CA1121682A - Catheter assembly for intermittent intravenous medicament delivery - Google Patents
Catheter assembly for intermittent intravenous medicament deliveryInfo
- Publication number
- CA1121682A CA1121682A CA000344471A CA344471A CA1121682A CA 1121682 A CA1121682 A CA 1121682A CA 000344471 A CA000344471 A CA 000344471A CA 344471 A CA344471 A CA 344471A CA 1121682 A CA1121682 A CA 1121682A
- Authority
- CA
- Canada
- Prior art keywords
- needle
- lumen
- cavity
- catheter
- hub
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/06—Haemostasis valves, i.e. gaskets sealing around a needle, catheter or the like, closing on removal thereof
- A61M39/0606—Haemostasis valves, i.e. gaskets sealing around a needle, catheter or the like, closing on removal thereof without means for adjusting the seal opening or pressure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/06—Haemostasis valves, i.e. gaskets sealing around a needle, catheter or the like, closing on removal thereof
- A61M2039/0673—Haemostasis valves, i.e. gaskets sealing around a needle, catheter or the like, closing on removal thereof comprising means actively pressing on the device passing through the seal, e.g. inflatable seals, diaphragms, clamps
Abstract
ABSTRACT OF THE DISCLOSURE
An intravenous catheter assembly comprises a catheter with an elongate hollow tube and a hub connected to the tube and having an interior cavity communicating with the lumen of the tube. A needle is slidably positioned in the lumen so that its point protrudes slightly beyond the distal end of the tube, whereas the other end of the needle extends through the hub and sealingly contacts the same so that the hub is effectively closed. A blocking device is contained in the cavity which is adapted to block the entrance of the lumen after the needle is withdrawn from the catheter tube to prevent ready re-insertion of an instrument into the lumen; however, flow of fluids into the lumen is not blocked. The hub includes an access provision to the cavity whereby fluids may be deposited into the cavity for delivery to a patient after the needle has been withdrawn from the catheter tube.
An intravenous catheter assembly comprises a catheter with an elongate hollow tube and a hub connected to the tube and having an interior cavity communicating with the lumen of the tube. A needle is slidably positioned in the lumen so that its point protrudes slightly beyond the distal end of the tube, whereas the other end of the needle extends through the hub and sealingly contacts the same so that the hub is effectively closed. A blocking device is contained in the cavity which is adapted to block the entrance of the lumen after the needle is withdrawn from the catheter tube to prevent ready re-insertion of an instrument into the lumen; however, flow of fluids into the lumen is not blocked. The hub includes an access provision to the cavity whereby fluids may be deposited into the cavity for delivery to a patient after the needle has been withdrawn from the catheter tube.
Description
llZ1~8Z
CATHETER ASSEMBLY FOR INTERMITTENT INTRAVENOUS
MEDICAMENT DELIVERY
. BACXGROUND OF THE INVENTION
The present invention relates to an intravenous catheter assembly, and more particularly, concerns a catheter assembly which is especially useful in situations where medicament is to be delivered in intermittent periods 5 to a patient.
For patients who require periodic intermittent medication by intravenous delivery it is desirable to ; make one venipuncture, insert an intravenous catheter and leave it in position for periodic use. This procedure, - 10 of course, eliminates repetitive piercing of the patient's veins each time he is to receive medication. A catheter ~t of this type whose purpose is to remain in the patient for a prolonged time period generally has to satisfy two : requirements: it must prevent blood and/or body fluids ';n' 15 from escaping out of the catheter both when being used and during the time period when the catheter is not in use;
and it must also have some provision so that the medicament can be deposited through the catheter and into the patient.
' Various reseal plugs are used in intravenous catheter s, 20 devices, and are well known for the purpose of preventing the escape of fluids from the catheter ln addition to allowing penetration by a needle for delivery of the ~' medicament of the patient. Some typical devices which ; include this reseal plug or a similar variant are described - 25 in U.S. Pat. Nos. 3,585,996; 3,313,299, and 3,097,646.
., ' ~, ~, , ,' :
A catheter with a reseal plug generally has the plug, such as a thin rubber diaphragm, covering the open end of the catheter hub. This type of diaphragm is self sealing so that each time the needle makes a puncture 5 through the diaphragm and then is withdrawn after deliver-ing the medication to the patient, the diaphragm seals again to prevent escape of blood or other fluids from the catheter. E30wever advantageous this type of device with reseal plug may be, some problems still arise.
In particular, many catheters which are expected to remain in the patient after initial insertion for periodic use are constructed wïth plastic catheter tubing. An introducer needle, inside the plastic catheter tube, is used to make the venipuncture, and 15 then the needle is withdrawn leaving the catheter tube in the vein of the patient. The plastic tubing, being generally flexible, minimizes trauma to the patient and does not include the very sharp points and edges such as a metal catheter tubing might have, thereby reducing the 20 risk of damage if the patient should move or roll over the catheter. In this type of catheter with plastic catheter tubing, a problem arises when medication is injected into the hub of the catheter~ The attendant or clinician pierces the reseal plug at the hub of the 25 catheter generally with a sharp pointed metal needle at the end of a syringe. If the needle penetrates too far into the catheter its sharp point may, and often times , does, puncture the wall of the plastic catheter tube.
This, of course, may not only damage the catheter tube ~l30 but may also leave a hole in the tube so that some of the medication may not be delivered to the patient.
Accordingly, while it is still desirable to permit the hypodermic needle to penetrate into the hub of the catheter for delivery of the medication, a means of 35 preventing inadvertent puncture of the catheter tube :"
:
i8Z
wall is also being sought. It is to this end and the solution of the problem of puncturing the catheter tube wall that the present invention is directed.
SUM2~IARY OF THE INVENTION
An intravenous catheter assembly comprises a 5 catheter with an elongate hollow tube and a hub connected to the tube. The hub has an interior cavity communica-ting with the lumen of the tube. A needle is slidably positioned in the lumen so that its point protrudes slightly beyond the distal end of the catheter tube, 10 the other end of the needle extending through the hub and being in sealing contact therewith so that the hub is effectively closed. Means in the cavity is adapted to block the entrance of the lumen after the needle is withdrawn from the catheter tube to prevent ready re-15 insertion of an instrument into the lumen, but is adapted to allow flow of fluids into the lumen. The hub includes means for access to the cavity whereby fluids may be ~, deposited into the cavity for delivery to the patient ; after the needle has been withdrawn from the catheter tube.
In a preferred embodiment of the present invention, the catheter tube is made of a flexible, plastic material and the blocking means is a ball having a diameter greater ' than the diameter of the lumen but smaller than the ; cross-sectional dimension of the cavity. These dimensional 25 relationships provide clearance for the needle upon ; original insertion into the catheter tube but prevent ready re-insertion of the needle into the catheter tube after it has been withdrawn. The ball is movable in the cavity ; so that fluids injected into the cavity will be permitted 30 to enter into the lumen for delivery to a patient. In this embodiment, the means for access to the cavity is a pierceable, self-sealing diaphragm placed over an open end of the hub. Upon original insertic~, the needle pierces the diaphragm; upon withdrawal of the needle, the ., diaphragrn is adapted to sealingly close to prevent escape of fluids from the hub.
In accordance with the principles of the present invention, a significant advantage lies in the blockage of the lumen of the catheter tube to prevent re-insertion of the needle or any like instrument into the catheter tube after the needle has been withdrawn. By preventing the needle from being re-inserted into the lumen of the catheter tube, any damage which could be caused by the ' 10 sharp point of the needle is avoided, in addition to any loss of fluid medicament should the catheter tube be ruptured ~y the sharp point of the needle. Further advantages are offered by the present invention as will ~- become more clear when reading the detailed description hereof.
~'~ BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a perspective view illustrating the preferred intravenous catheter assembly of the present - invention;
` Fig. 2 is a cross-sectional view taken along line , 20 2-2 of Fig. l;
Fig. 3 is a partial cross-sectional view illustrat-ing the interior of the catheter hu~ after the introducer needle has been withdrawn;
Fig. 4 is a partial cross-sectional view illustrat-ing the interior of the catheter hub when a needle from a syringe enters the cavity to deliver medicament;
Fig. 5 is a partial cross-sectional view illustrat-ing an alternate blocking means located inside the catheter hub; and Fig. 6 is an elevational view illustrating the blocking device of Fig. 5 ' . ' .
~ 168Z
DETAILED DES`CRIPTION
While this invention is satisfied by embodiments of many different forms there is shown in the drawings and will herein be described in detail a preferred ` embodiment of the invention, with the understanding : 5 that the present disclosure is to be considered as exem-plary of the principles of the inventian and is not intended to limit the invention to the embodiment illustrat-ing. The scope of the invention will be pointed out in the appended claims.
Adverting to the drawings, particularly Figs. 1 and ~ 2, there is illustrated an intravenous catheter assembly ,~ 10 particularly useful for periodic or intermittent intravenous medicament delivery~ Catheter assembly la is comprised of two general components, namely a catheter lS 12 and an introducer needle 14. Catheter 12 i5 constructed of an elongate hollow tube 15, preferably slender and smooth surfaced to provide minimal drag and discomfort upon insertion in the patient. Furthermore, to eliminate ; trauma to the patient and unnecessary rigidity, catheter 20 tube 15 is preferably made of a flexible, plastic material.
The distal end 16 of the catheter tube tapers inwardly in order to facilitate venipuncture and subsequent insertion '~ into the patient's vein. The hollow inside portion of the catheter tube forms a lumen 18 through which medicaments 25 pass on the way to the patient.
At or near the proximal end of catheter tube 15 hub 19 is connected. This hub is preferably a female Luer connection which is well known and commonly used as a catheter hub. The hub is formed so that its 30 interior is a cavity 20, and this cavity communicates with lumen 18 in a catheter tube. In most instances, cavity 2a has a much larger cross-sectional dimension than the diameter of lumen 18, in order for the cavity to be able to receive the medicament for eventual delivery to the il.'~:l6~Z
patient. In hub 19 being described, the end 21 opposite the connection to the catheter tube is an open end, and is covered by a pierceable, self-sealing diaphragm 22.
This diaphragm is preferably made of rubber or the like 5 material which will allow a sharp pointed instrument to pierce the material, but which serves to seal itself after the instrument is withdrawn so that no fluids may escape particularly through the hole or slit made by the piercing instrument. It is noted in Figure 2, that 10 diaphragm 22 includes two annular rims 24 and 25; these rims snugly fit around the wall of hub 19 and may be secured thèreto by various means such as adhesives,heat sealing and the like, if desired.
Located inside cavity 20 is a ball 26. Ball 26 is 15 free to move around inside the cavity inasmuch as it has a diameter smaller than the cross-sectional dimension - of the cavity. On the other hand, ball 26 has a diameter greater than the diameter of lumen 18. In this regard, the ball cannot enter lumen 18 of the catheter tube, but 20 is confined within the cavity 2Q inasmuch as diaphragm 22 serves to effectively enclose the cavity with the ball therein.
Introducer needle 14, the other general component of the present intravenous catheter assembly, includes 25 a long slender needle 28 the distal end 29 of which is pointed. Needle 28 may or may not be hollow depending upon choice of the fabricator. The opposite end of introducer needle 14 has a knob 30 which facilitates gripping by the operator in order to be able to manipulate 30 the needle.
Referring particularly to Fig. 2, catheter assembly 10 is illustrated in the relative positions of introducer needle 14 and catheter 12 upon being originally fabricat~d.
It can be seen that needle 28 is slidably positioned in 35 lumen 18 of the catheter tube, and that the distal - ' '`' , 168.'Z
7 .
pointed end 29 of the needle protrudes slightly beyond .: distal end 16 of th.e catheter tube. This., of course, ` facilitates venipuncture inasmuch as the point of the :l needle is the leading element in this.procedure. In 5 order to become positioned in lumen 18, the point of . the needle has had to pierce diaphragm 22. It should be pointed out that when needle point 29 pierces diaphragm 22 it is not attached to hub 19 nor is ball 26 in cavity 20. After the needle has pierced the diaphragm and is 10 inserted into lumen 18, ball 26 is positioned in the ~ cavity, and then the diaphragm is sealed to the hub.
; As seen in the drawings, the proximal end of the needle . extends beyond the open end of the tube, so that the knob can be easily grasped. In this completed package, ball 15 26 usually presses against the slender needle and may ~i even tend to slightly bend the needle barrel; this presents . no permanent distortion inasmuch.as the bend is slight and the needle is generally somewhat resilient. The catheter assembly, in the configuration illustrated in . 20 Figure 2, is used to effect venipuncture. so that catheter . tube 15 may be properly positioned in the vein of the patient. Once in proper position, introducer needle 14 is gripped by its knob 30 and slowly ~ithdrawn from the catheter while leaving catheter tube 15 in the patient.
25 Figure 3 of the drawings illustrates especially the interior of the catheter hub after intorducer needle 14 has been withdrawn.
It can be seen that, once the needle is completely removed from the catheter, th.e slit formed by the piercing 30 needle closes due to the self-sealing characteristics of ~ the diaphragm. Thi.s seal is important to prevent blood from flowing through.catheter tube lS and out of hub 19.
Thus, the catheter may now remain in the patient and be used for periodic delivery of medicament.. It is noted 35 when viewing Fig. 3, that ball 26 remains freely movable in cavity 20.
; .
"
11'~1682 -When it is time to use the catheter for delivering medicament to the patient, the operator merely pierces diaphragm 22 with the needle 32 of an appropriate syringe 34 or like device carrying the fluid medicament. This procedure is illustrated in Fig. 4. Once needle 32 passes through the diaphragm into the cavity, it encounters ball 26. The ball effectively blocks ready entrance by the hypodermic needle into lumen 18 of the catheter tube.
Thus, the point of needle 32 will penetrate no further ; 10 than cavity 20; moreover, this blockage can be felt by the operator to provide a clear indication that the needle is in the proper position for depositing the medicament~
~ Once the fluid medicament flows out of needle 32 when in - the cavity, it will flow around the ball and into lumen 18 of the catheter tube for eventual passage into the patient. Fluid flow motion in addition to the movability of the ball allows the fluid medicament to flow around the ball and into the lumen of the tube. When the - injection is complete, needle 32 is withdrawn and the diaphragm once again self seals, closing the hub and preventing any backflow of blood or fluids out of the catheter. It can be seen that not only is periodic delivery of medicament provided in this invention, but damage to the preferably plastic catheter tube is also eliminated by keeping the point of the hypodermic needle away from the plastic tube.
It is to be appreciated that other blocking devices may be incorporated in the cavity of the hub to serve the same purpose as the ball. For example, one alternate 3Q embodiment is illustrated in Figures 5 and 6. Instead of a ball, the blocking means in cavity 2Qa is a disc-like insert 35 with a hole 36 therethrough offset from the center of the insert.
Insert 35 is preferahly movahle within cavity 20a, but may be fixed to th~ inside surface of hub 19a in order -` 11;~1682 to be stationary, if desired. During fabrication of the catheter assembly, needle 28a pierces diaphragm 22a and is then carefully inserted through hole 36 in insert 35, whereupon the needle then is slidably positioned in lumen 18a. It is seen that the offset hole in the insert causes a slight bending of the needle when originally inserted into the lumen. This bend is not a problem, and serves to indicate the difficulty to be ; encountered upon subsequent re-insertion of the needle.
Diaphragm 22a is then sealed to hub l9a. Insert 35 performs its function substantially as described in the above embodiment; once the introducer needle has been withdrawn, especially when insert 35 is movable in the cavity, re-introduction of any needle into the cavity would encounter the insert which blocks entrance to the lumen. The chances of blindly locating hole 36 in the insert are very small due to the offset nature of the hole. Accordingly, the medicament needle is effectively prevented from entering the lumen of the catheter tube.
There are some instances when the catheter assembly is used without an introducer needle which is to be with-drawn after venipuncture. In that case, an elongate hollow needle having a pointed distal end replaces the catheter tube as described hereinbefore. The hub is directly connected to the hollow needle, with the blocking means and its various features being the same as previously described. Venipuncture is effected merely by inserting the hollow needle, generally a rigid, smooth surfaced metal, into the vein of the patient.
Thus, the present invention provides a catheter assembly for intermittent intravenous medicament delivery which advantageously protects the catheter tube from being damaged by the sharp point of the hypodermic needle which carries the medicament for the patient~
. .
CATHETER ASSEMBLY FOR INTERMITTENT INTRAVENOUS
MEDICAMENT DELIVERY
. BACXGROUND OF THE INVENTION
The present invention relates to an intravenous catheter assembly, and more particularly, concerns a catheter assembly which is especially useful in situations where medicament is to be delivered in intermittent periods 5 to a patient.
For patients who require periodic intermittent medication by intravenous delivery it is desirable to ; make one venipuncture, insert an intravenous catheter and leave it in position for periodic use. This procedure, - 10 of course, eliminates repetitive piercing of the patient's veins each time he is to receive medication. A catheter ~t of this type whose purpose is to remain in the patient for a prolonged time period generally has to satisfy two : requirements: it must prevent blood and/or body fluids ';n' 15 from escaping out of the catheter both when being used and during the time period when the catheter is not in use;
and it must also have some provision so that the medicament can be deposited through the catheter and into the patient.
' Various reseal plugs are used in intravenous catheter s, 20 devices, and are well known for the purpose of preventing the escape of fluids from the catheter ln addition to allowing penetration by a needle for delivery of the ~' medicament of the patient. Some typical devices which ; include this reseal plug or a similar variant are described - 25 in U.S. Pat. Nos. 3,585,996; 3,313,299, and 3,097,646.
., ' ~, ~, , ,' :
A catheter with a reseal plug generally has the plug, such as a thin rubber diaphragm, covering the open end of the catheter hub. This type of diaphragm is self sealing so that each time the needle makes a puncture 5 through the diaphragm and then is withdrawn after deliver-ing the medication to the patient, the diaphragm seals again to prevent escape of blood or other fluids from the catheter. E30wever advantageous this type of device with reseal plug may be, some problems still arise.
In particular, many catheters which are expected to remain in the patient after initial insertion for periodic use are constructed wïth plastic catheter tubing. An introducer needle, inside the plastic catheter tube, is used to make the venipuncture, and 15 then the needle is withdrawn leaving the catheter tube in the vein of the patient. The plastic tubing, being generally flexible, minimizes trauma to the patient and does not include the very sharp points and edges such as a metal catheter tubing might have, thereby reducing the 20 risk of damage if the patient should move or roll over the catheter. In this type of catheter with plastic catheter tubing, a problem arises when medication is injected into the hub of the catheter~ The attendant or clinician pierces the reseal plug at the hub of the 25 catheter generally with a sharp pointed metal needle at the end of a syringe. If the needle penetrates too far into the catheter its sharp point may, and often times , does, puncture the wall of the plastic catheter tube.
This, of course, may not only damage the catheter tube ~l30 but may also leave a hole in the tube so that some of the medication may not be delivered to the patient.
Accordingly, while it is still desirable to permit the hypodermic needle to penetrate into the hub of the catheter for delivery of the medication, a means of 35 preventing inadvertent puncture of the catheter tube :"
:
i8Z
wall is also being sought. It is to this end and the solution of the problem of puncturing the catheter tube wall that the present invention is directed.
SUM2~IARY OF THE INVENTION
An intravenous catheter assembly comprises a 5 catheter with an elongate hollow tube and a hub connected to the tube. The hub has an interior cavity communica-ting with the lumen of the tube. A needle is slidably positioned in the lumen so that its point protrudes slightly beyond the distal end of the catheter tube, 10 the other end of the needle extending through the hub and being in sealing contact therewith so that the hub is effectively closed. Means in the cavity is adapted to block the entrance of the lumen after the needle is withdrawn from the catheter tube to prevent ready re-15 insertion of an instrument into the lumen, but is adapted to allow flow of fluids into the lumen. The hub includes means for access to the cavity whereby fluids may be ~, deposited into the cavity for delivery to the patient ; after the needle has been withdrawn from the catheter tube.
In a preferred embodiment of the present invention, the catheter tube is made of a flexible, plastic material and the blocking means is a ball having a diameter greater ' than the diameter of the lumen but smaller than the ; cross-sectional dimension of the cavity. These dimensional 25 relationships provide clearance for the needle upon ; original insertion into the catheter tube but prevent ready re-insertion of the needle into the catheter tube after it has been withdrawn. The ball is movable in the cavity ; so that fluids injected into the cavity will be permitted 30 to enter into the lumen for delivery to a patient. In this embodiment, the means for access to the cavity is a pierceable, self-sealing diaphragm placed over an open end of the hub. Upon original insertic~, the needle pierces the diaphragm; upon withdrawal of the needle, the ., diaphragrn is adapted to sealingly close to prevent escape of fluids from the hub.
In accordance with the principles of the present invention, a significant advantage lies in the blockage of the lumen of the catheter tube to prevent re-insertion of the needle or any like instrument into the catheter tube after the needle has been withdrawn. By preventing the needle from being re-inserted into the lumen of the catheter tube, any damage which could be caused by the ' 10 sharp point of the needle is avoided, in addition to any loss of fluid medicament should the catheter tube be ruptured ~y the sharp point of the needle. Further advantages are offered by the present invention as will ~- become more clear when reading the detailed description hereof.
~'~ BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a perspective view illustrating the preferred intravenous catheter assembly of the present - invention;
` Fig. 2 is a cross-sectional view taken along line , 20 2-2 of Fig. l;
Fig. 3 is a partial cross-sectional view illustrat-ing the interior of the catheter hu~ after the introducer needle has been withdrawn;
Fig. 4 is a partial cross-sectional view illustrat-ing the interior of the catheter hub when a needle from a syringe enters the cavity to deliver medicament;
Fig. 5 is a partial cross-sectional view illustrat-ing an alternate blocking means located inside the catheter hub; and Fig. 6 is an elevational view illustrating the blocking device of Fig. 5 ' . ' .
~ 168Z
DETAILED DES`CRIPTION
While this invention is satisfied by embodiments of many different forms there is shown in the drawings and will herein be described in detail a preferred ` embodiment of the invention, with the understanding : 5 that the present disclosure is to be considered as exem-plary of the principles of the inventian and is not intended to limit the invention to the embodiment illustrat-ing. The scope of the invention will be pointed out in the appended claims.
Adverting to the drawings, particularly Figs. 1 and ~ 2, there is illustrated an intravenous catheter assembly ,~ 10 particularly useful for periodic or intermittent intravenous medicament delivery~ Catheter assembly la is comprised of two general components, namely a catheter lS 12 and an introducer needle 14. Catheter 12 i5 constructed of an elongate hollow tube 15, preferably slender and smooth surfaced to provide minimal drag and discomfort upon insertion in the patient. Furthermore, to eliminate ; trauma to the patient and unnecessary rigidity, catheter 20 tube 15 is preferably made of a flexible, plastic material.
The distal end 16 of the catheter tube tapers inwardly in order to facilitate venipuncture and subsequent insertion '~ into the patient's vein. The hollow inside portion of the catheter tube forms a lumen 18 through which medicaments 25 pass on the way to the patient.
At or near the proximal end of catheter tube 15 hub 19 is connected. This hub is preferably a female Luer connection which is well known and commonly used as a catheter hub. The hub is formed so that its 30 interior is a cavity 20, and this cavity communicates with lumen 18 in a catheter tube. In most instances, cavity 2a has a much larger cross-sectional dimension than the diameter of lumen 18, in order for the cavity to be able to receive the medicament for eventual delivery to the il.'~:l6~Z
patient. In hub 19 being described, the end 21 opposite the connection to the catheter tube is an open end, and is covered by a pierceable, self-sealing diaphragm 22.
This diaphragm is preferably made of rubber or the like 5 material which will allow a sharp pointed instrument to pierce the material, but which serves to seal itself after the instrument is withdrawn so that no fluids may escape particularly through the hole or slit made by the piercing instrument. It is noted in Figure 2, that 10 diaphragm 22 includes two annular rims 24 and 25; these rims snugly fit around the wall of hub 19 and may be secured thèreto by various means such as adhesives,heat sealing and the like, if desired.
Located inside cavity 20 is a ball 26. Ball 26 is 15 free to move around inside the cavity inasmuch as it has a diameter smaller than the cross-sectional dimension - of the cavity. On the other hand, ball 26 has a diameter greater than the diameter of lumen 18. In this regard, the ball cannot enter lumen 18 of the catheter tube, but 20 is confined within the cavity 2Q inasmuch as diaphragm 22 serves to effectively enclose the cavity with the ball therein.
Introducer needle 14, the other general component of the present intravenous catheter assembly, includes 25 a long slender needle 28 the distal end 29 of which is pointed. Needle 28 may or may not be hollow depending upon choice of the fabricator. The opposite end of introducer needle 14 has a knob 30 which facilitates gripping by the operator in order to be able to manipulate 30 the needle.
Referring particularly to Fig. 2, catheter assembly 10 is illustrated in the relative positions of introducer needle 14 and catheter 12 upon being originally fabricat~d.
It can be seen that needle 28 is slidably positioned in 35 lumen 18 of the catheter tube, and that the distal - ' '`' , 168.'Z
7 .
pointed end 29 of the needle protrudes slightly beyond .: distal end 16 of th.e catheter tube. This., of course, ` facilitates venipuncture inasmuch as the point of the :l needle is the leading element in this.procedure. In 5 order to become positioned in lumen 18, the point of . the needle has had to pierce diaphragm 22. It should be pointed out that when needle point 29 pierces diaphragm 22 it is not attached to hub 19 nor is ball 26 in cavity 20. After the needle has pierced the diaphragm and is 10 inserted into lumen 18, ball 26 is positioned in the ~ cavity, and then the diaphragm is sealed to the hub.
; As seen in the drawings, the proximal end of the needle . extends beyond the open end of the tube, so that the knob can be easily grasped. In this completed package, ball 15 26 usually presses against the slender needle and may ~i even tend to slightly bend the needle barrel; this presents . no permanent distortion inasmuch.as the bend is slight and the needle is generally somewhat resilient. The catheter assembly, in the configuration illustrated in . 20 Figure 2, is used to effect venipuncture. so that catheter . tube 15 may be properly positioned in the vein of the patient. Once in proper position, introducer needle 14 is gripped by its knob 30 and slowly ~ithdrawn from the catheter while leaving catheter tube 15 in the patient.
25 Figure 3 of the drawings illustrates especially the interior of the catheter hub after intorducer needle 14 has been withdrawn.
It can be seen that, once the needle is completely removed from the catheter, th.e slit formed by the piercing 30 needle closes due to the self-sealing characteristics of ~ the diaphragm. Thi.s seal is important to prevent blood from flowing through.catheter tube lS and out of hub 19.
Thus, the catheter may now remain in the patient and be used for periodic delivery of medicament.. It is noted 35 when viewing Fig. 3, that ball 26 remains freely movable in cavity 20.
; .
"
11'~1682 -When it is time to use the catheter for delivering medicament to the patient, the operator merely pierces diaphragm 22 with the needle 32 of an appropriate syringe 34 or like device carrying the fluid medicament. This procedure is illustrated in Fig. 4. Once needle 32 passes through the diaphragm into the cavity, it encounters ball 26. The ball effectively blocks ready entrance by the hypodermic needle into lumen 18 of the catheter tube.
Thus, the point of needle 32 will penetrate no further ; 10 than cavity 20; moreover, this blockage can be felt by the operator to provide a clear indication that the needle is in the proper position for depositing the medicament~
~ Once the fluid medicament flows out of needle 32 when in - the cavity, it will flow around the ball and into lumen 18 of the catheter tube for eventual passage into the patient. Fluid flow motion in addition to the movability of the ball allows the fluid medicament to flow around the ball and into the lumen of the tube. When the - injection is complete, needle 32 is withdrawn and the diaphragm once again self seals, closing the hub and preventing any backflow of blood or fluids out of the catheter. It can be seen that not only is periodic delivery of medicament provided in this invention, but damage to the preferably plastic catheter tube is also eliminated by keeping the point of the hypodermic needle away from the plastic tube.
It is to be appreciated that other blocking devices may be incorporated in the cavity of the hub to serve the same purpose as the ball. For example, one alternate 3Q embodiment is illustrated in Figures 5 and 6. Instead of a ball, the blocking means in cavity 2Qa is a disc-like insert 35 with a hole 36 therethrough offset from the center of the insert.
Insert 35 is preferahly movahle within cavity 20a, but may be fixed to th~ inside surface of hub 19a in order -` 11;~1682 to be stationary, if desired. During fabrication of the catheter assembly, needle 28a pierces diaphragm 22a and is then carefully inserted through hole 36 in insert 35, whereupon the needle then is slidably positioned in lumen 18a. It is seen that the offset hole in the insert causes a slight bending of the needle when originally inserted into the lumen. This bend is not a problem, and serves to indicate the difficulty to be ; encountered upon subsequent re-insertion of the needle.
Diaphragm 22a is then sealed to hub l9a. Insert 35 performs its function substantially as described in the above embodiment; once the introducer needle has been withdrawn, especially when insert 35 is movable in the cavity, re-introduction of any needle into the cavity would encounter the insert which blocks entrance to the lumen. The chances of blindly locating hole 36 in the insert are very small due to the offset nature of the hole. Accordingly, the medicament needle is effectively prevented from entering the lumen of the catheter tube.
There are some instances when the catheter assembly is used without an introducer needle which is to be with-drawn after venipuncture. In that case, an elongate hollow needle having a pointed distal end replaces the catheter tube as described hereinbefore. The hub is directly connected to the hollow needle, with the blocking means and its various features being the same as previously described. Venipuncture is effected merely by inserting the hollow needle, generally a rigid, smooth surfaced metal, into the vein of the patient.
Thus, the present invention provides a catheter assembly for intermittent intravenous medicament delivery which advantageously protects the catheter tube from being damaged by the sharp point of the hypodermic needle which carries the medicament for the patient~
. .
Claims (8)
1. An intravenous catheter assembly comprising: a catheter comprised of an elongate hollow tube and a hub connected at one end of said tube, the other end of said hub being an open end, said hub having an interior cavity communicating with the lumen of said tube; a needle slidably positioned in the lumen of the tube, the distal, pointed end of the needle adapted to protrude slightly beyond the distal end of said catheter tube, the proximal end of said needle extending beyond said open end of said hub; blocking means in said cavity adapted to block the entrance of said lumen after said needle is withdrawn from the catheter tube to prevent ready re-insertion of an instrument into said lumen but adapted to allow flow of fluids into said lumen; and means covering said open end of the hub to prevent fluid from flowing out of the hub after said needle has been withdrawn, said covering means adapted to provide access to said cavity whereby fluids may be deposited into said cavity for delivery to a patient after said needle has been withdrawn from the catheter tube.
2. An introducer catheter assembly as defined in Claim 1 wherein said blocking means is a ball having a diameter greater than the diameter of said lumen but smaller than the cross-sectional dimension of said cavity so that the ball may provide clearance for the needle upon original insertion but prevent ready re-insertion of an instrument into the catheter tube after the needle has been withdrawn, said ball being movable in said cavity so that fluid injected into said cavity will be permitted to enter said lumen for delivery to a patient.
3. An intravenous catheter assembly as defined in Claim 1 wherein said blocking means is a disc-like insert with a hole therethrough offset from its center, said needle being inserted through said hole upon its original insertion into the catheter, said offset hole serving to prevent ready re-insertion of an instrument into the catheter tube after the needle has been withdrawn, but permitting fluids injected into said cavity to enter said lumen for delivery to a patient.
4. An intravenous catheter assembly as defined in Claim 1 wherein said covering means is a pierceable self-sealing diaphragm over the open end of said hub, said diaphragm being pierced by said needle upon original insertion of the needle into the catheter, and adapted to sealingly close after the needle has been withdrawn.
5. An introducer catheter assembly as defined in Claim 1 wherein said catheter tube is made of flexible, plastic material.
6. An intravenous catheter assembly comprising: a catheter comprised of an elongate hollow tube and a hub connected to said tube having an interior cavity communication with the lumen of the tube; a needle slidably positioned in said lumen so that its point protrudes slight-ly beyond the distal end of the catheter tube, the other end of said needle extending through said hub and being in sealing contact therewith so that said hub is effectively closed; means in said cavity adapted to block the entrance of said lumen after said needle is withdrawn from the catheter tube to prevent ready re-insertion of an instrument into the lumen but adapted to allow flow of fluids into the lumen; said hub having means for access to said cavity whereby fluids may be deposited into said cavity for delivery to a patient after said needle has been withdrawn from the catheter tube.
7. An intravenous catheter comprising: an elongate hollow needle having a pointed distal end, and a hub connected to said needle and having an interior cavity communicating with the lumen of said needle, said hub forming an enclosure around said cavity to prevent flow of fluids out of said cavity; means for access through said hub into said cavity whereby fluids may be deposited into said cavity for delivery to a patient through the lumen of said needle; and means inside said cavity adapted to block the entrance of the lumen of said needle to prevent ready insertion of an instrument into said lumen, but adapted to allow flow of fluids into said lumen.
8. An intravenous catheter as defined in Claim 7 wherein said needle is substantially rigid and is made of metal.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7,137 | 1979-01-29 | ||
| US06/007,137 US4261357A (en) | 1979-01-29 | 1979-01-29 | Catheter assembly for intermittent intravenous medicament delivery |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1121682A true CA1121682A (en) | 1982-04-13 |
Family
ID=21724436
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000344471A Expired CA1121682A (en) | 1979-01-29 | 1980-01-28 | Catheter assembly for intermittent intravenous medicament delivery |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4261357A (en) |
| AU (1) | AU530522B2 (en) |
| CA (1) | CA1121682A (en) |
| DE (1) | DE3002915A1 (en) |
| DK (1) | DK35680A (en) |
| FI (1) | FI800239A (en) |
| FR (1) | FR2447201A1 (en) |
| GB (1) | GB2044106B (en) |
| IE (1) | IE49068B1 (en) |
| IT (1) | IT1128094B (en) |
| NZ (1) | NZ192581A (en) |
| SE (1) | SE8000638L (en) |
| ZA (1) | ZA80479B (en) |
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| US3853127A (en) * | 1973-04-03 | 1974-12-10 | R Spademan | Elastic sealing member |
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| US4126133A (en) * | 1977-07-13 | 1978-11-21 | Boris Schwartz | Intracorporeal catheter improvement |
-
1979
- 1979-01-29 US US06/007,137 patent/US4261357A/en not_active Expired - Lifetime
-
1980
- 1980-01-10 NZ NZ192581A patent/NZ192581A/en unknown
- 1980-01-25 FR FR8001613A patent/FR2447201A1/en active Pending
- 1980-01-28 IE IE153/80A patent/IE49068B1/en unknown
- 1980-01-28 CA CA000344471A patent/CA1121682A/en not_active Expired
- 1980-01-28 ZA ZA00800479A patent/ZA80479B/en unknown
- 1980-01-28 DE DE19803002915 patent/DE3002915A1/en not_active Withdrawn
- 1980-01-28 DK DK35680A patent/DK35680A/en not_active Application Discontinuation
- 1980-01-28 IT IT47726/80A patent/IT1128094B/en active
- 1980-01-28 FI FI800239A patent/FI800239A/en not_active Application Discontinuation
- 1980-01-28 SE SE8000638A patent/SE8000638L/en not_active Application Discontinuation
- 1980-01-28 GB GB8002777A patent/GB2044106B/en not_active Expired
- 1980-01-29 AU AU54995/80A patent/AU530522B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AU5499580A (en) | 1980-08-07 |
| IE800153L (en) | 1980-07-29 |
| FI800239A (en) | 1980-07-30 |
| IT1128094B (en) | 1986-05-28 |
| NZ192581A (en) | 1981-11-19 |
| ZA80479B (en) | 1981-09-30 |
| IT8047726A0 (en) | 1980-01-28 |
| SE8000638L (en) | 1980-07-30 |
| AU530522B2 (en) | 1983-07-21 |
| DK35680A (en) | 1980-07-30 |
| GB2044106B (en) | 1983-03-23 |
| FR2447201A1 (en) | 1980-08-22 |
| GB2044106A (en) | 1980-10-15 |
| DE3002915A1 (en) | 1980-07-31 |
| US4261357A (en) | 1981-04-14 |
| IE49068B1 (en) | 1985-07-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |