PCI (Peripheral Component Interconnect) postoperative rehabilitation support

Abstract

The utility model relates to the technical field of PCI (Peripheral Component Interconnect) postoperative rehabilitation supports, and discloses a PCI postoperative rehabilitation support, which comprises a main body component, an auxiliary body component and an auxiliary body component, the adjusting assembly is arranged in the supporting seat and comprises a moving part and a limiting part, the moving part is arranged in the supporting seat, and the limiting part is located on one side of the moving part. The wrist support has the advantages that by arranging the adjusting assembly, multi-angle adjustment can be conducted according to the position of the wrist of a patient, the support can meet different rehabilitation requirements, the comfort degree of the patient in the rehabilitation process is improved, the situation that the position of a traditional support is single is avoided, and the practicability and applicability of the support are enhanced.

Description

Technical Field

[0001] This utility model relates to the field of PCI postoperative rehabilitation stent technology, and in particular to a PCI postoperative rehabilitation stent. Background Technology

[0002] PCI, also known as percutaneous coronary intervention, is a treatment method that uses cardiac catheterization to open narrowed or even blocked coronary arteries, thereby improving myocardial blood perfusion. After PCI, it is necessary to restrict the patient's wrist movement (without affecting finger and elbow movement), but the restriction effect is poor. Elevating the hand to reduce swelling is often done clinically with soft pillows or cotton pads to elevate the affected limb, but these items have poor fixation, and the patient's arm often slips off. Furthermore, because the stent cannot be moved, its position is relatively fixed, making it impossible to adjust it at multiple angles according to the patient's wrist position, which is inconvenient and cannot meet the patient's comfort during the recovery process, further reducing the effectiveness of the stent. Utility Model Content

[0003] The purpose of this section is to outline some aspects of embodiments of the present invention and to briefly describe some preferred embodiments. Simplifications or omissions may be made in this section, as well as in the abstract and title of this application, to avoid obscuring the purpose of these documents; however, such simplifications or omissions should not be construed as limiting the scope of the present invention.

[0004] In view of the problems existing in the above and / or existing PCI postoperative rehabilitation stents, this utility model is proposed.

[0005] Therefore, the problem that this utility model aims to solve is that because the support cannot be moved, its position is relatively limited, making it impossible to adjust it at multiple angles according to the position of the patient's wrist. This makes it inconvenient to meet the patient's comfort during the rehabilitation process and further reduces the effectiveness of the support.

[0006] To solve the above-mentioned technical problems, this utility model provides the following technical solution: a postoperative rehabilitation support, comprising a main body component, including a base and a support base, wherein the support base is fixed to the top of the base; and,

[0007] An adjustment component, disposed within the support base, includes a movable component and a limiting component. The movable component is disposed within the support base, and the limiting component is located on one side of the movable component.

[0008] In a preferred embodiment of the postoperative rehabilitation support of this utility model, the movable component includes a push plate and a sliding block. The push plate slides within the support base, and the sliding block is fixed to the bottom of the push plate. A sliding groove is provided within the support base, and the sliding block slides within the sliding groove.

[0009] As a preferred embodiment of the postoperative rehabilitation bracket of this utility model, the movable component further includes a support plate and a movable rod. The support plate is fixed to the surface of the support base, and a guide groove is provided on the surface of the support plate. The movable rod slides in the guide groove.

[0010] In a preferred embodiment of the postoperative rehabilitation support of the present invention, the movable component further includes a partition block and a support rod, wherein the partition block is fixed to the surface of the movable rod and the support rod is rotatably connected to the surface of the movable rod.

[0011] In a preferred embodiment of the postoperative rehabilitation support described in this utility model, the movable component further includes a roller and a rack, the roller being rotatably connected to the surface of the movable rod, and the rack being fixed to one side of the push plate.

[0012] As a preferred embodiment of the postoperative rehabilitation support described in this utility model, the movable component further includes a connecting block and an arm sleeve. The connecting block is fixed to the top of the base, one end of the arm sleeve is rotatably connected to one side of the connecting block, and the other end of the arm sleeve is fixed to the top of the support rod.

[0013] As a preferred embodiment of the postoperative rehabilitation support of this utility model, the movable component further includes a rotating rod and a gear. The rotating rod is rotatably connected to the support plate, and the gear is fixed to the surface of the rotating rod. The gear can mesh with the rack.

[0014] In a preferred embodiment of the postoperative rehabilitation support described in this utility model, the movable component further includes a handle, which is fixed to one side of the rotating rod.

[0015] As a preferred embodiment of the postoperative rehabilitation bracket of this utility model, the limiting member includes a positioning block and a limiting block. The positioning block is fixed to one side of the support plate, and the limiting block slides within the positioning block. A positioning groove is provided on the surface of the rotating rod, and the limiting block is snapped and fixed within the positioning groove.

[0016] As a preferred embodiment of the postoperative rehabilitation bracket of this utility model, the limiting member further includes a compression spring and a handle. One end of the compression spring is fixed inside the positioning block, the other end of the compression spring is fixed to one side of the limiting block, and the handle is fixed to one side of the limiting block.

[0017] The beneficial effects of this utility model are as follows: by adjusting the settings of the components, the bracket can be adjusted at multiple angles according to the position of the patient's wrist, so that the bracket can adapt to different rehabilitation needs, thereby improving the patient's comfort during the rehabilitation process, thus avoiding the single position of the traditional bracket, thereby enhancing the practicality and applicability of the bracket. Attached Figure Description

[0018] To more clearly illustrate the technical solutions of the embodiments of this utility model, the drawings used in the description of the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this utility model. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort. Among them:

[0019] Figure 1 This is a structural diagram of a post-PCI rehabilitation stent.

[0020] Figure 2 This is a cross-sectional view of the arm sleeve of a post-PCI rehabilitation stent.

[0021] Figure 3 For PCI postoperative rehabilitation stents Figure 2 Enlarged structural diagram at point A in the diagram.

[0022] Figure 4 For PCI postoperative rehabilitation stents Figure 2 Enlarged structural diagram at point B in the image.

[0023] Figure 5 Another structural view of the PCI postoperative rehabilitation stent.

[0024] The diagram labels are as follows: 100, main component; 101, base; 102, support base; 200, adjustment component; 201, moving part; 201a, push plate; 201b, sliding block; V, sliding groove; 201c, support plate; 201d, moving rod; T, guide groove; 201e, partition block; 201f, support rod; 201g, roller; 201h, rack; 201i, connecting block; 201j, arm sleeve; 201k, rotating rod; 201l, gear; 201m, throttle; 202, limiting component; 202a, positioning block; 202b, limiting block; Y, positioning groove; 202c, compression spring; 202d, grip. Detailed Implementation

[0025] To make the above-mentioned objectives, features and advantages of this utility model more apparent and understandable, the specific embodiments of this utility model will be described in detail below with reference to the accompanying drawings.

[0026] Many specific details are set forth in the following description in order to provide a full understanding of the present invention. However, the present invention may also be implemented in other ways different from those described herein. Those skilled in the art can make similar extensions without departing from the spirit of the present invention. Therefore, the present invention is not limited to the specific embodiments disclosed below.

[0027] Secondly, the term "an embodiment" or "embodiment" as used herein refers to a specific feature, structure, or characteristic that may be included in at least one implementation of the present invention. The phrase "in one embodiment" appearing in different places in this specification does not necessarily refer to the same embodiment, nor is it a single or selective embodiment that excludes other embodiments.

[0028] Example 1

[0029] Reference Figures 1-3 and Figure 5 This is the first embodiment of the present invention, which provides a post-PCI rehabilitation stent. The post-PCI rehabilitation stent includes a main body component 100 and an adjustment component 200. Through the cooperation of the two, the stent can adapt to different rehabilitation needs, thereby improving the patient's comfort during the rehabilitation process and enhancing the practicality and applicability of the stent.

[0030] Specifically, the main component 100 includes a base 101 and a support 102, with the support 102 fixed to the top of the base 101.

[0031] The base 101 is used to ensure the position of the support 102, thereby ensuring that the support 102 will not become loose. The support 102 is used to ensure that the entire device can be used normally without loosening or other problems. The base 101 and the support 102 are existing technologies and will not be described in detail here.

[0032] Adjustment component 200 is disposed within support base 102 and includes movable component 201 and limiting component 202. Movable component 201 is disposed within support base 102 and limiting component 202 is located on one side of movable component 201.

[0033] The movable part 201 is used to ensure that the adjustment component 200 can be used normally and will not have problems such as displacement or loosening. The limiting part 202 is used to ensure the position of the movable part 201, thereby ensuring that the movable part 201 will not move on its own.

[0034] Specifically, the moving part 201 includes a push plate 201a and a sliding block 201b. The push plate 201a slides within the support base 102, and the sliding block 201b is fixed to the bottom of the push plate 201a. A sliding groove V is provided in the support base 102, and the sliding block 201b slides within the sliding groove V.

[0035] The push plate 201a is used to push the movable part 201 to move, thereby ensuring that the movable part 201 can be used normally and can be adjusted at multiple angles according to the position of the patient's wrist. The sliding block 201b slides in the sliding groove V in the support seat 102, thereby ensuring that the push plate 201a will not deviate when it moves, so that the sliding block 201b can limit the position of the push plate 201a.

[0036] Specifically, the movable component 201 also includes a support plate 201c and a movable rod 201d. The support plate 201c is fixed to the surface of the support base 102, and a guide groove T is provided on the surface of the support plate 201c. The movable rod 201d slides in the guide groove T.

[0037] The support plate 201c uses the guide groove T to limit the position of the moving rod 201d, thereby ensuring that the moving rod 201d can move with the guide groove T, so that the height of the moving part 201 can change, thus avoiding the problem of the traditional bracket having a single position.

[0038] Specifically, the movable component 201 also includes a partition block 201e and a support rod 201f. The partition block 201e is fixed to the surface of the movable rod 201d, and the support rod 201f is rotatably connected to the surface of the movable rod 201d.

[0039] The baffle block 201e is used to limit the position of the support rod 201f, thereby ensuring that the support rod 201f will not deviate when it rotates, and thus ensuring that the support rod 201f can cooperate with the moving rod 201d when the moving rod 201d moves, so that the height of the moving part 201 can change.

[0040] Example 2

[0041] Reference Figure 1 , Figure 2 , Figure 4 and Figure 5 This is the second embodiment of the present invention, which is based on the previous embodiment.

[0042] Specifically, the moving part 201 also includes a roller 201g and a rack 201h. The roller 201g is rotatably connected to the surface of the moving rod 201d, and the rack 201h is fixed to one side of the push plate 201a.

[0043] The roller 201g can contact the push plate 201a, so that when the push plate 201a moves, the roller 201g can push the moving rod 201d to move, so that the moving rod 201d can drive the moving part 201 to move upward. The rack 201h is used to push the push plate 201a to move, so that the push plate 201a can ensure the normal operation of the moving part 201.

[0044] Specifically, the movable component 201 also includes a connecting block 201i and an arm sleeve 201j. The connecting block 201i is fixed to the top of the base 101, one end of the arm sleeve 201j is rotatably connected to one side of the connecting block 201i, and the other end of the arm sleeve 201j is fixed to the top of the support rod 201f.

[0045] The connecting block 201i is used to support the position of the arm sleeve 201j, thereby ensuring that the arm sleeve 201j will not shift when it rotates. The arm sleeve 201j is used to fix and support the patient's arm, keeping it in a comfortable position that is conducive to rehabilitation.

[0046] Specifically, the moving part 201 also includes a rotating rod 201k and a gear 201l. The rotating rod 201k is rotatably connected to the support plate 201c, and the gear 201l is fixed to the surface of the rotating rod 201k. The gear 201l can mesh with the rack 201h.

[0047] The rotating rod 201k drives the gear 201l to rotate. Because the gear 201l and rack 201h mesh with each other, the gear 201l can push the push plate 201a to move. This allows the moving part 201 to be adjusted at multiple angles according to the patient's wrist position, enabling the support to adapt to different rehabilitation needs and thus improving the patient's comfort during rehabilitation.

[0048] Example 3

[0049] Reference Figure 4 This is the third embodiment of the present invention, which is based on the first two embodiments.

[0050] Specifically, the movable component 201 also includes a throttle 201m, which is fixed to one side of the rotating rod 201k.

[0051] The throttle 201m is used to drive the rotating rod 201k to rotate, so that the rotating rod 201k can drive the gear 201l to rotate, thereby ensuring that the moving part 201 can operate normally.

[0052] Specifically, the limiting component 202 includes a positioning block 202a and a limiting block 202b. The positioning block 202a is fixed to one side of the support plate 201c, and the limiting block 202b slides inside the positioning block 202a. The rotating rod 201k has a positioning groove Y on its surface, and the limiting block 202b is snapped and fixed inside the positioning groove Y.

[0053] The positioning block 202a is used to support the position of the limiting block 202b, thereby ensuring that the limiting block 202b can be engaged and fixed with the positioning groove Y on the surface of the rotating rod 201k, thereby ensuring that the rotating rod 201k will not rotate on its own.

[0054] Specifically, the limiting component 202 also includes a compression spring 202c and a handle 202d. One end of the compression spring 202c is fixed inside the positioning block 202a, and the other end of the compression spring 202c is fixed to one side of the limiting block 202b. The handle 202d is fixed to one side of the limiting block 202b.

[0055] Currently, the compression spring 202c is in a compressed state. The compression spring 202c is used to push the limit block 202b to move, thereby ensuring that the limit block 202b can restrict the position of the rotating rod 201k. The handle 202d is used to pull the limit block 202b to move, thereby allowing the limit block 202b to release the restriction on the rotating rod 201k.

[0056] When using this device, after PCI surgery when arm support is needed, first place the arm into the arm sleeve 201j. Then, the staff pulls the handle 202d, causing the handle 202d to move the limiting block 202b upwards. This releases the limiting block 202b from its restriction on the rotating rod 201k. Next, the handle 201m is rotated, causing it to drive the gear 201l via the rotating rod 201k. This allows the gear 201l to simultaneously push the rack 201h, thus enabling the rack 201h to move. The push plate 201a is moved, and when the push plate 201a moves, it can come into contact with the roller 201g, so that the roller 201g can push the moving rod 201d to move, which in turn can drive the support rod 201f to move. The support rod 201f can then drive the arm sleeve 201j to rise and fall, allowing for multi-angle adjustment according to the position of the patient's wrist. This enables the support to adapt to different rehabilitation needs, thereby improving the patient's comfort during the rehabilitation process.

[0057] It should be noted that the above embodiments are only used to illustrate the technical solution of this utility model and are not intended to limit it. Although this utility model has been described in detail with reference to preferred embodiments, those skilled in the art should understand that modifications or equivalent substitutions can be made to the technical solution of this utility model without departing from the spirit and scope of the technical solution of this utility model, and all such modifications or substitutions should be covered within the scope of the claims of this utility model.

Claims

1. A post-PCI rehabilitation stent, characterized in that: include, The main component (100) includes a base (101) and a support (102), the support (102) being fixed to the top of the base (101); and, An adjustment component (200) is disposed within the support base (102) and includes a movable component (201) and a limiting component (202). The movable component (201) is disposed within the support base (102), and the limiting component (202) is located on one side of the movable component (201).

2. The PCI postoperative rehabilitation stent as described in claim 1, characterized in that: The movable component (201) includes a push plate (201a) and a sliding block (201b). The push plate (201a) slides within the support base (102), and the sliding block (201b) is fixed to the bottom of the push plate (201a). A sliding groove (V) is provided in the support base (102), and the sliding block (201b) slides within the sliding groove (V).

3. The PCI postoperative rehabilitation stent as described in claim 2, characterized in that: The movable component (201) further includes a support plate (201c) and a movable rod (201d). The support plate (201c) is fixed to the surface of the support base (102). A guide groove (T) is provided on the surface of the support plate (201c), and the movable rod (201d) slides in the guide groove (T).

4. The PCI postoperative rehabilitation stent as described in claim 3, characterized in that: The movable component (201) further includes a partition block (201e) and a support rod (201f). The partition block (201e) is fixed to the surface of the movable rod (201d), and the support rod (201f) is rotatably connected to the surface of the movable rod (201d).

5. The PCI postoperative rehabilitation stent as described in claim 4, characterized in that: The moving part (201) further includes a roller (201g) and a rack (201h), the roller (201g) being rotatably connected to the surface of the moving rod (201d), and the rack (201h) being fixed to one side of the push plate (201a).

6. The PCI postoperative rehabilitation stent as described in claim 5, characterized in that: The movable component (201) also includes a connecting block (201i) and an arm sleeve (201j). The connecting block (201i) is fixed to the top of the base (101). One end of the arm sleeve (201j) is rotatably connected to one side of the connecting block (201i), and the other end of the arm sleeve (201j) is fixed to the top of the support rod (201f).

7. The PCI postoperative rehabilitation stent as described in claim 6, characterized in that: The moving part (201) further includes a rotating rod (201k) and a gear (201l). The rotating rod (201k) is rotatably connected to the support plate (201c), and the gear (201l) is fixed to the surface of the rotating rod (201k). The gear (201l) can mesh with the rack (201h).

8. The PCI postoperative rehabilitation stent as described in claim 7, characterized in that: The movable component (201) also includes a throttle (201m), which is fixed to one side of the rotating rod (201k).

9. The PCI postoperative rehabilitation stent as described in claim 7 or 8, characterized in that: The limiting component (202) includes a positioning block (202a) and a limiting block (202b). The positioning block (202a) is fixed to one side of the support plate (201c), and the limiting block (202b) slides within the positioning block (202a). A positioning groove (Y) is provided on the surface of the rotating rod (201k), and the limiting block (202b) is snapped and fixed within the positioning groove (Y).

10. The PCI postoperative rehabilitation stent as described in claim 9, characterized in that: The limiting member (202) also includes a compression spring (202c) and a grip (202d). One end of the compression spring (202c) is fixed inside the positioning block (202a), and the other end of the compression spring (202c) is fixed to one side of the limiting block (202b). The grip (202d) is fixed to one side of the limiting block (202b).

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