Nasal feeding device
By designing the pulling part in the nasogastric feeding device, and using a flexible cannula and a binding rope to connect the nasogastric tube and the connecting tube, the problem of the connection tube disengagement when the nasogastric tube is pulled externally is solved, and the stability of enteral nutrition infusion is achieved.
Patent Information
- Application Number
- CN202421674942.3
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-07-15
- Publication Date
- 2025-06-20
- Estimated Expiration
- 2034-07-15
AI Technical Summary
Prior art When the nasal intestinal tube is pulled externally, the connecting tube is prone to be released from the inlet end of the nasal intestinal tube, resulting in interruption of enteral nutrition infusion.
A nasofeeding device is designed, including a pulling part, which is connected to the naso-intestinal tube and the connecting tube through a flexible cannula and a binding rope to ensure that the connecting tube does not fall out when the naso-intestinal tube is pulled.
It effectively reduces the possibility of the connecting tube being released from the inlet end of the nasal intestinal tube, and avoids interruption of enteral nutrition infusion.
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Figure CN222998060U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of enteral nutrition infusion, and particularly relates to a nasogastric feeding device. Background Art
[0002] Enteral nutrition infusion is of great significance in the medical field. Currently, during enteral nutrition infusion, the outlet end of the nasointestinal tube is inserted through the nasal cavity, then passes through the pharynx, esophagus, and stomach and is placed into the duodenum or jejunum. Then, a bottle containing enteral nutrition suspension is hung on an infusion stand. One end of an infusion tube is connected to the bottle containing enteral nutrition suspension, and the other end is connected to the inlet end of the nasointestinal tube through a connecting tube. When connecting the infusion tube and the nasointestinal tube, one end of the connecting tube is inserted and connected inside the infusion tube, and the other end is inserted and connected inside the inner cavity of the inlet end of the nasointestinal tube. The enteral nutrition suspension in the bottle can sequentially enter the patient's intestine through the infusion tube, the connecting tube, and the nasointestinal tube. During the process of infusing enteral nutrition suspension into the patient's intestine in this way, when the nasointestinal tube is accidentally pulled by the patient, the connecting tube is likely to slip out from the inner cavity of the inlet end of the nasointestinal tube, easily interrupting enteral nutrition infusion. Content of the Utility Model
[0003] In view of this, the purpose of the utility model is to provide a nasogastric feeding device to solve the technical problem that when the nasointestinal tube is pulled externally, the connecting tube is likely to slip out from the inner cavity of the inlet end of the nasointestinal tube in the prior art.
[0004] The utility model is realized through the following technical solutions:
[0005] A nasogastric feeding device includes a container for containing enteral nutrition suspension, a tube body fixedly connected to the upper end of the container and communicating with the inner cavity of the container, a connecting tube fixedly connected to the lower end of the upper end of the tube body and communicating with the tube body, a nasointestinal tube with its inlet end inserted and connected to the lower end of the connecting tube, and a holding part fixedly connected to the lower end of the inlet end of the nasointestinal tube, and the holding part is used for detachably and fixedly connecting to the connecting tube.
[0006] Furthermore, the connecting tube includes an insertion section for being inserted into the inner cavity of the inlet end of the nasointestinal tube and being matched with the inner cavity of the inlet end of the nasointestinal tube, and a connecting section integrally formed at the upper end of the insertion section and fixedly connected to the lower end of the tube body. A plurality of annular grooves are formed by the outer peripheral surface of the connecting section being recessed inward.
[0007] The holding part includes a flexible sleeve fixedly connected to the outer surface of the inlet end of the nasointestinal tube at the lower end and sleeved on the inlet end of the nasointestinal tube, and a plurality of binding ropes fixedly arranged in the middle on the flexible sleeve. The flexible sleeve is sleeved around a plurality of the annular grooves, and the plurality of binding ropes correspond to the plurality of annular grooves one by one. The binding ropes are used to bind the flexible sleeve in the corresponding annular grooves.
[0008] Further, a first convex ring is formed by outward protrusion on the outer surface of the inlet end of the nasointestinal tube, and the lower end edge of the flexible sleeve is fixedly connected corresponding to the edge of the first convex ring.
[0009] Further, a second convex ring is formed by outward protrusion on the outer peripheral surface of the connecting section. The second convex ring is located above the uppermost annular groove. An external thread is further formed on the outer peripheral surface of the connecting section, and the external thread is located above the second convex ring;
[0010] The connecting tube further includes a threaded sleeve threadedly connected to the external thread;
[0011] The flexible sleeve is made of an airtight material. The lower end of the flexible sleeve is hermetically connected to the outer surface of the inlet end of the nasointestinal tube, and the upper part of the flexible sleeve is sleeved around the second convex ring and the threaded sleeve.
[0012] Further, it further includes a circular rubber band looped on the threaded sleeve. The rubber band is used to bind the flexible sleeve on the part of the connecting section between the second convex ring and the threaded sleeve.
[0013] Further, it further includes a medicine adding tube fixedly connected to the outer peripheral surface of the connecting tube and a valve arranged on the medicine adding tube. The inner cavity of the medicine adding tube communicates with the inner cavity of the connecting section.
[0014] Further, one end of the medicine adding tube is fixedly connected to the connecting section and the other end inclines downward.
[0015] Further, the container includes a circular barrel body with an open upper end and a closed lower end, a cylinder fixedly connected to the lower end surface of the barrel body, a through hole formed on the bottom plate of the barrel body and communicating the inner cavity of the cylinder and the inner cavity of the barrel body, and a soft rubber plug fixedly arranged in the cylinder and matched with the inner cavity of the cylinder; a bottle stopper puncture device is fixedly connected to the upper end of the tube body.
[0016] The beneficial effects of the present utility model are as follows:
[0017] During the process of using a nasogastric feeding device according to the present utility model to infuse enteral nutrition suspension into a patient's intestine, since the lower end of the pulling part is fixedly connected to the inlet end of the nasointestinal tube, the upper end of the pulling part is fixedly connected to the connecting tube, and the pulling part is used to pull the connecting tube towards the nasointestinal tube. When the nasointestinal tube is accidentally pulled by the patient, the pulling part can hold between the inlet end of the nasointestinal tube and the connecting tube, that is, the pulling part can pull the connecting tube towards the nasointestinal tube, which can reduce the possibility of the connecting tube coming out of the inlet end of the nasointestinal tube and reduce the possibility of the interruption of enteral nutrition infusion.
[0018] Other advantages, objectives and features of the present utility model will be described to some extent in the subsequent description, and to some extent, will be obvious to those skilled in the art based on the study of the following text, or can be taught from the practice of the present utility model. The objectives and other advantages of the present utility model can be realized and obtained through the following description. BRIEF DESCRIPTION OF THE DRAWINGS
[0019] Figure 1 is a schematic structural diagram of a nasogastric feeding device according to the present utility model;
[0020] Figure 2 is Figure 1 an enlarged view of a in;
[0021] Figure 3 is a schematic structural diagram of a container in a nasogastric feeding device according to the present utility model;
[0022] Figure 4 is a schematic structural diagram of the nasogastric feeding device according to the present utility model when the container is omitted;
[0023] Figure 5 is Figure 4 an enlarged view of a in;
[0024] Figure 6 is a schematic combined structural diagram of a connecting tube, a medicine adding tube and a valve in a nasogastric feeding device according to the present utility model.
[0025] The meanings of the numbers in the figures are as follows:
[0026] Tube body - 1; Nasointestinal tube - 2; Insertion section - 3; Connection section - 4; Annular groove - 5; Flexible sleeve - 6; Binding rope - 7; First convex ring - 8; Second convex ring - 9; External thread - 10; Thread sleeve - 11; Accommodation groove - 12; Rubber band - 13; Medicine adding tube - 14; Valve - 15; Barrel body - 16; Cylinder - 17; Soft rubber stopper - 18; Bottle stopper puncture device - 19; Screw cap - 20; Ventilation hole - 21; Drip kettle - 22; Speed regulator - 23. DETAILED DESCRIPTION OF THE EMBODIMENTS
[0027] To make the objectives, technical solutions and advantages of the embodiments of the present utility model clearer, the technical solutions in the embodiments of the present utility model will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present utility model. Apparently, the described embodiments are some, but not all, of the embodiments of the present utility model. The components of the embodiments of the present utility model described and illustrated in the accompanying drawings here can be arranged and designed in a variety of different configurations.
[0028] Therefore, the detailed description of the embodiments of the present utility model provided in the accompanying drawings is not intended to limit the scope of the present utility model claimed, but merely represents selected embodiments of the present utility model. All other embodiments obtained by those of ordinary skill in the art based on the embodiments of the present utility model without creative efforts fall within the scope of protection of the present utility model.
[0029] It should be noted that like reference numerals and letters denote like items in the following drawings. Therefore, once an item is defined in one drawing, it does not require further definition and explanation in subsequent drawings.
[0030] In the above description of the present utility model, it should be noted that the orientation or positional relationship indicated by terms such as "one side" and "the other side" is based on the orientation or positional relationship shown in the accompanying drawings, or the orientation or positional relationship in which the product of the present utility model is customarily placed during use. It is only for the convenience of describing the present utility model and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and therefore should not be construed as a limitation of the present utility model. In addition, terms such as "first" and "second" are only used for descriptive distinction and should not be construed as indicating or implying relative importance.
[0031] In addition, terms such as "identical" do not mean that the components are absolutely identical, but there may be slight differences. The term "perpendicular" only means that the positional relationship between components is more perpendicular relative to "parallel", and does not mean that the structure must be completely perpendicular, but may be slightly inclined.
[0032] Please refer to Figures 1-6, the present utility model provides a technical solution: a nasogastric feeding device, including a container, a tube body 1, a connecting tube, a nasointestinal tube 2 and a pulling part. The container is used for containing enteral nutrition suspension. The upper end of the tube body 1 is fixedly connected to the container, and the tube body 1 communicates with the inner cavity of the container. The upper end of the connecting tube is fixedly connected to the lower end of the tube body 1, and the connecting tube communicates with the tube body 1, that is, the inner cavity of the connecting tube communicates with the inner cavity of the tube body 1. The inlet end of the nasointestinal tube 2 is inserted and connected to the lower end of the connecting tube, and the inner cavity of the nasointestinal tube 2 communicates with the inner cavity of the connecting tube. The lower end of the pulling part is fixedly connected to the inlet end of the nasointestinal tube 2, and the pulling part is used for detachably and fixedly connecting to the connecting tube. The nasointestinal tube is a common medical supply on the current market, so its specific structure and usage method will not be elaborated here.
[0033] The initial state of the nasogastric feeding device described in the present utility model is: the upper end of the tube body 1 is fixedly connected to the container, and the upper end of the connecting tube is fixedly connected to the lower end of the tube body 1; the lower end of the pulling part is fixedly connected to the inlet end of the nasointestinal tube 2, the lower end of the connecting tube and the inlet end of the nasointestinal tube 2 are in a separated state, and the upper end of the abutting part is in a separated state from the connecting tube.
[0034] Before using the nasogastric feeding device described in the present utility model to infuse enteral nutrition suspension into the patient's intestine, insert the outlet end of the nasointestinal tube 2 into the patient's nasal cavity, so that the outlet end of the nasointestinal tube 2 passes through the pharynx, esophagus and stomach and enters the duodenum or jejunum, and the inlet end of the nasointestinal tube 2 is located outside the patient's body. Then hang the container filled with enteral nutrition suspension on the infusion stand. Then insert and connect the lower end of the connecting tube to the inlet end of the nasointestinal tube 2, specifically insert the lower end of the connecting tube into the inner cavity of the inlet end of the nasointestinal tube 2. Then fixedly connect the upper end of the pulling part to the connecting tube. Then enteral nutrition suspension can be infused into the patient's intestine, and the enteral nutrition suspension in the container can flow through the tube body 1, the connecting tube and the nasointestinal tube 2 in sequence and enter the patient's intestine.
[0035] During the process of using the nasogastric feeding device described in the present utility model to infuse enteral nutrition suspension into the patient's intestine, since the lower end of the pulling part is fixedly connected to the inlet end of the nasointestinal tube 2 and the upper end of the pulling part is fixedly connected to the connecting tube, the pulling part is used to pull the connecting tube towards the nasointestinal tube. When the nasointestinal tube 2 is accidentally pulled by the patient, the pulling part can be held between the inlet end of the nasointestinal tube 2 and the connecting tube, that is, the pulling part can pull the connecting tube towards the nasointestinal tube 2, which can reduce the possibility of the connecting tube slipping out of the inlet end of the nasointestinal tube 2 and reduce the possibility of the interruption of enteral nutrition infusion.
[0036] In this embodiment, the connecting tube includes an insertion section 3 and a connecting section 4. The insertion section 3 is used to be inserted into the inner cavity of the inlet end of the nasoenteric tube 2. The insertion section 3 is matched with the inner cavity of the inlet end of the nasoenteric tube 2. The lower end of the connecting section 4 is integrally formed with the upper end of the insertion section 3. The upper end of the connecting section 4 is fixedly connected to the lower end of the tube body 1. Specifically, the upper end of the connecting section 4 can be integrally formed with the lower end of the tube body 1. A plurality of annular grooves 5 are formed by inward depression on the outer peripheral surface of the connecting section 4;
[0037] The pulling part includes a flexible sleeve 7 fixedly connected to the outer surface of the inlet end of the nasoenteric tube 2 at the lower end and sleeved on the inlet end of the nasoenteric tube 2, and a plurality of binding ropes 8 fixedly arranged in the middle on the flexible sleeve 7. The flexible sleeve 7 has a circular tubular structure. The flexible sleeve 7 is made of rubber material. The flexible sleeve 7 is sleeved around a plurality of the annular grooves 5. A plurality of the binding ropes 8 correspond to a plurality of the annular grooves 5 one by one. Specifically, after the insertion section 3 is completely inserted into the inner cavity of the inlet end of the nasoenteric tube 2, and when the flexible sleeve 7 is in a state of being straightened but not stretched in its length direction, a plurality of the binding ropes 8 are directly opposite to a plurality of the annular grooves 5 one by one. The binding ropes 8 are used to bind the flexible sleeve 7 in the corresponding annular groove 5, that is, the binding ropes 8 are used to bind the flexible sleeve 7 in the annular groove 5 corresponding to the binding ropes 8.
[0038] Since the insertion section 3 is matched with the inner cavity of the inlet end of the nasoenteric tube 2, when the insertion section 3 is inserted into the inner cavity of the inlet end of the nasoenteric tube 2, the inlet end of the nasoenteric tube 2 can be inserted and connected with the insertion section 3, and the inlet end of the nasoenteric tube 2 can also be inserted and connected with the lower end of the connecting tube. Since the upper end of the connecting section 4 is integrally formed with the lower end of the tube body 1, the connecting section 4 can be stably fixedly connected with the tube body 1, so that the connecting tube is not easily detached from the tube body 1.
[0039] After the insertion section 3 is completely inserted into the inner cavity of the nasoenteric tube 2, a medical staff member holds the nasoenteric tube 2 with one hand and pulls the upper end of the flexible sleeve 7 upward with the other hand to make the flexible sleeve 7 in a straightened state and in a state of not being stretched. At this time, a plurality of the binding ropes 8 are directly opposite to a plurality of the annular grooves 5 one by one. Another medical staff member can tie the two ends of the binding rope 8 together to bind and fix the flexible sleeve 7 in the corresponding annular groove 5. At this time, the flexible sleeve 7 is fixedly connected to the connecting tube, and thus the pulling part can be fixedly connected to the connecting tube. It is more convenient to fixedly connect the pulling part to the connecting tube.
[0040] In this embodiment, a first convex ring 9 is formed by outward protrusion on the outer surface of the inlet end of the nasointestinal tube 2, and the lower edge of the flexible sleeve 7 is fixedly connected corresponding to the edge of the first convex ring 9.
[0041] Since the first convex ring 9 is formed by outward protrusion from the outer surface of the inlet end of the nasointestinal tube 2, that is, the first convex ring 9 is fixed on the outer surface of the inlet end of the nasointestinal tube 2, and the lower edge of the flexible sleeve 7 is fixedly connected corresponding to the edge of the first convex ring 9. With this structure, the flexible sleeve 7 can be fixedly connected to the outer surface of the inlet end of the nasointestinal tube 2.
[0042] In this embodiment, a second convex ring 10 is formed by outward protrusion on the outer peripheral surface of the connecting section 4. The second convex ring 10 is located above the uppermost annular groove 5. An external thread 11 is further formed on the outer peripheral surface of the connecting section 4, and the external thread 11 is located above the second convex ring 10;
[0043] The connecting pipe further includes a threaded sleeve 12 threadedly connected to the external thread 11; an annular receiving groove 13 is formed between the threaded sleeve 12 and the second convex ring 10.
[0044] The flexible sleeve 7 is made of an airtight material. Specifically, the flexible sleeve 7 is made of a rubber material. The lower end of the flexible sleeve 7 is hermetically connected to the outer surface of the inlet end of the nasointestinal tube 2, that is, air cannot enter the flexible sleeve 7 through the connection position between the lower end of the flexible sleeve 7 and the outer surface of the inlet end of the nasointestinal tube 2, and air or liquid cannot be discharged from the flexible sleeve 7 through the connection position between the lower end of the flexible sleeve 7 and the outer surface of the inlet end of the nasointestinal tube 2. The upper part of the flexible sleeve 7 is sleeved around the second convex ring 10 and the threaded sleeve 12.
[0045] After the flexible sleeve 7 is bundled and fixed in the corresponding annular groove 5 by the bundling rope 8, the part of the flexible sleeve 7 corresponding to the receiving groove 13 is pressed into the receiving groove 13. Then, the threaded sleeve 12 is rotated on the connecting section 4 to move the threaded sleeve 12 downward, that is, to move the threaded sleeve 12 toward the second convex ring 10. The part of the flexible sleeve 7 pressed into the receiving groove 13 can be pressed and held by the threaded sleeve 12 against the second convex ring 10. Since the flexible sleeve is made of an airtight material, the lower end of the flexible sleeve is hermetically connected to the outer surface of the inlet end of the nasointestinal tube 2. At this time, the part of the flexible sleeve 7 located below the threaded sleeve 12 can form a sealed space. When the connection between the connecting section 4 and the inlet end of the nasointestinal tube 2 becomes loose, even if enteral nutrition suspension enters the part of the flexible sleeve 7 located below the threaded sleeve 12, the enteral nutrition suspension entering the part of the flexible sleeve 7 located below the threaded sleeve 12 cannot leak out from the part of the flexible sleeve 7 located below the threaded sleeve 12.
[0046] Rotate the threaded sleeve 12 on the connecting section 4 to move the threaded sleeve 12 upward, that is, to move the threaded sleeve 12 away from the second convex ring 10, so as to release the abutment of the threaded sleeve 12 against the part of the flexible sleeve 7 pressed into the receiving groove 13. Then, untie the plurality of bundling ropes 8, and the flexible sleeve 7 can be detached from the connecting tube, that is, the pulling part can be detached from the connecting tube.
[0047] In this embodiment, a nasal feeding device of the present utility model further includes a rubber band 14 looped around the threaded sleeve 12. The rubber band 14 is circular. The rubber band 14 is used to bundle the flexible sleeve on the part of the connecting section 4 located between the second convex ring 10 and the threaded sleeve 12.
[0048] When the rubber band 14 is looped around the threaded sleeve 12, the ring formed by the rubber band 14 is in a state of being expanded by the threaded sleeve 12, that is, the rubber band 14 is in a stretched state. When the rubber band 14 is in an unstretched state, the diameter of the inner hole of the ring formed by the rubber band 14 is smaller than the diameter of the connecting section 4.
[0049] After the flexible sleeve 7 is bundled and fixed in the corresponding annular groove 5 by the bundling rope 8, the rubber band 14 can be moved downward to the position of the receiving groove 13. At this time, the rubber band 14 can press all the part of the flexible sleeve 7 corresponding to the receiving groove 13 into the receiving groove 13 under the action of its own elastic force, and the rubber band 14 can hoop the part of the flexible sleeve 7 corresponding to the receiving groove 13 on the part of the connecting section 4 corresponding to the receiving groove 13. In this way, the part of the flexible sleeve 7 corresponding to the receiving groove 13 can be pressed into the receiving groove 13, which is more convenient when pressing the part of the flexible sleeve 7 corresponding to the receiving groove 13 into the receiving groove 13.
[0050] In this embodiment, a nasal feeding device of the present utility model further includes a medicine adding tube 15 and a valve 16. The medicine adding tube 15 is fixedly connected to the outer peripheral surface of the connecting tube, the valve 16 is arranged on the medicine adding tube 15, and the inner cavity of the medicine adding tube 15 communicates with the inner cavity of the connecting section 4.
[0051] During the process of infusing enteral nutrition suspension into the patient's intestine, the nipple of a syringe containing medicine can also be inserted into the end of the medicine adding tube 15 facing away from the connecting tube, and then the valve 16 is opened. The medicine is injected into the connecting tube through the syringe and the medicine adding tube 15. The medicine entering the connecting tube can enter the patient's intestine through the nasointestinal tube 2, that is, the medicine adding tube 15 can play a role in adding medicine to the nasointestinal tube 2. After the medicine adding is completed, the valve 16 is closed, and then the nipple of the syringe is pulled out of the medicine adding tube 15. It is not necessary to pull out the connecting tube from the inlet end of the nasointestinal tube 2 and then add medicine from the inlet end of the nasointestinal tube 2, which is more convenient when adding medicine to the nasointestinal tube 2.
[0052] In this embodiment, one end of the medicine adding tube 15 is fixedly connected to the connecting section 4, and the other end of the medicine adding tube 15 inclines downward. With this structure, the nozzle at the end of the medicine adding tube 15 facing away from the connecting tube can face obliquely downward, so that dirt is not easily introduced into the medicine adding tube 15.
[0053] In this embodiment, the container includes a barrel 17, a cylinder 18, a through hole, and a soft rubber plug 19. The barrel 19 is a circular barrel. The upper end of the barrel 17 is open, and the lower end of the barrel 17 is closed. The cylinder 18 is fixedly connected to the lower end surface of the barrel 17. The through hole is formed in the bottom plate of the barrel 17, and the through hole communicates the inner cavity of the cylinder 18 and the inner cavity of the barrel 17. The soft rubber plug 19 is fixedly arranged in the cylinder 18, and the soft rubber plug 19 is matched with the inner cavity of the cylinder 18. The upper end of the tube body 1 is fixedly connected with a bottle stopper puncture device 20. The bottle stopper puncture device is a common medical supply component in the market. Specifically, the bottle stopper puncture device is relatively common in existing infusion sets, so the specific structure and usage method thereof will not be elaborated herein.
[0054] When the container holds the enteral nutrition suspension, the enteral nutrition suspension is contained in the barrel 17. When it is necessary to add the enteral nutrition suspension into the barrel 17, the enteral nutrition suspension can be added into the barrel 17 through the opening at the upper end of the barrel 17. By puncturing the soft rubber plug 19 from bottom to top with the bottle stopper puncture device 20, the upper end of the tube body 1 can be fixedly connected to the soft rubber plug 19, and the upper end of the tube body 1 can also be fixedly connected to the container.
[0055] In this embodiment, an external thread is formed on the outer peripheral surface of the upper end of the barrel 17. The container further includes a screw cap 21 threadedly connected to the upper end of the barrel 17. The screw cap 21 is used to close the opening at the upper end of the barrel 17. A ventilation hole 22 vertically penetrating the top plate is formed on the top plate of the screw cap 21. By providing the screw cap 21, the possibility of dirt falling into the barrel 17 can be reduced. By providing the ventilation hole 22, the inner cavity of the barrel 17 can be communicated with the external air. During the process of infusing the enteral nutrition suspension into the patient's intestine, negative pressure in the barrel 17 can be prevented, and the enteral nutrition suspension in the barrel 17 can flow out more smoothly.
[0056] In this embodiment, the nasal feeding device of the present utility model further includes a drip chamber 23 and a flow regulator provided on the tube body 1. The flow rate of the enteral nutrition suspension flowing through the tube body 1 can be adjusted by the flow regulator. The drip rate of the enteral nutrition suspension can be more intuitively observed through the drip chamber 23, and thus the speed of the enteral nutrition suspension flowing in the tube body can be observed. The drip chamber and the flow regulator are common structural components on existing infusion sets, so the specific structure and usage method of the drip chamber and the flow regulator will not be elaborated herein.
[0057] Finally, it should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention rather than to limit them. Although the present invention has been described in detail with reference to the preferred embodiments, those of ordinary skill in the art should understand that the technical solutions of the present invention can be modified or equivalently replaced without departing from the spirit and scope of the technical solutions of the present invention, and they should all be covered within the scope of the claims of the present invention.
Claims
1. A nasogastric feeding device, characterized in that: It includes a container for containing enteral nutrition suspension, a tube body whose upper end is fixedly connected to the container and communicated with the inner cavity of the container, a connecting tube whose upper end is fixedly connected to the lower end of the tube body and communicated with the tube body, a nasointestinal tube whose inlet end is pluggedly connected to the lower end of the connecting tube, and a holding portion whose lower end is fixedly connected to the inlet end of the nasointestinal tube, wherein the holding portion is used for detachably fixed connection to the connecting tube.
2. A nasogastric feeding device according to claim 1, characterized in that: The connecting tube includes an inserting section for inserting into the inner cavity of the inlet end of the nasointestinal tube and matching with the inner cavity of the inlet end of the nasointestinal tube, and a connecting section whose lower end is integrally formed with the upper end of the inserting section and whose upper end is fixedly connected to the lower end of the tube body, and whose outer circumference is inwardly concave to form a plurality of annular grooves; The holding portion includes a flexible sleeve whose lower end is fixedly connected to the outer surface of the inlet end of the nasointestinal tube and is sleeved on the inlet end of the nasointestinal tube, and a plurality of binding ropes fixedly arranged on the flexible sleeve in the middle portion. The flexible sleeve is sleeved around the plurality of annular grooves, and the plurality of binding ropes correspond one-to-one to the plurality of annular grooves. The binding ropes are used to bind the flexible sleeve in the corresponding annular grooves.
3. A nasogastric feeding device according to claim 2, characterized in that: The outer surface of the inlet end of the nasointestinal tube protrudes outward to form a first convex ring, and the lower end edge of the flexible sleeve is fixedly connected to the edge of the first convex ring accordingly.
4. A nasogastric feeding device according to claim 2, characterized in that: The outer circumference of the connecting section is formed with a second convex ring protruding outwards, and the second convex ring is located above the uppermost annular groove. The outer circumference of the connecting section is also formed with an external thread, and the external thread is located above the second convex ring. The connecting pipe also includes a threaded sleeve threadedly connected to the external thread; The flexible sleeve is made of airtight material, the lower end of the flexible sleeve is sealedly connected to the outer surface of the inlet end of the nasointestinal tube, and the upper part of the flexible sleeve is sleeved around the second convex ring and the threaded sleeve.
5. A nasogastric feeding device according to claim 4, characterized in that: It also includes a circular rubber band arranged on the threaded sleeve, and the rubber band is used to bind the flexible sleeve to the part of the connecting section located between the second convex ring and the threaded sleeve.
6. A nasogastric feeding device according to claim 2, characterized in that: It also includes a dosing pipe fixedly connected to the outer peripheral surface of the connecting pipe and a valve arranged on the dosing pipe, and the inner cavity of the dosing pipe is connected to the inner cavity of the connecting section.
7. A nasogastric feeding device according to claim 6, characterized in that: One end of the dosing tube is fixedly connected to the connecting section, and the other end is inclined downward.
8. A nasogastric feeding device according to claim 1, characterized in that: The container includes a circular barrel body with an open upper end and a closed lower end, a cylinder fixedly connected to the lower end surface of the barrel body, a through hole formed on the bottom plate of the barrel body and connecting the inner cavity of the cylinder and the inner cavity of the barrel body, and a soft rubber plug fixed in the cylinder and matched with the inner cavity of the cylinder; a bottle stopper piercer is fixedly connected to the upper end of the tube body.