Tapered intravenous cannula
AssigneeDSU Medical Corporation
InventorsDavid S. Utterberg, William J. Schnell
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AssigneeDSU Medical Corporation
InventorsDavid S. Utterberg, William J. Schnell
Estimating the term…
A cannula and method for providing an external connection with an implanted artificial port for communicating with a body lumen of a patient. The artificial port has an entrance conduit with an inwardly tapering section. The tapered cannula is sized and proportioned to substantially match and seal with the inwardly tapering section of the entrance conduit. Thus the cannula can form a readily removable seal with the inwardly tapering section. A typical angle of taper is one to three degrees.
A generally rigid cannula for communication through the skin with a body lumen of a patient including an entrance conduit, said cannula having a proximal end connected with a flow tube, said cannula having an inward taper of its outer wall extending at least most of the length between said proximal end and a distal end, whereby said distal end is of less diameter than said proximal end and said distal end being blunt wherein said tapered and blunt distal end is effectively incapable of cutting through living tissue and the tapered distal end adapted to be received by the entrance conduit that includes a generally corresponding shape to the tapered distal end forming a readily removable seal and locking connection with the entrance conduit.
A kit comprising at least one of a cannula and an implantable artificial port for communication with a body lumen of a patient, said artificial port having an entrance conduit which comprises a generally rigid, inwardly tapering section, said cannula having a proximal end connected with a fluid flow tube and a tapered distal end having a shape generally corresponding to said entrance conduit and being sized and proportioned to substantially match and seal with said inwardly tapering section of the entrance conduit, whereby said cannula can form a readily removable seal and locking connection with said inwardly tapering section;
Dependencies are inferred from the claim text.
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Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor: needles for infusions; Accessories therefor, e.g. for inserting…
Access sites: subcutaneous access sites
Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body: right-angle needle-type devices
Devices for delivering substances into the body
Term ended 20 Apr 2019 (estimated)
This invention relates to an improved cannula for communication with the vascular system in order to gain access to a supply of blood for extracorporeal blood processing, for example hemodialysis, hemoperfusion, or any other desired form of extracorporeal blood treatment.
In the early days of dialysis therapy, extracorporeal blood flows were moderate, at about 200 ml/min. with the result that a dialysis treatment took six hours or more. These treatments, while long, were often uneventful, not least because the extracorporeal pressures were moderate with the low flow rates, typically between −120 mm./Hg (arterial) and +120 mm./Hg (venous). Modern therapy has increased the flow rates to as much as 500 ml./min. or more, with corresponding increases in treatment efficiency. However, the operating pressures have also increased, even to as much as −400 mm./Hg (arterial) and as much +600 mm./Hg (post pump). At these pressures, undesirable events can take place more readily, for example, hemolysis, foaming or clotting of the blood, air emboli, and other alarm conditions, which may be frequent and sometimes severe.
While the operating pressures could be reduced by increasing the inner diameter of the patient access cannulae, which are typically the narrowest portion of the extracorporeal blood circuit, an increase in the size of the needles, which could significantly reduce pressures, is strongly objected to by the patients. A large needle results in a larger incision. Patients have historically shown reluctance to be penetrated in a fresh site by a needle with a cutting point larger than 15 G (gauge).
In the drawings, FIG. 1 is an elevational view of a cannula for communication with the vascular system of a patient, the cannula having a proximal end which is connected to a blood flow tube;
FIG. 1a is an elevational view of a modified cannula that is otherwise similar to FIG. 1;
FIG. 2 is a substantially sectional view of an implanted artificial port for communication with the vascular system of a patient, shown to be in connection with the cannula of FIG. 1;
Referring to FIG. 1, a cannula 10 is provided, typically for communication with the vascular system of a patient for high flow hemodialysis, or the like. The cannula 10 comprises a tapered stainless steel tube in this specific embodiment, having a larger proximal end 13 that terminates in a hub 12 and has an inner diameter of 2.85 mm in this specific embodiment. Cannula 10 also has a distal end 14 which has an inner diameter of 1.85 mm, with the bore 16 of cannula 10 tapering in substantially uniform manner along its length from proximal end 12 to distal end 14. However, if desired, a cylindrical segment 18 of the cannula may be provided adjacent to the proximal cannula end 12.
The outer diameter of cannula 10 at distal end 14 may be about 2.1 mm. The wall thickness of cannula 10 adjacent to distal end 14 and typically along the remainder of the length of the cannula can be about 0.12 mm.
Distal end 14 carries a bevel 98, or a multi-bevel or compound bevel and ends in a point 99 that is dulled or blunt to provide dilation of a preformed track through the skin.