Implant syringe

Details Implant syringe Implant syringe

2000-02-07

2002-11-12

Hayes, Michael J. (Department: 3763)

Surgery

Means for introducing or removing material from body for...

Treating material introduced into or removed from body...

C604S218000

Reexamination Certificate

active

06478768

ABSTRACT:

The present invention relates to an implant syringe from the needle of which a preferably elongated strand-shaped preparation with a sustained release substance is discharged by means of a plunger. Most of the time such a sustained release preparation is placed in a patient's abdominal wall which has previously been pierced with the needle of the implant syringe to form a receiving channel for the preparation.
So far one has proceeded such that after formation of the insertion channel the plunger of the implant syringe is pushed forward into the syringe needle while the entire implant syringe with the syringe needle is simultaneously retracted from the insertion channel, whereby the preparation slowly exits out of the syringe needle and finally leaves said needle. The problem arises here that the advance movement of the plunger and the retraction of the syringe needle have to be timed such that the preparation, which is a solid shaped body, is exactly placed in the insertion channel. In cases where the preparation is pressed out of the syringe needle at a pace faster than that at which the needle is retracted in the insertion channel, the preparation is violently pushed into the tissue of the abdominal wall, thereby causing great pain for the patient. On the other hand, if the syringe needle is retracted at a pace faster than that at which the preparation exists from the needle, this may have the consequence that the strand-shaped tablet is not completely received in the insertion channel.
It is the object of the present invention to provide an implant syringe by which it is ensured that the preparation is exactly placed in the insertion channel so that the placement is carried out without any pain, except for the one caused by the formation of the insertion channel.
According to the invention said object is achieved by the features of patent claim
1
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Advantageous developments of the invention are characterized in the subclaims.
The implant syringe according to the invention comprises a spacer which limits the advance movement of the plunger into the syringe needle in such a way that a distance equal to the length of the preparation to be discharged or slightly greater than said length remains between the outlet orifice of the syringe needle and the head end of the plunger in the forwardly pushed preparation-discharging position. Moreover, the syringe needle can be retracted by means of a grip member towards the spacer by a distance which is at least as great as or also greater than the length of the preparation.
Thus, in the implant syringe according to the invention, the plunger is pushed forward in a first step up to the abutment formed by the spacer after placement of the syringe and formation of the insertion channel, whereby the strand-shaped tablet contained in the implant syringe is pushed foward up to the tip of the needle, whereupon, while the plunger is immovably held, the syringe needle is retracted by means of an appliance or handle at least to such an extent that the preparation is exposed. It is thereby ensured in a reliable manner that the strand-shaped preparation is not pushed forward beyond the needle tip, i.e. beyond the end of the insertion channel, i.e. it is impossible to press the solid tablet strand into the tissue of a patient.
Since the preparation is moved by the advance movement of the plunger into a position in which it is located at the needle tip and thus at the end of the insertion channel, it is also ensured that it is placed over its entire length in the insertion channel as the preparation is not retracted while exiting from the syringe needle. Instead, the syringe needle is withdrawn from the preparation while the latter is held in its position by the plunger. While the syringe needle is retracted, the front surface of the syringe housing surrounding the rear portion of the syringe needle should remain in contact with the patient's skin when said front surface of the housing serves to limit the length or depth of the insertion channel, as is preferred.
In a preferred development of the present invention, the implant syringe according to the invention consists essentially of three main components, namely the spacer, the base plate preferably extending at a right angle relative to the longitudinal axis of the syringe, and a guide sleeve which is attached thereto and forms the above-mentioned syringe housing and whose front surface should limit the insertion depth of the syringe needle; furthermore, it consists of the grip member which as a handle preferably contains two tabs that are positioned in a plane parallel to the base plate of the spacer and project from an essentially tubular needle holder of the grip member that extends in the axial direction of the syringe, with the needle holder containing an axial through hole in which the syringe needle is seated, e.g. pressed thereinto, and of the plunger which has the shape of an elongated thin rod and which is centrally seated on an end plate that has molded thereon a sleeve which surrounds the end section of the plunger and limits the advance movement of the plunger as soon as its front face impinges on the base plate of the spacer.
In detail, it is advantageously suggested that the essentially tubular central attachment of the grip member, which forms the needle holder, should have an axial through hole engaged by the syringe needle. The syringe needle, however, extends preferably not entirely through the hole of the needle holder but leaves a rear end section of the through hole unoccupied which in this instance has a restricted free inner diameter slightly smaller than the inner diameter of the syringe needle and above all slightly smaller than the outer diameter of the strand-shaped preparation. The inner diameter of the end section of the through hole can be reduced by the measure that individual projections, which e.g. may be shaped in the form of beads or noses, slightly project inwards, the projections being dimensioned such that a strand-shaped tablet engaging into said end section of the through hole is prevented from entering into the syringe needle without the action of the plunger, and thus from unintentionally sliding out of the implant syringe. The preparation, however, is not so firmly retained in the end section of the through hole that the advance movement into the syringe needle as effected by the plunger would be impeded.
The grip member as a handle for retracting the syringe needle preferably comprises two opposite tabs projecting from the tubular needle holder, without the invention being limited to such a configuration.
The rear end of the essentially tubular needle holder is suitably connected to an element which is also essentially tubular and serves to receive the strand-shaped preparation, the preparation receiving element having a through hole which is in alignment with that of the needle holder. The two plastic elements may e.g. be put together or connected to each other in any other suitable manner by means of their front faces. Suitably, they have the same cross-sectional shape with a coinciding outer diameter, and the diameter of the through hole should here be slightly greater than the outer diameter of the preparation.
Suitably, the strand-shaped preparation is inserted into the through hole of the preparation receiving element before the grip member composed in the above-described manner is assembled with the spacer and the guide sleeve thereof.
The spacer suitably includes a base plate having a central hole in which in the initial state of the implant syringe the rear end of the preparation receiving element is seated, and a guide sleeve which extends in axial direction and projects from the base plate at a right angle. The guide sleeve preferably comprises two opposite and axially uninterrupted slots, i.e. it consists of two spaced-apart guide sleeve sections, with the tabs of the grip member passing through said slots and projecting outwards beyond the guide sleeve, so that they can be gripped from behind by the fingers of a user of the impl

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