US3856009A - Catheter placement unit - Google Patents

Abstract

A catheter for the administration of fluids into the body which includes a length of precurved, flexible tubing permanently attached to a gripping member having a winglike structure projecting therefrom. A catheter assembly comprising a catheter having a precurved distal portion and a gripping member permanently attached thereto, an introducer needle disposed partially in the catheter and a sleeve slidably disposed over the catheter tubing, said sleeve being operable to prevent internal skiving of the tubing when the introducer needle is moved forwardly within the catheter tubing. A detachable, rigid grip is provided which may be used to operatively connect the introducer needle with a syringe or other pressure indicating accessory.

Description

United States Patent [191 Winnie Dec. 24, 1974 1 CATHETER PLACEMENT UNIT [75] Inventor: Alon P. Winnie, Wilmette, Ill.

[73] Assignee: Johnson & Johnson, New

Brunswick, NJ.

22 Filed: May 29,1973

21 Appl. No.: 364,798

Related U.S. Application Data [62] Division of Ser. No. 202,256, Nov. 26, 1971, Pat. No.

3,565,074 2/1971 Foti 128/2144 3,610,240 10/1971 Harautuneian 128/221 3,680,562 8/1972 Wittes et a1 128/347 Primary ExaminerRichard A. Gaudet Assistant Examiner l. C. McGowan [57] ABSTRACT A catheter for the administration of fluids into the body which includes a length of precurved, flexible tubing permanently attached to a gripping member having a winglike structure projecting therefrom.

A catheter assembly comprising a catheter having a precurved distal portion and a gripping member permanently attached thereto, an introducer needle disposed partially in the catheter and a sleeve slidably disposed over the catheter tubing, said sleeve being operable to prevent internal skiving of the tubing when the introducer needle is moved forwardly within the catheter tubing. A detachable, rigid grip is provided which maybe used to operatively connect the introducer needle with a syringe or other pressure indicating accessory.

2 Claims, 10 Drawing Figures PATENTEU [JEEZ 4 I974 SHEET 1pg 3 CATHETER PLACEMENT UNIT This is a division of application Ser. No. 202,256, filed Nov. 26, 1971, now U.S. Pat. No. 3,782,381, issued Jan. 1, 1974.

FIELD OF THE INVENTION This invention relates to surgical instruments and, in particular, to improvements in catheter placement units. The catheter of the present invention is especially suited to the continuous or intermittent administration of caudal or epidural anesthesia, although it may likewise serve to introduce various desired fluids into, for example, the lumen of a blood vessel or a body cavity such as the abdomen. The present invention provides an improved catheter which is particularly adapted to follow the general conformation of the body at the site of administration of caudal or epidural anesthesia and which is free of structural parts which would, when the device is in use, endanger the patients safety and/or interfere with his comfort.

DESCRIPTION OF THE PRIOR ART Many devices have been made to aid in the administration or withdrawal of fluids from the body.

For example, U.S. Pat. No. 2,922,420 is directed to an epidural needle device which can be inserted into the epidural space without fear of puncturing the dura. The needle terminates in a blunt point whose inner face is sloped in a particular fashion. Adjacent the blunt point, and in the wall of the shaft, there is an elipsoidal opening facing in the lateral direction. As the catheter is fed through the lumen of the needle, the sloping internal face of the blunt point directs the distal end of the catheter through the elipsoidal opening into the epidural space. Since, however, the diameter of the puncture made in the tissue (corresponding to the outside diameter of the needle) is larger than the outside diameter of the catheter inserted therein, the surgeon must stitch the tissue around the catheter to prevent leakage from the puncture site. Additionally, once the needle is removed and the catheter is in place in the epidural space, there is a marked tendency for the catheter to revert from the curved configuration temporarily imparted thereto by the slope of the internal face of the needle to the straight line configuration characterizing the catheter before it was fed through the needle. This tendency of the catheter to revert to its former configuration may cause tissue irritation and/or discomfort to the patient.

U.S. Pat. No. 3,459,188 discloses a paracentesis stylet catheter comprising a precurved catheter and an elongated piercing element (stylet). The precurved portion of the catheter is straightened when the elongated piercing element is within the catheter and snaps back to its precurved configuration after removal of the piercing element. Unfortunately, the longer the piercing element is disposed within the curved portion of the catheter, the less likely is the catheter to take on its precurved configuration after removal of the piercing element. Additionally, when the piercing element is inserted within the precuved catheter, there is a tendency of the sharp point of the piercing element to skive (that is, cut into thin layers) the inner surface of the catheter within the curved portion. Subsequently, when the catheter is in place and is being used for the introduction of fluids, small pieces of catheter material may be inadvertently introduced into the patients body. Such an occurrence is particularly dangerous to the patients welfare where caudal or epidural anesthesia is being administered.

U.S. Pat. No. 3,463,152 discloses a catheter placement unit having a catheter within a needle which is slidably disposed in a sheath. The sheath has attached thereto a holding member which grasps the needle to facilitate the insertion thereof. Following venipuncture, the needle is retracted into the sheath, leaving the catheter in place. The sheath then surrounds the point of the needle to prevent inadvertent damage or discomfort to the patient. Such a unit is bulky in use and in addition suffers from the usual disadvantages of needle over the catheter devices.

U.S. Pat. No. 3,539,034 discloses a paracervical block anesthesia assembly comprising a catheter having a precurved, hook-shaped portion, a catheter stylet, a needle assembly, and an assembly guide. The catheter stylet is removably received within the catheter in order to straighten the curved portion thereof. When the catheter stylet is inserted, the internal walls of the precurved, distal portion of the catheter may be skived; and, if the stylet is left within the catheter for any substantial length of time, the curved portion of the catheter will begin to lose its preset character.

SUMMARY OF THE INVENTION In order to overcome the problems encountered in the use of prior art devices, the present invention provides a precurved, over the needle catheter wherein a wing assembly is permanently attached to the proximal end of a length of flexible tubing. This wing assembly functions initially to provide a gripping means by which the anesthesiologist can exercise improved control during the actual placement of the catheter in the patients body; thereafter, the wing assembly aids in the proper securement of the catheter at the site of the tissue puncture.

The present invention also provides an anti-skive device which can be operated to temporarily straighten the precurved portion of the catheter. When its presence is no longer required, the anti-skive device can be easily and quickly discarded. As its name suggests, this anti-skive device prevents the inadvertent cutting away of thin layers of the inner wall of the curved portion of the catheter during the insertion therein of the introducer needle. Thus the chance of small pieces of catheter material entering the patients body, and endangering his welfare, is eliminated.

Due to the presence of rigid, projecting elements and/or to their relative bulkiness, some of the catheter placement units of the prior art cause a significant amount of discomfort to the patient under treatment. More importantly, other devices, for example those wherein the introducer needle cannot be completely removed and discarded after placement of the catheter, present sources of potential danger to the patient. In order to eliminate patient discomfort and insure his physical safety, the present invention provides a catheter and extension tubing for use therewith which is completely free from any rigid projections such as hubs, ribs flanges, or handles, and which is relatively nonbulky. Once the catheter is secured in place, there are no needles which may accidentally puncture the catheter or injure the patient. Thus the catheter of the present invention permits a considerable degree of freedom in moving about, and the patient, if necessary or desirable, may actually lie on the catheter without any discomfort.

In order to further facilitate the catheter placement procedure, the present invention provides a detachable, rigid, grip, adapted at one end to fit into the introducer needle hub and at the other end to receive a pressure indicating device, as for example, a syringe. This rigid grip may be used in conjunction with the wing assembly during the catheter insertion step. The pressure indicating device is used to indicate when entry has been made into the epidural space.

Accordingly, one object of this invention is to provide a catheter placement unit useful in the continuous or intermittent administration of caudal or epidural anesthesia.

Another object of my invention is to provude a means for the prevention of internal skiving of a precurved catheter during the insertion therein of an introducer needle or a stylet.

Still another object of my invention is to provide an over the needle catheter having attached thereto means which initially facilitate the placement of a catheter within the desired part of the body and would subsequently assist in holding the catheter in its desired position.

Another object of this invention is to provide a special rigid grip which affords controlled insertion of an introducer needle and catheter and which is adapted to be used in conjunction with a syringe or other pressure indicating device to show entrance into the epidural space. I

Another object of this invention is to provide a catheter and auxiliary tubing and fittings in such form as to insure the safety and comfort of a patient during use thereof. Other objects and advantages of my invention will become apparent to those skilled in the art from a consideration of the following disclosure, claims and drawings.

In the appended drawings,

FIG. 1 is an exploded perspective view of the components of one embodiment of the epidural catheter placement unit of this invention.

FIG. 2 is a side view, with some portions in section, of a needle assembly partially inserted in a catheter over which an anti-skive device is shown in a first, nonoperative position.

FIG. 3 is a view, similar to that of FIG. 2, wherein the anti-skive device is shown in a second, operative position.

FIG. 4 is an enlarged detail section of the forward portion of FIG. 3 with the anti-skive device removed.

FIG. 5 is a detailed section of the needle hub, special grip, and pressure-indicating device in operative position.

FIG. 6 is a detailed view of the extension tubing attached to the gripping means at the distal end of the catheter.

FIG. 7 shows the needle assembly, with the catheter thereover, inserted into the tissue to the epidural space.

FIG. 8 shows the introducer needle with the grip and pressure indicating device attached thereto.

FIG. 9 shows the distal end of the catheter positioned in the epidural space and the extension tubing attached to the gripping means.

FIG. 10 is a perspective view of the catheter placed in the epidural space and secured to the patients back.

PREFERRED EMBODIMENT FIG. 1 shows, for the purpose of illustrating the present invention, a catheter placement unit which is particularly useful in the administration of epidural anesthesia. The placement unit includes a catheter 10, anintroducer needle 30, anobturator 40, a length ofextension tubing 50, ananti-skive device 60, arigid grip 65, and a penetration needle 70.

Catheter 10 includes a length offlexible tubing 14, the proximal end of which is permanently attached, as by epoxy or other suitable material, to a grippingmember 18. The distal portion offlexible tubing 14 is preset in a generally curved configuration and has abeveled tip 16. Grippingmember 18 hasflexible wings 20 and 21 extending laterally from ahousing 19 which defines a bore 22 (see FIG. 6). Bore 22 communicates and cooperates with the lumen offlexible tubing 14 to provide a continuous hollow portion in which the introducer needle may be removably received.

Introducer needle 30, consisting of ametal cannula 32 having apoint 34 at its distal end and aluer hub 36 permanently attached to its proximal end, is adapted to removably receive anobturator 40.Obturator 40 has asolid shank portion 42, with a point 44 at its distal end and ahub 46 permanently attached at its proximal end; it is provided as part of the catheter placement unit for use when it is desired to temporarily close off the lumen of the introducer needle. The outside diameter ofobturator shank 42 is sized so that it may be easily inserted into and removed fromintroducer needle 30. Point 44 ofobturator 40 andpoint 34 of introducer needle are simultaneously ground to insure that point 44 will substantially completely close the opening defined inintroducer needle 30 bypoint 34 thereof. Cooperating indexing means may be advantageously provided in the hubs of the introducer needle and obturator, respectively, to insure proper alignment when the obturator is disposed within the lumen of the introducer needle. For example, as can be seen in FIG. 1, when theprojection 48 onobturator hub 46 is seated in the notch 38 ofintroducer needle hub 36, obturator is properly aligned within the lumen ofintroducer needle 30. In accordance with the present invention, there is provided a rigid grip which may be advantageously constructed from any suitable plastic, for example polystyrene, polyvinyl chloride or polypropylene.

As can be seen in FIGS. 1 and 5,rigid grip 65 has acentral portion 66 defining a bore 68 running axially therethrough and projectingside portions 67. The distal end of thecentral portion 66 is tapered so that it may frictionally engage the female portion ofluer hub 36 ofintroducer needle 30, while the proximal end ofcentral portion 66 is adapted to receive a syringe or other pressure indicating device.

Referring now to FIG. 2, where some parts are in section, there is shown a side view of catheter I0,antiskive device 60,introducer needle 30 andobturator 40 as they would be assembled in a sealed, sterilized package.

Obturator 40 is placed entirely within the lumen ofintroducer needle 30.Projection 48 on the obturator engages the cooperating slot 38 in the introducer needle to secure proper alignment ofintroducer needle point 34 and obturator point 44, as previously explained.Introducer needle 30, withobturator 40 properly aligned therein, is inserted through the bore defined byhousing 19 and into the lumen ofcatheter tubing 14 to a point just short of the beginning of the precurved portion oftubing 14, so that there is no danger of the introducer needle point accidentally piercing or skiving the internal wall of the tubing.Anti-skive device 60 is placed overflexible tubing 14 of the catheter so that its one end rests just adjacent the distal end ofhousing 19 and its other end terminates at a point short of the beginning of the precurved portion of the flexible tubing. Preferably, as shown in FIG. 2,point 34 ofintroducer needle 30 and the distal end ofanti-skive device 60 are substantially co-terminating. Where this arrangement of the parts is used, there is no force exerted on the precurved distal portion oftubing 14 which would tend to straighten the precurved configuration.

As stated above, catheter comprises a length offlexible tubing 14 permanently attached to a gripping member 18 (FIG. 1).Flexible tubing 14 may be constructed, in whatever guage desired, from any of the plastics known to be useful and safe for placement in the human body. Teflon polytetrafluoroethylene is particularly suited for the purposes at hand because of its inherent lubricity and chemical inertness.

Distal portion oftubing 14 is preset, according to known methods, in a generally curved configuration; this is especially advantageous in the administration of epidural or caudal anesthesia. Referring to FIGS. 7-10 wherein placement of the flexible tubing for the purposes of administering epidural anesthesia is illustrated, it is seen that in such a procedure,distal portion 15 oftubing 14 is positioned within the epidural space at an angle of about 90 to the direction of entry into the patients back. The tubing, because of its preset configuration, easily and permanently conforms to the path that it must follow through the patients body. Thus, the stress and irritation that can result when an ordinary, straight length of flexible tubing is made to conform to two substantially different paths through the body is eliminated by use of the preset, curved flexible tubing of the present invention.

Grippingmember 18, to whichflexible tubing 14 is permanently attached, for example, by the use of an epoxy adhesive, includes ahousing 19 having wings, orlateral projections 20 and 21.Housing 19 may be best described as being semi-rigid, that is to say, it has more rigidity in its axial direction thanflexible tubing 14, but is nevertheless sufficiently flexible in its radial direction to yield upon the insertion, described later, of the distal portion ofextension tubing 50. Although the outside diameter ofhousing 19 is not critical, it is preferably kept small enough, consistent with its semi-rigid nature, to insure patient comfort.

Wings 20 and 21 are made from flexible plastic or elastomeric material and they are attached tohousing 19 so that they may be resiliently flexed through a variety of positions without breaking away from the housing. The wings may define openings, and their upper and/or lower surfaces may be appropriately scored to insure more positive gripping.

Referring now to FIG. 3, which is similar to FIG. 2 and where again some parts are in section, there is shown a side view of the parts of FIG. 2, withanti-skive device 60 in an operative position.Anti-skive device 60 has been slid forward over the precurved,distal portion 15 offlexible tubing 14, thus temporarily straightening it out, andintroducer needle 30, with its indwellingobturator 40 has been completely advanced by the anesthesiologist. The distal portion ofluer hub 36 ofintroducer needle 30 now abuts the proximal end ofhousing 19.

As seen in FIG. 4, thebeveled tip 16 offlexible tubing 14 is preferably co-terminating withpoint 34 of the introducer needle. Where the introducer needle is not needed to effect the primary tissue puncture,point 34 thereof may be of the Crawford type, that is,point 34 may be specially prepared to reduce the sharpness thereof.

Referring to FIG. 5, there is shown a detailed section of the rigidplastic grip 65 engagingluer hub 36 ofintroducer needle 30. The distal end of thecentral portion 66 ofgrip 65 frictionally engages the female socket defined byluer hub 36. At the opposite end thereof,central portion 66 is adapted to receive a syringe or other pressure indicating device.

The right-hand portion of FIG. 6 indicates howextension tubing 50 is detachably connected to the catheter. The end of the extension tubing having tubular blunt 52 therein is inserted into bore 22 defined byhousing 19. The extension tubing is held in place by frictional engagement of its outer surface with the inner wall ofhousing 19. When the catheter and extension tubing are thus connected, it will be seen that there is an uninterrupted passageway extending fromluer hub 54 attached to the extension tubing, through bore 22 defined byhousing 19 of grippingmember 18 to the distal end offlexible tubing 14.

One of the unique features of the present invention is the provision of an anti-skive device which serves to temporarily straighten the precurved portion ofcatheter tubing 14 prior to fully advancingintroducer needle 30 therethrough. The use of this device eliminates any possibility of the introducer needle skiving, or cutting away thin layers of, the internal wall of the precurved portion of the catheter tubing.Anti-skive device 60, seen in perspective in FIG. 1, comprises a length of plastic material having a bore axially therethrough and sufficient rigidity to hold the precurved portion of the catheter tubing in a straightened position when the anti-skive device is moved from a first, nonoperative position (FIG. 2) to a second, operative position (FIG. 3). The length ofanti-skive device 60 is not considered to be critical so long as it can effectively straightenprecurved portion 15 offlexible tubing 14. In order to do this, it is preferred that the length ofantiskive device 60 be substantially as long as the length ofprecurved portion 15. The internal diameter ofantiskive device 60 must be sufficiently larger than the outside diameter offlexible tubing 14 over which it is placed to facilitate axial movement along the flexible tubing; at the same time the internal diameter must be small enough so as to insure temporary straightening of the precurved portion of the flexible tubing.

In order to facilitate the introduction of fluids into the body, there is provided, as part of the catheter placement unit of the present invention, a length ofextension tubing 50, constructed in appropriate guage from a suitable flexible plastic or elastomeric material. In one end ofextension tubing 50, and partially extending therefrom, is a rigid tubular blunt 52, which may be of plastic or metallic construction. As can be seen in FIG. 6, the end oftubing 50 carrying blunt 52 can be inserted into the proximal portion of bore 22 ofhousing 19. The opposite end of the extension tubing is attached to aplastic luer hub 54 which is adapted to removably receive a puncturable, resealable diaphragm (not shown) or other accessory, for example, a syringe fitted with a male luer hub. Both the blunt 52 and theluer hub 54 are permanently attached by suitable means to the extension tubing to insure positive seal integrity.

Finally, there is provided a puncturing needle 70 having a point adapted for piercing the tissue of the patients body; this is used by the anesthesiologist to make the initial puncture at the site where the catheter is to be placed.

The procedure to be followed in using the catheter placement unit of the present invention for the administration of epidural anesthesia will now be described.

The site selected for insertion of the catheter is prepared according to standard procedures.

Puncturing needle 70 is then used to make the initial penetration of the body tissue to a point approaching theepidural space 76. When the initial puncture is completed, puncturing needle 70 is removed from the site.

Taking the catheter assembly as illustrated in FIG. 2 from the package, the anesthesiologist slidesanti-skive device 60 forwardly over the precurved, distal portion offlexible tubing 14, thereby temporarily straightening the precurved portion.Introducer needle 30, with its indwellingobturator 40, is then pushed forward until cannula 32 is completely inserted withinflexible tubing 14. The relationship of the various components at this stage is illustrated by FIG. 3, that is to say, the distal portion of theluer hub 36 ofintroducer needle 30 abuts the proximal end ofhousing 19,anti-skive device 60 is temporarily holding the precurved,distal portion 15 in a straightened alignment andpoint 34 ofintroducer needle 30 and beveledtip 16 offlexible tubing 14 are substantially co-terminating.

Anti-skive device 60 is completely removed and discarded. The anesthesiologist then folds theflexible wings 20 and 21 upwardly from their position as illustrated in FIG. 1 to the position illustrated in FIG. 7. Using the wings as thus folded in conjunction withobturator hub 40, the anesthesiologist then carefully inserts introducer needle with catheter 10 thereover, into the puncture previously made with the aid of needle 70. At this stage,introducer needle 30 is adjacent, but has not penetrated, epidural space 76 (FIG. 7). The anesthesiologist then removes obturator from within the introducer needle and, if desired, inserts the distal end ofcentral portion 66 ofrigid grip 65 into the socket ofluer hub 36. Asyringe 72, or other pressureindicating device, is then inserted into the proximal end of thecentral portion 66 of the rigid grip. The anesthesiologist then useswings 20 and 21, again folded upwardly as illustrated in FIG. 7, andrigid grip 65, to carefully insertintroducer needle 30 intoepidural space 76. Entrance into the epidural space will be shown bysyringe 72 or other pressure indicating device attached to the proximal end ofcentral portion 66. Afterepidural space 76 has been penetrated, the anesthesiologist removesintroducer needle 30,rigid grip 65, andsyringe 72 by holding the grippingmember 18 with one hand and pullingrigid grip 65 backw ardly. Alternatively, in the case where the anesthesiologist chooses not to employrigid grip 65,syringe 72 or the other pressure indicating device is connected directly to the proximal end ofluer hub 36 ofintroducer needle 30, the upwardly folded wings are then used in conjunction with syringe 72 (or the other pressure indicating device) to effect entrance intoepidural space 76. When that is done, syringe 72 (or the other pressure indicating device) is removed from withinluer hub 36, and the procedure is completed as indicated below.

The end of the extension tubing carrying rigid, tubular blunt 52 is then hooked up tohousing 19; the other end is connected, via thehub 54, to a syringe or other accessory containing the liquid to be infused.

As best seen in FIG. 9, the anesthesiologist then grasps the upwardly folded wings and movesflexible tubing 14 forwardly into position withinepidural space 76. As this is done, the preset curve is restored todistal portion 15 offlexible tubing 14 so that, as seen in FIGS. 9 and 10,flexible tubing 14 is properly and comfortably positioned inepidural space 76.

Wings 20 and 21 are then folded downwardly and fastened to the patients back 78 by strips ofadhesive tape 80.

What is claimed is:

1. A catheter assembly comprising: a length of flexible tubing precurved at its distal end; an introducer needle having a point at its distal end removably disposed within said tubing; and anti-skiving means mounted over said tubing and movable from a position overlying a portion of said tubing that is not precurved to a position overlying said precurved distal end so that said distal end may be temporarily straightened to pre-

Claims (2)

1. A catheter assembly comprising: a length of flexible tubing precurved at its distal end; an introducer needle having a point at its distal end removably disposed within said tubing; and anti-skiving means mounted over said tubing and movable from a position overlying a portion of said tubing that is not precurved to a position overlying said precurved distal end so that said distal end may be temporarily straightened to prevent internal skiving of said tubing when said introducer needle is fully positioned within said tubing.

2. The catheter assembly of claim 1 wherein said anti-skiving means is a sleeve having a length sufficient to substantially straighten the precurved end of said tubing.

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