EP0267947A1

EP0267947A1 - Protective devices for canulas

Info

Publication number: EP0267947A1
Application number: EP19870903670
Authority: EP
Inventors: Lola June Thurecht; Josephina Christina Maria Lenferink
Original assignee: Individual
Current assignee: Individual
Priority date: 1986-05-29
Filing date: 1987-05-27
Publication date: 1988-05-25
Also published as: WO1987007162A1

Abstract

Un dispositif protecteur pour canules (13, 53) se compose d'une enveloppe généralement tubulaire (10, 50) ayant une fente (16, 56) s'étendant depuis l'une de ses extrémités. L'enveloppe (10, 50) recouvre complètement la canule. La fente (16, 56) est plus large que le diamètre extérieur de la canule, de telle sorte que l'enveloppe peut être retirée de la canule et replacée sur celle-ci, sans que les mains de l'utilisateur de la canule s'approchent de la pointe de la canule. L'enveloppe peut être connectée par une attache (18, 58) à un couvercle (20) ou une bague (54) disposés sur le support de la canule.A protective device for cannulas (13, 53) consists of a generally tubular casing (10, 50) having a slot (16, 56) extending from one of its ends. The envelope (10, 50) completely covers the cannula. The slot (16, 56) is wider than the outside diameter of the cannula, so that the casing can be removed from the cannula and replaced thereon, without the hands of the user of the cannula s approach the tip of the cannula. The envelope can be connected by a clip (18, 58) to a cover (20) or a ring (54) arranged on the support of the cannula.

Description

TITLE: PROTECTIVE DEVICES FOR CANULAS

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TECHNICAL FIELD

This invention concerns the protection of the tips of the canulas (commonly called needles) used in 5 hypodermic syringes and in the equipment used to take blood samples and donations.

BACKGROUND ART

It has long been recognised that a person who uses a hypodermic syringe or a canula at the end of a tube

10 (for example, to administer a drug, to extract a blood sample or blood donation, to supply a drip to a patient or to effect a blood transfusion) is at some risk when the tip of the canula is exposed at the conclusion of the action being taken. The risk

15 arises because the viruses for some diseases, notably hepatitis B and acquired immune deficiency syndrome (AIDS), are carried by the blood, and if the tip of a sharp needle (canula) containing even a very small sample of the blood of an infected^' person punctures

20 the skin of the person handling the canula, that person handling the canula can become infected. So great is this risk to nurses, nursing sisters, doctors, paramedical personnel and laboratory staff that it is standard practice to cover the end (tip)

25 of a canula immediately after use.

V The covering of the end of a canula is effected with a cap or cover. Examples of protective caps have been described in the specification of U.K. patent No 1,514,725 and in the specifications of U.S. patents Nos 4,248,246 and 4,629,453. The cap or cover is normally positioned over the end of the new and sterile canula, is removed prior to the use of the canula, and is then replaced after the canula has been used. Unfortunately, the cap or cover usually has a small aperture into which the end of the canula must be fitted and it is not uncommon (even when a protective flange is fitted to the cover, as in the case of the invention of U.S. patent No 4,629,453) for the user of the canula to experience some difficulty in aligning this aperture with the end of the canula, and for the user to be pricked by the canula in the course of attempting to cover its tip.

Factors such as improper' room illumination, poor eyesight, lack of co-ordination or concentration, and working under stress are likely to cause problems when a person has to guide the canula tip into the small aperture in the over. In a hospital, when a member of the nursing staff accidentally punctures his or her skin with a potentially contaminated canula, the accident has to be reported as there may be a subsequent compensation claim if a serious and possibly incurable and/or fatal disease is contracted. The reporting requires the completion of * substantial documentation by the person who has been pricked by the needle, additional expenditure in administration and a general loss of productivity.

DISCLOSURE OF THE PRESENT INVENTION 5 It is an object of the present invention to overcome this disadvantage of the prior art protective covers for canulas.

This objective is achieved by providing a cover for a canula that is removeable from and replaceable over

10 the canula without the need for the user of the canula to be in close proximity to the tip of the canula. The cover for the canula comprises a generally tubular sheath which is adapted to fully cover the canula and which is provided with an

15 elongate slot through which the canula can pass. The

•provision of this slot enables the sheath to be moved laterally away from the canula to expose it for use, and enables the operator to restore the sheath to its protective position after the canula has been used,

20 without the operator's hands having to be close to the tip of the canula.

Thus, according to the present invention, there is provided a protective device for a canula, said device comprising an elongate, substantially rigid,. -^ 25 tubular sheath adapted to fit over the entire canula, characterised in that a) the sheath has an elongate slot formed therein and extending from one end thereof for at least part of the length thereof, the slot having a width which is greater than the diameter of the canula; and b) said one end of the sheath is adapted to fit- on to the support for the canula.

The support for the canula may be the conventional needle support of a hypodermic syringe or the end of a blood sampling flexible tube, in which case it is preferred that an annular retaining member, adapted to securely grasp said one end of the sheath, is fitted over the support for the canula.

Alternatively, the support for the canula may be provided with a cap which is firmly affixed (usually by manual pressure) over or into the end of the support for the canula, this cap having an aperture therein through which the canula projects. The end of the sheath which is .remote from the tip of the canula (that is, the end of the sheath from which the slot extends) will then be a press fit over or into this cap.

The sheath and the annular retaining member (or the cap) may be connected by a short strap or cord, or a hinge, which ensures that the sheath remains connected to the needle support while the canula is used, thus preventing misplacement of the protective sheath by the user of the canula. In this case, the length of the slot in the sheath will be approximately equal to the length of the canula.

Embodiments of the present invention will now be described, with reference to the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 is a perspective sketch of the present invention.

Figure 2 is a sectional view of an annular retaining member that may be used to secure the device of Figure 1 around a canula.

Figure 3 shows an alternative embodiment of the present invention fitted to a hypodermic syringe.

Figure 4 illustrates the removal and replacement of the protective sheath of the device illustrated in Figure 3.

Figure 5 is a perspective sketch of another embodiment of the present invention.

DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS The protective device illustrated in Figure 1 comprises a substantially rigid tubular member 10 which is tapered towards a closed end 11 and has an open end 12 which is adapted to fit over or into a support for a canula. The tubular member 10 has a slot 16 extending from the end 12 for a distance which, in the illustrated embodiment, is substantially equal to the length of the canula that it protects. The slot has a width which is at least slightly greater than the outside diameter of the

- canula. The tubular member 10 may be made from any suitable material which is rigid enough to be self supporting in the configuration illustrated in Figure 1. A number of plastics materials meet this requirement.

Preferably, the end 12 of the protective device illustrated in Figure 1 is firmly held in its protective position around a canula by an annular retaining member which fits on to the needle support. One form of retaining member is illustrated in Figure 2.

The retaining member 17 of Figure 2 is moulded as a single article from a resilient material, such as neoprene or a flexible and resilient plastics material. It comprises an annular body portion 14 from which an arm 15 extends. The arm 15 is generally C-shaped in cross-section, with the top of the "C" defining a circular aperture that is greater in diameter than the internal diameter of the body section 14. When the protective sheath 10 is placed over a needle mount on to which the retaining member 17 has been affixed, the end 12 deforms the circular end of the C-shaped arm 15 to force the top of the arm 15 outwards to permit the end 12 to bear against the top of the body portion 14. In this position, the resilient nature of the material from which the retaining member has been fabricated causes the arm 15 to revert, as far as possible, to its undeformed position, and thus to clamp the sheath 10 in the protective position, surrounding a canula.

To remove the tubular member 10 from its protective position around a canula, the tubular member is detached from the needle support on which it is mounted by a manual force applied at or near end 12 of the tubular member 10. After being detached from the needle support, the tubular member 10 is moved a distance away from the needle support until the tip of the canula can be passed through the slot 16. A sideways movement of the tubular member 10 (as shown in Figure 4, which is discussed below) enables the whole of canula to pass through the slot ^"16 as the tubular member 10 is removed. Replacement of the protective tubular member 10 is by the reverse of this sequence of steps.

When the retaining member 17 of Figure 2 (or a similar retaining device) is used to clamp the sheath 10 in its protective location, the force needed to prise sheath 10 out of the grip of the retaining member will be greater than when a retaining member of this type is not used.

The retaining member may be connected to the sheath 10 by a flexible strap, if desired, to prevent the removal of the sheath from the region of the canula.

A variation of the combination of the protective sheath 10 of Figure 1 and the retaining member 17 of Figure 2 is illustrated in Figures 3 and 4. In the embodiment of Figures 3 and 4, a cap 20 is a tight fit over the needle support. The cap 20 has an aperture in it to permit the canula 13 to project through the cap. The end of the sheath or tubular member 10 is a tight fit over the cap 20, and is removed from cap 20 in the same way as the tubular member 10 of Figure 1 is removed from its associated needle support or retaining member 17.

There are some optional - but preferred - features in the embodiment illustrated in Figures 3 and 4. These are a) the provision of a flexible strap 18 extending between a thickened region 19 of the tubular member 10 and the cap 20, to prevent the protective tubular member from being removed from the syringe assembly and possibly misplaced while the syringe is being used; and b) a series of flutes or ridges 21 to facilitate the holding of the tubular member 10 between the fingers of a user of the protective device when the canula is being passed through slot 16 during the removal or the replacement of the tubular member 10.

The protective devices shown in Figures 1, 2 and 3 are designed to be moulded as a single item from a suitable plastics material.

Figure 5 illustrates another embodiment of the present invention, consisting of a tapered, tubular sheath 50 having a slot 56 formed in it. A thickened end region 59 of the sheath 50 has a strap 58 affixed to it. Strap 58 connects the region 59 to a ring 54 which is adapted to be a tight fit over a support 55 for a canula 53 (shown in dashed outline to illustrate the way in which this embodiment of the invention is used). Flutes or ridges 57 assist in the manual gripping of the sheath 50. The operation of the embodiment of Figure 5 is essentially the same as the operation of the embodiment of Figures 3 and 4, and further explanation thereof is not necessary. The combination of sheath 50, strap 58 and ring 54 is designed to be moulded as a single item from a suitable plastics material, in which case the strap 58 will apply a bias to the sheath or cover 50 into the position shown in Figure 5. In this position, the cover will not interfere with the use of the canula to administer a drug or take a blood sample. It will be clear that all the protective devices illustrated and described above are suitable for use with canulas (needles) mounted in syringes and in the ends of tubes, whether for administering a drug or a drip, or for taking samples of blood or other liquid from a human or animal body or from a storage container of blood or other liquid. The present invention may also be adapted for use with catheters and other body probes if protection against contact with the ends of such probes is required.

It will also be apparent that although specific realisations of the present invention have been illustrated and described, modifications of those embodiments can be made without departing from the present inventive concept.

Claims

CLAIMS :

1. A protective device for a canula (13, 53), said device comprising an elongate, substantially rigid, tubular sheath (10, 50) adapted to fit over the entire canula, characterised in that a) the sheath has an elongate slot (16, 56) formed therein and extending from one end (12, 59) thereof for at least part of the length thereof, the slot having a width which is greater than the diameter of the canula; and b) said one end (12, 59) of the sheath (10, 50) is adapted to fit on to the support for the canula.

2. A protective device as defined in claim 1, in which an annular retaining member (17) is fitted over the support for the canula and said one end of the sheath (10) is adapted to be securely connected to said annular retaining member.

3. A protective device as defined in claim 2, in which said annular retaining member (17) has a body portion (14) from which an annular arm (15) of C-shaped cross-section extends, said annular arm (15) being adapted to grasp said one end of the sheath (10) .

4. A protective device as defined in claim 1, in which a cap (20) is affixed to the support for the canula and said sheath (10) is adapted to be connected to said cap.

5. A protective device as defined in claim 4, in which said cap (20) and said one end (12) of said sheath are connected by a flexible strap (18).

6. A protective device as defined in claim 1, including a ring (54) which is a tight fit over the support for the canula, and a flexible strap (58) connects said ring (54) to said one end (59) of said sheath (50).

7. A -protective device as defined in any preceding claim, including a plurality of flutes or ridges (21, 57) extending longitudinally on the surface of said sheath.

8. A protective device for a canula, substantially as hereinbefore described with reference to the accompanying drawings.