U.S. patent number 3,643,660 [Application Number 04/878,628] was granted by the patent office on 1972-02-22 for nasal cannula.
Invention is credited to Harold R. Havstad, Allan C. Hudson, John M. Kinnear.
United States Patent |
3,643,660 |
Hudson , et al. |
February 22, 1972 |
NASAL CANNULA
Abstract
A unified nasal cannula comprises a hollow tubular body having
an upper flat or plane surface and a pair of spaced and curved
elongated tubular extensions, having exterior orifices for
directing a gas flow which extensions project upwardly at an angle
from the surface.
Inventors: |
Hudson; Allan C. (Glendale,
CA), Kinnear; John M. (Walnut, CA), Havstad; Harold
R. (Lakewood, CA) |
Family
ID: |
25372443 |
Appl.
No.: |
04/878,628 |
Filed: |
November 21, 1969 |
Current U.S.
Class: |
128/207.18 |
Current CPC
Class: |
A61M
25/02 (20130101); A61M 16/0672 (20140204); A61M
2025/0226 (20130101) |
Current International
Class: |
A61M
16/06 (20060101); A61M 25/02 (20060101); A61m
015/08 () |
Field of
Search: |
;128/205,14N,198,199,200,205,207,142.3,145.5,348,342,350 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Gaudet; Richard A.
Assistant Examiner: Mitchell; J. B.
Claims
We claim:
1. A nasal cannula comprising:
an elongated body adapted to have minimal contact with a patient's
upper lip, said body having a tunnel extending through the length
thereof terminating in an oxygen supply opening at each end, the
body having a length sufficient to span the width of an average
patient's nostrils and an upper essentially flat surface portion
being relatively thin in cross section for resting against a
patient's anterior nares and a pair of spaced hollow tubular
extensions integral with and projecting upwardly from said flat
surface which extensions terminate at a gas directing orifice and
which hollow portion of said extensions communicate with said
tunnel.
2. The cannula of claim 1 wherein the tubular extensions are
curved.
3. The cannula of claim 2 wherein the tubular extensions join said
flat surface at an obtuse angle.
4. The cannula of claim 1 wherein the hollow portion of each of
said extensions communicates with said tunnel at a first orifice
and terminates at its opposite end in a gas directing orifice said
gas directing orifice being larger than said first orifice.
5. The cannula of claim 4 wherein said hollow portion of said
extensions is flared uniformly between said first and said gas
directing orifice.
6. The cannula of claim 1 having a flexible oxygen supply tube
extending from each tunnel opening.
7. The cannula of claim 1 composed of a flexible material.
8. The cannula of claim 8 wherein the flexible material comprises a
thermoplastic resin.
9. The cannula of claim 8 wherein the resin composition is selected
from the group consisting of polyvinyl chloride and polyvinyl
acetate.
10. The cannula of claim 1 wherein the length of said body is
between about 11/2 and about 2 inches.
11. A nasal cannula for delivering oxygen containing gas
comprising:
a. a generally flattened upper body portion having a flat upper
surface for resting against a patient's anterior nares said upper
surface having a length sufficient to span the width of an average
patient's nostrils, said body portion being thin in cross section
so as to have minimal contact with a patient's upper lip,
b. a hollow tunnel portion of substantially the same length as said
upper body portion and attached to the underside of said upper body
portion and terminating in an oxygen supply opening at each end,
and
c. a pair of spaced hollow tubular extensions projecting upwardly
from and integral with said flat surface, each end of said
extensions communicating with said tunnel at a first orifice and
terminating at its opposite end in a gas directing orifice.
12. The cannula of claim 11 wherein the length of said upper body
portion is between about 11/2 and about 2 inches.
13. The cannula of claim 11 having a flexible oxygen supply tube
extending from said tunnel ends.
Description
BACKGROUND OF THE INVENTION
One of the most efficient methods of administering therapeutic
oxygen to patients has been accomplished by the use of nasal
cannulae. Early cannula models were somewhat cumbersome due not
only to their relatively large sizes, but also in the manner by
which they were affixed to the patient. For example, devices were
attached to the user's forehead or utilized strap means which
extended around the cheeks to the back of the patient's head. With
the advent of plastic tubing, a number of improvements were
realized, both as to the more efficient oxygen administration, as
well as to the patient's comfort, for example, as disclosed in U.S.
Pat. Nos. 2,735,432 and 2,868,199. These cannulae are designed so
that gases flow directly into the patient's nasal passages and
pharynx. This object was achieved by tilting a flattened portion of
the cannula which lies against the patient's face or cheeks, with
respect to the plane of the elongated nasal extensions and by
curving these extensions in a manner so as to conform with the
shape of the nasal passageways.
Notwithstanding such improvements, there remained some
disadvantages notably in the area of patient discomfort. The
above-noted cannulae, as well as others, in view of their design,
generally have been placed on the user so as to be primarily
positioned or seated in the nasolabial area, i.e., the area between
the patient's upper lip and the nostrils. Even though such devices
are made of soft, flexible plastic or rubber, in attempts to
minimize skin irritation at the points of contact, some discomfort
is known to persist. For example, when a patient is required to
have prolonged oxygen administration thereby necessitating constant
wearing of the cannula, both during awakening as well as sleeping
hours, continued contact of the cannula, especially at the philtrum
and around the unprotected upper lip and cheek areas causes
inflammation and irritation. Not only does the wearer inadvertently
move the cannula while sleeping as the head moves from side to
side, but when eating and/or talking, further movement occurs.
There is also associated discomfort and inconvenience, particularly
in talking or eating where the device is firmly positioned against
the upper lip area and across the cheeks. As in the case in any
instances of prolonged contact of the patient's skin with an
object, not only does irritation result, but inflammation and
ulcerous conditions may occur after a period of time.
A further disadvantage associated with prior cannulae is in the
method in which they are placed on the patient. Where a strap or
elastic band is required to be secured around the back of the
patient's head, the head must be lifted. In cases where the patient
suffers from a serious back, head or neck injury, movement of the
head is quite undesirable and could cause additional injury. It is
to the reduction or elimination of the above-noted disadvantages
that the preset invention is directed.
SUMMARY OF THE INVENTION
The nasal cannula described herein comprises a body portion having
a hollow tunnel or tubular area extending therethrough and which
body portion has an upper generally flat surface. A pair of spaced
elongated tubular extensions extend from the flat surface. The
extensions have an outer orifice for directing a gas flow to the
nasal passageways of the patient and a lower interior orifice
communicating with the tubular area of the body portion. The
termination of the tubular area extending through the body provides
an opening at each end, which openings may be connected to an
oxygen supply tube. The tubular extensions are preferably curved so
that they intersect the flat surface of the body portion at an
angle. In use, the cannula when fitted to the patient is positioned
so that the flat surface lies across the nostrils (anterior nares)
and the approximate center thereof between the spaced tubular
extensions rests upon the exterior nasal septum. In this manner,
contact of the cannula with the upper lip area is essentially
avoided with patient discomfort and skin irritation minimized.
These, as well as other advantages will be described and become
more evident from the following detailed description.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a perspective view of the nasal cannula of the
invention;
FIG. 2 is a view in front elevation of the cannula of FIG. 1;
FIG. 3 is a sectional view through the cannula of FIG. 2 taken
along line A--A showing its relative position when secured to the
patient with its extensions inserted into the nasal cavity; and
FIG. 4 illustrates a preferred method by which the cannula is
secured to the patient utilizing the oxygen supply tubes.
DETAILED DESCRIPTION OF THE INVENTION
Referring to FIGS. 1 and 2, the construction of the nasal cannula
10 includes a body portion 11, having a hollow tunnel 17 through
the entire length of the body portion 11. Exterior openings 16 of
the tunnel 17 are located at each end of the body portion 11. The
size or diameter of the tunnel 17 is not particularly critical so
long as it is essentially uniform throughout and sufficient to
allow for unrestricted passage of gas therethrough. However, the
diameter of the tunnel opening 16 should be great enough to allow
for insertion of oxygen supply tubes 24 and 25. These supply tubes
are preferably of catheter size, for example, having an external
diameter of about 0.125 inches. The upper surface 12 of the body
portion 11 is flattened so as to provide a smooth surface for
contacting the patient's nostrils and exterior nasal septum,
although it may be slightly outwardly curved. The surface 12 not
only provides for patient comfort, but, in addition and of more
importance, prevents the cannula from turning or rotating thereby
maintaining its proper position during use. Thus, with the flat
surface engaging the anterior nares, the cannula does not tend to
roll which would otherwise cause the tubular extensions to be
displaced from within the nostrils. The rear edge 20 of the upper
surface 12 is preferably rounded to provide a smooth surface should
it contact the nasolabial area between a patient's upper lip and
nostrils. This feature is also shown in FIG. 3. The underside of
lower surface 18 of the cannula body 11 as shown is shaped as the
exterior diameter of the tunnel 17, but may have alternate form.
However, in the interest of being lightweight and flexible, by
molding the cannula 10 to have a general shape as shown, material
requirements are minimized and simplified molding techniques may be
utilized.
Integral with the cannula body 11 and protruding or extending from
the upper flat surface 12 are a pair of spaced tubular extensions
14. These extensions 14 are desirably curved, as shown, so that
when placed within the nasal cavities (Note FIG. 3) they conform to
the shape of the passageway as well as providing a smooth surface
which may contact the delicate nasal membranes. It will be noted in
FIG. 3 that the lower internal orifice 30 of each of the tubular
extensions 14 open to the hollow tunnel 17 of the cannula body 11.
Then, as oxygen is introduced into the cannula 10 through the
oxygen supply tubes 24 and 25, there is an unrestricted passageway
for entry of the oxygen through the orifices 30 of each of the
tubular extensions 14 which oxygen then passes upward through the
tubular extensions 14 and out of the upper external orifices 15.
Thus, the oxygen is directly introduced into the patient's nasal
cavity and pharynx.
As best seen in FIGS. 1 and 3, the tubular extensions 14 intersect
with the upper flat surface 12 of the cannula body 11 at an angle
which is preferably obtuse with the plane of the surface 12. The
tubular extensions 14 are also preferably located at or near the
forward edge of 22 of the surface 12, which location combined with
the angle of intersection of the tubular extensions 14 with that
surface provide maximum comfort to the patient and easy placement
of the cannula extensions 14 into the nasal passageways. Although
the extensions 14 may be curved to any desired extent, it has also
been found that for most patients having normal nasal passageway
contours where the plane of the external gas directing orifices 15
is essentially normal to the plane of the flat surface 12, proper
gas flow direction and maximum patient comfort will be achieved.
However, the greater or lesser curvatures of these tubular
extensions 14 may be utilized depending on individual patient
requirements. Yet, due to the flexibility of these extensions 14
small angle deviation is possible by inserting the cannula
extensions into the patient's nostrils with concomitant movement of
the extensions so as to conform to the patient's nasal cavity.
Another preferred feature is in utilizing flared extensions 14. The
flaring is preferably uniform between the lower internal orifice 30
and upper exterior orifice 15, resulting in a reduced velocity gas
flow from the external orifice 15 as compared to the velocity at
which the gas enters the lower orifice 30. Thus, although the same
volume of gas will be delivered to the patient, the reduced gas
velocity entering the nasal cavity avoids high-velocity impingement
on the delicate nasal cavity membrane which could cause oxygen
burn, irritation and discomfort. The amount of flaring between the
external orifice 15 and the internal orifice 30 may be varied to
any desired extent with diameter ratios between about 2:1 and about
4:1 respectively being preferred.
The size of the cannula is not particularly critical with the
provision that the length and width of the upper flat surface 12 to
be such that it will rest comfortably when placed on the patient.
Thus, for example, a length of the surface 12 being between about
11/2 and about 2 inches will ensure that it will span the width of
the nostrils. Further, the width of the flat surface 12, i.e., the
distance between the edges 22 and 20 should be sufficient to
provide a comfortable contact area with the nostrils and nasal
septum, while at the same time, holding the cannula firmly in place
when on the patient. However, it should also be understood that
this distance should not be excessive which would otherwise cause
edge 20 to engage the upper lip area excessively, resulting in
discomfort or irritation. In addition, the tubular extensions 14
should be separated or spaced so that they are comfortable and can
be easily inserted into the nasal passages. It will be appreciated
that such dimensional requirements will vary between individual
patients depending on age, size, facial features, etc. Thus,
cannula model sizes may be varied accordingly.
FIG. 4 illustrates a preferred manner in which the cannula is worn
by a patient. The cannula 10 rests across the patient's nostril
area (anterior nares) and the flexible oxygen supply tubes 24 and
25 are brought across the patient's face, over and behind the ears,
down the jaw areas and brought together under the chin. A hollow
sliding member 28 of sufficient size to encompass both tubes 24 and
25, may then be adjusted so that the cannula 10 will remain firmly
in place without the tubes being unduly taunt. The cannula 10 may
be easily removed by sliding the member 28 downwardly so that the
supply tubes 24 and 25 become loosened. In this manner the cannula
can be easily placed on a patient and removed without moving the
patient's head. The oxygen supply tubes 24 and 25 may be fitted
into a larger oxygen supply tube which in turn is connected to an
oxygen source as will be understood by those skilled in the
art.
The above-described invention provides an oxygen administration
device which not only can be easily fitted to and removed from a
patient, but which is of minimum discomfort and irritation to the
patient. Thus, since the cannula essentially contacts only the
exterior nostril area, its presence is realized to the minimum
possible extent. Further, the patient may eat, talk, and move his
head while the cannula remains firmly, yet comfortably, in place.
The fat upper surface which rests comfortably against the patient's
anterior nares prevents cannula rotation thereby maintaining its
proper position with the gas directing tubular extensions located
within the nostrils rather than slipping out even though the supply
tubes are rolled or turned somewhat. The cannula also offers the
advantage of being simple in design, and in expensive to fabricate.
The composition of the cannula is preferably of the thermoplastic
composition such as polyvinyl chloride or polyvinyl acetate which
materials are understood to be quite pliable or flexible.
Alternatively, the cannula may be fabricated from a rubber
composition or other flexible synthetic materials. The cannula
obviates the requirement of straps or bands thereby also
simplifying manufacturing techniques and reducing costs. The
unitary device may be produced by a simple molding operation with
the oxygen supply tubes then attached prior to or at the time of
use.
* * * * *