1. Field of the Invention
This invention relates to an intravenous catheter introducing device, more particularly to an intravenous catheter introducing device with a tubular plunger which is operable to draw blood for facilitating a catheter introducing operation, and a needle cannula which is retractable into the tubular plunger for safe disposal.
2. Description of the Related Art
Intravenous catheter introducing devices are generally used to administer a medication fluid into or to draw blood from a patient's vein. Referring to
Moreover, the conventional intravenous catheter introducing device 9 is specifically not suitable for patients whose blood pressure is not sufficient to permit flow of blood therethrough, such as an emergency case, aged people, and pediatrics patients, and for patients whose target vein is barely visible due to abundant adipose tissue, such as women and obese patients, since the health care worker will have difficulty determining whether the catheter 93 has been successfully introduced into the target vein, and may need to locate the vein by moving the needle cannula 94 in the skin of the patient, thereby complicating and prolonging the cannulation procedure and causing great discomfort to the patient.
Furthermore, although conventional self-retracting IV catheter introducers permit self-retraction of the used needle cannula into the syringe barrel after introduction of the catheter is completed, the blood in the barrel may be forced out of the barrel during the retraction of the used needle cannula, so that blood contamination may occur.
Therefore, in U.S. patent application Ser. No. 11/652,281, the applicants disclosed an intravenous catheter introducing device which includes a tubular plunger with outlets to communicate an accommodation compartment in the plunger with the ambient air so as to prevent blood from being forced out of the device during a needle retraction operation.
It is desirable to improve the aforesaid intravenous catheter introducing device to rapidly indicate whether a needle cannula has been inserted precisely into the vein of a patient for introduction of a tubular catheter.
One object of the present invention is to provide an intravenous catheter introducing device which can rapidly indicate whether a needle cannula has been inserted precisely into the vein of a patient to introduce a tubular catheter, which can be operated easily and safely to retract the used needle cannula with one hand, and which can prevent the flashback blood from being forced out thereof.
According to this invention, the intravenous catheter introducing device includes:
a barrel having a surrounding barrel wall which surrounds an axis, and which defines a passage with rearward and forward openings, the surrounding barrel wall including a smaller-diameter portion which has an inner abutment surface facing rearwards, and a larger-diameter portion which has a retaining area that is spaced apart from the smaller-diameter portion;
a needle cannula having a tip end and a rear connecting end;
a tubular needle seat including a front hub portion which confronts the inner abutment surface so as to be engageable therewith, and a rear fitting portion which is configured to fix the rear connecting end;
a hollow tubular member which includes a front open end formed with the rear fitting portion to be in fluid communication with the rear connecting end, and tubular monitoring and gripped segments, the tubular monitoring segment defining a pre-chamber for flashback blood, the tubular member further including a rear plug portion which has an internal duct extending therethrough to be communicated with the pre-chamber;
a tubular grip member which, in a position of use, is disposed to hold, with a holding force, the gripped segment in a position of immovability along the axis relative to the retaining area;
a tubular plunger which is movable in the passage along the larger-diameter portion, the plunger having a front end wall which is movable to abut against the grip member, a rear end wall which extends outwardly of the rearward opening so as to be manually operable, and an intermediate surrounding wall which defines an accommodation compartment; and
a tubular receptacle which has a socket end, an air-permeable end, and a tubular wall segment confining a flashback chamber, the tubular receptacle being disposed to be retained in the accommodation compartment by a friction force, with the socket end and the air-permeable end respectively confronting the rear plug portion and the rear end wall, thereby establishing air communication between the internal duct and the flashback chamber,
such that, when the front end wall is brought to abut against the grip member, the socket end is engaged with the rear plug portion to thereby permit the front hub portion to be placed in a pre-disposal position,
such that, when the grip member is pushed forward by virtue of a forward movement of the front end wall against the holding force, the pre-disposal position facilitates release of the gripped segment from the grip member, thereby permitting an axial and rearward movement of the gripped segment relative to the retaining area, and
such that continued forward movement of the front end wall against the friction force results in movement of the needle seat, and movement of the tubular receptacle together therewith through the engagement of the rear plug portion with the socket end, towards the rear end wall by virtue of a prodding force so as to place the needle seat and the needle cannula in a disposal position, where the tip end of the needle cannula is retracted into the passage, and where the socket end is closer to the rear end wall than in the position of use.
Other features and advantages of the present invention will become apparent in the following detailed description of the preferred embodiments of the invention, with reference to the accompanying drawings, in which:
Before the present invention is described in greater detail, it should be noted that same reference numerals have been used to denote like elements throughout the specification.
Referring to
The barrel 1 has a surrounding barrel wall 12 which surrounds an axis, and which defines a passage 11 therein. The passage 11 has rearward and forward openings 121, 122 which are opposite to each other in a longitudinal direction. The surrounding barrel wall 12 includes a larger-diameter portion 123 and a smaller-diameter portion 124 which are disposed proximate to the rearward and forward openings 121, 122, respectively, and a shoulder 125 interposed therebetween. The smaller-diameter portion 124 has an inner abutment surface 127 which faces rearwards. The larger-diameter portion 123 has a retaining area 120 which is spaced apart from the smaller-diameter portion 124 in the longitudinal direction. The smaller-diameter portion 124 has first and second step segments 128, 129 proximate to the forward opening 122 and the shoulder 125, respectively.
In addition, the barrel 1 has a surrounding segment 13 which extends forwardly from the rearward opening 121 to terminate at a finger flange 132, and which surrounds the larger-diameter portion 123. The surrounding segment 13 has a narrow sleeved portion 131.
The needle cannula 23 has a tip end 232 and a rear connecting end 231 opposite to each other along the axis in the longitudinal direction.
The tubular needle seat 29 includes a front hub portion 291 which confronts the inner abutment surface 127 so as to be engageable therewith, and a rear fitting portion 292 which is opposite to the front hub portion 291 in the longitudinal direction, and which is configured to fix the rear connecting end 231 of the needle cannula 23. Preferably, with reference to
The tubular member 22 is integrally formed with the tubular needle seat 29, and is made from a light transmissible material. The tubular member 22 includes a front open end 221 formed with the rear fitting portion 292 and in fluid communication with the rear connecting end 231, and tubular monitoring and gripped segments 224, 227 that are proximate to and distal from the front open end 221, respectively. The tubular monitoring segment 224 defines a pre-chamber 223 for flashback blood. The tubular member 22 further includes a rear plug portion 222 which extends from the gripped segment 227, which is distal from the front open end 221, and which has an internal duct 225 extending therethrough to be communicated with the pre-chamber 223.
The tubular grip member 21 is retained at the retaining area 120 in a position of use so as to hold the gripped segment 227 of the tubular member 22 in a position of immovability along the axis relative to the retaining area 120 by virtue of a holding force. Moreover, the rear plug portion 222 of the tubular member 22 is disposed rearwardly and outwardly of the grip member 21, and has a radial inlet 226 which extends radially to communicate the passage 11 with the pre-chamber 223.
The tubular plunger 3 is disposed to be movable in the passage 11 along the larger-diameter portion 123. The plunger 3 has an opened front end wall 321 which is movable to abut against the grip member 21, an opened rear end wall 322 which is disposed opposite to the front end wall 321, and which extends outwardly of the rearward opening 121 so as to be manually operable, and an intermediate surrounding wall 32 which is interposed between the front and rear end walls 321, 322, and which defines an accommodation compartment 31. The intermediate surrounding wall 32 has a plurality of ribs 324 which are formed on an outer surface thereof and adjacent to the rear end wall 322. The rear end wall 322 defines an access opening for insertion of the tubular receptacle 34 into the accommodation compartment 31. An end cap 37 is detachably mounted to the rear end wall 322 to close the access opening.
The plunger 3 further has a deformable annular sealing member 36 which is configured to surround the front end wall 321, and which is in air-tight sliding engagement with the larger-diameter portion 123 of the barrel 1.
The tubular receptacle 34 has a socket end 343 and an air-permeable end 344 opposite to each other in the longitudinal direction, and a tubular wall segment 341 interposed therebetween to confine a flashback chamber 342. The tubular receptacle 34 is retained in the accommodation compartment 31 by a friction force that is generated between protrusion and recess portions 3411, 323, with the socket end 343 and the air-permeable end 344 respectively confronting the rear plug portion 222 and the rear end wall 322, thereby establishing air communication between the internal duct 225 and the flashback chamber 342. The protrusion portion 3411 abuts against a shoulder 326 formed adjacent to the front end wall 321. An air-permeable member 35 is made from a porous material, and is integrally formed with the air-permeable end 344 so as to prevent flashback blood from trickling out of the flashback chamber 342.
The plunger 3 has two outlets 33 which communicate the accommodation compartment 31 with the ambient air, and which are disposed downstream of the air permeable end 344. In this embodiment, the outlets 33 are formed in the intermediate surrounding wall 32 adjacent to the rear end wall 322 to facilitate closing by an operator's fingers when the operator grips and moves the tubular plunger 3.
The coil spring 26 is disposed within the smaller-diameter portion 124 to surround the needle cannula 23, and is compressed between the forward opening 122 and the front hub portion 291 of the needle seat 29 so as to provide a prodding force for moving the needle seat 29 rearwardly.
The catheter hub 24 defines therein a duct that permits extension of the needle cannula 23 therethrough.
The tubular catheter 25 has a proximate segment which is inserted into the duct, and a distal segment which extends from the proximate segment and which surrounds and sheathes the needle cannula 23 while permitting the tip end 232 of the needle cannula 23 to project forwardly of the distal segment for piercing a patient's skin.
The front protector 14 is sleeved on the second step segment 129 to surround the smaller-diameter portion 124 for shielding the needle cannula 23. The rear protector 15 is sleeved on the sleeved portion 131 to surround the larger-diameter portion 123 for shielding the plunger 3.
A front sealing strip 16 is disposed to peelably adhere the front protector 14 to the larger-diameter portion 123 adjacent to the smaller-diameter portion 124. Specifically, the front sealing strip 16 includes small front and rear adhesive layers 162 which are adhered to the front protector 14 and the larger-diameter portion 123, respectively, and a film layer 161 which is peelably attached to the front and rear adhesive layers 162 and which is formed with a weakened line 163 such that, when the front protector 14 is turned to break the film layer 161 along the weakened line 163, only the rear adhesive layer 162 and a portion of the film layer 161 will remain on the larger-diameter portion 123, thereby permitting viewing inside of the larger-diameter portion 123.
The rear protector 15 is detachably sleeved on the surrounding segment 13. A rear sealing strip 17 is disposed to peelably adhere the rear protector 15 to the surrounding segment 13.
Referring to
Referring to
When the grip member 21 is pushed forward by virtue of forward movement of the front end wall 321 against the holding force, the grip member 21 is moved to disengage from the retaining area 120, and the front hub portion 291 is moved past the friction diminishing area 1241 to abut against the inner abutment surface 127, thereby shifting static frictions between the needle seat 29 and the smaller-diameter portion 124 and between the grip member 21 and the retaining area 120 to kinetic frictions. This facilitates a triggering action for retraction of the needle cannula 24 (to be described in detail hereinafter). Specifically, a material-sticking action and the engagement between the grip member 21 and the retaining area 120 can be minimized at this stage, so that the operator can push the plunger 3 effortlessly.
The needle seat 29, the tubular member 22 and the tubular receptacle 34 remain unmoved due to the abutment of the front hub portion 291 against the inner abutment surface 127 such that, once the plunger 3 is pressed further forward to cause movement of the plunger 3 relative to the tubular receptacle 34 against the friction force, the protrusion portion 3411 of the receptacle 34 is disengaged from the recess portion 323 in the plunger 3 so as to permit releasing of the coil spring 26. Also, the air in the barrel 1 can be released through the accommodation compartment 31 and be discharged from the outlets 33.
Therefore, as shown in
Referring to
It is noted that, with the provision of the radial inlet 226, the blood flowing into the passage 11 between the front end wall 321 and the grip member 21 can be guided into the internal duct 225 and the flashback chamber 342.
Referring to
In an IV catheter introducing stroke, the front and rear protectors 14, 15 and the spacer 18 are removed, and the plunger 3 is subsequently pressed forward to bring the receptacle 34 into engagement with the tubular member 22. Thus, the operator can hold the surrounding barrel wall 12 of the barrel 1 and pierce the patient's vein with one hand.
Subsequently, referring to
As shown in
Referring to
Referring to
Referring to
Referring to
Referring to
As illustrated, according to the intravenous catheter introducing device of this invention, the used needle cannula 23 can be retracted into the plunger 3 to thereby avoid occurrence of an accidental needle stick. Further, during the forward pressing of the plunger 3 to retract the needle cannula 23, since the pre-chamber 223 is air communicated with the ambient air, the flashback blood may flow into the pre-chamber 223 and the flashback chamber 342, and the air-permeable member 35 can prevent the flashback blood from trickling out. Thus, blood will not be forced out of the barrel 1.
Moreover, during the IV catheter introducing operation, once flashback blood is not observed in the pre-chamber 223, the operator can close the outlet(s) 33 and pull the plunger 3 rearwardly to generate a reduced pressure in the passage 11 to thereby facilitate flow of indicator blood into the passage 11. Thus, the operator can easily check whether the tubular catheter 25 has been successfully introduced into a target vein of the patient. Furthermore, the indicator blood flow is visible immediately through the pre-chamber 223 so as to shorten the time needed for the IV catheter introducing operation. By providing the front and rear protectors 14, 15 and the front and rear sealing strips 16, the air and water tightness of the device of the present invention can be maintained, and packing cost can be reduced.
While the present invention has been described in connection with what are considered the most practical and preferred embodiments, it is understood that this invention is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretations and equivalent arrangements.
Number | Date | Country | Kind |
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095121678 | Jun 2006 | TW | national |
097101762 | Jan 2008 | TW | national |
This application claims priority of Taiwanese Application No. 097101762, filed on Jan. 17, 2008. This application is a continuation-in-part of U.S. patent application Ser. No. 11/652,281, which was filed on Jan. 10, 2007, and which claims priority of Taiwanese Application No. 095121678, filed on Jun. 16, 2006. The contents of the above referenced applications are herein incorporated by reference in their entirety.
Number | Date | Country | |
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Parent | 11652281 | Jan 2007 | US |
Child | 12218887 | US |