WO2007108540A1 - Implant tube for injecting body fluid leakage-preventing agent for dead body and apparatus for caring dead body by using the same - Google Patents

Implant tube for injecting body fluid leakage-preventing agent for dead body and apparatus for caring dead body by using the same Download PDF

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Publication number
WO2007108540A1
WO2007108540A1 PCT/JP2007/056036 JP2007056036W WO2007108540A1 WO 2007108540 A1 WO2007108540 A1 WO 2007108540A1 JP 2007056036 W JP2007056036 W JP 2007056036W WO 2007108540 A1 WO2007108540 A1 WO 2007108540A1
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WO
WIPO (PCT)
Prior art keywords
insertion tube
fluid leakage
preventing agent
body fluid
main body
Prior art date
Application number
PCT/JP2007/056036
Other languages
French (fr)
Japanese (ja)
Inventor
Tooru Kojima
Original Assignee
Axis International Co., Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Axis International Co., Ltd. filed Critical Axis International Co., Ltd.
Publication of WO2007108540A1 publication Critical patent/WO2007108540A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N1/00Preservation of bodies of humans or animals, or parts thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/31Details
    • A61M2005/3117Means preventing contamination of the medicament compartment of a syringe
    • A61M2005/3118Means preventing contamination of the medicament compartment of a syringe via the distal end of a syringe, i.e. syringe end for mounting a needle cannula
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/28Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle

Definitions

  • the present invention relates to an insertion tube for injecting a bodily fluid leakage preventive agent for preventing leakage of bodily fluid from the corpse by loading and sealing the body cavity of the corpse, particularly the body cavity of the mouth, nose, ear, etc.
  • V related to corpse treatment equipment.
  • the injector 1 containing the jelly-like body fluid leakage preventing agent 2 has an injection port in which the piston 3 is slidably inserted from the rear end portion and the front end thereof is covered with the protective cap 5. 4 and is sealed in a film pack (not shown).
  • the insertion tube 6 to be inserted into a body cavity such as the throat B has a connection part 7 connected to the injection port 4 of the injector 1 at one end and an opening part 8 inserted into the nostril A at the other end. .
  • FIG. 1 A is the nostril, B is the throat, C is the tongue, D is the trachea, and E is the esophagus.
  • A is the nostril
  • B is the throat
  • C is the tongue
  • D is the trachea
  • E is the esophagus.
  • take out the injector 1 from the film pack remove the protective cap 5 of the inlet 4 of the injector 1, fit the connecting portion 7 of the insertion tube 6 to the inlet 4, and connect the insertion tube 6.
  • the opening 8 of the insertion tube 6 is inserted from the nostril A toward the throat B, and the insertion is stopped when the stopper portion 9 of the insertion tube 6 hits the nose tip B.
  • the piston 3 of the injector 1 is pressed, and the gel-like body fluid leakage preventing agent 2 in the injector 1 is injected into the throat B via the insertion tube 6.
  • the fluid leakage preventive agent 2 in the injector 1 After extruding and filling the fluid leakage preventive agent 2 in the injector 1, remove the injector 1 and the insertion tube 6 from the nostril A.
  • the jelly-like body fluid leakage preventing agent as described above does not scatter even if it is easily filled and injected with a syringe even in a narrow body cavity such as a nostril or an ear hole having high fluidity. It has the advantages. In particular, in the case of a jelly in which many highly water-absorbing polymer powders are dispersed, the water absorption performance is high. This makes it possible to prevent the body fluid from absorbing body fluid that leaks and preventing it from leaking outside. However, in the case of the combination of the conventional injector and the insertion tube, there is a problem in its operability and there is a mark or stopper portion indicating the insertion stop position in the middle portion of the elongated insertion tube.
  • Patent Document 1 Japanese Patent Laid-Open No. 10-298001
  • Patent Document 2 Japanese Patent Laid-Open No. 7-265367
  • Patent Document 3 JP-A-8-133901
  • Patent Document 4 Japanese Patent Laid-Open No. 2001-288002
  • Patent Document 5 Japanese Patent No. 3586207
  • the object of the present invention is excellent in operability, and without requiring skill in inserting the insertion tube, it is possible to reliably inject and load the body fluid leakage preventing agent with good workability into a constant application site.
  • An object of the present invention is to provide an insertion tube for injecting a body fluid leakage preventing agent for a corpse and a corpse treatment apparatus using the same.
  • an insertion tube for injecting a bodily fluid leakage preventing agent for a corpse is provided, and a first aspect thereof is a flexible synthetic resin insertion tube.
  • an insertion tube main body having a front end portion closed in a substantially hemispherical shape and having a plurality of apertures on its side surface, and a body fluid leakage preventing agent injector provided at the rear end portion of the insertion tube main body A connecting portion for connecting to the discharge tube portion, and having a stagger portion protruding radially outward at a predetermined position on the insertion tube main body side of the connecting portion.
  • the second aspect is a flexible synthetic resin insertion tube, the tip of which is formed in a substantially hemispherical shape by a plurality of tongue pieces extending outwardly curved toward the radial center. And, at the same time, an opening formed by the ends of the plurality of tongue pieces and a slit between the tongue pieces.
  • An insertion tube main body formed, and a connection portion for connecting to a discharge cylinder portion of a body fluid leakage preventing agent injector provided at a rear end portion of the insertion tube main body, and the insertion tube main body of the connection portion
  • the insertion tube main body is curved at a position separated from the tip by a predetermined distance. Part.
  • the insertion tube for injecting the body fluid leakage preventive agent; and a discharge cylinder portion for connecting to the connection portion of the insertion tube at the tip, and for hooking a finger on the rear end portion
  • a body fluid leakage preventive injector having a cylindrical main body having a flange projecting radially outward and a piston slidably inserted into the cylindrical main body from the rear end side;
  • a corpse treatment device is provided.
  • the cylindrical main body of the body fluid leakage preventing agent injector comprises a cylindrical member having a discharge cylinder at the tip and a cover member covered on the outer periphery thereof, and the collar is The cover member is provided, and the piston is slidably inserted into the cylindrical member.
  • the distal end portion of the flexible synthetic resin insertion tube main body is formed in a substantially hemispherical shape.
  • the side surface has a plurality of apertures, the insertion tube can be smoothly inserted from the nostril to the throat, and when the tip opening comes into contact with the application site, it is blocked and injected with a body fluid leakage prevention agent.
  • the body fluid leakage preventive agent can be injected and loaded smoothly without problems such as difficulty.
  • connection part for connecting to the discharge cylinder part of the body fluid leakage preventing agent injector provided at the rear end part of the insertion pipe body, and the connection part is arranged in a radial direction at a predetermined position on the insertion pipe body side. Because it has an outer protruding stagger portion, the length between inserts can be shortened compared to the case where a steep flange portion is provided in the middle of the elongated insertion tube, and insertion of the insertion tube is not required for skill. It can be carried out smoothly, and it is possible to inject and load the body fluid leakage preventing agent with the hole portion being surely positioned at a constant application site.
  • the distal end portion of the flexible synthetic resin insertion tube main body is formed in a substantially hemispherical shape by a plurality of tongue pieces extending outwardly toward the radial center, and the plurality of tongue pieces Since the opening formed by the opening formed by the tip and the slit between the tongue pieces is formed, when the bodily fluid leakage preventing agent filled in the injector is pushed out by the piston, the bodily fluid leakage preventing agent has a plurality of tongue pieces. As it comes out of the slit between the expanded tongue pieces, its surface area increases.
  • connection part for connecting to the discharge cylinder part of the body fluid leakage preventing agent injector provided at the rear end part of the insertion pipe body, and this connection part has a radial direction at a predetermined position on the insertion pipe body side. Because it has a protruding strobe part, the length between insertions can be shortened compared to the case where a stubbing part is provided in the middle part of an elongated insertion tube, and the insertion of the insertion tube is smooth without requiring skill. In addition, it is possible to reliably inject and load the bodily fluid leakage preventing agent with the opening portion positioned at a constant application site.
  • the insertion tube main body has a curved portion at a position a predetermined distance away from the distal end.
  • the insertion tube can be inserted smoothly without resistance.
  • the treatment apparatus for a corpse of the present invention includes the above-described insertion tube for injecting a bodily fluid leakage preventing agent; a discharge cylinder portion for connecting to the connection portion of the insertion tube at the tip, and a rear end portion.
  • An injector for a body fluid leakage preventing agent having a cylindrical main body having a flange projecting outward in the radial direction for hooking a finger, and a piston slidably inserted into the cylindrical main body at the rear end side.
  • the cylindrical main body of the body fluid leakage preventing agent injector includes a cylindrical member having a discharge cylindrical portion at a tip and a crowned outer periphery thereof. Since the cover is provided on the cover member and the piston is slidably inserted into the cylindrical member, the cost is lower than in the case of integral molding. Can easily manufacture a cylindrical body and the cover member has a polygonal cross section. Or by coloring the cover member or coloring it differently from other members to make it a colorful syringe, so that nurses can easily distinguish between ordinary syringes at the hospital. You can do it, or you can make it clear so that you can see where it is applied. Brief Description of Drawings
  • FIG. 1 is a schematic cross-sectional view showing a usage state of a conventional body treatment apparatus.
  • FIG. 2 shows one embodiment of a corpse treatment apparatus according to the present invention, in which (A) is a front view, (B) is a left side view, and (C) is a right side view.
  • FIG. 3 is a longitudinal sectional view taken along the central axis of the body treatment apparatus shown in FIG.
  • FIG. 4 is a cross-sectional view taken along the central axis of the corpse treatment apparatus shown in FIG.
  • FIG. 5 is a longitudinal sectional view showing an insertion tube of the corpse treatment apparatus according to the present invention.
  • FIG. 6 is a partial side view showing another embodiment of the distal end of the insertion tube of the corpse treatment apparatus according to the present invention.
  • FIG. 7 is a side view showing another embodiment of the insertion tube of the corpse treatment apparatus according to the present invention.
  • FIG. 8 is a partial cross-sectional view showing still another embodiment of the insertion tube of the corpse treatment apparatus according to the present invention.
  • the first feature of the insertion tube for injecting a bodily fluid leakage preventing agent according to the present invention is that the distal end portion of the flexible synthetic resin insertion tube body is formed in a substantially hemispherical shape.
  • the insertion tube can be smoothly inserted from the nostril to the throat.
  • the distal end portion of the insertion tube main body is formed to be closed in a substantially hemispherical shape and has a plurality of apertures on the side surface thereof, it is blocked when the distal end opening comes into contact with the body fluid. The problem of difficulty in injecting the leakage preventive agent can be sufficiently injected.
  • the distal end portion of the insertion tube main body is formed in a substantially hemispherical shape by a plurality of tongue pieces that are curved and extended outward toward the center in the radial direction.
  • An opening formed by an opening formed by the tip of the tongue piece and a slit between the tongue pieces is formed. Therefore, body fluid leakage prevention agent can be sufficiently injected and filled into the injector
  • the body fluid leakage preventing agent pushes out the plurality of tongue pieces and also comes out from the slits between the widened tongue pieces, so that the surface area becomes large. . Therefore, when it comes into contact with the body fluid in the body cavity, an additional effect is obtained that the fluid is quickly sucked into a solid gel having no fluidity, and the body fluid leakage can be prevented more effectively and quickly.
  • the second feature common to the insertion pipe for injecting bodily fluid leakage prevention agent is that the discharge cylinder of the bodily fluid leakage prevention agent injector provided at the rear end portion of the insertion tube main body.
  • the opening portion is surely positioned at the applied site and the body fluid leakage preventing agent can be injected and loaded. Further, when inserting from the nostril to the back of the pharynx, it is preferable to provide a curved portion at a position where the distal end force of the insertion tube main body is separated by a predetermined distance so that the insertion tube can be smoothly inserted without resistance.
  • the insertion tube main body and the connection portion may be integrally formed or may be separate. In the case of a separate body, it is preferable that the connecting portion is formed of a rigid synthetic resin.
  • the connecting portion and the insertion tube main body are joined by an appropriate means such as an adhesive or welding. Further, the stagger portion 44 may be formed at the tip of the connecting portion or may be formed at the intermediate portion of the connecting portion.
  • the corpse treatment apparatus of the present invention has a first feature of using the above-described insertion tube for injecting a bodily fluid leakage preventive agent. This is in that it has a flange projecting outward in the radial direction for hooking a finger on the rear end of the cylindrical body. By providing such a buttocks, a finger can be hooked on this, so that the pouring operation is facilitated.
  • the conventional syringe for preventing leakage of body fluid has a similar external shape to a general syringe, there is a possibility that a nurse may mistake the general syringe in a hospital. In the unlikely event that it is mistaken for a general syringe, it will cause a serious medical accident and must be avoided.
  • the cover member has a polygonal cross section, the cover member is colored, or the color of the other member is different from that of other members.
  • Figs. 2 to 5 show treatment devices for inserting and loading the fluid leakage preventive agent into the throat by inserting through the nostril.
  • Figs. 2 to 4 show the injector 10 and
  • Fig. 5 shows The insertion tube 40 is shown, and the symbol X indicates the body fluid leakage preventing agent accommodated in the injector 10.
  • FIGS. 2 to 4 show the injector 10, and FIG. 4 shows a cross-sectional view of the injector 10 rotated from the state shown in FIG. 2 by 90 ° around the center line.
  • the injector 10 is composed of a cylindrical body 20 and a piston 30, all of which are made of plastic force such as high-density polyethylene, polyester, and polyamide.
  • the cylindrical main body 20 includes a cylindrical member 21 having a discharge cylindrical portion 22 at the tip, and a cover member 25 covered on the outer periphery thereof.
  • the cover member 25 is a cylinder having an octagonal cross section as is apparent from FIG. 2, and is configured so that a nurse can easily discriminate it from a general syringe in a hospital, and the distal end side is It is formed in a slightly tapered shape so that it does not easily fall off when the cylindrical member 21 is inserted. It is also possible to make it possible to clearly grasp the place of application by coloring the cover member or coloring it differently from the color of other members to make a colorful injector. As clearly shown in FIG. 4, the cover member 25 has a pair of flange portions 26 protruding outward in the radial direction for hooking a finger to the rear end portion.
  • the distal end portion of the collar portion 26 is curved in the direction of the discharge cylinder portion 22 so that the finger can easily be hooked. It is preferable to set the height of the flange portion 26 from the outer peripheral surface of the cylindrical member 21 to about 5 to 18 mm, and the degree of curvature of the tip portion within a range of 0 to 50 °. Further, a pair of convex locking portions 23 are formed at the rear end of the cylindrical member 21, and when the collar portion 26 comes into contact with the locking portion 23, a finger is bowed on the collar portion 26. And do the injection operation In this case, the cover member 25 is configured not to move rearward from the rear end of the cylindrical member 21.
  • a protective cap 29 is removably crowned at the distal end opening of the discharge cylinder portion 22 after the body fluid leakage preventing agent of the present invention is filled in the injector 10.
  • the cylindrical member 21 and the cover member 25 are formed separately, but may be formed as a single body.
  • the cylindrical member 21 and the cover member 25 may be joined with an adhesive, or at the contact portion of their tip portions, a hole is fitted into one member and the other member is fitted into the hole. Claw portions may be formed and fixed to each other by their engagement.
  • the piston 30 is slidably inserted into the cylindrical member 21 of the cylindrical main body 20 from the rear end side.
  • the length of the piston 30 is designed to be longer than the length of the cylindrical member 21 so that the entire body fluid leakage preventing agent X in the contents can be pushed out.
  • the piston 30 includes a piston rod 31 having a cross-shaped cross section, and a circular flange portion 32 having a diameter slightly larger than the cross-sectional dimension of the piston rod is formed at the tip of the piston 30.
  • a gasket 34 made of synthetic resin or rubber is also covered.
  • a disc-like portion 35 for touching the finger is formed at the rear end of the piston rod 31 so that the piston rod 31 can be easily pressed with the finger.
  • the piston 30 is formed in the cylindrical member 21 in a state where the gasket 34 is in contact with the inner peripheral surface of the cylindrical member 21 of the injector 10 when a rear end side force is also inserted into the cylindrical member 21 of the cylindrical body 20. It is configured to slide. Furthermore, a ring-shaped ridge 24 protruding slightly inward is formed on the inner peripheral surface in the vicinity of the rear end portion of the cylindrical member 21, and the circular flange portion of the piston rod 31 is formed on the ridge 24.
  • the piston 30 is configured not to easily come out of the cylindrical main body 20 when it hits 32.
  • the piston rod 31 has a cross-shaped cross section, but may have a rod shape such as a circular cross section.
  • the insertion tube 40 is made of a flexible synthetic resin such as a polyester elastomer, a soft chlorinated resin, a rubber, etc., which has the flexibility to rub along the shape of the nasal cavity when inserted into the nostril.
  • the insertion tube 40 is composed of an insertion tube body 40a and a connection portion 43, and the distal end portion 41 of the insertion tube body 40a is formed in a substantially hemispherical shape so as to be easily inserted, and is closed. On the side and in two directions shifted in the direction perpendicular to each other.
  • Each has a pair of opening portions 42, and a rearward end portion is provided with a tapered connection portion 43 that is slightly expanded on the rear side for connection to the discharge cylinder portion 22 of the injector 10. ing. Further, at a predetermined position on the insertion tube main body side of the connection portion 43 (preferably the tip position of the connection portion 43), a cross section having a circular cross section protruding outward in the radial direction so as to surround the outer periphery is formed. .
  • the diameter of the stopper portion 44 needs to be sized so as not to be inserted into a desired body cavity such as a nostril.
  • the opening 42 at the distal end of the insertion tube 40 can be a hole having a desired shape such as a circle or an ellipse, and the position of the distal end force of the insertion tube is preferably about 5 to 30 mm. . Further, the number of the opening portions 42 may be an arbitrary number of about 2 to 6 forces, which is four in this embodiment.
  • the strobe portion 44 determines the length (injection position) that the opening portion 42 reaches when the insertion tube body is inserted into the pharynx through the nostril.
  • the length to the stagger portion 44 is preferably about 100 to 140 mm, and the outer diameter of the insertion tube body 40a is preferably about 3.5 to 7 mm, and the inner diameter is preferably about 2 to 5 mm.
  • the protective cap 29 of the discharge tube portion 22 of the injector 10 is removed, and the discharge tube portion 22 is fitted into the connection portion 43 of the insert tube 40 to insert the insert tube 40. And connect the injector 10.
  • the insertion tube body 40a is inserted from the nostril A (see FIG. 1) toward the throat B, and the insertion is stopped when the stopper portion 44 of the insertion tube 40 hits the nose tip.
  • a lubricant may be applied to the insertion tube main body 40a.
  • the piston 30 of the injector 10 is pressed, and the jelly-like body fluid leakage preventing agent X in the injector 10 is injected into the throat B through the insertion tube 40.
  • the injector 10 and the insertion tube 40 are extracted from the nostril A.
  • the insertion tube 40 is inserted into the nostril A while being connected to the injector 10.
  • the insertion tube 40 is first inserted into the nostril A, and then the injector 10 is connected to the insertion tube 40. May be.
  • FIG. 6 shows a modification of the distal end portion of the insertion tube for injecting a bodily fluid leakage preventing agent according to the present invention.
  • the distal end portion of the insertion tube main body 40a is formed in a substantially hemispherical shape by a plurality of tongue pieces 45 extending outwardly curved toward the center in the radial direction.
  • a mouth is formed.
  • Each tongue 45 has such flexibility that it can be bent outward. Therefore, when the fluid leakage preventive agent filled in the injector is pushed out by the piston, the fluid leakage preventing agent pushes out the plurality of tongue pieces and also comes out from the slit between the expanded tongue pieces. The surface area becomes large.
  • FIG. 7 shows another embodiment of the insertion tube for injecting a bodily fluid leakage preventing agent according to the present invention.
  • the insertion tube main body 40a is curved at a predetermined position from the distal end portion. Except this, it is the same as the insertion tube shown in FIG. By forming such a curved portion 46, when inserting from the nostril to the back of the pharynx, it can be smoothly inserted without resistance.
  • the distal end force of the insertion tube main body 40a is also preferably about 22 to 45 mm, more preferably any part with a distance of about 20 to 30 mm, and the bending angle is preferably 0 ° to 95 °. More preferably, it is 30 to 70 °.
  • the connecting portion 43 is formed as a body at the rear end portion of the insertion tube main body 40a.
  • the connecting portion 43 may be a separate body. An example is shown in Fig. 8.
  • connection portion 43 is separately prepared in advance, but the rear end portion 47 of the insertion tube main body 40a is inserted into the recessed portion 48 formed at the distal end portion of the connection portion 43, for example, an adhesive, Join by appropriate means such as welding.
  • connection portion 43 is preferably formed of a rigid synthetic resin.
  • the stopper portion 44 is formed at the tip of the connecting portion 43.
  • a liquid nonionic surfactant (A) that generates heat when mixed with water and is rapidly soluble in water
  • a specific dispersion stabilizer B It is desirable to use an oil jelly-like body fluid leakage preventing agent obtained by dispersing the superabsorbent coagulant powder (C) in a viscous liquid base containing When such a bodily fluid leakage preventing agent is used, due to the exothermic action of the nonionic surfactant (A) when in contact with bodily fluids, the liquid absorption speed of the superabsorbent resin powder (C) is increased, As a whole, it quickly absorbs and swells the body fluid and solidifies into a solid jelly having no fluidity, thereby effectively preventing leakage of the body fluid.
  • Nonionic surfactants (A) which are liquid at room temperature include coconut oil fatty acid monoethanolamide, coconut oil fatty acid diethanolamide 1: 1 type, coconut oil fatty acid diethanolamide 1: 2 type, polyoxy Ethylene coconut oil fatty acid monoethanolamide, lauric acid diethanolamide, polyoxyethylene lauryl ether, polyoxyethylene cetyl ether, polyoxyethylene higher alcohol ether, polyethylene glycol (average molecular weight of polymerization degree 600 or less), polyoxyethylene poly Oxypropylene glycol (pull nick type nonionic surfactant with addition of ethylene oxide to polypropylene glycol), polyoxyethylene alkyl (alkyl group having 12 to 14 carbon atoms) ether (number of moles of ethylene oxide attached: 7-12 mol) Polyoxyethylene alkyl ether, sorbitan fatty acid esters, surfactants such as polyoxyethylene sorbitan fatty acid esters and the like, may be used in combination either alone or in combination. Among these nonionic surfact
  • liquid nonionic surfactants (A), particularly liquid polyethylene glycol (average molecular weight of the degree of polymerization of about 200 to 600) are the dispersion stabilizer (B) described below, particularly polyalkylene oxide.
  • the thermoplastic non-ionic water-absorbent powder can be easily dissolved at low temperatures (about 30 ° C to 50 ° C), and when mixed with water, it is clear from the following test examples. In addition, when it comes into contact with water, it generates heat and the water temperature rises (increased by about 10 ° C to 12 ° C). Furthermore, since it is a surfactant, it easily mixes and dissolves in water that is compatible with water. As described above, the water-absorbing speed of the highly water-absorbing resin can be increased and quickly solidified into a solid jelly having no fluidity to prevent leakage of body fluids.
  • Test example (exothermic temperature measurement test of test material)
  • Measuring instrument DATA COLLECTOR liquid temperature sensor manufactured by Anritsu Keiki Co., Ltd.
  • PEG200 a liquid nonionic surfactant, immediately generated heat when mixed with water, quickly became soluble in water, and maintained its temperature level for some time.
  • PEG200 a liquid nonionic surfactant
  • PEG200 is a body fluid leakage prevention agent that increases the water absorption rate of highly water-absorbent resin and quickly solidifies into a solid jelly with no fluidity to prevent body fluid leakage. It turns out that it is optimal as a base.
  • the content of the nonionic surfactant (A) is preferably about 10 to 85% by mass, more preferably about 20 to 80% by mass, and still more preferably about 10% to 85% by mass of the total amount of the body fluid leakage preventing agent. 30 to 70% by mass. If the content of the non-ionic surfactant (A) exceeds 85% by mass, there will be no problem with the dispersibility of the superabsorbent resin powder, but there will be no jelly-like liquid. The state is not preferable because it is close to an aqueous solution. On the other hand, if the content of the nonionic surfactant (A) is too low, it is difficult to obtain a good jelly state. In addition to the above-described surfactant (A), a surfactant can be contained as needed in a quantitative ratio that does not impair the above-described effects.
  • the dispersion stabilizer (B) is intended to maintain a uniform dispersion state of the superabsorbent resin powder, and can absorb various aqueous electrolyte solutions, and is hardly affected by the electrolyte concentration.
  • polyalkylene oxide-based thermoplastic non-one water-absorbing resins are preferable, and these resins can absorb various aqueous electrolyte solutions and are almost influenced by the electrolyte concentration. In addition, it can absorb acid and aqueous alkali solution.
  • the content of the dispersion stabilizer (B) is preferably about 0.5 to 40% by mass, more preferably about 1 to 30% by mass, based on the total amount of the body fluid leakage preventing agent. If the content of the dispersion stabilizer (B) is too low, it will be difficult to maintain the uniform dispersibility of the superabsorbent oil-absorbent powder. There is no improvement, and the economic point is favorable.
  • the highly water-absorbent resin powder (C) various kinds of highly water-absorbent resin powders known in the art can be used and are not limited to specific ones.
  • Polyvinyl acrylate, polyacrylate, alginate, cross-linked acrylic acid graft copolymer, copolymer of butyl alcohol and polyacrylic acid, polyethylene glycol polymer, polyacrylamide resin, polyacrylic maleic acid It is possible to suitably use at least one selected from the group consisting of a polymer, a polyethylene oxide polymer, and a polyalginate polymer.
  • the superabsorbent resin powder (C) preferably has a mean particle size of about 18 mesh to 160 mesh (according to Tyler display), more preferably about 30 mesh to 140 mesh.
  • the content of the superabsorbent rosin powder (C) must be the amount necessary to create a non-flowable gel by immediately absorbing and expanding the body fluid without leaking from the body cavity.
  • the content of the superabsorbent rosin powder is preferably about 5 to 50% by mass, more preferably about 15 to 35% by mass, based on the total amount of the body fluid leakage preventing agent.
  • the body fluid leakage preventing agent further includes water-soluble ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, glycerin, methinorea nolecore, ethenolenole nolecore as an auxiliary solvent.
  • Organic solvent (D) such as isopropylenorenoreconole and sodium carboxymethylcellulose for improving fluidity
  • Carboxymethylcellulose, methenorescenellose, polyvinyl alcohol, polyvinylinol pyrrolidone, sora gum, sodium alginate, and / or other thickeners (E) should be included to facilitate viscosity adjustment and improve fluidity.
  • the viscosity of the body fluid leakage preventive agent containing each of the above components is preferably about 6,000 to 50, OOOcPs force S, more preferably about ⁇ to have good fluidity. , 000 to 40,000 c Ps.
  • the viscosity used here is a viscometer (manufactured by Brookfield, USA, “Digital Viscometer” model: DV-1 +), spindle No. 07, rotation speed: 20 rpm, body fluid leakage prevention agent temperature: 20 Force measured at the measurement condition of ° C. If it is a measured value measured under similar conditions, it is not limited to this.
  • the amount of the bodily fluid leakage preventing agent injected and filled into the body cavity can be appropriately set according to the application site.
  • the water absorption capability of the highly water-absorbent resin contained in the oil jelly-like body fluid leakage prevention agent is solidified into 3,000 ml of water to prevent water leakage from inside the body cavity.
  • 5 to 60 g is preferable, and 10 to 40 g is more preferable.
  • the filling amount of the bodily fluid leakage preventive agent (containing 5 to 50% by mass of superabsorbent fat) injected into the throat from the nostril of the corpse is preferably about 8 to 40 g, more preferably about 10 to 25 g.
  • the insertion tube for injecting a bodily fluid leakage preventive agent and the corpse treatment apparatus using the same of the present invention can be easily used for a treatment for preventing body fluid leakage of body cavities, particularly body cavities such as mouth, nose and ear.

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  • Life Sciences & Earth Sciences (AREA)
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  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
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  • Environmental Sciences (AREA)
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  • Infusion, Injection, And Reservoir Apparatuses (AREA)

Abstract

An implant tube for injecting a body fluid leakage-preventing agent into a dead body aiming at achieving excellent handling properties and ensuring the convenient injection and loading of the body fluid leakage-preventing agent constantly at a definite application site, which is an implant tube (40) made of a synthetic resin consisting of an implant tube body (40a) having an almost hemispherically closed front end and a plural number of openings (42) in the side face thereof, a connector part (43) located at the back end part of the implant tube body for connecting to a discharge syringe (22) of an injector (10) for the body fluid leakage-preventing agent, and a stopper part (44) projecting outward in the radius direction at a definite position in the implant tube body side of the connector part. In another embodiment mode, the front end of the implant tube body has an almost hemispherical shape formed by a plural number of curved tongue flaps projecting outward toward the radius direction and openings each formed by a slit between the opening and the tongue flap are provided byt the front end of the individual tongue flaps.

Description

明 細 書  Specification
遺体用の体液漏出防止剤注入用揷入管及びそれを用いた遺体処置装 置  Infusion tube for injecting body fluid leakage prevention agent for corpse and corpse treatment device using the same
技術分野  Technical field
[0001] 本発明は、遺体の体腔、特に口、鼻、耳などの体腔に装填して封止することにより、 遺体からの体液漏出を防止するための体液漏出防止剤注入用挿入管及びそれを用 [0001] The present invention relates to an insertion tube for injecting a bodily fluid leakage preventive agent for preventing leakage of bodily fluid from the corpse by loading and sealing the body cavity of the corpse, particularly the body cavity of the mouth, nose, ear, etc. For
V、た遺体処置装置に関する。 V, related to corpse treatment equipment.
背景技術  Background art
[0002] 一般に、ヒトゃ動物の死亡後には体腔各部の筋肉が弛緩し、胃液、肺液、腹水、排 泄物などの体液が漏出することが多ぐ悪臭や、病原菌による感染の原因ともなって いる。このため、例えば病院では、死亡確認後、遺体の口、鼻、耳、肛門、女性の膣 等の体腔に多量のガーゼ、脱脂綿等を装填し、体液の漏出を防ぐことが行なわれて おり、また、事故や手術後の遺体の開口部にも同様な処置がとられている。しかしな がら、体腔へのガーゼ、脱脂綿等の装填作業の多くは、従業者や看護師等の手によ つて行われることが多ぐその作業の煩雑さや不衛生さと同時に、ガーゼ、脱脂綿等 は吸水能力が低いため、作業中もしくは作業後にしばしば体液が漏出してしまうとい う問題や、作業従事中にこの漏出物質による死後感染の可能性もあり、その解決が 強く求められていた。  [0002] In general, after the death of a human animal, muscles in various parts of the body cavity relax, causing bodily fluids such as gastric fluid, lung fluid, ascites, and excreta to leak, which also causes infection by pathogenic bacteria. Yes. For this reason, for example, in hospitals, after confirming death, body cavities such as the mouth, nose, ears, anus, and woman's vagina are loaded with a large amount of gauze, cotton wool, etc. to prevent leakage of bodily fluids. Similar measures are also taken for the opening of the body after an accident or surgery. However, many of the operations for loading gauze and cotton wool into body cavities are often carried out by the hands of employees and nurses. Due to the low water absorption capacity, there was a problem that body fluids often leaked during or after work, and there was a possibility of postmortem infection due to this leaked substance during work, and there was a strong need for a solution.
[0003] このようなことから、ガーゼ、脱脂綿等に代えて高吸水性榭脂粉末を口、鼻、耳、咽 喉などに装填することが知られており、例えば、注射器を使って口、鼻、耳に高吸水 性榭脂粉末を装填する方法や (特許文献 1:特開平 10— 298001号公報参照)、安 定ィ匕二酸ィ匕塩素を含む吸水性榭脂粉末を、咽喉には粉末のまま、耳孔、鼻孔には 水溶性シートに包んで使用する方法 (特許文献 2 :特開平 7— 265367号公報参照) などが知られている。ところが、このような高吸水性榭脂粉末を装填しょうとしても、流 動性が悪いため、狭い体腔、例えば咽喉部、肛門等には装填することが困難である 。また、鼻孔や耳孔の入口部分だけであれば、このような微粉末を注射器のような注 入器で充填できるが、奥までは充填できない。また、奥まで充填するために注入器を 動力しながら充填しょうとすると、先端から出る微粉末が飛び散り、力えって遺体周辺 を汚すだけである。 [0003] Because of this, it is known to load superabsorbent greave powder in the mouth, nose, ears, throat, etc. instead of gauze, absorbent cotton, etc. For example, using a syringe, A method of loading the nose and ear with a highly water-absorbing fat powder (see Patent Document 1: Japanese Patent Application Laid-Open No. 10-298001), and a water-absorbing fat powder containing stable sodium diacid and chlorine are applied to the throat. There is known a method in which the powder is used in the form of a powder and the ear canal and nostril are wrapped in a water-soluble sheet (see Patent Document 2: JP-A-7-265367). However, even when trying to load such a superabsorbent coagulant powder, it is difficult to load into narrow body cavities such as the throat and anus because of poor fluidity. Moreover, if it is only the entrance part of a nostril or an ear canal, such a fine powder can be filled with an injection device such as a syringe, but cannot be filled to the back. Also, inject the syringe to fill If you try to fill it with power, the fine powder coming out from the tip will splatter and force it to just stain the area around the body.
[0004] このような高吸水性榭脂粉末の充填性や作業性の悪さや、飛散等の問題を解決す るために、近年、粉体でなぐゼリーを用いることが提案されており、例えば、消臭剤 入りの粉末ポリマーを適当量の水で溶かし適当に混合してゼリー状にしたものを用い る方法 (特許文献 3:特開平 8— 133901号公報参照)や、ジメチルアクリルアミドを主 成分とする両親媒性ゲルを用いる方法 (特許文献 4:特開 2001— 288002号公報参 照)、アルコールを主成分とするゼリーの中に高吸水性ポリマー粉体を多数分散させ たものを用いる方法 (特許文献 5:特許第 3586207号公報参照)が知られて 、る。  [0004] In order to solve the problems such as poor filling property and workability of such a superabsorbent resin powder and scattering, it has recently been proposed to use a jelly made of powder. In addition, a method of using a powder polymer containing a deodorant dissolved in an appropriate amount of water and mixing appropriately to form a jelly (see Patent Document 3: JP-A-8-133901) or dimethylacrylamide as a main component (Patent Document 4: Japanese Patent Laid-Open No. 2001-288002), and a method in which a large number of superabsorbent polymer powders are dispersed in an alcohol-based jelly (See Patent Document 5: Japanese Patent No. 3586207).
[0005] このようなゼリー状の体液漏出防止剤を、例えば鼻孔奥の咽喉部に充填する場合 の充填方法について図 1を参照しながら説明すると、特許第 3586207号公報 (特許 文献 5)に記載のように、ゼリー状の体液漏出防止剤 2が収容されている注入器 1は、 後端部からピストン 3が摺動自在に挿入されていると共に、その先端に保護キャップ 5 を被せた注入口 4を備え、フィルムパック(図示せず)で包んでシールした状態にされ ている。咽喉部 B等の体腔に挿入される挿入管 6は、一端に注入器 1の注入口 4に接 続される接続部 7を有し、他端に鼻孔 Aに挿入される開口部 8を有する。  [0005] The filling method in the case of filling such a jelly-like body fluid leakage preventing agent into the throat of the nostril, for example, will be described in Japanese Patent No. 3586207 (Patent Document 5). As shown, the injector 1 containing the jelly-like body fluid leakage preventing agent 2 has an injection port in which the piston 3 is slidably inserted from the rear end portion and the front end thereof is covered with the protective cap 5. 4 and is sealed in a film pack (not shown). The insertion tube 6 to be inserted into a body cavity such as the throat B has a connection part 7 connected to the injection port 4 of the injector 1 at one end and an opening part 8 inserted into the nostril A at the other end. .
[0006] 次に、このようにして用意された遺体処置装置を使用する方法を説明する。図 1〖こ おいて、 Aは鼻孔、 Bは咽喉部、 Cは舌、 Dは気管、 Eは食道である。使用時には、フ イルムパックから注入器 1を取り出し、注入器 1の注入口 4の保護キャップ 5を取り外し 、挿入管 6の接続部 7を注入口 4に嵌め合わせて挿入管 6を接続する。次いで、挿入 管 6の開口部 8を鼻孔 Aから咽喉部 Bに向けて挿入し、挿入管 6のストッパ部 9が鼻先 Bに当たった時点で挿入を停止する。そして、注入器 1のピストン 3を押圧し、注入器 1内のゼリ一状の体液漏出防止剤 2を挿入管 6を経由して咽喉部 Bに注入する。注入 器 1内の体液漏出防止剤 2を押出し、充填した後は、注入器 1と挿入管 6を鼻孔 Aか ら取り除く。  [0006] Next, a method of using the corpse treatment apparatus prepared in this way will be described. In Fig. 1, A is the nostril, B is the throat, C is the tongue, D is the trachea, and E is the esophagus. At the time of use, take out the injector 1 from the film pack, remove the protective cap 5 of the inlet 4 of the injector 1, fit the connecting portion 7 of the insertion tube 6 to the inlet 4, and connect the insertion tube 6. Next, the opening 8 of the insertion tube 6 is inserted from the nostril A toward the throat B, and the insertion is stopped when the stopper portion 9 of the insertion tube 6 hits the nose tip B. Then, the piston 3 of the injector 1 is pressed, and the gel-like body fluid leakage preventing agent 2 in the injector 1 is injected into the throat B via the insertion tube 6. After extruding and filling the fluid leakage preventive agent 2 in the injector 1, remove the injector 1 and the insertion tube 6 from the nostril A.
[0007] 前記したようなゼリー状の体液漏出防止剤は、流動性が高ぐ鼻孔、耳穴等の狭い 体腔であっても充填され易ぐ注入器で圧入しても飛散することがな 、と 、う利点を有 する。特に、高吸水性ポリマー粉体を多数分散させたゼリーの場合、吸水性能が高く 、このポリマーが体腔力 漏出する体液を吸収し、外部へ漏出することを防止すること が可能となる。しカゝしながら、従来の注入器と挿入管の組合せの場合、その操作性に 問題があると共に、細長い挿入管の中間部に挿入停止位置を示すマーク又はストッ パ部を有しているため、挿入管の挿入に熟練を要し、常に一定した施用部位に確実 に体液漏出防止剤を注入'装填することが難しいという問題がある。また、挿入管の 先端に開口があるため、施用部位に先端開口が当接した時に塞がれ、体液漏出防 止剤を注入し難くなると ヽぅ問題もある。 [0007] The jelly-like body fluid leakage preventing agent as described above does not scatter even if it is easily filled and injected with a syringe even in a narrow body cavity such as a nostril or an ear hole having high fluidity. It has the advantages. In particular, in the case of a jelly in which many highly water-absorbing polymer powders are dispersed, the water absorption performance is high. This makes it possible to prevent the body fluid from absorbing body fluid that leaks and preventing it from leaking outside. However, in the case of the combination of the conventional injector and the insertion tube, there is a problem in its operability and there is a mark or stopper portion indicating the insertion stop position in the middle portion of the elongated insertion tube. However, there is a problem that it requires difficulty in inserting the insertion tube, and it is difficult to reliably inject and load the body fluid leakage preventing agent at a constant application site. In addition, since there is an opening at the distal end of the insertion tube, there is a problem if the distal end opening comes into contact with the application site and is blocked, making it difficult to inject the bodily fluid leakage preventing agent.
特許文献 1:特開平 10— 298001号公報  Patent Document 1: Japanese Patent Laid-Open No. 10-298001
特許文献 2:特開平 7— 265367号公報  Patent Document 2: Japanese Patent Laid-Open No. 7-265367
特許文献 3 :特開平 8— 133901号公報  Patent Document 3: JP-A-8-133901
特許文献 4:特開 2001— 288002号公報  Patent Document 4: Japanese Patent Laid-Open No. 2001-288002
特許文献 5:特許第 3586207号公報  Patent Document 5: Japanese Patent No. 3586207
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0008] 従って、本発明の目的は、操作性に優れ、挿入管の挿入に熟練を要することなぐ 常に一定した施用部位に確実に体液漏出防止剤を作業性良く注入'装填することが できる、遺体用の体液漏出防止剤注入用挿入管及びそれを用いた遺体処置装置を 提供することにある。 [0008] Therefore, the object of the present invention is excellent in operability, and without requiring skill in inserting the insertion tube, it is possible to reliably inject and load the body fluid leakage preventing agent with good workability into a constant application site. An object of the present invention is to provide an insertion tube for injecting a body fluid leakage preventing agent for a corpse and a corpse treatment apparatus using the same.
課題を解決するための手段  Means for solving the problem
[0009] 前記目的を達成するために、本発明によれば、遺体用の体液漏出防止剤注入用 挿入管が提供され、その第一の態様は、可撓性の合成樹脂製挿入管であって、先 端部が略半球状に閉鎖されて形成され、且つその側面に複数の開孔部を有する挿 入管本体と、挿入管本体の後端部に設けられた体液漏出防止剤の注入器の吐出筒 部に接続するための接続部とを有し、該接続部の挿入管本体側の所定位置に半径 方向外側に突出したストツバ部を有していることを特徴としている。  [0009] In order to achieve the above object, according to the present invention, an insertion tube for injecting a bodily fluid leakage preventing agent for a corpse is provided, and a first aspect thereof is a flexible synthetic resin insertion tube. In addition, an insertion tube main body having a front end portion closed in a substantially hemispherical shape and having a plurality of apertures on its side surface, and a body fluid leakage preventing agent injector provided at the rear end portion of the insertion tube main body A connecting portion for connecting to the discharge tube portion, and having a stagger portion protruding radially outward at a predetermined position on the insertion tube main body side of the connecting portion.
[0010] また、第二の態様は、可撓性の合成樹脂製挿入管であって、先端部が半径方向中 心へ向けて外側に湾曲して延びる複数の舌片により略半球状に形成されて!、ると共 に、該複数の舌片の先端により形成される開口と舌片間のスリットからなる開口部が 形成されている挿入管本体と、挿入管本体の後端部に設けられた体液漏出防止剤 の注入器の吐出筒部に接続するための接続部とを有し、該接続部の挿入管本体側 の所定位置に半径方向外側に突出したストツバ部を有していることを特徴としている 前記いずれについても好適な態様によれば、前記挿入管本体は、先端から所定距 離離れた位置に湾曲部を有する。 [0010] Further, the second aspect is a flexible synthetic resin insertion tube, the tip of which is formed in a substantially hemispherical shape by a plurality of tongue pieces extending outwardly curved toward the radial center. And, at the same time, an opening formed by the ends of the plurality of tongue pieces and a slit between the tongue pieces. An insertion tube main body formed, and a connection portion for connecting to a discharge cylinder portion of a body fluid leakage preventing agent injector provided at a rear end portion of the insertion tube main body, and the insertion tube main body of the connection portion According to a preferred aspect of any of the above, the insertion tube main body is curved at a position separated from the tip by a predetermined distance. Part.
[0011] さらに本発明によれば、前記体液漏出防止剤注入用挿入管と;先端に上記挿入管 の接続部に接続するための吐出筒部を有すると共に、後端部に指を引っ掛けるため の半径方向外側に突出した鍔部を有する筒状本体と、該筒状本体に後端部側から 摺動自在に挿入されているピストンとを有する体液漏出防止剤用注入器とを備えて [0011] Further, according to the present invention, the insertion tube for injecting the body fluid leakage preventive agent; and a discharge cylinder portion for connecting to the connection portion of the insertion tube at the tip, and for hooking a finger on the rear end portion A body fluid leakage preventive injector having a cylindrical main body having a flange projecting radially outward and a piston slidably inserted into the cylindrical main body from the rear end side;
V、ることを特徴とする遺体の処置装置が提供される。 V. A corpse treatment device is provided.
好適な態様においては、前記体液漏出防止剤用注入器の筒状本体は、先端に吐 出筒部を有する円筒状部材と、その外周に被冠されたカバー部材とからなり、前記鍔 部は上記カバー部材に設けられており、また前記ピストンは上記円筒状部材に摺動 自在に挿入されている。  In a preferred embodiment, the cylindrical main body of the body fluid leakage preventing agent injector comprises a cylindrical member having a discharge cylinder at the tip and a cover member covered on the outer periphery thereof, and the collar is The cover member is provided, and the piston is slidably inserted into the cylindrical member.
発明の効果  The invention's effect
[0012] 本発明に係る遺体用の体液漏出防止剤注入用挿入管の第一の態様によれば、可 橈性の合成樹脂製挿入管本体の先端部が略半球状に閉鎖されて形成され、且つそ の側面に複数の開孔部を有するため、鼻孔から咽喉部にかけてスムーズに挿入管を 挿入できると共に、施用部位に先端開口が当接した時に塞がれて体液漏出防止剤 を注入し難くなるというような問題はなぐスムーズに体液漏出防止剤を注入'装填す ることができる。また、挿入管本体の後端部に設けられた体液漏出防止剤の注入器 の吐出筒部に接続するための接続部を有し、この接続部の挿入管本体側の所定位 置に半径方向外側に突出したストツバ部を有して 、るため、細長 、挿入管の中間部 にストツバ部を設けた場合に比べて挿入間の長さを短くでき、挿入管の挿入を熟練を 要することなくスムーズに行うことができ、且つ、常に一定した施用部位に確実に開孔 部が位置して体液漏出防止剤を注入'装填することができる。  [0012] According to the first aspect of the insertion tube for injecting a bodily fluid leakage preventing agent for a corpse according to the present invention, the distal end portion of the flexible synthetic resin insertion tube main body is formed in a substantially hemispherical shape. In addition, since the side surface has a plurality of apertures, the insertion tube can be smoothly inserted from the nostril to the throat, and when the tip opening comes into contact with the application site, it is blocked and injected with a body fluid leakage prevention agent. The body fluid leakage preventive agent can be injected and loaded smoothly without problems such as difficulty. Also, it has a connection part for connecting to the discharge cylinder part of the body fluid leakage preventing agent injector provided at the rear end part of the insertion pipe body, and the connection part is arranged in a radial direction at a predetermined position on the insertion pipe body side. Because it has an outer protruding stagger portion, the length between inserts can be shortened compared to the case where a steep flange portion is provided in the middle of the elongated insertion tube, and insertion of the insertion tube is not required for skill. It can be carried out smoothly, and it is possible to inject and load the body fluid leakage preventing agent with the hole portion being surely positioned at a constant application site.
[0013] 一方、本発明に係る遺体用の体液漏出防止剤注入用挿入管の第二の態様によれ ば、可撓性の合成樹脂製挿入管本体の先端部が半径方向中心へ向けて外側に湾 曲して延びる複数の舌片により略半球状に形成されていると共に、該複数の舌片の 先端により形成される開口と舌片間のスリットからなる開口部が形成されているため、 注入器に充填されている体液漏出防止剤がピストンにより押し出される時、体液漏出 防止剤が複数の舌片を押し広げて出ると共に、拡開された舌片間のスリットからも出 るためにその表面積が広くなる。そのため、体腔内の体液と接触した際、素早く吸液 して流動性の無い固いゲルになり、より効果的に迅速に体液漏出の防止が可能とな る。また、挿入管本体の後端部に設けられた体液漏出防止剤の注入器の吐出筒部 に接続するための接続部を有し、この接続部の挿入管本体側の所定位置に半径方 向外側に突出したストツバ部を有しているため、細長い挿入管の中間部にストツバ部 を設けた場合に比べて挿入間の長さを短くでき、挿入管の挿入を熟練を要することな くスムーズに行うことができ、且つ、常に一定した施用部位に確実に開孔部が位置し て体液漏出防止剤を注入'装填することができる。 On the other hand, according to the second aspect of the insertion tube for injecting a bodily fluid leakage preventing agent for a corpse according to the present invention. For example, the distal end portion of the flexible synthetic resin insertion tube main body is formed in a substantially hemispherical shape by a plurality of tongue pieces extending outwardly toward the radial center, and the plurality of tongue pieces Since the opening formed by the opening formed by the tip and the slit between the tongue pieces is formed, when the bodily fluid leakage preventing agent filled in the injector is pushed out by the piston, the bodily fluid leakage preventing agent has a plurality of tongue pieces. As it comes out of the slit between the expanded tongue pieces, its surface area increases. Therefore, when it comes into contact with bodily fluid in the body cavity, the liquid is quickly sucked into a solid gel having no fluidity, and it is possible to prevent bodily fluid leakage more effectively and quickly. Also, it has a connection part for connecting to the discharge cylinder part of the body fluid leakage preventing agent injector provided at the rear end part of the insertion pipe body, and this connection part has a radial direction at a predetermined position on the insertion pipe body side. Because it has a protruding strobe part, the length between insertions can be shortened compared to the case where a stubbing part is provided in the middle part of an elongated insertion tube, and the insertion of the insertion tube is smooth without requiring skill. In addition, it is possible to reliably inject and load the bodily fluid leakage preventing agent with the opening portion positioned at a constant application site.
[0014] また、前記遺体用の体液漏出防止剤注入用挿入管の好適な態様によれば、前記 挿入管本体は、先端カゝら所定距離離れた位置に湾曲部を有するため、鼻孔から咽 頭部奥まで挿入する際、抵抗なくスムーズに挿入管を挿入できる。  [0014] Further, according to a preferred aspect of the insertion tube for injecting a bodily fluid leakage preventing agent for a corpse, the insertion tube main body has a curved portion at a position a predetermined distance away from the distal end. When inserting to the back of the head, the insertion tube can be inserted smoothly without resistance.
[0015] さらに、本発明の遺体の処置装置は、前記した体液漏出防止剤注入用挿入管と; 先端に上記挿入管の接続部に接続するための吐出筒部を有すると共に、後端部に 指を引っ掛けるための半径方向外側に突出した鍔部を有する筒状本体と、該筒状本 体に後端部側力 摺動自在に挿入されているピストンとを有する体液漏出防止剤用 注入器とを備えているため、前記した挿入管使用の効果を発揮すると共に、筒状本 体の後端部に指を引っ掛けるための鍔部を有するため、遺体の体腔への体液漏出 防止剤の注入操作をより簡便に作業性良く行うことができる。  [0015] Furthermore, the treatment apparatus for a corpse of the present invention includes the above-described insertion tube for injecting a bodily fluid leakage preventing agent; a discharge cylinder portion for connecting to the connection portion of the insertion tube at the tip, and a rear end portion. An injector for a body fluid leakage preventing agent having a cylindrical main body having a flange projecting outward in the radial direction for hooking a finger, and a piston slidably inserted into the cylindrical main body at the rear end side. In addition to exerting the effects of using the insertion tube described above, and having a buttocks for hooking a finger to the rear end of the cylindrical main body, injection of a body fluid leakage preventing agent into the body cavity of the corpse The operation can be performed more easily and with good workability.
[0016] さらに、遺体処置装置の好適な態様にお!、ては、前記体液漏出防止剤用注入器 の筒状本体は、先端に吐出筒部を有する円筒状部材と、その外周に被冠されたカバ 一部材とからなり、前記鍔部は上記カバー部材に設けられており、また前記ピストン は上記円筒状部材に摺動自在に挿入されているため、一体成形の場合に比べて低 コストで容易に筒状本体を製造できると共に、カバー部材を断面多角形の外形にし たり、カバー部材を着色したり、あるいはその色を他の部材の色と異なるように着色し てカラフルな注入器とすることにより、病院で看護師が一般の注射器と間違えずに容 易に判別できる、あるいはまた施用場所を鮮明に把握できるよう〖こすることができる。 図面の簡単な説明 [0016] Further, according to a preferred aspect of the corpse treatment apparatus, the cylindrical main body of the body fluid leakage preventing agent injector includes a cylindrical member having a discharge cylindrical portion at a tip and a crowned outer periphery thereof. Since the cover is provided on the cover member and the piston is slidably inserted into the cylindrical member, the cost is lower than in the case of integral molding. Can easily manufacture a cylindrical body and the cover member has a polygonal cross section. Or by coloring the cover member or coloring it differently from other members to make it a colorful syringe, so that nurses can easily distinguish between ordinary syringes at the hospital. You can do it, or you can make it clear so that you can see where it is applied. Brief Description of Drawings
[図 1]従来の遺体処置装置の使用状態を示す概略断面図である。 FIG. 1 is a schematic cross-sectional view showing a usage state of a conventional body treatment apparatus.
[図 2]本発明に係る遺体処置装置の一実施態様を示し、(A)は正面図、(B)は左側 面図、(C)は右側面図である。  FIG. 2 shows one embodiment of a corpse treatment apparatus according to the present invention, in which (A) is a front view, (B) is a left side view, and (C) is a right side view.
[図 3]図 2に示す遺体処置装置の中心軸線に沿った縦断面図である。  3 is a longitudinal sectional view taken along the central axis of the body treatment apparatus shown in FIG.
[図 4]図 2に示す遺体処置装置の中心軸線に沿った横断面図である。  4 is a cross-sectional view taken along the central axis of the corpse treatment apparatus shown in FIG.
[図 5]本発明に係る遺体処置装置の挿入管を示す縦断面図である。  FIG. 5 is a longitudinal sectional view showing an insertion tube of the corpse treatment apparatus according to the present invention.
[図 6]本発明に係る遺体処置装置の挿入管の先端の他の実施態様を示す部分側面 図である。  FIG. 6 is a partial side view showing another embodiment of the distal end of the insertion tube of the corpse treatment apparatus according to the present invention.
[図 7]本発明に係る遺体処置装置の挿入管の他の実施態様を示す側面図である。  FIG. 7 is a side view showing another embodiment of the insertion tube of the corpse treatment apparatus according to the present invention.
[図 8]本発明に係る遺体処置装置の挿入管のさらに他の実施態様を示す部分断面 図である。 FIG. 8 is a partial cross-sectional view showing still another embodiment of the insertion tube of the corpse treatment apparatus according to the present invention.
符号の説明 Explanation of symbols
1,: 10 注入器  1: 10 injector
20 筒状本体  20 Tubular body
21 円筒状部材  21 Cylindrical member
22 吐出筒部  22 Discharge cylinder
23 係止部  23 Locking part
24 突条部  24 ridge
25 カバー部材  25 Cover member
26 鍔部  26 Buttocks
27 ストツバ部  27 Stubbing section
28 舌片  28 Tongue pieces
29 保護キャップ  29 Protective cap
30 ピストン 31 ピストンロッド 30 pistons 31 Piston rod
32 円形フランジ杳  32 Round flange 杳
33 フランジ部  33 Flange
34 ガスケット  34 Gasket
35 円板状部  35 Disc-shaped part
40 挿入管  40 Insertion tube
40a 挿入管本体  40a Insertion tube body
42 開孔部  42 Openings
43 接続部  43 Connection
45 舌片  45 Tongue
46 湾曲部  46 Curved part
X 体液漏出防止剤  X Body fluid leakage prevention agent
A 鼻孔  A nostril
B 咽喉部  B Throat
C 舌  C tongue
D 気管  D trachea
E 食道  E esophagus
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0019] 本発明に係る遺体用の体液漏出防止剤注入用挿入管の第一の特徴は、可撓性の 合成樹脂製挿入管本体の先端部が略半球状に形成されている点にあり、これにより 鼻孔から咽喉部にかけてスムーズに挿入管を挿入できる。第一の態様によれば、挿 入管本体の先端部が略半球状に閉鎖されて形成され、且つその側面に複数の開孔 部を有するため、先端開口が当接した時に塞がれて体液漏出防止剤を注入し難くな るというような問題はなぐ体液漏出防止剤を充分に注入することができる。 [0019] The first feature of the insertion tube for injecting a bodily fluid leakage preventing agent according to the present invention is that the distal end portion of the flexible synthetic resin insertion tube body is formed in a substantially hemispherical shape. Thus, the insertion tube can be smoothly inserted from the nostril to the throat. According to the first aspect, since the distal end portion of the insertion tube main body is formed to be closed in a substantially hemispherical shape and has a plurality of apertures on the side surface thereof, it is blocked when the distal end opening comes into contact with the body fluid. The problem of difficulty in injecting the leakage preventive agent can be sufficiently injected.
[0020] 一方、第二の態様においては、挿入管本体の先端部が半径方向中心へ向けて外 側に湾曲して延びる複数の舌片により略半球状に形成されて 、ると共に、該複数の 舌片の先端により形成される開口と舌片間のスリットからなる開口部が形成されてい る。そのため、体液漏出防止剤を充分に注入することができると共に、注入器に充填 されている体液漏出防止剤がピストンにより押し出される時、体液漏出防止剤が複数 の舌片を押し広げて出ると共に、拡開された舌片間のスリットからも出るためにその表 面積が広くなる。そのため、体腔内の体液と接触した際、素早く吸液して流動性の無 い固いゲルになり、より効果的に迅速に体液漏出の防止が可能となる、という付加的 な効果が得られる。 [0020] On the other hand, in the second aspect, the distal end portion of the insertion tube main body is formed in a substantially hemispherical shape by a plurality of tongue pieces that are curved and extended outward toward the center in the radial direction. An opening formed by an opening formed by the tip of the tongue piece and a slit between the tongue pieces is formed. Therefore, body fluid leakage prevention agent can be sufficiently injected and filled into the injector When the body fluid leakage preventing agent is pushed out by the piston, the body fluid leakage preventing agent pushes out the plurality of tongue pieces and also comes out from the slits between the widened tongue pieces, so that the surface area becomes large. . Therefore, when it comes into contact with the body fluid in the body cavity, an additional effect is obtained that the fluid is quickly sucked into a solid gel having no fluidity, and the body fluid leakage can be prevented more effectively and quickly.
[0021] また、前記いずれの態様の体液漏出防止剤注入用挿入管にも共通する第二の特 徴は、挿入管本体の後端部に設けられた体液漏出防止剤の注入器の吐出筒部に接 続するための接続部を有し、この接続部の挿入管本体側の所定位置に半径方向外 側に突出したストッパ部を有している点にある。このため、細長い挿入管の中間部に ストツバ部を設けた場合に比べて挿入間の長さを短くでき、挿入管の挿入を熟練を要 することなくスムーズに行うことができ、且つ、常に一定した施用部位に確実に開孔部 が位置して体液漏出防止剤を注入'装填することができる。また、鼻孔から咽頭部奥 まで挿入する際、抵抗なくスムーズに挿入管を挿入できるように、挿入管本体の先端 力も所定距離離れた位置に湾曲部を設けることが好ましい。なお、挿入管本体と接 続部は一体成形してもよぐあるいは別体としてもよい。別体とする場合、接続部は剛 性な合成樹脂で形成することが好ましぐこの接続部と挿入管本体は接着剤、溶着 等の適当な手段により接合する。また、ストツバ部 44は接続部の先端に形成してもよ ぐあるいは接続部の中間部に形成してもよい。  [0021] Further, the second feature common to the insertion pipe for injecting bodily fluid leakage prevention agent according to any of the above aspects is that the discharge cylinder of the bodily fluid leakage prevention agent injector provided at the rear end portion of the insertion tube main body. A connecting portion for connecting to the connecting portion, and a stopper portion protruding radially outward at a predetermined position on the insertion tube main body side of the connecting portion. For this reason, the length between insertions can be shortened compared to the case where a staggered portion is provided in the middle of the elongated insertion tube, the insertion tube can be inserted smoothly without requiring skill, and always constant. The opening portion is surely positioned at the applied site and the body fluid leakage preventing agent can be injected and loaded. Further, when inserting from the nostril to the back of the pharynx, it is preferable to provide a curved portion at a position where the distal end force of the insertion tube main body is separated by a predetermined distance so that the insertion tube can be smoothly inserted without resistance. The insertion tube main body and the connection portion may be integrally formed or may be separate. In the case of a separate body, it is preferable that the connecting portion is formed of a rigid synthetic resin. The connecting portion and the insertion tube main body are joined by an appropriate means such as an adhesive or welding. Further, the stagger portion 44 may be formed at the tip of the connecting portion or may be formed at the intermediate portion of the connecting portion.
[0022] さらに、本発明の遺体処置装置は、前記した体液漏出防止剤注入用挿入管を用い ることを第一の特徴としているが、第二の特徴として、体液漏出防止剤用注入器の筒 状本体の後端部に指を引っ掛けるための半径方向外側に突出した鍔部を有する点 にある。このような鍔部を設けることにより、これに指を引っ掛けることができるため注 入操作がし易くなる。  [0022] Furthermore, the corpse treatment apparatus of the present invention has a first feature of using the above-described insertion tube for injecting a bodily fluid leakage preventive agent. This is in that it has a flange projecting outward in the radial direction for hooking a finger on the rear end of the cylindrical body. By providing such a buttocks, a finger can be hooked on this, so that the pouring operation is facilitated.
[0023] さらに、従来の体液漏出防止剤用注入器は一般の注射器と類似の外形を有するた め、病院で看護師が一般の注射器と間違える恐れがある。万が一、一般の注射器と 間違えた場合、重大な医療事故となるので絶対に避けなければならない。そのため には、体液漏出防止剤用注入器の筒状本体を、先端に吐出筒部を有する円筒状部 材と、その外周に被冠されたカバー部材とに分けることが好ましい。これにより、一体 成形の場合に比べて低コストで容易に筒状本体を製造できるという利点の他に、カバ 一部材を断面多角形の外形にしたり、カバー部材を着色したり、あるいはその色を他 の部材の色と異なるように着色してカラフルな注入器とすることにより、病院で看護師 が一般の注射器と間違えずに容易に判別できる、あるいはまた施用場所を鮮明に把 握でさるよう〖こすることがでさる。 [0023] Furthermore, since the conventional syringe for preventing leakage of body fluid has a similar external shape to a general syringe, there is a possibility that a nurse may mistake the general syringe in a hospital. In the unlikely event that it is mistaken for a general syringe, it will cause a serious medical accident and must be avoided. For that purpose, it is preferable to divide the cylindrical main body of the injector for body fluid leakage preventing agent into a cylindrical member having a discharge cylinder at the tip and a cover member covered by the outer periphery thereof. This makes it one In addition to the advantage that a cylindrical body can be easily manufactured at a lower cost compared to the case of molding, the cover member has a polygonal cross section, the cover member is colored, or the color of the other member is different from that of other members. By coloring it differently from the color and making it a colorful syringe, nurses can easily distinguish it from ordinary syringes in the hospital, or they should be able to grasp the place of application clearly. It is out.
実施例  Example
[0024] 以下、添付図面を参照しながら、本発明の体液漏出防止剤注入用挿入管及びそ れを用いた遺体処置装置の各態様の具体例につ!、て説明する。  [0024] Hereinafter, specific examples of each aspect of a body fluid leakage preventing agent injection insertion tube and a corpse treatment apparatus using the same according to the present invention will be described with reference to the accompanying drawings.
図 2〜図 5は、鼻孔から挿入して咽喉部に前記体液漏出防止剤を注入 '装填するた めの処置装置を示しており、図 2〜図 4はその注入器 10を、図 5は挿入管 40を示して おり、符号 Xは注入器 10内に収容された体液漏出防止剤を示している。  Figs. 2 to 5 show treatment devices for inserting and loading the fluid leakage preventive agent into the throat by inserting through the nostril. Figs. 2 to 4 show the injector 10 and Fig. 5 shows The insertion tube 40 is shown, and the symbol X indicates the body fluid leakage preventing agent accommodated in the injector 10.
[0025] 図 2〜図 4は注入器 10を示しているが、図 4は図 2に示す状態から中心線のまわり に 90° 回転した状態の断面図を示している。図 2〜図 4に示されるように、注入器 10 は、いずれも高密度ポリエチレン、ポリエステル、ポリアミド等のプラスチック力も作製 された筒状本体 20とピストン 30とから構成されている。筒状本体 20は、先端に吐出 筒部 22を有する円筒状部材 21と、その外周に被冠されたカバー部材 25とからなる。  FIGS. 2 to 4 show the injector 10, and FIG. 4 shows a cross-sectional view of the injector 10 rotated from the state shown in FIG. 2 by 90 ° around the center line. As shown in FIGS. 2 to 4, the injector 10 is composed of a cylindrical body 20 and a piston 30, all of which are made of plastic force such as high-density polyethylene, polyester, and polyamide. The cylindrical main body 20 includes a cylindrical member 21 having a discharge cylindrical portion 22 at the tip, and a cover member 25 covered on the outer periphery thereof.
[0026] カバー部材 25は、図 2から明らかなように断面八角形の筒体であり、病院で看護師 が一般の注射器と間違えずに容易に判別できるように構成されていると共に、先端 側がやや先細のテーパ状に形成され、円筒状部材 21を嵌入したときに容易に脱落 しないように構成されている。なお、カバー部材を着色したり、あるいはその色を他の 部材の色と異なるように着色してカラフルな注入器とすることにより、施用場所を鮮明 に把握できるようにすることも可能である。図 4に明瞭に示されているように、カバー部 材 25は、その後端部に指を引っ掛けるための半径方向外側に突出した一対の鍔部 26を有する。鍔部 26の先端部分は、吐出筒部 22の方向に湾曲しており、指が容易 に引っ掛力り易いようになつている。鍔部 26の円筒状部材 21の外周面からの高さは 約 5〜18mm、先端部の湾曲の程度は 0〜50° の範囲内に設定することが好ましい 。さらに、円筒状部材 21の後端には一対の凸状の係止部 23が形成されており、鍔部 26がこの係止部 23に当接することによって、鍔部 26に指を弓 Iつ掛けて注入操作をし た時に、カバー部材 25が円筒状部材 21の後端より後方向に移動しな 、ように構成さ れている。また、吐出筒部 22の先端開口部には、注入器 10内に本発明の体液漏出 防止剤が充填された後に保護キャップ 29が取り外し可能に被冠される。なお、本実 施態様においては、円筒状部材 21とカバー部材 25は別体に形成されているが、一 体成形してもよい。また、円筒状部材 21とカバー部材 25は、接着剤により接合しても よぐあるいはそれらの先端部分の接触箇所において、一方の部材に孔部を、他方 の部材に該孔部に嵌合する爪部を形成してこれらの係合により互いに固定されるよう にしてもよい。 [0026] The cover member 25 is a cylinder having an octagonal cross section as is apparent from FIG. 2, and is configured so that a nurse can easily discriminate it from a general syringe in a hospital, and the distal end side is It is formed in a slightly tapered shape so that it does not easily fall off when the cylindrical member 21 is inserted. It is also possible to make it possible to clearly grasp the place of application by coloring the cover member or coloring it differently from the color of other members to make a colorful injector. As clearly shown in FIG. 4, the cover member 25 has a pair of flange portions 26 protruding outward in the radial direction for hooking a finger to the rear end portion. The distal end portion of the collar portion 26 is curved in the direction of the discharge cylinder portion 22 so that the finger can easily be hooked. It is preferable to set the height of the flange portion 26 from the outer peripheral surface of the cylindrical member 21 to about 5 to 18 mm, and the degree of curvature of the tip portion within a range of 0 to 50 °. Further, a pair of convex locking portions 23 are formed at the rear end of the cylindrical member 21, and when the collar portion 26 comes into contact with the locking portion 23, a finger is bowed on the collar portion 26. And do the injection operation In this case, the cover member 25 is configured not to move rearward from the rear end of the cylindrical member 21. In addition, a protective cap 29 is removably crowned at the distal end opening of the discharge cylinder portion 22 after the body fluid leakage preventing agent of the present invention is filled in the injector 10. In this embodiment, the cylindrical member 21 and the cover member 25 are formed separately, but may be formed as a single body. In addition, the cylindrical member 21 and the cover member 25 may be joined with an adhesive, or at the contact portion of their tip portions, a hole is fitted into one member and the other member is fitted into the hole. Claw portions may be formed and fixed to each other by their engagement.
[0027] 一方、ピストン 30は、上記筒状本体 20の円筒状部材 21に、後端部側から摺動自 在に挿入されている。ピストン 30の長さは、内容物の体液漏出防止剤 Xを全て押し出 せるように、円筒状部材 21の長さよりも長くなるように設計されている。ピストン 30は、 断面十字形のピストンロッド 31を有し、その先端部には該ピストンロッドの断面寸法よ りも若干大きな直径の円形フランジ部 32が形成されている。該円形フランジ部 32か ら突出して形成されたフランジ部 33周囲には、合成樹脂やゴム等力も作製されたガ スケット 34が被冠されている。また、ピストンロッド 31の後端には、ピストンロッド 31を 指で押圧し易いように、指を当てる円板状部 35が形成されている。ピストン 30は、筒 状本体 20の円筒状部材 21に後端部側力も挿入したときに、上記ガスケット 34が注 入器 10の円筒状部材 21内周面に接触した状態で円筒状部材 21内を摺動するよう に構成されている。さらに、円筒状部材 21の後端部近傍の内周面には僅かに内方 に突出したリング状の突条部 24が形成されており、この突条部 24にピストンロッド 31 の円形フランジ部 32が当たることによって、ピストン 30が筒状本体 20から容易に抜け 出ないように構成されている。なお、本実施態様ではピストンロッド 31は断面十字形 であるが、断面円形等の棒状であってもよい。  On the other hand, the piston 30 is slidably inserted into the cylindrical member 21 of the cylindrical main body 20 from the rear end side. The length of the piston 30 is designed to be longer than the length of the cylindrical member 21 so that the entire body fluid leakage preventing agent X in the contents can be pushed out. The piston 30 includes a piston rod 31 having a cross-shaped cross section, and a circular flange portion 32 having a diameter slightly larger than the cross-sectional dimension of the piston rod is formed at the tip of the piston 30. Around the flange portion 33 formed so as to protrude from the circular flange portion 32, a gasket 34 made of synthetic resin or rubber is also covered. In addition, a disc-like portion 35 for touching the finger is formed at the rear end of the piston rod 31 so that the piston rod 31 can be easily pressed with the finger. The piston 30 is formed in the cylindrical member 21 in a state where the gasket 34 is in contact with the inner peripheral surface of the cylindrical member 21 of the injector 10 when a rear end side force is also inserted into the cylindrical member 21 of the cylindrical body 20. It is configured to slide. Furthermore, a ring-shaped ridge 24 protruding slightly inward is formed on the inner peripheral surface in the vicinity of the rear end portion of the cylindrical member 21, and the circular flange portion of the piston rod 31 is formed on the ridge 24. The piston 30 is configured not to easily come out of the cylindrical main body 20 when it hits 32. In this embodiment, the piston rod 31 has a cross-shaped cross section, but may have a rod shape such as a circular cross section.
[0028] 挿入管 40は、鼻孔に挿入した際、鼻腔形状に沿って橈む柔軟性を有するポリエス テルエラストマー、軟質塩化ビュル榭脂、ゴム等の可撓性の合成樹脂から作製され ている。図 5に示されるように、挿入管 40は挿入管本体 40aと接続部 43とからなり、 挿入管本体 40aの先端部 41は鼻孔力も挿入し易いように略半球状に形成されて閉 鎖されており、且つその側面に、位置をずらした 2ケ所に、互いに直行する方向のそ れぞれ一対の開孔部 42を有すると共に、後端部には、前記注入器 10の吐出筒部 2 2に接続するための後側にやや拡開したテーパ状の接続部 43が設けられている。ま た、接続部 43の挿入管本体側の所定位置 (好ましくは接続部 43の先端位置)には、 外周を囲繞するように半径方向外側に突出した断面円形のストツバ部 44が形成され ている。ストッパ部 44の直径は、鼻孔等の所望の体腔に挿入されないようなサイズと する必要がある。 [0028] The insertion tube 40 is made of a flexible synthetic resin such as a polyester elastomer, a soft chlorinated resin, a rubber, etc., which has the flexibility to rub along the shape of the nasal cavity when inserted into the nostril. As shown in FIG. 5, the insertion tube 40 is composed of an insertion tube body 40a and a connection portion 43, and the distal end portion 41 of the insertion tube body 40a is formed in a substantially hemispherical shape so as to be easily inserted, and is closed. On the side and in two directions shifted in the direction perpendicular to each other. Each has a pair of opening portions 42, and a rearward end portion is provided with a tapered connection portion 43 that is slightly expanded on the rear side for connection to the discharge cylinder portion 22 of the injector 10. ing. Further, at a predetermined position on the insertion tube main body side of the connection portion 43 (preferably the tip position of the connection portion 43), a cross section having a circular cross section protruding outward in the radial direction so as to surround the outer periphery is formed. . The diameter of the stopper portion 44 needs to be sized so as not to be inserted into a desired body cavity such as a nostril.
[0029] 上記挿入管 40の先端部の開孔部 42は、円形、楕円形等の所望の形状をした孔と することができ、その位置は挿入管先端力も約 5〜30mmの距離が好ましい。また、 開孔部 42の数は、本実施態様では 4個である力 2〜6個程度の任意の数でよい。ま た、上記ストツバ部 44は、挿入管本体を鼻孔から通して咽頭部に挿入する際の開孔 部 42の到達する長さ(注入位置)を決めるが、挿入管本体 40aの先端カゝらストツバ部 44までの長さは約 100〜 140mmが好ましぐまた、挿入管本体 40aの外径は約 3. 5〜7mm、内径は約 2〜5mmであることが好ましい。  [0029] The opening 42 at the distal end of the insertion tube 40 can be a hole having a desired shape such as a circle or an ellipse, and the position of the distal end force of the insertion tube is preferably about 5 to 30 mm. . Further, the number of the opening portions 42 may be an arbitrary number of about 2 to 6 forces, which is four in this embodiment. The strobe portion 44 determines the length (injection position) that the opening portion 42 reaches when the insertion tube body is inserted into the pharynx through the nostril. The length to the stagger portion 44 is preferably about 100 to 140 mm, and the outer diameter of the insertion tube body 40a is preferably about 3.5 to 7 mm, and the inner diameter is preferably about 2 to 5 mm.
[0030] 上記遺体処置装置の使用に際しては、まず、注入器 10の吐出筒部 22の保護キヤ ップ 29を取り外し、挿入管 40の接続部 43に吐出筒部 22を嵌め合わせて挿入管 40 と注入器 10を接続する。次いで、挿入管本体 40aを鼻孔 A (図 1参照)から咽喉部 B に向けて挿入し、挿入管 40のストッパ部 44が鼻先に当たった時点で挿入を停止する 。この際、挿入抵抗を軽減するために、挿入管本体 40aに潤滑剤を塗布してもよい。 そして、注入器 10のピストン 30を押圧し、注入器 10内のゼリー状の体液漏出防止剤 Xを挿入管 40を経由して咽喉部 Bに注入する。注入器 10内の体液漏出防止剤 Xを 押出し、充填した後は、注入器 10と挿入管 40を鼻孔 Aカゝら抜き出す。なお、上記操 作方法では、挿入管 40を注入器 10に接続した状態で鼻孔 Aに挿入したが、挿入管 40を先に鼻孔 Aに挿入し、次いで挿入管 40に注入器 10を接続してもよい。  [0030] When using the above corpse treatment apparatus, first, the protective cap 29 of the discharge tube portion 22 of the injector 10 is removed, and the discharge tube portion 22 is fitted into the connection portion 43 of the insert tube 40 to insert the insert tube 40. And connect the injector 10. Next, the insertion tube body 40a is inserted from the nostril A (see FIG. 1) toward the throat B, and the insertion is stopped when the stopper portion 44 of the insertion tube 40 hits the nose tip. At this time, in order to reduce insertion resistance, a lubricant may be applied to the insertion tube main body 40a. Then, the piston 30 of the injector 10 is pressed, and the jelly-like body fluid leakage preventing agent X in the injector 10 is injected into the throat B through the insertion tube 40. After the body fluid leakage preventing agent X in the injector 10 is extruded and filled, the injector 10 and the insertion tube 40 are extracted from the nostril A. In the above operation method, the insertion tube 40 is inserted into the nostril A while being connected to the injector 10. However, the insertion tube 40 is first inserted into the nostril A, and then the injector 10 is connected to the insertion tube 40. May be.
[0031] 図 6は、本発明に係る体液漏出防止剤注入用挿入管の先端部の変形例を示して いる。  [0031] Fig. 6 shows a modification of the distal end portion of the insertion tube for injecting a bodily fluid leakage preventing agent according to the present invention.
この変形例においては、図 6に示すように、挿入管本体 40aの先端部が半径方向 中心へ向けて外側に湾曲して延びる複数の舌片 45により略半球状に形成されて!ヽ ると共に、該複数の舌片 45の先端により形成される開口と舌片間のスリットからなる開 口部が形成されている。各舌片 45は、外側に曲げることができるような柔軟性を有す る。そのため、注入器に充填されている体液漏出防止剤がピストンにより押し出される 時、体液漏出防止剤は複数の舌片を押し広げて出ると共に、拡開された舌片間のス リットからも出るためにその表面積が広くなる。 In this modified example, as shown in FIG. 6, the distal end portion of the insertion tube main body 40a is formed in a substantially hemispherical shape by a plurality of tongue pieces 45 extending outwardly curved toward the center in the radial direction. An opening formed by the tips of the plurality of tongue pieces 45 and a slit between the tongue pieces. A mouth is formed. Each tongue 45 has such flexibility that it can be bent outward. Therefore, when the fluid leakage preventive agent filled in the injector is pushed out by the piston, the fluid leakage preventing agent pushes out the plurality of tongue pieces and also comes out from the slit between the expanded tongue pieces. The surface area becomes large.
[0032] 図 7は、本発明に係る体液漏出防止剤注入用挿入管の他の実施態様を示している この実施態様においては、前記した挿入管本体 40aを先端部から所定位置で湾曲 させたこと以外は、前記図 5に示す挿入管と同じである。このような湾曲部 46を形成 することにより、鼻孔から咽頭部奥まで挿入する際、抵抗なくスムーズに挿入すること ができる。湾曲させる位置は、挿入管本体 40aの先端力も約 22〜45mm、より好まし くは約 20〜30mmの距離の任意の部分が好ましぐまた、湾曲角度は 0度〜 95° が 好ましぐより好ましくは 30〜70° である。 FIG. 7 shows another embodiment of the insertion tube for injecting a bodily fluid leakage preventing agent according to the present invention. In this embodiment, the insertion tube main body 40a is curved at a predetermined position from the distal end portion. Except this, it is the same as the insertion tube shown in FIG. By forming such a curved portion 46, when inserting from the nostril to the back of the pharynx, it can be smoothly inserted without resistance. As for the bending position, the distal end force of the insertion tube main body 40a is also preferably about 22 to 45 mm, more preferably any part with a distance of about 20 to 30 mm, and the bending angle is preferably 0 ° to 95 °. More preferably, it is 30 to 70 °.
[0033] 前記した各実施態様では、挿入管本体 40aの後端部に接続部 43がー体成形され ているが、接続部 43を別体としてもよい。その一例を図 8に示す。  [0033] In each of the above-described embodiments, the connecting portion 43 is formed as a body at the rear end portion of the insertion tube main body 40a. However, the connecting portion 43 may be a separate body. An example is shown in Fig. 8.
挿入管本体 40aと接続部 43は予め別個に作製されるが、接続部 43の先端部に形 成された凹陥部 48に、挿入管本体 40aの後端部 47を挿入し、例えば接着剤、溶着 等の適当な手段により接合する。このように挿入管本体 40aと接続部 43を別体とする 場合、接続部 43は剛性な合成樹脂で形成することが好ましい。なお、この実施態様 の場合、ストツバ部 44は接続部 43の先端に形成されて 、る。  The insertion tube main body 40a and the connection portion 43 are separately prepared in advance, but the rear end portion 47 of the insertion tube main body 40a is inserted into the recessed portion 48 formed at the distal end portion of the connection portion 43, for example, an adhesive, Join by appropriate means such as welding. Thus, when the insertion tube main body 40a and the connection portion 43 are separated, the connection portion 43 is preferably formed of a rigid synthetic resin. In the case of this embodiment, the stopper portion 44 is formed at the tip of the connecting portion 43.
[0034] 前記した本発明の遺体処置装置により遺体の口、鼻、耳等の体腔に注入 '装填す る体液漏出防止剤としては、従来公知のゼリー状の各種体液漏出防止剤を用 Vヽるこ とができる力 特に好ましくは、水と混和すると発熱し、速やかに水に可溶な液状のノ ユオン性界面活性剤 (A)と、これに溶解した後述する特定の分散安定剤 (B)とを含 有する粘稠液基剤に、高吸水性榭脂粉末 (C)を分散させてなるオイルゼリー状の体 液漏出防止剤を用いることが望ましい。このような体液漏出防止剤を用いた場合、体 液と接触した時の上記ノニオン性界面活性剤 (A)の発熱作用により、上記高吸水性 榭脂粉末 (C)の吸液速度を高め、全体的に速やかに体液を吸収'膨潤して流動性 の無い固いゼリー状に固化し、体液漏出防止を効果的に行うことができる。 [0035] 室温で液状のノ-オン性界面活性剤 (A)としては、ヤシ油脂肪酸モノエタノールァ ミド、ヤシ油脂肪酸ジエタノールアミド 1: 1型、ヤシ油脂肪酸ジエタノールアミド 1: 2型 、ポリオキシエチレンヤシ油脂肪酸モノエタノールアミド、ラウリン酸ジエタノールアミド 、ポリオキシエチレンラウリルエーテル、ポリオキシエチレンセチールエーテル、ポリオ キシエチレン高級アルコールエーテル、ポリエチレングリコール(重合度の平均分子 量が 600以下)、ポリオキシエチレンポリオキシプロピレングリコール(ポリプロピレング リコールにエチレンォキシドを付加したプル口ニック型非イオン界面活性剤)、ポリオ キシエチレンアルキル (アルキル基の炭素数 12〜 14)エーテル (エチレンオキサイド の付カ卩モル数: 7〜 12モル)等のポリオキシエチレンアルキルエーテル系、ソルビタン 脂肪酸エステル系、ポリオキシエチレンソルビタン脂肪酸エステル系などの界面活性 剤が挙げられ、これらを単独で又は 2種以上を組み合わせて用いることができる。こ れらのノ-オン性界面活性剤 (A)の中でも、液状のポリエチレングリコール (重合度 の平均分子量が約 200〜600)が好まし!/、。 [0034] As a bodily fluid leakage preventive agent that is injected and loaded into a body cavity such as the mouth, nose, and ear of the corpse by the corpse treatment apparatus of the present invention described above, various conventionally known jelly-like bodily fluid leakage preventive agents are used. Particularly preferred is a liquid nonionic surfactant (A) that generates heat when mixed with water and is rapidly soluble in water, and a specific dispersion stabilizer (B It is desirable to use an oil jelly-like body fluid leakage preventing agent obtained by dispersing the superabsorbent coagulant powder (C) in a viscous liquid base containing When such a bodily fluid leakage preventing agent is used, due to the exothermic action of the nonionic surfactant (A) when in contact with bodily fluids, the liquid absorption speed of the superabsorbent resin powder (C) is increased, As a whole, it quickly absorbs and swells the body fluid and solidifies into a solid jelly having no fluidity, thereby effectively preventing leakage of the body fluid. [0035] Nonionic surfactants (A) which are liquid at room temperature include coconut oil fatty acid monoethanolamide, coconut oil fatty acid diethanolamide 1: 1 type, coconut oil fatty acid diethanolamide 1: 2 type, polyoxy Ethylene coconut oil fatty acid monoethanolamide, lauric acid diethanolamide, polyoxyethylene lauryl ether, polyoxyethylene cetyl ether, polyoxyethylene higher alcohol ether, polyethylene glycol (average molecular weight of polymerization degree 600 or less), polyoxyethylene poly Oxypropylene glycol (pull nick type nonionic surfactant with addition of ethylene oxide to polypropylene glycol), polyoxyethylene alkyl (alkyl group having 12 to 14 carbon atoms) ether (number of moles of ethylene oxide attached: 7-12 mol) Polyoxyethylene alkyl ether, sorbitan fatty acid esters, surfactants such as polyoxyethylene sorbitan fatty acid esters and the like, may be used in combination either alone or in combination. Among these nonionic surfactants (A), liquid polyethylene glycol (average molecular weight of the degree of polymerization is about 200 to 600) is preferred! /.
[0036] これらの液状のノ-オン性界面活性剤 (A)、特に液状のポリエチレングリコール (重 合度の平均分子量が約 200〜600)は、後述する分散安定剤 (B)、特にポリアルキ レンオキサイド系の熱可塑性ノ-オン型吸水性榭脂粉末を、低温 (約 30°C〜50°C) で容易に溶解することができ、また、水との混和時、以下に示す試験例から明らかな ように、水に接触すると発熱して水温が上昇し(10°C〜12°C程度上昇)、さらに、界 面活性剤なので水との相性が良ぐ水と容易に混和、溶解し、前記したように高吸水 性榭脂の吸水速度を高め、速やかに流動性の無い固いゼリー状に固化して体液漏 出防止をすることができる。 [0036] These liquid nonionic surfactants (A), particularly liquid polyethylene glycol (average molecular weight of the degree of polymerization of about 200 to 600) are the dispersion stabilizer (B) described below, particularly polyalkylene oxide. The thermoplastic non-ionic water-absorbent powder can be easily dissolved at low temperatures (about 30 ° C to 50 ° C), and when mixed with water, it is clear from the following test examples. In addition, when it comes into contact with water, it generates heat and the water temperature rises (increased by about 10 ° C to 12 ° C). Furthermore, since it is a surfactant, it easily mixes and dissolves in water that is compatible with water. As described above, the water-absorbing speed of the highly water-absorbing resin can be increased and quickly solidified into a solid jelly having no fluidity to prevent leakage of body fluids.
[0037] 試験例 (供試原料の発熱温度測定試験) [0037] Test example (exothermic temperature measurement test of test material)
試験方法:  Test method:
30mlのビーカーに表 1に示す各原料 10gを秤量して入れ、次にイオン交換水 8gを 注入したときの混合液の発熱温度を、以下の条件で測定した。  10 g of each raw material shown in Table 1 was weighed into a 30 ml beaker, and then the exothermic temperature of the mixed solution when 8 g of ion exchange water was injected was measured under the following conditions.
測定器:安立計器 (株)製 DATA COLLECTORの液体用温度センサー。  Measuring instrument: DATA COLLECTOR liquid temperature sensor manufactured by Anritsu Keiki Co., Ltd.
測定時の室温: 22. 3°C。  Room temperature during measurement: 22.3 ° C.
試験結果を表 1に併せて示す。 [0038] [表 1] The test results are also shown in Table 1. [0038] [Table 1]
Figure imgf000016_0001
上記表 1に示すように、液状のノ-オン性界面活性剤である PEG200の場合、水と 混和すると直ちに発熱し、速やかに水に可溶となり、またその温度レベルをある程度 の時間維持できた。これに対して、アルコール系溶剤である無水グリセリン、エチレン グリコール、エチルアルコールの場合、水と混和した後に僅かに発熱する力 その温 度レベルがかなり低レ、。このことから、液状のノニオン性界面活性剤である PEG200 は、高吸水性榭脂の吸水速度を高め、速やかに流動性の無い固いゼリー状に固化 して体液漏出防止を図る体液漏出防止剤の基剤として最適であることがわかる。
Figure imgf000016_0001
As shown in Table 1, PEG200, a liquid nonionic surfactant, immediately generated heat when mixed with water, quickly became soluble in water, and maintained its temperature level for some time. . On the other hand, in the case of anhydrous glycerin, ethylene glycol, and ethyl alcohol, which are alcoholic solvents, the ability to generate a slight heat after mixing with water has a fairly low temperature level. Therefore, PEG200, a liquid nonionic surfactant, is a body fluid leakage prevention agent that increases the water absorption rate of highly water-absorbent resin and quickly solidifies into a solid jelly with no fluidity to prevent body fluid leakage. It turns out that it is optimal as a base.
[0039] 上記ノ-オン性界面活性剤 (A)の含有量は、体液漏出防止剤全体量の約 10〜85 質量%が好ましぐより好ましくは約 20〜80質量%、さらに好ましくは約 30〜70質量 %である。ノ-オン性界面活性剤 (A)の含有量が 85質量%を越えて多量に配合さ れると、高吸水性榭脂粉末の分散性には問題ないが、ゼリー状になり難ぐ液の状態 は水溶液に近くなるので好ましくない。一方、ノニオン性界面活性剤 (A)の含有量が 低すぎると、良好なゼリー状態とすることが困難になるので好ましくない。また、前記し たノ-オン性界面活性剤 (A)の他に、前記した効果を損わない量的割合で必要に応 じてァ-オン性界面活性剤を含有することもできる。  [0039] The content of the nonionic surfactant (A) is preferably about 10 to 85% by mass, more preferably about 20 to 80% by mass, and still more preferably about 10% to 85% by mass of the total amount of the body fluid leakage preventing agent. 30 to 70% by mass. If the content of the non-ionic surfactant (A) exceeds 85% by mass, there will be no problem with the dispersibility of the superabsorbent resin powder, but there will be no jelly-like liquid. The state is not preferable because it is close to an aqueous solution. On the other hand, if the content of the nonionic surfactant (A) is too low, it is difficult to obtain a good jelly state. In addition to the above-described surfactant (A), a surfactant can be contained as needed in a quantitative ratio that does not impair the above-described effects.
[0040] 前記分散安定剤 (B)は、高吸水性榭脂粉末の均一な分散状態を保持させるため のものであり、各種電解質水溶液の吸収が可能で、電解質濃度の影響を殆ど受けな 、ポリアルキレンオキサイド系の熱可塑性ノ-オン型吸水性榭脂、アクリル酸の共重 合体のカルボキシビュルポリマー、アクリル酸の共重合体のカルボキシビュルポリマ 一 Zアルカリ中和剤、親油性スメクタイト、合成へクトライト、天然へクトライト、及びべ ントナイトよりなる群力 選ばれた少なくとも 1種が用いられる。これらの分散安定剤 (B )の中でも、ポリアルキレンオキサイド系の熱可塑性ノ-オン型吸水性榭脂が好ましく 、この榭脂は、各種電解質水溶液の吸収が可能で、電解質濃度の影響を殆ど受け ず、酸やアルカリ水溶液の吸収が可能である。 [0040] The dispersion stabilizer (B) is intended to maintain a uniform dispersion state of the superabsorbent resin powder, and can absorb various aqueous electrolyte solutions, and is hardly affected by the electrolyte concentration. , Polyalkylene oxide thermoplastic non-ionic water-absorbent resin, carboxybule polymer of acrylic acid copolymer, carboxybule polymer of acrylic acid copolymer 1 Z alkali neutralizer, lipophilic smectite, synthesis At least one selected from group power consisting of hectorite, natural hectorite, and bentonite is used. Among these dispersion stabilizers (B), polyalkylene oxide-based thermoplastic non-one water-absorbing resins are preferable, and these resins can absorb various aqueous electrolyte solutions and are almost influenced by the electrolyte concentration. In addition, it can absorb acid and aqueous alkali solution.
[0041] 分散安定剤 (B)の含有量は、体液漏出防止剤全体量の約 0. 5〜40質量%が好ま しぐより好ましくは約 1〜30質量%である。分散安定剤 (B)の含有量が低すぎると、 高吸水性榭脂粉末の均一な分散性を保持し難くなり、一方、 40質量%を越えて多量 に配合してもそれ以上の効果の改善は見られず、経済性の点力 好ましくな 、。  [0041] The content of the dispersion stabilizer (B) is preferably about 0.5 to 40% by mass, more preferably about 1 to 30% by mass, based on the total amount of the body fluid leakage preventing agent. If the content of the dispersion stabilizer (B) is too low, it will be difficult to maintain the uniform dispersibility of the superabsorbent oil-absorbent powder. There is no improvement, and the economic point is favorable.
[0042] 前記高吸水性榭脂粉末 (C)としては、従来知られて!/ヽる各種高吸水性榭脂の粉末 を用いることができ、特定のものに限定されないが、それらの中でも、ポリビニルアタリ レート、ポリアクリル酸塩、アルギン酸塩、アクリル酸グラフト共重合体架橋物、ビュル アルコールとポリアクリル酸の共重合物、ポリエチレングリコール系ポリマー、ポリアク リルアミド系榭脂、ポリアクリル酸マレイン酸の共重合物、ポリエチレンオキサイド系ポ リマー、及びポリアルギン酸塩系ポリマーよりなる群力も選ばれた少なくとも 1種を好 適に用いることができる。  [0042] As the highly water-absorbent resin powder (C), various kinds of highly water-absorbent resin powders known in the art can be used and are not limited to specific ones. Polyvinyl acrylate, polyacrylate, alginate, cross-linked acrylic acid graft copolymer, copolymer of butyl alcohol and polyacrylic acid, polyethylene glycol polymer, polyacrylamide resin, polyacrylic maleic acid It is possible to suitably use at least one selected from the group consisting of a polymer, a polyethylene oxide polymer, and a polyalginate polymer.
[0043] 前記高吸水性榭脂粉末 (C)は、平均粒度が約 18メッシュ〜 160メッシュ (Tyler表 示による)の粉体が好ましぐより好ましくは約 30メッシュ〜 140メッシュである。  [0043] The superabsorbent resin powder (C) preferably has a mean particle size of about 18 mesh to 160 mesh (according to Tyler display), more preferably about 30 mesh to 140 mesh.
また、高吸水性榭脂粉末 (C)の含有量は、遺体内の体液を体腔から漏出すること なく直ちに吸収,膨脹して流動性のないゲルを作成する必要な量でなければならな い。高吸水性榭脂粉末の含有量は、体液漏出防止剤全体量の約 5〜50質量%が好 ましぐより好ましくは約 15〜35質量%である。  In addition, the content of the superabsorbent rosin powder (C) must be the amount necessary to create a non-flowable gel by immediately absorbing and expanding the body fluid without leaking from the body cavity. . The content of the superabsorbent rosin powder is preferably about 5 to 50% by mass, more preferably about 15 to 35% by mass, based on the total amount of the body fluid leakage preventing agent.
[0044] また、前記体液漏出防止剤は、さらに補助溶剤としての水に可溶なエチレングリコ ール、プロピレングリコール、ジエチレングリコール、トリエチレングリコール、グリセリン 、メチノレアノレコーノレ、ェチノレアノレコーノレ、イソプロピノレアノレコーノレ等のァノレコーノレ系 有機溶剤 (D)及び流動性を向上させるためのカルボキシメチルセルロースナトリウム 、カルボキシメチルセルロース、メチノレセノレロース、ポリビニルアルコール、ポリビニノレ ピロリドン、ソラガム、アルギン酸ナトリウム等の増粘剤 (E)のいずれか又は両方を含 有することにより、粘度調整が容易となり、流動性を向上させることができ、咽喉部等 の狭い体腔でも、よりスムーズに注入'装填することが可能となる。さらに、殺菌剤、防 カビ ·防腐剤、消臭剤及び香料よりなる群から選ばれた少なくとも 1種を含有すること により、これらの所望の効果も併せて発揮することができる。 [0044] Further, the body fluid leakage preventing agent further includes water-soluble ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, glycerin, methinorea nolecore, ethenolenole nolecore as an auxiliary solvent. , Organic solvent (D) such as isopropylenorenoreconole and sodium carboxymethylcellulose for improving fluidity , Carboxymethylcellulose, methenorescenellose, polyvinyl alcohol, polyvinylinol pyrrolidone, sora gum, sodium alginate, and / or other thickeners (E) should be included to facilitate viscosity adjustment and improve fluidity. It is possible to inject and load more smoothly even in narrow body cavities such as the throat. Furthermore, by containing at least one selected from the group consisting of bactericides, fungicides / preservatives, deodorants, and fragrances, these desired effects can also be exhibited.
[0045] 以上のような各成分を含有する体液漏出防止剤の粘度は、良好な流動性を持った めに ίま、約 6, 000〜50, OOOcPs力 S好ましく、より好ましく ίま約 10, 000〜40, 000c Psである。 [0045] The viscosity of the body fluid leakage preventive agent containing each of the above components is preferably about 6,000 to 50, OOOcPs force S, more preferably about ί to have good fluidity. , 000 to 40,000 c Ps.
なお、ここでいう粘度は、粘度計 (米国ブルックフィールド社製、「デジタル粘度計」 型式: DV— 1 + )を用い、スピンドル No. 07、回転数: 20rpm、使用体液漏出防止 剤温度: 20°Cの測定条件で測定した値である力 これに限定されるものではなぐ同 様な条件で測定した測定値であればょ 、。  The viscosity used here is a viscometer (manufactured by Brookfield, USA, “Digital Viscometer” model: DV-1 +), spindle No. 07, rotation speed: 20 rpm, body fluid leakage prevention agent temperature: 20 Force measured at the measurement condition of ° C. If it is a measured value measured under similar conditions, it is not limited to this.
なお、前記ノ-オン性界面活性剤 (A)の含有量が低くなるほど、従って高吸水性榭 脂粉末 (C)の含有量が高くなるほど、体液漏出防止剤がゼリー状になる時間は短く なり、また液の粘度は上昇するので、これらの配合量を調節することにより、ゼリー状 になる時間や所望の用途 (施用部位)に応じた液粘度となるように調節することができ る。  The lower the content of the nonionic surfactant (A), and thus the higher the content of the superabsorbent resin powder (C), the shorter the time it takes for the bodily fluid leakage preventing agent to form a jelly. Moreover, since the viscosity of the liquid rises, by adjusting the blending amount of these liquids, it is possible to adjust the liquid viscosity according to the jelly-like time and the desired application (application site).
[0046] 前記体液漏出防止剤を体腔に注入して充填する量は、施用部位に応じて適宜設 定できる。また、オイルゼリー状の体液漏出防止剤中に含有されている高吸水性榭 脂の吸水性能にもよる力 水 3, 000mlをゲル状に固め、体腔内から体液の漏出を 防止する吸水能力がある程度であればよぐ一般に 5〜60gが好ましぐより好ましく は 10〜40gである。例えば、遺体の鼻孔から咽喉部に注入する体液漏出防止剤(高 吸水性榭脂 5〜50質量%含有)の充填量は約 8〜40gが好ましぐより好ましくは 10 〜25g程度である。オイルゼリー状の体液漏出防止剤の注入量が多すぎると、注入 器具が大きくなるので取り扱いが難しぐコストアップになる。一方、注入量が少なす ぎると、体液をゲル状に固めることが困難になり、体液が漏出する危険性があるので 好ましくない。 産業上の利用可能性 [0046] The amount of the bodily fluid leakage preventing agent injected and filled into the body cavity can be appropriately set according to the application site. In addition, the water absorption capability of the highly water-absorbent resin contained in the oil jelly-like body fluid leakage prevention agent is solidified into 3,000 ml of water to prevent water leakage from inside the body cavity. In general, 5 to 60 g is preferable, and 10 to 40 g is more preferable. For example, the filling amount of the bodily fluid leakage preventive agent (containing 5 to 50% by mass of superabsorbent fat) injected into the throat from the nostril of the corpse is preferably about 8 to 40 g, more preferably about 10 to 25 g. If the amount of oil jelly-like body fluid leakage prevention agent injected is too large, the injection device will become large, which will increase the cost of handling. On the other hand, if the injection amount is too small, it becomes difficult to solidify the body fluid into a gel, and there is a risk of the body fluid leaking out, which is not preferable. Industrial applicability
本発明の体液漏出防止剤注入用挿入管及びそれを用いた遺体処置装置は、遺体 の体腔、特に口、鼻、耳などの体腔力 の体液漏出を防止するための処置に簡便に 使用できる。  The insertion tube for injecting a bodily fluid leakage preventive agent and the corpse treatment apparatus using the same of the present invention can be easily used for a treatment for preventing body fluid leakage of body cavities, particularly body cavities such as mouth, nose and ear.

Claims

請求の範囲 The scope of the claims
[1] 可撓性の合成樹脂製挿入管であって、先端部が略半球状に閉鎖されて形成され、 且つその側面に複数の開孔部を有する挿入管本体と、挿入管本体の後端部に設け られた体液漏出防止剤の注入器の吐出筒部に接続するための接続部とを有し、該 接続部の挿入管本体側の所定位置に半径方向外側に突出したストツバ部を有して いることを特徴とする遺体用の体液漏出防止剤注入用挿入管。  [1] A flexible synthetic resin insertion tube, the distal end portion of which is formed in a substantially hemispherical shape, and an insertion tube body having a plurality of apertures on its side surface; And a connecting portion for connecting to the discharge cylinder portion of the body fluid leakage preventing agent injector provided at the end portion, and a stagger portion protruding outward in the radial direction at a predetermined position on the insertion tube main body side of the connecting portion. An insertion tube for injecting a bodily fluid leakage preventing agent for a corpse characterized by comprising:
[2] 可撓性の合成樹脂製挿入管であって、先端部が半径方向中心へ向けて外側に湾 曲して延びる複数の舌片により略半球状に形成されていると共に、該複数の舌片の 先端により形成される開口と舌片間のスリットからなる開口部が形成されている挿入 管本体と、挿入管本体の後端部に設けられた体液漏出防止剤の注入器の吐出筒部 に接続するための接続部とを有し、該接続部の挿入管本体側の所定位置に半径方 向外側に突出したストツバ部を有していることを特徴とする遺体用の体液漏出防止剤 注入用挿入管。  [2] A flexible synthetic resin insertion tube, the tip portion of which is formed in a substantially hemispherical shape by a plurality of tongue pieces extending outwardly toward the center in the radial direction. An insertion tube main body in which an opening formed by an opening formed by the tip of the tongue piece and a slit between the tongue pieces is formed, and a discharge cylinder of a body fluid leakage preventing agent injector provided at the rear end portion of the insertion tube main body Body fluid leakage prevention, characterized in that it has a connecting portion for connecting to the connecting portion, and has a stagger portion protruding outward in the radial direction at a predetermined position on the insertion tube main body side of the connecting portion. Agent Injection tube.
[3] 前記挿入管本体は、先端から所定距離離れた位置に湾曲部を有することを特徴と する請求項 1又は 2に記載の体液漏出防止剤注入用挿入管。  [3] The insertion tube for injecting a body fluid leakage preventing agent according to claim 1 or 2, wherein the insertion tube main body has a curved portion at a position separated from the tip by a predetermined distance.
[4] 前記請求項 1乃至 3のいずれか一項に記載の体液漏出防止剤注入用挿入管と;先 端に上記挿入管の接続部に接続するための吐出筒部を有すると共に、後端部に指 を引っ掛けるための半径方向外側に突出した鍔部を有する筒状本体と、該筒状本体 に後端部側から摺動自在に挿入されて!ヽるピストンとを有する体液漏出防止剤用注 入器とを備えて 、ることを特徴とする遺体の処置装置。  [4] The body fluid leakage preventing agent injection insertion tube according to any one of claims 1 to 3; and a discharge tube portion for connecting to a connection portion of the insertion tube at the front end, and a rear end A body fluid leakage preventing agent having a cylindrical main body having a flange protruding outward in the radial direction for hooking a finger on the portion, and a piston which is slidably inserted into the cylindrical main body from the rear end side! A corpse treatment device comprising an infusion device.
[5] 前記体液漏出防止剤用注入器の筒状本体は、先端に吐出筒部を有する円筒状部 材と、その外周に被冠されたカバー部材とからなり、前記鍔部は上記カバー部材に 設けられており、また前記ピストンは上記円筒状部材に摺動自在に挿入されているこ とを特徴とする請求項 4に記載の処置装置。  [5] The cylindrical main body of the injector for body fluid leakage preventing agent includes a cylindrical member having a discharge cylinder part at the tip and a cover member covered on the outer periphery thereof, and the collar part is the cover member. 5. The treatment device according to claim 4, wherein the piston is slidably inserted into the cylindrical member.
PCT/JP2007/056036 2006-03-23 2007-03-23 Implant tube for injecting body fluid leakage-preventing agent for dead body and apparatus for caring dead body by using the same WO2007108540A1 (en)

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Citations (3)

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Publication number Priority date Publication date Assignee Title
JPS6442051U (en) * 1987-09-07 1989-03-14
JP2001212241A (en) * 2000-02-01 2001-08-07 Suugan Kk Catheter
JP2001288002A (en) * 2000-04-03 2001-10-16 Tsukasa:Kk Body liquid leakage preventive gel and method for preventing body liquid from leaking by using the same

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JPWO2004093540A1 (en) * 2003-04-21 2006-07-13 梨沙 西原 Body fluid leakage prevention device

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6442051U (en) * 1987-09-07 1989-03-14
JP2001212241A (en) * 2000-02-01 2001-08-07 Suugan Kk Catheter
JP2001288002A (en) * 2000-04-03 2001-10-16 Tsukasa:Kk Body liquid leakage preventive gel and method for preventing body liquid from leaking by using the same

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