|Publication number||US3878869 A|
|Publication date||Apr 22, 1975|
|Filing date||May 29, 1973|
|Priority date||May 29, 1972|
|Publication number||US 3878869 A, US 3878869A, US-A-3878869, US3878869 A, US3878869A|
|Inventors||Tsuyoshi Tsuji, Itsuro Yamanouchi|
|Original Assignee||Atomu Kabushiki Kaisha|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (20), Classifications (17)|
|External Links: USPTO, USPTO Assignment, Espacenet|
LIQUID TRANSFUSION PIPE FOR A VERY SMALL QUANTITY United States Patent Yamanouchi et al.
PATENTEUAPRza |975 FIG. 5
LIQUID TRANSFUSION PIPE FOR A VERY SMALL QUANTITY The invention relates to a liquid transfusion pipe for transfusing a small quantity of liquid, and more particularly to a pipe of the kind terminating in connectors and having a capillary passage for controlling the flow rate through a liquid transfusion system adapted to inject Ringers solution or other liquids into the human body.
For transfusing very small quantities of liquid, it is known to adjustably squeese a rubber tube with a pinch cock for obtaining flow rate, down to 120 ml per day or ml per hour. It is, however, difficult with this procedure to control the flow rate when below 5 ml per hour. This is true because at flow rates of less than 5 rnl per hour, precision adjustment of the pinch cock is extremely difficult, and moreover the flow loses its steady state nature. There is frequent need for transfusion at a rate less than 5 ml per hour particularly when treating a newly born baby.
Therefore, it is an object of the invention to provide a liquid transfusion pipe for transfusing a very small quantity of liquid, which pipe includes a capillary passage for maintaining a steady state flow.
It is another object of the invention to provide a liquid transfusion pipe having connectors which permit ready connection with and removal from a liquid transfusion system.
In accordance with the invention, there is provided a liquid transfusion pipe for a very small quantity having a capillary passage the cross-sectional area and the length of which can be varied. Thus, when the liquid transfusion pipe according to the invention is connected in a liquid transfusion system, the flow rate of the liquid to be transfused can be controlled to a desired value so that only an extremely small quantity is injected.
The above and other objects and features of the invention will become apparent from the following detailed description of the embodiments thereof illustrated in the drawings, in which:
FIG. l is a longitudinal section of the liquid transfusion pipe according to the invention,
FIG. 2 is a cross section, to an enlarged scale, taken along the line II-II shown in FIG. 1,
FIG. 3 is a similar cross section of another embodiment,
FIG. 4 is an elevational view of a liquid transfusion system incorporating the pipe according to the invention, and
FIG. 5 is a graph illustrating several examples of the relationship between the available head of the liquid transfusion system of FIG. 4 and the liquid transfusion rate.
n Referring to the drawings the liquid transfusion pipe according to the invention is shown as comprising a tubular member generally denoted by l, which includes a number of axially assembled filaments 2 surrounded by a sleeve 3. The tubular member 1 includes a number of capillary passages 4 defined between adjacent filaments 2. As will clearly be noted from FIG. 2 which shows one example of the tubular member l, the sleeve 3 is moulded from resin so as to firmly encase a number of filaments. 2 surrounded thereby. The filaments 2, which when assembled form capillary passages 4 as mentioned previously, may be formed of synthetic resin such as nylon or polypropylene or of fibre glass. FIG.
3 shows another embodiment of the tubular member having filaments of a shape different from that of the filaments shown in FIG. 2. Each filament of FIG. 3 has axially extending grooves 2a formed therein, which serve as the capillary passages 4. When the filaments are formed of synthetic resin, it is known that any desired cross-sectional shape may be achieved for the filaments in their spinning process, and therefore it should be understood that the profile of the filaments is not limited to those illustrated in FIGS. 2 and 3. Where grooved filaments are used, their apparent diameter is generally greater than the diameter of other shapped filaments. However, it is the total cross-sectional area of capillary passages 4 which is controlling. The crosssectional area depends on the thickness of the filaments, the size of any groove formed therein, the number as well disposition of the filaments, and the degree to which the filaments are compressed when they are encased in the sleeve 3.
The procedure for moulding resin around a bundle of filaments 2 to form the sleeve 3 is not part ofthe invention. A bundle of filaments 2 may, for example, be coated with moulded resin as they are drawn out of thin nozzles.
The tubular member 1 may have a length of I0 cm. and is provided with a pair of connectors 5 and 6 on its opposite ends to permit connection of the tubular member 1 in a liquid transfusion system. One of the connectors comprises a socket 7 while the other connector comprises a plug 8 which is adapted to be in serted into a socket similar to socket 7 of another tubular member permitting thereby connection of a series of tubular members in tandem. The socket 7 is formed with a helical ridge 7a on its inner wall, and the plug 8 is formed on its outer end with a flange 8a which is adapted to engage threadably with the helical ridge 7a of another tubular member. The tubular member 1 and each of the connectors 5 and 6 are assembled by fitting the opposite ends of the tubular member 1 into hollow cylindrical portions 9 and 10 respectively part of connectors 5 and 6, respectively. Each of the connectors 5 and 6 has a path ll or 12 which communicates with the capillary passages formed in the tubular member 1. One of the paths, 1l, is formed in and extends through an axially extending guide member 13 which is integrally formed with the socket 5 and centrally located therein. The other path 12 communicates with an axially extending guide bore 14 centrally formed within the plug 8. The guide member 13 and the guide bore 14 are dimensioned to permit interfitting therebetween. In the FIG. 1 embodiment, a filter l5 is posi tioned in the connector 6 between path 12 and guide bore 14, and advantageously prevents clogging of capillary passages 4.
FIG. 4 is a diagrammatic illustration of a liquid transfusion system. As will be noted, the liquid transfusion pipe or the tubular pipe 1 constructed in accordance with the invention is connected between an irrigator 18 and a cannula 19 by way of a pair of rubber tubes 20 and 21. The interconnection takes place by separately preparing connectors similar to those shown at 5 and 6 and inserting their hollow cylindrical portions similar to those shown at 9 and 10 into the respective tubes 20 and 21. To ensure against inadvertent separation of these cylindrical portions 9 and 10 from tubes 20, 2l, the cylindrical portions are formed with wedge-shaped tabs 9a and 10a thereabout.
With the liquid transfusion pipe ofthe invention, the flow rate therethrough is determined principally by the length of the tubular member 1, the cross-sectional area of its capillary passages, the pressure of the irrigator 18, or the distance between the irrigator and the cannula 19, and the viscosity ofthe liquid to be transfused.
FIG. graphically shows the experimental results in terms of the relationship between the flow rate and the distance between thc irrigator and cannula. For rectilinear curves 1 to 3, the tubular members 1 had a length of cm and substantially similar cross-sectional arca of the capillary passages 4. The curve 4 represents the result obtained with a pair of the transfusion pipes used in plotting the curves 1 to 3, the pair of pipes being connected in parallel. In plotting curves 1 and 4 distilled water was used, for curve 2 ringer lactate and for curve 3 l0 percent glucose. As far as the data shown in FIG. 5 are concerned, it is considered that the flow rate through the liquid transfusion pipe of the invention obeys the Poiseuille-Hagens formula:
As will be readily understood from the foregoing description, a varying flow rate can be obtained using a liquid transfusion pipe having a fixed cross-sectional area for the capillary passages 4, by varying the length of the tube l or by varying the height of the irrigator 18. The use ofa liquid transfusion pipe having different cross-sectional areas for the capillary passages 4 permits even greater control ofthe flow rate. It will be apparent from the foregoing that the use of a liquid transfusion pipe according to the invention assures a steady state flow rate and maintains liquid pressure transfused in the cannula 19 constant, thereby avoiding possibility of coagulation which may occur due to reverse flow through the cannula.
What is claimed is:
1. A liquid transfusion pipe for transfusing a small quantity of liquid and comprising an elongate tubular member having an axially extending capillary passage therein, and a pair of connectors, one at one end of the tubular member and the other at the opposite end of the tubular member, said one of said pair of connectors comprising a socket having a helical ridge on its inner wall and said other of said pair of connectors comprising a plug having a flange, said helical ridge and said flange being adapted for respective engagement with a flange and a helical ridge ofa like plug and a like socket provided on separate connecting lines.
2. A liquid transfusion pipe according to claim l in which the tubular member contains a plurality of filaments between which are defined a plurality of capillary passages, an elongate sleeve encasing the filaments.
3. A liquid transfusion pipe according to claim 2 in which the filaments are substantially circular in cross section.
4. A liquid transfusion pipe according to claim 2 in which the filaments have axially extending grooves formed in their outer periphery, said capillary passages being defined between said filaments in spaces provided by the grooves.
5. A liquid transfusion pipe according to claim 2 in which the sleeve comprises resin moulded around the assembled filaments.
6. A liquid transfusion pipe according to claim 2 in which the filaments are formed of synthetic resin.
7. A liquid transfusion pipe according to claim 2 in which the filaments are formed of fibre glass.
8. A liquid transfusion pipe according to claim 2 in which each of the connectors has a space which cornmunicates with the capillary passages of the tubular
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US1165564 *||Dec 19, 1912||Dec 28, 1915||Schaeffer & Budenberg Mfg Co||Thermometer.|
|US3078878 *||May 25, 1959||Feb 26, 1963||Penn Controls||Capillary element|
|US3250469 *||Aug 5, 1963||May 10, 1966||Bowles Eng Corp||Pure fluid function generating system|
|US3529632 *||Nov 21, 1968||Sep 22, 1970||Moore & Co Samuel||Composite tubing|
|US3630229 *||Apr 9, 1970||Dec 28, 1971||Us Navy||Quiet fluid flow regulator|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4034754 *||Aug 7, 1975||Jul 12, 1977||Baxter Travenol Laboratories, Inc.||Intravenous solution set having a constricted inner diameter portion|
|US4037596 *||Dec 3, 1975||Jul 26, 1977||Burron Medical Products, Inc.||Parenteral administration set with internal valve and flow restrictor|
|US4105029 *||Apr 28, 1977||Aug 8, 1978||Baxter Travenol Laboratories, Inc.||Intravenous solution set having an air access site and constricted inner diameter portion|
|US4146028 *||Mar 29, 1977||Mar 27, 1979||Burron Medical Products, Inc.||Intravenous system having an accumulator tube therein|
|US4621989 *||Jul 15, 1980||Nov 11, 1986||Herwig Burgert||Support disc for pump diaphragm|
|US4781698 *||Apr 9, 1987||Nov 1, 1988||Parren Mark L||Selectable drop size infusion metering device|
|US4892524 *||Oct 30, 1987||Jan 9, 1990||Gordon Smith||Intravenous administration system|
|US5081737 *||Jun 13, 1988||Jan 21, 1992||Gebruder Schmeing Gmbh & Co.||Apparatus for eliminating deposits of floating fibers|
|US6013184 *||Sep 19, 1996||Jan 11, 2000||Asahi Medical Co., Ltd.||Device for depletion of leukocytes|
|US7455072 *||Sep 18, 2003||Nov 25, 2008||I-Flow Corporation||Device for selectively regulating the flow rate of a fluid|
|US7661440 *||Feb 16, 2010||I-Flow Corporation||Device for selectively regulating the flow rate of a fluid|
|US8118061||Jun 19, 2008||Feb 21, 2012||Acacia, Inc.||Variable flow rate controller|
|US8403004||Mar 26, 2013||Medical Product Specialists||Variable flow rate controller|
|US20030054300 *||Sep 15, 2001||Mar 20, 2003||Castaldi Marco J.||Apparatus having similar interstitial passages|
|US20060070669 *||Sep 18, 2003||Apr 6, 2006||I-Flow||Device for selectively regulating the flow rate of a fluid|
|US20090099504 *||Oct 24, 2008||Apr 16, 2009||Eric Mabry||Device for selectively regulating the flow rate of a fluid|
|US20090314352 *||Jun 19, 2008||Dec 24, 2009||Hyun Dongchul D||Variable flow rate controller|
|WO1989001065A1 *||Jun 13, 1988||Feb 9, 1989||Gebrüder Schmeing Gmbh & Co. Kg||Device for preventing the deposit of fly fibre|
|WO1996002289A1 *||Jul 10, 1995||Feb 1, 1996||Abbott Laboratories||Anti-squirting orifice flow control device|
|WO1996020744A1 *||Dec 21, 1995||Jul 11, 1996||Volker Lang||Micro-infusion system|
|U.S. Classification||138/40, 604/246, 138/111|
|International Classification||A61M5/165, A61M39/10, A61M39/08, F16L55/027, A61M5/14|
|Cooperative Classification||A61M2039/1027, F16L55/02763, A61M39/10, A61M5/141, A61M39/08|
|European Classification||A61M39/10, A61M39/08, F16L55/027L, A61M5/14C|