GB2083364A

GB2083364A - Inserting needles into body spaces

Info

Publication number: GB2083364A
Application number: GB8127063A
Authority: GB
Original assignee: Smiths Group PLC
Current assignee: Smiths Group PLC
Priority date: 1980-09-12
Filing date: 1981-09-08
Publication date: 1982-03-24
Also published as: GB2083364B

Abstract

An instrument for detecting penetration of the epidural space comprises a barrel 1 within which a plunger 2 is urged forward by a resilient strap 3. The barrel 1 has a nose 10 on which a Tuohy needle 12 is mounted. The inner surface of the barrel has a groove 13 that extends along the barrel, being spaced from the nose 10. In operation the assembly is pushed forward until the tip 13 of the needle 10 contacts the spinal ligaments. The plunger 2 is then pulled rearwardly past the end of the groove 13 so that air enters the barrel 1 and becomes trapped when the plunger is released and urged forwards by the strap 3. Penetration of the epidural space by the tip 13 of the needle 12 allows the trapped air to escape through the needle thereby providing an indication of penetration of the epidural space by causing the plunger to be moved forwards. <IMAGE>

Description

SPECIFICATION Medical-Surgical Instruments This invention relates to medico-surgical instruments. The invention is, more particularly, concerned with instruments for use in detecting the epidural, or other body, space.

In epidural anaesthesia an anaesthetic drug is administered through a small-bore cannula or needle, one end of which is located within the patient's epidural space. The cannula is correctly positioned by means of a hollowbore Tuohy needle that is pushed through the spinal ligaments into the epidural space, the cannula then being fed through the bore of the needle which is subsequently withdrawn to leave the cannula in place. In the past, difficulties have been experienced in correctly position the Tuohy needle. If the Tuohy needle is pushed too far it penetrates the matter underlying the epidural space and discomfort can be caused to the patient.

It is an object of the present invention to provide an instrument that can be used to facilitate positioning of the Tuohy needle and reduce the risk of it being inserted too far.

According to one aspect of the present invention there is provided a medico-surgical instrument for use in inserting a hollow-bored needle into a body space, the instrument including a barrel member; a plunger moveable within said barrel member, the barrel member and the plunger together defining a cavity of variable volume that is arranged to open into the bore of said needle; and reslient means acting to urge said plunger and barrel member together so as to tend to reduce the volume of said cavity and thereby force fluid from said cavity through said bore when said needle penetrates said body space, the instrument being arranged to permit flow of fluid from outside said instrument into said cavity upon increasing the volume of said cavity.

The barrel member may be formed with passage means permitting flow of fluid from outside said instrument into said cavity when said cavity exceeds a predetermined volume.

According to another aspect of the present invention there is provided a medico-surgical instrument for use in inserting a hollow-bored needle into a body space, the instrument including a barrel member; a plunger moveable within said barrel member, the barrel member and the plunger together defining a cavity of variable volume that opens into the bore of said needle; resilient means acting to urge said plunger and barrel member together so as to tend to reduce the volume of said cavity and thereby force fluid in said cavity through said bore when said needle penetrates said body space; and passage means arranged to permit flow of fluid from outside said instrument into said cavity when said cavity exceeds a predetermined volume.

The passage means may include a groove formed along the inside of said barrel member, said groove being spaced from the end of the barrel member proximate said needle.

Alternatively, said passage means may include an aperture formed through the wall of said barrel member and spaced from the end of the barrel member proximate said needle.

In use, fluid flow through the needle is prevented by contact of the spinal ligaments, or other body tissue, with the opening at the tip of the needle. The plunger and barrel are pulled away from one another to increase the volume of the cavity and permit entry of air.

The resilient means then urges the plunger and barrel together trapping the air in the cavity. The plunger and barrel remain extended, because of the volume of trapped air, until the tip of the needle is unblocked on entry into the epidural, or other body, space.

At this time, air is forced out of the tip of the needle by the re-resilient means, thereby causing relative movement of the plunger with respect to the barrel. By observing this movement the surgeon recognizes that the needle has entered the epidural, or other body, space.

An epidural space detector instrument, in accordance with the present invention, will now be described, by way of example, with reference to the accompanying drawings, in which: Figure 1 is a partially sectional side elevation, to an enlarged scale of the instrument mounted on a Tuohy nedle; Figure 2 is a cross-section of the instrument along the line Il-Il; and Figures 3A to SE illustrate, on a reduced scale, the instrument in use.

With reference to Figs. 1 and 2, the epidural space detector instrument comprises a barrel 1 within which a plunger 2 is urged forwardly by a resilient strap 3.

The barrel 1 is of cylindrical shape and circular cross-section being about 8 cm long and 1.5 cm in diameter, although any alternative cross-sectional shape could be used. The barrel is made of a rigid polypropylene plastics material. A reduced-diameter nose portion 10 projects from the forward end of the barrel, the nose portion being inserted within the rear end 11 of a standard Tuohy needle 12. About 2 cm to the rear of the forward end of the barrel 1 the inner surface of the barrel is formed with a passage or groove 13 of rectangular section which extends rearwardly along the length of the barrel. Towards the rear end 14 of the barrel 1 there is formed an inwardly-directed lip 15 that prevents inadvertent withdrawal of the plunger from the barrel.Two lugs 16 project radially outwards at the rear end 14, each lug being provided with a slot 17 for receiving opposite ends of the strap 3.

The plunger 2 is approximately 9 cm long having a plastics stem 20 of cruciform section. The stem 20 is provided with five radially reinforcing discs 21 to 25 spaced apart along the stem. The discs 21 to 25 are circular, the middle disc 23 and the rear disc 25 being of increased diameter. The middle disc 23 is located about 5 cm from the forward end of the plunger 2 and is arranged to limit withdrawal of the plunger, by engagement with the lip 15, to not more than about 2.5 cm. The rear disc 25 limits insertion of the plunger 2, by engagement with the rear end 14 of the barrel 1, so that the forward end of the plunger is prevented from contacting the forward end of the barrel 1.The forward disc 21 supports a sealing head 27 mounted at the forward end of the plunger The head 27 is of a resilient elastomeric substance and is of a generally cylindrical shape being slightly smaller in diameter than the interior of the barrel 1. The forward end of the head 27 has a radial lip 28 that forms a seal about its circumference with the inner surface of the barrel wall. At the rear end of the plunger 2 there is provided a radiallyextending finger grip 32 by which the plunger may be held and moved within the barrel 1.

The grip 32 is formed with two slots 29 which receive the strap 3.

The strap 3 is of a resilient elastomeric material, such as thermoset rubber, and is about 4 cm long in its unstretched state. The ends of the strap 3 are formed into enlarged balls 30 which serve to prevent the strap being pulled from the slots 17 in the lugs 16.

The resilience of the strap 3 is sufficient to urge the plunger 2 and barrel 1 together so that the plunger is forced to the forward end of the barrel against the action of any friction with the barrel.

In operation, the epidural space detector instrument is fitted to the rear end 11 of a Tuohy needle 12 and, with the plunger 2 in its normal position at the forward end of the barrel 1, the assembly is pushed forwardly so that the needle passes through the patient's skin 40 and underlying tissue, and into the spinal ligaments 41 (Figs. 3A and 3B). The spinal ligaments are of a dense and grissly nature, the presence of which is readily apparent to the surgeon by the increased resistance to forward movement of the needle 12. In this position, the aperture 31 at the tip of the needle 12 is blocked by the surrounding spinal ligaments 41. The surgeon then pulls the plunger 2 rearwardly out of the cylinder 1 (Fig. 3C) thereby further stretching the strap 3.As the surgeon begins to do this, the cavity formed between the plunger 2 and the barrel 1 increases in volume, but without initially permitting entry of fluid to the cavity, thereby forming a reduced pressure within the cavity that resists displacement of the plunger. The resistance is not, however, sufficient to prevent movement over a short distance and, as soon as the lip 28 of the plunger head 27 clears the forward end of the groove 13, air flows from outside the instrument, along the groove, between the plunger head and the wall of the barrel 1. In this way, pressure in the cavity is equalised with that outside the cavity. When this happens, the surgeon releases the plunger 2 so that it is urged forwards by the resilience of the strap 3 as far as the forward end of the groove 13 where the trapped air prevents further movement.

The surgeon then continues pushing the assembly forwards (Fig. 3D) through the spinal ligaments 41. As soon as the aperture 31 at the tip of the needle 12 clears the spinal ligaments 41 the air trapped in the barrel 1 is forced by the resilience of the strap 3 through the bore of the needle 12 and out of its aperture 31. The plunger 1 therefore moves forwards rapidly (Fig. 3E) alerting the surgeon that the nedle 12 is in the correct location.

The epidural detector instrument is then removed, leaving the needle 12 in position. An epidural cannula (not shown) is subsequently pushed through the bore of the needle 12 in the normal way, after which the needle is removed by sliding rearwardly along the cannula.

It will be appreciated that the instrument could be used in applications other than for detecting the location of the epidural space.

The instrument need not have a groove or grooves formed along the inner surface of the barrel, instead, apertures extending through the wall of the barrel could be used. Alternatively, the cylinder could have a bore that tapers, or is stepped to, a larger diameter to permit air passage around the plunger head when it is in a rearward position. The instrument could be provided with a one way valve that is arranged to allow air to enter the cavity from externally of the instrument when the plunger is pulled rearwardly, but to prevent air leaving the cavity on forward movement of the plunger, except through the bore of the attached Tuohy needle. The plunger could be urged forwardly by a helical spring or other resilient means.

Claims

1. A medico-surgical instrument for use in inserting a hollow-bored needle into a body space, the instrument including a barrel member; a plunger moveable within said barrel member, the barrel member and the plunger together defining cavity of variable volume that is arranged to open into the bore of said needle; and resilient means acting to urge said plunger and barrel member together so as to tend to reduce the volume of said cavity and thereby force fluid from said cavity through said bore when said needle penetrates said body space, the instrument being arranged to permit flow of fluid from outside said instrument into said cavity upon increas ing the volume of said cavity.

2. A medico-surgical instrument according to Claim 1, wherein said barrel member is formed with passage means permitting flow of fluid from outside said instrument into said cavity when said cavity exceeds a predetermined volume.

3. A medico-surgical instrument for use in inserting a hollow-bored needle into a body space, the instrument including a barrel member; a plunger moveable within said barrel member, the barrel member and the plunger together defining a cavity of variable volume that opens into the bore of said needle; resilient means acting to urge said plunger and barrel member together so as to tend to reduce the volume of said cavity and thereby force fluid in said cavity through said bore when said needle penetrates said body space; and passage means arranged to permit flow of fluid from outside said instrument into said cavity when said cavity exceeds a predetermined volume.

4. A medico-surgical instrument according to Claim 2 or 3, wherein said passage means includes a groove formed along the inside of said barrel member, said groove being spaced from the end of the barrel member proximate said needle.

5. A medico-surgical instrument accordng to Claim 2 or 3, wherein said passage means includes an aperture formed through the wall of said barrel member and spaced from the end of the barrel member proximate said needle.

6. A medico-surgical instrument according to Claim 2 or 3, wherein the internal diameter of said barrel member is greater at a greater volume of said cavity.

7. A medico-surgical instrument according to any one of the preceding claims, wherein said resilient means includes a strap of elastic material that is stretched on increasing the volume of said cavity.

8. A medico-surgical instrument according to Claim 7, wherein said strap is secured at opposite ends with said barrel member and is engaged by said plunger intermediate its said ends.

9. A medico-surgical instrument according to any one of the preceding claims, wherein said needle is mounted with said barrel member.

10. A medico-surgical instrument according to any one of the preceding claims, wherein said needle is adapted for insertion into the epidural space through the spinar ligaments, the tip of said needle being blocked while being inserted through said spinal ligaments so that said fluid is trapped in said cavity, and being opened on penetration of said epidural space so that fluid is forced out of said cavity causing displacement of said plunger relative to said barrel member and thereby giving an indication of penetration of said epidural space.

11. A medico-surgical instrument substantially as hereinbefore described with reference to the accompanying drawings.