U.S. patent number 3,726,275 [Application Number 05/207,930] was granted by the patent office on 1973-04-10 for nasal cannulae.
This patent grant is currently assigned to SAID Sheridan, by said Jackson. Invention is credited to Isaac S. Jackson, David S. Sheridan.
United States Patent |
3,726,275 |
Jackson , et al. |
April 10, 1973 |
NASAL CANNULAE
Abstract
Nasal cannulae are formed of two flexible narine tubes which are
permanently bent near their outlet ends and fixed together at the
bends in a cross-over arrangement that creates a nares entrance
unit without use of a bridge member or similar tube holding means.
Such nasal cannulae are extremely light and inconspicuous providing
maximum comfort during use for administration of oxygen or other
gas into the nares of a person.
Inventors: |
Jackson; Isaac S. (Greenwich,
NY), Sheridan; David S. (Argyle, NY) |
Assignee: |
SAID Sheridan, by said Jackson
(04) N/A)
|
Family
ID: |
22772546 |
Appl.
No.: |
05/207,930 |
Filed: |
December 14, 1971 |
Current U.S.
Class: |
128/207.18 |
Current CPC
Class: |
A61M
16/0666 (20130101); A61M 16/0672 (20140204) |
Current International
Class: |
A61M
16/06 (20060101); A61m 015/08 () |
Field of
Search: |
;128/206,207,14N,348,350,198,199,200,185,250,342,142.3,145.5
;138/111,112,113,114,115,116,117 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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|
|
|
|
|
791,798 |
|
Dec 1935 |
|
FR |
|
98,119 |
|
Feb 1940 |
|
SW |
|
Primary Examiner: Gaudet; Richard A.
Assistant Examiner: Cohen; Lee S.
Claims
The embodiments of the invention in which an exclusive property or
right is claimed are defined as follows:
1. A nasal cannula comprising a pair of narine tubes made of
flexible plasticized vinyl chloride polymer comprising inlet and
outlet ends, said tubes being fitted at their inlet ends to a
tubing connector molded of rigid plastic material having a male
connector member on one end and a pair of sockets on the other end
into which the inlet ends of said narine tubes are fixed, the
periphery of the outlet end of each tube of said pair being
smoothly rounded, one of said tubes being permanently bent a short
distance from said outlet end at an acute angle to the longitudinal
axis of the tube forming a first nares insertion member, the other
of said tubes being similarly bent at its outlet end forming a
second nares insertion member, said tubes being fixed together in
cross-over arrangement at the position of said permanent bends by a
ring of plastic material that encircles said tubes at said
position, said ring being cemented to both said tubes with said
ring and said insertion members substantially parallel to each
other and a plastic ring that slidably encircles said pair of tubes
between said tubing connector and said fixed together position.
2. A nasal cannula as claimed in claim 1 wherein the opening of the
outlet end of each of said tubes is flared.
3. A nasal cannula as claimed in claim 1 wherein said first and
second nares insertion members extend outwardly at an angle between
about 35.degree. and 45.degree. relative to the plane defined by
the longitudinal axis of said tubes proximal to the bends in said
tubes.
4. A nasal cannula as claimed in claim 1 wherein said periphery of
the outlet end of each tube defines a plane that is at an angle to
the bore of the tube.
Description
BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to nasal cannulae to be used in
administering oxygen or other gases to persons via their nostrils.
More particularly, it concerns nasal cannulae made of plastic
materials that are light, inconspicuous, and inherently form
fitting.
2. Description of the Prior Art
Certain ailments of people, e.g., lung emphysema, may require
inhaling of oxygen by the afflicted person over extended periods of
time. Also, there are numerous occasions where bed-ridden patients
in hospitals, nursing homes, etc. require extended administration
of oxygen or other gases to sustain the patient's breathing or for
some other medical purpose. Various methods and apparatus are
available to accomplish such gas administration. In order to
mitigate discomfort of the person receiving gas administration over
long periods, there has been extensive development of socalled
nasal cannulae, e.g., see U.S. Pats. Nos. 2,499,650; 2,663,297 and
2,735,432. Such devices are not only used with bed-ridden cases,
but also ambulatory cases, e.g., see U.S. Pat. No. 3,400,712.
In the nasal cannulae, there is some means to direct a stream of
gas into the nares of the person requiring gas. This may be merely
two holes in a section of tubing, but usually such means comprises
a pair of tubes or nozzles that project into the nares. Such tubes
may be of preformed shape or may include metal inserts, etc. to
provide a desired shape, e.g., see U.S. Pats. Nos. 2,693,800 and
3,513,844. Frequently, the nasal cannula includes a bridge member
to hold the narine tubes apart for nares insertion and the
arrangement of the narine tubes and the bridge member may permit
adjustment of tube spacing, etc., e.g., see U.S. Pat. Nos.
2,931,358 and 3,172,407. Such cannulae may include other features
to improve patient comfort or effectiveness of the device such as
flared ends of the narine tubes to modify gas flow, e.g., see U.S.
Pat. No. 3,400,714.
In spite of the numerous developments in nasal cannulae such as
those described above and others, further improvements in these
devices are needed. Since existing nasal cannulae tend to be heavy
and relatively unyielding to facial shapes and movements, they
become annoying to the wearer when used over any extended period of
time. Also, their bulk makes then conspicuous and this adds to the
annoyance of the user. Hence, a need exists for nasal cannulae that
will be fully effective for the administration of gas to persons
while being extremely light in weight, form fitting, inconspicuous
and relatively highly comfortable.
OBJECTS
A principle object of this invention is the provision of improved
forms of nasal cannulae. Further objects include the provision
of:
1. Nasal cannulae which are inconspicuous when upon the face of a
user, comfortable and inherently form fitting.
2. Nasal cannulae that do not require a separate nares bridge
member or equivalent member.
3. Such nasal cannulae that are extremely light in weight because
they involve a minimum of parts.
4. Nasal cannulae that can be made so inexpensively they may be
treated as disposable, single-user items.
Other objects and further scope of applicability of the present
invention will become apparent from the de-tailed description given
hereinafter; it should be understood, however, that the detailed
description, while indicating preferred embodiments of the
invention, is given by way of illustration only, since various
changes and modifications within the spirit and scope of the
invention will become apparent to those skilled in the art from
this detailed description. It should also be understood the
foregoing abstract of the disclosure is for the purpose of
providing a non-legal brief statement to serve as a
searching-scanning tool for scientists, engineers and researchers
and is not intended to limit the scope of the invention as
disclosed herein nor is it intended it should be used in
interpreting or in any way limiting the scope or fair meaning of
the appended claims.
SUMMARY OF THE INVENTION
The foregoing objects are accomplished according to the present
invention, in part, by forming nasal cannulae from a pair of narine
tubes made of flexible plastic material with the tubes near the
outlet end fixed in a cross-over arrangement so that the tube which
would project into the left nostril of a user will pass across the
right side of the face of the user and, conversely, the tube which
will project into the right nostril of the user will pass across
the left portion of the face of the user. Such an arrangement can
be attained by creating a permanent bend in each tube about 2 cm.
from the outlet end, the bend in the tube being sufficient so that
the portion of the tube between the bend and the outlet end forms
an angle of about 90.degree. or less with the longitudinal axis of
the tube. The narines tubes are fixed together in the region of
said permanent bend, preferably by encircling the tubes at this
point with a small ring of plastic and cementing the tubes to such
ring.
The inlet end of the tubes will be joined for fluid flow to a
tubing connector. Preferably, the tubing connector will be formed,
such as by injection molding, from rigid plastic to include a male
connector on one end and a pair of tubing sockets at the other end
into which the inlet ends of the two flexible narine tubes are
cemented. The only other component of the new nasal cannulae is a
small plastic ring or sleeve slidably encircling the pair of
narines tubes so that it may be moved to any desired position
between the tubing connector and the cross-over portion of the
narine tubes. Consequently, the new nasal cannulae are formed of a
minimum of parts so as to be extremely light and relatively
inconspicuous when positioned on the head of a user.
Success of the present invention is due, in part, to the discovery
that a cross-over arrangement as described above provides a
positioning of the nostril projection portions of a nasal cannulae
which is inherently form fitting. This is accomplished without the
use of a bridge member or similar holder which has been employed in
prior known devices for obtaining the necessary position in the
narines tubes for satisfactory projection into the nares of a user.
In contrast to such prior devices involving bridge members, the
cross-over arrangement of the narine tubes of the new nasal
cannulae have an inherent form fitting feature which is relatively
yielding to facial shapes and movements of different users. This
permits the wearer to talk, eat, smile and make other facial
movements without annoyance and without substantial disturbance to
the appearance of the wearer. The flexibility of the assembly of
the new cannulae allow them to conform without any annoying
pressure points upon the face or nares region of the wearer.
BRIEF DESCRIPTION OF THE DRAWING
A more complete understanding of the improved nasal cannulae of the
invention and of their method of use may be had by reference to the
accompanying drawings in which:
FIG. 1 is an elevational front view of a nasal cannulae of the
invention positioned upon the face of a wearer.
FIG. 2 is an elevational side view comparable to FIG. 1.
FIG. 3 is a plan view, partially broken away, of one of the new
nasal cannulae shown in FIG. 1.
FIG. 4 is a side view, partially broken away, of the cannulae of
FIG. 3.
FIG. 5 is a fragmentary front elevational view of the outlet end
portion of the cannulae of FIG. 3.
FIG. 6 is a fragmentary bottom view of the portion of the cannulae
shown in FIG. 5.
Referring in detail to the drawings, the nasal cannulae 2 comprises
a pair of narine tubes 4 and 6, a tubing connector 8 and a ring
slide 10.
The outlet end 12 of tube 4 has a smoothly rounded periphery 14
that defines a plane that intersects the bore of the tube 4 at an
angle. The outlet end 16 of tube 6 similarly has a smoothly rounded
periphery 18 which also intersects the bore of the tube at an
angle. However, it is possible, if desired, to have the peripheries
14 and 18 of the tubes 4 and 6, respectively, square with the bore
of the tubes.
A permanent bend is formed in each of the narine tubes 4 and 6
about two cm. from their outlet ends 12 and 16 respectively.
Although the tubes 4 and 6 are formed of relatively flexible
plastic material so that the tubes can normally be flexed to
conform to desired shapes, the tubes do have a tendency to remain
in a relatively straight longitudinally extended position. A bend
20 in tube 4 and similar bend 22 in tube 6, however, can be
relatively permanently formed in the tubes such as by manipulation
of the tube while it is heated in that portion in which the bend is
desired, by application of solvent or in other ways known to those
skilled in the art of fabrication of flexible plastic tubing. The
portion 28 of tube 6 beyond bend 22 is longer than portion 26 of
tube 4 by the diameter of tube 4 so that when the tubes are crossed
(see FIG. 5) the outlet ends 12 and 16 will be even.
Tubes 4 and 6 are fixed together at the bends 20 and 22 in some
suitable manner, such as by cementing, solvent welding or the like.
Preferably, a narrow ring of plastic material 24 will encircle the
tubes 4 and 6 at the bends 20 and 22 respectively and this plastic
ring will be cemented to the tubes 4 and 6 at this point. The only
fixed part of the assembly is at the cross-over points of the tubes
4 and 6 where they and the ring 24 are joined together. As a
result, movement of tubes 4 and 6 about the cross-over point and
the outlet end portions 12 and 16 is possible. This allows the
tubes 4 and 6 and the portions 26 and 28 respectively, which in use
project into the nostrils of a wearer, to readily conform to the
nares of the user and to the shape of the wearer's face.
Consequently, the new nasal cannulae can move substantially
unrestrictedly with the face and head movements of the wearer. The
cross-over arrangement of the tubes 4 and 6 as described has an
inherent form fitting feature due to the fact that the only fixed
part of the assembly is where the tubes cross at the ring 24.
It will be apparent in the embodiment of the invention in which the
peripheries 14 and 18 of the tubes 4 and 6 form an acute angle with
the bores of the tubes, there is a right and left hand arrangement
between the tubes 4 and 6. Thus, when the new nasal cannulae is
positioned upon the face of the wearer 30, the slanted periphery 14
of the tube 4 will extend inwardly relative to the nares of the
wearer 30 (see FIG. 5). The tubing portion 26 of the tube 4 will
project into the right nostril of the wearer 30 while the portion
of the tube 4 which is distal of the ring 24 will pass across the
left side of the face of the wearer. Similarly, the slanted
periphery 18 of tubing 6 will face inwardly relative to the nares
with portion 28 projecting into the left nostril of the wearer
while the adjacent section of tube 6 distal of the ring 24 will
pass across the right portion of the face of the wearer.
Referring to FIG. 4, the tube portion 26 extends outwardly at an
acute angle, e.g., between about 20.degree.-85.degree., relative to
tubes 4 and 6. The portion 28 of the other tube 6 also extends
outwardly at a similar angle. Preferred results are obtained when
this angle is between 35.degree. and 45.degree..
As can be seen from the FIGS. 1 and 2, new nasal cannulae of the
invention can fit close under the nares of a user and the portions
of tubes 4 and 6 which pass across the face of the wearer will rest
high on the cheekbones. This provides a comfortable and
inconspicuous positioning of the cannula.
The ring or slide 10 can be adjusted in any suitable position along
with the tubes 4 and 6 to provide freedom of movement of the jaw
and head of the wearer. Advantageously, the plastic rings 10 and 24
may be cut from plastic tubing compounded from flexible plastic
material identical with or similar to that used to form extruded
tubes 4 and 6. Alternatively, the rings 10 and 24 could be molded
or otherwise shaped from flexible or rigid plastic material, rubber
or the like. It is advantageous, however, to have ring 24 made of
substantially the same material as tubes 4 and 6 so that good
connection can be made between them at the bends in tubes 4 and 6
by means of solvent welding, cementing or the like. Plasticized
vinyl chloride polymer is a preferred material from which to
fabricate tubes 4 and 6 and rings 10 and 24, but other flexible
thermoplastics can be used, e.g., polyethylene, polypropylene and
the like.
The tubing connector 8 is preferably injection molded from rigid
plastic material to have a male connector 32 at one end and a pair
of tubing sockets 34 and 36 at the other end into which the inlet
ends 38 and 40 of tubes 4 and 6 respectively are fitted and,
preferably, cemented. Nylon, polycarbonate resin, polystyrene or
the like are suitable thermoplastics from which to mold the tubing
connector.
In use, a nasal cannula of the invention can be positioned on the
head of a wearer as shown in FIGS. 1 and 2. When so used, the nares
tubes 4 and 6 pass across the side of the face, over the ears and
then down below the jaw and in front of the throat of the wearer.
The tubing connector 8 will be joined to a single gas conveying
tube which in turn will be connected to a source of oxygen or other
gas required for the treatment or medical procedure being applied
to the wearer of the cannula. In an alternative method of
positioning a cannula on the head of the patient, the pair of nares
tubes can pass over the ears to the back of the head of the wearer.
In this case, the ring or band 10 will be moved along the tubes 4
and 6 to the back of the head of the wearer.
* * * * *