BACKGROUND OF THE INVENTION1. Field of the Invention
This invention relates to a syringe having an inner cannula integral with the distal portion of said syringe and a piston sealably engaging said inner cannula with said piston integral with a plunger-conduit system. The inner cannula is integral with the distal portion of the syringe and positioned therein so as to allow a fluid to flow around said inner cannula and into the barrel of the syringe when said piston is advanced proximally and in so doing, this first obtained fluid is separate from a second fluid which can be obtained by inserting a vacuum glass tube into a fluid collection receptacle attached to the plunger conduit system. After a plurality of vacuum tubes are filled with the second obtained fluid, the first obtained fluid can be returned to the patient by simply advancing the piston distally.
2. Information Disclosure Statement
Since the advent of the Acquired Immune Deficiency Syndrome (AIDS), many disposable devices have been developed to prevent accidental needle sticks. However, prior art lacks simplicity and blood drawing procedures found traditionally cumbersome are now made unusually complex. Yet even further, as cost containment becomes more important, the additional blood drawing components found in prior art touted as being safe are now realized to be unusually complex, not universally applicable, and consequently not cost worthy.
Often, severely ill patients in the hospital will require central venous catheterization for administration of various medicinal preparations and arterial catheterization for monitoring of blood pressure.
Regarding central venous catheterization, often a triple lumen catheter will be placed in the patient's subclavian vein and at least one lumen of the catheter is used for the administration of fluid; the two remaining unused lumens may be used to draw blood for laboratory testing or alternately the administration of a variety of other medicinal preparations. If a given lumen of the central venous catheter is used to obtain a blood sample for laboratory testing, a syringe is attached to the unused lumen and this first obtained venous blood considered too dilute for laboratory testing is drawn into the barrel of the syringe, the syringe is then detached and discarded. A second syringe is then attached to this lumen and a second obtained volume of venous blood is drawn into the barrel of the syringe. The volume of venous blood obtained is limited by the volume of the syringe. This second obtained venous blood is then transferred to vacuum glass tubes by cumbersome traditional methods.
Regarding arterial catheterization, an arterial catheter is inserted into the patient's radial artery. The now inserted arterial catheter can then be attached to a blood pressure monitor. The connection to the blood pressure monitor is established with pressure tubing having at least one three-way valve proximal to the catheter insertion site. When monitoring blood pressure, heparinized solution fills the pressure tubing to the level of the catheter insertion site distally and a pressure transducer proximally. In the monitoring mode, the three-way valve is patent with the distal catheter and the proximal pressure transducer. Simultaneously, the three-way valve is closed to a blood sampling side port used to obtain blood samples for laboratory testing. To obtain blood for laboratory testing, the three-way valve is closed toward the proximal pressure transducer and patent toward the distal catheter and the blood sampling side port. Thereafter, a syringe is attached to the blood sampling side port and a first obtained volume of arterial blood considered too dilute for laboratory testing is drawn into the barrel of the syringe and the syringe is then detached. A second syringe is then attached to the blood sampling side port and a second obtained volume of arterial blood is drawn into the barrel of the syringe. This second obtained volume of arterial blood considered appropriate for laboratory testing is transferred to vacuum glass tubes in a traditional manner found to be cumbersome and unusually complex by those familiar with prior art. The three-way valve is then positioned to make patent the arterial catheter distally and the pressure transducer proximally so that the patient's blood pressure can be continuously monitored.
In view of the aforementioned cumbersome manipulations and unusually complex devices used to obtain a single sample of venous or arterial blood from an indwelling catheter, the objectives of the present invention are set forth and described herein.
In preparation for this application, a search was completed in Class 604, Subclass 231 and 187, Class 128, Subclass 214.4. In contradistinction to the patent application at hand U.S. Pat. No. 4,274,408 of Nimrod teaches a displaceable feeder tube contained within a syringe barrel having a function readily distinguishable from that which follows.
SUMMARY AND OBJECTS OF THE PRESENT INVENTIONIt is an object of the present invention to provide an improved method for obtaining a plurality of blood samples for vacuum glass tubes from indwelling arterial or venous catheters from a single syringe apparatus.
It is an object of the present invention to provide means for separating a first obtained volume of blood considered too dilute for laboratory testing from a second obtained volume of blood considered appropriate for laboratory testing using a single syringe.
It is an object of the present invention to provide a single syringe apparatus that can be attached to an indwelling central venous catheter or an indwelling arterial catheter for purposes of obtaining a plurality of blood samples.
SUMMARYThe invention describes a syringe apparatus having an inner cannula positioned securely in the distal portion of said syringe apparatus so as to allow fluid to flow past the inner cannula and into the barrel of the syringe. This first obtained fluid considered too dilute for testing remains separate from a second obtained fluid which passes through the inner cannula, a plunger-conduit system and into a plurality of vacuum glass tubes inserted into a blood collection receptacle integral with the plunger-conduit system. The piston of the syringe apparatus sealably engages the inner cannula and slides lengthwise about the inner cannula when the plunger-conduit system is advanced in a proximal or distal direction. The outer-diameter of the inner cannula is smaller than the inner diameter of the plunger-conduit system and thereby facilitates telescoping of the inner cannula within the plunger-conduit system when the plunger conduit system is advanced in a proximal or distal direction while the piston of the syringe apparatus keeps separate a first obtained fluid considered too dilute for laboratory testing from a second obtained fluid considered appropriate for laboratory testing induced to pass through the inner cannula and the plunger-conduit system when a plurality of vacuum glass tubes are inserted into a blood collection receptacle integral with the plunger-conduit system.
BRIEF DESCRIPTION OF THE DRAWINGSFIG. 1 is a sectional view of the syringe of the present invention with the piston thereof positioned proximally to show the inner cannula within the syringe tip distally and the plunger-conduit system proximally;
FIG. 2 is an exploded cross section view of the distal portion of the syringe of this invention;
FIG. 3 is a sectional view of the syringe of the present invention attached to arterial pressure tubing at a side blood sampling port;
FIG. 4 is a sectional view of the syringe of the present invention with first obtained fluid within the barrel of the syringe;
FIG. 5 is a sectional view of the syringe of the present invention showing a second obtained fluid within the inner cannula, the plunger-conduit system and a vacuum glass tube;
FIG. 6 is a sectional view of the syringe of the present invention showing the first obtained fluid having been returned to the patient;
FIG. 7 is a sectional view of the syringe of the present invention showing the three-way valve positioned to allow continuous monitoring of a patient's blood pressure;
FIG. 8 is an alternate embodiment of the distal portion of the syringe of the present invention with the inner cannula having a side opening within the fluid chamber.
DESCRIPTION OF THE PREFERRED EMBODIMENTSThe apparatus of the present invention is exemplified by the embodiment of FIG. 1, which shows a syringe type device with a customarycylindrical body 10 terminating at anend wall 82 integral with adistal hub 34. Integral with thedistal hub 34 is a supportingbar 30 which partially occludes a hub opening 32. Thesupport bar 30 rigidly holds and prevents axial or lateral movement of aninner cannula 28. Theinner cannula 28 has origin at thedistal hub 34 and not beyond and extends proximally and not beyond athumb rest 80 which is integral with thecylindrical body 10. Thepiston 14 is mounted to theplunger 20 at apiston mounting face 18 with thepiston 14 having been fitted into the proximal end of thecylindrical body 10 to establish a fluid seal at the juncture thereof and theinterior wall 12 of thecylindrical body 10. Thepiston 14 has a fluid-chamber face 16 which establishes afluid chamber 36 through which theinner cannula 28 passes. The outer diameter of theinner cannula 28 is substantially larger than the inner diameter of thecentral opening 24 of thepiston 14 so as to create a slidable fluid seal at the juncture thereof and the outer diameter of theinner cannula 28. Theinner cannula 28 has a substantially narrow inner diameter defined by a smoothinner wall 78. The outer diameter of theinner cannula 28 is substantially smaller than the inner diameter of theconduit 22 so as to allow telescoping of theinner cannula 28 into theconduit 22 of theplunger 20 when the plunger is advanced in a proximal or distal direction. At the proximal end of theconduit 22 is a funnel shapedopening 26 to which a bluntblood collection needle 46 integral with ablood collection receptacle 52 is sealably mounted. Often, blunt blood collection needles of this variety have aproximal needle 48 housed within arubber sleeve 50. The cooperative functional elements define thefluid chamber 36 which is substantially separate from afluid chamber 88.
Thedistal hub 34 is further exemplified in FIG. 2 to show thesupport bars 30 in cross section partially occluding the hub opening 32. The hub opening 32 freely communicates with thefluid chamber 36 as shown in FIG. 1.
The functional and operative position of the syringe apparatus is shown in FIG. 3 wherein a bloodsampling side port 40 is mounted to thedistal hub 34. A three-way valve 42 having anoff indicator tip 44 is integral with adistal port 54 andproximal port 62. In the operative position shown thedistal port 54 and theproximal port 62 freely communicate. Integral with thedistal port 54 is atransparent pressure tube 68 which is attached to a patient'sradial artery 64 of awrist 76. Thepressure tube 68 contains a first obtainedfluid 70 which is partially mixed with a second obtainedfluid 66. Integral with theproximal port 62 is thetransparent pressure tube 68 attached to afluid reservoir 74 and apressure transducer 72 with a blood pressure reading of 120/80.
FIG. 4 shows the three-way valve 42 with theoff indicator tip 44 directed toward theproximal port 62 thereby allowing thedistal port 54 to freely communicate with the bloodsampling side port 40. Thepiston 14 has been advanced proximally for purposes of drawing the first obtainedfluid 70 considered too dilute for laboratory testing into thefluid chamber 36 as shown in FIG. 1. A substantially minimal amount of first obtainedfluid 70 is drawn into theinner cannula 28 having a substantially narrow inner diameter defined by aninner wall 78. The second obtainedfluid 66 is now at rest at thedistal hub opening 32.
FIG. 5 shows the second obtainedfluid 66 considered appropriate for laboratory testing having passed through theinner cannula 28, theconduit 22 of theplunger 20 and into avacuum glass tube 82 having arubber plug 84 when theneedle 48 is caused to penetrate therubber plug 84. The first obtainedfluid 70 remains substantially separate from the second obtainedfluid 66 when thevacuum glass tube 82 is inserted into the proximal end of theblood collection receptacle 52.
FIG. 6 shows the first obtainedfluid 70 considered too dilute for laboratory testing having been returned to the patient's radial artery.
FIG. 7 shows the three-way valve 42 with theoff indicator tip 44 directed toward the bloodsampling side port 40 so as to allow thepressure transducer 72 to record the patient's blood pressure.
FIG. 8 is an exploded view of an alternative embodiment of thedistal hub 34. Theinner cannula 28 is integral with thedistal hub 34 such that only a singledistal opening 90 allows fluid to enter thefluid chamber 36 via aside opening 92 integral with theinner wall 78 of theinner cannula 28. The distinctive operative elements require manual positioning of theplunger 20 to prevent forward displacement of thepiston 14 when thevacuum glass tube 82 is inserted into the proximal end of the blood collection receptacle.
It will be appreciated that the method and apparatus illustrated above enable the benefits of obtaining a plurality of blood samples from second obtained fluid to be enjoyed using a single syringe. The collection of blood samples from indwelling catheters is universally made safe, simple, efficient and cost effective. The syringe apparatus of this invention makes a traditionally cumbersome and time consuming procedure a welcomed necessity.