The present invention relates to catheter removers, and, more particularly, to cuffed catheter removers.
In the US, there are more than 2 million central venous catheters (CVCs) inserted each year. CVCs are surgically implanted in a patient when it is necessary to deliver IV fluids, parenteral nutrition, antibiotics, chemotherapy, blood products, obtain blood samples, perform plasma pheresis and provide access for hemodialysis treatment. CVCs are available in several different configurations depending upon patient indication, patient anatomy and indwelling time requirements. Specific CVC configurations are PICCs lines, Tunneled or cuffed Catheters, Ports, Midline Catheters, and non-tunneled Catheters.
It is estimated there are approximately 567,000 tunneled or cuffed catheters in the US, of which 50% are used for hemodialysis treatment access. It is essential that tunneled catheters be anchored within the patient. One approach to anchoring the implanted catheter is the placement of a permeable member of the implanted catheter inside the patient to promote tissue in-growth within the permeable member. Typically, the permeable member is a cuff affixed around the catheter tube. These cuffs are commercially known as “Dacron” cuffs.
Implantation of a CVC involves surgically creating a subcutaneous tunnel through the skin and into a blood vessel of the patient, and positioning the cuff midway between the skin entry point and the blood vessel entry point. The catheter may include a single cuff or a double cuff (see, e.g.,
In order to remove a catheter from the ingrown subcutaneous tissue, the physician must surgically dissect around the cuff with a scalpel, cutting the subcutaneous tissue surrounding all edges of the cuff into which tissue has grown. Tissue growth occurs substantially transverse to the longitudinal axis of the cuff and around the outer circumference of the cuff. In addition, tissue growth occurs at angles oblique to the longitudinal axis of the cuff along both of the cuffs side edges. The physician must cut around the circumference of the cuff and both side edges to completely detach the cuff and free the indwelling catheter. This is a difficult and time-consuming surgical procedure that tends to result in increased patient bleeding. Prolonged surgical time also increases the risk of infection. The procedure may also contribute to an increased chance of scar tissue build-up within the subcutaneous tissue such that creation of additional subcutaneous catheter tunnels becomes increasingly difficult. Also, because cuffs are sized to provide a snug fit in the subcutaneous area, they are difficult to extract smoothly through the tunnel.
With catheters formed of softer materials, such as urethane and silicone, for example, the risk that the catheter will snap or break apart during the removal procedure increases. The use of such materials also increases the risk the affixed cuff will tend to result in the elongation of the tube and alter its dimensions while placing traction. The stress placed on the proximal end of the catheter during removal from the tunnel is concentrated at the location of the cuff. If the catheter breaks during removal, the physician may have to perform a further procedure to remove the severed distal portion of the catheter left within the patient.
The present invention provides a cuffed catheter remover which includes a handle and a shaft that will slide down through the entrance site of the catheter. The head of the cuffed catheter remover is used to cut and dissect away the fibrous tissue that is grown into the cuff. The cuffed catheter remover facilitates the removal of the catheter.
The present invention provides a one-handed, ergonomic surgical instrument that is placed over the exposed catheter shaft and effectively passes through the subcutaneous tunnel while dissecting the fibrous tissue away from the cuff and catheter shaft distal to the cuff. It also allows catheter removal through the exit tunnel and precludes the need for surgical “cut down”, thereby minimizing patient trauma and significantly decreasing catheter removal time and providing a catheter removal option that does not require the use of a scalpel and associated “sharp” risk factors.
The invention in one form is directed to a catheter remover, including a handle with an actuation mechanism. A shaft having a proximal end is attached to the handle. The shaft is a hollow shaft with an elongate member therein. The elongate member has a proximal end engaged with the actuation mechanism. A cutting head is attached to a distal end of the shaft. The cutting head includes a plurality of arcuate cutting segments, each attached to the distal end of the shaft. At least one of the cutting segments is pivotally attached to the distal end of the shaft.
The invention in another form is directed to a catheter remover, including a T-handle with an actuation mechanism. A shaft is attached and disposed generally perpendicular to the T-handle. The shaft is a hollow shaft with an elongate member therein. The elongate member has a proximal end engaged with the actuation mechanism. A cutting head is attached to a distal end of the shaft. The cutting head includes a plurality of arcuate cutting segments, with each cutting segment attached to a distal end of the shaft and including an outer cylindrical portion and a radially inner cutting portion. Each cutting portion has an arcuate cutting edge.
Non-inclusive advantages of the invention include reduced bleeding compared to traditional removal techniques, reduced likelihood of scar formation, reduced need for follow up, decreased procedure time, lower cost, improved patient comfort, and reduced chance for complications.
The above-mentioned and other features and advantages of this invention, and the manner of attaining them, will become more apparent and the invention will be better understood by reference to the following description of embodiments of the invention taken in conjunction with the accompanying drawings, wherein:
Corresponding reference characters indicate corresponding parts throughout the several views. The exemplifications set out herein illustrate embodiments of the invention, and such exemplifications are not to be construed as limiting the scope of the invention in any manner.
Referring now to the drawings, and more particularly to
Handle 12 is an ergonomically shaped T-handle which is disposed generally perpendicular to shaft 14. Handle 12 includes an outer housing 18 and an internal actuation mechanism 20. Actuation mechanism 20 preferably is configured as an elongate actuator which is axially movable along a longitudinal axis 22 within handle 12. Actuation mechanism 20 includes an end 24 which extends through housing 18 of handle 12 to define a push button which is actuatable by a user. Actuation mechanism 20 includes a ramped actuation surface 26 which is disposed at an acute angle relative to longitudinal axis 22.
Shaft 14 includes a proximal end 28 attached to handle 12, and a distal end 30 attached to cutting head 16. Shaft 14 is a hollow shaft with an elongate member 32 slidably positioned therein. Elongate member 32 preferably is in the form of a rod having a proximal end 34 which is engaged with ramped actuation surface 26 of actuation mechanism 20. More particularly, proximal end 34 of elongate member 32 is biased against ramped actuation surface 26, which in turn applies a tension force to elongate member 32 upon actuation of actuation mechanism 20.
Cutting head 16 includes a plurality of arcuate cutting segments 36 which are each attached to distal end 30 of shaft 14. One or more of the cutting segments 36 are pivotally attached to distal end 30 of shaft 14. In the embodiment shown in
As shown in more detail in
During use, the push button (end 24) of actuation mechanism 20 extending through housing 18 is depressed by a user to move arcuate cutting segments 36 to the open position as shown in
Referring now to
While this invention has been described with respect to at least one embodiment, the present invention can be further modified within the spirit and scope of this disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains and which fall within the limits of the appended claims.
This is a non-provisional application based upon U.S. provisional patent application Ser. No. 61/440,010, entitled “CUFFED-CATHETER REMOVAL INSTRUMENT”, filed Feb. 7, 2011, and U.S. provisional patent application Ser. No. 61/498,323, entitled “CUFFED-CATHETER REMOVER”, filed Jun. 17, 2011, each of which are incorporated herein by reference.
Number | Date | Country | |
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61440010 | Feb 2011 | US | |
61498323 | Jun 2011 | US |