U.S. patent application number 15/041196 was filed with the patent office on 2016-06-09 for integrated vascular delivery system.
The applicant listed for this patent is THE REGENTS OF THE UNIVERSITY OF MICHIGAN. Invention is credited to Adrienne HARRIS, Merrell SAMI, Elyse Kemmerer WHITE, Steven B. WHITE.
Application Number | 20160158498 15/041196 |
Document ID | / |
Family ID | 43586857 |
Filed Date | 2016-06-09 |
United States Patent
Application |
20160158498 |
Kind Code |
A1 |
WHITE; Steven B. ; et
al. |
June 9, 2016 |
Integrated Vascular Delivery System
Abstract
An integrated vascular delivery system having a frame configured
to receive a catheter insertable in a patient to deliver fluid at
an insertion site. The frame includes a first hub, a second hub,
and a pair of flexible lateral members extending between the hubs
and including a tubular lateral member. The system also includes a
fluidic channel that fluidically communicates with the catheter,
wherein the fluidic channel passes through the tubular lateral
member and at least one of the hubs, and includes a fixed turnabout
portion in which fluid flows in a direction different from that
within the catheter. The first and second hubs provide anchoring
points on the patient distributed around the insertion site and on
opposite ends of the catheter, thereby anchoring the frame to the
patient and stabilizing the catheter. A method is provided for
using an integrated vascular delivery system.
Inventors: |
WHITE; Steven B.; (Ann
Arbor, MI) ; HARRIS; Adrienne; (Clinton, MI) ;
SAMI; Merrell; (Arlington, VA) ; WHITE; Elyse
Kemmerer; (Ann Arbor, MI) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
THE REGENTS OF THE UNIVERSITY OF MICHIGAN |
Ann Arbor |
MI |
US |
|
|
Family ID: |
43586857 |
Appl. No.: |
15/041196 |
Filed: |
February 11, 2016 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14602735 |
Jan 22, 2015 |
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15041196 |
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|
13930797 |
Jun 28, 2013 |
8968252 |
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14602735 |
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|
13665162 |
Oct 31, 2012 |
8668674 |
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13930797 |
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12855013 |
Aug 12, 2010 |
8323249 |
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13665162 |
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Current U.S.
Class: |
604/174 |
Current CPC
Class: |
A61M 25/02 20130101;
A61M 5/158 20130101; A61M 5/162 20130101; A61M 25/0693 20130101;
B33Y 80/00 20141201; A61M 25/0606 20130101; B33Y 70/00 20141201;
A61M 25/0097 20130101 |
International
Class: |
A61M 25/02 20060101
A61M025/02; A61M 25/06 20060101 A61M025/06; A61M 5/158 20060101
A61M005/158; A61M 25/00 20060101 A61M025/00 |
Claims
1. An integrated vascular delivery system adapted to stabilize a
catheter inserted at an insertion site on a patient, comprising: a
catheter hub configured to conform to a surface of the patient and
configured to provide a first anchoring point on the patient,
wherein the catheter hub comprises a proximal side and a distal
side, and is configured to receive a catheter, at the proximal
side, to transfer a fluid at the insertion site; a fluidic channel
that fluidly communicates with the catheter, wherein the fluidic
channel is configured to pass through the catheter hub and provide
a fluid path into the catheter; a septum, coupled to the distal
side of the catheter hub, configured to receive a needle and to
direct the needle into a portion of the fluidic channel and into
the catheter, thereby facilitating insertion of the catheter at the
insertion site; and a fluid supply adapter, fluidically coupled to
the fluid channel by way of the catheter hub.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 14/602,735 filed on Jan. 22, 2015, which is a
continuation of U.S. patent application Ser. No. 13/930,797 filed
on Jun. 28, 2013 (now U.S. Pat. No. 8,968,252, issued on Mar. 3,
2015), which is a continuation of U.S. patent application Ser. No.
13/665,162 filed on Oct. 31, 2012 (now U.S. Pat. No. 8,668,674,
issued on Mar. 11, 2014), which is a continuation of U.S. patent
application Ser. No. 12/855,013, filed on Aug. 12, 2010 (now U.S.
Pat. No. 8,323,249, issued on Dec. 4, 2012). The entire disclosure
of each of the above applications is incorporated herein by
reference.
FIELD
[0002] The present disclosure relates generally to the medical care
field, and more specifically to an improved vascular delivery
system in the intravenous therapy field.
BACKGROUND
[0003] This section provides background information related to the
present disclosure which is not necessarily prior art.
[0004] Patients undergoing medical treatment often require a form
of intravenous (IV) therapy, in which a fluid is administered to
the patient through a vein of the patient. IV therapy is among the
fastest ways to deliver fluids and medications into the body of the
patient. Intravenously infused fluids, which typically include
saline, drugs, blood, and antibiotics, are conventionally
introduced to the patient through a flexible catheter positioned at
any of several venous routes, such as peripheral veins and central
veins.
[0005] To set up IV therapy with conventional devices and methods,
the caregiver positions the catheter over the selected vein and
uses a needle within the catheter to pierce the skin and allow
insertion of the catheter into the vein. The catheter is typically
positioned such that the distal inserted end of the catheter points
toward the midline of the patient (e.g., for a peripheral IV line
on the arm, the catheter body is positioned on the forearm and
points toward the elbow). The caregiver then withdraws the needle
from the catheter, leaving the catheter inserted in the vein. The
proximal end of the catheter, relative to the midline of the
catheter, is fixed to the end of a catheter hub that is proximal
relative to the midline of the patient. The caregiver connects the
catheter to a fluid supply through external tubing, including
extension tubing that is typically attached to the distal end of
the catheter hub relative to the midline of the patient, and that
the caregiver typically bends into a U-shape. To avoid unscheduled
IV line restarts, the catheter and tubing are typically secured
against the skin of the patient with tape or similar catheter
stabilization devices (CSDs) such as adhesive stabilizing pads that
restrain the catheter body.
[0006] However, conventional devices and methods for IV therapy
have drawbacks. The extension tubing may catch on nearby obstacles
during patient movement or caregiver manipulation, which may cause
painful vein irritation and compromise the IV. Tape and other
existing CSDs are not optimal for stabilization because securing
the round, rigid, and bulky components such as the catheter and
tubing against the skin can be difficult and ineffective. Tape and
other existing CSDs do not fully prevent the catheter from moving
within the vein, which leads to patient-endangering complications
including catheter dislodgement, infiltration (fluid entering
surrounding tissue instead of the vein), and phlebitis
(inflammation of the vein). Adhesive stabilizing pads tend to
result in other undesired effects, such as skin irritation and/or
breakdown due to prolonged concentrated adhesion to the skin.
Furthermore, tape and current CSDs restrain the catheter on only
one side of the catheter insertion site, and do not prevent the
catheter from painfully and dangerously pivoting around the
insertion site and moving within the vein.
[0007] Thus, there is a need in the intravenous therapy field to
create an improved vascular delivery system that overcomes one or
more of the drawbacks of the conventional vascular delivery
systems. This invention provides such an improved vascular delivery
system.
DRAWINGS
[0008] The drawings described herein are for illustrative purposes
only of selected embodiments and not all possible implementations,
and are not intended to limit the scope of the present
disclosure.
[0009] FIG. 1 is the integrated vascular delivery system of a
preferred embodiment;
[0010] FIG. 2 is a semi-transparent overhead view of the integrated
vascular delivery system of a preferred embodiment;
[0011] FIG. 3 is a semi-transparent view of the integrated vascular
delivery system of another preferred embodiment;
[0012] FIGS. 4A-4D are semi-transparent overhead views of
variations of the integrated vascular delivery system of another
preferred embodiment;
[0013] FIGS. 5A-5F are schematics of a method for using the
integrated vascular delivery system of a preferred embodiment;
and
[0014] FIGS. 6A-6C are overhead, side, and perspective views,
respectively, of a variation of the step of folding in a method for
using the integrated vascular delivery system of a preferred
embodiment.
[0015] Corresponding reference numerals indicate corresponding
parts throughout the several views of the drawings.
DETAILED DESCRIPTION
[0016] The following description of preferred embodiments of the
present teachings is not intended to limit the disclosure to these
preferred embodiments, but rather to enable any person skilled in
the art to make and use this invention.
[0017] 1. Integrated Vascular Delivery System
[0018] As shown in FIGS. 1 and 2, the integrated vascular delivery
system 100 of the preferred embodiments includes: a frame 110
configured to receive a catheter 170 insertable in a patient to
deliver fluid at an insertion site, in which the frame includes a
first hub 120, a second hub 130, and a pair of flexible lateral
members 140 extending between the hubs and including a tubular
lateral member 140'; and a fluidic channel 150 that fluidically
communicates with the catheter, wherein the fluidic channel 150
passes through the tubular lateral member 140' and at least one of
the hubs, and includes a fixed turnabout portion 156 in which fluid
flows in a direction different from that within the catheter 170.
The first and second hubs preferably provide first and second
anchoring points 122 and 132, respectively, on the patient such
that the anchoring points are distributed around the insertion site
112 and on opposite ends of the catheter, thereby anchoring the
frame to the patient and stabilizing the catheter 170. Fluid flow
in the turnabout portion 156 of the fluidic channel 150 is
preferably opposite of that within the catheter, and the turnabout
portion is preferably fixed in such a way as to reduce the
likelihood of snagging or catching on nearby objects. In one
preferred embodiment, the system includes a second tubular lateral
member 140' and a second fluidic channel 150 that fluidically
communicates with the catheter 170 and passes through the second
tubular lateral member 140'. In a preferred embodiment, the frame
110 is configured to receive the catheter as an integral part of
the system, in which the catheter 170 is embedded in a portion of
the frame, and more preferably in one of the hubs. However, in an
alternative embodiment the frame 110 is configured to receive a
separate catheter, which may snap fit into the frame.
[0019] In some versions of the system, the system further includes
at least one extension tube 180 and/or a fluid supply adapter 182
that delivers fluid from a fluid supply to the fluidic channel. The
system functions to enable access to the vein of a patient
undergoing intravenous (IV) therapy with an included catheter,
administer fluids intravenously through the catheter, and securely
and safely stabilize the catheter on the patient. The system is
preferably used to administer drugs, antibiotics, saline, or blood,
but may be used to administer any suitable fluid to a patient. The
system is preferably used to create, stabilize, and maintain an IV
line on a peripheral vein such as on the arm, hand, or leg, but may
alternatively be used for central or peripheral venous access on
the neck, chest, or abdomen, or any suitable intravenous
intra-arterial location. The system may further be used to create,
stabilize, and maintain any suitable catheter-based access to a
patient, such as for the transfer of cerebrospinal fluid.
[0020] In a preferred embodiment, the catheter 170, frame 110,
fluidic channel 150, extension tubing 180, and/or fluid supply
adapter 182 are pre-assembled during manufacture of the system to
provide an integrated system that is cost-efficient, reduces IV
setup time, and packaging waste. The system preferably stabilizes
the catheter 170 on the patient with anchoring points distributed
around the insertion site 112, more preferably on at least two
opposing sides of the insertion site 112, which may reduce or
eliminate painful and dangerous pivoting motions of the catheter
170 that may occur during normal patient movement and/or caregiver
manipulations. The system is preferably streamlined by aligning the
catheter with the fluid supply adapter and reducing external free
tubing, which reduces the likelihood of the system catching or
snagging on nearby obstacles. The system is preferably a closed
system that reduces possible points of contamination and fluid
leakage, which improves safety for both the patient and the
caregiver. The system is preferably compatible with existing
conventional catheter insertion and IV setup procedures, which
enables a caregiver to easily use the system without significant
additional training.
[0021] The frame 110 of the integrated vascular delivery system
functions to stabilize the system on the patient. As shown in FIGS.
1 and 2, the frame 110 preferably includes a first hub 120 on one
end of the frame that provides a first anchoring point 122 on the
patient, a second hub 130 on an end of the frame approximately
opposite to the first hub that provides a second anchoring point
132 on the patient, and two flexible lateral members 140 that
extend between and flexibly connect the first hub and the second
hub, such that the first hub and the second hub move relative to
one another with a significant number of degrees of freedom. In
particular, the lateral members 140 preferably are reversibly
bendable to fold one of the first and second hubs over the other
hub. As shown in FIG. 2, in a preferred embodiment, the lateral
members are substantially parallel such that the frame 110 forms an
approximately rectangular perimeter 114 around the catheter 170 and
insertion site 112. In variations of the frame 110, the frame may
include any suitable number of hubs and any suitable number of
lateral members, such that the frame forms a perimeter 114 of any
suitable shape and size around the insertion site 112. The frame
110 preferably allows visualization of the insertion site 112 of
the catheter, such as by leaving an open uncovered area around the
catheter, although alternatively the system may include a cover
that is transparent, translucent, opaque, or any suitable kind of
material, that extends over the frame to cover the insertion site
112 and/or catheter 170. As shown in FIG. 5E, the frame is
preferably secured to the patient by securing the first hub 120 and
second hub 130 to the patient at the first and second anchoring
points, respectively, on opposite sides of the insertion site 112
(preferably distal and proximal to the insertion site) and opposite
ends of the catheter 170, thereby stabilizing the catheter.
However, the frame 110 may additionally and/or alternatively be
secured by securing only the first hub, only the second hub, the
lateral members and/or or any other suitable portion of the frame.
The frame may alternatively stabilize the catheter at anchoring
points located at any suitable locations relative to the catheter
insertion site 112. The frame 110, when secured to the patient,
enables the integrated vascular system to stabilize the catheter
more effectively than conventional catheter securement devices that
stabilize the catheter on only one side of the insertion site 112,
because stabilizing the catheter on two opposite sides of the
insertion site reduces pivoting motions of the catheter that may
occur during normal patient movement and/or caregiver
manipulations.
[0022] The first hub 120 of the frame 110 functions to provide a
first anchoring point 122 for the frame. As shown in FIG. 2, in a
preferred embodiment, the first hub 120 further functions to house
a portion of the fluidic channel 150 within the first hub. The
first hub 120 is preferably located on the proximal end of the
frame relative to the midline of the patient, such that the first
hub provides a first anchoring point 122 proximal to the catheter
insertion site relative to the midline of the patient.
Alternatively, the first hub 120 may be located on any suitable
part of the frame relative to the insertion site 112 to provide a
first anchoring point 122 at any suitable location relative to the
insertion site 112. As shown in FIG. 5E, the first hub 120 is
preferably secured to the skin of the patient with tape, but may
additionally and/or alternatively be secured with an adhesive
located on the underside of the first hub 120; elastic straps;
straps fastened with fasteners such as hooks, hook and loop, or
magnets; or any suitable securement mechanism. The first hub may
alternatively not be secured to the skin of the patient. In one
specific embodiment, the first hub preferably has a relatively wide
and thin profile, with a width of approximately 20-30 mm and a
thickness of approximately 5 mm. However, the first hub may
alternatively be any suitable shape and size. A large width is
advantageous for distributing forces over a greater area on the
skin, which decreases the chances of the patient developing skin
irritations, sores, and other degradations. The thin profile, which
is approximately half as thick as conventional vascular access
devices, decreases the risk of the hub catching or snagging on bed
equipment or other nearby obstacles that could cause the catheter
to move within the vein and cause complications such as catheter
dislodgement, infiltration, and phlebitis. As shown in FIG. 1, the
first hub 120 preferably has rounded edges and preferably has an
upper surface that is slightly arched along its lateral axis. The
arched upper surface may adapt the first hub to receive tape along
the arch for securement to the patient. The first hub may
additionally have features that conform to the body of the patient,
such as an underside concavity to conform to a limb, finger, or
knuckle.
[0023] The first hub 120 is preferably made of a rigid or
semi-rigid material, such as nylon or silicone, to provide
structural support to the frame 110 for stabilizing the system.
However, the first hub may alternatively be made of any polymer,
metal, composite, or other suitable material. The first hub may be
transparent or semi-transparent to allow visualization of the fluid
channel 150. The first hub is preferably manufactured through
injection molding, but may alternatively be manufactured through
stereolithography, casting, milling, or any other suitable
manufacturing process known to one skilled in the art.
[0024] The first hub 120 and/or the second hub 130 may include a
sensor 116 that measures a biometric parameter such as temperature,
blood pressure, or pulse rate of the patient. The sensor 116 may
additionally and/or alternatively sense any suitable parameter such
one pertaining to the fluid, such as pH or flow rate.
[0025] The portion of the fluidic channel 150 fixed to the first
hub 120 may be coupled to an extension tube and/or fluid supply
adapter that function to deliver fluid from a fluid supply to the
fluidic channel 150 of the system. The fluid supply adapter
preferably includes a connector that attaches the extension tube to
a fluid supply, which is preferably a pole-mounted IV bag that
supplies fluid through tubing, but may alternatively be a syringe,
pump, or other suitable fluid supply. As shown in FIG. 4, the
connector is preferably a standard female luer lock connector or
Y-connector that commonly interfaces with conventional IV bags, as
known to one skilled in the art. Alternatively, the connector may
be any suitable male or female connector that is adapted to
interface with a fluid supply. The extension tube further functions
to provide stress relief if the system is jostled and is preferably
made of flexible tubing, such as polymer tubing, but may be a
passageway made of any other suitable material. Flexible tubing is
advantageous for relieving mechanical stress and reducing chances
of patient injury if the system is suddenly disturbed, such as
during patient movement or caregiver manipulations. The extension
tube is preferably long enough to provide stress relief if needed,
but short enough to reduce the chances of the extension tube
catching or snagging on nearby obstacles. The length of the
extension tube may alternatively be any suitable length, and may
depend on the specific application of the system. Other dimensions
of the fluid passageway, such as outer diameter and inner diameter,
may depend on the specific application of the system.
[0026] In alternative versions of the system, the system may
include more than one extension tube and/or connector, to
facilitate delivering fluid from multiple fluid supplies
simultaneously to the system. For example, in an embodiment of the
system that includes two fluidic channels 150, the system may
include a first extension tube that delivers a first fluid to a
first fluidic channel, and a second extension tube that delivers a
second fluid to the second fluidic channel. However, two extension
tubes may be useful in applications involving the administering of
two separate fluids through the same fluidic channel and
catheter.
[0027] The second hub 130 of the system is preferably similar to
the first hub 120, except as noted below. The second hub 130
functions to provide a second anchoring point 132 for the frame
110, preferably on a distal end of the frame relative to the
midline of the patient. The second hub is preferably secured distal
to the catheter insertion site 112 relative to the midline of the
patient, and in one specific embodiment, approximately 15 mm or
less distal to the insertion site. However, the second hub may
alternatively be secured in any suitable location relative to the
insertion site 112. As shown in FIG. 2, the second hub 130
preferably includes a self-sealing septum 134. The self-sealing
septum of the second hub functions to provide an opening for an
insertion needle to be inserted into the catheter 170 prior to
catheter insertion, and to seal the internal channel second hub
after withdrawal of the insertion needle within the catheter after
catheter insertion, to prevent escape or leakage of blood and other
potential biohazards or other fluids. As shown in FIG. 2, the
septum 134 is preferably located on the distal side of the second
hub 130 relative to the midline of the patient, and is
approximately concentric with the catheter 170. The septum is
preferably made of a flexible material that self-seals to form a
hermetic seal. This self-sealing septum prevents fluid from passing
through the distal side of the second hub relative to the midline
of the patient, contributing to a closed system in which blood and
other fluids will not exit the integrated vascular delivery device
after the needle punctures the patient. The septum 134 may
alternatively be sealed with a plug, such as a stopper or sealant
material applied to the septum.
[0028] The second hub 130 may additionally include a reservoir
between the septum 134 and the catheter 170. This reservoir may
serve as a flash chamber to contain any blood leakage during
withdrawal of the insertion needle from the catheter after catheter
insertion, or may serve any other suitable purpose.
[0029] The second hub 130 may additionally include features at the
connection between the second hub 130 and the lateral members that
reduce creasing, collapsing, fracture, or other damage in the
lateral members when the lateral members are folded to pass one of
the hubs over the other hub during insertion of the catheter into
the patient. As an example, the second hub may include rounded
edges that are contoured to the natural bend radius of the lateral
members, to prevent the lateral members from bending too sharply or
bending against a sharp edge. As another example, the second hub
may include relief cutouts and/or other reinforcements that
encourage the lateral members to bend to their natural bend
radius.
[0030] The lateral members 140 of the frame 110 function to provide
structural stability to the frame by stabilizing the first hub 120
relative to the second hub 130. As shown in FIGS. 1 and 2, the
frame 110 preferably includes two flexible lateral members,
including at least one tubular lateral member 140'. However, in
alternative versions of the frame, the frame may include fewer or
more lateral members. The lateral members preferably provide
structural stability to the frame, and the tubular lateral member
140' or members preferably house a portion of the fluidic channel
150. The lateral members are preferably parallel with one another
and preferably extend between the first and second hubs, to form a
perimeter 114 around the catheter 170. However, the lateral members
may be in any crossed, non-parallel or any suitable orientation.
The lateral members preferably allow the first hub and the second
hub to move relative to one another with a significant number of
degrees of freedom, including displacement in the compression
direction (and subsequent displacement in the tension direction)
along the axis of the catheter, displacement in both directions
along the other two axes, twisting in both directions along the
axis of the catheter, and bending in both directions along the
other two axes. In particular, the lateral members are preferably
reversibly bendable to fold one of the first and second hubs over
the other hub. As shown in FIGS. 5B and 6, during insertion of the
catheter into the patient, the lateral members are preferably
folded to fold the first hub 120 over the second hub 130, which
opens the perimeter 114 around the catheter and exposes the
penetrating distal tip of the catheter. The length of the lateral
members is preferably approximately 30%-50% longer than the
catheter, but may alternatively be shorter or longer depending on
the specific application. At least one lateral member 140 may
include markings, such as markings similar to those on a ruler, to
indicate the depth to which the catheter is inserted into the
patient. The lateral members are preferably made of an extruded
flexible polymer cut to length and molded to one or both hubs, but
may alternatively be made through any suitable manufacturing
process and/or out of any suitable material.
[0031] In a first preferred embodiment, the pair of lateral members
includes a tubular lateral member 140' and a solid lateral member
140''. The tubular lateral member is preferably a generally
straight, soft, and flexible hollow channel such as medical tubing,
but may alternatively be any suitable structure with an internal
fluid passageway that houses a portion of the fluidic channel 150.
The tubular lateral member is preferably rigid enough to provide
structural support to the frame 110, but flexible enough to bend
and fold across its length without damage during insertion of the
catheter. The tubular lateral member may include additional
features that enhance the ability to bend without damage. As an
example, the tubular lateral member may be tapered along its length
and include a thicker wall and/or larger outer diameter near the
bending stress point at the second hub 130. As another example, the
tubular lateral member may have an elliptical cross-section that is
more resistant to bending damage. As another example, at least a
portion of the first lateral member may include extendable and
foldable pleats, similar to an accordion, that allow curvature of
the lateral member with less bending stress.
[0032] As shown in FIG. 2, in the first preferred embodiment, the
solid lateral member is preferably similar in shape and size to the
first lateral member so that the frame 110 is structurally
symmetrical, but preferably is a "dummy" structure in that it does
not house a portion of the fluidic channel 150. The solid lateral
member 140'' preferably is approximately identical in flexibility
and strength as the tubular lateral member 140'. However, the solid
lateral member 140'' may alternatively have a different shape
(e.g., larger diameter or larger thickness) to further enhance
stabilization of the first hub 120 relative to the second hub.
Similar to the tubular lateral member 140', the solid lateral
member 140'' may additionally include features that enhance the
ability to bend without damage.
[0033] As shown in FIG. 3, in a second preferred embodiment, the
pair of lateral members includes two tubular lateral members 140',
similar to the tubular lateral member of the first preferred
embodiment. In this embodiment, the tubular lateral members 140'
are preferably identical and house two separate fluidic channels
that direct a first and a second fluid flow between the hubs.
However, the tubular lateral members may alternatively be different
for serving different purposes. For example, two tubular lateral
members 140' may house two separate fluidic channels that are
adapted to carry different types of fluids (e.g., different
densities), and the tubular lateral members may have different wall
thicknesses to compensate for the different fluids and achieve
structural symmetry in the frame. As another example, the tubular
lateral members may have different sized lumens.
[0034] In some alternative versions, the frame 110 may include
fewer or more than two lateral members, in any suitable combination
and permutation of tubular and solid lateral members. All of the
lateral members may be solid, tubular, or hollow, or any
combination thereof. In some alternative versions, the lateral
members may merge and/or branch upstream and/or downstream. For
example, in one alternative embodiment the lateral members may
include portions of a thin, flexible sheet that are merged proximal
and distal to the insertion site, such that the catheter tip passes
through a slot-like opening between the merged portions.
[0035] The fluidic channel 150 of the system functions to deliver
fluid from a fluid supply to the catheter, and in some embodiments,
deliver fluid to and from the catheter. The fluidic channel 150 may
additionally and/or alternatively deliver fluid from the catheter
170, such as transferring fluid removed from the patient through
the catheter to an external reservoir. As shown in FIG. 2, the
fluidic channel 150 preferably includes at least one portion that
is fixed within at least one of the hubs and/or within a tubular
lateral member 140'. More preferably, the fluidic channel 150
includes a first portion 152 fixed within the first hub 120, a
second portion 154 passing through a tubular lateral member 140',
and a turnabout portion 156 fixed within the second hub 130. In a
first variation, the fluidic channel 150 may be a continuous length
such as a single piece of tubing fixed in the first hub, passing
through or serving as the tubular lateral member 140', fixed in the
second hub 130 and fluidically coupled to the catheter. In a second
variation, the fluidic channel 150 includes separate lengths such
as separate tubing segments joined at various points such as
through heat sealing, other plastic welding methods, or fluidic
couplings. In a third variation, the fluidic channel 150 includes
tubular cavities within one or both hubs, to which a tubular
segment joins through a process similar to the second variation. In
the third variation, the tubular cavities in the first and/or
second hub may be formed by molding, drilling, laser cutting, or in
any suitable manufacturing process. In a fourth variation, the
fluidic channel 150 may be external to one or more of the hubs and
lateral members, such that at least a portion of the fluidic
channel is mounted to and passes over the exterior of a hub or
lateral member. Other variations of the fluidic channel include
every combination and permutation of these variations.
[0036] As shown in FIG. 2, the first portion 152 of the fluidic
channel 150 preferably includes an inlet located at the midline of
the proximal side of the first hub and an outlet located on the
distal side of the first hub, relative to the midline of the
patient. However, the inlet and outlet of the internal channel may
be located on any suitable position on the first hub. The inlet of
the first portion of the fluidic channel 150 preferably receives
fluid from the extension tubing 180, and the outlet of the internal
channel preferably delivers the fluid to at least one of the
lateral members of the frame 110, but fluid may alternatively flow
in reverse order. The first portion of the fluidic channel 150
preferably includes right angles to direct fluid from the midline
of the first hub to a tubular lateral member 140' located on the
side of the frame. However, the first portion of the fluidic
channel may alternatively be curved (shown in FIGS. 3 and 4),
curvilinear, or any suitable shape for fluid flow through the first
hub 120 to the lateral member. The first portion of the fluidic
channel may be connected to the extension tube by inserting the
extension tube into a hollow recess aligned with the fluidic
channel in the first hub and sealing the recess edge with epoxy,
but the first hub may alternatively be coupled to the extension
tube by press fitting the extension tube into the recess in the
first hub, sealing a butt joint with epoxy, or any suitable
coupling process.
[0037] As shown in FIG. 2, the second portion 154 of the fluidic
channel 150 preferably passes through a tubular lateral segment,
between the first portion in the first hub 120 and the turnabout
portion in the second hub 130.
[0038] As shown in FIG. 2, the turnabout portion 156 of the fluidic
channel 150 is preferably fixed in such a way to direct fluid flow
in a direction different from fluid flow within the catheter 170.
The turnabout portion preferably directs fluid flow to a direction
opposite of that within the catheter, or in an approximately
180-degree turn. The turnabout portion 156 may include right
angles, an elliptical, or a circular turn. The turnabout portion of
the fluidic channel is preferably fixed or embedded within the
second hub 130 (distal relative to the midline of the patient).
Since the catheter is typically inserted in the patient such that
its penetrating end points proximally towards the heart of the
patient, the approximate 180-degree turn of fluid flow within the
internal channel allows the extension tubing to lie proximal to the
insertion site 112 relative to the midline of the patient. This
position of the fluid supply channel advantageously allows a stand
supporting the IV bag or other fluid supply to be kept near the
head of a bed or otherwise proximal to the insertion site relative
to the midline of the patient, as is typically desired and
practiced in patient treatment settings. The internalized fluid
flow turn in the turnabout portion of the fluidic channel 150 also
is advantageous because it reduces external features that can get
caught or snagged on nearby obstacles and disturb the IV setup.
Another effect of the turnabout portion is that if the extension
tube and/or additional tubing from a fluid supply is pulled or
caught, the turnabout portion may enables the frame to stabilize
the catheter more effectively by causing the catheter to be pulled
further into the patient. For example, in a common catheter
placement where the catheter is placed on the forearm with its
distal tip pointing proximally towards the crook of the elbow of
the patient, if the extension tubing is accidentally pulled
posteriorly towards the patient, the tubing will in turn pull the
turnabout portion of the fluidic channel and the distal second hub
130 in a posterior direction, thereby pulling the catheter tip
proximally and further into the blood vessel of the patient.
[0039] In another preferred embodiment, as shown in FIGS. 3-4, the
system includes a second fluidic channel 150 that is preferably
similar to the first fluidic channel 150, but may alternatively be
any of the variations of the first fluidic channel. The second
fluidic channel preferably passes through a second tubular lateral
member 140'. The second fluidic channel preferably receives a
second fluid, which may be the same or different from the first
fluid supplied to the first fluidic channel. In this embodiment, as
shown in FIGS. 4A-4C, the system may further include a second
extension tube 180 that supplies a second fluid to the second
fluidic channel. However, as shown in FIG. 4D, the system may
include only one extension tube that supplies fluid to one or both
fluidic channels. The fluidic channels may have separate inlets on
the first hub or may share the same inlet on the first hub in which
flow may be regulated with valves or other fluid control means. In
one variation, the first and second fluidic channels preferably
fluidically communicate with the same catheter in the second hub
130, coupled to the catheter at the same (FIG. 4D) or different
points (FIG. 4C) along the length of the catheter. In this
variation, the system preferably includes a flow control system 160
that selectively restricts flow of one or both of the fluids to the
catheter and therefore to the patient. The flow control system may
include one or more valves 162, such as at the extension tubes
(FIGS. 4A-4B), at the junction with the catheter 170 (FIGS. 4C-4D),
or any suitable location. The flow control system 162 may
additionally and/or alternatively use pressure drops, vents, or any
suitable technique for controlling fluid flow among the fluidic
channels and catheter. The flow control system 162 may also be
present in an embodiment that includes only one fluidic channel. In
another variation, the first and second fluidic channels preferably
fluidically communicate with a catheter with dual lumens, such that
one catheter lumen is coupled to the first fluidic channel and
another catheter lumen is coupled to a second fluidic channel. In
yet another variation, the first and second fluidic channels
fluidically communicate with separate catheters. Additional
variations expand on these variations with three or more fluidic
channels.
[0040] Furthermore, the first hub 120 and/or second hub 130 may
include multiple internal channels that merge downstream, such that
the number of inlets is greater than the number of outlets in the
hub. In some variations, one of the hubs may include one or more
internal channels that branch downstream, such that the number of
inlets is less than the number of outlets. One of the hubs may
include one or more internal channels that both branch and merge
within the first hub. Multiple internal channels may deliver fluid
to multiple catheters or multiple lumens of a catheter.
[0041] In some embodiments, the system further includes a catheter
170 having a proximal portion embedded in a portion of the frame,
and more preferably in the first or second hub 130. The catheter
170 of the integrated vascular system functions to administer
fluids for IV therapy to the patient. The catheter 170 is
preferably a conduit insertable into a blood vessel of the patient,
but may be any suitable type of catheter. As shown in FIGS. 1-4,
the catheter is preferably fluidly connected to the turnabout
portion of the fluidic channel and located at the midline of the
proximal side of the second hub 130 relative to the midline of the
patient. The catheter 170 is preferably aligned with the extension
tubing, which reduces and streamlines extraneous external tubing
and other connections that may get caught or snagged on nearby
obstacles, which is painful and dangerous for the patient. However,
the catheter may be positioned at any suitable location on the
second hub. In some embodiments, the catheter may be positioned
such as having its proximal end fluidically connected to the first,
more proximal hub and pointing towards and such that the system
lacks a turnabout portion of the fluidic channel. For example, the
catheter may be fluidic connected to the first hub that is more
proximal to the patient, The catheter is preferably made of a soft,
flexible polymer but may be made out of any suitable material.
Dimensions of the catheter, including length, diameter, and cannula
size, will depend on the specific application. Catheters are known
and used in the art, such as that described in U.S. Pat. No.
5,358,493 entitled "Vascular access catheter and methods for
manufacture thereof", which is incorporated in its entirety by this
reference. The catheter may include markings, such as those similar
to a ruler, along its length to indicate the depth to which the
catheter is inserted into the patient.
[0042] 2. Method of Using an Integrated Vascular Delivery
System
[0043] As shown in FIGS. 5A-5F, the method 200 of an integrated
vascular delivery system preferably includes the steps of:
supplying a frame forming a perimeter S210, wherein the frame is
configured to receive a catheter having a distal end contained
within the perimeter and includes a first hub, a second hub, and a
fluidic channel; folding the frame to modify the perimeter of the
frame S220, thereby freeing the distal end of the catheter from the
perimeter of the frame; inserting the catheter into the patient at
an insertion site S230; unfolding the frame to restore the
perimeter of the frame around the distal end of the catheter and
insertion site S240; securing the frame to the patient at a
plurality of anchoring points distributed around the insertion site
S250, thereby stabilizing the catheter relative to the insertion
site; and allowing fluid to flow between the catheter and the
patient S260. The method 200 may be performed to obtain access to
the blood vessel of a patient, such as one undergoing intravenous
(IV) therapy. The method may be used to administer drugs,
antibiotics, saline, blood, or any suitable fluid to a patient,
and/or to remove fluid from the patient. The method may be used to
create, stabilize, and maintain an IV line at an insertion site on
a peripheral vein or artery such as on the arm, hand, or leg, or
for central venous access on the neck, chest, or abdomen, or any
suitable IV location. Furthermore, the method may be used to
create, stabilize, and maintain any suitable catheter-based access
to a patient, such as catheters for transfer of cerebrospinal
fluid.
[0044] As shown in FIG. 5A, the step of supplying a frame S210
preferably includes supplying an integrated vascular delivery
system such as that described above. However, the integrated
vascular delivery system may alternatively be any suitable system
with a frame, first hub and second hub, and a fluidic channel in
which the frame can be folded to pass the first hub towards the
second hub. For example, a frame forming a perimeter may include a
first hub and a second hub coupled with a hinged joint.
Furthermore, the integrated vascular delivery system may include
fewer or more hubs.
[0045] The step of folding a frame S220 functions to expose an
insertable end of the catheter and to provide visual clearance for
the catheter to be positioned at an insertion site and physical
clearance to access the insertion site. As shown in FIGS. 5B and
6A, the step of folding the frame preferably includes passing the
first hub of the frame over the second hub of the frame in a first
direction. The first hub of the frame is preferably a proximal
portion of the frame relative to the patient midline, and the
second hub of the frame is preferably a distal portion of the frame
relative to the patient midline, but the first hub and second hub
may be any suitable portions of the frame. For example, as shown in
FIG. 5F, relative to an insertion site at the crook of an elbow of
a patient, the first hub is preferably closer to the elbow and the
second hub is preferably closer to the hand, such that the step of
folding a frame folds the first hub away from the patient, and
typically towards a medical caregiver using the system who is
standing in front of the patient.
[0046] The step of inserting the catheter into the patient at an
insertion site S230 includes inserting a needle into a catheter,
penetrating the insertion site with the needle, positioning the
catheter within the insertion site, and withdrawing the needle from
the catheter. The step of inserting the catheter into the patient
functions to create a conduit through which fluid can be
administered to the patient. In performing the step of penetrating
the insertion site with the needle, the needle is preferably
pointed proximally relative to the midline of the patient. The step
of inserting a needle into a catheter preferably includes inserting
a needle through the second hub of the frame, which introduces a
piercing tool that is adapted to penetrate the insertion site for
catheter insertion. The steps of penetrating the insertion site,
positioning the catheter, and withdrawing the needle are known and
used by one ordinarily skilled in the art. As shown in FIG. 5C, in
a first variation, inserting a needle through the catheter includes
passing the needle over the first hub of the frame and through the
catheter S232, which maintains the folded orientation of the frame
during catheter insertion and to help hold the first hub in place
to prevent the first hub from obstructing needle access to the
second hub. As shown in FIGS. 6A-6C, in a second variation,
inserting a needle through the catheter includes passing the needle
under the first hub of the frame and through the catheter S234. In
this second variation, the first hub is preferably seated in, or
otherwise coupled to an additional mechanism such as a needle
housing.
[0047] The step of unfolding the frame S240 functions to restore
the perimeter of the frame around the distal end of the catheter
and insertion site. As shown in FIG. 5D, the step of unfolding the
frame preferably includes passing the first hub of the frame over
the second hub of the frame in a second direction. The second
direction is preferably opposite of the first direction, but may
alternatively be any suitable direction and restores the perimeter
of the frame around the insertion site. The step of unfolding the
frame is facilitated by the step of withdrawing the needle from the
catheter, since the needle or other mechanism to which the first
hub is coupled is no longer present to hold the first hub in
place.
[0048] The step of securing the frame to the patient S250 at a
plurality of anchoring points around the insertion site functions
to stabilize the catheter relative to the insertion site. As shown
in FIG. 5E, the step of securing the frame to the patient includes
securing the first hub of the frame to the patient at a first
anchoring point adjacent to the insertion site, and securing the
second hub of the frame to the patient at a second anchoring point
opposite the first anchoring point across the insertion site. The
plurality of anchoring points preferably include at least two
anchoring points approximately opposite to each other, and more
preferably include anchoring points distributed approximately
equally around the insertion site. In particular, the first
anchoring point is preferably distal to the insertion site and the
second anchoring point is preferably proximal to the insertion
site, relative to the patient. Securing the frame to the patient on
two opposite sides of the insertion site functions to effectively
reduce or eliminate motions of the catheter within the vein and
reduce or eliminate the occurrence of painful and
patient-endangering complications including catheter dislodgement,
infiltration, and phlebitis. In some variations, the step of
securing the frame includes securing any suitable number of hubs at
one anchoring point or three or more anchoring points. The first
anchoring point is preferably proximal to the insertion site
relative to the midline of the patient, and the second anchoring
point is preferably distal to the insertion site relative to the
midline of the patient, but the first anchoring point and second
anchoring point may be at any suitable location relative to the
insertion site. Each securing step may include taping the frame to
the patient, adhering the frame to the patient with adhesive,
strapping the frame to the patient, or any suitable securing
mechanism.
[0049] The step of allowing the fluid to flow between the catheter
and the patient S260 functions to administer fluid to the patient
and/or remove fluids from the patient. As shown in FIG. 5F, the
step of allowing the fluid to flow preferably includes connecting
the fluidic channel to a fluid supply or reservoir. The fluidic
channel is preferably connected to the fluid supply or reservoir by
fluidly connecting fluidic channel to extension tubing as is well
known in the art, but may alternatively be connected to the fluid
supply by connecting any suitable portion of the frame through any
suitable method. The fluid supply is preferably an IV bag, but may
alternatively be any suitable fluid supply. In some variations in
which the integrated vascular delivery system includes multiple
fluidic channels, the step of allowing the fluid to flow includes
connecting a second fluidic channel to a second fluid supply or
reservoir.
[0050] The method may additionally further include the step of
applying a dressing over the insertion site and the frame. The step
of applying a dressing functions to protect the insertion site
against bacteria, viruses, and other pathogens. The dressing is
preferably a breathable, sterile dressing such as Tegaderm, which
is known and used to one skilled in the art. As shown in FIG. 5F,
the dressing is preferably transparent to allow visualization of
the insertion site, and includes adhesive to attach to the skin of
the patient and to provide securement of the frame. However, the
dressing can include any suitable device or method to assist in the
protection of the insertion site.
[0051] As a person skilled in the art will recognize from the
previous detailed description and from the figures and claims,
modifications and changes can be made to the preferred embodiments
of the invention without departing from the scope of this invention
defined in the following claims.
* * * * *