserter according to claim 3, wherein the release lever is
biased in a second rotational direction opposite the first
rotational direction, such that movement of the retainer toward the
retracted position causes the second end portion of the release
lever to engage and hold the retainer.
5. An inserter according to claim 4, wherein the safety member
comprises a lower surface that, in a first locking position,
engages the second end portion of the release lever to block
movement of the release lever in the first rotational
direction.
6. An inserter according to claim 1, wherein the acute angle is in
a range of about 10 degrees to about 40 degrees.
7. An inserter according to claim 1, wherein the acute angle is
approximately 30 degrees.
8. An inserter for an infusion set, the inserter comprising: an
inserter housing defining an opening in a distal end thereof; a
retainer slideably connected to the inserter housing for movement
between retracted and extended positions, the retainer being
adapted to releasably receive the infusion set including a cannula
and an insertion needle, the cannula and the insertion needle
defining an insertion axis; a biasing member connected between the
retainer and the inserter housing for biasing the retainer toward
the extended position, said biasing member being expanded when said
retainer is in said retracted position, and contracted when said
retainer is in said extended position; a first release button for
releasing said biasing member from being expanded, movable in a
direction substantially normal to said insertion axis; and a base
attached to a lower surface of said inserter housing defining an
acute angle with respect to said inserter housing, for guiding the
insertion needle and the cannula to be inserted subcutaneously in
skin of a user, along the insertion axis and at the acute angle
with respect to the skin.
9. An inserter according to claim 8, further comprising a release
lever mounted for pivotal movement on the retainer, the release
lever including a first end portion exposed for manipulation by an
operator when the retainer is in the extended position and a second
end portion for engagement with the cannula assembly to hold the
cannula assembly on the retainer, wherein pivotal movement of the
release lever in a first rotational direction causes disengagement
of the second end portion of the release lever and the cannula
assembly to release the cannula assembly from the inserter.
10. An inserter according to claim 9, wherein the release lever is
biased in a second rotational direction opposite the first
rotational direction, such that movement of the retainer toward the
retracted position causes the second end portion of the release
lever to engage and hold the retainer.
11. A method for inserting an insertion needle and a cannula into
skin of a user, comprising the steps of: providing an inserter
housing having a bottom wall, a distal end defining an opening
therein, and a base member attached to the bottom wall proximate
the distal end, said base member including a lower surface adapted
to contact the skin and defining an acute angle with said bottom
wall; slideably mounting a retainer within said inserter housing,
movable between a retracted position and an extended position, said
extended position being substantially parallel with said bottom
wall of said inserter housing; mounting the cannula and the
insertion needle in said retainer to define an insertion axis;
providing a tension spring for biasing said retainer toward said
extended position, movable between an expanded position and a
contracted position; releasing said tension spring by pressing a
release button proximate said distal end of said inserter housing,
in a direction substantially normal to the insertion axis, thereby
releasing said spring to move from said expanded position to said
contracted position and move said retainer to said extended
position, whereby said insertion needle and said cannula are guided
to be inserted subcutaneously in the skin at said acute angle with
respect to the skin.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 10/024,894, filed Dec. 18, 2001, which claims the benefit of
U.S. application Ser. No. 60/256,573, filed Dec. 19, 2000.
BACKGROUND OF THE INVENTION
[0002] This invention relates to medical devices, and more
particularly to an automatic inserter for installing an angled or
low-profile infusion set in the skin of a person to subcutaneously
administer medication or other substances beneficial to health.
[0003] Frequent or continuous subcutaneous injection of medication
such as insulin is often accomplished through the use of an
infusion set or injection port which may remain in place for
several days. In the case of frequent injections, the infusion set
reduces the need to constantly puncture the skin, thereby
minimizing the risk of infection and the formation of scar tissue.
For continuous subcutaneous delivery of medication through portable
insulin pumps or the like, an infusion set is often used to provide
a method of temporarily detaching the pump and fluid line for
activities such as dressing or bathing. It is also desirable in
this instance to detach the fluid line from the pump as close to
the injection site as possible, thereby leaving a relatively small
component attached to the body which minimizes any interference
during dressing, bathing or other activities.
[0004] Angled infusion sets, such as disclosed in my copending U.S.
patent application Ser. No. 09/625,245 filed on Jul. 25, 2000, now
U.S. Pat. No. 6,572,586, the disclosure of which is herein
incorporated by reference, are especially advantageous due to their
low profile during use. See also U.S. Pat. No. 5,522,803 issued to
Tiessen-Simoney on Jun. 4, 1996. Such devices include a manual
inserter with a handle and an introducer needle that attach to a
cannula housing. A self-adhesive pad on the bottom surface of the
cannula housing secures the housing to the skin of a person. To
insert the infusion set, the user grasps the handle with one hand
while pinching a fold of skin between the thumb and forefinger of
the other hand. The introducer needle together with the outer end
of the cannula are then pushed by the user into the fold of skin.
The introducer needle is removed from the cannula housing leaving
the cannula inserted in the subcutaneous layer. The housing is then
adhesively secured to the skin. A tubing connector from an insulin
pump can then be connected to the cannula housing to deliver
insulin or other substances to the subcutaneous layer.
[0005] While this process is relatively straightforward for more
experienced persons, it does require manual dexterity. In addition,
the cannula may become kinked during an improper installation and
impede the flow of insulin, or may be positioned in an improper
skin layer. Surrounding tissue may also be damaged during attempts
to correctly position the cannula, causing added pain and trauma to
a user. Many users prefer to avoid the trauma associated with
self-inserting the introducer needle and cannula into their
bodies.
[0006] Accordingly, it would be desirous to provide an automatic
inserter for angled or low-profile infusion sets, thereby assuring
the correct placement of the cannula in the subcutaneous layer at
the correct angle while minimizing the trauma associated with
cannula installation.
SUMMARY OF THE INVENTION
[0007] According to one aspect of the invention, a low-profile
inserter for an angled infusion set comprises an inserter housing
having a bottom wall, a retainer slidably connected to the inserter
housing for movement between retracted and extended positions in a
direction substantially parallel with the bottom wall, and a base
member connected to the inserter housing. The retainer is adapted
to releasably receive a cannula assembly, including a cannula
connected to a cannula housing. The base member has a lower surface
that is adapted to contact an outer skin surface. The lower surface
and bottom wall together form an acute angle. With this
arrangement, the cannula can be inserted subcutaneously at the
acute angle with respect to the outer skin surface.
[0008] According to a further aspect of the invention, an inserter
for an infusion set comprises an inserter housing, and a retainer
slidably connected to the inserter housing for movement between
retracted and extended positions. The retainer is adapted to
releasably receive the cannula assembly. A biasing member is
connected between the retainer and the inserter housing for biasing
the retainer toward the extended position. A first release lever is
pivotally mounted to the inserter housing. The first release lever
includes a first end portion that is exposed through the housing
for manipulation by an operator and a second end portion for
engagement with the retainer to thereby hold the retainer in the
retracted position. In this manner, pivotal movement of the first
release lever in a first rotational direction causes disengagement
of the second end portion and the retainer to thereby release the
retainer.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] The foregoing summary, as well as the following detailed
description of preferred embodiments of the invention, will be
better understood when read in conjunction with the appended
drawings. For the purpose of illustrating the invention, there is
shown in the drawings embodiments which are presently preferred. It
should be understood, however, that the invention is not limited to
the precise arrangements and instrumentalities shown. In the
drawings:
[0010] FIG. 1 is a side elevational view of a low-profile inserter
assembly according to the invention in a retracted or cocked
position;
[0011] FIG. 2 is a side elevational view of the inserter assembly
of FIG. 1 in an extended position with an insertion needle and
cannula inserted in the skin (shown in cross section);
[0012] FIG. 3 is a front elevational view of the inserter
assembly;
[0013] FIG. 4 is top plan view in partial cross section of the
inserter assembly;
[0014] FIG. 5 is an enlarged cross sectional view of the inserter
assembly taken along line 5-5 of FIG. 3;
[0015] FIG. 6 is an enlarged cross sectional view of a portion of
the inserter assembly taken along line 6-6 of FIG. 5;
[0016] FIG. 7 is an isometric view of a low-profile inserter
assembly according to a second embodiment of the invention;
[0017] FIG. 8 is a top plan view of the inserter assembly second
embodiment;
[0018] FIG. 9 is top plan view in partial cross section of a
low-profile inserter assembly according to a third embodiment of
the invention;
[0019] FIG. 10 is an enlarged cross sectional view of the inserter
assembly second embodiment taken along line 10-10 of FIG. 9;
[0020] FIG. 11 is an enlarged cross sectional view of a portion of
the inserter assembly taken along line 11-11 of FIG. 10;
[0021] FIG. 12 is a side elevational view of a low-profile inserter
assembly according to a fourth embodiment of the invention;
[0022] FIG. 13 is a top plan view of the inserter assembly fourth
embodiment; and
[0023] FIG. 14 is a front elevational view in partial cross section
of the inserter assembly fourth embodiment.
[0024] It is noted that the drawings are intended to represent only
typical embodiments of the invention and therefore should not be
construed as limiting the scope thereof. The invention will now be
described in greater detail with reference to the drawings, wherein
like parts throughout the drawing figures are represented by like
numerals.
DETAILED DESCRIPTION OF THE INVENTION
[0025] Referring now to the drawings, and to FIGS. 1-3 in
particular, a low-profile inserter assembly 10 according to the
invention includes a housing 12 with an upper housing portion 14
connected to a lower housing portion 16. An angled alignment guide
in the form of a triangular-shaped base 18 is preferably integrally
formed with the lower housing portion 16 and includes a lower
surface 20 that is adapted to contact an outer surface 22 of skin
24 during use. The lower surface 20 extends at an acute angle 0
with respect to a bottom wall 25 of the lower housing portion 16 so
that an insertion needle 27 and cannula 26 of a low-profile cannula
housing 28 placed in the inserter assembly 10 can be inserted into
the skin 24 at the proper angle. The angle 0 is in the range of
approximately 10.degree. to 40.degree., and preferably in the range
of 15.degree. to 35.degree., depending on the particular
configuration of the cannula housing 28 to be installed. In one
preferred embodiment, the angle 0 is approximately 30.degree. to
accommodate a cannula housing and accompanying cannula that will
extend into the subcutaneous layer at approximately 30.degree. with
respect to the skin outer surface 22. The housing portions may be
constructed of any suitable material, and can be retained together
through screws 23 (FIG. 5), interlocking tabs, adhesive,
heat-staking, or a combination thereof, or any other well-known
fastening means.
[0026] With reference now to FIGS. 4-6, a retainer 30 is slidably
mounted in the housing 12 between the upper housing portion 14 and
the lower housing portion 16. The retainer 30 includes a main body
40 and a pair of side flanges 42 (only one shown in FIG. 6) that
extend laterally from the main body and a pair of bottom flanges 44
(only one shown in FIG. 6) that extend downwardly from the main
body. A pair of spaced guide ribs 32 extend downwardly from an
upper wall 34 of the upper housing portion 14. Each guide rib 32
includes a lower surface 36 that slidably contacts an upper surface
46 of one of the side flanges 42. A pair of spaced shoulders 48
(only one shown in FIG. 6) are formed at the intersection of the
bottom wall 25 and opposite side walls 52 of the lower housing
portion 16. Each bottom flange 44 includes a side surface 50 and a
lower surface 54 that slidably contact a shoulder side surface 56
and an inner surface 58 of the bottom wall 25, respectively, to
guide sliding movement of the retainer 30 in a substantially linear
direction between a retracted position (FIG. 1) and an extended
position (FIG. 2).
[0027] As best shown in FIG. 5, an infusion set release lever 60 is
pivotally connected to a forward end of the retainer 30 at a pivot
joint 64. The pivot joint 64 may include fingers (not shown) on the
lever 60 that extend in opposite directions and fit into opposed
depressions (not shown) in the retainer 30. A release button 66 is
formed at a forward end of the lever 60 for manipulation by a user.
A downwardly-extending catch 68 is formed on the lever 60
rearwardly of the pivot joint 64 and normally seats against a
depression 70 in the top of a handle portion 72 of the cannula
housing 28. A lower ramped surface 62 extends from the release
button 66 to the catch 68 to facilitate connection of the cannula
housing 28 to the retainer 30. A slot 74 is formed in the forward
end of the retainer 30 for receiving the handle portion 72. A slot
78 (FIG. 4) is also formed in the housing 12 between the upper
housing portion 14 and the lower housing portion 16 to accommodate
an adhesive-backed mounting pad 80 associated with the cannula
housing 28 since, as shown in FIGS. 3 and 4, the pad is wider than
the housing 12. In a further embodiment, the housing may be wide
enough to completely receive the mounting pad 80, as will be
described in further detail below.
[0028] The release button 66 is normally biased upwardly by means
of a tension spring 82 connected between a forwardly extending hook
84 of the retainer 30 and a rearwardly extending hook 86 of the
release lever 60. In this position, the cannula housing 28 is
locked to the retainer 30 and is slidable therewith along the
housing 12 between the extended and retracted positions. Since the
release lever 60 is pivotally connected to the retainer 30, it is
also slidable with the retainer to maintain the cannula housing in
a locked position until the housing is released by depressing the
release button 66. When the retainer 30 is retracted, the release
button 66 is located within the housing 12 and therefore cannot be
accessed until the retainer is extended to expose the release
button. In this manner, the cannula housing 28 cannot be
inadvertently released during handling or positioning of the
inserter assembly 10, to thereby reduce the possibility of cannula
contamination and/or injury. Depression of the release button 66
when the retainer 30 is extended causes the release lever 60 to
rotate (clockwise as viewed in FIG. 5) about the pivot joint 64
against bias from the spring 82 until the catch 68 clears the
handle portion 72 of the cannula housing 28. In this position, the
cannula housing and inserter assembly can be separated.
[0029] As shown in FIG. 4, a pair of cocking levers 90 extend in
opposite directions from opposite sides of the retainer 30 and into
the housing slot 78. The cocking levers 90 can be grasped by a user
to move the retainer 30 and attached cannula housing 28 into the
retracted position. A pair of tension springs 92 (only one shown in
FIGS. 4 and 6) are located on opposite sides of the retainer 30.
Each tension spring 92 has one end connected to a hook 94
projecting downwardly from a rear end of the retainer side flange
42 and an opposite end connected to a hook 96 extending from the
guide flange 32 of the upper housing portion 14. In this manner,
the retainer 30 is normally biased toward the extended position. In
an alternative arrangement, a single, centrally mounted tension or
compression spring may be used to bias the retainer 30 toward the
extended position. In a further embodiment, the one or both tension
springs may be replaced with other biasing means, such as an
elastomeric member, an air cylinder, and so on.
[0030] A retainer release lever 98 (FIG. 5) is pivotally connected
to the upper housing portion 14 by a pivot pin 100 that extends
between the guide flanges 32 and through the lever 98. A release
button 102 is located at a forward end of the release lever 98 and
projects upwardly through an opening 104 in an upper wall 105 of
the upper housing portion 14. A catch 106 is located at a rearward
end of the release lever 98 and projects downwardly therefrom. The
catch 106 is arranged to fit within a recess 108 of the retainer 30
and hold the retainer in the retracted position under bias from the
tension spring 92. A compression spring 114 is positioned in a bore
110 formed in the rearward end of the release lever 98 and extends
to a corresponding depression 112 formed in the upper wall 105 of
the upper housing portion 14 to normally bias the catch 106 toward
the recess 108.
[0031] In order to retract the retainer 30, including the attached
cannula housing 12, to a cocked position, the levers 90 (FIG. 4)
are grasped by a user to slide the retainer 30 rearwardly in the
housing 12. A rear end of the retainer is initially in contact with
a lower ramped surface 110 of the catch 106 and rearward movement
of the retainer causes the catch 106 to rotate upwardly about the
pivot pin 100 (clockwise as viewed in FIG. 5) against bias force
from the spring 114 until the catch 106 is clear of the retainer.
Further rearward movement of the retainer causes the catch 106 to
snap into the recess 108 with a clear audible sound to thereby
indicate to a user that the retainer 30 is properly cocked.
[0032] Once in the retracted position, the inserter assembly can be
placed on the skin of a patient with the lower surface 20 of the
base 18 positioned against a user's or patient's outer skin 22. The
release button 102 can be depressed to rotate the catch 106 out of
the recess 108, which causes the retainer 30 to slide forwardly to
the extended position under force from the springs 92 at a
relatively rapid rate. Forward movement of the retainer in this
manner causes the needle 27 and cannula 26 to pierce the skin at
the proper angle and enter into the subcutaneous layer at the
proper distance. The cannula housing 28 can then be released from
the inserter assembly 10 by depressing the release button 66, as
previously described. The mounting pad 80 can then be secured to
the skin and the needle 27 removed in a well-known manner, thus
leaving the cannula 26 in place.
[0033] A safety button 120 is mounted in the upper housing portion
14 between the guide flanges 32 for limited forward and rearward
sliding movement. The safety button 120 includes an upper portion
122 that extends through a rear opening 124 in the top wall 105 for
grasping by a user. A pair of resilient arms 126 (only one shown in
FIG. 4) extend from a lower portion 130 of the button 120. A head
128 is formed at the free end of each arm and is positioned to
engage one of two detents 132, 134 formed in the guide flanges 32
which define unlocked and locked positions, respectively, of the
safety button 120. In the locked position, the lower portion 130 of
the safety button 120 is adjacent a ledge 136 of the catch 106
(FIG. 5), to prevent upward movement of the catch 106 and thus
inadvertent release of the retainer 30 and the attached cannula
housing 28. In the unlocked position, the ledge 136 is clear of the
lower portion 130 to move upwardly when the release button 102 is
depressed or when the retainer 30 is moved to the retracted
position.
[0034] With reference now to FIGS. 7 and 8, a low-profile inserter
assembly 140 according to a second embodiment of the invention is
illustrated, wherein like parts in the previous embodiment are
represented by like numerals. The inserter assembly 140 is similar
in construction to the inserter assembly 10, with the exception
that an upper housing portion 142 and lower housing portion 144 are
narrowed in width behind the release button 102 to form a narrowed
handle portion 146 that is easier to hold and manipulate. This
narrower width necessitates moving the tension springs 92 (not
shown in FIG. 7) inward, closer to the longitudinal centerline of
the housing. These springs will now be located under the retainer
30 rather than on each side as shown in FIGS. 4 and 5. However they
are attached to the retainer side flange 42 and guide flange 32 of
the upper housing portion 142 in a similar manner.
[0035] With reference now to FIGS. 9-11, a low-profile inserter
assembly 150 according to a third embodiment of the invention is
illustrated, wherein like parts in the previous embodiments are
represented by like numerals. In this embodiment, a slot 152 is
formed in the bottom wall 25 of the lower housing portion 16. A
single cocking lever 154 extends downwardly through the slot 152
from the retainer 30. As shown, the cocking lever 154 includes a
head portion 156 that is larger than the slot and a neck portion
158 that extends through the slot. The neck portion 158 is
preferably integrally formed with the retainer 30. A fastener 160
is countersunk in the head portion 156 and extends through the head
and neck portions 156, 158 and into the retainer 30 for securing
the head portion to the retainer.
[0036] The bottom wall 25 is formed in a depression 162 of the
lower housing portion 16 and is defined by a pair of inner side
walls 164 (only one shown in FIG. 9) that extend downwardly from
the bottom wall 25. An L-shaped guide flange 166 is formed at each
longitudinal side of the retainer 30 and contacts the bottom wall
25 and inner side wall 164 to guide sliding movement of the
retainer in a substantially linear direction.
[0037] Operation of the inserter assembly 150 is similar to the
operation of the inserter assembly 10, with the exception that a
user sets the retainer in a retracted position by pushing the head
portion 156 of the cocking lever 154 rearwardly until the catch 106
is located in the recess 108 of the retainer to thereby hold the
retainer in the retracted position under bias force from the
springs 92. The head portion 156 is preferably entirely located
within the depression 162 of the lower housing portion 16 to
prevent interference between the head portion and other objects,
such as the skin or clothing of a user, and thus possible injury or
misplacement of the cannula assembly in the skin during release of
the retainer 30.
[0038] With reference now to FIGS. 12-14, a low-profile inserter
assembly 170 according to a fourth embodiment of the invention is
illustrated, wherein like parts in the previous embodiments are
represented by like numerals. The inserter assembly 170 includes a
housing 172 that is relatively wide in comparison to the previous
embodiments. The housing 172 has an upper housing portion 174
connected to a lower housing portion 176 in a manner as previously
described. A bifurcated base 178 is preferably integrally formed
with the lower housing portion 176 and includes spaced feet 180,
182. Each foot has a lower surface 184 that extends at an acute
angle 0 with respect to a lower surface 186 of the lower housing
portion 176 so that an insertion needle 17 and cannula 26 of a
low-profile cannula housing 28 placed in the inserter assembly 170
can be inserted into the skin 24 at the proper angle, as previously
described. In one preferred embodiment, the angle 0 is
approximately 30.degree. to accommodate a cannula that will extend
approximately 30.degree. with respect to the outer skin surface 22.
However, the actual angle can vary depending on the shape of the
cannula housing, as well as the length of the needle and cannula
assembly 26. The spaced-apart feet offer greater stability over the
previous embodiment and permit a fold of skin to be inserted
therebetween during insertion of the needle and cannula assembly 26
into the subcutaneous layer.
[0039] A generally vertically extending channel 190 is formed in a
forward end of the housing 172. Preferably, the channel is wide
enough to receive the cannula housing 28 and the mounting pad 80. A
generally horizontally extending slot 192 is formed between the
upper housing portion 174 and lower housing portion 176 and
intersects with the channel 190. The slot 192 is dimensioned to
receive the cannula housing 28, the mounting pad 80, and the
release button 66 so that the cannula housing and mounting pad can
be releasably connected to the retainer and moved into and out of
the housing 172 without obstruction.
[0040] It will be understood that the terms relating to orientation
and/or position, such as upper, lower, forward, rearward, downward,
bottom, and side, including their respective derivatives, as may be
used throughout the specification, refer to relative rather than
absolute orientations and/or positions.
[0041] While the invention has been taught with specific reference
to the above-described embodiments, those skilled in the art will
recognize that changes can be made in form and detail without
departing from the spirit and the scope of the invention. For
example, although the present invention has been described for use
with a low profile or angled infusion set, it will be understood
that the invention may be used to insert straight infusion sets or
other types of needles and/or cannulas. Thus, the described
embodiments are to be considered in all respects only as
illustrative and not restrictive. The scope of the invention is,
therefore, indicated by the appended claims rather than by the
foregoing description. All changes that come within the meaning and
range of equivalency of the claims are to be embraced within their
scope.
* * * * *