The invention relates to intravenous drip lines which can extend and retract over a distance of many tens of feet.
Medical patients are often placed on an intravenous (i.v.) drip line. Typically this i.v. line is fed from a source such as a 1 liter bag of some per-cent saline or some percent glucose. Typically the line has junction points and insertion points. The junction points allow one i.v. drip line to attach to another line. An insertion points, sometimes combined with one or more junction points, allows for the injection into the line of medication, typically by a syringe adapted to be inserted temporarily into the insertion point.
One goal which doesn't appear to be satisfactorily solved is to make the i.v. drip line extensible so that a patient, for example, is able to get out of bed, while attached to the i.v. drip line and traverse a distance to a bathroom and then return to bed, without having to roll along an i.v. source (“bag”) holder. The bag holder is typically a relatively large and heavy object extending upward and on rollers or wheels. If the patient currently needs to move around, the patient must move the i.v. bag holder along with him or her. This tends to be awkward, especially for a quick trip to the bathroom.
An ideal approach to solving this problem would to have an extensible i.v. tube that could extend and return to its place of origin. This ideal approach would use existing i.v. tubing and such junction points and insertion points which already exist, are approved for medical use by the Food and Drug Administration.
One difficulty can be noted up front: the i.v. tubing is very flexible and relatively of small diameter and relatively thin walled. This difficulty may preclude some direct approaches to answering the question of how to translate the desired result into a workable apparatus.
It is of interest to review prior art. In this conjunction it is noted that at least in one's typical experience in a modern hospital, no such extensible i.v. lines have been encountered. This is based on the inventor's anecdotal experiences.
This mechanical composition invention fulfills a long felt need. Although a number of inventors have turned their hands to proving a solution to the problem outlined in the “Background of the Invention” section above, and no doubt many Medical Doctors and scientists, engineers and inventors have been subject to hospitalization or observations of those hospitalized, the invention herein, if it were obvious, would have already been invented. Therefore, hindsight alone would not be enough to render this invention obvious.
The invention herein uses a helical accordion support structure (“backbone”) backbone on which the i.v. tubing is attached or held. The helical accordion backbone has some tendency to spring back, but this is not relied upon to extend and return the i.v. tubing it carries. The carrier structures keeps the i.v. tubing from getting tangle or kinked.
Instead a centrally located line retractable line, which is located within the center of the helical accordion structure, acts as the retracting mechanism, as it tends to allow the accordion structure to be pulled into an extended position, while upon rewinding the central cord, the helical accordion support structure.
An additional feature to help insure safety, so the i.v. line does not encounter and strain between it and the point of entry of the i.v. line into the patient, is one or more wrist and or armbands to which the i.v. carrier is attached by a short, strong, typically fabric, line The wrist/armband typically uses a Velcro closure, or as will be a double Velcro closure.
This method and apparatus may be used also for patient oxygen lines and for gastro-intestinal tubing, although not necessarily limited to these uses.
For a more complete understanding of the present invention, and the advantages thereof, reference is now made to the following descriptions taken in conjunction with the accompanying drawings, in which:
a shows one method of attaching i.v. drip line to the accordion carrying structure with closed arches;
b shows a second method of attaching i.v. drip line to the accordion carrying structure with open arches;
c shows a the protective tendency of the open or closed arches, tending to protect the i.v. drip line from compression;
d shows a third method of attaching i.v. drip line to the accordion carrying structure with glue;
e shows a fourth method of attaching i.v. drip line to the accordion carrying structure with heat welding;
f shows a fifth method of attaching i.v. drip line to the accordion carrying structure with tape;
a shows the patient “in bed” with the i.v. extensible system in a collapsed mode;
b shows the patient with the i.v. extensible system in an extended position;
a shows one of many possible systems for integrating the invention with other existing i.v. drip line joint elements and existing i.v. drip line injection elements, with bifurcation into male and female blades;
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b shows a male blade with raised bumps;
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c shows a female doubled blade with receptor holes;
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d mated male and female blade; and
The following description is of the best mode presently contemplated for carrying out the invention. This description is not to be taken in a limiting sense, but is merely made for the purpose of describing the general principles of the invention.
The helical accordion support structure 101 provides an indexing topological base such that the sequential ordering of the i.v. drip line 201 is maintained: a first point remains ordered behind a second point in a linear ordering of the i.v. drip line.
The accordion support structure is necessary but not sufficient to have the extensible i.v. drip line apparatus operate. Before coming to the next component, however,
With the molded arches 301 (
In another variation of the molded arches 301 of
As shown in
d shows the i.v. drip tubing 201 attached to the helical accordion support structure 101 by “glue” 310. The glue 310 needs to be compatible with the i.v. drip tubing 201 so as not to result in penetration and contamination of the i.v. drip tubing 201 by the glue 310. The glue 310 also must not cause structural degradation of the helical accordion support structure 101.
e shows the i.v. drip tubing 201 attached to the helical accordion support structure 101 by “adhesive tape” 311. The adhesive of the tape 311 needs to be compatible with the i.v. drip tubing 201 so as not to result in penetration and contamination of the i.v. drip tubing 201 by the tape 31. The tape also must not cause structural degradation of the helical accordion support structure 101.
f shows the i.v. drip tubing 201 attached to the helical accordion support structure 101 by a thermoplastic heat welding method. In this thermoplastic heat welding method, a strip of thermoplastic material 312 is attached to the center of one side of the helical accordion support structure 10 and heat s applied to the thermoplastic material 312 and to the i.v. drip tubing 201. The thermoplastic material 312 may be of the same type plastic as the i.v. drip line 201.
The springiness of the accordion aspect of the helical accordion support structure 101 is easily pulled apart and easily aided in compression by attaching the end 502 of the helical accordion support structure 101, which may be closest to the insertion point of the i.v. line into an arm or wrist vein, to an control element 501 (See
As shown in
By allowing the control element 501 to pay out line length, a person can walk forward and the accordion aspect of the helical accordion support structure 101 will open up, carrying with it the i.v. drip line 201. Thus the i.v. drip line 201 extends out carried by the accordion structure of helical accordion support structure 101. As the person walks back toward the i.v. drip stand and allows control element 501 to allow the central line to retract, the accordion aspect of the helical accordion support structure 101 tend to close up, contracting with the i.v. drip line 201 attached to it.
The retraction ability of central line 401 rewinding into the control element 501 is fairly weak, but combined with the slight compression ability of the accordion aspect of the helical accordion support structure 101, the helical accordion support structure 101 with the attached i.v. drip line 201 are easily pushed backed to a compressed situation where the total length of the helical accordion support structure 101 is shortened to an fully compressed condition. Similarly, the helical accordion support structure 101 and the attached i.v. drip line are easily extensible by releasing the central line 401 by causing the control element to release and pulling on the control element which is attached to one end of the helical accordion support structure 101.
Similarly, depending upon the location of the vein insertion point, a similar Velcro armband 511 with a short line 512 may be attached to a patient's arm and a location on the helical accordion support structure 101.
These two situations are illustrated in
In order to incorporate current drip line 201 devices (dotted “object” in
a shows a bifurcation of the helical accordion support structure 101. The helical accordion support structure 101 branched out into two wings 701, 702. The wings come in male/female pairs.
d shows the mated blade of the male blade 701 with the mated female double 704 blade 702. It shows the protrusions or bumps 703 on the male blade 701 seated in the holes 705 of the female blade 702 in its doubled configuration 704.
Smallest diameter compatible with radius of curvature of i.v. drip line 201 is best because the extra length is 2πr, which compared with the spacing (about h=o.d. of i.v. drip tubing. But one wants also to keep ease of expansion.
Additionally, to complete a kit for installation on existing i.v. stands 503, an attachable bracket 801, which provides for anchoring of the end (
Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations can be made herein without departing from the spirit and scope of the invention as defined by the appended claims. Moreover, the scope of the present application is not intended to be limited to the particular embodiments of the process, machine, manufacture, composition of matter, means, methods and steps described in the specification. As one of ordinary skill in the art will readily appreciate from the disclosure of the present invention, processes, machines, manufacture, compositions of matter, means, methods, or steps, presently existing or later to be developed that perform substantially the same function or achieve substantially the same result as the corresponding embodiments described herein may be utilized according to the present invention.