CN211132000U

CN211132000U - Neck rehabilitation nursing device after tumor operation

Info

Publication number: CN211132000U
Application number: CN201921838908.4U
Authority: CN
Inventors: 李一华
Original assignee: Individual
Current assignee: Individual
Priority date: 2019-10-28
Filing date: 2019-10-28
Publication date: 2020-07-31
Anticipated expiration: 2029-10-28

Abstract

The postoperative head and neck rehabilitation nursing device for the tumor effectively solves the problem that the rehabilitation training effect is poor due to insufficient neck strength of a patient after the head and neck tumor operation; the device comprises a T-shaped base, wherein front and rear ends of the base are respectively provided with front and rear axial arch supports, the two arch supports are coaxial, the upper ends of the two arch supports are respectively provided with a left and right supporting plate which can swing up and down, the upper ends of the two supporting plates are fixedly connected through a baffle, the middle part of the baffle is provided with a half-football-shaped placing sleeve, the left and right ends of the baffle are respectively provided with a vertical connecting plate, the two connecting plates are respectively provided with a left and right through circular groove, a left and right axial worm is arranged below the baffle, the left and right ends of the worm respectively extend out of the circular grooves on the corresponding sides of the worm and are rotatably connected with the circular grooves on the corresponding sides of the; the structure is simple, the operation is convenient, the conception is novel, and the practicability is strong.

Description

Neck rehabilitation nursing device after tumor operation

Technical Field

The utility model relates to a tumour postoperative nursing auxiliary instrument technical field, concretely relates to tumour postoperative neck rehabilitation and nursing ware.

Background

The head and neck tumor comprises three major parts of neck tumor, otorhinolaryngology tumor and oral cavity maxillofacial tumor. Neck tumour belongs to the department of general surgery in comprehensive hospital, more common be exactly the thyroid gland tumour, otolaryngology department tumour is common has laryngeal carcinoma, paranasal sinus cancer etc. and the tumour that neck portion took place, its primary site and pathological type are many, live in whole body tumour first, to this type of disease surgical resection be a common and effectual treatment method, patient's postoperative a period, need carry out certain rehabilitation training to the head and neck, usually for patient oneself rotate the neck or make medical personnel carry out the adjunctie nursing to it, but the effect when some patient's neck strength are not enough to lead to the training is not good.

SUMMERY OF THE UTILITY MODEL

To the above situation, for overcoming the defect of prior art, the utility model aims at providing a tumour postoperative neck rehabilitation and nursing ware, effectual solved head neck tumour postoperative patient because of the neck strength problem that the not good effect of rehabilitation training is not enough leaded to.

The technical scheme of its solution is, the utility model discloses a base of T shape, axial arch support around both ends are equipped with respectively around the base, two arch support are coaxial, but two arch support upper ends are equipped with left right direction and luffing motion's backup pad respectively, but two backup pad upper ends are through baffle fixed connection, the baffle middle part is equipped with half football shape places the cover, both ends are equipped with the connecting plate of upper and lower direction respectively about the baffle, set up the circular recess that link up about respectively on two connecting plates, axial worm about the baffle below is equipped with, both ends are stretched out its circular recess that corresponds the side respectively and are rotated rather than the circular recess that corresponds the side and be connected about the worm, the base upper end is fixed with the worm wheel with worm meshing, both ends twine respectively about the worm.

Compared with the prior art, the beneficial effects of the utility model are that: it is rational in infrastructure, convenient to use sets up stretching strap, baffle, places cover and worm gear mechanism, makes the patient can be according to self demand when using, and manual drive neck carries out the rehabilitation training, and it is not good to have avoided the patient to lead to the training effect inadequately because of neck strength, is equipped with gasbag and pull ring simultaneously, makes this device more comfortable convenient when using, this simple structure, and convenient operation conceives the novelty, and the practicality is strong.

Drawings

Fig. 1 is an isometric view of the present invention.

Fig. 2 is a rear perspective view of the present invention.

Figure 3 is the utility model discloses a partially cut right side and look the axonometric drawing.

Figure 4 is the utility model discloses a partially cut owner and look axonometric drawing.

Detailed Description

The following describes the embodiments of the present invention in further detail with reference to the accompanying drawings.

The novel multifunctional adjustable support is characterized by being given by comprising a T-shaped base 1, front and rear axial arched supports 2 are arranged at the front end and the rear end of the base 1 respectively, the two arched supports 2 are coaxial, supporting plates 3 which can swing up and down in the left and right directions are arranged at the upper ends of the two arched supports 2 respectively, the upper ends of the two supporting plates 3 are fixedly connected through a baffle 4, a half-football-shaped placing sleeve 5 is arranged at the middle part of the baffle 4, connecting plates 6 in the up and down directions are arranged at the left end and the right end of the baffle 4 respectively, round grooves 7 which are communicated in the left and right directions are formed in the two connecting plates 6 respectively, a worm 8 in the left and right axial directions is arranged below the baffle 4, the round grooves 7 of the corresponding sides of the worm 8 are extended out at the left and right ends of the worm 8 respectively and are.

In order to facilitate the swinging of the baffle 4, the two support plates 3 are respectively provided with arc-shaped sliding grooves 10 which are through from front to back and have downward openings, and the two arc-shaped supports 2 are in sliding connection with the arc-shaped sliding grooves 10 on the corresponding sides.

In order to limit the left-right sliding of the worm 8, limiting rings 12 are coaxially fixed on the left side and the right side of the worm 8 respectively, and the two limiting rings 12 are positioned between the two connecting plates 6 and are in contact with the connecting plates 6 on the corresponding sides.

In order to increase the comfort of the patient, the placing sleeve 5 is internally provided with an air bag 13 attached to the inner side wall of the placing sleeve, the rear end of the air bag 13 is provided with a connecting pipe 14, and the upper end of the connecting pipe 14 is provided with an air stop plug 15.

In order to pull the pull belt 9 conveniently, the left end and the right end of the baffle 4 are respectively provided with a fixing sleeve 16, and the free end of the pull belt 9 penetrates through the fixing sleeves 16 and is provided with a pull ring 17.

In order to prevent the device from swinging left and right due to self gravity, the outer edge surfaces of the left side and the right side of the arched support 2 at the front side are respectively provided with a front through slot and a rear through slot, the two slots are respectively connected with the insertion blocks 18 in a detachable manner, and the upper end surfaces of the two insertion blocks 18 can be in contact with the lower end surface of the support plate 3.

For ease of patient use, the anterior stent arch 2 has an outer diameter that is smaller than the posterior stent arch 2.

When the utility model is used, the right drawstring 9 is arranged to be wound on the worm 8, the left drawstring 9 is not completely wound on the worm 8, the air bag 13 is not inflated, the two insertion blocks 18 are inserted into the corresponding side slots, the upper ends of the two insertion blocks 18 are contacted with the support plate 3, the device is placed on a bed, a patient puts the head into the placing sleeve 5, the air stop plug 15 is pulled out upwards, the air bag 13 is inflated through the connecting pipe 14 according to the requirement of the patient, the air stop plug 15 is sleeved on the upper end of the connecting pipe 14 after being inflated, and the head of the patient is fixed at the moment;

after the head of a patient is fixed, the insertion blocks 18 are pushed forwards or backwards, the two insertion blocks 18 are moved out of the slots, the limitation on the supporting plate 3 is removed, at the moment, the patient pulls the right pull belt 9, the right pull belt 9 drives the worm 8 to rotate clockwise, the left end of the worm 8 swings downwards along the axis of the worm wheel 11 under the meshing of the worm wheel 11 and the worm 8, due to the limitation of the limiting ring 12, the worm 8 drives the baffle plate 4 to swing downwards along the arched support 2 through the connecting plate 6, the baffle plate 4 drives the head of the patient to swing leftwards, the left pull belt 9 is wound on the worm 8 along with the clockwise rotation of the worm 8, and when the head of the patient swings to a proper position or the rear end of the left pull ring 17 contacts with the fixing;

when the pull belt 9 on the right side is stopped to be pulled, the patient pulls the pull belt 9 on the left side, the pull belt 9 on the left side drives the worm 8 to rotate anticlockwise, the right end 8 of the worm swings upwards along the axis of the worm wheel 11 under the meshing of the worm wheel 11 and the worm 8, due to the limitation of the limiting ring 12, the worm 8 drives the baffle 4 to swing rightwards along the arch-shaped support 2 through the connecting plate 6, the baffle 4 drives the head of the patient to swing rightwards, the pull belt 9 on the right side is wound on the worm 8 along with the anticlockwise rotation of the worm 8, when the head of the patient swings to a proper position or the rear end of the pull ring 17 on the right side is contacted with the fixed sleeve 16;

after the patient does not need to train, the air stop plug 15 is pulled out to discharge the gas in the air bag 13, the head of the patient is separated from the placing sleeve 5, the drawstring 9 is pulled to enable the baffle 4 of the device to recover to the initial position, the inserting block 18 is inserted into the inserting groove, the upper end of the inserting block 18 is in contact with the supporting plate 3, and the position of the baffle 4 is fixed.

Claims

1. A rehabilitation nursing device for head and neck after tumor operation comprises a T-shaped base (1) and is characterized in that front and back ends of the base (1) are respectively provided with front and back axial arched supports (2), the two arched supports (2) are coaxial, the upper ends of the two arched supports (2) are respectively provided with a support plate (3) which can swing up and down in the left-right direction, the upper ends of the two support plates (3) are fixedly connected through a baffle plate (4), the middle part of the baffle plate (4) is provided with a half-football-shaped placing sleeve (5), the left and right ends of the baffle plate (4) are respectively provided with a vertical connecting plate (6), the two connecting plates (6) are respectively provided with a left-right through circular groove (7), a left-right axial worm (8) is arranged below the baffle plate (4), the left and right ends of the worm (8) respectively extend out of the circular groove (, a worm wheel (11) meshed with the worm (8) is fixed at the upper end of the base (1), and pull belts (9) are respectively wound at the left end and the right end of the worm (8).

2. The head and neck rehabilitation nursing device after tumor operation according to claim 1, wherein the two supporting plates (3) are respectively provided with arc chutes (10) which are through from front to back and open downwards, and the two arc brackets (2) are slidably connected with the arc chutes (10) on the corresponding sides.

3. The head and neck rehabilitation nursing device after tumor operation as claimed in claim 1, wherein the worm (8) is coaxially fixed with two limit rings (12) on the left and right sides respectively, and the two limit rings (12) are located between the two connecting plates (6) and are in contact with the connecting plates (6) on the corresponding sides.

4. The head and neck rehabilitation and nursing device after tumor operation as claimed in claim 1, wherein the placing sleeve (5) is internally provided with an air bag (13) attached to the inner side wall thereof, the rear end of the air bag (13) is provided with a connecting pipe (14), and the upper end of the connecting pipe (14) is provided with an air stop plug (15).

5. The head and neck rehabilitation nursing device after tumor operation as claimed in claim 1, wherein the baffle (4) is provided with fixing sleeves (16) at the left and right ends respectively, and the free end of the pull belt (9) passes through the fixing sleeves (16) and is provided with a pull ring (17).

6. The head and neck rehabilitation nursing device after tumor operation as claimed in claim 1, wherein the outer edge surfaces of the left and right sides of the arched bracket (2) at the front side are respectively provided with slots which are through from front to back, the two slots are respectively connected with the insertion blocks (18) in a detachable manner, and the upper end surfaces of the two insertion blocks (18) can be in contact with the lower end surface of the support plate (3).

7. The head and neck rehabilitation care device after tumor operation as claimed in claim 1, characterized in that the external diameter of the arched stent (2) on the anterior side is smaller than the external diameter of the arched stent (2) on the posterior side.